US20110312974A1 - Heteroaryl antagonists of prostaglandin d2 receptors - Google Patents

Heteroaryl antagonists of prostaglandin d2 receptors Download PDF

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Publication number
US20110312974A1
US20110312974A1 US13/121,398 US200913121398A US2011312974A1 US 20110312974 A1 US20110312974 A1 US 20110312974A1 US 200913121398 A US200913121398 A US 200913121398A US 2011312974 A1 US2011312974 A1 US 2011312974A1
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Prior art keywords
substituted
unsubstituted
alkyl
compound
phenyl
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US13/121,398
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Inventor
John Howard Hutchinson
Brian Andrew Stearns
Nicholas Simone Stock
Yen Pham Truong
Jeffrey Roger ROPPE
Deborah VOLKOTS
Jill Melissa Scott
Timothy Andrew Parr
Bowei Wang
Thomas Jon SEIDERS
Ryan Clark
Heather Renee Coate
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Panmira Pharmaceuticals LLC
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Amira Pharmaceuticals Inc
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Priority to US13/121,398 priority Critical patent/US20110312974A1/en
Assigned to AMIRA PHARMACEUTICALS, INC. reassignment AMIRA PHARMACEUTICALS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CLARK, RYAN, COATE, HEATHER RENEE, PARR, TIMOTHY, ROPPE, JEFFREY ROGER, STOCK, NICHOLAS SIMON, VOLKOTS, DEBORAH, SEIDERS, THOMAS JON, STEARNS, BRIAN ANDREWS, HUTCHINSON, JOHN HOWARD, SCOTT, JILL MELISSA, TRUONG, YEN PHAM, WANG, BOWEI
Assigned to PANMIRA PHARMACEUTICALS, LLC reassignment PANMIRA PHARMACEUTICALS, LLC ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: AMIRA PHARMACEUTICALS, INC.
Publication of US20110312974A1 publication Critical patent/US20110312974A1/en
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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Definitions

  • Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or diagnose diseases, disorders or conditions associated with prostaglandin D 2 .
  • Prostaglandins are acidic lipids derived from the metabolism of arachidonic acid by the action of cyclooxygenase enzymes and downstream synthases. Prostaglandins have a diverse range of activities and have a well recognized role in pain and inflammation.
  • Prostaglandin D 2 (PGD 2 ) is an acidic lipid mediator derived from the metabolism of arachidonic acid by cyclooxygenases and PGD 2 synthases.
  • PGD 2 is produced by mast cells, macrophages and Th2 lymphocytes in response to local tissue damage as well as allergic inflammation in diseases such as asthma, rhinitis, and atopic dermatitis. Exogenous PGD 2 applied to bronchial airways elucidates many characteristics of an asthmatic response suggesting that PGD 2 plays an important pro-inflammatory role in allergic diseases.
  • PGD 2 binds to a number of receptors, which include the thromboxane-type prostanoid (TP) receptor, PGD 2 receptor (DP, also known as DP 1 ) and chemoattractant receptor-homologous molecule expressed on Th2 cells (CRTH2; also known as DP 2 ).
  • TP thromboxane-type prostanoid
  • DP PGD 2 receptor
  • CRTH2 chemoattractant receptor-homologous molecule expressed on Th2 cells
  • the methods, compounds, pharmaceutical compositions, and medicaments described herein comprise antagonists of PGD 2 receptors.
  • the methods, compounds, pharmaceutical compositions, and medicaments described herein comprise antagonists of DP 2
  • PGD 2 -dependent conditions or diseases including, but not limited to, asthma, rhinitis, chronic obstructive pulmonary disease, pulmonary hypertension, interstitial lung fibrosis, arthritis, allergy, psoriasis, inflammatory bowel disease, adult respiratory distress syndrome, myocardial infarction, aneurysm, stroke, cancer, endotoxic shock, proliferative disorders and inflammatory conditions.
  • PGD 2 -dependent conditions or diseases include those wherein an absolute or relative excess of PGD 2 is present and/or observed.
  • substituents can be selected from among from a subset of the listed alternatives.
  • Q is —C( ⁇ O)-Q 1 ;
  • Q 1 is OR B ;
  • R B is H or C 1 -C 6 alkyl.
  • Q is —C( ⁇ O)—OH.
  • Q 1 is —OH.
  • R B is H or C 1 -C 4 alkyl.
  • R B is H.
  • each R 1 is independently selected from H, F, and —CH 3 . In some other embodiments, each R 1 is H.
  • ring A is a substituted or unsubstituted 5-membered or 6-membered heteroaryl, wherein if ring A is substituted, then ring A is substituted with 1 to 4 R A .
  • ring A is a substituted or unsubstituted 5-membered heteroaryl or a substituted or unsubstituted 6-membered heteroaryl, wherein ring A includes 0 or 1 O atoms, 0 or 1 S atoms, 0-3 N atoms, and at least 2 carbon atoms, wherein if ring A is substituted, then ring A is substituted with 1 to 3 R A .
  • ring A is a substituted or unsubstituted 5-membered or 6-membered heteroaryl selected from among furanyl, thienyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, 1,3,4-thiadiazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, and triazinyl, wherein if ring A is substituted then ring A is substituted with 1 to 3 R A .
  • ring A is a substituted or unsubstituted 5-membered heteroaryl, wherein ring A includes 0 or 1 O atoms, 0 or 1 S atoms, 1-3 N atoms, and at least 2 carbon atoms, wherein if ring A is substituted then ring A is substituted with 1 to 3 R A .
  • ring A is a substituted or unsubstituted 5-membered heteroaryl selected from among pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, 1,3,4-thiadiazolyl, wherein if ring A is substituted then ring A is substituted with 1 to 3 R A .
  • ring A is a substituted or unsubstituted 6-membered heteroaryl containing 1-3 N atoms in the ring, wherein if ring A is substituted then ring A is substituted with 1 to 3 R A .
  • ring A is a substituted or unsubstituted 6-membered heteroaryl selected from among pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, and triazinyl, wherein if ring A is substituted then ring A is substituted with 1 or 2 R A .
  • each R A is independently selected from H, halogen, —CN, —OH, —OR 12 , —S( ⁇ O) 2 R 12 , —C( ⁇ O)R 12 , —CO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)R 12 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, and C 1 -C 6 heteroalkyl; each of R 5 , R 6 , R 7 , and R 8 is independently selected from H, halogen, —CN, —NO 2 , —OH, —OR 12 , —SR 12 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —N(R 13 )S( ⁇ O) 2 R 12 ,
  • each of R 5 , R 7 , and R 8 is independently selected from H, halogen, —CN, —OH, —OR 12 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, and C 1 -C 6 heteroalkyl.
  • each of R 5 , R 7 , and R 8 is independently selected from H, F, Cl, Br, I, —CN, —OH, —OCH 3 , —OCH 2 CH 3 , —CH 3 , —CH 3 CH 3 , —CF 3 , CHF 2 , CH 2 F, and —OCF 3 .
  • At least one of R 5 , R 7 , and R 8 is H.
  • At least two of R 5 , R 7 , and R 8 is H.
  • each of R 5 , R 7 , and R 8 is H.
  • the compound of Formula (I) has the structure of Formula (II):
  • R B is H; each R 1 is independently selected from H and —CH 3 .
  • ring A is a substituted or unsubstituted 6-membered heteroaryl selected from among pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, and triazinyl, wherein if ring A is substituted then ring A is substituted with 1 or 2 R A .
  • ring A is a substituted or unsubstituted pyridinyl, wherein if ring A is substituted then ring A is substituted with 1 or 2 R A .
  • ring A is a substituted or unsubstituted pyridinyl, wherein if ring A is substituted then ring A is substituted with 1 or 2 R A ; each R A is independently H, halogen, —CN, —OH, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, or C 1 -C 4 alkoxy; R 10 is —C( ⁇ O)R 14 , —C( ⁇ O)OR 15 , or —C( ⁇ O)N(R 16 ) 2 ; R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 4 alkyl
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 4 alkyl-(substituted or unsubstituted C 3 -C 10 cycloalkyl), —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 4 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 10 is —C( ⁇ O)R 14 ;
  • R 14 is C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 4 alkyl-(C 3 -C 6 cycloalkyl), —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 4 alkyl-(substituted or unsubstituted monocyclic heteroaryl); or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkyl; X 3 is —O—, —S—, —S( ⁇ O)—, or —S( ⁇ O)
  • R 14 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl); or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkyl; X 3 is —O—; Q 3 is a C 1 -C 6 alkyl, a substituted or unsubstituted phenyl, —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl), or C 1 -C 4 alkyl-(substituted or unsubstituted or unsubsti
  • R 14 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 14 is C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl). In some embodiments, R 14 is C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl. In some embodiments, R 14 is C 1 -C 4 alkyl. In some embodiments, R 14 is C 3 -C 6 cycloalkyl.
  • R 14 is —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl). In some embodiments, R 14 is —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl). In some embodiments, R 14 is -L 3 -X 3 -Q 3 .
  • R 11 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl);
  • R 14 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl); or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkyl; X 3 is — —
  • R 11 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl
  • R 14 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl); or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkyl; X 3 is —O—; Q 3 is a C 1 -C 6 alkyl.
  • R 11 is —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl);
  • R 14 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl; or R 14 is -L 3 -X 3 -Q 3 ;
  • L 3 is a C 1 -C 4 alkyl;
  • X 3 is —O—;
  • Q 3 is a C 1 -C 6 alkyl.
  • R 10 is —C( ⁇ O)OR 15 ;
  • R 15 is C 1 -C 6 alkyl, —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 4 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 10 is —C( ⁇ O)OR 15 ;
  • R 15 is C 1 -C 4 alkyl, or —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl).
  • R 10 is —C( ⁇ O)OR 15 ;
  • R 11 is C 1 -C 6 alkyl;
  • R 15 is —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl).
  • R 10 is C( ⁇ O)OR 15 ;
  • R 11 is C 1 -C 4 alkyl;
  • R 15 is —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl).
  • R 10 is —C( ⁇ O)N(R 16 ) 2 ; each R 16 is independently H, C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 10 is —C( ⁇ O)N(R 16 ) 2 ; one R 16 is C 1 -C 6 alkyl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl); and the other R 16 is H or C 1 -C 6 alkyl.
  • R 10 is —C( ⁇ O)N(R 16 ) 2 ;
  • R 11 is C 1 -C 6 alkyl;
  • one R 16 is C 1 -C 6 alkyl, or —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl); and the other R 16 is H or C 1 -C 6 alkyl.
  • R 10 is C( ⁇ O)N(R 16 ) 2 ;
  • R 11 is C 1 -C 4 alkyl;
  • one R 16 is C 1 -C 4 alkyl, or —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl); and the other R 16 is H or C 1 -C 4 alkyl.
  • R 6 is selected from H, halogen, —CN, —NO 2 , —OH, —OR 12 , —SR 12 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —N(R 13 )S( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —C( ⁇ O)R 12 , —OC( ⁇ O)R 12 , —CO 2 R 13 , —OCO 2 R 13 , —N(R 13 ) 2 , —NHCH 2 CO 2 R 13 , —OCH 2 CO 2 R 13 , —SCH 2 CO 2 R 13 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)R 12 , —NR 13 C( ⁇ O)R 12 ,
  • R 6 is H, halogen, —OH, —SR 13 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —NHS( ⁇ O) 2 R 12 , —C( ⁇ O)R 12 , —OC( ⁇ O)R 12 , —CO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)R 12 , C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, C 1 -C 4 alkoxy, or C 1 -C 4 heteroalkyl.
  • R 6 is halogen, —CN, —OH, —SR 13 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —NHS( ⁇ O) 2 R 12 , —C( ⁇ O)R 12 , —OC( ⁇ O)R 12 , —CO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)R 12 , C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, C 1 -C 4 alkoxy, or C 1 -C 4 heteroalkyl.
  • R 6 is halogen, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, or C 1 -C 4 alkoxy.
  • R 6 is selected from a substituted or unsubstituted C 3 -C 10 cycloalkyl, a substituted or unsubstituted C 2 -C 10 heterocycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted naphthyl, and a substituted or unsubstituted monocyclic heteroaryl.
  • R 6 is selected from a substituted or unsubstituted C 3 -C 6 cycloalkyl, a substituted or unsubstituted C 2 -C 10 heterocycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted naphthyl, and a substituted or unsubstituted monocyclic heteroaryl.
  • R 6 is C 3 -C 6 cycloalkyl. In some embodiments, R 6 is a substituted or unsubstituted C 2 -C 10 heterocycloalkyl. In some embodiments, R 6 is a substituted or unsubstituted C 3 -C 6 heterocycloalkyl. In some embodiments, R 6 is a substituted or unsubstituted phenyl, or a substituted or unsubstituted monocyclic heteroaryl. In some embodiments, R 6 is a substituted or unsubstituted phenyl. In some embodiments, R 6 is a substituted or unsubstituted monocyclic heteroaryl.
  • the compound of Formula (I) has the structure of Formula (III):
  • each of A 1 , A 2 , A 3 , and A 4 is independently selected from among —N—, —N + (—O ⁇ )— and —C(R A )—, where one or two of A 1 , A 2 , A 3 , and A 4 is —N— or —N + (—O ⁇ )—.
  • each R A is independently selected from H, halogen, —CN, —OH, —OR 12 , —N(R 13 ) 2 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, and C 1 -C 6 heteroalkyl.
  • each R A is independently selected from H, halogen, —CN, —OH, —OR 12 , C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, C 1 -C 4 alkoxy, and C 1 -C 4 heteroalkyl;
  • a 1 is —N—, —N + (—O ⁇ )— or —CH—;
  • each of A 2 , A 3 , and A 4 is independently selected from among —N—, —N + (—O ⁇ )- and —C(R A )—, where one or two of A 1 , A 2 , A 3 , and A 4 is —N— or —N + (—O ⁇ )—
  • each R A is independently selected from H, halogen, —CN, —OH, —OR 12 , C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, C 1 -C 4 alkoxy, and C 1 -C 4 heteroalkyl.
  • one of A 1 , A 2 , A 3 , and A 4 is —N— or —N + (—O ⁇ )—.
  • a 1 is —N— or —N + (—O ⁇ )—.
  • a 2 is —N— or —N + (—O ⁇ )—.
  • a 3 is —N— or —N + (—O ⁇ )—.
  • a 4 is —N— or —N + (—O ⁇ )—.
  • a 1 is —CH—.
  • a 1 is CH;
  • a 3 is —N— or —N + (—O ⁇ )—; and each of A 2 and A 4 is —C(R A )—; each R A is independently selected from H, F, Cl, Br, I, —CN, —OH, —OCH 3 , —OCH 2 CH 3 , —CH 3 , —CH 2 CH 3 , —CF 3 , —CHF 2 , —CH 2 F, and —OCF 3 .
  • each R 1 is independently selected from H and —CH 3 .
  • R B is H, methyl, ethyl, propyl, or butyl.
  • each of R 5 , R 7 , and R 8 is independently selected from H, F, Cl, Br, I, —CN, —OH, —OCH 3 , —OCH 2 CH 3 , —CH 3 , —CH 3 CH 3 , —CF 3 , CHF 2 , CH 2 F, and —OCF 3 .
  • At least one of R 5 , R 7 , and R 8 is H.
  • each of R 5 , R 7 , and R 8 is H.
  • the compound of Formula (III) has the structure of Formula (IV):
  • each R 1 is independently selected from H and —CH 3 ;
  • a 1 is CH;
  • a 3 is —N— or —N + (—O ⁇ )—; and
  • each of A 2 and A 4 is —C(R A )—;
  • each R A is independently selected from H, halogen, —CN, —OH, —OR 12 , C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, C 1 -C 4 alkoxy, and C 1 -C 4 heteroalkyl.
  • each R 1 is H; each R A is independently selected from H, F, Cl, Br, I, —CN, —OH, —OCH 3 , —OCH 2 CH 3 , —CH 3 , —CH 2 CH 3 , —CF 3 , —CHF 2 , —CH 2 F, and —OCF 3 .
  • At least one R A is H.
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 4 alkyl-(C 3 -C 6 cycloalkyl), —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 4 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 10 is —C( ⁇ O)R 14 , —C( ⁇ O)OR 15 , or —C( ⁇ O)N(R 16 ) 2 .
  • R 10 is —C( ⁇ O)R 14 , —C( ⁇ O)OR 15 , or —C( ⁇ O)N(R 16 ) 2 ;
  • R 14 is C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 4 alkyl-(substituted or unsubstituted monocyclic heteroaryl); or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkylene or a substituted or unsubstituted phenyl; X 3 is a bond, —O—O—
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 heteroalkyl, or C 3 -C 6 cycloalkyl.
  • R 11 is —C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 heteroalkyl.
  • R 11 is C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl.
  • R 11 is a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 4 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 11 is —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 4 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 10 is —C( ⁇ O)R 14 , —C( ⁇ O)OR 15 , or —C( ⁇ O)N(R 16 ) 2 ;
  • R 14 is C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, or a C 3 -C 6 cycloalkyl;
  • R 15 is C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, or a C 3 -C 6 cycloalkyl;
  • each R 16 is independently H, C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, or a C 3 -C 6 cycloalkyl; or two R 16 groups attached to the same N atom are taken together with the N atom to which they are attached to form an optionally substituted heterocycloalkyl.
  • R 10 is —C( ⁇ O)R 14 ;
  • R 14 is —C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 4 alkyl-(C 3 -C 6 cycloalkyl), —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 4 alkyl-(substituted or unsubstituted monocyclic heteroaryl); or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkyl; X 3 is —O—, —S—, —S( ⁇ O)—, or —S(S(
  • R 14 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl); or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkyl; X 3 is —O—; Q 3 is a C 1 -C 6 alkyl, a substituted or unsubstituted phenyl, —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl), or C 1 -C 4 alkyl-(substituted or unsubstituted or unsubsti
  • R 14 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl); or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkyl; X 3 is —O—; Q 3 is a C 1 -C 6 alkyl.
  • R 14 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl) or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl); or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkyl; X 3 is —O—; Q 3 is a C 1 -C 6 alkyl.
  • R 14 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl; or R 14 is -L 3 -X 3 -Q 3 ; L 3 is a C 1 -C 4 alkyl; X 3 is —O—; Q 3 is a C 1 -C 6 alkyl. In some embodiments, R 14 is C 1 -C 6 alkyl, or C 3 -C 6 cycloalkyl.
  • R 10 is —C( ⁇ O)OR 15 ;
  • R 15 is C 1 -C 6 alkyl, —C 1 -C 4 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 4 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 10 is —C( ⁇ O)OR 15 ;
  • R 15 is C 1 -C 4 alkyl, or —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl).
  • R 10 is —C( ⁇ O)OR 15 ;
  • R 15 is —C 1 -C 2 alkyl—(substituted or unsubstituted phenyl).
  • R 10 is —C( ⁇ O)N(R 16 ) 2 ; each R 16 is independently H, C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, C 3 -C 6 cycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted monocyclic heteroaryl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl).
  • R 10 is —C( ⁇ O)N(R 16 ) 2 ; one R 16 is C 1 -C 6 alkyl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), or —C 1 -C 2 alkyl-(substituted or unsubstituted monocyclic heteroaryl); and the other R 16 is H or C 1 -C 6 alkyl.
  • R 10 is —C( ⁇ O)N(R 16 ) 2 ; one R 16 is C 1 -C 6 alkyl, or —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl); and the other R 16 is H or C 1 -C 6 alkyl.
  • R 10 is —C( ⁇ O)N(R 16 ) 2 ; one R 16 is C 1 -C 4 alkyl, or —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl); and the other R 16 is H or C 1 -C 6 alkyl.
  • R 10 is —C( ⁇ O)N(R 16 ) 2 ; one R 16 is C 1 -C 4 alkyl, or —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl); and the other R 16 is H.
  • R 6 is selected from halogen, —CN, —NO 2 , —OH, —OR 12 , —SR 12 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —N(R 13 )S( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —C( ⁇ O)R 12 , —OC( ⁇ O)R 12 , —CO 2 R 13 , —OCO 2 R 13 , —N(R 13 ) 2 , —NHCH 2 CO 2 R 13 , —OCH 2 CO 2 R 13 , —SCH 2 CO 2 R 13 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)R 12 , —NR 13 C( ⁇ O)R 12 , —NR
  • R 6 is selected from halogen, —CN, —NO 2 , —OH, —OR 12 , —SR 12 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —NHS( ⁇ O) 2 R 12 , —N(C 1 -C 4 alkyl)S( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —C( ⁇ O)R 12 , —OC( ⁇ O)R 12 , —CO 2 R 13 , —OCO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)N(R 13 ) 2 , —N(C 1 -C 4 alkyl)C( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)R 12 , —N
  • R 6 is selected from halogen, —CN, —NO 2 , —OH, —OR 12 , —S( ⁇ O) 2 R 12 , —NHS( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —CO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)N(R 13 ) 2 , —N(C 1 -C 6 alkyl)C( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)R 12 , —N(C 1 -C 6 alkyl)C( ⁇ O)R 12 , —NHC 1 -C 4 alkyl-C( ⁇ O)R 12 , —C 1 -C 4 alkyl-N(R 13 ) 2 , —C 1 -C 4 al
  • R 6 is selected from —NHS( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —CO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)N(R 13 ) 2 , —N(C 1 -C 6 alkyl)C( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)R 12 , —N(C 1 -C 6 alkyl)C( ⁇ O)R 12 , —NHC 1 -C 4 alkyl-C( ⁇ O)R 12 , —C 1 -C 4 alkyl-N(R 13 ) 2 , —NHC( ⁇ O)OR 12 , —N(C 1 -C 6 alkyl)C( ⁇ O)OR 12 .
  • R 6 is selected from halogen, —OH, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, or C 1 -C 4 alkoxy.
  • R 6 is C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted phenyl, substituted or unsubstituted napthyl, substituted or unsubstituted monocyclic heteroaryl, or substituted or unsubstituted bicyclic heteroaryl.
  • R 6 is cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or a substituted or unsubstituted group selected from pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, thiomorpholinyl, phenyl, naphthyl, furanyl, thienyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, triazolyl, tetrazolyl, pyridinyl, pyridazinyl, pyrazinyl, pyrimidinyl, triazinyl, indolyl, benzofuranyl, benzothienyl, indazolyl, benzimidaolyl, benzthiazolyl, quinolinyl
  • R 6 is a substituted or unsubstituted group selected from phenyl, naphthyl, furanyl, thienyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, triazolyl, tetrazolyl, pyridinyl, pyridazinyl, pyrazinyl, pyrimidinyl, triazinyl, indolyl, benzofuranyl, benzothienyl, indazolyl, benzimidaolyl, benzthiazolyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, and quinoxalinyl.
  • R 6 is a substituted or unsubstituted group selected from pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, triazolyl, tetrazolyl, pyridinyl, pyridazinyl, pyrazinyl, pyrimidinyl, triazinyl, indolyl, indazolyl, benzimidaolyl, benzthiazolyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl, and quinoxalinyl.
  • R 6 is a substituted or unsubstituted group selected from pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, tetrazolyl, isoxazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrazinyl, pyrimidinyl, quinolinyl, and isoquinolinyl.
  • R 6 is a substituted or unsubstituted group selected from pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, tetrazolyl, isoxazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrazinyl, and pyrimidinyl.
  • the compound of Formula (I) has the structure of Formula (V).
  • R 10 is —C( ⁇ O)R 20 , where R 20 is as defined herein.
  • each R A is independently R A is H, F, Cl, Br, —CN, —OH, —CH 3 , —CF 3 , —OCF 3 , —OCH 2 CF 3 , —OCH 3 or —OCH 2 CH 3 ;
  • R 6 is H, F, Cl, Br, —CN, —OH, —SR 13 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —NHS( ⁇ O) 2 R 12 , —CO 2 R 13 , —C( ⁇ O)NH(R 13 ), —NHC( ⁇ O)R 12 , —CH 3 , —CF 3 , —OCF 3 , or —OCH 3 ;
  • R 12 is C 1 -C 4 alkyl;
  • R 13 is H, C 1 -C 4 alkyl, or substituted or unsubstituted benzyl.
  • R 20 is C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), —C 1 -C 2 alkyl-(substituted or unsubstituted 6-membered heteroaryl containing 1 or 2 N atom), —C 1 -C 2 alkyl-O—C 1 -C 4 alkyl, —O—C 1 -C 4 alkyl, —O—C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), —NR 16 C 1 -C 4 alkyl, or —NR 16 C 1 -C 2 alkyl-(substituted or unsubstituted phenyl); R 11 is C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl or substituted or unsubstituted phenyl);
  • R 20 is —CH 3 , —CH 2 CH 3 , —CH(CH 3 ) 2 , —C(CH 3 ) 3 , cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, —CH 2 OCH 3 , —CH 2 OCH 2 CH 3 , —C 1 -C 2 alkyl-(substituted or unsubstituted phenyl), —C 1 -C 2 alkyl-(substituted or unsubstituted 6-membered heteroaryl containing 1 or 2 N atom); where each substituted phenyl or substituted heteroaryl is substituted with 1 or 2 R C , where each R C is independently selected from halogen, —OH, —CH 3 , —CH 2 CH 3 , —OCH 3 , —OCH 2 CH 3 , and —CF 3 ; R 11 is —CH 3 , —CH 2
  • At least one R A is H;
  • R 6 is F, Cl, Br, —CH 3 , —CF 3 , —OCF 3 , or —OCH 3 ;
  • R 20 is —CH 3 , cyclopropyl, —CH 2 OCH 3 , or —CH 2 OCH 2 CH 3 .
  • At least one R A is H; R 11 is —CH 2 CH 3 .
  • R 20 is C 1 -C 4 alkyl, or C 3 -C 6 cycloalkyl; R 11 is substituted or unsubstituted benzyl.
  • At least one R A is H;
  • R 6 is F, Cl, Br, —CN, —OH, —SR 13 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —NHS( ⁇ O) 2 R 12 , —CO 2 R 13 , —C( ⁇ O)NH(R 13 ), —NHC( ⁇ O)R 12 , —CH 3 , —CF 3 , —OCF 3 , or —OCH 3 ;
  • R 20 is —CH 3 , or cyclopropyl;
  • R 11 is substituted or unsubstituted benzyl.
  • R 20 is —O—C 1 -C 4 alkyl or —O—C 1 -C 2 alkyl-(substituted or unsubstituted phenyl).
  • R 20 is —O—CH 2 — (substituted or unsubstituted phenyl) or —O—CH(CH 3 )—(substituted or unsubstituted phenyl); where each substituted phenyl is substituted with 1 or 2 R C , where each R C is independently selected from halogen, —OH, —CH 3 , —CH 2 CH 3 , —OCH 3 , —OCH 2 CH 3 , and —CF 3 ; R 11 is C 1 -C 4 alkyl or C 3 -C 6 cycloalkyl.
  • At least one R A is H;
  • R 6 is F, Cl, Br, —CH 3 , —CF 3 , —OCF 3 , or —OCH 3 ;
  • R 20 is —O—CH 2 — (substituted or unsubstituted phenyl), where the substituted phenyl is substituted with 1 or 2 R C , where each R C is independently selected from F, Cl, Br, —OH, —CH 3 , —OCH 3 , and —CF 3 ;
  • R 11 is C 1 -C 4 alkyl.
  • one R A is H, F, Cl, —CH 3 , —CF 3 , —OCF 3 , or —OCH 3 , and the other R A is H; R 6 is —CF 3 ; R 11 is —CH 2 CH 3 .
  • R 20 is —NR 16 C 1 -C 4 alkyl, or —NR 16 C 1 -C 2 alkyl-(substituted or unsubstituted phenyl); R 16 is H, —CH 3 or —CH 2 CH 3 .
  • R 20 is —NR 16 —CH 2 — (substituted or unsubstituted phenyl) or —NR 16 —CH(CH 3 )—(substituted or unsubstituted phenyl), where the substituted phenyl is substituted with 1 or 2 R C , where each R C is independently selected from F, Cl, Br, —OH, —CH 3 , —OCH 3 , and —CF 3 ; R 11 is C 1 -C 4 alkyl or C 3 -C 6 cycloalkyl; R 16 is H, —CH 3 or —CH 2 CH 3 .
  • At least one R A is H;
  • R 6 is F, Cl, Br, —CH 3 , —CF 3 , —OCF 3 , or —OCH 3 ;
  • R 20 is —NR 16 —CH 2 — (substituted or unsubstituted phenyl); where the substituted phenyl is substituted with 1 or 2 R C , where each R C is independently selected from F, Cl, Br, —OH, —CH 3 , —OCH 3 , and —CF 3 ; R 11 is C 1 -C 4 alkyl.
  • one R A is H, F, Cl, —CH 3 , —CF 3 , —OCF 3 , or —OCH 3 , and the other R A is H; R 6 is —CF 3 ; R 11 is —CH 2 CH 3 .
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), and Formula (V) are antagonists of DP 2 .
  • the antagonist of DP 2 is selective for DP 2 .
  • the antagonist of DP 2 is also an antagonist of DP 1 .
  • the antagonist of DP 2 is also an antagonist of TP (thromboxane receptor).
  • presented herein are compounds selected from active metabolites, solvates, pharmaceutically acceptable salts or pharmaceutically acceptable prodrugs of a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • a pharmaceutical composition comprising a therapeutically effective amount of a compound provided herein.
  • the pharmaceutical composition also contains a pharmaceutically acceptable excipient.
  • presented herein are methods for treating a PGD 2 -dependent condition or disease in a patient comprising administering to the patient a therapeutically effective amount of an antagonist of DP 2 having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • provided herein is a method for treating inflammation in a mammal comprising administering a therapeutically effective amount of a compound provided herein to the mammal in need.
  • provided herein is a method for treating asthma in a mammal comprising administering a therapeutically effective amount of a compound provided herein to the mammal in need.
  • a method for treating asthma in a mammal comprising administering a therapeutically effective amount of a compound provided herein, such as, for example, a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V), to the mammal in need.
  • PGD 2 -dependent conditions or diseases including, but not limited to, asthma, rhinitis, chronic obstructive pulmonary disease, pulmonary hypertension, interstitial lung fibrosis, arthritis, allergy, psoriasis, inflammatory bowel disease, adult respiratory distress syndrome, myocardial infarction, aneurysm, stroke, cancer
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V), including pharmaceutically acceptable salts, pharmaceutically acceptable prodrugs, and pharmaceutically acceptable solvates thereof are antagonists of CRTH2.
  • these compounds are used to treat patients suffering from one or more PGD 2 -dependent conditions or diseases, including, but not limited to, asthma, rhinitis, chronic obstructive pulmonary disease, pulmonary hypertension, interstitial lung fibrosis, rhinitis, allergy, and adult respiratory distress syndrome.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are antagonists of DP 2 .
  • such antagonists of DP 2 also antagonize other related PGD 2 receptors.
  • Related PGD 2 receptors include, but are not limited to, DP 1 and TP.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered with a TP antagonist.
  • TP antagonists inhibit bronchoconstriction, vasoconstriction, and platelet aggregation.
  • co-administration of a TP antagonist with a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) inhibits bronchoconstrictor effects of PGD 2 and other prostanoids.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are included into pharmaceutical compositions or medicaments used for treating a PGD 2 -dependent or PGD 2 mediated condition or disease in a patient.
  • compositions described herein are administrable to a subject in a variety of by multiple administration routes, including but not limited to, oral, parenteral (e.g., intravenous, subcutaneous, intramuscular), intranasal, buccal, topical or transdermal administration routes.
  • the pharmaceutical formulations described herein include, but are not limited to, aqueous liquid dispersions, self-emulsifying dispersions, solid solutions, liposomal dispersions, aerosols, solid dosage forms, powders, immediate release formulations, controlled release formulations, fast melt formulations, tablets, capsules, pills, delayed release formulations, extended release formulations, pulsatile release formulations, multiparticulate formulations, and mixed immediate and controlled release formulations.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered orally.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered topically.
  • the compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) is formulated into a variety of topically administrable compositions, such as solutions, suspensions, lotions, gels, pastes, shampoos, scrubs, rubs, smears, medicated sticks, medicated bandages, balms, creams or ointments.
  • Such pharmaceutical compounds can contain solubilizers, stabilizers, tonicity enhancing agents, buffers and preservatives.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered by intranasal administration.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are formulated for intranasal administration.
  • Such formulations include nasal sprays, nasal mists, and the like.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are formulated as eye drops.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered topically to the skin.
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are used to treat or prevent inflammatory conditions.
  • Inflammatory conditions include, but are not limited to, asthma, rhinitis, chronic obstructive pulmonary disease, pulmonary hypertension, interstitial lung fibrosis, atherosclerosis, aortic aneurysm, myocardial infarction, and stroke.
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are used to treat or prevent immunological disorders.
  • the immunological disorders include, but are not limited to, allergy or to excessive or inappropriate response to an endogenous or exogenous antigen.
  • the immunological disorder that is characterized by immune dysregulation that is not accompanied by inflammation.
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are used to treat or prevent proliferative disorders.
  • the proliferative disorders include, but are not limited to, cancer and noncancerous disorders, including, but not limited to, those involving the skin or lymphatic tissues.
  • such conditions are iatrogenic and increases in, or abnormal localization of, PGD 2 is induced by other therapies or medical or surgical procedures.
  • the PGD 2 -dependent or PGD 2 mediated condition or disease is caused by surgery.
  • the methods, compounds, pharmaceutical compositions, and medicaments described herein are used to prevent the cellular activity of PGD 2 .
  • such methods, compounds, pharmaceutical compositions, and medicaments comprise DP 2 antagonists disclosed herein for the treatment of asthma by modulating the activity of enzymes or proteins in a patient wherein such enzymes or proteins are involved in the PGD 2 pathway such as, by way of example, DP 2 .
  • the methods, compounds, pharmaceutical compositions, and medicaments described herein are used in combination with other medical treatments or surgical modalities.
  • methods for reducing/antagonizing the PGD 2 activation of DP 2 in a mammal comprising administering to the mammal at least once an effective amount of a compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • a mammal in another aspect, presented herein are methods for modulating, including reducing and/or antagonizing the activity of PGD 2 in a mammal, directly or indirectly, comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • methods for treating PGD 2 -dependent or PGD 2 mediated conditions or diseases comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • methods for treating inflammation comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • methods for treating immunological abnormalities comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • a respiratory disease comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • the respiratory disease is asthma.
  • the respiratory disease includes, but is not limited to, adult respiratory distress syndrome and allergic (extrinsic) asthma, non-allergic (intrinsic) asthma, acute severe asthma, chronic asthma, clinical asthma, nocturnal asthma, allergen-induced asthma, aspirin-sensitive asthma, exercise-induced asthma, isocapnic hyperventilation, child-onset asthma, adult-onset asthma, cough-variant asthma, neutrophilic asthma, occupational asthma, steroid-resistant asthma, seasonal asthma.
  • a respiratory disease comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • the respiratory disease is rhinitis.
  • the respiratory disease includes, but is not limited to, allergic (extrinsic) rhinitis, non-allergic (intrinsic) rhinitis, chronic rhinitis, allergen-induced rhinitis, aspirin-sensitive rhinitis, child-onset rhinitis, adult-onset rhinitis, occupational rhinitis, steroid-resistant rhinitis, seasonal rhinitis, perennial rhinitis, rhinosinusitis, and rhinopolyposis.
  • chronic obstructive pulmonary disease in another aspect, includes administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • chronic obstructive pulmonary disease includes, but is not limited to, chronic bronchitis and/or emphysema, pulmonary hypertension, interstitial lung fibrosis and/or airway inflammation and cystic fibrosis.
  • a disease or condition comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • methods for treating organ reperfusion injury following organ ischemia and/or endotoxic shock comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • eosinophil and/or basophil and/or dendritic cell and/or neutrophil and/or monocyte or TH2 cell recruitment comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • a further aspect are methods for the prevention or treatment of abnormal bone remodeling, loss or gain, including diseases or conditions as, by way of example, osteopenia, osteoporosis, Paget's disease, cancer, trauma, surgery, and other diseases comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • diseases or conditions as, by way of example, osteopenia, osteoporosis, Paget's disease, cancer, trauma, surgery, and other diseases comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • compositions for preventing ocular inflammation and allergic conjunctivitis, vernal keratoconjunctivitis, and papillary conjunctivitis comprising administering to the mammal at least once an effective amount of at least one having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • CNS disorders include, but are not limited to, multiple sclerosis, Parkinson's disease, Alzheimer's or other degenerative disease, stroke, cerebral ischemia, retinal ischemia, post-surgical cognitive dysfunction, migraine, peripheral neuropathy/neuropathic pain, spinal cord injury, cerebral edema and head injury.
  • a further aspect are methods for the treatment of cancer comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • the type of cancer includes, but is not limited to, pancreatic cancer and other solid or hematological tumors.
  • methods for treating endotoxic shock and septic shock comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • methods for treating rheumatoid arthritis and osteoarthritis comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • gastrointestinal diseases comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • diseases include, by way of example only, chronic gastritis, eosinophilic gastroenteritis, and gastric motor dysfunction.
  • a further aspect are methods for treating kidney diseases comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • diseases include, by way of example only, acute tubular necrosis, glomerulonephritis, cyclosporine nephrotoxicity, renal ischemia, and reperfusion injury.
  • methods for preventing or treating acute or chronic renal insufficiency comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • methods for treating pain including neuropathic pain comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • non-steroidal anti-inflammatory drugs including selective or non-selective cyclooxygenase-1 or -2 inhibitors
  • administering comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • a further aspect are methods for the prevention or treatment of rejection or dysfunction in a transplanted organ or tissue comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • inflammatory responses of the skin comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • inflammatory responses of the skin include, by way of example, dermatitis, contact dermatitis, eczema, urticaria, rosacea, and scarring.
  • methods for reducing psoriatic lesions in the skin, joints, or other tissues or organs comprising administering to the mammal an effective amount of a first compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • a further aspect are methods for the treatment of cystitis, including, by way of example only, interstitial cystitis, comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • a further aspect are methods for the treatment of Familial Mediterranean Fever comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • hepatorenal syndrome comprising administering to the mammal at least once an effective amount of at least one compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • a further aspect are methods to treat acute or chronic allergic responses to exogenous substances that have been ingested such as foods (e.g., peanuts) or drugs (e.g., penicillin, non-steroidal anti-inflammatory drugs or the like).
  • foods e.g., peanuts
  • drugs e.g., penicillin, non-steroidal anti-inflammatory drugs or the like.
  • a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) in the manufacture of a medicament for treating an inflammatory disease or condition in an animal in which the activity of at least one PGD 2 -associated protein contributes to the pathology and/or symptoms of the disease or condition.
  • the PGD 2 pathway protein is CRTH2.
  • the inflammatory disease or conditions are respiratory, cardiovascular, or proliferative diseases.
  • any of the aforementioned aspects are further embodiments in which: (a) the effective amount of the compound is systemically administered to the mammal; and/or (b) the effective amount of the compound is administered orally to the mammal; and/or (c) the effective amount of the compound is intravenously administered to the mammal; and/or (d) the effective amount of the compound administered by inhalation; and/or (e) the effective amount of the compound is administered by nasal administration; or and/or (f) the effective amount of the compound is administered by injection to the mammal; and/or (g) the effective amount of the compound is administered topically (dermal) to the mammal; and/or (h) the effective amount of the compound is administered by ophthalmic administration; and/or (i) the effective amount of the compound is administered rectally to the mammal.
  • the mammal is a human, including embodiments wherein the human has an asthmatic condition or one or more other condition(s) selected from the group consisting of allergic (extrinsic) asthma, non-allergic (intrinsic) asthma, acute severe asthma, chronic asthma, clinical asthma, nocturnal asthma, allergen-induced asthma, aspirin-sensitive asthma, exercise-induced asthma, isocapnic hyperventilation, child-onset asthma, adult-onset asthma, cough-variant asthma, neutrophilic asthma, occupational asthma, steroid-resistant asthma, or seasonal asthma, or chronic obstructive pulmonary disease, or pulmonary hypertension or interstitial lung fibrosis.
  • the mammal is an animal model for pulmonary inflammation, examples of which are provided herein.
  • any of the aforementioned aspects are further embodiments comprising single administrations of the effective amount of the compound, including further embodiments in which (i) the compound is administered once; (ii) the compound is administered to the mammal multiple times over the span of one day; (iii) continually; or (iv) continuously.
  • any of the aforementioned aspects are further embodiments comprising multiple administrations of the effective amount of the compound, including further embodiments in which (i) the compound is administered continuously or intermittently: as in a single dose; (ii) the time between multiple administrations is every 6 hours; (iii) the compound is administered to the mammal every 8 hours.
  • the method comprises a drug holiday, wherein the administration of the compound is temporarily suspended or the dose of the compound being administered is temporarily reduced; at the end of the drug holiday, dosing of the compound is resumed.
  • the length of the drug holiday varies from 2 days to 1 year.
  • any of the aforementioned aspects are further embodiments comprising multiple administrations of the effective amount of the compound, including further embodiments in which (i) the compound is administered once daily; (ii) the compound is administered twice daily; (iii) the compound is administered in cycles that include daily administration for a period of time followed by at least 1 day without administration; (iv) the compound is administered in cycles that include daily administration for a period of time followed by at least 1 day that includes a dose reduction in the daily amount of compound that is administered.
  • any of the aforementioned aspects involving the treatment of PGD 2 dependent diseases or conditions are further embodiments comprising administering at least one additional agent in addition to the administration of a compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • each agent is administered in any order, including simultaneously.
  • the at least one additional agent is, by way of example only, an anti-inflammatory agent, a different compound having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V), a DP 1 receptor antagonist, a TP receptor antagonist, or a different DP 2 receptor antagonist.
  • a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) is combined with an additional agent that is a respiratory agent, including, but not limited to antihistamines (e.g., Zyrtec®), bronchodilators, LABAs (e.g., salmeterol), theophylline, IgE modulators (e.g., Xolair® and omalizumab), steroids (e.g., fluticasone).
  • antihistamines e.g., Zyrtec®
  • LABAs e.g., salmeterol
  • IgE modulators e.g., Xolair® and omalizumab
  • steroids e.g., fluticasone
  • the anti-inflammatory agent is, by way of example only, a leukotriene pathway modulator such as a CysLT1 receptor antagonists (e.g., montelukast), a CysLT2 receptor antagonist, a 5-lipoxygenase inhibitor (e.g., zileuton), a 5-lipoxygenase-activating protein inhibitor (e.g., MK-0591, MK-886, DG-031 (BAY X1005), 3-[3-tert-butylsulfanyl-1-[4-(6-methoxy-pyridin-3-yl)-benzyl]-5-(pyridin-2-ylmethoxy)-1H-indol-2-yl]-2,2-dimethyl-propionic acid, 3-[3-tert-butylsulfanyl-1-[4-(6-ethoxy-pyridin-3-yl)-benzyl]-5-(5-methyl-pyri
  • any of the aforementioned aspects involving the treatment of proliferative disorders, including cancer are further embodiments comprising administering at least one additional agent, including by way of example only alemtuzumab, arsenic trioxide, asparaginase (pegylated or non-), bevacizumab, cetuximab, platinum-based compounds such as cisplatin, cladribine, daunorubicin/doxorubicin/idarubicin, irinotecan, fludarabine, 5-fluorouracil, gemtuzumab, methotrexate, PaclitaxelTM, taxol, temozolomide, thioguanine, or classes of drugs including hormones (an antiestrogen, an antiandrogen, or gonadotropin releasing hormone analogues), interferons such as alpha interferon, nitrogen mustards such as busulfan or melphalan or mechlorethamine, retinoids such as tretinoin
  • any of the aforementioned aspects involving the therapy of an immunological disorder requiring immunosuppression or involving the therapy of transplanted organs or tissues or cells are further embodiments comprising administering at least one additional agent, including by way of example only azathioprine, a corticosteroid, cyclophosphamide, cyclosporin, dacluzimab, mycophenolate mofetil, OKT3, rapamycin, tacrolimus, or thymoglobulin.
  • at least one additional agent including by way of example only azathioprine, a corticosteroid, cyclophosphamide, cyclosporin, dacluzimab, mycophenolate mofetil, OKT3, rapamycin, tacrolimus, or thymoglobulin.
  • any of the aforementioned aspects involving the therapy of interstitial cystitis are further embodiments comprising administering at least one additional agent selected from, e.g., dimethylsulfoxide, omalizumab, and pentosan polysulfate.
  • at least one additional agent selected from, e.g., dimethylsulfoxide, omalizumab, and pentosan polysulfate.
  • any of the aforementioned aspects involving the therapy of disorders of bone are further embodiments comprising administering at least one additional agent such as, by way of example only, minerals, vitamins, bisphosphonates, anabolic steroids, parathyroid hormone or analogs, and cathepsin K inhibitors dronabinol.
  • at least one additional agent such as, by way of example only, minerals, vitamins, bisphosphonates, anabolic steroids, parathyroid hormone or analogs, and cathepsin K inhibitors dronabinol.
  • any of the aforementioned aspects involving the prevention or treatment of inflammation are further embodiments comprising: (a) monitoring inflammation in a mammal; (b) measuring bronchoconstriction in a mammal; (c) measuring eosinophil and/or basophil and/or dendritic cell and/or neutrophil and/or monocyte and/or lymphocyte recruitment in a mammal; (d) monitoring mucosal secretion in a mammal; (e) measuring mucosal edema in a mammal.
  • the PGD 2 -dependent or PGD 2 mediated diseases or conditions include, but are not limited to, asthma, rhinitis, chronic obstructive pulmonary disease, pulmonary hypertension, interstitial lung fibrosis, arthritis, allergy, inflammatory bowel disease, adult respiratory distress syndrome, myocardial infarction, aneurysm, stroke, cancer, and endotoxic shock.
  • Prostaglandin D 2 is an acidic lipid derived from the metabolism of arachidonic acid by cyclooxygenases and PGD 2 synthases. PGD 2 is produced by mast cells, macrophages and Th2 lymphocytes in response to local tissue damage as well as in response allergic inflammation observed in diseases such as asthma, rhinitis, and atopic dermatitis. More specifically, exogenous PGD 2 applied to bronchial airways elicits many responses that are characteristic of acute asthma.
  • PGD 2 is a major mast cell product that acts via two receptors, the D-type prostanoid (DP, also known as DP 1 ) and the chemoattractant receptor-homologous molecule expressed on Th2 cells (CRTH2, also known as DP 2 ) receptors.
  • DP 2 mediates the chemotaxis of eosinophils, basophils, and Th2 lymphocytes, and DP 1 receptor plays an important role in eosinophil trafficking DP 1 antagonists do not inhibit the release of eosinophils when induced by the DP 2 -selective agonists.
  • eosinophils in human bone marrow specimens express DP 1 and DP 2 receptors at similar levels and human peripheral blood expresses both DP 1 and DP 2 , but the DP 1 receptor is expressed at lower levels.
  • the chemotaxis of human peripheral blood eosinophils is inhibited by both DP 1 and DP 2 antagonists. Accordingly, DP 1 , DP 2 and dual DP 1 /DP 2 antagonists are useful in the treatment of allergic inflammation.
  • Activation of DP 2 is associated with chemotaxis and activation of Th2 lymphocytes, eosinophils and basophils.
  • PGD 2 binds to DP 2 and mediates many of its effects through a G i -dependent elevation of intracellular calcium levels and reduction of cyclic AMP.
  • IL4, IL5 and IL13 cytokine production are also stimulated by DP 2 activation.
  • cytokines have been implicated in numerous biological actions including, by way of example only, immunoglobulin E production, airway response, mucous secretion, and eosinophil recruitment.
  • CRTH2 and DP 2 refer to the same receptor and are used interchangeably herein.
  • DP 1 another common name for DP is DP 1 , and the two terms are used interchangeably herein.
  • Prostaglandins are recognized physiological lipid acid mediators produced by the release of arachidonic acid from cell membrane phospholipids and converted to prostaglandins by the action of COX 1 and COX 2 cyclooxygenases and PG synthases.
  • the cyclooxygenases sequentially convert arachidonic acid to cyclic endoperoxide prostaglandin G 2 (PGG 2 ) and subsequently, prostaglandin H 2 (PGH 2 ).
  • PGH 2 can be converted to numerous different prostaglandins, such as PGE 2 , PGD 2 , PGF 2 ⁇ , and PGI 2 as well as thromboxane A 2 , another eicosanoid signaling molecule. These mediators then elicit a wide variety of physiological responses including vasoconstriction or dilation, platelet aggregation, calcium transport, pain sensitization, hormone release, inflammatory and immune response, and cellular growth.
  • Prostaglandin D 2 is a major metabolite produced from the PGH 2 intermediate via hematopoietic PGD 2 synthase or lipocalin PGD 2 synthase.
  • PGD 2 is produced and thought to function in pain perception and sleep regulation.
  • PGD 2 is produced primarily in immunoglobulin E (IgE) activated mast cells and to a lesser extent, in macrophages, dendritic cells, T helper 2 (Th2) lymphocytes and other leukocytes.
  • IgE immunoglobulin E
  • PGD 2 is rapidly metabolized and converted to other downstream effectors including ⁇ 12 PGJ 2 , 9 ⁇ 11 ⁇ PGF 2 , 13,14-dihydro-15-keto-PGD 2 , and 15-deoxy- ⁇ 12,14 PGD 2 .
  • Mast-cell-derived PGD 2 is produced in high concentrations in response to an allergen challenge. Studies in preclinical species have observed the following features when PGD 2 is applied to in vivo preparations, or its overproduction is engineered by genetic manipulation:
  • the main receptors that are activated by PGD 2 or its metabolites and mediate its effects are DP 1 , CRTH2 (or DP 2 ) and TP.
  • DP 1 (or DP) is a G-protein coupled seven-transmembrane receptor that, upon activation by PGD 2 binding, leads to an increase in intracellular cAMP levels.
  • DP 1 is expressed in the brain, bronchial smooth muscle, vascular and airway smooth muscle, dendritic cells, and platelets and induces PGD 2 dependent bronchodilation, vasodilation, platelet aggregation inhibition, and suppression of cytokine production.
  • Genetic analysis of DP 1 function using knock-out mice has shown that mice lacking DP do not develop asthmatic responses in an ovalbumin-induced asthma model.
  • DP antagonism alleviate allergen-induced plasma exudation in the conjunctiva in a guinea pig allergic conjuctivitis model and antigen-induced eosinophil infiltration into the lung in a guinea pig asthma model.
  • DP 2 is a G-protein coupled receptor and is typically highly expressed in Th2 lymphocytes, eosinophils and basophils. DP 2 activation functions to directly activate and recruit Th2 lymphocytes and eosinophils. Activated Th2 lymphocytes produce and secrete inflammatory cytokines including IL4, IL5, and IL13.
  • DP 2 is not structurally related to DP 1 and signals through a different mechanism—the effects of DP 2 are mediated through Gi-dependent elevation in intracellular calcium levels and reduction in intracellular levels of cyclic AMP.
  • DP 2 activation is important in eosinophil recruitment in response to allergic challenge in such tissues as nasal mucosa, bronchial airways, and skin.
  • the application of either PGD 2 or selective DP 2 agonists both exacerbate and enhance allergic responses in lung and skin.
  • DP 2 activation appears to have a crucial role in mediating allergic responses, and thus the use of antagonists of PGD 2 activation of the DP 2 receptor are an attractive approach to treat the inflammatory component of allergic diseases such as asthma, rhinitis, and dermatitis.
  • TP receptors primarily function to antagonize DP 1 receptor's effects such as promoting bronchoconstriction, vasoconstriction, and platelet aggregation. While TP receptor's main ligand is thromboxane A 2 , it also binds and is activated by the PGD 2 derivative, 9 ⁇ 11 ⁇ PGF 2 . TP is a Gq-coupled prostanoid receptor that binds thromboxane with high affinity, promoting platelet aggregation and constriction of both vascular and airway smooth muscle. PGD 2 activates the TP receptor in human bronchial muscle, probably through the formation of the 11-ketoreductase metabolite 9 ⁇ 11 ⁇ PGF2. The bronchoconstrictor effects of TP dominate over the bronchodilator effects of DP 1 in the airways.
  • DP 1 and DP 2 have crucial, and complementary, roles in the physiological response of animals to PGD 2 and blockade of either one or both of these receptors may prove beneficial in alleviating allergic diseases or conditions triggered by PGD 2 , such as, but not limited to, allergic rhinitis, asthma, dermatitis, and allergic conjunctivitis.
  • blockade of DP 2 and TP activity is beneficial in alleviating allergic diseases or conditions triggered by PGD 2 , such as, but not limited to, allergic rhinitis, asthma, dermatitis, and allergic conjunctivitis.
  • blockade of DP 1 , DP 2 and TP activity is beneficial in alleviating allergic diseases or conditions triggered by PGD 2 , such as, but not limited to, allergic rhinitis, asthma, dermatitis, and allergic conjunctivitis.
  • substituents can be selected from among from a subset of the listed alternatives.
  • Q is —C( ⁇ O)-Q 1 , or tetrazolyl.
  • Q is selected from —CO 2 H, —CO 2 Me, —CO 2 Et, —C( ⁇ O)NH 2 , —C( ⁇ O)NHOH, —C( ⁇ O)NH—CN, tetrazolyl, —C( ⁇ O)—NHSO 2 R 12 , or
  • Q is selected from —CO 2 H, —CO 2 Me, —CO 2 Et, —C( ⁇ O)NH 2 , —C( ⁇ O)—NHSO 2 CH 3 , —C( ⁇ O)—NHSO 2 CH 2 CH 3 .
  • Q is —C( ⁇ O)-Q 1 .
  • Q is —CO 2 H.
  • Q 1 is —OH, —OR 13 , —NHSO 2 R 12 , or —N(R 13 ) 2 . In some other embodiments, Q 1 is —OH, —OCH 3 , —OCH 2 CH 3 , or —NHSO 2 CH 3 . In some other embodiments, Q 1 is —OH, —OCH 3 , or —OCH 2 CH 3 .
  • Q is tetrazolyl or —C( ⁇ O)-Q 1 ;
  • Q 1 is —OH, —OR B , —NHSO 2 R 12 , or —N(R 13 ) 2 .
  • Q is —C( ⁇ O)-Q 1 ; Q 1 is —OH or —OR B .
  • R B is H, —CH 3 or —CH 2 CH 3 . In other embodiments, R B is H.
  • each R 1 is independently selected from H, F, or C 1 -C 4 alkyl; or both R 1 groups are taken together with the carbon atom to which they are attached form a cyclopropyl, cyclobutyl, cyclophenyl, or cyclohexyl.
  • each R 1 is independently selected from H, F, and —CH 3 . In one aspect, each R 1 is H.
  • Q is —C( ⁇ O)-Q 1 ;
  • Q 1 is —OH, or —OR B ;
  • R B is H or C 1 -C 6 alkyl.
  • each R 1 is independently selected from H, F, and C 1 -C 4 alkyl; each R 9 is each independently selected from H and —CH 3 .
  • ring A is a substituted or unsubstituted monocyclic heteroaryl, wherein if ring A is substituted then each substituent on ring A is independently selected from among H and R A .
  • each R 1 is independently selected from H and C 1 -C 4 alkyl.
  • each R 9 is H.
  • ring A is a substituted or unsubstituted 5-membered heteroaryl or a substituted or unsubstituted 6-membered heteroaryl, wherein ring A includes 0 or 1 O atoms, 0 or 1 S atoms, 0-3 N atoms, and at least 2 carbon atoms, wherein if ring A is substituted then each substituent on ring A is independently selected from among H and R A .
  • ring A is a substituted or unsubstituted 5-membered or 6-membered heteroaryl selected from among furanyl, thienyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, 1,3,4-thiadiazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, and triazinyl, wherein if ring A is substituted then each substituent on ring A is independently selected from H and R A .
  • ring A is a substituted or unsubstituted 5-membered heteroaryl, wherein ring A includes 0 or 1 O atoms, 0 or 1 S atoms, 1-3 N atoms, and at least 2 carbon atoms, wherein if ring A is substituted then each substituent on ring A is independently selected from among H and R A .
  • ring A is a substituted or unsubstituted 5-membered heteroaryl selected from among pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, 1,3,4-thiadiazolyl, wherein if ring A is substituted then each substituent on ring A is independently selected from H and R A .
  • ring A is a substituted or unsubstituted 6-membered heteroaryl containing 1-3 N atoms in the ring, wherein if ring A is substituted then each substituent on ring A is independently selected from among H and R A .
  • ring A is a substituted or unsubstituted 6-membered heteroaryl selected from among pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, and triazinyl, wherein if ring A is substituted then each substituent on ring A is independently selected from among H and R A .
  • each of R 5 , R 6 , R 7 , and R 8 is independently selected from H, halogen, —CN, —NO 2 , —OH, —OR 12 , —SR 12 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —N(R 13 )S( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —C( ⁇ O)R 12 , —OC( ⁇ O)R 12 , —CO 2 R 13 , —OCO 2 R 13 , —N(R 13 ) 2 , —NHCH 2 CO 2 R 13 , —OCH 2 CO 2 R 13 , —SCH 2 CO 2 R 13 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)N(
  • each of R 5 , R 7 , and R 8 is independently selected from H, halogen, —CN, —OH, —OR 12 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, and C 1 -C 6 heteroalkyl.
  • each of R 5 , R 7 , and R 8 is independently selected from H, F, Cl, Br, I, —CN, —OH, —OCH 3 , —OCH 2 CH 3 , —CH 3 , —CH 3 CH 3 , —CF 3 , CHF 2 , CH 2 F, and —OCF 3 .
  • At least one of R 5 , R 7 , and R 8 is H. In some embodiments, at least two of R 5 , R 7 , and R 8 is H. In some embodiments, each of R 5 , R 7 , and R 8 is H.
  • the compound of Formula (I) has the following structure:
  • the compound of Formula (I) has the structure of Formula (III):
  • each R A is independently selected from H, halogen, —CN, —OH, —OR 12 , —S( ⁇ O) 2 R 12 , —C( ⁇ O)R 12 , —CO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)R 12 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, and C 1 -C 6 heteroalkyl.
  • each R A is independently selected from H, halogen, —CN, —OH, —OR 12 , —N(R 13 ) 2 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, and C 1 -C 6 heteroalkyl.
  • each R A is independently selected from H, F, Cl, Br, I, —CN, —OH, —OCH 3 , —OCH 2 CH 3 , —CH 3 , —CH 2 CH 3 , —CF 3 , —CHF 2 , —CH 2 F, and —OCF 3 .
  • one of A 1 , A 2 , A 3 , and A 4 is —N— or —N + (—O ⁇ )—. In some embodiments, two of A 1 , A 2 , A 3 , and A 4 is —N— or —N + (—O ⁇ )—. In some embodiments, two of A 1 , A 2 , A 3 , and A 4 is —N—.
  • a 1 is —N— or —N + (—O ⁇ )—. In some embodiments, A 1 is N. In some embodiments, A 2 is —N— or —N + (—O ⁇ )—. In some embodiments, A 2 is N. In some embodiments, A 3 is —N— or —N + (—O ⁇ )—. In some embodiments, A 3 is N. In some embodiments, A 4 is —N— or —N + (—O ⁇ )—. In some embodiments, A 4 is N.
  • a 4 is —C(H)—.
  • a 1 is CH;
  • a 3 is —N— or —N + (—O ⁇ )—; and each of A 2 and A 4 is —C(R A )—.
  • each R 1 is independently selected from H and —CH 3 . In some embodiments, each R 1 is H.
  • R B is H, methyl, ethyl, propyl, or butyl. In some embodiments, R B is H.
  • the compound of Formula (I) has the structure of Formula (IV):
  • the compound of Formula (I) has the structure of Formula (V):
  • R 10 is —C( ⁇ O)—R 20 , where R 20 is —R 14 , —OR 15 , or —N(R 16 ) 2 .
  • R 20 is —R 14 .
  • R 20 is —OR 15 .
  • R 20 is —N(R 16 ) 2 .
  • R 6 is selected from halogen, —CN, —NO 2 , —OH, —OR 12 , —SR 12 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —N(R 13 )S( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —C( ⁇ O)R 12 , —OC( ⁇ O)R 12 , —CO 2 R 13 , —OCO 2 R 13 , —N(R 13 ) 2 , —NHCH 2 CO 2 R 13 , —OCH 2 CO 2 R 13 , —SCH 2 CO 2 R 13 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)N(R 13 ) 2 , —NR 13 C( ⁇ O)R 12 , —NR 13 C( ⁇ O)R 12 , —NR
  • R 6 is selected from halogen, —CN, —NO 2 , —OH, —OR 12 , —SR 12 , —S( ⁇ O)R 12 , —S( ⁇ O) 2 R 12 , —NHS( ⁇ O) 2 R 12 , —N(C 1 -C 6 alkyl)S( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —C( ⁇ O)R 12 , —OC( ⁇ O)R 12 , —CO 2 R 13 , —OCO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)N(R 13 ) 2 , —N(C 1 -C 6 alkyl)C( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)R 12 , —N
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 heteroalkyl, a substituted or unsubstituted cycloalkyl, a substituted or unsubstituted heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, a substituted or unsubstituted —C 1 -C 4 alkyl-cycloalkyl, a substituted or unsubstituted —C 1 -C 4 alkyl-heterocycloalkyl, a substituted or unsubstituted —C 1 -C 4 alkyl-aryl, a substituted or unsubstituted —C 1 -C 4 alkyl-heteroaryl, —C 1 -C 6 alkylene-O—R 17 , —C 1 -C 6 alkylene-N
  • R 10 is —C( ⁇ O)R 14 , —C( ⁇ O)OR 15 , or —C( ⁇ O)N(R 16 ) 2 .
  • R 10 is —C( ⁇ O)R 14 , —C( ⁇ O)OR 15 , or —C( ⁇ O)N(R 16 ) 2 ;
  • R 14 is C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, a substituted or unsubstituted C 3 -C 10 cycloalkyl, a substituted or unsubstituted heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, a substituted or unsubstituted —C 1 -C 4 alkyl-cycloalkyl, a substituted or unsubstituted —C 1 -C 4 alkyl-heterocycloalkyl, a substituted or unsubstituted —C 1 -C 4 alkyl-aryl or a substituted or unsubstituted —C
  • R 14 is —C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, a substituted or unsubstituted C 3 -C 10 cycloalkyl, a substituted or unsubstituted heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, a substituted or unsubstituted —C 1 -C 4 alkyl-cycloalkyl, a substituted or unsubstituted —C 1 -C 4 alkyl-heterocycloalkyl, a substituted or unsubstituted —C 1 -C 4 alkyl-aryl or a substituted or unsubstituted —C 1 -C 4 alkyl-heteroaryl.
  • R 14 is C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, a substituted or unsubstituted C 3 -C 10 cycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, a substituted or unsubstituted —C 1 -C 4 alkyl-aryl or a substituted or unsubstituted —C 1 -C 4 alkyl-heteroaryl.
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 heteroalkyl.
  • R 11 is C 1 -C 6 alkyl, or C 1 -C 6 haloalkyl.
  • R 10 is —C( ⁇ O)R 14 , —C( ⁇ O)OR 15 , or —C( ⁇ O)N(R 16 ) 2 ;
  • R 14 is C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, or a C 3 -C 6 cycloalkyl;
  • R 15 is C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, or a C 3 -C 6 cycloalkyl;
  • each R 16 is independently H, C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 heteroalkyl, or a C 3 -C 6 cycloalkyl; or two R 16 groups attached to the same N atom are taken together with the N atom to which they are attached to form an optionally substituted heterocycloalkyl;
  • R 11
  • R 11 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, or C 1 -C 6 heteroalkyl.
  • R 11 is C 1 -C 6 alkyl, or a C 1 -C 6 haloalkyl.
  • R 10 is —C( ⁇ O)R 14 , —C( ⁇ O)OR 15 , or —C( ⁇ O)N(R 16 ) 2 ;
  • R 14 is a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, a substituted or unsubstituted —C 1 -C 4 alkyl-aryl or a substituted or unsubstituted —C 1 -C 4 alkyl-heteroaryl; or R 14 is -L 3 -X 3 -Q 3 ;
  • L 3 is a C 1 -C 6 alkylene or a substituted or unsubstituted aryl;
  • X 3 is a bond, —O—, —S—, —S( ⁇ O)—, —S( ⁇ O) 2 —, —NR 13 S( ⁇ O) 2 —, or —NR 13 —;
  • Q 3 is a substituted or un
  • R 14 is a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, a substituted or unsubstituted —C 1 -C 4 alkyl-aryl or a substituted or unsubstituted —C 1 -C 4 alkyl-heteroaryl;
  • R 15 is a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, a substituted or unsubstituted —C 1 -C 4 alkyl-aryl, or a substituted or unsubstituted —C 1 -C 4 alkyl-heteroaryl;
  • each R 16 is independently H, C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, a substituted or unsubstituted —
  • R 6 is selected from halogen, —CN, —NO 2 , —OH, — 0 R 12 , —S( ⁇ O) 2 R 12 , —NHS( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —CO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)N(R 13 ) 2 , —N(C 1 -C 6 alkyl)C( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)R 12 , —N(C 1 -C 6 alkyl)C( ⁇ O)R 12 , —NHC 1 -C 4 alkyl-C( ⁇ O)R 12 , —C 1 -C 4 alkyl-N(R 13 ) 2 , —C 1 -C
  • R 6 is selected from —NHS( ⁇ O) 2 R 12 , —S( ⁇ O) 2 N(R 13 ) 2 , —CO 2 R 13 , —N(R 13 ) 2 , —C( ⁇ O)N(R 13 ) 2 , —OC( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)N(R 13 ) 2 , —N(C 1 -C 6 alkyl)C( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)R 12 , —N(C 1 -C 6 alkyl)C( ⁇ O)R 12 , —NHC 1 -C 4 alkyl-C( ⁇ O)R 12 , —C 1 -C 4 alkyl-N(R 13 ) 2 , —NHC( ⁇ O)OR 12 , —N(C 1 -C 6 alkyl)C( ⁇ O)OR 12 .
  • R 6 is —NO 2 , —N(C 1 -C 4 alkyl)S( ⁇ O) 2 R 12 , —NHS( ⁇ O) 2 R 12 , —N(R 13 ) 2 , —N(C 1 -C 4 alkyl)C( ⁇ O)N(R 13 ) 2 , —NHC( ⁇ O)N(R 13 ) 2 , —N(C 1 -C 4 alkyl)C( ⁇ O)R 12 , —NHC( ⁇ O)R 12 , —NH—C 1 -C 4 alkyl-C( ⁇ O)R 12 , —N(C 1 -C 4 alkyl)C( ⁇ O)OR 12 , or —NHC( ⁇ O)OR 12 .
  • R 6 is F, Cl, Br, I, —CN, —NO 2 , —OH—CH 3 , —CH 2 CH 3 , i-propyl, -tert-butyl, —CF 3 , —CH 2 CF 3 , —OCH 3 , —OCHF 2 , —OCF 3 , —S( ⁇ O) 2 (C 1 -C 6 alkyl), —S( ⁇ O) 2 (substituted or unsubstituted phenyl), —C( ⁇ O)—(C 1 -C 6 alkyl), —C( ⁇ O)-(substituted or unsubstituted phenyl), —C( ⁇ O)-(substituted or unsubstituted heteroaryl containing 0-3 N atoms), —C( ⁇ O)-(substituted or unsubstituted C 2 -C 10 heterocycloalkyl), —C( ⁇ O)
  • R 6 is Cl, Br, —CF 3 , —CH 3 , NO 2 , —NH 2 , —CO 2 H, —CO 2 CH 3 , —CO 2 CH 2 CH 3 , —SO 2 CH 3 , —SO 2 CH 2 CH 3 , —C( ⁇ O)CH 3 , —C( ⁇ O)CH 3 CH 3 , —C( ⁇ O)CH(CH 3 ) 2 , —C( ⁇ O)(CH 3 ) 3 , —C( ⁇ O)CH 2 (CH 3 ) 3 , —C( ⁇ O)NHCH 3 , —C( ⁇ O)NHCH 2 CH 3 ,
  • cyclopentyl cyclohexyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, thiomorpholinyl.
  • R 10 is —C( ⁇ O)R 14 .
  • R 10 is —C( ⁇ O)OR 15 .
  • R 10 is —C( ⁇ O)N(R 16 ) 2 .
  • ring A is selected from:
  • R 1 is as defined in Table 1.
  • R 11 is as defined in Table 1.
  • R 10 is as defined in Table 1.
  • R 6 is as defined in Table 1.
  • a 1 is as defined in Table 1.
  • a 2 is as defined in Table 1.
  • a 3 is as defined in Table 1.
  • a 4 is as defined in Table 1.
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) include, but are not limited to, those described in Table 1:
  • the starting material used for the synthesis of the compounds of Formula (I) described in the prior section are either synthesized or obtained from commercial sources, such as, but not limited to, Aldrich Chemical Co. (Milwaukee, Wis.), or Sigma Chemical Co. (St. Louis, Mo.).
  • the compounds described herein, and other related compounds having different substituents are synthesized using known techniques and materials, including those found in March, A DVANCED O RGANIC C HEMISTRY 4 th Ed., (Wiley 1992); Carey and Sundberg, A DVANCED O RGANIC C HEMISTRY 4 th Ed., Vols.
  • 2-halo-benzaldehydes such as 2-bromobenzaldehydes of structure I are reacted with amines of structure II under reductive amination conditions to provide secondary amines of structure III. Secondary amines of structure III are then reacted with acid chlorides, chloroformates, isocyantes, sulfonylchlorides and the like, to provide 2-bromobenzylamines of structure V.
  • amines of structure III are reacted with, but not limited to, a carboxylic acid and coupling reagent such as EDC, DCC, BOP, HATU or the like, or a carboxylic acid activated ester or an acid halide, alkylchloroformates, arylchloroformates, benzylchloroformates, alkylisocyanates, benzylisocyanates, arylisocyanates, alkylsulfonyl chlorides, arylsulfonyl chlorides, heteroarylsulfonyl chlorides, or the like in dichloromethane, dichloroethane, tetrahydrofuran, dimethoxyethane or the like in the presence of a hindered base such as triethylamine, diisopropylethylamine, N-methylmorpholine, pyridine or the like, to afford compounds of structure V.
  • 2-Bromobenzylamines of structure V are converted to boronic esters of structure VI via metal-mediated reactions with boranes.
  • Other methods of borylation are known, including but not limited to the Miyaura borylation reaction and other magnesium, lithium, copper, irridium and palladium mediated reactions of triflates or halides with boranes (T. Ishiyama, et al., J. Org. Chem., 1995, 60, 7508-7510; X.-J. Wang, et al., Org. Lett., 2006, 8, 305-307; M. Murata, et al., Synlett, 2006, 1867-1870; W. Zhu, D. Ma, Org. Lett., 2006, 8, 261-263).
  • Boronic esters of structure VI are coupled to halogen containing heteroaryl compounds of structure VII under palladium mediated coupling conditions to provide esters of structure VIII.
  • Other metal mediated coupling reactions to form phenyl-heteroaryl compounds of structure VIII include, but are not limited to Suzuki reactions, Stille cross couplings, Negishi couplings, Kumada couplings, Ullmann reactions, Hiyama Coupling, and variants thereof (Metal-Catalyzed Cross-Coupling Reactions, Armin de Meijere (Editor), François Diederich (Editor), John Wiley & Sons; 2nd edition, 2004; ⁇ zdemir, et al., Tetrahedron, 2005, 61, 9791-9798; Ackermann, et al., Org.
  • ester group of amides of structure VIII is then hydrolyzed to form carboxylic acid compounds of structure IX.
  • amides of structure XII are prepared as outlined in Scheme 2.
  • benzylamines of structure III are reacted with acid chlorides to provide amides of structure X.
  • Amides of structure X are used in the synthesis of compounds of Formula (I) as outlined in Scheme 1.
  • benzylamines (compounds of structure V) are treated with phosgene or a phosgene equivalent, such as, for example, trichloromethyl chloroformate or carbonyldiimidazole, to yield an intermediate, which is then treated with a hydroxy containing compound R 15 —OH to provide carbamates of structure XIII.
  • phosgene or a phosgene equivalent such as, for example, trichloromethyl chloroformate or carbonyldiimidazole
  • ureas of structure XVIII are prepared as depicted in Scheme 4:
  • ureas include the following procedures: C. Han, J. A. Porco, Jr, Org. Lett., 2007, 9, 1517-1520; H. Lebel, O. Leogane, Org. Lett., 2006, 8, 5717-5720; M. B. Bertrand, J. P. Wolfe, Tetrahedron, 2005, 61, 6447-6459; M. McLaughlin, M. Palucki, I. W. Davies, Org. Lett., 2006, 8, 3311-3314; J. A. Fritz, et al., Org.
  • sulfonamides of structure XXI are prepared as depicted in Scheme 5:
  • 2-bromobenzaldehydes of structure I are converted to boronic esters of structure XXII via palladium metal-mediated reactions with boranes.
  • Boronic esters of structure XXII are coupled with halogen containing heteroaryl compounds of structure VII under palladium mediated coupling conditions to provide phenyl-heteroaryl compounds of structure XXIII.
  • Other metal mediated coupling reactions to form phenyl-heteroaryl compounds are known in the art.
  • the aldehyde group of the phenyl-heteroaryl compounds of structure XXIII are reacted with amines (i.e.
  • metal mediated coupling reactions may be used to introduce other groups at R 6 .
  • Metal mediated coupling reactions include, but are not limited to Suzuki reactions, Stille cross couplings, Negishi couplings, Kumada couplings, Ullmann reactions, Hiyama Coupling, and variants thereof (Metal-Catalyzed Cross-Coupling Reactions, Armin de Meijere (Editor), Veronica Diederich (Editor), John Wiley & Sons; 2nd edition, 2004; ⁇ zdemir, et al., Tetrahedron, 2005, 61, 9791-9798; Ackermann, et al., Org.
  • R 6 in any of Schemes 1 to 8 is a nitro group (—NO 2 ).
  • Reduction of the nitro group provides the amine (i.e. R 6 is —NH 2 ).
  • Typical reaction conditions for the reduction of nitro groups include treatment of the nitro compound with iron trichloride in the presence of hydrazine.
  • Other reaction conditions exist for the reduction of nitrobenzenes to anilines such as, but not limited to, catalytic hydrogenation using palladium-on-carbon (Bavin, P. M. G. (1973). Org. Synth.; Coll. Vol. 5: 30), platinum oxide, or Raney nickel (Allen, C. F. H.; VanAllan, J. (1955)). Org. Synth.; Coll. Vol.
  • R 6 is —NHC( ⁇ O)R 12 ); (2) reacted with chloroformates to provide carbamates (i.e. R 6 is —NHC( ⁇ O)OR 12 ); (3) reacted with isocyanates to provide ureas (i.e. R 6 is —NHC( ⁇ O)N(R 13 ) 2 ; (4) reacted with sulfonyl chlorides to provide sulfonamides (i.e. R 6 is —SO 2 R 12 ); or reacted with a variety of other electrophiles to provide derivatized amino groups.
  • acetic acid moiety of compounds of Formula (I) are introduced using the chemistry outlined in Scheme 7.
  • Phenyl-heteroaryl compounds of structure XXV that contain a halide are coupled with trimethylsilylacetylene in the presence of a palladium catalyst and a copper co-catalyst to provide acetylene compounds of structure XXVI.
  • Hydroboration of acetylene compounds of structure XXVI is followed by treatment with sodium hydroxide and hydrogen peroxide to provide the compounds of Formula (I).
  • benzyl halides of structure XXVII are reacted with heterocycles of structure XXVIII to form benzyl heterocycles of structure XXIX.
  • Boronate compounds of structure XXX are reacted with bromo heterocycles of structure VII under palladium mediated coupling conditions to form phenyl-heteroaryl compounds of structure XXXI.
  • the ester group of the phenyl-heteroaryl compounds of structure XXXI is then hydrolyzed to form carboxylic acid compounds of structure XXXII.
  • Each R13 in Scheme 8 is independently defined as described herein.
  • each of A 1 , A 2 , A 3 and A 4 are independently selected from N,N(—O) and C(R A ). It will be understood that the preceding Schemes are applicable to cases where ring A is as defined herein.
  • compounds of Formula (I) are synthesized as outlined in the Examples.
  • the compounds described herein are modified using various electrophiles or nucleophiles to form new functional groups or substituents.
  • Table 4 entitled “Examples of Covalent Linkages and Precursors Thereof” lists selected, non-limiting examples of covalent linkages and precursor functional groups that are used to prepare the modified compounds. Precursor functional groups are shown as electrophilic groups and nucleophilic groups.
  • protective groups are used to block some or all reactive moieties and prevent such groups from participating in chemical reactions until the protective group is removed.
  • each protective group is removable by a different means.
  • Protective groups that are cleaved under totally disparate reaction conditions fulfill the requirement of differential removal.
  • protective groups are removed by acid, base, and/or hydrogenolysis.
  • Groups such as trityl, dimethoxytrityl, acetal and t-butyldimethylsilyl are acid labile and are used in certain embodiments to protect carboxy and hydroxy reactive moieties in the presence of amino groups protected with Cbz groups, which are removable by hydrogenolysis, and/or Fmoc groups, which are base labile.
  • carboxylic acid and hydroxy reactive moieties are blocked with base labile groups such as, but not limited to, methyl, ethyl, and acetyl in the presence of amines blocked with acid labile groups such as t-butyl carbamate or with carbamates that are both acid and base stable but hydrolytically removable.
  • carboxylic acid and hydroxy reactive moieties are blocked with hydrolytically removable protective groups such as the benzyl group, while amine groups capable of hydrogen bonding with acids are blocked with base labile groups such as Fmoc.
  • carboxylic acid reactive moieties are protected by conversion to simple ester compounds as exemplified herein, or they are, in yet another embodiment, blocked with oxidatively-removable protective groups such as 2,4-dimethoxybenzyl, while co-existing amino groups are blocked with fluoride labile silyl carbamates.
  • Allyl blocking groups are useful in the presence of acid- and base-protecting groups since the former are stable and can be subsequently removed by metal or pi-acid catalysts.
  • an allyl-blocked carboxylic acid can be deprotected with a Pd(0)-catalyzed reaction in the presence of acid labile t-butyl carbamate or base-labile acetate amine protecting groups.
  • Yet another form of protecting group is a resin to which a compound or intermediate is attached. As long as the residue is attached to the resin, that functional group is blocked and cannot react. Once released from the resin, the functional group is available to react.
  • blocking/protecting groups are, by way of example only:
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are prepared as a pharmaceutically acceptable acid addition salt (which is a type of a pharmaceutically acceptable salt) by reacting the free base form of the compound with a pharmaceutically acceptable inorganic or organic acid, including, but not limited to, inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid metaphosphoric acid, and the like; and organic acids such as acetic acid, propionic acid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, p-toluenesulfonic acid, tartaric acid, trifluoroacetic acid, citric acid, benzoic acid, 3-(4-hydroxybenzoyl)benzoic acid, cinnamic acid, mande
  • pharmaceutically acceptable refers to a material, such as a carrier or diluent, which does not abrogate the biological activity or properties of the compound, and is relatively nontoxic, i.e., the material may be administered to an individual without causing undesirable biological effects or interacting in a deleterious manner with any of the components of the composition in which it is contained.
  • pharmaceutically acceptable salt refers to a formulation of a compound that does not cause significant irritation to an organism to which it is administered and does not abrogate the biological activity and properties of the compound.
  • pharmaceutically acceptable salts are obtained by reacting a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) with acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like.
  • Pharmaceutically acceptable salts are also obtained by reacting a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) with a base to form a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, and salts with amino acids such as arginine, lysine, and the like.
  • a salt such as an ammonium salt, an alkali metal salt, such as a sodium or a potassium salt, an alkaline earth metal salt, such as a calcium or a magnesium salt, a salt of organic bases such as dicyclohexylamine, N-methyl-D-glucamine, tris(hydroxymethyl)methylamine, and salts with amino acids such as arginine, lysine, and
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are prepared as a pharmaceutically acceptable salts by reacting the free acid form of the compound with a pharmaceutically acceptable inorganic or organic base, including, but not limited to organic bases such as ethanolamine, diethanolamine, triethanolamine, tromethamine, N-methylglucamine, and the like, or with an inorganic base such as aluminum hydroxide, calcium hydroxide, potassium hydroxide, sodium carbonate, sodium hydroxide, and the like.
  • organic bases such as ethanolamine, diethanolamine, triethanolamine, tromethamine, N-methylglucamine, and the like
  • an inorganic base such as aluminum hydroxide, calcium hydroxide, potassium hydroxide, sodium carbonate, sodium hydroxide, and the like.
  • a reference to a pharmaceutically acceptable salt includes the solvent addition forms or crystal forms thereof, particularly solvates or polymorphs.
  • Solvates contain either stoichiometric or non-stoichiometric amounts of a solvent, and are optionally formed during the process of crystallization with pharmaceutically acceptable solvents such as water, ethanol, and the like. Hydrates are formed when the solvent is water, or alcoholates are formed when the solvent is alcohol.
  • Solvates of compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are conveniently prepared or formed during the processes described herein.
  • hydrates of compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are conveniently prepared by recrystallization from an aqueous/organic solvent mixture, using organic solvents including, but not limited to, dioxane, tetrahydrofuran, ethanol, or methanol.
  • organic solvents including, but not limited to, dioxane, tetrahydrofuran, ethanol, or methanol.
  • the compounds provided herein can exist in unsolvated as well as solvated forms. In general, the solvated forms are considered equivalent to the unsolvated forms for the purposes of the compounds and methods provided herein.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are prepared in various forms, including but not limited to, amorphous forms, milled forms and nano-particulate forms.
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) include crystalline forms, also known as polymorphs.
  • Polymorphs include the different crystal packing arrangements of the same elemental composition of a compound. Polymorphs usually have different X-ray diffraction patterns, infrared spectra, melting points, density, hardness, crystal shape, optical and electrical properties, stability, and solubility. Various factors such as the recrystallization solvent, rate of crystallization, and storage temperature may cause a single crystal form to dominate.
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are prepared as prodrugs.
  • a “prodrug” refers to an agent that is converted into the parent drug in vivo. Prodrugs are often useful because, in some situations, they may be easier to administer than the parent drug. They may, for instance, be bioavailable by oral administration whereas the parent is not. The prodrug may also have improved solubility in pharmaceutical compositions over the parent drug.
  • prodrug a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) which is administered as an ester (the “prodrug”) to facilitate transmittal across a cell membrane where water solubility is detrimental to mobility but which then is metabolically hydrolyzed to the carboxylic acid, the active entity, once inside the cell where water-solubility is beneficial.
  • prodrug a short peptide (polyaminoacid) bonded to an acid group where the peptide is metabolized to reveal the active moiety.
  • Prodrugs are generally drug precursors that, following administration to a subject and subsequent absorption, are converted to an active, or a more active species via some process, such as conversion by a metabolic pathway. Some prodrugs have a chemical group present on the prodrug that renders it less active and/or confers solubility or some other property to the drug. Once the chemical group has been cleaved and/or modified from the prodrug the active drug is generated. Prodrugs are often useful because, in some situations, they are easier to administer than the parent drug. In certain embodiments, the prodrug of a compound described herein is bioavailable by oral administration whereas the parent is not. Furthermore, in some embodiments, the prodrug of a compound described herein has improved solubility in pharmaceutical compositions over the parent drug.
  • prodrugs are designed as reversible drug derivatives, for use as modifiers to enhance drug transport to site-specific tissues.
  • the design of prodrugs to date is to increase the effective water solubility of the therapeutic compound for targeting to regions where water is the principal solvent.
  • prodrug derivatives of compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are prepared, if desired (e.g., for further details see Saulnier et al., (1994), Bioorganic and Medicinal Chemistry Letters , Vol. 4, p. 1985).
  • appropriate prodrugs are prepared by reacting a non-derivatized compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) with a suitable carbamylating agent, such as, but not limited to, 1,1-acyloxyalkylcarbanochloridate, para-nitrophenyl carbonate, or the like.
  • Prodrug forms of the herein described compounds, wherein the prodrug is metabolized in vivo to produce a derivative as set forth herein are included within the scope of the claims. Indeed, some of the herein-described compounds are a prodrug for another derivative or active compound.
  • sites on the aromatic ring portion of compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are susceptible to various metabolic reactions Therefore incorporation of appropriate substituents on the aromatic ring structures will reduce, minimize or eliminate this metabolic pathway.
  • the appropriate substituent to decrease or eliminate the susceptibility of the aromatic ring to metabolic reactions is, by way of example only, a halogen, or an alkyl group.
  • the compounds described herein are labeled isotopically (e.g. with a radioisotope) or by another other means, including, but not limited to, the use of chromophores or fluorescent moieties, bioluminescent labels, or chemiluminescent labels.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) possess one or more stereocenters and each center exists independently in either the R or S configuration.
  • the compounds presented herein include all diastereomeric, enantiomeric, and epimeric forms as well as the appropriate mixtures thereof.
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are prepared as their individual stereoisomers by reacting a racemic mixture of the compound with an optically active resolving agent to form a pair of diastereoisomeric compounds, separating the diastereomers and recovering the optically pure enantiomers.
  • resolution of enantiomers is carried out using covalent diastereomeric derivatives of the compounds described herein.
  • dissociable complexes are utilized (e.g., crystalline diastereomeric salts).
  • Diastereomers have distinct physical properties (e.g., melting points, boiling points, solubilities, reactivity, etc.) and are, in specific embodiments, separated by taking advantage of these dissimilarities.
  • the diastereomers are separated by chiral chromatography or by separation/resolution techniques based upon differences in solubility.
  • the optically pure enantiomer is then recovered, along with the resolving agent, by any practical means that does not result in racemization. Jean Jacques, Andre Collet, Samuel H. Wilen, “Enantiomers, Racemates and Resolutions”, John Wiley and Sons, Inc., 1981.
  • the compounds provided herein exist as geometric isomers.
  • the compounds and methods provided herein include all cis, trans, syn, anti,
  • E
  • Z
  • the compounds described herein exist as tautomers. All tautomers are intended to be within the scope of the molecular formulas described herein.
  • mixtures of enantiomers and/or diastereoisomers, resulting from a single preparative step, combination, or interconversion are envisioned.
  • alkyl refers to an aliphatic hydrocarbon group.
  • the alkyl moiety may be a saturated alkyl group (which means that it does not contain any units of unsaturation, e.g. carbon-carbon double bonds or carbon-carbon triple bonds) or the alkyl moiety may be an unsaturated alkyl group (which means that it contains at least one unit of unsaturation).
  • the alkyl moiety, whether saturated or unsaturated, may be branched, straight chain, or include a cyclic portion. The point of attachment of an alkyl is at a carbon atom that is not part of a ring.
  • alkyl moiety may have 1 to 10 carbon atoms (whenever it appears herein, a numerical range such as “1 to 10” refers to each integer in the given range; e.g., “1 to 10 carbon atoms” means that the alkyl group may consist of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc., up to and including 10 carbon atoms, although the present definition also covers the occurrence of the term “alkyl” where no numerical range is designated).
  • the alkyl group of the compounds described herein may be designated as “C 1 -C 6 alkyl” or similar designations.
  • C 1 -C 6 alkyl indicates that there are one, two, three, four, five, or six carbon atoms in the alkyl chain, i.e., the alkyl chain is selected from the group consisting of methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, and t-butyl.
  • Typical alkyl groups include, but are in no way limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tertiary butyl, pentyl, neopentyl, hexyl, allyl, but-2-enyl, but-3-enyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, and the like.
  • an alkyl is a C 1 -C 6 alkyl.
  • alkoxy refers to a (alkyl)O— group, where alkyl is as defined herein.
  • An “amide” is a chemical moiety with formula —C( ⁇ O)NHR or —NHC( ⁇ O)R, where R is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl (bonded through a ring carbon) and heteroalicyclic (bonded through a ring carbon).
  • An amide may be an amino acid or a peptide molecule attached to a compound of Formula (I), thereby forming a prodrug. Any amine, or carboxyl side chain on the compounds described herein is optionally amidified, as desired. See, e.g., Greene and Wuts, Protective Groups in Organic Synthesis, 3 rd Ed., John Wiley & Sons, New York, N.Y., 1999, is incorporated herein by reference for such disclosure.
  • aromatic refers to a planar ring having a delocalized ⁇ -electron system containing 4n+2 ⁇ electrons, where n is an integer. Aromatic rings can be formed from five, six, seven, eight, nine, ten, or more than ten atoms. Aromatics are optionally substituted.
  • aromatic includes both carbocyclic aryl (“aryl”, e.g., phenyl) and heterocyclic aryl (or “heteroaryl” or “heteroaromatic”) groups (e.g., pyridine).
  • aryl e.g., phenyl
  • heterocyclic aryl or “heteroaryl” or “heteroaromatic” groups
  • pyridine monocyclic or fused-ring polycyclic (i.e., rings which share adjacent pairs of carbon atoms) groups.
  • Carbocyclic refers to a ring or ring system where the atoms forming the backbone of the ring are all carbon atoms. The term thus distinguishes carbocyclic from heterocyclic rings in which the ring backbone contains at least one atom which is different from carbon.
  • aryl refers to an aromatic ring wherein each of the atoms forming the ring is a carbon atom.
  • Aryl rings are formed by five, six, seven, eight, nine, or more than nine carbon atoms.
  • Aryl groups are optionally substituted.
  • an aryl is a phenyl or a naphthalenyl.
  • an aryl group can be a monoradical or a diradical (i.e., an arylene group).
  • an aryl is a C 6 -C 10 aryl.
  • cycloalkyl refers to a monocyclic or polycyclic aliphatic, non-aromatic radical, wherein each of the atoms forming the ring (i.e. skeletal atoms) is a carbon atom. Cycloalkyls may be saturated, or partially unsaturated. Cycloalkyls may be fused with an aromatic ring, and the point of attachment is at a carbon that is not an aromatic ring carbon atom. Cycloalkyl groups include groups having from 3 to 10 ring atoms. Illustrative examples of cycloalkyl groups include, but are not limited to, the following moieties:
  • cycloalkyl groups are selected from among cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl.
  • bicyclic cycloalkyl groups are selected from among indanyl, indenyl, and 1,2,3,4-tetrahydronaphthalenyl. Cycloalkyl groups may be substituted or unsubstituted.
  • a cycloalkyl group can be a monoradical or a diradical (i.e., an cycloalkylene group, such as, but not limited to, cyclopropan-1,1-diyl, cyclobutan-1,1-diyl, cyclopentan-1,1-diyl, cyclohexan-1,1-diyl, cyclohexan-1,4-diyl, cycloheptan-1,1-diyl, and the like).
  • an cycloalkylene group such as, but not limited to, cyclopropan-1,1-diyl, cyclobutan-1,1-diyl, cyclopentan-1,1-diyl, cyclohexan-1,1-diyl, cyclohexan-1,4-diyl, cycloheptan-1,1-diyl, and the like).
  • esters refers to a chemical moiety with formula —COOR, where R is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl (bonded through a ring carbon) and heteroalicyclic (bonded through a ring carbon). Any hydroxy, or carboxyl side chain on the compounds described herein is esterified, if desired. Examples of procedures and specific groups to make such esters are found in sources such as Greene and Wuts, Protective Groups in Organic Synthesis, 3 rd Ed., John Wiley & Sons, New York, N.Y., 1999.
  • halo or, alternatively, “halogen” or “halide” means fluoro, chloro, bromo or iodo.
  • haloalkyl refers to an alkyl group in which one or more hydrogen atoms are replaced by one or more halide atoms.
  • a haloalkyl is a C 1 -C 4 haloalkyl.
  • fluoroalkyl refers to a alkyl in which one or more hydrogen atoms are replaced by a fluorine atom.
  • a fluoroalkyl is a C 1 -C 4 fluoroalkyl.
  • heteroalkyl refers to an alkyl group in which one or more skeletal atoms of the alkyl are selected from an atom other than carbon, e.g., oxygen, nitrogen, sulfur, phosphorus or combinations thereof.
  • a heteroalkyl is a C 1 -C 6 heteroalkyl.
  • heterocycle refers to heteroaromatic rings (also known as heteroaryls) and heterocycloalkyl rings (also known as heteroalicyclic groups) containing one to four heteroatoms in the ring(s), where each heteroatom in the ring(s) is selected from O, S and N, wherein each heterocyclic group has from 4 to 10 atoms in its ring system, and with the proviso that the any ring does not contain two adjacent O or S atoms.
  • Non-aromatic heterocyclic groups also known as heterocycloalkyls
  • the heterocyclic groups include benzo-fused ring systems.
  • An example of a 3-membered heterocyclic group is aziridinyl.
  • An example of a 4-membered heterocyclic group is azetidinyl.
  • An example of a 5-membered heterocyclic group is thiazolyl.
  • An example of a 6-membered heterocyclic group is pyridyl, and an example of a 10-membered heterocyclic group is quinolinyl.
  • non-aromatic heterocyclic groups are pyrrolidinyl, tetrahydrofuranyl, dihydrofuranyl, tetrahydrothienyl, oxazolidinonyl, tetrahydropyranyl, dihydropyranyl, tetrahydrothiopyranyl, piperidinyl, morpholinyl, thiomorpholinyl, thioxanyl, piperazinyl, aziridinyl, azetidinyl, oxetanyl, thietanyl, homopiperidinyl, oxepanyl, thiepanyl, oxazepinyl, diazepinyl, thiazepinyl, 1,2,3,6-tetrahydropyridinyl, pyrrolin-2-yl, pyrrolin-3-yl, indolinyl, 2H-pyranyl, 4H-pyranyl, dioxanyl,
  • aromatic heterocyclic groups are pyridinyl, imidazolyl, pyrimidinyl, pyrazolyl, triazolyl, pyrazinyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, oxazolyl, isothiazolyl, pyrrolyl, quinolinyl, isoquinolinyl, indolyl, benzimidazolyl, benzofuranyl, cinnolinyl, indazolyl, indolizinyl, phthalazinyl, pyridazinyl, triazinyl, isoindolyl, pteridinyl, purinyl, oxadiazolyl, thiadiazolyl, furazanyl, benzofurazanyl, benzothiophenyl, benzothiazolyl, benzoxazolyl, quinazolinyl, quinox
  • the foregoing groups may be C-attached or N-attached where such is possible.
  • a group derived from pyrrole may be pyrrol-1-yl (N-attached) or pyrrol-3-yl (C-attached).
  • a group derived from imidazole may be imidazol-1-yl or imidazol-3-yl (both N-attached) or imidazol-2-yl, imidazol-4-yl or imidazol-5-yl (all C-attached).
  • the heterocyclic groups include benzo-fused ring systems. Non-aromatic heterocycles may be substituted with one or two oxo ( ⁇ O) moieties, such as pyrrolidin-2-one.
  • heteroaryl or, alternatively, “heteroaromatic” refers to an aryl group that includes one or more ring heteroatoms selected from nitrogen, oxygen and sulfur.
  • heteroaryl groups include the following moieties:
  • Monocyclic heteroaryls include pyridinyl, imidazolyl, pyrimidinyl, pyrazolyl, triazolyl, pyrazinyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, oxazolyl, isothiazolyl, pyrrolyl, pyridazinyl, triazinyl, oxadiazolyl, thiadiazolyl, and furazanyl.
  • a heteroaryl contains 0-3 N atoms.
  • a heteroaryl contains 1-3 N atoms.
  • a heteroaryl contains 0-3 N atoms, 0-1 O atoms, and 0-1 S atoms.
  • a heteroaryl is a monocyclic or bicyclic heteroaryl.
  • a heteroaryl is a C 1 -C 9 heteroaryl.
  • a heteroaryl is a C 1 -C 5 heteroaryl.
  • a heteroaryl is a C 6 -C 9 heteroaryl.
  • heterocycloalkyl or “heteroalicyclic” group refers to a cycloalkyl group that includes at least one heteroatom selected from nitrogen, oxygen and sulfur.
  • the radicals may be fused with an aryl or heteroaryl.
  • heterocycloalkyl groups also referred to as non-aromatic heterocycles, include:
  • the heterocycloalkyl is selected from oxazolidinonyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothienyl, tetrahydropyranyl, tetrahydrothiopyranyl, piperidinyl, morpholinyl, thiomorpholinyl, piperazinyl, and indolinyl.
  • the term heteroalicyclic also includes all ring forms of the carbohydrates, including but not limited to the monosaccharides, the disaccharides and the oligosaccharides.
  • a heterocycloalkyl is a C 2 -C 10 heterocycloalkyl.
  • a heterocycloalkyl is a C 4 -C 10 heterocycloalkyl. In another aspect, a heterocycloalkyl is a C 3 -C 6 heterocycloalkyl. In one aspect, a heterocycloalkyl contains 0-2 N atoms. In another aspect, a heterocycloalkyl contains 0-2 N atoms, 0-2 O atoms or 0-1 S atoms.
  • bond refers to a chemical bond between two atoms, or two moieties when the atoms joined by the bond are considered to be part of larger substructure.
  • bond when a group described herein is a bond, the referenced group is absent thereby allowing a bond to be formed between the remaining identified groups.
  • membered ring includes any cyclic structure.
  • membered is meant to denote the number of skeletal atoms that constitute the ring.
  • cyclohexyl, pyridinyl, pyranyl and thiopyranyl are 6-membered rings and cyclopentyl, pyrrolyl, furanyl, and thienyl are 5-membered rings.
  • moiety refers to a specific segment or functional group of a molecule. Chemical moieties are often recognized chemical entities embedded in or appended to a molecule.
  • carboxylic acid bioisostere refers to a functional group or moiety that exhibits similar physical and/or chemical properties as a carboxylic acid moiety.
  • a carboxylic acid bioisostere has similar biological properties to that of a carboxylic acid group.
  • a compound with a carboxylic acid moiety can have the carboxylic acid moiety exchanged with a carboxylic acid bioisostere and have similar physical and/or biological properties when compared to the carboxylic acid-containing compound.
  • a carboxylic acid bioisostere would ionize at physiological pH to roughly the same extent as a carboxylic acid group.
  • bioisoteres of a carboxylic acid include, but are not limited to,
  • optionally substituted or “substituted” means that the referenced group may be substituted with one or more additional group(s) individually and independently selected from alkyl, cycloalkyl, aryl, heteroaryl, heteroalicyclic, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, alkylsulfoxide, arylsulfoxide, alkylsulfone, arylsulfone, cyano, halo, carbonyl, thiocarbonyl, nitro, haloalkyl, fluoroalkyl, and amino, including mono- and di-substituted amino groups, and the protected derivatives thereof.
  • an optional substituents may be halide, —CN, —NO 2 , or L s R s , wherein each L s is independently selected from a bond, —O—, —C( ⁇ O)—, —C( ⁇ O)O—, —S—, —S( ⁇ O)—, —S( ⁇ O) 2 —, —NH—, —NHC( ⁇ O)—, —C( ⁇ O)NH—, S( ⁇ O) 2 NH—, —NHS( ⁇ O) 2 , —OC( ⁇ O)NH—, —NHC( ⁇ O)O—, or —(C 1 -C 6 alkyl)-; and each R s is selected from H, alkyl, fluoroalkyl, heteroalkyl, cycloalkyl, aryl, heteroaryl, or heterocycloalkyl.
  • substituents are selected from halogen, —CN, —NH 2 , —OH, —N(CH 3 ) 2 , alkyl, fluoroalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkoxy, aryloxy, alkylthio, arylthio, alkylsulfoxide, arylsulfoxide, alkylsulfone, and arylsulfone.
  • an optional substituents is halogen, —CN, —NH 2 , —OH, —NH(CH 3 ), —N(CH 3 ) 2 , alkyl, fluoroalkyl, heteroalkyl, alkoxy, —S-alkyl, or —S( ⁇ O) 2 alkyl.
  • substituted groups are substituted with one or more substituents selected from halogen, —OH, —OC 1 -C 4 alkyl, C 1 -C 4 alkyl, C 1 -C 4 heteroalkyl, C 1 -C 4 fluoroalkyl and —OC 1 -C 4 fluoroalkyl.
  • substituted groups are substituted with one or more substituents selected from F, Cl, Br, —OH, —OCH 3 , —CH 3 , and —CF 3 .
  • substituted groups are substituted with one or two of the preceding groups.
  • the protecting groups that may form the protective derivatives of the above substituents may be found in sources such as Greene and Wuts, above
  • the compounds presented herein possess one or more stereocenters and each center independently exists in either the R or S configuration.
  • the compounds presented herein include all diastereomeric, enantiomeric, and epimeric forms as well as the appropriate mixtures thereof.
  • Stereoisomers are obtained, if desired, by methods such as, the separation of stereoisomers by chiral chromatographic columns.
  • the methods and formulations described herein include the use of N-oxides (if appropriate), crystalline forms (also known as polymorphs), or pharmaceutically acceptable salts of compounds having the structure of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V), as well as active metabolites of these compounds having the same type of activity.
  • compounds may exist as tautomers. All tautomers are included within the scope of the compounds presented herein.
  • the compounds described herein exist in solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like. In other embodiments, the compounds described herein exist in unsolvated form.
  • module means to interact with a target either directly or indirectly so as to alter the activity of the target, including, by way of example only, to enhance the activity of the target, to inhibit the activity of the target, to limit the activity of the target, or to extend the activity of the target.
  • modulator refers to a molecule that interacts with a target either directly or indirectly.
  • the interactions include, but are not limited to, the interactions of an agonist, partial agonist, an inverse agonist and antagonist.
  • a modulator is an antagonist.
  • agonist refers to a molecule such as a compound, a drug, an enzyme activator or a hormone modulator that binds to a specific receptor and triggers a response in the cell.
  • An agonist mimics the action of an endogenous ligand (such as prostaglandin, hormone or neurotransmitter) that binds to the same receptor.
  • Antagonist refers to a molecule such as a compound, which diminishes, inhibits, or prevents the action of another molecule or the activity of a receptor site. Antagonists include, but are not limited to, competitive antagonists, non-competitive antagonists, uncompetitive antagonists, partial agonists and inverse agonists.
  • Non-competitive antagonists also known as allosteric antagonists
  • Non-competitive antagonists do not compete with agonists for binding.
  • the bound antagonists may result in a decreased affinity of an agonist for that receptor, or alternatively may prevent conformational changes in the receptor required for receptor activation after the agonist binds.
  • Uncompetitive antagonists differ from non-competitive antagonists in that they require receptor activation by an agonist before they can bind to a separate allosteric binding site.
  • Partial agonists are defined as drugs which, at a given receptor, might differ in the amplitude of the functional response that they elicit after maximal receptor occupancy. Although they are agonists, partial agonists can act as a competitive antagonist if co-administered with a full agonist, as it competes with the full agonist for receptor occupancy and producing a net decrease in the receptor activation observed with the full agonist alone.
  • An inverse agonist can have effects similar to an antagonist, but causes a distinct set of downstream biological responses.
  • Constitutively active receptors which exhibit intrinsic or basal activity can have inverse agonists, which not only block the effects of binding agonists like a classical antagonist, but inhibit the basal activity of the receptor.
  • PGD 2 -dependent refers to conditions or disorders that would not occur, or would not occur to the same extent, in the absence of PGD 2 .
  • PGD 2 -mediated refers to refers to conditions or disorders that might occur in the absence of PGD 2 but can occur in the presence of PGD 2 .
  • asthma refers to any disorder of the lungs characterized by variations in pulmonary gas flow associated with airway constriction of whatever cause (intrinsic, extrinsic, or both; allergic or non-allergic).
  • the term asthma may be used with one or more adjectives to indicate cause.
  • rhinitis refers to any disorder of the nose in which there is inflammation of the mucous lining of the nose by whatever cause (intrinsic, extrinsic or both; allergic or non-allergic).
  • bone disease refers to a disease or condition of the bone, including, but not limited to, inapproriate bone remodeling, loss or gain, osteopenia, osteomalacia, osteofibrosis, and Paget's disease.
  • cardiovascular disease refers to diseases affecting the heart or blood vessels or both, including but not limited to: arrhythmia (atrial or ventricular or both); atherosclerosis and its sequelae; angina; cardiac rhythm disturbances; myocardial ischemia; myocardial infarction; cardiac or vascular aneurysm; vasculitis, stroke; peripheral obstructive arteriopathy of a limb, an organ, or a tissue; reperfusion injury following ischemia of the brain, heart or other organ or tissue; endotoxic, surgical, or traumatic shock; hypertension, valvular heart disease, heart failure, abnormal blood pressure; shock; vasoconstriction (including that associated with migraines); vascular abnormality, inflammation, insufficiency limited to a single organ or tissue.
  • arrhythmia atrial or ventricular or both
  • atherosclerosis and its sequelae angina
  • cardiac rhythm disturbances myocardial ischemia
  • myocardial infarction myocardial infarction
  • cancer refers to an abnormal growth of cells which tend to proliferate in an uncontrolled way and, in some cases, to metastasize (spread).
  • types of cancer include, but is not limited to, solid tumors (such as those of the bladder, bowel, brain, breast, endometrium, heart, kidney, lung, lymphatic tissue (lymphoma), ovary, pancreas or other endocrine organ (thyroid), prostate, skin (melanoma) or hematological tumors (such as the leukemias).
  • carrier refers to relatively nontoxic chemical compounds or agents that facilitate the incorporation of a compound into cells or tissues.
  • co-administration are meant to encompass administration of the selected therapeutic agents to a single patient, and are intended to include treatment regimens in which the agents are administered by the same or different route of administration or at the same or different time.
  • dermatological disorder refers to a skin disorder.
  • dermatological disorders include, but are not limited to, proliferative or inflammatory disorders of the skin such as, atopic dermatitis, bullous disorders, collagenoses, contact dermatitis eczema, Kawasaki Disease, rosacea, Sjogren-Larsso Syndrome, urticaria.
  • dilute refers to chemical compounds that are used to dilute the compound of interest prior to delivery. Diluents can also be used to stabilize compounds because they can provide a more stable environment. Salts dissolved in buffered solutions (which also can provide pH control or maintenance) are utilized as diluents in the art, including, but not limited to a phosphate buffered saline solution.
  • an “effective amount” or “therapeutically effective amount,” as used herein, refer to a sufficient amount of an agent or a compound being administered which will relieve to some extent one or more of the symptoms of the disease or condition being treated. The result can be reduction and/or alleviation of the signs, symptoms, or causes of a disease, or any other desired alteration of a biological system.
  • an “effective amount” for therapeutic uses is the amount of the composition comprising a compound as disclosed herein required to provide a clinically significant decrease in disease symptoms.
  • An appropriate “effective” amount in any individual case may be determined using techniques, such as a dose escalation study.
  • an “enhance” or “enhancing,” as used herein, means to increase or prolong either in potency or duration a desired effect.
  • the term “enhancing” refers to the ability to increase or prolong, either in potency or duration, the effect of other therapeutic agents on a system.
  • An “enhancing-effective amount,” as used herein, refers to an amount adequate to enhance the effect of another therapeutic agent in a desired system.
  • fibrosis refers to conditions that follow acute or chronic inflammation and are associated with the abnormal accumulation of cells and/or collagen and include but are not limited to fibrosis of individual organs or tissues such as the heart, kidney, joints, lung, or skin, and includes such disorders as idiopathic pulmonary fibrosis and cryptogenic fibrosing alveolitis.
  • iatrogenic means a PGD 2 -dependent or PGD 2 -mediated condition, disorder, or disease created or worsened by medical or surgical therapy.
  • inflammation disorders refers to those diseases or conditions that are characterized by one or more of the signs of pain, heat, redness, swelling, and loss of function (temporary or permanent). Inflammation takes many forms and includes, but is not limited to, inflammation that is one or more of the following: acute, adhesive, atrophic, catarrhal, chronic, cirrhotic, diffuse, disseminated, exudative, fibrinous, fibrosing, focal, granulomatous, hyperplastic, hypertrophic, interstitial, metastatic, necrotic, obliterative, parenchymatous, plastic, productive, proliferous, pseudomembranous, purulent, sclerosing, seroplastic, serous, simple, specific, subacute, suppurative, toxic, traumatic, and/or ulcerative.
  • Inflammatory disorders further include, without being limited to those affecting the blood vessels (polyarteritis, temporal arteritis); joints (arthritis: crystalline, osteo-, psoriatic, reactive, rheumatoid, Reiter's); gastrointestinal tract (colitis); skin (dermatitis); or multiple organs and tissues (systemic lupus erythematosus).
  • immunological disorders refers to those diseases or conditions that are characterized by inappropriate or deleterious response to an endogenous or exogenous antigen that may result in cellular dysfunction or destruction and consequently dysfunction or destruction of an organ or tissue and which may or may not be accompanied by signs or symptoms of inflammation.
  • a “metabolite” of a compound disclosed herein is a derivative of that compound that is formed when the compound is metabolized.
  • active metabolite refers to a biologically active derivative of a compound that is formed when the compound is metabolized.
  • metabolized refers to the sum of the processes (including, but not limited to, hydrolysis reactions and reactions catalyzed by enzymes) by which a particular substance is changed by an organism. Thus, enzymes may produce specific structural alterations to a compound.
  • cytochrome P450 catalyzes a variety of oxidative and reductive reactions while uridine diphosphate glucuronyltransferases catalyze the transfer of an activated glucuronic-acid molecule to aromatic alcohols, aliphatic alcohols, carboxylic acids, amines and free sulphydryl groups.
  • Metabolites of the compounds disclosed herein are optionally identified either by administration of compounds to a host and analysis of tissue samples from the host, or by incubation of compounds with hepatic cells in vitro and analysis of the resulting compounds.
  • neurogenerative disease or “nervous system disorder,” as used herein, refers to conditions that alter the structure or function of the brain, spinal cord or peripheral nervous system, including but not limited to Alzheimer's Disease, cerebral edema, cerebral ischemia, multiple sclerosis, neuropathies, Parkinson's Disease, those found after blunt or surgical trauma (including post-surgical cognitive dysfunction and spinal cord or brain stem injury), as well as the neurological aspects of disorders such as degenerative disk disease and sciatica.
  • CNS refers to disorders of the central nervous system, i.e., brain and spinal cord.
  • Ocular disease refers to diseases which affect the eye or eyes and potentially the surrounding tissues as well.
  • Ocular or ophthalmic diseases include, but are not limited to, conjunctivitis, retinitis, scleritis, uveitis, allergic conjuctivitis, vernal conjunctivitis, papillary conjunctivitis.
  • interstitial cystitis refers to a disorder characterized by lower abdominal discomfort, frequent and sometimes painful urination that is not caused by anatomical abnormalites, infection, toxins, trauma or tumors.
  • pharmaceutical combination means a product that results from the mixing or combining of more than one active ingredient and includes both fixed and non-fixed combinations of the active ingredients.
  • fixed combination means that the active ingredients, e.g. a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) and a co-agent, are both administered to a patient simultaneously in the form of a single entity or dosage.
  • non-fixed combination means that the active ingredients, e.g.
  • a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) and a co-agent are administered to a patient as separate entities either simultaneously, concurrently or sequentially with no specific intervening time limits, wherein such administration provides effective levels of the two compounds in the body of the patient.
  • cocktail therapy e.g. the administration of three or more active ingredients.
  • pharmaceutical composition refers to a mixture of a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) with other chemical components, such as carriers, stabilizers, diluents, dispersing agents, suspending agents, thickening agents, and/or excipients.
  • the pharmaceutical composition facilitates administration of the compound to an organism. Multiple techniques of administering a compound exist in the art including, but not limited to: intravenous, oral, aerosol, parenteral, ophthalmic, pulmonary and topical administration.
  • respiratory disease refers to diseases affecting the organs that are involved in breathing, such as the nose, throat, larynx, eustachian tubes, trachea, bronchi, lungs, related muscles (e.g., diaphragm and intercostals) and nerves.
  • Respiratory diseases include, but are not limited to, asthma, adult respiratory distress syndrome and allergic (extrinsic) asthma, non-allergic (intrinsic) asthma, acute severe asthma, chronic asthma, clinical asthma, nocturnal asthma, allergen-induced asthma, aspirin-sensitive asthma, exercise-induced asthma, isocapnic hyperventilation, child-onset asthma, adult-onset asthma, cough-variant asthma, neutrophilic asthma, occupational asthma, steroid-resistant asthma, seasonal asthma, seasonal allergic rhinitis, perennial allergic rhinitis, chronic obstructive pulmonary disease, including chronic bronchitis or emphysema, pulmonary hypertension, interstitial lung fibrosis and/or airway inflammation and cystic fibrosis, and hypoxia.
  • subject or “patient” encompasses mammals.
  • mammals include, but are not limited to, any member of the Mammalian class: humans, non-human primates such as chimpanzees, and other apes and monkey species; farm animals such as cattle, horses, sheep, goats, swine; domestic animals such as rabbits, dogs, and cats; laboratory animals including rodents, such as rats, mice and guinea pigs, and the like.
  • the mammal is a human.
  • treat include alleviating, abating or ameliorating at least one symptom of a disease disease or condition, preventing additional symptoms, inhibiting the disease or condition, e.g., arresting the development of the disease or condition, relieving the disease or condition, causing regression of the disease or condition, relieving a condition caused by the disease or condition, or stopping the symptoms of the disease or condition either prophylactically and/or therapeutically.
  • Suitable routes of administration include, but are not limited to, oral, intravenous, rectal, aerosol, parenteral, ophthalmic, pulmonary, transmucosal, transdermal, vaginal, otic, nasal, and topical administration.
  • parenteral delivery includes intramuscular, subcutaneous, intravenous, intramedullary injections, as well as intrathecal, direct intraventricular, intraperitoneal, intralymphatic, and intranasal injections.
  • a compound as described herein is administered in a local rather than systemic manner, for example, via injection of the compound directly into an organ, often in a depot preparation or sustained release formulation.
  • long acting formulations are administered by implantation (for example subcutaneously or intramuscularly) or by intramuscular injection.
  • the drug is delivered in a targeted drug delivery system, for example, in a liposome coated with organ-specific antibody.
  • the liposomes are targeted to and taken up selectively by the organ.
  • the compound as described herein is provided in the form of a rapid release formulation, in the form of an extended release formulation, or in the form of an intermediate release formulation.
  • the compound described herein is administered topically.
  • the compounds described herein are formulated into pharmaceutical compositions.
  • pharmaceutical compositions are formulated in a conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically. Proper formulation is dependent upon the route of administration chosen. Any pharmaceutically acceptable techniques, carriers, and excipients are used as suitable to formulate the pharmaceutical compositions described herein: Remington: The Science and Practice of Pharmacy , Nineteenth Ed (Easton, Pa.: Mack Publishing Company, 1995); Hoover, John E., Remington's Pharmaceutical Sciences , Mack Publishing Co., Easton, Pa. 1975; Liberman, H. A. and Lachman, L., Eds., Pharmaceutical Dosage Forms , Marcel Decker, New York, N.Y., 1980; and Pharmaceutical Dosage Forms and Drug Delivery Systems, Seventh Ed. (Lippincott Williams & Wilkins 1999).
  • compositions comprising a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) and a pharmaceutically acceptable diluent(s), excipient(s), or carrier(s).
  • the compounds described are administered as pharmaceutical compositions in which a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) is mixed with other active ingredients, as in combination therapy.
  • the pharmaceutical compositions include one or more compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • a pharmaceutical composition refers to a mixture of a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) with other chemical components, such as carriers, stabilizers, diluents, dispersing agents, suspending agents, thickening agents, and/or excipients.
  • the pharmaceutical composition facilitates administration of the compound to an organism.
  • therapeutically effective amounts of compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered in a pharmaceutical composition to a mammal having a disease or condition to be treated.
  • the mammal is a human.
  • therapeutically effective amounts vary depending on the severity of the disease, the age and relative health of the subject, the potency of the compound used and other factors.
  • the compounds described herein are used singly or in combination with one or more therapeutic agents as components of mixtures.
  • one or more compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) is formulated in an aqueous solution.
  • the aqueous solution is selected from, by way of example only, a physiologically compatible buffer, such as Hank's solution, Ringer's solution, or physiological saline buffer.
  • one or more compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) is formulated for transmucosal administration.
  • transmucosal formulations include penetrants that are appropriate to the barrier to be permeated.
  • appropriate formulations include aqueous or nonaqueous solutions.
  • such solutions include physiologically compatible buffers and/or excipients.
  • compounds described herein are formulated for oral administration.
  • Compounds described herein, including compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are formulated by combining the active compounds with, e.g., pharmaceutically acceptable carriers or excipients.
  • the compounds described herein are formulated in oral dosage forms that include, by way of example only, tablets, powders, pills, dragees, capsules, liquids, gels, syrups, elixirs, slurries, suspensions and the like.
  • pharmaceutical preparations for oral use are obtained by mixing one or more solid excipient with one or more of the compounds described herein, optionally grinding the resulting mixture, and processing the mixture of granules, after adding suitable auxiliaries, if desired, to obtain tablets or dragee cores.
  • Suitable excipients are, in particular, fillers such as sugars, including lactose, sucrose, mannitol, or sorbitol; cellulose preparations such as: for example, maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methylcellulose, microcrystalline cellulose, hydroxypropylmethylcellulose, sodium carboxymethylcellulose; or others such as: polyvinylpyrrolidone (PVP or povidone) or calcium phosphate.
  • disintegrating agents are optionally added. Disintegrating agents include, by way of example only, cross-linked croscarmellose sodium, polyvinylpyrrolidone, agar, or alginic acid or a salt thereof such as sodium alginate.
  • dosage forms such as dragee cores and tablets, are provided with one or more suitable coating.
  • concentrated sugar solutions are used for coating the dosage form.
  • the sugar solutions optionally contain additional components, such as by way of example only, gum arabic, talc, polyvinylpyrrolidone, carbopol gel, polyethylene glycol, and/or titanium dioxide, lacquer solutions, and suitable organic solvents or solvent mixtures.
  • Dyestuffs and/or pigments are also optionally added to the coatings for identification purposes. Additionally, the dyestuffs and/or pigments are optionally utilized to characterize different combinations of active compound doses.
  • Oral dosage forms include push-fit capsules made of gelatin, as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol.
  • push-fit capsules contain the active ingredients in admixture with one or more filler.
  • Fillers include, by way of example only, lactose, binders such as starches, and/or lubricants such as talc or magnesium stearate and, optionally, stabilizers.
  • soft capsules contain one or more active compound that is dissolved or suspended in a suitable liquid. Suitable liquids include, by way of example only, one or more fatty oil, liquid paraffin, or liquid polyethylene glycol.
  • stabilizers are optionally added.
  • therapeutically effective amounts of at least one of the compounds described herein are formulated for buccal or sublingual administration.
  • Formulations suitable for buccal or sublingual administration include, by way of example only, tablets, lozenges, or gels.
  • the compounds described herein are formulated for parental injection, including formulations suitable for bolus injection or continuous infusion.
  • formulations for injection are presented in unit dosage form (e.g., in ampoules) or in multi-dose containers. Preservatives are, optionally, added to the injection formulations.
  • the pharmaceutical composition of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are formulated in a form suitable for parenteral injection as a sterile suspensions, solutions or emulsions in oily or aqueous vehicles.
  • Parenteral injection formulations optionally contain formulatory agents such as suspending, stabilizing and/or dispersing agents.
  • pharmaceutical formulations for parenteral administration include aqueous solutions of the active compounds in water-soluble form.
  • suspensions of the active compounds are prepared as appropriate oily injection suspensions.
  • Suitable lipophilic solvents or vehicles for use in the pharmaceutical compositions described herein include, by way of example only, fatty oils such as sesame oil, or synthetic fatty acid esters, such as ethyl oleate or triglycerides, or liposomes.
  • aqueous injection suspensions contain substances which increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol, or dextran.
  • the suspension contains suitable stabilizers or agents which increase the solubility of the compounds to allow for the preparation of highly concentrated solutions.
  • the active ingredient is in powder form for constitution with a suitable vehicle, e.g., sterile pyrogen-free water, before use.
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are prepared as solutions for parenteral injection as described herein or known in the art and administered with an automatic injector.
  • Automatic injectors such as those disclosed in U.S. Pat. Nos. 4,031,893, 5,358,489; 5,540,664; 5,665,071, 5,695,472 and WO/2005/087297 (each of which are incorporated herein by reference for such disclosure) are known.
  • all automatic injectors contain a volume of solution that includes a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) to be injected.
  • automatic injectors include a reservoir for holding the solution, which is in fluid communication with a needle for delivering the drug, as well as a mechanism for automatically deploying the needle, inserting the needle into the patient and delivering the dose into the patient.
  • Exemplary injectors provide about 0.3 mL of solution at about a concentration of 0.5 mg to 10 mg of compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) per 1 mL of solution. Each injector is capable of delivering only one dose of the compound.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered topically.
  • the compounds described herein are formulated into a variety of topically administrable compositions, such as solutions, suspensions, lotions, gels, pastes, medicated sticks, balms, creams or ointments.
  • Such pharmaceutical compositions optionally contain solubilizers, stabilizers, tonicity enhancing agents, buffers and preservatives.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are formulated for transdermal administration.
  • transdermal formulations employ transdermal delivery devices and transdermal delivery patches and can be lipophilic emulsions or buffered, aqueous solutions, dissolved and/or dispersed in a polymer or an adhesive.
  • patches are constructed for continuous, pulsatile, or on demand delivery of pharmaceutical agents.
  • the transdermal delivery of the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) is accomplished by means of iontophoretic patches and the like.
  • transdermal patches provide controlled delivery of the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • the rate of absorption is slowed by using rate-controlling membranes or by trapping the compound within a polymer matrix or gel.
  • absorption enhancers are used to increase absorption.
  • Absorption enhancers or carriers include absorbable pharmaceutically acceptable solvents that assist passage through the skin.
  • transdermal devices are in the form of a bandage comprising a backing member, a reservoir containing the compound optionally with carriers, optionally a rate controlling barrier to deliver the compound to the skin of the host at a controlled and predetermined rate over a prolonged period of time, and means to secure the device to the skin.
  • Transdermal formulations described herein may be administered using a variety of devices which have been described in the art.
  • such devices include, but are not limited to, U.S. Pat. Nos. 3,598,122, 3,598,123, 3,710,795, 3,731,683, 3,742,951, 3,814,097, 3,921,636, 3,972,995, 3,993,072, 3,993,073, 3,996,934, 4,031,894, 4,060,084, 4,069,307, 4,077,407, 4,201,211, 4,230,105, 4,292,299, 4,292,303, 5,336,168, 5,665,378, 5,837,280, 5,869,090, 6,923,983, 6,929,801 and 6,946,144.
  • transdermal dosage forms described herein may incorporate certain pharmaceutically acceptable excipients which are conventional in the art.
  • the transdermal formulations described herein include at least three components: (1) a formulation of a compound of Formula (I); (2) a penetration enhancer; and (3) an aqueous adjuvant.
  • transdermal formulations can include additional components such as, but not limited to, gelling agents, creams and ointment bases, and the like.
  • the transdermal formulation further include a woven or non-woven backing material to enhance absorption and prevent the removal of the transdermal formulation from the skin.
  • the transdermal formulations described herein maintain a saturated or supersaturated state to promote diffusion into the skin.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are formulated for administration by inhalation.
  • Various forms suitable for administration by inhalation include, but are not limited to, aerosols, mists or powders.
  • Pharmaceutical compositions of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are conveniently delivered in the form of an aerosol spray presentation from pressurized packs or a nebuliser, with the use of a suitable propellant (e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas).
  • a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
  • the dosage unit of a pressurized aerosol is determined by providing a valve to deliver a metered amount.
  • capsules and cartridges of, such as, by way of example only, gelatin for use in an inhaler or insufflator are formulated containing a powder mix of the compound and a suitable powder base such as lactose or starch.
  • Intranasal formulations are known in the art and are described in, for example, U.S. Pat. Nos. 4,476,116, 5,116,817 and 6,391,452, each of which is specifically incorporated by reference.
  • Formulations, which include a compound of Formula (I), which are prepared according to these and other techniques well-known in the art are prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, fluorocarbons, and/or other solubilizing or dispersing agents known in the art. See, for example, Ansel, H. C. et al., Pharmaceutical Dosage Forms and Drug Delivery Systems, Sixth Ed. (1995). Preferably these compositions and formulations are prepared with suitable nontoxic pharmaceutically acceptable ingredients.
  • nasal dosage form e.g., solutions, suspensions, ointments, or gels.
  • Nasal dosage forms generally contain large amounts of water in addition to the active ingredient. Minor amounts of other ingredients such as pH adjusters, emulsifiers or dispersing agents, preservatives, surfactants, gelling agents, or buffering and other stabilizing and solubilizing agents may also be present.
  • the nasal dosage form should be isotonic with nasal secretions.
  • the compounds described herein may be in a form as an aerosol, a mist or a powder.
  • Pharmaceutical compositions described herein are conveniently delivered in the form of an aerosol spray presentation from pressurized packs or a nebuliser, with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
  • a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
  • the dosage unit may be determined by providing a valve to deliver a metered amount.
  • Capsules and cartridges of, such as, by way of example only, gelatin for use in an inhaler or insufflator may be formulated containing a powder mix of the compound described herein and a suitable powder base such as lactose or starch.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are formulated in rectal compositions such as enemas, rectal gels, rectal foams, rectal aerosols, suppositories, jelly suppositories, or retention enemas, containing conventional suppository bases such as cocoa butter or other glycerides, as well as synthetic polymers such as polyvinylpyrrolidone, PEG, and the like.
  • a low-melting wax such as, but not limited to, a mixture of fatty acid glycerides, optionally in combination with cocoa butter is first melted.
  • compositions are formulated in any conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically. Proper formulation is dependent upon the route of administration chosen. Any pharmaceutically acceptable techniques, carriers, and excipients is optionally used as suitable and as understood in the art.
  • Pharmaceutical compositions comprising a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) may be manufactured in a conventional manner, such as, by way of example only, by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or compression processes.
  • compositions include at least one pharmaceutically acceptable carrier, diluent or excipient and at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) described herein as an active ingredient.
  • the active ingredient is in free-acid or free-base form, or in a pharmaceutically acceptable salt form.
  • the methods and pharmaceutical compositions described herein include the use of N-oxides, crystalline forms (also known as polymorphs), as well as active metabolites of these compounds having the same type of activity. All tautomers of the compounds described herein are included within the scope of the compounds presented herein. Additionally, the compounds described herein encompass unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like.
  • compositions optionally include other medicinal or pharmaceutical agents, carriers, adjuvants, such as preserving, stabilizing, wetting or emulsifying agents, solution promoters, salts for regulating the osmotic pressure, buffers, and/or other therapeutically valuable substances.
  • adjuvants such as preserving, stabilizing, wetting or emulsifying agents, solution promoters, salts for regulating the osmotic pressure, buffers, and/or other therapeutically valuable substances.
  • compositions comprising the compounds described herein include formulating the compounds with one or more inert, pharmaceutically acceptable excipients or carriers to form a solid, semi-solid or liquid.
  • Solid compositions include, but are not limited to, powders, tablets, dispersible granules, capsules, cachets, and suppositories.
  • Liquid compositions include solutions in which a compound is dissolved, emulsions comprising a compound, or a solution containing liposomes, micelles, or nanoparticles comprising a compound as disclosed herein.
  • Semi-solid compositions include, but are not limited to, gels, suspensions and creams.
  • compositions described herein include liquid solutions or suspensions, solid forms suitable for solution or suspension in a liquid prior to use, or as emulsions. These compositions also optionally contain minor amounts of nontoxic, auxiliary substances, such as wetting or emulsifying agents, pH buffering agents, and so forth.
  • composition comprising at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) illustratively takes the form of a liquid where the agents are present in solution, in suspension or both.
  • a liquid composition includes a gel formulation.
  • the liquid composition is aqueous.
  • pharmaceutical aqueous suspensions include one or more polymers as suspending agents.
  • Polymers include water-soluble polymers such as cellulosic polymers, e.g., hydroxypropyl methylcellulose, and water-insoluble polymers such as cross-linked carboxyl-containing polymers.
  • Certain pharmaceutical compositions described herein include a mucoadhesive polymer, selected from, for example, carboxymethylcellulose, carbomer (acrylic acid polymer), poly(methylmethacrylate), polyacrylamide, polycarbophil, acrylic acid/butyl acrylate copolymer, sodium alginate and dextran.
  • compositions also, optionally include solubilizing agents to aid in the solubility of a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • solubilizing agent generally includes agents that result in formation of a micellar solution or a true solution of the agent.
  • Certain acceptable nonionic surfactants for example polysorbate 80, are useful as solubilizing agents, as can ophthalmically acceptable glycols, polyglycols, e.g., polyethylene glycol 400, and glycol ethers.
  • compositions optionally include one or more pH adjusting agents or buffering agents, including acids such as acetic, boric, citric, lactic, phosphoric and hydrochloric acids; bases such as sodium hydroxide, sodium phosphate, sodium borate, sodium citrate, sodium acetate, sodium lactate and tris-hydroxymethylaminomethane; and buffers such as citrate/dextrose, sodium bicarbonate and ammonium chloride.
  • acids such as acetic, boric, citric, lactic, phosphoric and hydrochloric acids
  • bases such as sodium hydroxide, sodium phosphate, sodium borate, sodium citrate, sodium acetate, sodium lactate and tris-hydroxymethylaminomethane
  • buffers such as citrate/dextrose, sodium bicarbonate and ammonium chloride.
  • acids, bases and buffers are included in an amount required to maintain pH of the composition in an acceptable range.
  • compositions optionally include one or more salts in an amount required to bring osmolality of the composition into an acceptable range.
  • salts include those having sodium, potassium or ammonium cations and chloride, citrate, ascorbate, borate, phosphate, bicarbonate, sulfate, thiosulfate or bisulfite anions; suitable salts include sodium chloride, potassium chloride, sodium thiosulfate, sodium bisulfite and ammonium sulfate.
  • compositions optionally include one or more preservatives to inhibit microbial activity.
  • Suitable preservatives include mercury-containing substances such as merfen and thiomersal; stabilized chlorine dioxide; and quaternary ammonium compounds such as benzalkonium chloride, cetyltrimethylammonium bromide and cetylpyridinium chloride.
  • compositions include one or more surfactants to enhance physical stability or for other purposes.
  • Suitable nonionic surfactants include polyoxyethylene fatty acid glycerides and vegetable oils, e.g., polyoxyethylene (60) hydrogenated castor oil; and polyoxyethylene alkylethers and alkylphenyl ethers, e.g., octoxynol 10, octoxynol 40.
  • compositions may include one or more antioxidants to enhance chemical stability where required.
  • Suitable antioxidants include, by way of example only, ascorbic acid and sodium metabisulfite.
  • pharmaceutical aqueous suspension compositions are packaged in single-dose non-reclosable containers.
  • multiple-dose reclosable containers are used, in which case it is typical to include a preservative in the composition.
  • hydrophobic pharmaceutical compounds are employed. Liposomes and emulsions are examples of delivery vehicles or carriers herein. In certain embodiments, organic solvents such as N-methylpyrrolidone are also employed. In additional embodiments, the compounds described herein are delivered using a sustained-release system, such as semipermeable matrices of solid hydrophobic polymers containing the therapeutic agent. Various sustained-release materials are useful herein. In some embodiments, sustained-release capsules release the compounds for a few hours up to over 24 hours. Depending on the chemical nature and the biological stability of the therapeutic reagent, additional strategies for protein stabilization may be employed.
  • the formulations described herein include one or more antioxidants, metal chelating agents, thiol containing compounds and/or other general stabilizing agents.
  • stabilizing agents include, but are not limited to: (a) about 0.5% to about 2% w/v glycerol, (b) about 0.1% to about 1% w/v methionine, (c) about 0.1% to about 2% w/v monothioglycerol, (d) about 1 mM to about 10 mM EDTA, (e) about 0.01% to about 2% w/v ascorbic acid, (f) 0.003% to about 0.02% w/v polysorbate 80, (g) 0.001% to about 0.05% w/v.
  • polysorbate 20 (h) arginine, (i) heparin, (j) dextran sulfate, (k) cyclodextrins, (1) pentosan polysulfate and other heparinoids, (m) divalent cations such as magnesium and zinc; or (n) combinations thereof.
  • the compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are used in the preparation of medicaments for the treatment of PGD 2 -dependent or PGD 2 -mediated diseases or conditions.
  • a method for treating any of the diseases or conditions described herein in a subject in need of such treatment involves administration of pharmaceutical compositions containing at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or a pharmaceutically acceptable salt, pharmaceutically active metabolite, pharmaceutically acceptable prodrug, or pharmaceutically acceptable solvate thereof, in therapeutically effective amounts to said subject.
  • compositions containing the compound(s) described herein are administered for prophylactic and/or therapeutic treatments.
  • the compositions are administered to a patient already suffering from a disease or condition, in an amount sufficient to cure or at least partially arrest the symptoms of the disease or condition. Amounts effective for this use depend on the severity and course of the disease or condition, previous therapy, the patient's health status, weight, and response to the drugs, and the judgment of the treating physician. Therapeutically effective amounts are optionally determined by methods including, but not limited to, a dose escalation clinical trial.
  • compositions containing the compounds described herein are administered to a patient susceptible to or otherwise at risk of a particular disease, disorder or condition. Such an amount is defined to be a “prophylactically effective amount or dose.”
  • a patient susceptible to or otherwise at risk of a particular disease, disorder or condition is defined to be a “prophylactically effective amount or dose.”
  • dose a pharmaceutically effective amount or dose.
  • the precise amounts also depend on the patient's state of health, weight, and the like.
  • effective amounts for this use will depend on the severity and course of the disease, disorder or condition, previous therapy, the patient's health status and response to the drugs, and the judgment of the treating physician.
  • the administration of the compounds are administered chronically, that is, for an extended period of time, including throughout the duration of the patient's life in order to ameliorate or otherwise control or limit the symptoms of the patient's disease or condition.
  • the dose of drug being administered may be temporarily reduced or temporarily suspended for a certain length of time (i.e., a “drug holiday”).
  • the length of the drug holiday is between 2 days and 1 year, including by way of example only, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 10 days, 12 days, 15 days, 20 days, 28 days, 35 days, 50 days, 70 days, 100 days, 120 days, 150 days, 180 days, 200 days, 250 days, 280 days, 300 days, 320 days, 350 days, and 365 days.
  • the dose reduction during a drug holiday is, by way of example only, by 10%-100%, including by way of example only 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, and 100%.
  • a maintenance dose is administered if necessary. Subsequently, in specific embodiments, the dosage or the frequency of administration, or both, is reduced, as a function of the symptoms, to a level at which the improved disease, disorder or condition is retained. In certain embodiments, however, the patient requires intermittent treatment on a long-term basis upon any recurrence of symptoms.
  • the amount of a given agent that corresponds to such an amount varies depending upon factors such as the particular compound, disease condition and its severity, the identity (e.g., weight, sex) of the subject or host in need of treatment, but can nevertheless be determined according to the particular circumstances surrounding the case, including, e.g., the specific agent being administered, the route of administration, the condition being treated, and the subject or host being treated.
  • doses employed for adult human treatment are typically in the range of 0.02 mg-5000 mg per day, preferably 1-1500 mg per day.
  • the desired dose is conveniently presented in a single dose or in divided doses administered simultaneously (or over a short period of time) or at appropriate intervals, for example as two, three, four or more sub-doses per day.
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered chronically. In some embodiments, compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered intermittently (e.g. drug holiday that includes a period of time in which the compound is not administered or is administered in a reduced amount).
  • compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are administered in cycles that include: (a) a first period that includes daily administration of the compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V); followed by (b) a second period that includes a dose reduction of the daily amount of the compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) that is administered.
  • the compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) is not administered in the second period.
  • the duration of the first and second periods, as well as the dose amounts are determined using methods described herein or known in the art.
  • a drug holiday or a dose reduction period is appropriate depending on the pharmacodynamic profile of the active agent, e.g., the ‘off’ rate of the active agent is significantly slower than the ‘off’ rate of prostaglandin D 2 from the DP 2 receptor.
  • the pharmaceutical composition described herein is in unit dosage forms suitable for single administration of precise dosages.
  • the formulation is divided into unit doses containing appropriate quantities of one or more compound.
  • the unit dosage is in the form of a package containing discrete quantities of the formulation.
  • Non-limiting examples are packaged tablets or capsules, and powders in vials or ampoules.
  • Aqueous suspension compositions are optionally packaged in single-dose non-re-closeable containers.
  • multiple-dose re-closeable containers are used, in which case it is typical to include a preservative in the composition.
  • formulations for parenteral injection are, in some embodiments, presented in unit dosage form, which include, but are not limited to ampoules, or in multi-dose containers, with an added preservative.
  • the daily dosages appropriate for the compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) described herein are from about 0.01 to about 10 mg/kg per body weight.
  • an indicated daily dosage in a large mammal including, but not limited to, humans, is in the range from about 0.5 mg to about 1000 mg, conveniently administered in divided doses, including, but not limited to, up to four times a day.
  • the daily dosage is administered in extended release form.
  • suitable unit dosage forms for oral administration comprise from about 1 to 500 mg active ingredient.
  • the daily dosage or the amount of active in the dosage form are lower or higher than the ranges indicated herein, based on a number of variables in regard to an individual treatment regime.
  • the daily and unit dosages are altered depending on a number of variables including, but not limited to, the activity of the compound used, the disease or condition to be treated, the mode of administration, the requirements of the individual subject, the severity of the disease or condition being treated, and the judgment of the practitioner.
  • Toxicity and therapeutic efficacy of such therapeutic regimens are determined by standard pharmaceutical procedures in cell cultures or experimental animals, including, but not limited to, the determination of the LD 50 (the dose lethal to 50% of the population) and the ED 50 (the dose therapeutically effective in 50% of the population).
  • the dose ratio between the toxic and therapeutic effects is the therapeutic index and it is expressed as the ratio between LD 50 and ED 50 .
  • the data obtained from cell culture assays and animal studies are used in formulating the therapeutically effective daily dosage range and/or the therapeutically effective unit dosage amount for use in mammals, including humans.
  • the daily dosage amount of the compounds described herein lies within a range of circulating concentrations that include the ED 50 with minimal toxicity.
  • the daily dosage range and/or the unit dosage amount varies within this range depending upon the dosage form employed and the route of administration utilized.
  • the therapy of PGD 2 -dependent or PGD 2 -mediated diseases or conditions is designed to modulate the activity of DP 2 , DP 1 and/or TP.
  • modulation includes, in some embodiments, antagonizing DP 2 activity.
  • such modulation includes antagonizing DP 2 and DP 1 .
  • a DP 2 antagonist is administered in order to decrease signal transduction initiated by PGD 2 within the individual.
  • compositions and methods described herein include compositions and methods for treating, preventing, reversing, halting or slowing the progression of PGD 2 -dependent or PGD 2 mediated diseases or conditions once it becomes clinically evident, or treating the symptoms associated with or related to PGD 2 -dependent or PGD 2 mediated diseases or conditions, by administering to the subject a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • the subject already has a PGD 2 -dependent or PGD 2 mediated disease or condition at the time of administration, or is at risk of developing a PGD 2 -dependent or PGD 2 mediated disease or condition.
  • the activity of DP 2 in a mammal is directly or indirectly modulated by the administration of (at least once) an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof to a mammal.
  • modulation includes, but is not limited to, reducing and/or inhibiting the activity of DP 2 .
  • the activity of PGD 2 in a mammal is directly or indirectly modulated, including reducing and/or inhibiting, by the administration of (at least once) an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof to a mammal.
  • Such modulation includes, but is not limited to, reducing and/or inhibiting the activity of DP 2 .
  • prevention and/or treatment of PGD 2 -dependent or PGD 2 mediated diseases or conditions comprises administering to a mammal at least once a therapeutically effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • the compound administered to the mammal is a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V).
  • PGD 2 -dependent or PGD 2 mediated diseases or conditions that include, but are not limited to, bone diseases and disorders, cardiovascular diseases and disorders, inflammatory diseases and disorders, immunological diseases or disorders, dermatological diseases and disorders, ocular diseases and disorders, cancer and other proliferative diseases and disorders, respiratory diseases and disorder, and non-cancerous disorders.
  • the respiratory disease is asthma.
  • respiratory diseases include, but are not limited to, adult respiratory distress syndrome and allergic (extrinsic) asthma, non-allergic (intrinsic) asthma, acute severe asthma, chronic asthma, clinical asthma, nocturnal asthma, allergen-induced asthma, aspirin-sensitive asthma, exercise-induced asthma, isocapnic hyperventilation, child-onset asthma, adult-onset asthma, cough-variant asthma, neutrophilic asthma, occupational asthma, steroid-resistant asthma, seasonal asthma, allergic rhinitis, vascular responses, endotoxin shock, fibrogenesis, pulmonary fibrosis, allergic diseases, chronic inflammation, and adult respiratory distress syndrome.
  • chronic obstructive pulmonary disease comprising administering to the mammal at least once an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • chronic obstructive pulmonary disease includes, but is not limited to, chronic bronchitis or emphysema, pulmonary hypertension, interstitial lung fibrosis and/or airway inflammation and cystic fibrosis.
  • compositions or medicament comprising administering to the mammal at least once an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • aortic aneurysm included in the prevention/treatment methods described herein are methods for preventing or treating vasoconstriction, atherosclerosis and its sequelae myocardial ischemia, myocardial infarction, aortic aneurysm, vasculitis and stroke comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • eosinophil and/or basophil and/or dendritic cell and/or neutrophil and/or monocyte and/or T-cell recruitment comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • ⁇ included in the prevention/treatment methods described herein are methods for the prevention or treatment of abnormal bone remodeling, loss or gain, including diseases or conditions as, by way of example, osteopenia, osteoporosis, Paget's disease, cancer and other diseases comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • diseases or conditions as, by way of example, osteopenia, osteoporosis, Paget's disease, cancer and other diseases comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • ocular inflammation and allergic conjunctivitis comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • otitis otitis media
  • methods for preventing otitis, otitis media comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • CNS disorders include, but are not limited to, multiple sclerosis, Parkinson's disease, Alzheimer's disease, stroke, cerebral ischemia, retinal ischemia, post-surgical cognitive dysfunction, migraine, peripheral neuropathy/neuropathic pain, spinal cord injury, cerebral edema and head injury.
  • compositions or medicaments comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • the type of cancer may include, but is not limited to, pancreatic cancer and other solid or hematological tumors.
  • gastrointestinal diseases include, by way of example only, inflammatory bowel disease (IBD), colitis and Crohn's disease.
  • a method for the reduction or treatment of inflammation and/or preventing, reducing the incidences of or treating acute or chronic transplant rejection (including any vascular abnormality associated with acute or chronic rejection) or preventing or treating tumors or accelerating the healing of wounds comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • inflammatory responses of the skin comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • inflammatory responses of the skin include, by way of example, psoriasis, dermatitis, contact dermatitis, eczema, urticaria, rosacea, wound healing and scarring.
  • compositions or medicaments comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • cystitis including, e.g., interstitial cystitis, comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • Familial Mediterranean Fever comprising administering at least once to the mammal an effective amount of at least one compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof.
  • Compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are DP 2 antagonists.
  • compounds of Formula (I) are used in the treatment of PGD 2 -dependent or PGD 2 -mediated diseases, disorders or conditions as disclosed herein.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) show higher selectivity for DP 2 versus other receptors, such as for example DP 1 , CETP and/or PPAR receptors.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) show higher affinity for DP 2 versus other receptors, such as for example DP 1 , CETP and/or PPAR receptors.
  • the therapeutic effectiveness of one of the compounds described herein is enhanced by administration of an adjuvant (i.e., by itself the adjuvant may have minimal therapeutic benefit, but in combination with another therapeutic agent, the overall therapeutic benefit to the patient is enhanced).
  • the benefit of experienced by a patient is increased by administering one of the compounds described herein with another therapeutic agent (which also includes a therapeutic regimen) that also has therapeutic benefit.
  • another therapeutic agent which also includes a therapeutic regimen
  • the therapeutic benefit of treating asthma by administering at least one of the compounds described herein is increased by also providing the patient with other therapeutic agents or therapies for asthma.
  • the overall benefit experienced by the patient may simply be additive of the two therapeutic agents or the patient may experience a synergistic benefit.
  • different therapeutically-effective dosages of the compounds disclosed herein will be utilized in formulating pharmaceutical composition and/or in treatment regimens when the compounds disclosed herein are administered in combination with one or more additional agent, such as an additional therapeutically effective drug, an adjuvant or the like.
  • additional agent such as an additional therapeutically effective drug, an adjuvant or the like.
  • Therapeutically-effective dosages of drugs and other agents for use in combination treatment regimens can be determined by means similar to those set forth hereinabove for the actives themselves.
  • the methods of prevention/treatment described herein encompasses the use of metronomic dosing, i.e., providing more frequent, lower doses in order to minimize toxic side effects.
  • a combination treatment regimen encompasses treatment regimens in which administration of a DP 2 antagonist described herein is initiated prior to, during, or after treatment with a second agent described above, and continues until any time during treatment with the second agent or after termination of treatment with the second agent. It also includes treatments in which a DP 2 antagonist described herein and the second agent being used in combination are administered simultaneously or at different times and/or at decreasing or increasing intervals during the treatment period. Combination treatment further includes periodic treatments that start and stop at various times to assist with the clinical management of the patient. For example, in one embodiment, a DP 2 antagonist described herein in the combination treatment is administered weekly at the onset of treatment, decreasing to biweekly, and decreasing further as appropriate.
  • compositions and methods for combination therapy are provided herein.
  • the pharmaceutical compositions disclosed herein are used to treat PGD 2 -dependent or PGD 2 mediated conditions.
  • the pharmaceutical compositions disclosed herein are used to treat respiratory diseases (e.g., asthma), where treatment with a DP 2 antagonist is indicated and to induce bronchodilation in a subject.
  • the pharmaceutical compositions disclosed herein are used to treat airways or nasal inflammation diseases such as asthma and rhinitis.
  • compositions disclosed herein are used to treat a subject suffering from a vascular inflammation-driven disorder. In one embodiment, the pharmaceutical compositions disclosed herein are used to treat skin inflammation diseases such as atopic dermatitis.
  • combination therapies described herein are used as part of a specific treatment regimen intended to provide a beneficial effect from the co-action of a DP 2 described herein and a concurrent treatment. It is understood that the dosage regimen to treat, prevent, or ameliorate the condition(s) for which relief is sought, is modified in accordance with a variety of factors. These factors include the type of respiratory disorder and the type of bronchoconstriction or inflammation from which the subject suffers, as well as the age, weight, sex, diet, and medical condition of the subject. Thus, in some instances, the dosage regimen actually employed varies and, in some embodiments, deviates from the dosage regimens set forth herein.
  • dosages of the co-administered compounds vary depending on the type of co-drug employed, on the specific drug employed, on the disease or condition being treated and so forth.
  • the compound provided herein when co-administered with one or more biologically active agents, is administered either simultaneously with the biologically active agent(s), or sequentially. If administered sequentially, the attending physician decides on the appropriate sequence of administering protein in combination with the biologically active agent(s).
  • the multiple therapeutic agents are administered in any order or even simultaneously. If administration is simultaneous, the multiple therapeutic agents are, by way of example only, provided in a single, unified form, or in multiple forms (e.g., as a single pill or as two separate pills). In one embodiment, one of the therapeutic agents is given in multiple doses, and in another, two (or more if present) are given as multiple doses. In some embodiments of non-simultaneous administration, the timing between the multiple doses vary from more than zero weeks to less than four weeks. In addition, the combination methods, compositions and formulations are not to be limited to the use of only two agents; the use of multiple therapeutic combinations is also envisioned.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) are used in combination with procedures that provide additional or synergistic benefit to the patient.
  • patients are expected to find therapeutic and/or prophylactic benefit in the methods described herein, wherein pharmaceutical composition of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) and/or combinations with other therapeutics are combined with genetic testing to determine whether that individual is a carrier of a mutant gene that is known to be correlated with certain diseases or conditions.
  • the compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) and combination therapies are administered before, during or after the occurrence of a disease or condition, and the timing of administering the composition containing a compound varies.
  • the compounds described herein are used as a prophylactic and are administered continuously to subjects with a propensity to develop conditions or diseases in order to prevent the occurrence of the disease or condition.
  • the compounds and compositions are administered to a subject during or as soon as possible after the onset of the symptoms.
  • the administration of the compounds are initiated within the first 48 hours of the onset of the symptoms, preferably within the first 48 hours of the onset of the symptoms, more preferably within the first 6 hours of the onset of the symptoms, and most preferably within 3 hours of the onset of the symptoms.
  • the initial administration is accomplished via any practical route, such as, for example, by intravenous injection, a bolus injection, infusion over 5 minutes to about 5 hours, a pill, a capsule, transdermal patch, buccal delivery, and the like, or combination thereof.
  • a compound described herein is administered as soon as is practicable after the onset of a disease or condition is detected or suspected, and for a length of time necessary for the treatment of the disease, such as, for example, from about 1 month to about 3 months.
  • the length required for effective treatment varies, and the treatment length is adjusted to suit the specific needs of each subject.
  • a compound described herein or a formulation containing the compound is administered for at least 2 weeks, about 1 month to about 5 years, or from about 1 month to about 3 years.
  • therapies which combine compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) with inhibitors of PGD 2 synthesis or PGD 2 receptor antagonists, either acting at the same or other points in the PGD 2 synthesis pathway, are encompassed herein for treating PGD 2 -dependent or PGD 2 mediated diseases or conditions.
  • encompassed herein are therapies that combine compounds of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) with inhibitors of inflammation for treating PGD 2 -dependent or PGD 2 mediated diseases or conditions.
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases include administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with an anti-inflammatory agent including, but not limited to, non-steroidal anti-inflammatory drugs (NSAIDs) and corticosteroids (glucocorticoids).
  • Anti-inflammatory agents include, but are not limited to: arthrotec, mesalamine, auralglan, sulfasalazine, daypro, etodolac, ponstan, and solumedrol; non-steroidal anti-inflammatory agents; corticosteroids; and leukotriene pathway modulators (e.g. montelukast, zilueton).
  • asthma is a chronic inflammatory disease characterized by pulmonary eosinophilia and airway hyperresponsiveness.
  • PGD 2 is released from mast cells, eosinophils, and basophils.
  • PGD 2 is involved in contraction of airway smooth muscle, an increase in vascular permeability and mucus secretions, and has been reported to attract and activate inflammatory cells in the airways of asthmatics.
  • the methods for treatment of respiratory diseases include administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with an anti-inflammatory agent.
  • NSAIDs include, but are not limited to: aspirin, salicylic acid, gentisic acid, choline magnesium salicylate, choline salicylate, choline magnesium salicylate, choline salicylate, magnesium salicylate, sodium salicylate, diflunisal, carprofen, fenoprofen, fenoprofen calcium, fluorobiprofen, ibuprofen, ketoprofen, nabutone, ketolorac, ketorolac tromethamine, naproxen, oxaprozin, diclofenac, etodolac, indomethacin, sulindac, tolmetin, meclofenamate, meclofenamate sodium, mefenamic acid, piroxicam, meloxicam, COX-2 specific inhibitors (such as, but not limited to, celecoxib, rofecoxib, valdecoxib, parecoxib, etoricoxib
  • Corticosteroids include, but are not limited to: betamethasone (Celestone), prednisone (Deltasone), alclometasone, aldosterone, amcinonide, beclometasone, betamethasone, budesonide, ciclesonide, clobetasol, clobetasone, clocortolone, cloprednol, cortisone, cortivazol, deflazacort, deoxycorticosterone, desonide, desoximetasone, desoxycortone, dexamethasone, diflorasone, diflucortolone, difluprednate, fluclorolone, fludrocortisone, fludroxycortide, flumetasone, flunisolide, fluocinonide, fluocortin, fluocortolone, fluorometholone, fluperolone, flupred
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases include administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination in combination with NSAIDs and NO-donors or NSAIDs and proton-pump inhibitors.
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases includes administering to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with other PGD 2 receptor antagonists including, but are not limited to, DP 1 receptor antagonists and TP receptor antagonists.
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases includes administered to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with a DP 1 receptor antagonist.
  • DP 1 receptor antagonists include, but are not limited to, BWA868C (Sharif et al., Br. J.
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases includes administering to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with a TP receptor antagonist.
  • TP receptor antagonists include, but are not limited to, Ramatroban (“BayerTM”), GR32191 (Beasley et al., J. Appl. Physiol., 1989 April; 66(4):1685-93), IC1192605 (Boersma et al., Br. J. Pharmacol., 1999 December; 128(7):1505-12) and derivatives or analogs thereof.
  • Such combinations may be used to treat PGD 2 -dependent or PGD 2 mediated disorders, including respiratory disorders.
  • the co-administration of a DP 2 receptor antagonist with a DP 1 receptor antagonist or a TP receptor antagonist has therapeutic benefit over and above the benefit derived from the administration of a either a DP 2 antagonist, DP 1 antagonist or a TP antagonist alone.
  • a DP 2 antagonist, DP 1 antagonist or a TP antagonist alone.
  • partial inhibition of this pathway through the amelioration of the effects of the proinflammatory agonists combined with the block of the DP 1 receptor, TP receptor and/or DP 2 receptor may afford substantial therapeutic benefits, particularly for respiratory diseases.
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases comprises administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one additional agent selected, by way of example only, alemtuzumab, arsenic trioxide, asparaginase (pegylated or non-), bevacizumab, cetuximab, platinum-based compounds such as cisplatin, cladribine, daunorubicin/doxorubicin/idarubicin, irinotecan, fludarabine, 5-fluorouracil, gemtuzumab, methotrexate, PaclitaxelTM, taxol, temozolomide, thioguanine, or classes of drugs including hormones (an antiestrogen, an antiandrogen, or gonadotropin releasing hormone analogues, interferons such as alpha interferon, nitrogen mustard
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases comprises administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one additional agent selected from, by way of example only, azathioprine, a corticosteroid, cyclophosphamide, cyclosporin, dacluzimab, mycophenolate mofetil, OKT3, rapamycin, tacrolimus, thymoglobulin.
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases comprises administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one additional agent selected, by way of example only, HMG-CoA reductase inhibitors (e.g., statins in their lactonized or dihydroxy open acid forms and pharmaceutically acceptable salts and esters thereof, including but not limited to lovastatin; simvastatin; dihydroxy open-acid simvastatin, particularly the ammonium or calcium salts thereof; pravastatin, particularly the sodium salt thereof; fluvastatin, particularly the sodium salt thereof; atorvastatin, particularly the calcium salt thereof; nisvastatin, also referred to as NK-104; rosuvastatin); agents that have both lipid-altering effects and other pharmaceutical activities; HMG-CoA synthase inhibitors; cholesterol absorption inhibitors such as ezetimibe; cholesterol ester transfer
  • HMG-CoA reductase inhibitors
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases comprises administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one additional agent selected from, by way of example only, COX-2 inhibitors; nitric oxide synthase inhibitors, such as N-(3-(aminomethyl)benzyl)acetamidine; Rho kinase inhibitors, such as fasudil; angiotension II type-1 receptor antagonists, including candesartan, losartan, irbesartan, eprosartan, telmisartan and valsartan; glycogen synthase kinase 3 inhibitors; sodium or calcium channel blockers, including crobenetine; p38 MAP kinase inhibitors, including SKB 239063; thromboxane AX-synthetase inhibitors, including isbogrel, ozagrel,
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases comprises administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one additional agent selected from, by way of example only, anti-inflammatory agents, such as corticosteroids, azathioprine or cyclophosphamide.
  • additional agent selected from, by way of example only, anti-inflammatory agents, such as corticosteroids, azathioprine or cyclophosphamide.
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases comprises administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one additional agent selected from, by way of example only, dimethylsulfoxide, omalizumab, and pentosan polysulfate.
  • methods for treatment of PGD 2 -dependent or PGD 2 mediated conditions or diseases comprises administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one additional agent selected from the, by way of example only, minerals, vitamins, bisphosphonates, anabolic steroids, parathyroid hormone or analogs, and cathepsin K inhibitors.
  • methods for treating PGD 2 -dependent or PGD 2 mediated conditions or diseases comprises administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one respiratory agent.
  • Respiratory agents include, but are not limited to, bronchodilators (e.g., sympathomimetic agents and xanthine derivatives), leukotriene receptor antagonists, leukotriene formation inhibitors, leukotriene modulators, nasal decongestants, respiratory enzymes, lung surfactants, antihistamines (e.g., Mepyramine (pyrilamine), Antazoline, Diphenhydramine, Carbinoxamine, Doxylamine, Clemastine, Dimenhydrinate, Pheniramine, Chlorphenamine (chlorpheniramine), Dexchlorpheniramine, Brompheniramine, Triprolidine, cetirizine, Cyclizine, Chlorcyclizine, Hydroxyzine, Meclizine, loratadine, desloratidine, Promethazine, Alimemazine (trimeprazine), Cyproheptadine, Azatadine, Ketotifen, Acrivastine, Astemizole, Ce
  • methods for treating PGD 2 -dependent or PGD 2 mediated conditions or diseases, such as the therapy of asthma and/or COPD comprises administration to a patient anti-inflammatory agents.
  • methods for treating PGD 2 -dependent or PGD 2 mediated conditions or diseases, such as the therapy of asthma and/or COPD comprise administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one additional agent selected from, but not limited to, epinephrine, isoproterenol, orciprenaline, bronchodilators, glucocorticoids, leukotriene modifiers, mast-cell stabilizers, xanthines, anticholinergics, 13-2 agonists, FLAP inhibitors, FLAP modulators or 5-LO inhibitors.
  • ⁇ -2 agonists include, but are not limited to, short-acting ⁇ -2 agonists (e.g., salbutamol (albuterol), levalbuterol, terbutaline, pirbuterol, procaterol, metaproterenol, fenoterol and bitolterol mesylate) and long-acting ⁇ -2 agonists (e.g., salmeterol, formoterol, bambuterol and clenbuterol).
  • short-acting ⁇ -2 agonists e.g., salbutamol (albuterol), levalbuterol, terbutaline, pirbuterol, procaterol, metaproterenol, fenoterol and bitolterol mesylate
  • long-acting ⁇ -2 agonists e.g., salmeterol, formoterol, bambuterol and clenbuterol.
  • FLAP inhibitors and/or FLAP modulators include, but are not limited to, 3-[3-tert-butylsulfanyl-1-[4-(6-methoxy-pyridin-3-yl)-benzyl]-5-(pyridin-2-ylmethoxy)-1H-indol-2-yl]-2,2-dimethyl-propionic acid, 3-[3-tert-butylsulfanyl-1-[4-(6-ethoxy-pyridin-3-yl)-benzyl]-5-(5-methyl-pyridin-2-ylmethoxy)-1H-indol-2-yl]-2,2-dimethyl-propionic acid, MK-886, MK-0591, DG-031 (BAY-x1005) and compounds found in US 2007/0225285, US 2007/0219206, US 2007/0173508, US 2007/0123522 and US 2007/0105866 (each of which are hereby incorporated by reference).
  • Glucocorticoids include, but are not limited to, beclometasone, budesonide, ciclesonide, fluticasone and mometasone.
  • Anticholinergics include, but are not limited to, ipratropium and tiotropium.
  • Mast cell stabilizers include, but are not limited to, cromoglicate and nedocromil.
  • Xanthines include, but are not limited to, amminophylline, theobromine and theophylline.
  • Leukotriene antagonists include, but are not limited to, montelukast, tomelukast, pranlukast and zafirlukast.
  • 5-LO inhibitors include, but are not limited to, zileuton, VIA-2291 (ABT761), MK-0633, CJ-13,610 (PF-4191834), AZ-4407 and ZD-2138 and compounds found in US 2007/0149579, WO2007/016784.
  • methods for treating PGD 2 -dependent or PGD 2 mediated conditions or diseases comprises administration to a patient compounds, pharmaceutical compositions, or medicaments described herein in combination with at least one additional agent selected from, by way of example only, antihistamines, leukotriene antagonists, corticosteroids and decongestants.
  • Leukotriene antagonists include, but are not limited to, montelukast, tomelukast, pranlukast and zafirlukast.
  • methods for treating PGD 2 -dependent or PGD 2 mediated conditions or diseases include administering a DP 2 antagonist described herein in combination with other agents to treat respiratory diseases or conditions.
  • Therapeutic agents used in the treatment of respiratory conditions and disorders include: glucocorticoids, such as, ciclesonide, beclomethasone, budesonide, flunisolide, fluticasone, mometasone, and triamcinolone; leukotriene modifiers, such as, montelukast, zafirlukast, pranlukast, and zileuton; mast cell stabilizers, such as, cromoglicate (cromolyn), and nedocromil; antimuscarinics/anticholinergics, such as, ipratropium, oxitropium, and tiotropium; methylxanthines, such as, theophylline and aminophylline; antihistamine, such as, me
  • DP 2 anatogonists described herein are administered in combination with one or more agents used to treat used to treat asthma, including, but not limited to: combination inhalers (fluticasone and salmeterol oral inhalation (e.g. Advair)); inhaled Beta-2 agonists (albuterol inhaler; albuterol nebulizer solution; formoterol; isoproterenol oral inhalation; levalbuterol; metaproterenol inhalation; pirbuterol acetate oral inhalation; salmeterol aerosol inhalation; salmeterol powder inhalation; terbutaline inhaler); inhaled corticosteroids (beclomethasone oral inhalation; budesonide inhalation solution; budesonide inhaler; flunisolide oral inhalation; fluticasone inhalation aerosol; fluticasone powder for oral inhalation; mometasone inhalation powder; triamcinolone oral
  • DP 2 anatogonists described herein are administered in combination with one or more agents used to treat allergy, including, but not limited to: antihistamine and decongestant combinations (cetirizine and pseudoephedrine; desloratadine and pseudoephedrine ER; fexofenadine and pseudoephedrine; loratadine and pseudoephedrine); antihistamines (azelastine nasal spray; brompheniramine; brompheniramine oral suspension; carbinoxamine; cetirizine; chlorpheniramine; clemastine; desloratadine; dexchlorpheniramine ER; dexchlorpheniramine oral syrup; diphenhydramine oral; fexofenadine; loratadine; promethazine); decongestants (pseudoephedrine); leukotriene modifiers (montelukast; montelukast granule
  • DP 2 anatogonists described herein are administered in combination with one or more agents used to treat chronic obstructive pulmonary disease (COPD), including, but not limited to: anticholinergics—ipratropium bromide oral inhalation); combination Inhalers (albuterol and ipratropium (e.g. Combivent, DuoNeb); fluticasone and salmeterol oral inhalation (e.g.
  • COPD chronic obstructive pulmonary disease
  • corticosteroids (dexamethasone tablets; fludrocortisone acetate; hydrocortisone tablets; methylprednisolone; prednisolone liquid; prednisone oral; triamcinolone oral); inhaled Beta-2 Agonists (albuterol inhaler; albuterol nebulizer solution; formoterol; isoproterenol oral inhalation; levalbuterol; metaproterenol inhalation; pirbuterol acetate oral inhalation; salmeterol aerosol inhalation; salmeterol powder inhalation; terbutaline inhaler); inhaled Corticosteroids (beclomethasone oral inhalation; budesonide inhalation solution; budesonide inhaler; flunisolide oral inhalation; fluticasone inhalation aerosol; fluticasone powder for oral inhalation; triamcinolone oral inhalation); mukolytics
  • DP 2 anatogonists described herein are administered to a patient in combination with inhaled corticosteroids.
  • DP 2 anatogonists described herein are administered to a patient in combination with beta2-adrenergic receptor agonists. In one embodiment, DP 2 anatogonists described herein are administered to a patient in combination with short acting beta2-adrenergic receptor agonists. In one embodiment, DP 2 anatogonists described herein are administered to a patient in combination with long-acting beta2-adrenergic receptor agonists.
  • the administration of compounds of any of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) is designed to anatagonize the activity of DP 2 .
  • the administration of a DP 2 inhibitor decreases signal transduction initiated by PGD 2 within the individual.
  • methods described herein include the diagnosis or determination of whether or not a patient is suffering from a PGD 2 -dependent or PGD 2 mediated disease or condition by administering to the subject a compound of Formula (I), Formula (II), Formula (III), Formula (IV), or Formula (V) or pharmaceutical composition or medicament thereof and determining whether or not the patient responds to the treatment.
  • kits and articles of manufacture are also described herein.
  • Such kits can comprise a carrier, package, or container that is compartmentalized to receive one or more containers such as vials, tubes, and the like, each of the container(s) comprising one of the separate elements to be used in a method described herein.
  • Suitable containers include, for example, bottles, vials, syringes, and test tubes.
  • the containers are formed from any acceptable material including, e.g., glass or plastic.
  • the container(s) can comprise one or more compounds described herein, optionally in a composition or in combination with another agent as disclosed herein.
  • the container(s) optionally have a sterile access port (for example the container can be an intravenous solution bag or a vial having a stopper pierceable by a hypodermic injection needle).
  • kits optionally comprising a compound with an identifying description or label or instructions relating to its use in the methods described herein.
  • a kit will typically comprise one or more additional containers, each with one or more of various materials (such as reagents, optionally in concentrated form, and/or devices) desirable from a commercial and user standpoint for use of a compound described herein.
  • materials include, but not limited to, buffers, diluents, filters, needles, syringes; carrier, package, container, vial and/or tube labels listing contents and/or instructions for use, and package inserts with instructions for use.
  • a set of instructions will also typically be included.
  • a label can be on or associated with the container.
  • a label can be on a container when letters, numbers or other characters forming the label are attached, molded or etched into the container itself; a label can be associated with a container when it is present within a receptacle or carrier that also holds the container, e.g., as a package insert.
  • a label can be used to indicate that the contents are to be used for a specific therapeutic application. The label can also indicate directions for use of the contents, such as in the methods described herein.
  • Step 1 (5-Bromo-pyridin-3-yl)-acetic acid ethyl ester
  • Step 5 3-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-bromo-benzoic acid ethyl ester
  • Step 6 3-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-bromo-benzoic acid
  • Step 7 3-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-bromo-benzoic acid benzyl ester
  • Step 8 3-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzoic acid benzyl ester
  • Step 9 3-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-(5-carboxymethyl-pyridin-3-yl-benzoic acid benzyl ester
  • Tetrakis(triphenylphosphine)palladium(0) (0.427 g, 0.37 mmol) was added, and the reaction was stirred at 70° C. overnight.
  • Analytical LCMS indicated that the ethyl ester had been hydrolyzed during the reaction, so the mixture was quenched with 1N aqueous HCl (13 mL) and extracted with EtOAc. The combined organic layers were washed with H 2 O, and then dried and concentrated to give the title compound.
  • Step 10 3-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-(5-carboxymethyl-pyridin-3-yl-benzoic acid
  • Step 1 3-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-(5-ethoxycarbonylmethyl-pyridin-3-yl)-benzoic acid ethyl ester
  • Step 2 4-(5-Ethoxycarbonylmethyl-pyridin-3-yl)-3-ethylaminomethyl-benzoic acid
  • Step 3 4-(5-Carboxymethyl-pyridin-3-yl)-3-[(N-cyclopropanecarbonyl-N-ethyl-amino)-methyl]-benzoic acid
  • Step 4 Cyclopropanecarboxylic acid benzyl-(2-bromo-5-cyano-benzyl)-amide
  • Step 5 Cyclopropanecarboxylic acid benzyl-[5-cyano-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]-amide
  • Step 6 (5- ⁇ 2-[(Benzyl-cyclopropanecarbonyl-amino)-methyl]-4-cyano-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester
  • Tetrakis(triphenylphosphine)palladium(0) (0.370 g, 0.35 mmol) was added, and the reaction was stirred at 70° C. for 1 hour. Once no starting material was present by analytical LCMS, the mixture was diluted with H 2 O and 1N aqueous HCl (15 mL), and extracted with EtOAc. The combined organic layers were concentrated and purified by preparative HPLC to give the title compound, as well as the some of the hydrolyzed ester product.
  • Step 7 (5- ⁇ 2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-cyano-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 1 ⁇ 5-[2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-(2H-tetrazol-5-yl)-phenyl]-pyridin-3-yl ⁇ -acetic acid ethyl ester
  • Step 2 ⁇ 5-[2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-(2H-tetrazol-5-yl)-phenyl]-pyridin-3-yl ⁇ -acetic acid
  • Step 1 4-Bromo-3-dibromomethyl-benzoic acid ethyl ester
  • Step 2 4-Bromo-3-formyl-benzoic acid ethyl ester
  • the aqueous layer was separated and extracted with EtOAc, and the combined organic layers were concentrated to give a mixture of the title compound and the diethyl acetal product.
  • the mixture was dissolved in MeOH (100 mL) and treated with 2N aqueous H 2 SO 4 (15 mL) for 1 hour at room temperature. After work-up, the crude material was purified by silica gel chromatography to give a mixture of the title compound and the dimethyl acetal.
  • the mixture was dissolved in 1,4-dioxane and treated with 2N aqueous H 2 SO 4 (80 mL), and stirred overnight at room temperature.
  • the solution was diluted with EtOAc and H 2 O, and the organic layer was separated, dried, and concentrated to give the title compound.
  • Step 4 3-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-bromo-benzoic acid ethyl ester
  • Step 5 3-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-bromo-benzoic acid
  • Step 7 N-Benzyl-3-[(N-benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide
  • Step 8 (5- ⁇ 4-Benzylcarbamoyl-2-[(N-benzyl-N-cyclopropanecarbonyl-amino)-methyl]-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester
  • Step 9 (5- ⁇ 4-Benzylcarbamoyl-2-[(N-benzyl-N-cyclopropanecarbonyl-amino)-methyl]-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 1 3-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-bromo-N-methyl-benzamide
  • Step 2 3-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-N-methyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide
  • Step 3 (5- ⁇ 2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-methylcarbamoyl-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester
  • Step 4 (5- ⁇ 2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-methylcarbamoyl-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 1 3-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-bromo-N-tert-butyl-benzamide
  • Step 2 3-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-N-tert-butyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide
  • Step 3 (5- ⁇ 2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-tert-butylcarbamoyl-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester
  • Step 4 (5- ⁇ 2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-tert-butylcarbamoyl-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 1 Cyclopropanecarboxylic acid benzyl-[2-bromo-5-(pyrrolidine-1-carbonyl)-benzyl]-amide
  • Step 2 Cyclopropanecarboxylic acid benzyl-[5-(pyrrolidine-1-carbonyl)-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzyl]-amide
  • Step 3 ⁇ 5-[2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-(pyrrolidine-1-carbonyl)-phenyl]-pyridin-3-yl ⁇ -acetic acid ethyl ester
  • Step 4 ⁇ 5-[2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-(pyrrolidine-1-carbonyl)-phenyl]-pyridin-3-yl ⁇ -acetic acid
  • Step 1 (5- ⁇ 4-Aminomethyl-2-[(N-benzyl-N-cyclopropanecarbonyl-amino)-methyl]-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester
  • Step 2 (5- ⁇ 4-(Acetylamino-methyl)-2-[(N-benzyl-N-cyclopropanecarbonyl-amino)-methyl]-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester
  • Step 3 (5-[4-(Acetylamino-methyl)-2-[(N-benzyl-N-cyclopropanecarbonyl-amino)-methyl]-phenyl]-pyridin-3-yl)-acetic acid
  • Step 1 ⁇ 5-[2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-(methanesulfonylamino-methyl)-phenyl]-pyridin-3-yl ⁇ -acetic acid ethyl ester
  • Step 2 ⁇ 5-[2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-(methanesulfonylamino-methyl)-phenyl]-pyridin-3-yl ⁇ -acetic acid
  • Step 4 2-[5-(4-Fluoro-2-formyl-phenyl)-pyridin-3-yl]-propionic acid methyl ester
  • Step 5 2-[5-(2-Ethylaminomethyl-4fluoro-phenyl)-pyridin-3-yl]-propionic acid methyl ester
  • Step 6 2-(5- ⁇ 2-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4fluoro-phenyl ⁇ -pyridin-3-yl)-propionic acid methyl ester
  • Step 7 2-(5- ⁇ 2-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4fluoro-phenyl ⁇ -pyridin-3-yl)-propionic acid
  • Step 1 2- ⁇ 5-[2-(3-Benzyl-1-ethyl-ureidomethyl)-4fluoro-phenyl]-pyridin-3-yl ⁇ -propionic acid methyl ester
  • Step 2 2- ⁇ 5-[2-(3-Benzyl-1-ethyl-ureidomethyl)-4fluoro-phenyl]-pyridin-3-yl ⁇ -propionic acid
  • Step 1 2-(5- ⁇ 2-[(N-Cyclopropanecarbonyl-N-ethyl-amino)-methyl]-4fluoro-phenyl ⁇ -pyridin-3-yl)-propionic acid methyl ester
  • Step 2 2-(5- ⁇ 2-[(N-Cyclopropanecarbonyl-N-ethyl-amino)-methyl]-4fluoro-phenyl ⁇ -pyridin-3-yl)-propionic acid
  • Step 2 (2-Bromo-5-trifluoromethyl-benzyl)-ethyl-carbamic acid tert-butyl ester
  • Step 3 Ethyl-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-5-trifluoromethyl-benzyl]-carbamic acid tert-butyl ester
  • Step 4 (5- ⁇ 2-[(N-tert-Butoxycarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid methyl ester
  • Step 5 [5-(2-Ethylaminomethyl-4-trifluoromethyl-phenyl)-pyridin-3-yl]-acetic acid methyl ester, dihydrochloride
  • Step 6 (5- ⁇ 2-[(N-Cyclopropanecarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid methyl ester
  • Step 7 (5- ⁇ 2-[(N-Cyclopropanecarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 1 (5-Bromo-1-oxy-pyridin-3-yl)-acetic acid ethyl ester
  • Step 2 (5-Bromo-2-chloro-pyridin-3-yl)-acetic acid ethyl ester and (5-Bromo-6-chloro-pyridin-3-yl)-acetic acid ethyl ester
  • Step 4 [2-Chloro-5-(2-formyl-4-trifluoromethyl-phenyl)-pyridin-3-yl]-acetic acid ethyl ester
  • Step 5 [2-Chloro-5-(2-ethylaminomethyl-4-trifluoromethyl-phenyl)-pyridin-3-yl]-acetic acid ethyl ester
  • Step 6 (2-Chloro-5- ⁇ 2-[(N-cyclopropanecarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester
  • Step 7 (2-Chloro-5- ⁇ 2-[(N-cyclopropanecarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 4 Cyclopropanecarboxylic acid [2-(5-bromo-2-methoxy-pyridin-3-yl)-5-trifluoromethyl-benzyl]-ethyl-amide
  • Step 5 Cyclopropanecarboxylic acid ethyl-[2-(2-methoxy-5-trimethylsilanylethynyl-pyridin-3-yl)-5-trifluoromethyl-benzyl]-amide
  • Step 5 (5- ⁇ 2-[(N-Cyclopropanecarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -6-methoxy-pyridin-3-yl)-acetic acid
  • Step 3 Cyclopropanecarboxylic acid ethyl-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-5-trifluoromethyl-benzyl]-amide
  • Step 4 (6-Chloro-5- ⁇ 2-[(N-cyclopropanecarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester
  • Tetrakis(triphenylphosphine)palladium(0) (0.338 g, 0.20 mmol) was added, and the reaction was stirred at 85° C. for 2 hours. After cooling to room temperature, the mixture was worked-up with EtOAc, H 2 O, and brine, and the organic layer was separated, dried, filtered, and concentrated. The residue was purified by silica gel chromatography (0-100% EtOAc in hexanes) to give the title compound.
  • Step 5 (6-Chloro-5- ⁇ 2-[(N-cyclopropanecarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 3 (5- ⁇ 2-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid methyl ester
  • Step 4 (5- ⁇ 2-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 1 (5- ⁇ 2-[(N-tert-Butoxycarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 1 ⁇ 5-[2-(3-Benzyl-1-ethyl-ureidomethyl)-4-trifluoromethyl-phenyl]-pyridin-3-yl ⁇ -acetic acid methyl ester
  • Step 2 ⁇ 5-[2-(3-Benzyl-1-ethyl-ureidomethyl)-4-trifluoromethyl-phenyl]-pyridin-3-yl ⁇ -acetic acid
  • Step 1 (5- ⁇ 2-[(N-Benzyloxycarbonyl-N-ethyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -1-oxy-pyridin-3-yl)-acetic acid
  • Methyl phenylacetate (5.03 g, 33.5 mmol) was treated with 1N aqueous NaOH (22 mL, 22 mmol) in THF (40 mL) and MeOH (4 mL), and stirred overnight at room temperature. Additional 1N aqueous NaOH (22 mL, 22 mmol) was added, and the reaction was stirred for 6 hours at room temperature, until no starting material was seen by analytical LCMS. The mixture was acidified with 1N aqueous HCl to pH 3-4 and extracted with EtOAc three times. The combined organic layers were dried and concentrated to give the title compound.
  • Step 2 (5- ⁇ 2-[(N-Ethyl-N-phenylacetyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid methyl ester
  • Step 3 (5- ⁇ 2-[(N-Ethyl-N-phenylacetyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 1 Benzyl-(2-bromo-5-trifluoromethyl-benzyl)-amine
  • Step 2 Cyclopropanecarboxylic acid benzyl-(2-bromo-5-trifluoromethyl-benzyl)-amide
  • Step 3 Cyclopropanecarboxylic acid benzyl-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-5-trifluoromethyl-benzyl]-amide
  • Step 4 (5- ⁇ 2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester
  • Cyclopropanecarboxylic acid benzyl-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-5-trifluoromethyl-benzyl]-amide (60% pure; 1.07 g, 1.4 mmol), (5-bromo-pyridin-3-yl)-acetic acid ethyl ester (0.375 g, 1.5 mmol), and potassium carbonate (0.484 g, 3.5 mmol) were combined in DME (8 mL) and H 2 O (4 mL), and the solution was purged with N 2 for 15 minutes.
  • Tetrakis(triphenylphosphine)palladium(0) (0.162 g, 0.14 mmol) was added, and the reaction was stirred at 90° C. overnight.
  • Analytical LCMS indicated that some of the ester had been hydrolyzed during the coupling reaction, so the mixture was diluted with saturated aqueous NH 4 Cl and EtOAc. The aqueous layer was separated and extracted twice with EtOAc, and the combined organic layers were dried and concentrated. The residue was purified by preparative HPLC to give the title compound, which was then hydrolyzed in the following step, as well as the hydrolyzed product.
  • Step 5 (5- ⁇ 2-[(N-Benzyl-N-cyclopropanecarbonyl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid
  • Step 3 Cyclopropanecarboxylic acid indan-2-yl-[2-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-5-trifluoromethyl-benzyl]-amide
  • Step 4 (5- ⁇ 2-[(N-Cyclopropanecarbonyl-N-indan-2-yl-amino)-methyl]-4-trifluoromethyl-phenyl ⁇ -pyridin-3-yl)-acetic acid ethyl ester

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9797903B2 (en) 2012-10-24 2017-10-24 Winthrop-University Hospital Non-invasive biomarker to identify subject at risk of preterm delivery
US11112403B2 (en) 2019-12-04 2021-09-07 Progenity, Inc. Assessment of preeclampsia using assays for free and dissociated placental growth factor
US11333672B2 (en) 2017-09-13 2022-05-17 Progenity, Inc. Preeclampsia biomarkers and related systems and methods

Families Citing this family (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BRPI0907364A2 (pt) 2008-02-01 2015-07-14 Amira Pharmaceuticals Inc Antagonistas aminoalquilbifenil n,n-disubstituídos de receptores d2 de prostaglandina
WO2009099901A1 (en) * 2008-02-01 2009-08-13 Amira Pharmaceuticals, Inc. N,n-disubstituted aminoalkylbiphenyl antagonists of prostaglandin d2 receptors
WO2009102893A2 (en) * 2008-02-14 2009-08-20 Amira Pharmaceuticals, Inc. CYCLIC DIARYL ETHER COMPOUNDS AS ANTAGONISTS OF PROSTAGLANDIN D2 receptors
JP2011513242A (ja) 2008-02-25 2011-04-28 アミラ ファーマシューティカルズ，インク． プロスタグランジンｄ２受容体アンタゴニスト
US8426449B2 (en) * 2008-04-02 2013-04-23 Panmira Pharmaceuticals, Llc Aminoalkylphenyl antagonists of prostaglandin D2 receptors
US8710163B2 (en) 2008-07-25 2014-04-29 Exxonmobil Chemical Patents Inc. Pyridyldiamido transition metal complexes, production and use thereof
US8674040B2 (en) 2008-07-25 2014-03-18 Exxonmobil Chemical Patents Inc. Pyridyldiamido transition metal complexes, production and use thereof
GB2463788B (en) 2008-09-29 2010-12-15 Amira Pharmaceuticals Inc Heteroaryl antagonists of prostaglandin D2 receptors
US8378107B2 (en) 2008-10-01 2013-02-19 Panmira Pharmaceuticals, Llc Heteroaryl antagonists of prostaglandin D2 receptors
US8524748B2 (en) 2008-10-08 2013-09-03 Panmira Pharmaceuticals, Llc Heteroalkyl biphenyl antagonists of prostaglandin D2 receptors
WO2010057118A2 (en) 2008-11-17 2010-05-20 Amira Pharmaceuticals, Inc. Heterocyclic antagonists of prostaglandin d2 receptors
US20100173313A1 (en) * 2009-01-08 2010-07-08 Amira Pharmaceuticals, Inc. Biomarkers of inflammation
WO2011014588A2 (en) * 2009-07-31 2011-02-03 Amira Pharmaceuticals, Inc. Dermal formulations of dp2 receptor antagonists
CN102596199A (zh) 2009-07-31 2012-07-18 潘米拉制药公司 Dp2受体拮抗剂的眼用医药组合物
CN102596902A (zh) 2009-08-05 2012-07-18 潘米拉制药公司 Dp2拮抗剂及其用途
EP2457900A1 (en) 2010-11-25 2012-05-30 Almirall, S.A. New pyrazole derivatives having CRTh2 antagonistic behaviour
TWI527809B (zh) * 2011-01-24 2016-04-01 百靈佳殷格翰國際股份有限公司 作為ｃｒｔｈ２拮抗劑之吡唑化合物
US8623974B2 (en) 2011-03-25 2014-01-07 Exxonmobil Chemical Patents Inc. Branched vinyl terminated polymers and methods for production thereof
US8399724B2 (en) 2011-03-25 2013-03-19 Exxonmobil Chemical Patents Inc. Vinyl terminated higher olefin copolymers and methods to produce thereof
US8318998B2 (en) 2011-03-25 2012-11-27 Exxonmobil Chemical Patents Inc. Enhanced catalyst performance for production of vinyl terminated propylene and ethylene/propylene macromers
US8841397B2 (en) 2011-03-25 2014-09-23 Exxonmobil Chemical Patents Inc. Vinyl terminated higher olefin polymers and methods to produce thereof
US8940839B2 (en) 2011-03-25 2015-01-27 Exxonmobil Chemical Patents Inc. Diblock copolymers prepared by cross metathesis
US8835563B2 (en) 2011-03-25 2014-09-16 Exxonmobil Chemical Patents Inc. Block copolymers from silylated vinyl terminated macromers
DK2697207T3 (en) 2011-04-12 2017-03-27 Chong Kun Dang Pharmaceutical Corp 3- (2-ARYL-CYCLOALKENYLMETHYL) -OXAZOLIDIN-2-ON DERIVATIVES AS CHOLESTEROL ESTER-TRANSFER PROTEIN (CETP) INHIBITORS
US9102773B2 (en) 2013-02-06 2015-08-11 Exxonmobil Chemical Patents Inc. Process for controlling molecular weight of polyolefins prepared using pyridyl diamide catalyst systems
US9290519B2 (en) 2013-11-15 2016-03-22 Exxonmobil Chemical Patents Inc. Pyridyldiamido transition metal complexes, production and use thereof
US9315593B2 (en) 2013-11-15 2016-04-19 Exxonmobil Chemical Patents Inc. Catalyst systems comprising pyridyldiamido transition metal complexes and chain transfer agent and use thereof
US9260552B2 (en) 2013-11-15 2016-02-16 Exxonmobil Chemical Patents Inc. Process to produce polymers from pyridyldiamido transition metal complexes and use thereof
WO2015073157A1 (en) 2013-11-15 2015-05-21 Exxonmobil Chemical Patents Inc. Process to produce polymers from pyridyldiamido transition metal complexes and use thereof
US9315526B2 (en) 2014-03-03 2016-04-19 Exxonmobil Chemical Patents Inc. Pyridyldiamido transition metal complexes, production and use thereof
US9598444B2 (en) 2015-06-30 2017-03-21 Exxonmobil Chemical Patents Inc. Transition metal complexes of tridentate dianionic CNN ligands, production and use thereof
CN107922441A (zh) 2015-06-30 2018-04-17 埃克森美孚化学专利公司 三齿双阴离子cnn配体的过渡金属络合物及其生产和用途
TWI704139B (zh) * 2015-08-17 2020-09-11 日商日本煙草產業股份有限公司 羥基三化合物及其醫藥用途
US10618988B2 (en) 2015-08-31 2020-04-14 Exxonmobil Chemical Patents Inc. Branched propylene polymers produced via use of vinyl transfer agents and processes for production thereof
JP2018525507A (ja) 2015-08-31 2018-09-06 エクソンモービル・ケミカル・パテンツ・インク ビニル連鎖移動剤の使用によって製造されたポリマー
US10676547B2 (en) 2015-08-31 2020-06-09 Exxonmobil Chemical Patents Inc. Aluminum alkyls with pendant olefins on clays
CN107922527A (zh) 2015-08-31 2018-04-17 埃克森美孚化学专利公司 用于聚烯烃反应的具有悬垂烯烃的铝烷基
US9982067B2 (en) 2015-09-24 2018-05-29 Exxonmobil Chemical Patents Inc. Polymerization process using pyridyldiamido compounds supported on organoaluminum treated layered silicate supports
WO2018005201A1 (en) 2016-06-30 2018-01-04 Exxonmobil Chemical Patents Inc. Quinolinyldiamido transition metal complexes, production and use thereof
US10208140B2 (en) 2016-06-30 2019-02-19 Exxonmobil Chemical Patents Inc. Quinolinyldiamido transition metal complexes, production and use thereof
US10562987B2 (en) 2016-06-30 2020-02-18 Exxonmobil Chemical Patents Inc. Polymers produced via use of quinolinyldiamido transition metal complexes and vinyl transfer agents
US10927196B2 (en) 2016-06-30 2021-02-23 Exxonmobil Chemical Patents Inc. Long chain branched polypropylene via polymerization with aluminum vinyl transfer agent
WO2018022249A1 (en) 2016-07-29 2018-02-01 Exxonmobil Chemical Patents Inc. Heterocyclic amido transition metal complexes, production and use thereof
US10150821B2 (en) 2016-07-29 2018-12-11 Exxonmobil Chemical Patents Inc. Heterocyclic amido transition metal complexes, production and use thereof
US10882932B2 (en) 2016-10-05 2021-01-05 Exxonmobil Chemical Patents Inc. Sterically hindered metallocenes, synthesis and use
US10626200B2 (en) 2017-02-28 2020-04-21 Exxonmobil Chemical Patents Inc. Branched EPDM polymers produced via use of vinyl transfer agents and processes for production thereof
US10676551B2 (en) 2017-03-01 2020-06-09 Exxonmobil Chemical Patents Inc. Branched ethylene copolymers produced via use of vinyl transfer agents and processes for production thereof
CN109485664B (zh) * 2017-09-12 2022-03-08 北京凯莱天成医药科技有限公司 一种抗真菌药物他伐硼罗的制备工艺
US11578155B2 (en) 2018-03-08 2023-02-14 Exxonmobil Chemical Patents Inc. Ethylene-propylene linear copolymers as viscosity modifiers
US11479625B2 (en) 2018-03-08 2022-10-25 Exxonmobil Chemical Patents Inc. Ethylene-propylene branched copolymers as viscosity modifiers with enhanced fuel economy
CN109266735A (zh) * 2018-06-15 2019-01-25 天津医科大学 Crth2作为肺动脉高压免疫治疗药物靶标及其应用
US20220289882A1 (en) 2019-08-27 2022-09-15 Chevron Oronite Company Llc Ethylene copolymers and use as viscosity modifiers
CN110878043B (zh) * 2019-11-18 2020-08-14 南京哈柏医药科技有限公司 一种地平类降压药物中间体6-甲氧基吡啶-3-甲醛的合成方法

Family Cites Families (86)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5239084A (en) * 1990-06-29 1993-08-24 Hoffmann-La Roche Inc. Substituted aminoalkyl biphenyl compounds
US5827868A (en) * 1991-10-07 1998-10-27 E. R. Squibb & Sons, Inc. Prostaglandin analogs
US5334598A (en) * 1993-03-19 1994-08-02 Merck & Co., Inc. Six-membered ring fused imidazoles substituted with phenoxyphenylacetic acid derivatives
US5565485A (en) * 1993-03-19 1996-10-15 Merck & Co., Inc. Biphenyl compounds useful or endothelin antagonists
US5391566A (en) 1993-07-20 1995-02-21 Merck & Co., Inc. Benzimidazolinones substituted with phenoxyphenylacetic acid derivatives
DE19601782A1 (de) * 1996-01-19 1997-07-24 Merck Patent Gmbh Chinolin-2-(1H)one
CO4960662A1 (es) 1997-08-28 2000-09-25 Novartis Ag Ciertos acidos 5-alquil-2-arilaminofenilaceticos y sus derivados
US6617351B1 (en) * 1998-07-31 2003-09-09 Eli Lilly And Company Amide, carbamate, and urea derivatives
DE19937537A1 (de) * 1999-08-09 2001-03-08 Gruenenthal Gmbh Substituierte 2-Dialkylaminoalkylbiphenyl-Derivate
EP1211513B1 (en) * 1999-08-23 2006-01-04 BML, Inc. Method of identifying modulators of prostaglandin d2 receptors
US6617361B2 (en) * 1999-11-05 2003-09-09 Be Able, Llc Behavior chemotherapy
US20010047027A1 (en) * 2000-04-12 2001-11-29 Marc Labelle Prostaglandin D2 receptor antagonists
US6878522B2 (en) 2000-07-07 2005-04-12 Baiyong Li Methods for the identification of compounds useful for the treatment of disease states mediated by prostaglandin D2
EP1395590B1 (en) * 2001-05-23 2006-09-27 Merck Frosst Canada & Co. Dihydropyrrolo¬1,2-a|indole and tetrahydropyrido¬1,2-a|indole derivatives as prostaglandin d2 receptor antagonists
EP1394147A4 (en) * 2001-06-04 2007-10-24 Eisai R&D Man Co Ltd CARBOXYLENE DERIVATIVE AND A SALT OR AN ESTER CONTAINING MEDICINE
WO2003006011A1 (en) 2001-07-09 2003-01-23 Axys Pharmaceuticals, Inc. 2-[5-(5-carbamimidoyl-1h-heteroaryl)-6-hydroxybiphenyl-3-yl]-succinic acid derivatives as factor viia inhibitors
AR038136A1 (es) 2002-01-24 2004-12-29 Merck Frosst Canada Inc Cicloalcanindoles con sustitucion con fluor composiciones que contienen estos compuestos y metodos de tratamiento
EP2423190A1 (en) * 2002-05-16 2012-02-29 Shionogi&Co., Ltd. Compounds Exhibiting PGD 2 Receptor Antagonism
JP2006511486A (ja) 2002-10-21 2006-04-06 ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー Ｃｒｔｈ２拮抗剤としてのテトラヒドロキノリン誘導体
MXPA05004715A (es) * 2002-10-30 2005-08-03 Merck Frosst Canada Inc Derivados de piridopirrolizina y piridoindolizina.
JP2004182657A (ja) 2002-12-04 2004-07-02 Eisai Co Ltd Ｈｄｌレベル上昇促進剤
AU2003297398B2 (en) 2002-12-20 2009-09-24 Amgen Inc. Asthma and allergic inflammation modulators
EP1471057B1 (en) 2003-04-25 2006-01-18 Actimis Pharmaceuticals, Inc. Pyrimidinylacetic acid derivatives useful for the treatment of diseases mediated by CRTH2
US7205329B2 (en) * 2003-05-30 2007-04-17 Microbia, Inc. Modulators of CRTH2 activity
JP4553899B2 (ja) 2003-08-21 2010-09-29 メルク フロスト カナダ リミテツド カテプシンシステインプロテアーゼ阻害剤
AU2004278382B2 (en) * 2003-09-30 2008-09-18 Amgen Inc. Vanilloid receptor ligands and their use in treatments
US20070232681A1 (en) 2003-10-14 2007-10-04 Oxagen Limited Compounds Having Crth2 Antagonist Activity
GB0324763D0 (en) 2003-10-23 2003-11-26 Oxagen Ltd Use of compounds in therapy
WO2005051373A1 (ja) 2003-11-26 2005-06-09 Takeda Pharmaceutical Company Limited 受容体機能調節剤
US7019022B2 (en) * 2003-12-15 2006-03-28 Merck Frosst Canada & Co. Substituted tetrahydrocarbazole and cyclopentanoindole derivatives
US20060014737A1 (en) * 2004-03-09 2006-01-19 Varghese John Methods of treatment of amyloidosis using bi-aryl aspartyl protease inhibitors
JP4922924B2 (ja) * 2004-04-13 2012-04-25 メルク・シャープ・エンド・ドーム・コーポレイション Ｃｅｔｐ阻害薬
AU2005257999B2 (en) 2004-06-18 2011-12-08 Millennium Pharmaceuticals, Inc. Factor Xa inhibitors
DOP2005000123A (es) 2004-07-02 2011-07-15 Merck Sharp & Dohme Inhibidores de cetp
GB0415320D0 (en) 2004-07-08 2004-08-11 Astrazeneca Ab Novel compounds
EP1773792A1 (en) 2004-07-30 2007-04-18 Merck & Co., Inc. Indanone potentiators of metabotropic glutamate receptors
CA2581338A1 (en) * 2004-09-21 2006-03-30 Athersys, Inc. Indole acetic acids exhibiting crth2 receptor antagonism and uses thereof
AU2005286717A1 (en) * 2004-09-21 2006-03-30 Wyeth Benzimidazole acetic acids exhibiting CRTH2 receptor antagonism and uses thereof
GB0422057D0 (en) * 2004-10-05 2004-11-03 Astrazeneca Ab Novel compounds
GT200500284A (es) * 2004-10-15 2006-03-27 Aventis Pharma Inc Pirimidinas como antagonistas del receptor de prostaglandina d2
WO2006052798A2 (en) 2004-11-08 2006-05-18 Merck & Co., Inc. Method of treating pathological blushing
CA2587545C (en) * 2004-11-19 2013-10-22 Galderma Research & Development, S.N.C. Novel compounds that modulate ppar.gamma. type receptors, and use thereof in cosmetic or pharmaceutical compositions
EP1817297A1 (en) 2004-11-23 2007-08-15 Pfizer Products Inc. Dibenzyl amine compounds and derivatives
NZ556657A (en) 2004-12-27 2010-10-29 Actelion Pharmaceuticals Ltd 2,3,4,9-tetrahydro-1H-carbazole derivatives as CRTH2 receptor antagonists
US7960417B2 (en) 2005-02-24 2011-06-14 Merck Sharp & Dohme Corp. Benzazole potentiators of metabotropic glutamate receptors
CA2598934A1 (en) * 2005-02-25 2006-08-31 Takeda Pharmaceutical Company Limited Pyridyl acetic acid compounds
GB0510584D0 (en) 2005-05-24 2005-06-29 Novartis Ag Organic compounds
BRPI0615133A2 (pt) 2005-08-23 2011-05-03 Irm Llc compostos imunossupressores, composições farmacêuticas contendo os mesmos assim como referido uso
GB0518783D0 (en) * 2005-09-14 2005-10-26 Argenta Discovery Ltd Indolizine compounds
RU2405770C2 (ru) 2005-09-27 2010-12-10 Сионоги Энд Ко., Лтд. Производное сульфонамида, обладающее антагонистической активностью в отношении рецептора pgd2
US8148572B2 (en) * 2005-10-06 2012-04-03 Astrazeneca Ab Compounds
GT200600457A (es) * 2005-10-13 2007-04-27 Aventis Pharma Inc Sal de fosfato dihidrogeno como antagonistas del receptor de prostaglandina d2
ES2380683T3 (es) 2005-12-15 2012-05-17 Astrazeneca Ab Difenil-éteres, -amidas, -sulfuros y - metanos sustituidos para el tratamiento de la enfermedad respiratoria
UY30117A1 (es) 2006-01-31 2007-06-29 Tanabe Seiyaku Co Compuesto amina trisustituido
GB0605743D0 (en) 2006-03-22 2006-05-03 Oxagen Ltd Salts with CRTH2 antagonist activity
GB0611695D0 (en) 2006-06-13 2006-07-26 Novartis Ag Organic compounds
NZ574705A (en) 2006-08-07 2011-12-22 Actelion Pharmaceuticals Ltd (3-amino-1,2,3,4-tetrahydro-9h-carbazol-9-yl)-acetic acid derivatives
NZ575507A (en) 2006-08-21 2011-10-28 Array Biopharma Inc 4-substituted phenoxyphenylacetic acid derivatives
WO2008033455A2 (en) 2006-09-13 2008-03-20 The Institutes For Pharmaceutical Discovery, Llc Biphenyl and heteroaryl phenyl derivatives as protein tyrosine phosphatases inhibitors
US7629258B2 (en) * 2006-11-22 2009-12-08 Clarkson University Method for one-to-one polishing of silicon nitride and silicon oxide
WO2008082567A1 (en) 2006-12-29 2008-07-10 Merck & Co., Inc. Process for synthesizing a cetp inhibitor
US7960567B2 (en) 2007-05-02 2011-06-14 Amgen Inc. Compounds and methods useful for treating asthma and allergic inflammation
WO2008156780A1 (en) 2007-06-21 2008-12-24 Actimis Pharmaceuticals, Inc. Particulates of a crth2 antagonist
UA100983C2 (ru) 2007-07-05 2013-02-25 Астразенека Аб Бифенилоксипропановая кислота как модулятор crth2 и интермедиаты
GB0719521D0 (en) 2007-10-05 2007-11-14 Argenta Discovery Ltd Compounds
WO2009061681A2 (en) * 2007-11-06 2009-05-14 Amira Pharmaceuticals, Inc Antagonists of pgd2 receptors
WO2009061676A2 (en) * 2007-11-06 2009-05-14 Amira Pharmaceuticals, Inc. Antagonists of pgd2 receptors
GB0722203D0 (en) 2007-11-13 2007-12-19 Oxagen Ltd Use of CRTH2 antagonist compounds
GB0722216D0 (en) 2007-11-13 2007-12-27 Oxagen Ltd Use of crth2 antagonist compounds
US20110136877A1 (en) 2008-01-07 2011-06-09 Ligand Pharmaceuticals Inc. 2-phenyl phenoxyacetic acids useful for treating inflammatory disorders
CN101932571B (zh) * 2008-01-18 2014-04-23 奥克萨根有限公司 具有crth2拮抗活性的化合物
WO2009099901A1 (en) 2008-02-01 2009-08-13 Amira Pharmaceuticals, Inc. N,n-disubstituted aminoalkylbiphenyl antagonists of prostaglandin d2 receptors
BRPI0907364A2 (pt) * 2008-02-01 2015-07-14 Amira Pharmaceuticals Inc Antagonistas aminoalquilbifenil n,n-disubstituídos de receptores d2 de prostaglandina
WO2009102893A2 (en) 2008-02-14 2009-08-20 Amira Pharmaceuticals, Inc. CYCLIC DIARYL ETHER COMPOUNDS AS ANTAGONISTS OF PROSTAGLANDIN D2 receptors
JP2011513242A (ja) 2008-02-25 2011-04-28 アミラ ファーマシューティカルズ，インク． プロスタグランジンｄ２受容体アンタゴニスト
US8426449B2 (en) 2008-04-02 2013-04-23 Panmira Pharmaceuticals, Llc Aminoalkylphenyl antagonists of prostaglandin D2 receptors
UY31956A (es) 2008-07-03 2010-01-29 Amira Pharmaceuticals Inc Antagonistas de heteroalquilo de receptores de prostaglandina d2
GB2463788B (en) 2008-09-29 2010-12-15 Amira Pharmaceuticals Inc Heteroaryl antagonists of prostaglandin D2 receptors
US8378107B2 (en) 2008-10-01 2013-02-19 Panmira Pharmaceuticals, Llc Heteroaryl antagonists of prostaglandin D2 receptors
US8524748B2 (en) 2008-10-08 2013-09-03 Panmira Pharmaceuticals, Llc Heteroalkyl biphenyl antagonists of prostaglandin D2 receptors
GB2465062B (en) * 2008-11-06 2011-04-13 Amira Pharmaceuticals Inc Cycloalkane(B)azaindole antagonists of prostaglandin D2 receptors
WO2010057118A2 (en) 2008-11-17 2010-05-20 Amira Pharmaceuticals, Inc. Heterocyclic antagonists of prostaglandin d2 receptors
US20100173313A1 (en) * 2009-01-08 2010-07-08 Amira Pharmaceuticals, Inc. Biomarkers of inflammation
WO2011014588A2 (en) 2009-07-31 2011-02-03 Amira Pharmaceuticals, Inc. Dermal formulations of dp2 receptor antagonists
CN102596199A (zh) 2009-07-31 2012-07-18 潘米拉制药公司 Dp2受体拮抗剂的眼用医药组合物
CN102596902A (zh) * 2009-08-05 2012-07-18 潘米拉制药公司 Dp2拮抗剂及其用途

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9797903B2 (en) 2012-10-24 2017-10-24 Winthrop-University Hospital Non-invasive biomarker to identify subject at risk of preterm delivery
EP3382391A1 (en) 2012-10-24 2018-10-03 NYU Winthrop Hospital Non-invasive biomarker to identify subjects at risk of preterm delivery
US10408838B2 (en) 2012-10-24 2019-09-10 Nyu Winthrop Hospital Non-invasive biomarker to identify subject at risk of preterm delivery
US11333672B2 (en) 2017-09-13 2022-05-17 Progenity, Inc. Preeclampsia biomarkers and related systems and methods
US11112403B2 (en) 2019-12-04 2021-09-07 Progenity, Inc. Assessment of preeclampsia using assays for free and dissociated placental growth factor
US11327071B2 (en) 2019-12-04 2022-05-10 Progenity, Inc. Assessment of preeclampsia using assays for free and dissociated placental growth factor

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Owner name: PANMIRA PHARMACEUTICALS, LLC, CALIFORNIA

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Effective date: 20110902

STCB Information on status: application discontinuation

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