WO2005123680A1 - Six-membered heterocycles useful as serine protease inhibitors - Google Patents
Six-membered heterocycles useful as serine protease inhibitors Download PDFInfo
- Publication number
- WO2005123680A1 WO2005123680A1 PCT/US2005/020971 US2005020971W WO2005123680A1 WO 2005123680 A1 WO2005123680 A1 WO 2005123680A1 US 2005020971 W US2005020971 W US 2005020971W WO 2005123680 A1 WO2005123680 A1 WO 2005123680A1
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- WIPO (PCT)
- Prior art keywords
- phenyl
- substituted
- alkyl
- occurrence
- independently
- Prior art date
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- 125000004070 6 membered heterocyclic group Chemical group 0.000 title description 6
- 239000003001 serine protease inhibitor Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 227
- 238000000034 method Methods 0.000 claims abstract description 99
- 150000003839 salts Chemical group 0.000 claims abstract description 61
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- 239000012453 solvate Chemical group 0.000 claims abstract description 29
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 23
- 208000027866 inflammatory disease Diseases 0.000 claims abstract description 14
- -1 carbocycle Chemical group 0.000 claims description 301
- 125000000217 alkyl group Chemical group 0.000 claims description 282
- 125000000623 heterocyclic group Chemical group 0.000 claims description 257
- 229910052760 oxygen Inorganic materials 0.000 claims description 154
- 125000004432 carbon atom Chemical group C* 0.000 claims description 137
- 229910052717 sulfur Inorganic materials 0.000 claims description 132
- 125000005842 heteroatom Chemical group 0.000 claims description 129
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 109
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- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 62
- 229910052794 bromium Inorganic materials 0.000 claims description 62
- 125000003118 aryl group Chemical group 0.000 claims description 56
- 229910052740 iodine Inorganic materials 0.000 claims description 56
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 56
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 50
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- 125000001072 heteroaryl group Chemical group 0.000 claims description 25
- 125000001624 naphthyl group Chemical group 0.000 claims description 24
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- 125000001424 substituent group Chemical group 0.000 claims description 23
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- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 4
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/16—Central respiratory analeptics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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Definitions
- the present invention relates generally to compounds that inhibit serine proteases.
- it is directed to novel six-membered heterocycle derivatives of Formula (I):
- the compounds of Formula (I) are useful as selective inhibitors of serine protease enzymes of the coagulation cascade and/or contact activation system; for example thrombin, factor XIa, factor Xa, factor IXa, factor Vila, and/or plasma kallikrein.
- thrombin thrombin
- factor XIa serine protease enzymes of the coagulation cascade and/or contact activation system
- factor XIa factor Xa
- factor IXa factor Vila
- plasma kallikrein relates to compounds that are selective factor XIa inhibitors or dual inhibitors of fXIa and plasma kallikrein.
- This invention also relates to pharmaceutical compositions comprising these compounds and methods of using the same.
- Factor XIa is a plasma serine protease involved in the regulation of blood coagulation. While blood coagulation is a necessary and important part of the regulation of an organism's homeostasis, abnormal blood coagulation can also have deleterious effects. For instance, thrombosis is the formation or presence of a blood clot inside a blood vessel or cavity of the heart. Such a blood clot can lodge in a blood vessel blocking circulation and inducing a heart attack or stroke. Thromboembolic disorders are the largest cause of mortality and disability in the industrialized world.
- TF Factor VII
- FVIIa Factor Vila
- FIX Factor IX
- FXa Factor Xa
- the FXa that is generated catalyzes the transformation of prothrombin into small amounts of thrombin before this pathway is shut down by tissue factor pathway inhibitor (TFPI).
- TFPI tissue factor pathway inhibitor
- the process of coagulation is then further propagated via the feedback activation of Factors V, VIII and XI by catalytic amounts of thrombrn.
- Factor XIa plays a key role in propagating this amplification loop and is thus an attractive target for anti-thrombotic therapy.
- Contact activation is a surface mediated process responsible in part for the regulation of thrombosis and inflammation, and is mediated, at least in part, by fibrinolytic-, complement-, kmmogen/kinin-, and other humoral and cellular pathways (for review, Coleman, R. Contact Activation Pathway, pages 103-122 in Hemostasis and Thrombosis, Lippincott Williams & Wilkins 2001; Schmaier A.H. Contact Activation, pages 105-128 in Thrombosis and Hemorrhage, 1998).
- Factor XI is a zymogen of a trypsin-like serine protease and is present in plasma at a relatively low concentration. Proteolytic activation at an internal R369- 1370 bond yields a heavy chain (369 amino acids) and a light chain (238 amino acids). The latter contains a typical trypsin-like catalytic triad (H413, D464, and S557). Activation of factor XI by thrombin is believed to occur on negatively charged surfaces, most likely on the surface of activated platelets.
- Platelets contain high affinity (0.8 nM) specific sites (130-500/platelef) for activated factor XL After activation, factor XIa remains surface bound and recognizes factor IX as its normal macromolecular substrate.
- thrombin activates thrombin activated fibrinolysis inhibitor (TAFI), a plasma carboxypeptidase that cleaves C-terminal lysine and arginine residues on fibrin, reducing the ability of fibrin to enhance tissue-type plasminogen activator (tPA) dependent plasminogen activation.
- TAFI thrombin activated fibrinolysis inhibitor
- tPA tissue-type plasminogen activator
- factor XI is not required for normal homeostasis, implying a superior safety profile of the factor XI mechanism compared to competing antithrombotic mechanisms.
- hemophilia A factor VIII deficiency
- hemophilia B factor IX deficiency
- mutations of the factor XI gene causing factor XI deficiency result in only a mild to moderate bleeding diathesis characterized primarily by postoperative or posttraumatic, but rarely spontaneous hemorrhage.
- Postoperative bleeding occurs mostly in tissue with high concentrations of endogenous fibrinolytic activity (e.g., oral cavity, and urogenital system). The majority of the cases are fortuitously identified by preoperative prolongation of APTT (intrinsic system) without any prior bleeding history.
- factor XI activation can be determined by complex formation with either CI inhibitor or alpha 1 antitrypsin.
- AMI acute myocardial infarction
- approximately 25% of the patients had values above the upper normal range of the complex ELISA.
- This study can be viewed as evidence that at least in a subpopulation of patients with AMI, factor XI activation contributes to thrombin formation (Minnema, M.C. et al. Arterioscler.
- Plasma kallikrein is a zymogen of a trypsin-like serine protease and is present in plasma at 35 to 50 ⁇ g/mL.
- the gene structure is similar to that of factor XI, overall, the amino acid sequence of plasma kallikrein has 58% homology to factor XL
- Proteolytic activation by factor Xlla at an internal I 389- R390 bond yields a heavy chain (371 amino acids) and a light chain (248 amino acids).
- the active site of kallikrein is contained in the light chain.
- the light chain of plasma kallikrein reacts with protease inhibitors, including alpha 2 macroglobulin and CI- inhibitor.
- HMWK high molecular weight kininogen
- WO 01/27079 There are advantages in using small organic compounds, however, in preparing pharmaceuticals, e.g., small compounds generally have better oral bioavailability and compatibility in making formulations to aid in delivery of the drug as compared with large proteins or peptides.
- Small molecule inhibitors of Factor XIa are disclosed in U.S. Patent Application Publication US20040235847A1 and US Patent Application Publication US20040220206A1.
- new compounds with improved plasma kallikrein inhibitory activity and selectivity for plasma kallikrein versus other serine proteases are preferred. It is also desirable and preferable to find compounds with advantageous and improved characteristics in one or more of the following categories, but are not limited to: (a) pharmaceutical properties; (b) dosage requirements; (c) factors which decrease blood concentration peak-to-trough characteristics; (d) factors that increase the concentration of active drug at the receptor; (e) factors that decrease the liability for clinical drug-drug interactions; (f) factors that decrease the potential for adverse side-effects; and (g) factors that improve manufacturing costs or feasibility.
- the present invention provides novel six-membered heterocycle derivatives, and analogues thereof, which are useful as selective inhibitors of serine protease enzymes, especially factor XIa and/or plasma kallikrein, or stereoisomers or pharmaceutically acceptable salts, solvates, or prodrugs thereof.
- the present invention also provides processes and intermediates for making the compounds of the present invention or a stereoisomer or a pharmaceutically acceptable salt, solvate, or prodrug form thereof.
- the present invention also provides pharmaceutical compositions comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt, solvate or prodrug form thereof.
- the present invention also provides a method for modulation of the coagulation cascade and/or the contact activation system comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt, solvate, or prodrug form thereof.
- the present invention also provides a method for treating thromboembolic disorders comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt, solvate, or prodrug form thereof.
- the present invention also provides a method for treating inflammatory diseases disorders comprising adn ⁇ iistering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt, solvate, or prodrug form thereof.
- the present invention also provides novel six-membered heterocycle derivatives, and analogues thereof, for use in therapy.
- the present invention also provides the use of six-membered heterocycle derivatives, and analogues thereof, for the manufacture of a medicament for the treatment of a thromboembolic disorder.
- the present invention also provides the use of six-membered heterocycle derivatives, and analogues thereof, for the manufacture of a medicament for the treatment of an inflammatory disorder.
- the present invention provides, inter alia, a compound of Formula (I):
- A is C3.7 cycloalkyl substituted with 0-1 R 1 and 0-2 R 2 , C3-7 cycloalkenyl substituted with 0-1 R 1 and 0-2 R 2 , phenyl substituted with 0-1 R 1 and 0-3 R 2 , naphthyl substituted with 0-1 R 1 and 0-3 R 2 , or a 5- to 12-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted 0-1 R 1 and 0-3 R 2 ;
- X 1 , X 2 , X 3 , and X 4 are independently CR 3 , CR 4 , N, NR 6 , N ⁇ O, or C(O); provided that at least one of X 1 , X 2 , X 3 , and X 4 is CR 3 ;
- X 5 is N, NR 6 or N ⁇ O;
- Z is -CH(R n )- or NR 13 ;
- L is -C(O)NR10-, -NR 10 C(O)-, -CH 2 C(O)NR 10 -, -CH 2 NR 10 C(O)-,
- R 1 is, independently at each occurrence, -NH2, -NH(C ⁇ _3 alkyl),
- R 1 and R 2 when R 1 and R 2 are substituted on adjacent ring atoms, they can be taken together with the ring atoms to which they are attached to form a 5- to 7-membered carbocycle or heterocycle comprising: carbon atoms and 0-4 heteroatoms selected from N, O, and S(O) p , wherein said carbocycle or heterocycle is substituted with 0-2 R 2b ;
- R 3 is, independently at each occurrence, -(CH 2 ) r C(O)NR 8 R9,
- R 3b is, independently at each occurrence, H, C ⁇ _6 alkyl substituted with
- R 3c is, independently at each occurrence, C1.-6 alkyl substituted with
- R 3 and R 4 groups when located on adjacent atoms can be taken together to form a C3_ ⁇ o carbocycle substituted with 0-2 R 3d or a 5- to 10- membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-2 R 3d ;
- R 6 is, independently at each occurrence, H, C ⁇ -6 alkyl, C1-4 haloalkyl,
- R 7 is, independently at each occurrence, H, alkyl, -(CH 2 ) n -C3-io carbocycle, -(CH 2 ) n -(5-10 membered heteroaryl), -C(O)R c , -CHO, -C(O) 2 R c , -S(O) 2 R c , -CONR Rc, -OCONHRc, -C(O)O-(C]-4 alkyl)OC(O)-(C ⁇ _4 alkyl), or -C(O)O-(Ci_4 alkyl)OC(O)-(C6-io aryl); wherein said alkyl, carb
- R 7 and R 8 when attached to the same nitrogen, combine to form a 5- to 10-membered heterocycle comprising: carbon atoms and 0-2 additional heteroatoms selected from N, O, and S(O) P; wherein said heterocycle is substituted with 0-2 R d ;
- R 8a is, independently at each occurrence, R 7 , OH, C ⁇ _ 6 alkyl,
- R 9a is, independently at each occurrence, H, alkyl, or
- R 8 and R 9 when attached to the same nitrogen, combine to form a 5- to 10-membered heterocycle comprising: carbon atoms and 0-2 additional heteroatoms selected from N, O, and S(O) Pj wherein said heterocycle is substituted with 0-2 R d ;
- R 10 is, independently at each occurrence, H, C ⁇ _g alkyl substituted with
- Rl * is C1-4 haloalkyl, -(CH 2 ) r -C(O)NR 8 R9, CI_ 6 alkyl substituted with
- R 1 lb is, independently at each occurrence
- R 1 lb groups when two R 1 lb groups are substituents on adjacent atoms they may be taken together with the atoms to which they are attached to form a 5- to 7-membered heterocycle comprising carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p and substituted with 0-2 R ⁇ ;
- R 13 is H, C ⁇ _ 6 alkyl, -C(O)R c , -C(O)OR c , -CONR 8 R c , -OCONR 8 R ,
- R a is, independently at each occurrence, H, CF3, Ci-6 alkyl,
- cycloalkyl -(CH 2 ) r -C3-7 cycloalkyl, -(CH ) r -C6-io aryl, or -(CH 2 ) r -5- to 10-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p ; wherein said cycloalkyl, aryl and heterocycle groups are optionally substituted with 0-2 R f ;
- R b is, independently at each occurrence, CF3, OH, C1.4 alkoxy,
- R8 is, independently at each occurrence, H, C g alkyl, or -(CH 2 ) n -phenyl;
- n at each occurrence, is selected from 0, 1, 2, 3, and 4;
- p at each occurrence, is selected from 0, 1, and 2;
- r at each occurrence, is selected from 0, 1, 2, 3, and 4;
- s at each occurrence, is selected from 1, 2, 3, and 4.
- the present invention includes a compound of
- the present invention includes a compound of
- A is substituted with 0-1 R 1 and 0-2 R 2 and selected from; C3-7 cycloalkyl, phenyl, naphthyl, pyridyl, 1,2,3,4-tetrahydronaphthyl, indazolyl, benzimidazolyl, benzisoxazolyl, isoquinolinyl, 5,6,7,8-tetrahydroisoquinolinyl, 1,2,3,4-tetrahydroisoquinolinyl, quinazolinyl, lH-quinazolin-4-onyl, 2H-isoquinolin-l-onyl, 3H-quinazolin-4-onyl, 3,4-dihydro-2H-isoquinolin-l-onyl, 2,3-dmydroisoindolinonyl, and phthalazinyl;
- L is -C(O)NR 10 -, or -NR 10 C(O)-;
- Z is CHR 11 ;
- R 4 is, independently at each occurrence, H, F, CI, Br, I, OCF3, CF3,
- R J ° is, independently at each occurrence, H, C ⁇ _6 alkyl substituted with
- R 10a -(CH 2 ) r -phenyl substituted with 0-2 R d , or -(CH 2 ) r -5-10 membered heterocycle comprising carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-2 R d ; and [0083]
- R 1 1 is C1-4 haloalkyl, -(CH 2 ) r -CONR 8 R 9 , C ⁇ - 6 alkyl substituted with
- the present invention includes a compound of
- R 1 is, independently at each occurrence, F, CI, Me, Et, -NH 2 ,
- R 3 is -CO 2 H, -CO 2 Me, -C(O)NHCH 2 CO 2 H, -C(O)NHCH 2 CO 2 Et,
- R 4 is H, F, CI, Br, OMe, NH 2 , CF 3 , CO 2 H, CO 2 Me, CO 2 Et,
- R 10 is H
- R 1 1 is C ⁇ -6 alkyl, -(CH 2 ) r -C(O)NR 8 R 9 , -CH 2 OBn, -CH 2 SBn, -(CH 2 ) S - cyclohexyl substituted with 0-2 R 1 lb , -(CH 2 ) s - ⁇ henyl substituted with 0-2 R 1 lb , - (CH2) s -naphthyl substituted with 0-2 R l lb , -(CH 2 ) s -5-to 10-membered heteroaryl substituted with 0-1 R 1 lb ; wherein said heteroaryl selected from thiazolyl, imidazolyl, pyridyl, indolyl benzimidazolyl, and benzothiazolyl.
- the present invention includes a compound of Formula
- L is -C(O)NH-
- R 1 ! is phenylmethyl, 4-imidazolylmethyl, 4-tl ⁇ iazolylmethyl,
- 2-benzthiazolylmethyl 2- pyridylmethyl, 3- pyridylmethyl, 4- pyridyhnethyl, 3-indolylmethyl, 2-benzimidazolylmethyl, 1 -naphthyhnethyl, 2- naphthyhnethyl, cyclohexylmethyl, -CH 2 C(O)NHCH 2 -py ⁇ idin-2-yl or
- R 1 lb is, independently at each occurrence, H, F, CI, Br, CF3, OMe, OCF3, OCHF 2 , OPh, OBn, NO 2 , -NH 2 , -C(O)Ph, -NHC(O)Bn, -NHC(O)CH 2 CH 2 Ph,
- the present invention includes a compound of
- R 3 is phenyl substituted with 0-2 R 3a , naphthyl substituted with 0-2
- R 3a indanone substituted with 0-2 R 3a , or a 5- to 10-membered heterocycle substituted with 0-2 R 3a and selected from: pyridine, pyridinone, pyrimidine, pyrrole, pyrazole, indole, 2-oxoindole, indazole, benzofuran, benzothiophene, benzimidazole, benzisoxazole, benzoxazole, quinazoline, 5H-quinazolin-4-one, phthalazine, 2H-phthalazin-l-one, iH-quinolin-4-one, isoquinoline, and 2H-3 ,4-dihydroisoquinolin- 1 -one.
- the present invention includes a compound of
- A is 4-aminomethyl-cyclohexyl, 4-carbamoyl-cyclohexyl,
- R 3 is phenyl, 3-OH-phenyl, 3,4-methylenedioxyphenyl, 2-naphthyl,
- 2-NH 2 -pyrid-4-yl 2-NH 2 -pyrid-4-yl, 2-NH 2 -pyrid-5-yl, 2-NH 2 -pyrid-6-yl, 2-NHMe-pyrid-4-yl, 2-NMe 2 -pyrid-4-yl, 2-CONH 2 -pyrid-4-yl, 2-CO 2 H-pyrid-4-yl, 2-CONH 2 -pyrid-5-yl, 2-OMe-6-NH2-pyridyl-4-yl, 4-NH 2 -pyrimidin-6-yl, 4-NH 2 -pyrimidin-2-yl, 2-NH 2 -pyrixnidin-4-yl, 2-NH 2 -pyrimidin-5-yl, indol-5-yl, indol-6-yl, indazol-5-yl, indazol-6-yl, 3-OH-indazol-5-yl, 3-OH-indazol-6-yl, 3-OMe-
- 3-OMe-indazol-6-yl 3-NH 2 -indazol-5-yl, 3-NH 2 -indazol-6-yl, benzisoxalol-6-yl, benzisoxazol-5-yl, 3-NH 2 -benzoisoxazol-5-yl, 3-NH 2 -benzoisoxazol-6-yl, 4-OMe-quinolin-6-yl, l-NH 2 -phthalazin-6-yl, l-NH 2 -phthalazin-7-yl, 4-NH 2 -quinazolin-6-yl, 2-Me-4-amino-quinazolin-6-yl, 4-NH 2 -quinazolin-7-yl, 2-Me-4-NH 2 -quinazolin-7-yl, 2,4-di-NH 2 -quinazolin-7-yl,
- the present invention provides a compound of
- A is C3.7 cycloalkyl substituted with 0-1 R 1 and 0-2 R 2 , C3.7 cycloalkenyl substituted with 0-1 R 1 and 0-2 R 2 , phenyl substituted with 0-1 R 1 and 0-3 R 2 , naphthyl substituted with 0-1 R 1 and 0-3 R 2 , or a 5- to 10-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted 0-1 R 1 and 0-3 R 2 ;
- the group is selected from:
- L is -C(O)NR 10 -, -NR ⁇ O)-, -CH 2 C(O)NR 1 0-, -CH 2 NRlOC(O)-,
- R 1 is, independently at each occurrence, -NH , -NH(C ⁇ _3 alkyl),
- R 1 and R 2 when R 1 and R 2 are substituted on adjacent ring atoms, they can be taken together with the ring atoms to which they are attached to form a 5- to 7-membered carbocycle or heterocycle comprising: carbon atoms and 0-4 heteroatoms selected from N, O, and S(O) p , wherein said carbocycle or heterocycle is substituted with 0-2 R 2b ;
- R 3 is, independently at each occurrence, -(CH 2 ) r C(O)NR 8 R 9 ,
- R 3a groups when two R 3a groups are substituted on adjacent atoms, they can be taken together with the atoms to which they are attached to form a C3-10 carbocycle substituted with 0-2 R 3d or a 5- to 10-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-2 R 3d ;
- R 3b is, independently at each occurrence, H, _6 alkyl substituted with 0-2 R 3d , C 2 _6 alkenyl substituted with 0-2 R 3d , C 2 _6 alkynyl substituted with 0-2 R 3 -(CH2) r -C3-io carbocycle substituted with 0-3 R 3d or -(CH 2 ) r -5- to 10-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-3 R 3d ; [00114] R 3c is, independently at each occurrence, alkyl substituted with 0-2 R 3d , C 2 -6 alkenyl substituted with 0-2 R 3d C 2 _6 alkynyl substituted with 0-2 R 3d -(CH2) r -C3_ ⁇ o carbocycle substituted with 0-3 R 3d ;
- R 3 and R 4 groups when located on adjacent atoms can be I taken together to form a C3-10 carbocycle substituted with 0-2 R 3d or a 5- to 10- membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-2 R 3d ;
- R 6 is, independently at each occurrence, H, Ci-6 alkyl, C1-4 haloalkyl,
- R 7 is, independently at each occurrence, H, alkyl, -(CH 2 ) n -C3-io carbocycle, -(CH 2 ) n -(5-10 membered heteroaryl), -C(O)R c , -CHO, -C(O) 2 R c , -S(O) 2 R c , -CONR 8 R c , -OCONHR c , -C(O)O-(C ⁇ _ 4 alkyl)OC(O)-(C ⁇ .
- R 8 is, independently at each occurrence, H, C ⁇ _g alkyl, -(CH 2 ) n -phenyl, or -(CH 2 ) n -5-10 membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected fromN, O, and S(O) p ; wherein said alkyl, phenyl and heterocycle are optionally substituted with 0-2 R f ;
- R 7 and R 8 when attached to the same nitrogen, combine to form a 5- to 10-membered heterocycle comprising: carbon atoms and 0-2 additional heteroatoms selected from N, O, and S(O)p 5 wherein said heterocycle is substituted with 0-2 R d ;
- R 8a is, independently at each occurrence, R 7 , OH, C 1-6 alkyl,
- R9 is, independently at each occurrence, H, C ⁇ g alkyl, or
- R 9 is, independently at each occurrence, H, C ⁇ _6 alkyl, or
- R 8 and R 9 when attached to the same nitrogen, combine to form a 5- to 10-membered heterocycle comprising: carbon atoms and 0-2 additional heteroatoms selected from N, O, and S(O) P; wherein said heterocycle is substituted with 0-2 R d ;
- R 10 is, independently at each occurrence, H, C ⁇ _6 alkyl substituted with 0-2 R 10a , -(CH 2 ) phenyl substituted with 0-3 R d , or -(CH 2 ) r -5- to 10-membered heterocycle comprising carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-3 R d ;
- R 1 1 is C1-4 haloalkyl, -(CH 2 ) r -C(O)NR 8 R 9 , C ⁇ _ 6 alkyl substituted with
- R 1 lb groups when two R 1 lb groups are substituents on adjacent atoms they may be taken together with the atoms to which they are attached to form a 5- to 7-membered heterocycle comprising carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p and substituted with 0-2 R ⁇ ;
- R 3 is H, C 6 alkyl, -C(O)R c , -C(O)OR c , -CONR 8 R c , -OCONR R c ,
- R a is, independently at each occurrence, H, CF3, alkyl,
- R b is, independently at each occurrence, CF3, OH, C1-4 alkoxy, C ⁇ _6 alkyl, -(CH 2 ) r -C3. ⁇ o carbocycle substituted with 0-3 R d , or -(CH ) r 5- to 10- membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p and substituted with 0-2 R d ;
- R c is, independently at each occurrence, CF3, Cj
- RS is, independently at each occurrence, H, C g alkyl, or
- n at each occurrence, is selected from 0, 1, 2, 3, and 4
- p at each occurrence, is selected from 0, 1, and 2;
- r at each occurrence, is selected from 0, 1, 2, 3, and 4;
- s at each occurrence, is selected from 1, 2, 3, and 4.
- the present invention includes compounds of Formula (la), within the scope of the eighth aspect wherein: [00147] A is substituted with 0-1 R 1 and 0-2 R 2 and selected from; C3.7 cycloalkyl, phenyl, naphthyl, pyridyl, 1,2,3,4-tetrahydronaphthyl, indazolyl, benzimidazolyl, benzisoxazolyl, isoquinolinyl, 5,6,7,8-tetrahydroisoquinolinyl, 1,2,3,4-tetral ⁇ ydroisoquinolinyl, quinazolinyl, 1 H-quinazolin-4-onyl, 2H-isoquinolin-l-onyl, 3H-quinazolin-4-onyl, 3,4-dihydro-2H-isoquinolin-l-onyl, 2,3-du ⁇ ydroisoindolinonyl
- R 4 is, independently at each occurrence, H, F, CI, Br, I, CF3, CN, NO2,
- R 6 is H, or C ⁇ _ 4 alkyl.
- the present invention includes compounds of Formula (la), within the scope of the ninth aspect wherein:
- R 1 is, independently at each occurrence, F, CI, Me, Et, -NH2,
- R 2 is, independently at each occurrence, F, CI, Me, OMe, OEt, Bn,
- R 3 is -CO 2 H, -CO 2 Me, -C(O)NHCH 2 CO 2 H, -C(O)NHCH 2 CO 2 Et,
- R 10 is H
- R 1 1 is -(CH 2 ) r -C(O)NR 8 R9, -CH 2 OBn, -CH 2 SBn, -(CH 2 ) s -cyclohexyl substituted with 0-2 R l lb , -(CH 2 ) s - ⁇ henyl substituted with 0-2 R l lb , -(CH 2 ) s -naphthyl substituted with 0-2 R l lb , -(CH2) s -5-to 10-membered heteroaryl substituted with 0-1 R 1 lb ; wherein said heteroaryl selected from thiazolyl, imidazolyl, pyridyl, indolyl benzimidazolyl, and benzothiazolyl.
- the present invention includes compounds of
- R 1 ! is phenylmethyl, 4-imidazolylmethyl, 4-thiazolylmethyl,
- the present invention includes compounds of
- R 3 is phenyl substituted with 0-2 R 3a , naphthyl substituted with 0-2
- R 3a indanone substituted with 0-2 R 3a , or a 5- to 10-membered heterocycle substituted with 0-2 R 3a and selected from: pyridine, pyridinone, pyrimidine, pyrrole, pyrazole, indole, 2-oxoindole, indazole, benzofuran, benzothiophene, benzimidazole, benzisoxazole, benzoxazole, quinazoline, 3H-quinazolin-4-one, phthalazine, 2H-phthalazin-l-one, iH-quinolin-4-one, isoquinoline, and 2H-3,4-dihydroisoquinolin-l -one.
- the present invention includes compounds of Formula (la), within the scope of the twelfth aspect wherein:
- A is 4-aminomethyl-cyclohexyl, 4-carbamoyl-cyclohexyl,
- R 3 is phenyl, 3-OH-phenyl, 3,4-methylenedioxyphenyl, 2-naphthyl,
- the present invention includes compounds of
- the present invention provides a compound selected from the exemplified examples or stereoisomers or pharmaceutically acceptable salts, solvates, or prodrugs thereof.
- the present invention includes, inter alia, compounds of Formula (III):
- A is C3.10 carbocycle substituted with 0-1 R 1 and 0-3 R 2 , or a 5- to 10- membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from
- X is C, CH, or N
- X 1 , X 2 , X 3 , X 4 , and ⁇ 5 are independently CR 3 , CR 4 , CR 5 , CR 4 R 5 , O,
- CH at least one of ⁇ l, X 2 , X 3 , X 4 , and X 5 is selected from N, NR 3 , NR 6 , and N ⁇ O;
- Z is -C(R! l )(R 12 )- or -NR 13 -;
- L is -C(O)NR!0-, -NR* 0 C(O)-, -CH 2 C(O)NR 10 -, -CH2JNR 10 C(O)-,
- R 1 is, independently at each occurrence, -NH 2 , -NH(C ⁇ _3 alkyl),
- R 3a groups when two R 3a groups are substituted on adjacent atoms, they can be taken together with the atoms to which they are attached to form a C3.10 carbocycle substituted with 0-2 R 3d , or a 5- to 10-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-2 R 3d ;
- R 3b is, independently at each occurrence, H, C ⁇ _6 alkyl substituted with
- R 3d C 2 -6 alkenyl substituted with 0-2 R 3d , C 2 _6 alkynyl substituted with 0-2 R 3d , -(CH 2 ) r -C3-io carbocycle substituted with 0-3 R 3d , or -(CH 2 ) r -5- to 10-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-3 R 3d ; [00190] R 3c is, independently at each occurrence, C ⁇ _6 alkyl substituted with
- R 3e is, independently at each occurrence, H, -(CH 2 ) r OR a , F, CI, Br, I,
- R 3 and R 4 groups when located on adjacent atoms, can be taken together to form a C3-10 carbocycle substituted with 0-2 R 3d or a 5- to 10- membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(0) p , wherein said heterocycle is substituted with 0-2 R 3d ;
- R 5 is, independently at each occurrence, H, F, CI, Br, I, OCF3, CF 3 , OR a , SR a , CN, NO 2 , -C(O)R a , -C(O)OR , -OC(O)R a , -NR 7 R 8 , -C(O)NR 7 R 8 ,
- alkyl substituted with 0-2 R 5a C 2 _6 alkenyl substituted with 0-2 R 5a , C 2 _6 alkynyl substituted with 0-2 R 5a , -(CH 2 ) r -C 3 . ⁇ o carbocycle substituted with 0-3 R 5b , or -(CH 2 ) r -5- to 10- membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , and substituted with 0-3 R 5b ;
- R 3 , R 4 , or R 5 are substituted on adjacent atoms, two of them can be taken together with the carbon atoms to which they are attached to form a 5- to 7-membered carbocycle or heterocycle substituted with 0-3 R 3a and 0-1 R ;
- R 6 is, independently at each occurrence, H, C1-6 alkyl substituted with
- R 7 is, independently at each occurrence, H, C ⁇ _6 alkyl, -(CH 2 )n-C 3 _ ⁇ 0 carbocycle, -(CH 2 ) n -(5-l 0 membered heteroaryl), -CHO, -C(O)R c , -C(O)OR c , -CONR 8 R c , -OC(O)NHR c , -S(O) 2 R c , -C(O)O-(C ⁇ _4 alkyl)-OC(O)-(Ci- 4 alkyl),
- R 8 is, independently at each occurrence, H, C g alkyl, or
- R 7 and R 8 when attached to the same nitrogen, combine to form a 5- to 10-membered heterocycle comprising: carbon atoms and 0-2 additional heteroatoms selected from N, O, and S(O) P) wherein said heterocycle is substituted with 0-2 R d ;
- R 8a is, independently at each occurrence, R 7 , OH, C1-4 alkoxy,
- R 9 is, independently at each occurrence, H, alkyl, or
- R 9a is, independently at each occurrence, H, C ⁇ _6 alkyl, or
- R 8 and R 9 when attached to the same nitrogen, combine to form a 5- to 10-membered heterocycle comprising: carbon atoms and 0-2 additional heteroatoms selected from N, O, and S(O) P; wherein said heterocycle is substituted with 0-2 R d ;
- R 10 is, independently at each occurrence, H, C ⁇ -6 alkyl substituted with 0-3 R 10a , C 2 -6 alkenyl substituted with 0-3 R 10a , C 2 -6 alkynyl substituted with 0-3 R 10a , -(CH2) r -C 3 _io carbocycle substituted with 0-3 R d , or -(CH ) r -5- to 10- membered heterocycle comprising carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-3 R d ;
- Rl 1 is C1.4 haloalkyl, -(CH 2 ) r -C(O)NR 7 R 8 , C ⁇ _ 6 alkyl substituted with
- R 1 lb groups when two R 1 lb groups are substituents on adjacent atoms they may be taken together with the atoms to which they are attached to form a 5- to 7-membered carbocycle or heterocycle comprising carbon atoms and 0-4 heteroatoms selected from N, O, and S(O) p and substituted with 0-2 R8;
- R 12 is H, F, C haloalkyl, C ⁇ _ 6 alkyl substituted with 0-3 R 1 a ,
- R 1 * and R 12 can be taken together to form a C3.10 carbocycle substituted with 0-2 R 12b , or a 5- to 10-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected fromN, O, and S(O) p , wherein said heterocycle is substituted with 0-2 R 1 b ; [00220] alternately, R 11 or
- R 13 is H, C ⁇ _ 6 alkyl, -C(O)R c , -C(O)OR c , -CONR 8 R c , -OCONR 8 R c ,
- R 13 can be taken together with R 10 to form a 5- to 10- membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-2 R d ;
- R 14 is, independently at each occurrence, H, CM a lky ⁇ > OR a , F, CN,
- R a is, independently at each occurrence, H, CF3, C ⁇ _6 alkyl,
- R b is, independently at each occurrence, CF3, OH, CM alkoxy,
- Rg is, independently at each occurrence, H, C ⁇ _g alkyl, or -(CH 2 ) n -phenyl;
- n at each occurrence, is selected from 0, 1, 2, 3, and 4;
- p at each occurrence, is selected from 0, 1, and 2;
- r at each occurrence, is selected from 0, 1, 2, 3, and 4;
- s at each occurrence, is selected from 1, 2, 3, and 4.
- the present invention includes compounds of
- A is C3.8 cycloalkyl substituted with 0-1 R 1 and 0-3 R 2
- A is C3-8 cycloalkenyl substituted with 0-1 R 1 and 0-3 R 2 , phenyl substituted with 0-1 R 1 and 0-3 R 2 , naphthyl substituted with 0-1 R 1 and 0-3 R 2 , or a 5- to 10- membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected fromN, O, and S(O) p , wherein said heterocycle is substituted 0-1 R 1 and 0-3 R 2 ;
- Z is -C(R ⁇ XR 12 )-;
- L is -C(O)NR 10 -, -NR 10 C(O)-, -CH 2 C(O)NR 10 -, -
- R 3 is, independently at each occurrence, -(CH 2 ) r C(O)NR 8 R 9 ,
- R 6 is, independently at each occurrence, H, alkyl substituted with 0-2 R 6a , C 2 _6 alkenyl substituted with 0-2 R 6a , C _ 6 alkynyl substituted with 0-2 R 6a , (C
- R 10 is, independently at each occurrence, H, C ⁇ _6 alkyl substituted with
- R 10a 0-3 R 10a , -(CH 2 ) r -C 3 _ ⁇ o carbocycle substituted with 0-3 R d , or -(CH 2 ) r -5- to 10- membered heterocycle comprising carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , and substituted with 0-3 R d ; and [00245]
- R 11 is CM haloalkyl, C ⁇ _ 6 alkyl substituted with 0-3 R 1 la , C 2 .
- the present invention includes compounds of
- A is C 5 _ 6 cycloalkyl substituted with 0-1 R 1 and 0-2 R 2 , A is
- R 3 is, independently at each occurrence, -(CH 2 ) r C(O)NR 8 R 9 ,
- R 6 is, independently at each occurrence, H, or C ⁇ _6 alkyl substituted with 0-2 R 6a ;
- R 10 is, independently at each occurrence, H, C ⁇ _6 alkyl substituted with
- R 11 is C ⁇ _6 alkyl substituted with 0-3 R 1 la -(CH 2 ) r -phenyl substituted with 0-3 R l l , or -(CH 2 ) r -5- to 10-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, O, and S(O) p , wherein said heterocycle is substituted with 0-3 R 1 lb ; and
- R 12 is H, F, CM haloalkyl, C ⁇ _ 6 alkyl, phenyl, or benzyl.
- the present invention provides a novel pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound of the present invention or a stereoisomer or a pharmaceutically acceptable salt, solvate or prodrug form thereof.
- the present invention provides a novel process for making a compound of the present invention or a stereoisomer or pharmaceutically acceptable salt, solvate or prodrug form thereof.
- the present invention provides a novel intermediate for making a compound of the present invention or a stereoisomer or pharmaceutically acceptable salt, solvate or prodrug form thereof.
- the present invention provides a pharmaceutical composition further comprising additional therapeutic agent(s) selected from potassium channel openers, calcium channel blockers, sodium hydrogen exchanger inhibitors, antiarrhythmic agents, antiatherosclerotic agents, anticoagulants, antithrombotic agents, prothrombolytic agents, fibrinogen antagonists, diuretics, antihypertensive agents, ATPase inhibitors, mineralocorticoid receptor antagonists, phospodiesterase inhibitors, antidiabetic agents, anti-inflammatory agents, antioxidants, angiogenesis modulators, antiosteoporosis agents, hormone replacement therapies, hormone receptor modulators, oral contraceptives, antiobesity agents, antidepressants, antianxiety agents, antipsychotic agents, antiproliferative agents, antitumor agents, antiulcer and gastroesophageal reflux disease agents, growth hormone agents and/or growth hormone secretagogues, thyroid mimetics, anti- infective agents, antiviral agents, antibacterial agents, antifungal agents,
- the present invention provides a pharmaceutical composition further comprising additional therapeutic agent(s) selected from an anti-arrhythmic agent, an anti-hypertensive agent, an anti-coagulant agent, an anti-platelet agent, a thrombin inhibiting agent, a thrombolytic agent, a fibrinolytic agent, a calcium channel blocker, a cholesterol/lipid lowering agent, or a combination thereof.
- additional therapeutic agent(s) selected from an anti-arrhythmic agent, an anti-hypertensive agent, an anti-coagulant agent, an anti-platelet agent, a thrombin inhibiting agent, a thrombolytic agent, a fibrinolytic agent, a calcium channel blocker, a cholesterol/lipid lowering agent, or a combination thereof.
- the present invention provides a pharmaceutical composition further comprising additional therapeutic agent(s) selected from warfarin, unfractionated heparin, low molecular weight heparin, synthetic pentasaccharide, hirudin, argatroban, aspirin, ibuprofen, naproxen, sulindac, indomethacin, mefenamate, dipyridamol, droxicam, diclofenac, sulfinpyrazone, piroxicam, ticlopidine, clopidogrel, tirofiban, eptifibatide, abciximab, melagatran, ximelagatran, disulfatohirudin, tissue plasminogen activator, modified tissue plasminogen activator, anistreplase, urokinase, and streptokinase, or a combination thereof.
- additional therapeutic agent(s) selected from warfarin, unfractionated heparin, low molecular weight heparin
- the present invention provides a pharmaceutical composition wherein the additional therapeutic agent is an antihypertensive agent selected from ACE inhibitors, AT-1 receptor antagonists, ET receptor antagonists, dual ET/AII receptor antagonists, and vasopepsidase inhibitors, an antiarrythmic agent selected from IKur inhibitors, or an antithrombotic agent selected from anticoagulants selected from thrombin inhibitors, other factor XIa inhibitors, other kallikrein inhibitors, factor Vila inhibitors and factor Xa inhibitors, and antiplatelet agents selected from GPIIb/IIIa blockers, P2YJ and P2Y 12 antagonists, thromboxane receptor antagonists, and aspirin, or a combination thereof.
- the present invention provides pharmaceutical composition, wherein the additional therapeutic agent(s) are an anti- platelet agent or a combination thereof.
- the present invention provides a pharmaceutical composition, wherein the additional therapeutic agent is the anti- platelet agent clopidogrel.
- the present invention provides a method for modulation of the coagulation cascade and/or contact activation system comprising administering to a patient in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt, solvate or prodrug form thereof.
- the present invention provides a novel method for treating thromboembolic disorders comprising: administering to a patient in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt, solvate or prodrug form' thereof.
- the present invention provides a novel method, wherein the thromboembolic disorder is selected from the group consisting of arterial cardiovascular thromboembolic disorders, venous cardiovascular thromboembolic disorders, arterial cerebrovascular thromboembolic disorders, and venous cerebrovascular thromboembolic disorders.
- the present invention provides a novel method, wherein the thromboembolic disorder is selected unstable angina, an acute coronary syndrome, atrial fibrillation, first myocardial infarction, recurrent myocardial infarction, ischemic sudden death, transient ischemic attack, stroke, atherosclerosis, peripheral occlusive arterial disease, venous thrombosis, deep vein thrombosis, thrombophlebitis, arterial embolism, coronary arterial thrombosis, cerebral arterial thrombosis, cerebral embolism, kidney embolism, pulmonary embolism, and tlirombosis resulting from (a) prosthetic ' valves or other implants, (b) indwelling catheters, (c) stents, (d) cardiopulmonary bypass, (e) hemodialysis, and (f) other procedures in which blood is exposed to an artificial surface that promotes thrombosis.
- the thromboembolic disorder is selected unstable angina, an acute coronary syndrome,
- the present invention provides a method for treating inflammatory disorders comprising: administering to a patient in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or a pharmaceutically acceptable salt or prodrug form thereof.
- the present invention provides a method, wherein the inflammatory disorder is selected from the group consisting of sepsis, acute respiratory dystress syndrome, and systemic inflammatory response syndrome.
- the present invention provides a novel method of treating a patient in need of thromboembolic disorder treatment, comprising: administering a compound of the present invention or a pharmaceutically acceptable salt, solvate, or prodrug form thereof in an amount effective to treat a thromboembolic disorder.
- the present invention provides a method of treating a patient in need of inflammatory disorder treatment, comprising: administering a compound of the present invention or a pharmaceutically acceptable salt form thereof in an amount effective to treat an inflammatory disorder.
- the present invention provides a novel article of manufacture, comprising: (a) a first container; (b) a pharmaceutical composition located within the first container, wherein the composition, comprises: a first therapeutic agent, comprising: a compound of the present invention or a pharmaceutically acceptable salt, solvate, or prodrug form thereof; and (c) a package insert stating that the pharmaceutical composition can be used for the treatment of a thromboembolic and/or inflammatory disorder.
- the present invention provides a novel article of manufacture, further comprising: (d) a second container; wherein components (a) and (b) are located within the second container and , component (c) is located within or outside of the second container.
- the present invention provides a novel article of manufacture, comprising: (a) a first container; (b) a pharmaceutical composition located within the first container, wherein the composition, comprises: a first therapeutic agent, comprising: a compound of the present invention or a pharmaceutically acceptable salt, solvate, or prodrug form thereof; and (c) a package insert stating that the pharmaceutical composition can be used in combination with a second therapeutic agent to treat a thromboembolic and/or inflammatory disorder.
- the present invention provides a novel article of manufacture, further comprising: (d) a second container; wherein components (a) and (b) are located within the second container and component (c) is located within or outside of the second container.
- the present invention provides a novel method, comprising: administering a compound of the present invention or a pharmaceutically acceptable salt, solvate, or prodrug form thereof in an amount effective to treat a thromboembolic and/or inflammatory disorder.
- the present invention provides a compound of the present invention or a pharmaceutically acceptable salt, solvate, or prodrug form thereof, for use in therapy.
- the present invention also provides the use of a compound of the present invention or a pharmaceutically acceptable salt, solvate, or prodrug form thereof, for the manufacture of a medicament for the treatment of a thromboembolic and/or inflarnmatory disorder.
- the molecular weight of compounds of the present invention is less than about 500, 550, 600, 650, 700, 750, or 800 grams per mole.
- the molecular weight is less than about 800 grams per mole. More preferably, the molecular weight is less than about 750 grams per mole. Even more preferably, the molecular weight is less than about 700 grams per mole.
- alkyl or “alkylene” is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms.
- C1-C10 alkyl or “C1-10 alkyl” (or alkylene) is intended to include Ci, C 2 , C3, C4, C5, C , C ⁇ , Cs, C9, and C10 alkyl groups.
- alkyl denotes alkyl having 1 to 6 carbon atoms.
- Alkyl groups can be unsubstituted or substituted so that one or more of its hydrogens are replaced by another chemical group.
- Example alkyl groups include, but are not limited to, methyl (Me), ethyl (Et), propyl (e.g., n-propyl and isopropyl), butyl (e.g., n-butyl, isobutyl, t-butyl), pentyl (e.g., n-pentyl, isopentyl, neopentyl), and the like.
- Alkenyl or “alkenylene” is intended to include hydrocarbon chains of either straight or branched configuration having one or more double carbon-carbon bonds that may occur in any stable point along the chain.
- C2-6 alkenyl (or alkenylene) is intended to include C2, C3, C4, C5, and C ⁇ alkenyl groups.
- alkenyl examples include, but are not limited to, ethenyl, 1-propenyl, 2- propenyl, 2-butenyl, 3-butenyl, 2-pentenyl, 3, pentenyl, 4-pentenyl, 2-hexenyl, 3- hexenyl, 4-hexenyl, 5-hexenyl, 2-methyl-2-propenyl, 4-methyl-3-pentenyl, and the like.
- Alkynyl or “alkynylene” is intended to include hydrocarbon chains of either straight or branched configuration and having one or more triple carbon-carbon bonds that may occur in any stable point along the chain.
- C2-6 alkynyl (or alkynylene), is intended to include C2, C3, C4, C5, and C ⁇ alkynyl groups; such as ethynyl, propynyl, butynyl, pentynyl, hexynyl and the like.
- Halo or "halogen” includes fluoro, chloro, bromo, and iodo.
- Haloalkyl refers to branched and straight-chained, having one or more halogen substituents.
- Example haloalkyl groups include, but are not limited to, CF3, C 2 F5, CHF 2 , CCI3, CHC1 2 , C 2 C 5 , and the like.
- alkoxy refers to an -O-alkyl group.
- C ⁇ _ 6 alkoxy (or alkyloxy), is intended to include Ci, C 2 , C3, C4, C5, and C alkoxy groups.
- Example alkoxy groups include, but are not limited to, methoxy, ethoxy, propoxy (e.g., n-propoxy and isopropoxy), and t-butoxy, and the like.
- alkylthio or “thioalkoxy” represents an alkyl group as defined above with the indicated number of carbon atoms attached through a sulphur bridge; for example methyl-S-, ethyl-S-, and the like.
- Haloalkoxy or "haloalkyloxy” represents a haloalkyl group as defined above with the indicated number of carbon atoms attached through an oxygen bridge.
- C ⁇ _6 haloalkoxy is intended to include Ci, C 2 , C3, C4, C5, and C haloalkoxy groups.
- haloalkoxy include, but are not limited to, trifluoromethoxy, 2,2,2-trifluoroethoxy, pentafluorothoxy, and the like.
- haloalkylthio or “thiohaloalkoxy” represents a haloalkyl group as defined above with the indicated number of carbon atoms attached through a sulphur bridge; for example trifluoromethyl-S-, pentafluoroethyl-S-, and the like.
- cycloalkyl refers to cyclized alkyl groups, including mono-, bi- or poly-cyclic ring systems. C3-7 cycloalkyl is intended to include C3, C4, C5, C ⁇ , and C7 cycloalkyl groups.
- Example cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, norbornyl, and the like.
- “carbocycle” or “carbocyclic residue” is intended to mean any stable 3, 4, 5, 6, or 7-membered monocyclic or bicyclic or 7, 8, 9, 10, 11, 12, or 13 -membered bicyclic or tricyclic ring, any of which may be saturated, partially unsaturated, unsaturated or aromatic.
- carbocycles include, but are not limited to, cyclopropyl, cyclobutyl, cyclobutenyl, cyclopentyl, cyclopentenyl, cyclohexyl, cycloheptenyl, cycloheptyl, cycloheptenyl, adamantyl, cyclooctyl, cyclooctenyl, cyclooctadienyl, [3.3.0]bicyclooctane, [4.3.0]bicyclononane,
- bridged rings are also included in the definition of carbocycle (e.g., [2.2.2]bicyclooctane).
- Preferred carbocycles are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, phenyl, and indanyl.
- carbocycle unless otherwise specified, are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, phenyl, and indanyl.
- a bridged ring occurs when one or more carbon atoms link two non-adjacent carbon atoms.
- Preferred bridges are one or two carbon atoms. It is noted that a bridge always converts a monocyclic ring into a tricyclic ring. When a ring is bridged, the substituents recited for the ring may also be present on the bridge.
- Aryl refer to monocyclic or polycyclic aromatic hydrocarbons, including, for example, phenyl, naphthyl, phenanthranyl, and the like. Aryl moieties are well known and described, for example, in Hawley's Condensed Chemical Dictionary (13 ed.), R.J. Lewis, ed., J.
- heterocycle or “heterocyclic group” is intended to mean a stable 5, 6, or 7- membered monocyclic or bicyclic or 7, 8, 9, 10, 11, 12, 13, or 14-membered bicyclic heterocyclic ring which is saturated, partially unsaturated or fully unsaturated, and which consists of carbon atoms and 1, 2, 3 or 4 heteroatoms independently selected fromN, O and S; and including any bicyclic group in which any of the above-defined heterocyclic rings is fused to a benzene ring.
- the nitrogen and sulfur heteroatoms may optionally be oxidized (i.e., N ⁇ O and S(O)p).
- the nitrogen atom may be substituted or unsubstituted (i.e., N or NR wherein R is H or another substituent, if defined).
- the heterocyclic ring may be attached to its pendant group at any heteroatom or carbon atom that results in a stable structure.
- the heterocyclic rings described herein may be substituted on carbon or on a nitrogen atom if the resulting compound is stable.
- a nitrogen in the heterocycle may optionally be quatemized. It is preferred that when the total number of S and O atoms in the heterocycle exceeds 1, then these heteroatoms are not adjacent to one another.
- heterocycle it is intended to include heteroaryl.
- heterocycles include, but are not limited to, acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzoxazolyl, benzoxazolinyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazolinyl, carbazolyl, 4aH-carbazolyl, carbolinyl, chromanyl, chromenyl, cinnolinyl, decahydroquinolinyl, 2H,6H-l,5,2-dithiazinyl, dmydrofuro[2,3-b]tefrahydrofuran,
- Preferred 5 to 10 membered heterocycles include, but are not limited to, pyridinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, pyrazinyl, piperazinyl, piperidinyl, imidazolyl, imidazolidinyl, indolyl, tetrazolyl, isoxazolyl, morpholinyl, oxazolyl, oxazolidinyl, tetrahydrofuranyl, thiadiazinyl, thiadiazolyl, thiazolyl, triazinyl, triazolyl, benzimidazolyl, lH-indazolyl, benzofuranyl, benzothiofuranyl, benztetrazolyl, benzotriazolyl, benzisoxazolyl, benzoxazolyl, oxindolyl, benzoxazolinyl, benzthiazoly
- Preferred 5 to 6 membered heterocycles include, but are not limited to, pyridinyl, furanyl, thienyl, pyrrolyl, pyrazolyl, pyrazinyl, piperazinyl, piperidinyl, imidazolyl, imidazolidinyl, indolyl, tetrazolyl, isoxazolyl, morpholinyl, oxazolyl, oxazolidinyl, tetrahydrofuranyl, thiadiazinyl, thiadiazolyl, thiazolyl, triazinyl, and triazolyl.
- fused ring and spiro compounds containing, for example, the above heterocycles are also included.
- aromatic heterocyclic group or “heteroaryl” is intended to mean a stable monocyclic and polycyclic aromatic hydrocarbons that include at least one heteroatom ring member such as sulfur, oxygen, or nitrogen.
- Heteroaryl groups include, without limitation, pyridyl, pyrimidinyl, pyrazinyl, pyridazinyl, triazinyl, furyl, quinolyl, isoquinolyl, thienyl, imidazolyl, thiazolyl, indolyl, pyrroyl, oxazolyl, benzofuryl, benzothienyl, benzthiazolyl, isoxazolyl, pyrazolyl, triazolyl, tetrazolyl, indazolyl, 1,2,4-thiadiazolyl, isothiazolyl, purinyl, carbazolyl, benzimidazolyl, indolinyl, benzodioxolanyl, benzodioxane, and the like.
- Heteroaryl groups can be substituted or unsubstituted.
- the nitrogen atom may be substituted or unsubstituted (i.e., N or NR wherein R is H or another substituent, if defined).
- the nitrogen and sulfur heteroatoms may optionally be oxidized (i.e., N ⁇ O and S(O)p). It is to be noted that total number of S and O atoms in the aromatic heterocycle is not more than 1.
- Bridged rings are also included in the definition of heterocycle. A bridged ring occurs when one or more atoms (i.e., C, O, N, or S) link two non-adjacent carbon or nitrogen atoms.
- Preferred bridges include, but are not limited to, one carbon atom, two carbon atoms, one nitrogen atom, two nitrogen atoms, and a carbon-nitrogen group. It is noted that a bridge always converts a monocyclic ring into a tricyclic ring. When a ring is bridged, the substituents recited for the ring may also be present on the bridge.
- counterion is used to represent a small, negatively charged species such as chloride, bromide, hydroxide, acetate, and sulfate.
- a ring system e.g., carbocyclic or heterocyclic
- a carbonyl group or a double bond it is intended that the carbonyl group or double bond be part (i.e., within) of the ring.
- any variable e.g., R 2a , R b , etc.
- its definition at each occurrence is independent of its definition at every other occurrence.
- R 2b the definition of R 2b
- R 2b at each occurrence is selected independently from the definition of R 2b .
- combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.
- a dotted ring When a dotted ring is used within a ring structure, this indicates that the ring structure may be saturated, partially saturated or unsaturated.
- pharmaceutically acceptable is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of hximan beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
- pharmaceutically acceptable salt refers to acid or base salts of the compounds described herein.
- Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like.
- Pharmaceutically acceptable salts of the compounds of the invention can be prepared by reacting the free acid or base forms of these compounds with a stoichiometric amount of the appropriate base or acid in water or in an organic solvent, or in a mixture of the two; generally, nonaqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile are preferred. Lists of suitable salts are found in Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, PA, 1985, p.
- Examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acid salts of basic residues such as amines; alkali or organic salts of acidic residues such as carboxylic acids; and the like.
- Pharmaceutically acceptable salts include the conventional non-toxic salts or the quaternary ammonium salts of the parent compound formed, for example, from non-toxic inorganic or organic acids.
- Such conventional non-toxic salts include those derived from inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric, and the like; and the salts prepared from organic acids such as acetic, propionic, succinic, glycolic, stearic, lactic, malic, tartaric, citric, ascorbic, pamoic, maleic, hydroxymaleic, phenylacetic, glutamic, benzoic, salicylic, sulfanilic, 2-acetoxybenzoic, fumaric, toluenesulfonic, methanesulfonic, ethane disulfonic, oxalic, isethionic, and the like.
- inorganic acids such as hydrochloric, hydrobromic, sulfuric, sulfamic, phosphoric, nitric, and the like
- organic acids such as acetic, propionic, succinic, glycolic, stearic,
- compounds of formula I may have prodrug forms. Any compound that will be converted in vivo to provide the bioactive agent (i.e., a compound of formula I) is a prodrug within the scope and spirit of the invention.
- a prodrug within the scope and spirit of the invention.
- Various forms of prodrugs are well known in the art. For examples of such prodrug derivatives, see: a) Design of Prodrugs, edited by H. Bundgaard, (Elsevier, 1985), and Methods in Enzymology, Vol. 42, at pp. 309-396, edited by K. Widder, et. al. (Academic Press, 1985); b) A Textbook of Drug Design and Development, edited by Krosgaard-Larsen and H.
- Bundgaard Chapter 5, "Design and Application of Prodrugs " by H. Bundgaard, at pp. 113-191 (1991); c) H. Bundgaard, Advanced Drug Delivery Reviews, Vol. 8, p. 1-38 (1992); d) H. Bundgaard, et al, Journal of Pharmaceutical Sciences, Vol. 77, p. 285 (1988); and e) N. Kakeya, et. al, Chem Phar Bull, Vol. 32, p. 692 (1984).
- prodrugs are well known in the art and described in, for example, Medicinal Chemistry: Principles and Practice, ed. F. D. King, The Royal Society of Chemistry, Cambridge, UK, 1994, which is incorporated herein by reference in its entirety.
- Radiolabelled compounds of the present invention i.e., wherein one or more of the atoms described are replaced by a radioactive isotope of that atom (e.g., C replaced by 13 C or by 1 C; and isotopes of hydrogen include tritium and deuterium), are also provided herein.
- a radioactive isotope of that atom e.g., C replaced by 13 C or by 1 C; and isotopes of hydrogen include tritium and deuterium
- Such compounds have a variety of potential uses, e.g., as standards and reagents in determining the ability of a potential pharmaceutical to bind to target proteins or receptors, or for imaging compounds of this invention bound to biological receptors in vivo or in vitro.
- Compounds of the present invention are, subsequent to their preparation, preferably isolated and purified to obtain a composition containing an amount by weight equal to or greater than 98%, preferably 99%, compound of the present invention ("substantially pure"), which is then used or formulated as described herein. Such “substantially pure” compounds are also contemplated herein as part of the present invention.
- “Stable compound” and “stable structure” are meant to indicate a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent. It is preferred that compounds of the present invention do not contain a N-halo, S(O) 2 H, or S(O)H group.
- solvates e.g., hydrates
- Methods of solvation are generally known in the art.
- treating cover the treatment of a disease-state in a mammal, particularly in a human, and include: (a) preventing the disease-state from occurring in a mammal, in particular, when such mammal is predisposed to the disease-state but has not yet been diagnosed as having it; (b) inhibiting the disease-state, i.e., arresting it development; and/or (c) relieving the disease-state, i.e., causing regression of the disease state.
- Therapeutically effective amount is intended to include an amount of a compound of the present invention that is effective when administered alone or in combination to inhibit factor XIa and/or plasma kallikrein.
- “Therapeutically effective amount” is also intended to include an amount of the combination of compounds claimed that is effective to inhibit factor XIa and/or plasma kallikrein.
- the combination of compounds is preferably a synergistic combination. Synergy, as described, for example, by Chou and Talalay, Adv.
- Enzyme Regul 1984, 22:27-55 occurs when the effect (in this case, inhibition of factor XIa and/or plasma kallikrein) of the compounds when administered in combination is greater than the additive effect of the compounds when administered alone as a single agent.
- a synergistic effect is most clearly demonstrated at sub-optimal concentrations of the compounds. Synergy can be in terms of lower cytotoxicity, increased antithrombotic and/or anti-inflammatory effect, or some other beneficial effect of the combination compared with the individual components.
- the present invention further includes compositions comprising one or more compounds of the present invention and a pharmaceutically acceptable carrier.
- a "pharmaceutically acceptable carrier” refers to media generally accepted in the art for the delivery of biologically active agents to animals, in particular, mammals.
- Pharmaceutically acceptable carriers are formulated according to a number of factors well within the purview of those of ordinary skill in the art. These include, without limitation: the type and nature of the active agent being formulated; the subject to which the agent-containing composition is to be administered; the intended route of administration of the composition; and the therapeutic indication being targeted.
- Pharmaceutically acceptable carriers include both aqueous and non-aqueous liquid media, as well as a variety of solid and semi- solid dosage forms.
- Such carriers can include a number of different ingredients and additives in addition to the active agent, such additional ingredients being included in the formulation for a variety of reasons, e.g., stabilization of the active agent, binders, etc., well known to those of ordinary skill in the art.
- suitable pharmaceutically acceptable carriers, and factors involved in their selection are found in a variety of readily available sources such as, for example, Remington's Pharmaceutical Sciences, 17th ed., Mack Publishing Company, Easton, PA, 1985, which is incorporated herein by reference in its entirety.
- the compounds of the present invention can be prepared in a number of ways known to one skilled in the art of organic synthesis.
- the compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or by variations thereon as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below.
- the reactions are performed in a solvent appropriate to the reagents and materials employed and suitable for the transformations being effected. It will be understood by those skilled in the art of organic synthesis that the functionality present on the molecule should be consistent with the transformations proposed. This will sometimes require a judgment to modify the order of the synthetic steps or to select one particular process scheme over another in order to obtain a desired compound of the invention.
- Representative pyridine compounds of this invention can be prepared as shown in Scheme 1. Suzuki coupling between an appropriately functionalized pyridine, such as la and an appropriately substituted aryl or heteroaryl boronic acid or ester lb in the presence of a base such as anhydrous potassium carbonate in a solvent such as methanol or THF using a catalyst such as PXPd2 provides the biaryl compound.
- a base such as anhydrous potassium carbonate
- a catalyst such as PXPd2
- the 2-chloropyridine derivative is treated with trimethylsilyl bromide in propionitrile at elevated temperature in a microwave to give the 2-bromopyridine derivative lc.
- Metal- halogen exchange with n-butyllithium and quenching the intermediate anion with a suitable formyl source such as 1-formyl piperidine or DMF provides aldehyde Id.
- the R 3 moiety can be introduced via a Suzuki coupling strategy later in the synthesis as shown in Scheme 2.
- Compound 2c can be prepared , in three steps according to a modified procedure described by Negi (Negi, S. et al Synthesis, 1996, 991). Addition of Grignard or lithium reagents to a suitably substituted ester or Weinreb amide 2a yields ketone 2b. Condensation of 2b with hydroxylamine hydrochloride generates the oxime which can be reduced to the primary amine 2c with zinc dust and TFA. Amide coupling between 2c and carboxylic acid If employing suitable coupling reagents as described in Scheme 1 gives 2d.
- Suzuki coupling between 4-chloropyridine 2d and an appropriately substituted aryl or heteroaryl boronic acid or ester lb in the presence of a base such as anhydrous cesium carbonate, potassium fluoride, or potassium phosphate in a solvent, such as dioxane, dimethylsulfoxide, or dimemylformamide, using a catalyst such as tetr ⁇ te(friphenylphosphine)palladium(0), tra(dibenzylideneacetone)dipalladiiim(0) and tri-t-butylphosphonium tetrafluoroborate or Pd(dppf) 2 Cl 2 *CH 2 Cl 2 complex provides the biaryl compound lg.
- a base such as anhydrous cesium carbonate, potassium fluoride, or potassium phosphate in a solvent, such as dioxane, dimethylsulfoxide, or dimemylformamide
- a catalyst such as tetr ⁇ te(
- [l,3,2]dioxaborolane intermediate using the method of Ishiyama, T. et al. (J. Org. Chem. 1995, 60(23), 7508-7510).
- this same intermediate can be prepared by reaction of the intermediate halide with the corresponding dialkoxyhydroborane as described by Murata et ⁇ /. (J. Org. Chem. 1997, 67(19), 6458-6459).
- the boron pinacolate intermediates can be used in place of boronic acids for coupling to the aryl/heteroaryl halides or triflates or the boron pinacolate intermediate can be converted to the boronic acids.
- the corresponding boronic acids can be prepared by metal-halogen exchange of the aryl/heteroaryl halide, quenching with a trialkoxyborate reagent, and aqueous workup to provide the boronic acids (Miyaura, N.; Suzuki, A. Chem. Review, 1995, 95, 2457).
- a suitably substituted amino nitrile 3 a can be converted to the corresponding amidine 3b by treatment with N- acetylcysteine and ammonium acetate in the presence of dithiothreitol.
- Condensation of amidine 3b with an appropriately substituted aryl propynone 3g in the presence of a base such as sodium carbonate and in a solvent such as acetonitrile provides the pyrimidine compound 3c (Bagley, C. Synlett 2003, 2, 259-261).
- the amine is coupled with carboxylic acid If employing suitable amide coupling conditions as described in Scheme 1 to yield 3d.
- the pyrimidone derivatives 3e can be prepared similarly by condensation of amidine 3b with an appropriately substituted aryl propiolate 3h in the presence of a base such as Hunig's base and in a solvent such as ethanol (Gupta, K.A, et al. Indian J. Chem., 1983, 22B, 384). After deprotection with TFA, the amine is coupled with carboxylic acid If as described above to yield 3f. Further manipulation of functional groups on A and R 3 using methods known to one skilled in the art of organic synthesis will give additional compounds of the invention.
- Representative pyridone compounds of this invention can be prepared as shown in Scheme 4.
- Compound 4d can be prepared in two steps according to a modified procedure described by Resmini (Resmini, M. et al, Tetrahedron Asymmetry, 2004, 15, 1847).
- a suitably substituted amino ester 4a can be converted to the corresponding ⁇ -ketophosphonate 4b by treatment with lithium dimethylmethylphosphonate.
- Horner-Wadsworth-Emmons reaction of 4b and a suitably substituted aldehyde 4c in the presence of base such as potassium carbonate in a solvent such as ethanol or tetrahydrofuran gives the ⁇ , ⁇ -unsaturated ketone 4d.
- pyridine and pyridone compounds of this invention can be prepared as shown in Scheme 5.
- Compound 5c can be prepared in two steps from ⁇ - ketophosphonate 5a as described Scheme 4.
- Selective O-alkylation as described by Rao can be achieved with silver carbonate and an alkyl iodide, such as methyl iodide, i a solvent, such as benzene or chloroform, to give 5d.
- 5c can be treated with phosphorus oxychloride to give chloropyridine 5e.
- Carboxylic acids suitable for use in preparing compounds of this invention may be obtained through oxidation of the corresponding alcohol 7a or aldehyde 7b as taught in "Advanced Organic Chemistry” (Jerry March, Wiley Interscience, 4 th Edition, pg 1196 and 701-703 and references therein). Alternately, oxidation of aromatic side chains in 7c gives aromatic carboxylic acids as taught in “Advanced Organic Chemistry” (Jerry March, Wiley Interscience, 4 th Edition, pg 1183-1184 and references therein).
- esters 7d or nitriles 7e yields the carboxylic acid as taught in "Advanced Organic Chemistry” (Jerry March, Wiley Interscience, 4 Edition, pg 378-383 and 887-889 and references therein).
- carbonylation of bromide 7f gives the carboxylic acid as taught in "Advanced Organic Chemistry” (Jerry March, Wiley Interscience, 4 Edition, pg 484-486, 546-547, and 664-665 and references therein).
- the R 1 and R 2 groups can be further manipulated using methods known in the art to provide additional compounds of this invention.
- R 1 when R 1 is a cyano group, it can be reduced to give CH 2 NH with a suitable reducing agent.
- the nitrile can also be converted to an amidine by reaction with hydroxylamine followed hydrogenolysis with a palladium catalyst under a hydrogen atmosphere or via a Pinner reaction followed by ammonolysis.
- Scheme 9 describes the synthesis of specific examples of A-CO 2 H (If) when A is the 4-amino-qumazoline moiety.
- aldehydes 4c when R 3 is phenyl, suitable for use in preparing compounds of this invention may be obtained through oxidation of the corresponding alcohols or halides 10a as taught in "Advanced Organic Chemistry” (Jerry March, Wiley Interscience, 4 th Edition, pp. 1167-1171, 1190, and 1193 and references therein).
- suitable aldehydes may be prepared by hydrogenation of the corresponding carboxylic acids 10b in the presence of palladium complexes and pivalic anhydride (Nagayama et al. Chemistry Letters 1998, 27, 1143-1144) or by reduction of the corresponding carboxylic acid 10b with borane followed by oxidation of the intermediate alcohol with manganese dioxide or Dess-Martin periodinane.
- Additional aryl aldehydes may be obtained from the corresponding toluene derivatives 10c by direct oxidation or by a two step procedure which involves formation of the dibromide intermediate and subsequent conversion to the aldehyde with a silver salt, hexamethylenetetramine, or morpholine (with silver: Demir, A.S.; Reis, O. Tetrahedron, 2004, 60, 3803; hexamethylenetetramine: Tidwell, R.R.; et al. J. Med. Chem., 1978, /(7), 613; mo holine: published WO patent WO2002/32884). Additional suitable aldehydes may be prepared through formylation of the aromatic ring lOd as taught in "Advanced Organic Chemistry" (Jerry March, Wiley Interscience, 4 th Edition, pp. 542-546 and references therein).
- Scheme 11 A modification of Scheme 2 is shown in Scheme 11. Reacting 4- chloropyridine 2b with TMSBr or acetyl bromide at elevated temperatures as described in Scheme 1 provides 4-bromopyridine lla. Compound lla can be carried through the sequence described in Scheme 2 to give lg. Alternately, the Suzuki coupling strategy can be reversed. The 4-bromopyridine lie can be converted to either the boronate or boronic acid derivative as described previously to yield lid.
- a base such as anhydrous cesium carbonate, potassium fluoride, or potassium phosphate
- a solvent such as dioxane, dimethylsulfoxide, or dimethylforniamide
- a catalyst such as tetr
- Fluoropyridhie 12a can be displaced with amines, such as ammonium hydroxide, to give ammopyridine 12b, alkoxides, such as sodium methoxide, to give 12c, or sodium hydroxide to give 12d according to a modified procedures described by Queguiner (Queguiner, G. et al. J. Org. Chem., 1988, 53, 2740.) Scheme 12
- amines such as ammonium hydroxide
- R 3 is a pyrimidine ring system
- Condensation of amidine 13b, which can be synthesized from cyanopyridine 13a via the Pinner reaction, with an appropriately substituted propiolate can provide pyrimidone 13c.
- Pyrimidone 13c can be converted to the aminopyrimidine 13d in two steps.
- a regioisomeric pyrimidine synthesis is described in Scheme 14.
- the ⁇ -ketonitrile 14b can be prepared from the acid 14a according to a modified procedure described by Katritzky (Katritzky, A. R. et al. J. Org. Chem., 2003, 68, 4932).
- Na 2 SO4 sodium sulfate
- PXPd2 Bis[di-tert-butyl phosphinous chloride- P]di-m-chlorodichloro dipalladium
- ESI electrospray ionization mass spectroscopy
- HPLC high performance liquid chromatography
- MS mass spectrometry
- LC/MS liquid chromatography mass spectrometry
- NMR nuclear magnetic resonance spectroscopy
- TLC thin layer chromatography
- ⁇ , " ⁇ ”, “R”, “S”, “E”, and “Z” are stereochemical designations familiar to one skilled in the art.
- One stereoisomer of a compound of Formula I may display superior activity compared with the others.
- each stereoisomer of a compound of Formula I is considered to be a part of the present invention.
- separation of the racemic material can be achieved by HPLC using a chiral column or by a resolution using a resolving agent such as described in Wilen, S. H. Tables of Resolving Agents and Optical Resolutions 1972, 308 or using enantiomerically pure acids and bases.
- Example 1 To a clear, colorless solution of ID (0.086 g, 0.167 mmol) in CH 2 C1 2 (3.0 mL) was added TFA (0.9 mL). After 1 h, the reaction was concentrated. CH 2 C1 was added and the reaction was concentrated again.
- Example 2 (0.0328 g, 45%) as a white solid.
- LH-NMR (500 MHz, MeOD 4 ) ⁇ : 8.40 (d, J 6.6
- Example 3 To a flame-dried 1 dram vial (with a teflon cap) was added 3D (0.050 g, 0.106 mmol), 3-(methoxycarbonyl)phenylboronic acid (0.0248 g, 0.138 mmol), tr ⁇ (dibeij2ylideneacetone)dipalladium (0) (0.0048 g, 0.0053 mmol), tri-t-butylphosphonium tetrafluoroborate (0.0037 g, 0.0127 mmol), and cesium carbonate (0.069 g, 0.212 mmol).
- the vial was purged with argon for several minutes and degassed dioxane (0.53 mL) was added.
- the vial was capped with a Teflon- coated cap under a blanket of argon.
- the purple suspension was stirred at rt for lh and then placed in a preheated (90 °C) shaker or oil bath. After 15.5 h, the reaction was cooled to rt, diluted with CH 2 C1 , and filtered through a 0.45 ⁇ m nylon filter and the filtrate was concentrated to yield a yellow residue.
- the residue was dissolved in CH 2 C1 2 (2.5 mL) followed by the addition of TFA (0.75 mL). The bright yellow solution stirred at rt for 45 min and then concentrated.
- Example 3 (0.035 g, 47%) as a white solid.
- Example 7F was treated according to the procedure described for IE. The crude product was re-dissolved in MeOH/H 2 O (9:1) containing 0.1%
- Example 8B Example 8: 8A (16 mg, 0.041 mmol) was converted to Example 8 using the procedures described in 7D-F with the exception that HOAt was used in place of HOBt.
- H NMR 500 MHz, d 4 -MeOH
- Example 10 (0.013 g, quantitative) as a white solid.
- 1H NMR 500 MHz, CD 3 OD
- HRMS m/z calc'd for C
- 13A 4-Aminomethyl-cyclohexanecarboxylic acid ⁇ 2-phenyl-l-[4- (l-triisopropylsilanyl-l£T-pyrrol-3-yI)-pyridin-2-yl]-ethyl ⁇ -amide, bistrifluoroacetic acid salt: This compound was prepared from 3D following the procedures described in example 3E using l-(Triisopropylsilyl)pyrrole-3 -boronic acid in place of 3-(methoxycarbonyl)phenylboronic acid to give 13 A (0.013 g, 16%) as a brown residue. MS 559.3 (M+H) + .
- the purple suspension was stirred at rt for lh and then placed in a preheated (90 °C) oil bath.- After 14 h, the reaction was cooled to rt, diluted with CH 2 C1 2 , and filtered through a 0.45 ⁇ m nylon filter and the filtrate was concentrated to yield a yellow solid.
- the solid was dissolved in CH 2 CI 2 and NH OH was added and the biphasic mixture was stirred vigorously for 10 min. The layers were separated and the organic layer was washed with brine, dried over MgSO 4 , filtered, and concentrated to give an off-white solid weighing 0.200 g.
- the solid was dissolved in 30% TFA in CH 2 C1 2 (10 mL).
- Example 21 (0.146 g, 67%) as a white solid.
- Example 25 (0.0195 g, 63%) as a yellow solid.
- a suspension of Example 23 (0.095 g) in n-butanol (3.0 mL) and hydrazine monohydrate (1.0 mL) was microwaved at 150 °C for 10 min. The resulting clear, bright yellow solution was concentrated.
- Example 27 (0.0073 g, 20%) as a pale, yellow solid.
- 1H NMR 500 MHz, CD 3 OD
- (+)-4-Aminomethyl-cyclohexanecarboxyIic acid ⁇ l-[4-(3-amino ⁇ l,2-benzisoxazol- 6-yl)-pyridin-2-yl]-2-phenyl-ethyl ⁇ -amide, bis-trifluoroacetic acid
- Example 29 (-)-4-Aminomethyl-cycIohexanecarboxylic acid ⁇ l-[4-(3-amino-l,2-benzisoxazol- 6-yI)-pyridin-2-yI]-2-phenyl-ethyl ⁇ -amide, bis-trifluoroacetic acid [00373]
- Example 29 was prepared from 23 following the procedures described in Example 27.
- Example 33 Alternative preparation of Example 33: A mixture of Example 52 in 1-butanol and hydrazine monohydrate was micro waved at 160 °C for 1 h.
- 34A (0.14 g, 70%) as a clear, colorless oil. MS 200.2 (M+H) + .
- 34B 6-Methoxy-4-phenyl-pyridine-2-carbaldehyde: A solution of compound of 34A (0.14 g, 0.7 mmol), N-bromosuccinimide (0.25 g, 1.4 mmol), and benzoyl peroxide (0.0085 g, 0.035 mmol) in CC (3 mL) was heated at 80 °C.
- Example 34 To a solution of 34C (0.067 g, 0.13 mmol) in DMF (2 mL) was added Boc-tranexamic acid (0.036 mL, 0.14 mmol), triethylamine (0.088 mL, 0.63 mmol), HOBt (0.026 g, 0.19 mmol), and EDCI (0.036 g, 0.19 mmol). The reaction mixture was stirred at rt for 2 h, at 40 °C for 2 h, and then at rt for 18 h. The reaction mixture was diluted with EtOAc (25 mL), washed with water, sat. NaHCU 3 , brine, dried over Na 2 SO 4 , filtered and concentrated to give the amide (0.090 g) as a yellow solid. MS 544.4 (M+H) + .
- Example 35 4-Aminomethyl-cyclohexanecarboxylic acid [l-(6-oxo-4-phenyl-l,6-dihydro- pyridin-2-yl)-2-phenyl-ethyl] -amide, trifluoroacetic acid salt [00384] To a cooled (0 °C) solution of the amide from 34D (0.045 g, 0.08 mmol) in CH 2 C1 2 (1 mL) was added BBr 3 (0.078 mL, 0.8 mmol). The reaction was warmed to rt. After 2 h, the reaction was cooled to 0 °C, quenched with MeOH, and then concentrated. Prep.
- Example 36 4-Aminomethyl-cyclohexanecarboxylic acid [l-(l-methyl-6-oxo-4-phenyl-l,6- dihydro-pyridin-2-yl)-2-phenyl-ethyl]-amide, trifluoroacetic acid salt [00386] 36A. 6-(l-Amino-2-phenyl-ethyl)-l-methyl-4-phenyl-lH-pyridin-
- Example 36 Compound 36A was converted to Example 36 according to the procedures described in 34D.
- 1H NMR 500 MHz, CD 3 OD
- Example 37 To a sealable tube was added 37C (0.045 g, 0.082 mmol), benzophenone imine (0.028 mL, 0.16 mmol), Pd(OAc) 2 (0.0018 g, 0.0082 mmol), BINAP (0.0077 g, 0.012 mmol),Cs 2 CO 3 (0.064 g, 0.2 mmol) and DMSO (0.55 mL). The mixture was degassed by bubbling argon for 10 min, the tube was sealed, and the reaction was heated at 85 °C. After 18h, the reaction was cooled to rt, poured into water and extracted with CH 2 C1 2 (3 x).
- Example 38 can be prepared by deprotection of the Boc-protected 37C with TFA as was previously described.
- 1H NMR 500 MHz, CD 3 OD
- HRMS m/z Calc'd for C 27 H 31 Cl
- Example 39 4-Aminomethyl-cyclohexanecarboxylic acid ⁇ l-[4-(3-amino-lJ ⁇ -indazol-6-yl)-6- oxo-l,6-dihydro-pyridin-2-yl]-2-phenyl-ethyl ⁇ -amide, trifluoroacetic acid salt [00396] 39A.
- Example 39 A suspension of 39C (0.125 g), 1-butanol (3 mL) and hydrazine monohydrate (1 mL) was micro waved at 150 °C for 10 min. The reaction mixture was cooled to rt and concentrated to give a residue. Prep. HPLC (30 x 250 mm, 20 min.
- Example 39 (0.029 g, 33% over three steps) as a white solid.
- 1H NMR 500 MHz, CD 3 OD
- Example 40 4-Aminomethyl-cyclohexanecarboxylic acid ⁇ l-[4-(3-amino-l,2-benzisoxazol-6- yI)-6-oxo-l,6-dihydro-pyridin-2-yl] -2-phenyl-ethyl ⁇ -amide, trifluoroacetic acid salt
- Example 52 was prepared from 3D following the procedures described in 3E using 3-carboxy-4-fluorophenylboronic acid in place of 3-
- Example 57 was prepared from 3D following the procedures described in 3E using 6-(5,5-Dimethyl- 1 ,3,2-dioxaborman-2-yl)-4-methoxy-quinoline, prepared following the procedure in 54 A, in place of 3-(methoxycarbonyl)phenylboronic acid.
- 58A 6-[2-(l-Amino-2-phenyl-ethyl)-pyridm-4-yl]-lH-quinolin-4- one, £r ⁇ -trifluoroaeetic acid salt: A mixture of 57 (0.062 g, 0.074 mmol) in concentrated HCI (0.5 mL) and 1,2-dichloroethane (1.0 mL) was heated to 130 °C in a sealed tube. After 22 h, the reaction was concentrated. Prep. HPLC (Phenomenex Luna 5u 21.2 x 100 mm; 8 min. gradient, 20 tol00% B; 20 mL/min.) gave 58A (0.031 g, 92%) as a clear, colorless oil. MS 342.2 (M + H) + .
- the compounds of this invention are inhibitors of factor XIa and are useful as anticoagulants for the treatment or prevention of thromboembolic disorders in mammals (i.e., factor XIa-associated disorders).
- a thromboembolic disorder is a circulatory disease caused by blood clots (i.e., diseases involving fibrin formation, platelet activation, and/or platelet aggregation).
- blood clots i.e., diseases involving fibrin formation, platelet activation, and/or platelet aggregation.
- thromboembolic disorders as used herein includes arterial cardiovascular thromboembolic disorders, venous cardiovascular or cerebovascular thromboembolic disorders, and thromboembolic disorders in the chambers of the heart.
- thromboembolic disorders also includes specific disorders selected from, but not limited to, unstable angina or other acute coronary syndromes, atrial fibrillation, first or recurrent myocardial infarction, ischemic sudden death, fransient ischemic attack, stroke, atherosclerosis, peripheral occlusive arterial disease, venous thrombosis, deep vein thrombosis, thrombophlebitis, arterial embolism, coronary arterial thrombosis, cerebral arterial thrombosis, cerebral embolism, kidney embolism, pulmonary embolism, and thrombosis resulting from (a) prosthetic valves or other implants, (b) indwelling catheters, (c) stents, (d) cardiopulmonary bypass, (e) hemodialysis, or (f) other procedures in which blood is exposed to an artificial surface that promotes thrombosis.
- thrombosis includes occlusion (e.g., after a bypass) and reocclusion (e.g., during or after percutaneous tr ⁇ r ⁇ ginanal coronary angioplasty).
- the thromboembolic disorders may result from conditions including but not limited to atherosclerosis, surgery or surgical complications, prolonged immobilization, arterial fibrillation, congenital thrombophilia, cancer, diabetes, effects of medications or hormones, and complications of pregnancy.
- the anticoagulant effect of compounds of the present invention is believed to be due to inhibition of serine proteases involved in the coagulation cascade and/or contact activation system, more specifically, inhibition of the coagulation factors: factor XIa, factor Vila, factor IXa, factor Xa, plasma kallikrein or thrombin.
- the compounds of this invention also are inhibitors of plasma kallikrein and are useful as anti-inflammatory agents for the treatment or prevention of diseases associated with an activation of the contact activation system (i.e., plasma kallikrein associated disorders).
- a contact activation system disorder is a disease caused by activation of blood on artificial surfaces, including prosthetic valves or other implants, indwelling catheters, stents, cardiopulmonary bypass, hemodialysis, microorganism (e.g., bacteria, virus), or other procedures in which blood is exposed to an artificial surface that promotes contact activation, blood clots (i.e., diseases involving fibrin formation, platelet activation, and/or platelet aggregation).
- the rate of hydrolysis of the chromogenic or fluorogenic substrate by the relevant serine protease was measured both in the absence and presence of compounds of the present invention. Hydrolysis of the substrate resulted in the release of pNA (para nitroaniline), which was monitored spectrophotometrically by measuring the increase in absorbance at 405 nm, or the release of AMC (amino methylcoumarin, which was monitored spectrofluorometrically by measuring the increase in emission at 460 nm with excitation at 380 nm. A decrease in the rate of absorbance or fluorescence change in the presence of inhibitor is indicative of enzyme inhibition. Such methods are known to one skilled in the art. The results of this assay are expressed as the inhibitory constant, Kj. [00417] Factor XIa determinations were made in 50 mM HEPES buffer at pH
- Factor XIa assay, thereby demonstrating the utility of the compounds of the present invention as especially effective inhibitors of coagulation Factor XIa. More preferred compounds have Kj's of equal to or less than 5 ⁇ M, preferably equal to or less than 1 ⁇ M, more preferably equal to or less than 0.5 ⁇ M. [00418] Factor Vila determinations were made in 0.005 M calcium chloride,
- Factor IXa determinations were made in 0.005 M calcium chloride, 0.1 M sodium chloride, 0.05 M TRIS base and 0.5% PEG 8000 at a pH of 7.4.
- PCIXA2100-B CenterChem
- Pefafluor IXa 3688 H-D-Leu-Ph'Gly-Arg-AMC
- Factor Xa determinations were made in 0.1 M sodium phosphate buffer at apH of 7.4 containing 0.2 M sodium chloride and 0.5% PEG 8000. Determinations were made using purified human Factor Xa (Haematologic Technologies) at a final assay concentration of 150-1000 pM and the synthetic substrate S-2222 (Bz-Ile-Glu (gamma-OMe, 50%>)-Gly-Arg-pNA; Chromogenix) at a concentration of 0.0002-0.0003 M.
- Plasma kallikrein determinations were made in 0.1 M sodium phosphate buffer at a pH of 7.4 containing 0.2 M sodium chloride and 0.5% PEG 8000. Determinations were made using purified human kallikrein (Enzyme Research Laboratories) at a final assay concentration of 200 pM and the synthetic substrate S- 2302 (H-(D)-Pro-Phe-Arg-pNA; Chromogenix) at a concentration of 0.00008-0.0004 M. The Km value used for calculation of Ki was 0.00005 to 0.00007 M. In general, Compounds tested in the plasma kallikrein assay are considered to be active if they exhibit a Kj of equal to or less than 15 ⁇ M.
- Thrombin determinations were made in 0.1 M sodium phosphate buffer at apH of 7.4 containing 0.2 M sodium chloride and 0.5% PEG 8000. Determinations were made using purified human alpha thrombin (Haematologic Technologies or Enzyme Research Laboratories) at a final assay concentration of 200- 250 pM and the synthetic substrate S-2366 (pyroGlu-Pro-Arg-pNA; Chromogenix) at a concentration of 0.0002 M. hi general, compounds tested in the thrombin assay are considered to be active if they exhibit a Ki of equal to or less than 15 ⁇ M.
- preferred compounds of the present invention have demonstrated Ki values of equal to or less than 15 ⁇ M in at least one of the above assays, thereby confirming the utility of the compounds of the present invention as effective inhibitors of the coagulation cascade and/or contact activation system, and useful as anticoagulants for the prevention or treatment of thromboembolic disorders in mammals and/or as anti-inflammatory agents for the prevention or treatment of inflammatory disorders in mammals.
- the Michaelis constant,K m for substrate hydrolysis by each protease was determined at 25 °C using the method of Lineweaver and Burk. Values of Kj were determined by allowing the protease to react with the substrate in the presence of the inhibitor.
- the effectiveness of compounds of the present invention as inhibitors of the coagulation factors XIa, Vila, IXa, Xa, or thrombin can be determined using relevant in vivo thrombosis models, including In Vivo Electrically-induced Carotid Artery Thrombosis Models and In Vivo Rabbit Arterio-venous Shunt Thrombosis Models.
- ECAT electrically-induced carotid artery thrombosis
- rabbits are anesthetized with a mixture of ketamine (50 mg/kg i.m.) and xylazine (10 mg/kg i.m.).
- a femoral vein and a femoral artery are isolated and catheterized.
- the carotid artery is also isolated such that its blood flow can be measured with a calibrated flow probe that is linked to a flowmeter.
- a stainless steel bipolar hook electrode is placed on the carotid artery and positioned caudally in relationship to the flow probe as a means of applying electrical stimulus. In order to protect the surrounding tissue, a piece of Parafilm is placed under the electrode.
- Test compounds are considered to be effective as anticoagulants based on their ability to maintain blood flow in the carotid artery following the induction of thrombosis by an electrical stimulus.
- a test compound or vehicle is given as continuous intravenous infusion via the femoral vein, starting 1 hour before electrical stimulation and continuing to the end of the test.
- Thrombosis is induced by applying a direct electrical current of 4 mA for 3 min to the external arterial surface, using a constant current unit and a d.c. stimulator.
- the carotid blood flow is monitored and the time to occlusion (decrease of blood flow to zero following induction of thrombosis) in niinutes is noted.
- the change in observed blood flow is calculated as a percentage of the blood flow prior to induction of thrombosis and provides a measure of the effect of a test compound when compared to the case where no compound is administered. This information is used to estimate the ED50 value, the dose that increases blood flow to 50% of the control (blood flow prior to induction of thrombosis) and is accomplished by nonlinear least square regression.
- AV arterio-venous shunt thrombosis model
- rabbits weighing 2-3 kg anesthetized with a mixture of xylazine (10 mg/kg i.m.) and ketamine (50 mg/kg i.m.) are used.
- a saline-filled AV shunt device is connected between the femoral arterial and the femoral venous cannulae.
- the AV shunt device consists of a piece of 6-cm tygon tubing that contains a piece of silk thread.
- Blood will flow from the femoral artery via the AV-shunt into the femoral vein.
- the exposure of flowing blood to a silk thread will induce the formation of a significant thrombus.
- Test agents or vehicle will be given (i.v., i.p., s.c, or orally) prior to the opening of the AV shunt.
- the percentage inhibition of thrombus formation is determined for each treatment group.
- the ID 5 0 values dose which produces 50% inhibition of thrombus formation) are estimated by linear regression.
- the anti-inflammatory effect of these compounds can be demonstrated in an Evans Blue dye extravasation assay using Cl-esterase inhibitor deficient mice. In this model, mice are dosed with a compound of the present invention, Evans Blue is injected via the tail vein, and extravasation of the blue dye is determined by spectrophotometric means from tissue extracts.
- the ability of the compounds of the current invention to reduce or prevent the systemic inflammatory response syndrome can be tested in in vitro perfusion systems, or by on-pump surgical procedures in larger mammals, including dogs and baboons.
- Read-outs to assess the benefit of the compounds of the present invention include for example reduced platelet loss, reduced platelet / white blood cell complexes, reduced neutrophil elastase levels in plasma, reduced activation of complement factors, and reduced activation and/or consumption of contact activation proteins (plasma kallikrein, factor XII, factor XI, high molecular weight krninogen, Cl-esterase inhibitors).
- the utility of the compounds of the current invention to reduce or prevent the morbidity and/or mortality of sepsis can be assessed by injecting a mammalian host with bacteria or viruses or extracts there of and compounds of the present invention.
- Typical read-outs of the efficacy include changes in the LD50 and blood pressure preservation.
- the compounds of the present invention may also be useful as inhibitors of additional serine proteases, notably human thrombin, human plasma kallikrein and human plasmin. Because of their inhibitory action, these compounds are indicated for use in the prevention or treatment of physiological reactions, including blood coagulation, fibrinolysis, blood pressure regulation and inflammation, and wound healing catalyzed by the aforesaid class of enzymes. Specifically, the compounds have utility as drugs for the treatment of diseases arising from elevated thrombin activity of the aforementioned serine proteases, such as myocardial infarction, and as reagents used as anticoagulants in the processing of blood to plasma for diagnostic and other commercial purposes.
- additional serine proteases notably human thrombin, human plasma kallikrein and human plasmin. Because of their inhibitory action, these compounds are indicated for use in the prevention or treatment of physiological reactions, including blood coagulation, fibrinolysis, blood pressure regulation and inflammation, and wound healing catalyzed by the afores
- the compounds of the present invention can be administered alone or in combination with one or more additional therapeutic agents. These include other anti-coagulant or coagulation inhibitory agents, anti-platelet or platelet inhibitory agents, anti-inflammatory agents, thrombin inhibitors, or thrombolytic or fibrinolytic agents.
- the compounds are administered to a mammal in a therapeutically effective amount.
- therapeutically effective amount it is meant an amount of a compound of the present invention that, when administered alone or in combination with an additional therapeutic agent to a mammal, is effective to treat (i.e. prevent, inhibit or ameliorate) the thromboembolic and/or inflammatory disease condition or treat the progression of the disease in a host.
- the compounds of the invention are preferably administered alone to a mammal in a therapeutically effective amount.
- the compounds of the invention can also be administered in combination with an additional therapeutic agent, as define below, to a mammal in a therapeutically effective amount.
- the combination of compounds is preferably, but not necessarily, a synergistic combination. Synergy, as described for example by Chou and Talalay, Adv. Enzyme Regul 1984, 22, 27-55, occurs when the effect (in this case, inhibition of the desired target) of the compounds when administered in combination is greater than the additive effect of the compounds when administered alone as a single agent. In general, a synergistic effect is most clearly demonstrated at suboptimal concentrations of the compounds.
- Synergy can be in terms of lower cytotoxicity, increased anticoagulant effect, or some other beneficial effect of the combination compared with the individual components.
- administered in combination or “combination therapy” it is meant that the compound of the present invention and one or more additional therapeutic agents are administered concurrently to the mammal being treated.
- each component may be administered at the same time or sequentially in any order at different points in time.
- each component may be administered separately but sufficiently closely in time so as to provide the desired therapeutic effect.
- Compounds which can be administered in combination with the compounds of the present invention include, but are not limited to, anticoagulants, anti-thrombin agents, anti-platelet agents, fibrinolytics, hypolipidemic agents, antihypertensive agents, and anti-ischemic agents.
- anticoagulant agents include warfarin, heparin (either unfractionated heparin or any commercially available low molecular weight heparin, for example LOVENOXTM), aprotinin, synthetic pentasaccharide, direct acting thrombin inhibitors including hirudin and argatroban, as well as other factor Vila, Villa, IXa, Xa, XIa, thrombin, TAFI, and fibrinogen inhibitors known in the art.
- warfarin heparin (either unfractionated heparin or any commercially available low molecular weight heparin, for example LOVENOXTM)
- aprotinin synthetic pentasaccharide
- direct acting thrombin inhibitors including hirudin and argatroban, as well as other factor Vila, Villa, IXa, Xa, XIa, thrombin, TAFI, and fibrinogen inhibitors known in the art.
- anti-platelet agents denotes agents that inhibit platelet function, for example, by inhibiting the aggregation, adhesion or granular secretion of platelets.
- agents include, but are not limited to, the various known non-steroidal anti-inflammatory drugs (NS AIDS) such as aspirin, ibuprofen, naproxen, sulindac, indomethacin, mefenamate, droxicam, diclofenac, sulfinpyrazone, and piroxicam, cluding pharmaceutically acceptable salts or prodrugs thereof.
- NS AIDS non-steroidal anti-inflammatory drugs
- NSAIDS acetylsalicylic acid or ASA
- piroxicam are preferred.
- Other suitable platelet inhibitory agents include Ilb/IIIa antagonists (e.g., tirofiban, eptifibatide, and abciximab), thromboxane-A2-receptor antagonists (e.g., ifetroban), thromboxane-A2-synthetase inhibitors, phosphodiesterase-III (PDE-III) inhibitors (e.g., dipyridamole, cilostazol), and PDE V inhibitors (such as sildenafil), and pharmaceutically acceptable salts or prodrugs thereof.
- Ilb/IIIa antagonists e.g., tirofiban, eptifibatide, and abciximab
- thromboxane-A2-receptor antagonists e.g., ifetroban
- anti-platelet agents or platelet inhibitory agents
- ADP adenosine diphosphate
- Preferred P2Y12 receptor antagonists include ticlopidine and clopidogrel, including pharmaceutically acceptable salts or prodrugs thereof.
- Clopidogrel is an even more preferred agent.
- Ticlopidine and clopidogrel are also preferred compounds since they are known to be gentle on the gastro-intestinal tract in use.
- the compounds of the present invention may also be dosed in combination with aprotinin.
- thrombin inhibitors denotes inhibitors of the serine protease thrombin.
- various thrombin-mediated processes such as thrombin-mediated platelet activation (that is, for example, the aggregation of platelets, and/or the granular secretion of plasminogen activator inhibitor- 1 and/or serotonin), endothelial cell activation, inflammatory reactions, and/or fibrin formation are disrupted.
- thrombin inhibitors are known to one of skill in the art and these inhibitors are contemplated to be used in combination with the present compounds.
- Such inhibitors include, but are not limited to, boroarginine derivatives, boropeptides, heparins, hirudin and argatroban, including pharmaceutically acceptable salts and prodrugs thereof.
- Boroarginine derivatives and boropeptides include N-acetyl and peptide derivatives of boronic acid, such as C- terminal alpha-arninoboronic acid derivatives of lysine, or thine, arginine, homoarginine and corresponding isothiouronium analogs thereof.
- hirudin includes suitable derivatives or analogs of hirudin, referred to herein as hirulogs, such as disulfatohirudin.
- thrombolytic agents denotes agents that lyse blood clots (thrombi).
- agents include tissue plasminogen activator (TPA, natural or recombinant) and modified forms thereof, anistreplase, urokinase, streptokinase, tenecteplase (TNK), lanoteplase (nPA), factor Vila inhibitors, PAI-I inhibitors (i.e., inactivators of tissue plasminogen activator inhibitors), alpha-2-antiplasmin inhibitors, and anisoylated plasminogen streptokinase activator complex, including pharmaceutically acceptable salts or prodrugs thereof.
- TPA tissue plasminogen activator
- TNK tenecteplase
- nPA lanoteplase
- PAI-I inhibitors i.e., inactivators of tissue plasminogen activator inhibitors
- alpha-2-antiplasmin inhibitors alpha-2-antiplasmin inhibitors
- anistreplase refers to anisoylated plasminogen streptokinase activator complex, as described, for example, in European Patent Application No. 028,489, the disclosure of which is hereby incorporated herein by reference herein.
- iirokinase as used herein, is intended to denote both dual and single chain urokinase, the latter also being referred to herein as prourokinase.
- Suitable anti-arrythmic agents for use in combination with the present compounds include: Class I agents (such as propafenone); Class II agents (such as carvadiol and propranolol); Class III agents (such as sotalol, dofetilide, amiodarone, azimilide and ibutilide); Class LV agents (such as ditiazem and verapamil); K + channel openers such as 1 ⁇ inhibitors, and 1 ⁇ inhibitors (e.g., compounds such as those disclosed in WO01/40231).
- Class I agents such as propafenone
- Class II agents such as carvadiol and propranolol
- Class III agents such as sotalol, dofetilide, amiodarone, azimilide and ibutilide
- Class LV agents such as ditiazem and verapamil
- K + channel openers such as 1 ⁇ inhibitors, and 1 ⁇ inhibitors (e.g., compounds such as those disclosed in WO
- antihypertensive agents include: alpha adrenergic blockers; beta adrenergic blockers; calcium channel blockers (e.g., diltiazem, verapamil, nifedipine, amlodipine and mybefradil); diruetics (e.g., chlorothiazide, hydrochlorothiazide, flumethiazide, hydroflumethiazide, bendroflumethiazide, methylchlorothiazide, trichloromethiazide, polythiazide, benzthiazide, ethacrynic acid tricrynafen, chlorthalidone, furosemide, musolimine, bumetanide, triamtrenene, amiloride, spironolactone); renin inhibitors; angiotensin- converting enzyme (ACE) inhibitors (e.g., captopril) inhibitors (e.g., captopri
- DNP neutral endopeptidase
- vasopepsidase inhibitors dual ACE/NEP inhibitors, e.g., omapatrilat, gemopatrilat, nitrates
- ⁇ -blockers e.g., propanolol, nadolo, or carvedilol.
- suitable cardiac glycosides for use in combination with the compounds of the present invention include digitalis and ouabain.
- Examples of suitable mineralocorticoid receptor antagonists for use in combination with the compounds of the present invention include sprionolactone and eplirinone.
- Examples of suitable cholesterol/lipid lowering agents and lipid profile therapies for use in combination with the compounds of the present invention include: HMG-CoA reductase inhibitors (e.g., pravastatin, lovastatin, atorvastatin, simvastatin, fluvastatin, NK-104 (a.k.a. itavastatin, or nisvastatin or nisbastatin) and ZD-4522 (a.k.a.
- rosuvastatin, or atavastatin or visastatin rosuvastatin, or atavastatin or visastatin
- squalene synthetase inhibitors include fibrates; bile acid sequestrants (such as questran); ACAT inhibitors; MTP inhibitors; lipooxygenase inhibitors; choesterol absorption inhibitors; and cholesterol ester transfer protein inhibitors (e.g., CP-529414).
- Suitable anti-diabetic agents for use in combination with the compounds of the present invention include: biguanides (e.g., metformin); glucosidase inhibitors (e.g., acarbose); insulins (including insulin secretagogues or insulin sensitizers); meglitinides (e.g., repaglinide); sulfonylureas (e.g., glimepiride, glyburide and glipizide); biguanide/glyburide combinations (e.g., glucovance), thiozolidinediones (e.g., troglitazone, rosiglitazone and pioglitazone), PPAR-alpha agonists, PPAR-gamma agonists, PPAR alpha gamma dual agonists, SGLT2 inhibitors, inhibitors of fatty acid binding protein (aP2) such as those disclosed in WO00/59506,
- Examples of suitable anti-depressant agents for use in combination with the compounds of the present invention include nefazodone and sertraline.
- Examples of suitable anti-inflammatory agents for use in combination with the compounds of the present invention include: prednisone; dexamethasone; enbrel; protein tyrosine kinase (PTK) inhibitors; cyclooxygenase inhibitors (including NSAIDs, and COX-1 and/or COX-2 inhibitors); aspirin; indomethacin; ibuprofen; prioxicam; naproxen; celecoxib; and/or rofecoxib.
- Examples of suitable anti-osteoporosis agents for use in combination with the compounds of the present invention include alendronate and raloxifene.
- Examples of suitable hormone replacement therapies for use in combination with the compoxmds of the present invention include estrogen (e.g., congugated estrogens) and estradiol.
- Suitable anti-obesity agents for use in combination with the compounds of the present invention include orlistat and aP2 inhibitors (such as those disclosed in WO00/59506).
- Examples of suitable anti-anxiety agents for use in combination with the compounds of the present invention include diazepam, lorazepam, buspirone, and hydroxyzine pamoate.
- Examples of suitable anti-anxiety agents for use in combination with the compounds of the present invention include diazepam, lorazepam, buspirone, and hydroxyzine pamoate.
- Examples of suitable anti-proliferative agents for use in combination with the compounds of the present invention include cyclosporin A, paclitaxel, adriamycin; epithilones, cisplatin, and carboplatin.
- Suitable anti-ulcer and gastroesophageal reflux disease agents for use in combination with the compounds of the present invention include famotidine, ranitidine, and omeprazole.
- Administration of the compounds of the present invention i.e., a first therapeutic agent in combination with at least one additional therapeutic agent (i.e., a second therapeutic agent), preferably affords an efficacy advantage over the compounds and agents alone, preferably while permitting the use of lower doses of each.
- a lower dosage minimizes the potential of side effects, thereby providing an increased margin of safety.
- at least one of the therapeutic agents is administered in a sub-therapeutic dose. It is even more preferred that all of the therapeutic agents be administered in sub-therapeutic doses.
- Sub-therapeutic is intended to mean an amount of a therapeutic agent that by itself does not give the desired therapeutic effect for the condition or disease being treated.
- the compoxmds of the present invention are also useful as standard or reference compounds, for example as a quality standard or control, in tests or assays involving the inhibition of thrombin, Factor Vila, IXa, Xa, XIa, and/or plasma kallikrein.
- Such compounds may be provided in a commercial kit, for example, for use in pharmaceutical research involving thrombin, Factor Vila, IXa, Xa, XIa, and/or plasma kallikrein.
- XIa for use in pharmaceutical research involving thrombin, Factor Vila, IXa, Xa, XIa, and/or plasma kallikrein.
- a compound of the present invention could be used as a reference in an assay to compare its known activity to a compoxmd with an unknown activity. This would ensure the experimentor that the assay was being performed properly and provide a basis for comparison, especially if the test compound was a derivative of the reference compound.
- compounds according to the present invention could be used to test their effectiveness.
- the compounds of the present invention may also be used in diagnostic assays involving thrombin, Factor Vila, IXa, Xa, XIa, and/or plasma kallikrein.
- thrombin, Factor Vila, LXa, Xa XIa, and/or plasma kallikrein in an unknown sample could be detemiined by addition of the relevant chromogenic substrate, for example S2366 for Factor XIa, to a series of solutions containing test sample and optionally one of the compounds of the present invention. If production of pNA is observed in the solutions containing test sample, but not in the presence of a compound of the present invention, then one would conclude Factor XIa was present.
- Extremely potent and selective compounds of the present invention those having Ki values less than or equal to 0.001 ⁇ M against the target protease and greater than or equal to 0.1 ⁇ M against the other proteases, may also be used in diagnostic assays involving the quantitation of thrombin, Factor Vila, IXa, Xa, XIa, and or plasma kallikrein in serum samples.
- the amount of Factor XIa in serum samples could be determined by careful titration of protease activity in the presence of the relevant chromogenic substrate, S2366, with a potent and selective Factor XIa inhibitor of the present invention.
- the present mvention also encompasses an article of manufacture.
- article of manufacture is intended to include, but not be limited to, kits and packages.
- the article of manufacture of the present invention comprises: (a) a first container; (b) a pharmaceutical composition located within the first container, wherein the composition, comprises: a first therapeutic agent, comprising: a compound of the present invention or a pharmaceutically acceptable salt form thereof; and, (c) a package insert stating that the pharmaceutical composition can be used for the treatment of a thromboembolic and/or inflammatory disorder (as defined previously).
- the package insert states that the pharmaceutical composition can be used in combination (as defined previously) with a second therapeutic agent to treat a thromboembolic and/or mflarnmatory disorder.
- the article of manufacture can further comprise: (d) a second container, wherein components (a) and (b) are located within the second container and component (c) is located within or outside of the second container. Located within the first and second containers means that the respective container holds the item wi1 jin its boundaries.
- the first container is a receptacle used to hold a pharmaceutical composition.
- This container can be for manufacturing, storing, shipping, and/or individual/bulk selling.
- First container is intended to cover a bottle, jar, vial, flask, syringe, tube (e.g., for a cream preparation), or any other container used to manufacture, hold, store, or distribute a pharmaceutical product.
- the second container is one used to hold the first container and, optionally, the package insert. Examples of the second container include, but are not limited to, boxes (e.g., cardboard or plastic), crates, cartons, bags (e.g., paper or plastic bags), pouches, and sacks.
- the package insert can be physically attached to the outside of the first container via tape, glue, staple, or another method of attachment, or it can rest inside the second container without any physical means of attachment to the first container.
- the package msert is located on the outside of the second container.
- the package insert is physically attached via tape, glue, staple, or another method of attachment.
- it can be adjacent to or touching the outside of the second container without being physically attached.
- the package insert is a label, tag, marker, etc. that recites information relating to the pharmaceutical composition located within the first container.
- the package insert specifically recites the indications for which the pharmaceutical composition has been approved.
- the package insert may be made of any material on which a person can read information contained therein or thereon.
- the package insert is a printable material (e.g., paper, plastic, cardboard, foil, adhesive-backed paper or plastic, etc.) on which the desired information has been formed (e.g., printed or applied).
- the compounds of this invention can be administered in such oral dosage forms as tablets, capsules (each of which includes sustained release or timed release formulations), pills, powders, granules, elixirs, tinctures, suspensions, syrups, and emulsions. They may also be administered in intravenous (bolus or infusion), intraperitoneal, subcutaneous, or intramuscular form, all using dosage forms well known to those of ordinary skill in the pharmaceutical arts. They can be administered alone, but generally will be administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice.
- the dosage regimen for the compounds of the present invention will, of course, vary depending upon known factors, such as the pharmacodynamic characteristics of the particular agent and its mode and route of administration; the species, age, sex, health, medical condition, and weight of the recipient; the nature and extent of the symptoms; the kind of concurrent treatment; the frequency of treatment; the route of administration, the renal and hepatic function of the patient, and the effect desired.
- a physician or veterinarian can determine and prescribe the effective amount of the drag required to prevent, counter, or arrest the progress of the thromboembolic disorder.
- the daily oral dosage of each active ingredient when used for the indicated effects, will range between about 0.001 to 1000 mg kg of body weight, preferably between about 0.01 to 100 mg kg of body weight per day, and most preferably between about 1.0 to 20 mg/kg/day. Intravenously, the most preferred doses will range from about 1 to about 10 mg/kg/minute during a constant rate infusion.
- Compounds of this invention may be administered in a single daily dose, or the total daily dosage may be administered in divided doses of two, three, or four times daily.
- Compounds of this invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal routes, using transdermal skin patches.
- the dosage administration When administered in the form of a transdermal delivery system, the dosage administration will, of course, be continuous rather than intermittent throughout the dosage regimen.
- the compounds are typically administered in ad ⁇ iixture with suitable pharmaceutical diluents, excipients, or carriers (collectively referred to herein as pharmaceutical carriers) suitably selected with respect to the intended form of administration, that is, oral tablets, capsules, elixirs, syrups and the like, and consistent with conventional pharmaceutical practices.
- the active drug component can be combined with an oral, non-toxic, pharmaceutically acceptable, inert carrier such as lactose, starch, sucrose, glucose, methyl cellulose, magnesium stearate, dicalcium phosphate, calcium sulfate, mannitol, sorbitol and the like; for oral administration in liquid form, the oral drug components can be combined with any oral, non-toxic, pharmaceutically acceptable inert carrier such as ethanol, glycerol, water, and the like. Moreover, when desired or necessary, suitable binders, lubricants, disintegrating agents, and coloring agents can also be incorporated into the mixture.
- suitable binders, lubricants, disintegrating agents, and coloring agents can also be incorporated into the mixture.
- Suitable binders include starch, gelatin, natural sugars such as glucose or beta-lactose, com sweeteners, natural and synthetic gums such as acacia, tragacanth, or sodium alginate, carboxymethylcellulose, polyethylene glycol, waxes, and the like.
- Lubricants used in these dosage forms include sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride, and the like.
- Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum, and the like.
- the compounds of the present invention can also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles, and multilamellar vesicles.
- Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine, or phosphatidylcholines.
- Compounds of the present invention may also be coupled with soluble polymers as targetable drug carriers.
- Such polymers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropyhnethacrylamide-phenol, polyhydroxyethylaspartamidephenol, or polyethyleneoxide-polylysine substituted with palmitoyl residues.
- compoxmds of the present invention may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, poly lactic acid, polyglycolic acid, copolymers of polylactic and polyglycolic acid, polyepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacylates, and crosslinked or amphipathic block copolymers of hydrogels.
- biodegradable polymers useful in achieving controlled release of a drug
- a drug for example, poly lactic acid, polyglycolic acid, copolymers of polylactic and polyglycolic acid, polyepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacylates, and crosslinked or amphipathic block copolymers of hydrogels.
- Dosage forms suitable for administration may contain from about 1 milligram to about 100 milligrams of active ingredient per dosage unit. In these pharmaceutical compositions the active ingredient will ordinarily be present in an amount of about 0.5-95% by weight based on the total weight of the composition.
- Gelatin capsules may contain the active ingredient and powdered carriers, such as lactose, starch, cellulose derivatives, magnesium stearate, stearic acid, and the like. Similar diluents can be used to make compressed tablets. Both tablets and capsules can be manufactured as sustained release products to provide for continuous release of medication over a period of hours. Compressed tablets can be sugar coated or film coated to mask any unpleasant taste and protect the tablet from the atmosphere, or enteric coated for selective disintegration in the gastrointestinal tract.
- Liquid dosage forms for oral administration can contain coloring and flavoring to increase patient acceptance.
- water, a suitable oil, saline, aqueous dextrose (glucose), and related sugar solutions and glycols such as propylene glycol or polyethylene glycols are suitable carriers for parenteral solutions.
- Solutions for parenteral administration preferably contain a water soluble salt of the active ingredient, suitable stabilizing agents, and if necessary, buffer substances.
- Antioxidizing agents such as sodium bisulfite, sodium sulfite, or ascorbic acid, either alone or combined, are suitable stabilizing agents.
- citric acid and its salts and sodium EDTA are also used.
- parenteral solutions can contain preservatives, such as benzalkonium chloride, methyl-or propyl-paraben, and chlorobutanol.
- Suitable pharmaceutical carriers are described in Remington's
- a daily dosage maybe about 0.1 to 100 milligrams of the compound of the present invention and about 1 to 7.5 milligrams of the second anticoagulant, per kilogram of patient body weight.
- the compounds of this invention generally may be present in an amount of about 5 to 10 milligrams per dosage unit, and the second anti-coagulant in an amount of about 1 to 5 milligrams per dosage unit.
- a daily dosage may be about 0.01 to 25 milligrams of the compound of the present invention and about 50 to 150 milligrams of the anti-platelet agent, preferably about 0.1 to 1 milligrams of the compound of the present invention and about 1 to 3 milligrams of antiplatelet agents, per kilogram of patient body weight.
- a daily dosage may be about 0.1 to 1 milligrams of the compound of the present invention, per kilogram of patient body weight and, in the case of the thrombolytic agents, the usual dosage of the thrombolyic agent when administered alone may be reduced by about 70-80% when administered with a compound of the present invention.
- the amount of each component in a typical daily dosage and typical dosage form may be reduced relative to the usual dosage of the agent when administered alone, in view of the additive or synergistic effect of the therapeutic agents when administered in combination.
- the compound of Formula I and a second therapeutic agent are combined in a single dosage unit they are formulated such that although the active ingredients are combined in a single dosage unit, the physical contact between the active ingredients is minimized (that is, reduced).
- one active ingredient may be enteric coated. By enteric coating one of the active ingredients, it is possible not only to minimize the contact between the combined active ingredients, but also, it is possible to control the release of one of these components in the gastrointestinal tract such that one of these components is not released in the stomach but rather is released in the intestines.
- One of the active ingredients may also be coated with a material that affects a sustained-release throughout the gastrointestinal tract and also serves to minimize physical contact between the combined active ingredients.
- the sustained-released component can be additionally enteric coated such that the release of this component occurs only in the intestine.
- Still another approach would involve the formulation of a combination product in which the one component is coated with a sustained and/or enteric release polymer, and the other component is also coated with a polymer such as a low viscosity grade of hydroxypropyl methylcellulose (HPMC) or other appropriate materials as known in the art, in order to further separate the active components.
- HPMC hydroxypropyl methylcellulose
- the polymer coating serves to form an additional barrier to interaction with the other component.
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Abstract
Description
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Priority Applications (7)
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CN2005800274852A CN101010299B (en) | 2004-06-15 | 2005-06-14 | Six-membered heterocycles useful as serine protease inhibitors |
AT05787697T ATE520662T1 (en) | 2004-06-15 | 2005-06-14 | SIX-MEMBERED HETEROCYCLENES AS SERINE PROTEASE INHIBITORS |
JP2007516646A JP4834663B2 (en) | 2004-06-15 | 2005-06-14 | 6-membered heterocycles useful as serine protease inhibitors |
AU2005255029A AU2005255029A1 (en) | 2004-06-15 | 2005-06-14 | Six-membered heterocycles useful as serine protease inhibitors |
MXPA06014799A MXPA06014799A (en) | 2004-06-15 | 2005-06-14 | Six-membered heterocycles useful as serine protease inhibitors. |
EP05787697A EP1773775B1 (en) | 2004-06-15 | 2005-06-14 | Six-membered heterocycles useful as serine protease inhibitors |
NO20070201A NO20070201L (en) | 2004-06-15 | 2007-01-11 | Six-membered heterocycles useful as serine protease inhibitors |
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US11/151,627 | 2005-06-13 |
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Cited By (92)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006089005A2 (en) * | 2005-02-17 | 2006-08-24 | Bristol-Myers Squibb Company | Combination of selective factor viia and/or xia and plasma kallikrein inhibitors |
WO2007070818A1 (en) * | 2005-12-14 | 2007-06-21 | Bristol-Myers Squibb Company | Six-membered heterocycles useful as serine protease inhibitors |
WO2007070816A2 (en) * | 2005-12-14 | 2007-06-21 | Bristol-Myers Squibb Company | Thiophene derivatives as factor xia inhibitors |
WO2007082264A2 (en) * | 2006-01-11 | 2007-07-19 | Bristol-Myers Squibb Company | Human glucagon-like-peptide-1 modulators and their use in the treatment of diabetes and related conditions |
WO2008076805A3 (en) * | 2006-12-15 | 2008-08-14 | Bristol Myers Squibb Co | Arylpropionamide, arylacrylamide, arylpropynamide, or arylmethylurea analogs as factor xia inhibitors |
WO2010009029A2 (en) * | 2008-07-15 | 2010-01-21 | Wyeth | Methods for the preparation of azole compounds |
JP2010529137A (en) * | 2007-06-08 | 2010-08-26 | アボット・ラボラトリーズ | 5-Heteroaryl-substituted indazoles as kinase inhibitors |
WO2012017020A1 (en) * | 2010-08-04 | 2012-02-09 | Novartis Ag | N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides as inhibitors of plasma kallikrein |
WO2013006738A1 (en) * | 2011-07-06 | 2013-01-10 | Gilead Sciences, Inc. | Compounds for the treatment of hiv |
WO2013130976A1 (en) * | 2012-03-01 | 2013-09-06 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
US8648069B2 (en) | 2007-06-08 | 2014-02-11 | Abbvie Inc. | 5-substituted indazoles as kinase inhibitors |
US8828983B2 (en) | 2010-02-11 | 2014-09-09 | Bristol-Myers Squibb Company | Macrocycles as factor XIa inhibitors |
WO2014188211A1 (en) * | 2013-05-23 | 2014-11-27 | Kalvista Pharmaceuticals Limited | Heterocyclic derivates |
US8901115B2 (en) | 2011-08-05 | 2014-12-02 | Bristol-Myers Squibb Company | Cyclic P1 linkers as factor XIa inhibitors |
WO2015022546A1 (en) * | 2013-08-14 | 2015-02-19 | Kalvista Pharmaceuticals Limited | Inhibitors of plasma kallikrein |
US9000172B2 (en) | 2011-10-14 | 2015-04-07 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
US9072842B2 (en) | 2002-04-19 | 2015-07-07 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US9079929B2 (en) | 2011-10-14 | 2015-07-14 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
US9089294B2 (en) | 2002-04-19 | 2015-07-28 | Sanofi-Aventis Deutschland Gmbh | Analyte measurement device with a single shot actuator |
US9108951B2 (en) | 2011-10-14 | 2015-08-18 | Bristol-Myers Squibb Company | Substituted 5,6,7,8-tetrahydro-1,6-naphthyridines as factor XIa inhibitors |
WO2015123091A1 (en) | 2014-02-11 | 2015-08-20 | Merck Sharp & Dohme Corp. | Factor xia inhibitors |
WO2015123093A1 (en) | 2014-02-11 | 2015-08-20 | Merck Sharp & Dohme Corp. | Factor xia inhibitors |
US9133187B2 (en) | 2011-02-28 | 2015-09-15 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
WO2015164308A1 (en) | 2014-04-22 | 2015-10-29 | Merck Sharp & Dohme Corp. | FACTOR XIa INHIBITORS |
US9187462B2 (en) | 2011-08-04 | 2015-11-17 | Array Biopharma Inc. | Substituted quinazolines as serine/threonine kinase inhibitors |
US9221818B2 (en) | 2011-08-05 | 2015-12-29 | Bristol-Myers Squibb Company | Macrocycles as factor XIa inhibitors |
US9248267B2 (en) | 2002-04-19 | 2016-02-02 | Sanofi-Aventis Deustchland Gmbh | Tissue penetration device |
WO2016015593A1 (en) | 2014-07-28 | 2016-02-04 | Merck Sharp & Dohme Corp. | FACTOR XIa INHIBITORS |
US9261476B2 (en) | 2004-05-20 | 2016-02-16 | Sanofi Sa | Printable hydrogel for biosensors |
US9315519B2 (en) | 2012-10-12 | 2016-04-19 | Bristol-Myers Squibb Company | Guanidine substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
WO2016083816A1 (en) | 2014-11-27 | 2016-06-02 | Kalvista Pharmaceuticals Limited | N-((heteroarylmethyl)-heteroaryl-carboxamide derivatives as plasma kallikrein inhibitors |
US9376444B2 (en) | 2012-08-03 | 2016-06-28 | Bristol-Myers Squibb Company | Dihydropyridone P1 as factor XIa inhibitors |
US9388171B2 (en) | 2012-08-27 | 2016-07-12 | Genetech, Inc. | Serine/threonine kinase inhibitors |
US9403774B2 (en) | 2012-10-12 | 2016-08-02 | Bristol-Myers Squibb Company | Guanidine and amine substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
US9409908B2 (en) | 2012-08-03 | 2016-08-09 | Bristol-Myers Squibb Company | Dihydropyridone p1 as factor XIa inhibitors |
US9427532B2 (en) | 2001-06-12 | 2016-08-30 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
US9453018B2 (en) | 2014-10-01 | 2016-09-27 | Bristol-Myers Squibb Company | Pyrimidinones as factor XIa inhibitors |
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US10696657B2 (en) | 2018-02-16 | 2020-06-30 | Gilead Sciences, Inc. | Methods and intermediates for preparing therapeutic compounds |
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Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7453002B2 (en) | 2004-06-15 | 2008-11-18 | Bristol-Myers Squibb Company | Five-membered heterocycles useful as serine protease inhibitors |
CN101137412B (en) * | 2005-01-13 | 2012-11-07 | 布里斯托尔-迈尔斯·斯奎布公司 | Substituted biaryl compounds as factor xia inhibitors |
AU2006257646A1 (en) * | 2005-06-16 | 2006-12-21 | Pfizer Inc. | N-(pyridin-2-YL)-sulfonamide derivatives |
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Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992002513A1 (en) * | 1990-08-06 | 1992-02-20 | Fujisawa Pharmaceutical Co., Ltd. | Heterocyclic compounds |
WO2002042273A2 (en) | 2000-11-07 | 2002-05-30 | Bristol-Myers Squibb Company | Acid derivatives useful as serine protease inhibitors |
WO2002064559A2 (en) * | 2001-02-09 | 2002-08-22 | Merck & Co., Inc. | Thrombin inhibitors |
US20030225131A1 (en) * | 2002-04-05 | 2003-12-04 | Burgey Christopher S. | Thrombin inhibitors |
WO2004014844A2 (en) | 2002-08-09 | 2004-02-19 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds and methods to modulate coagulation |
WO2004019868A2 (en) * | 2002-08-29 | 2004-03-11 | Merck & Co., Inc. | N-biarylmethyl aminocycloalkanecarboxamide derivatives |
WO2005007627A1 (en) | 2003-07-18 | 2005-01-27 | Nihon Nohyaku Co., Ltd. | Phenylpyridine derivative, intermediate therefor, and herbicide containing the same as active ingredient |
WO2005063690A1 (en) | 2003-12-22 | 2005-07-14 | Merck & Co., Inc. | Alpha-hydroxy amides as bradykinin antagonists or inverse agonists |
WO2005085198A2 (en) | 2004-03-02 | 2005-09-15 | Merck & Co., Inc. | Amino cyclopropane carboxamide derivatives as bradykinin antagonists |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9409882D0 (en) | 1994-05-18 | 1994-07-06 | Sandoz Ltd | Organic compounds |
US6593291B1 (en) | 1997-02-06 | 2003-07-15 | Entremed, Inc. | Compositions and methods of use of ligands that bind components of the blood coagulation/clotting pathway for the treatment of cancer and angiogenic-based disease |
TW575562B (en) | 1998-02-19 | 2004-02-11 | Agrevo Uk Ltd | Fungicides |
EP1140901A2 (en) | 1998-12-24 | 2001-10-10 | Aventis Pharmaceuticals Products Inc. | Substituted (aminoiminomethyl or aminomethyl)benzoheteroaryl compounds as factor xa inhibitors |
JP2002541253A (en) | 1999-04-09 | 2002-12-03 | スミスクライン・ビーチャム・コーポレイション | Triarylimidazole |
AU5158100A (en) | 1999-05-24 | 2000-12-12 | Cor Therapeutics, Inc. | Inhibitors of factor xa |
US6448281B1 (en) | 2000-07-06 | 2002-09-10 | Boehringer Ingelheim (Canada) Ltd. | Viral polymerase inhibitors |
PL363757A1 (en) | 2000-11-29 | 2004-11-29 | Vantico Ag | Filled epoxy resin system having high mechanical strength values |
WO2002098840A1 (en) | 2001-06-04 | 2002-12-12 | Eisai Co., Ltd. | Carboxylic acid derivative and medicine comprising salt or ester of the same |
DK1441734T3 (en) * | 2001-10-26 | 2007-06-11 | Angeletti P Ist Richerche Bio | Dihydroxypyrimidine carboxamide inhibitors and HIV integrase |
JP2003277362A (en) | 2002-01-21 | 2003-10-02 | Nippon Nohyaku Co Ltd | Pyrazolecarboxamide, intermediate of the same and pest- controlling agent with the same as active ingredient |
US7138412B2 (en) | 2003-03-11 | 2006-11-21 | Bristol-Myers Squibb Company | Tetrahydroquinoline derivatives useful as serine protease inhibitors |
US7129264B2 (en) | 2003-04-16 | 2006-10-31 | Bristol-Myers Squibb Company | Biarylmethyl indolines and indoles as antithromboembolic agents |
US7417063B2 (en) | 2004-04-13 | 2008-08-26 | Bristol-Myers Squibb Company | Bicyclic heterocycles useful as serine protease inhibitors |
US7453002B2 (en) | 2004-06-15 | 2008-11-18 | Bristol-Myers Squibb Company | Five-membered heterocycles useful as serine protease inhibitors |
CN101137412B (en) | 2005-01-13 | 2012-11-07 | 布里斯托尔-迈尔斯·斯奎布公司 | Substituted biaryl compounds as factor xia inhibitors |
-
2005
- 2005-06-13 US US11/151,627 patent/US7429604B2/en active Active
- 2005-06-14 EP EP05787697A patent/EP1773775B1/en active Active
- 2005-06-14 AT AT05787697T patent/ATE520662T1/en not_active IP Right Cessation
- 2005-06-14 MX MXPA06014799A patent/MXPA06014799A/en not_active Application Discontinuation
- 2005-06-14 JP JP2007516646A patent/JP4834663B2/en not_active Expired - Fee Related
- 2005-06-14 WO PCT/US2005/020971 patent/WO2005123680A1/en active Application Filing
- 2005-06-14 AU AU2005255029A patent/AU2005255029A1/en not_active Abandoned
- 2005-06-14 CN CN2005800274852A patent/CN101010299B/en not_active Expired - Fee Related
-
2007
- 2007-01-11 NO NO20070201A patent/NO20070201L/en not_active Application Discontinuation
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1992002513A1 (en) * | 1990-08-06 | 1992-02-20 | Fujisawa Pharmaceutical Co., Ltd. | Heterocyclic compounds |
WO2002042273A2 (en) | 2000-11-07 | 2002-05-30 | Bristol-Myers Squibb Company | Acid derivatives useful as serine protease inhibitors |
WO2002064559A2 (en) * | 2001-02-09 | 2002-08-22 | Merck & Co., Inc. | Thrombin inhibitors |
US20030225131A1 (en) * | 2002-04-05 | 2003-12-04 | Burgey Christopher S. | Thrombin inhibitors |
WO2004014844A2 (en) | 2002-08-09 | 2004-02-19 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds and methods to modulate coagulation |
WO2004019868A2 (en) * | 2002-08-29 | 2004-03-11 | Merck & Co., Inc. | N-biarylmethyl aminocycloalkanecarboxamide derivatives |
WO2005007627A1 (en) | 2003-07-18 | 2005-01-27 | Nihon Nohyaku Co., Ltd. | Phenylpyridine derivative, intermediate therefor, and herbicide containing the same as active ingredient |
WO2005063690A1 (en) | 2003-12-22 | 2005-07-14 | Merck & Co., Inc. | Alpha-hydroxy amides as bradykinin antagonists or inverse agonists |
WO2005085198A2 (en) | 2004-03-02 | 2005-09-15 | Merck & Co., Inc. | Amino cyclopropane carboxamide derivatives as bradykinin antagonists |
Non-Patent Citations (13)
Title |
---|
"Comprehensive Heterocyclic Chemistry", vol. 2, 1984, PERGAMON PRESS, pages: 165 - 524 |
"Comprehensive Heterocyclic Chemistry", vol. 5, 1996, PERGAMON PRESS, pages: 1 - 300 |
"Design of Prodrugs", 1985, ELSEVIER |
"Medicinal Chemistry: Principles and Practice", 1994, THE ROYAL SOCIETY OF CHEMISTRY |
"Methods in Enzymology", vol. 42, 1985, ACADEMIC PRESS, pages: 309 - 396 |
"Remington's Pharmaceutical Sciences", 1985, MACK PUBLISHING COMPANY |
"The Chemistry of Heterocyclic Compounds", vol. 14, 1974, JOHN WILEY AND SONS, article "Pyridine and Its Derivatives" |
GREENE; WUTS: "Protective Groups In Organic Synthesis", 1999, WILEY-INTERSCIENCE |
H. BUNDGAARD ET AL., JOURNAL OF PHARMACEUTICAL SCIENCES, vol. 77, 1988, pages 285 |
H. BUNDGAARD, ADVANCED DRUG DELIVERY REVIEWS, vol. 8, 1992, pages 1 - 38 |
H. BUNDGAARD: "A Textbook of Drug Design and Development", 1991, article "Design and Application of Prodrugs", pages: 113 - 191 |
KROHNKE, F., SYNTHESIS, 1976, pages 1 |
N. KAKEYA, CHEM PHAR BULL., vol. 32, 1984, pages 692 |
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EA021359B1 (en) * | 2010-08-04 | 2015-05-29 | Новартис Аг | N-((6-aminopyridin-3-yl)methyl)heteroaryl-carboxamides as inhibitors of plasma kallikrein |
CN103080104A (en) * | 2010-08-04 | 2013-05-01 | 诺瓦提斯公司 | N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides as inhibitors of plasma kallikrein |
CN103080104B (en) * | 2010-08-04 | 2015-04-08 | 诺华股份有限公司 | N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides as inhibitors of plasma kallikrein |
US9290485B2 (en) | 2010-08-04 | 2016-03-22 | Novartis Ag | N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides |
US9133187B2 (en) | 2011-02-28 | 2015-09-15 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
US10370358B2 (en) | 2011-07-06 | 2019-08-06 | Gilead Sciences, Inc. | Compounds for the treatment of HIV |
US9540343B2 (en) | 2011-07-06 | 2017-01-10 | Gilead Sciences, Inc. | Compounds for the treatment of HIV |
WO2013006738A1 (en) * | 2011-07-06 | 2013-01-10 | Gilead Sciences, Inc. | Compounds for the treatment of hiv |
US11034668B2 (en) | 2011-07-06 | 2021-06-15 | Gilead Sciences, Inc. | Compounds for the treatment of HIV |
US9944619B2 (en) | 2011-07-06 | 2018-04-17 | Gilead Sciences, Inc. | Compounds for the treatment of HIV |
US9187462B2 (en) | 2011-08-04 | 2015-11-17 | Array Biopharma Inc. | Substituted quinazolines as serine/threonine kinase inhibitors |
US9902742B2 (en) | 2011-08-05 | 2018-02-27 | Bristol-Myers Squibb Company | Macrocycles as factor XIa inhibitors |
US9221818B2 (en) | 2011-08-05 | 2015-12-29 | Bristol-Myers Squibb Company | Macrocycles as factor XIa inhibitors |
US10208068B2 (en) | 2011-08-05 | 2019-02-19 | Bristol-Myers Squibb Company | Macrocycles as factor XIa inhibitors |
US8901115B2 (en) | 2011-08-05 | 2014-12-02 | Bristol-Myers Squibb Company | Cyclic P1 linkers as factor XIa inhibitors |
US9108981B2 (en) | 2011-08-05 | 2015-08-18 | Bristol-Myers Squibb Company | Cyclic P1 linkers as factor XIa inhibitors |
US9611274B2 (en) | 2011-08-05 | 2017-04-04 | Bristol-Myers Squibb Company | Macrocycles as factor XIa inhibitors |
US9079929B2 (en) | 2011-10-14 | 2015-07-14 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
US9192607B2 (en) | 2011-10-14 | 2015-11-24 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
US9108951B2 (en) | 2011-10-14 | 2015-08-18 | Bristol-Myers Squibb Company | Substituted 5,6,7,8-tetrahydro-1,6-naphthyridines as factor XIa inhibitors |
US9000172B2 (en) | 2011-10-14 | 2015-04-07 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
US9725435B2 (en) | 2011-10-14 | 2017-08-08 | Bristol-Myers Squibb Company | Substituted 4,5,6,7-tetrahydropyrazolo[4,3-c]pyridines as factor XIa inhibitors |
US9447110B2 (en) | 2011-10-14 | 2016-09-20 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
US10208021B2 (en) | 2011-10-14 | 2019-02-19 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
US9944625B2 (en) | 2011-10-14 | 2018-04-17 | Bristol-Myers Squibb Company | Substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
US10906886B2 (en) | 2011-10-14 | 2021-02-02 | Bristol-Myers Squibb Company | Substituted 5,6,7,8-tetrahydroimidazo[1,5-a]pyrazines as factor xia inhibitors |
US10000466B2 (en) | 2011-10-14 | 2018-06-19 | Bristol-Myers Squibb Company | Substituted 4,5,6,7-tetrahydropyrazolo[3,4-c]pyridines as factor XIa inhibitors |
US9394276B2 (en) | 2011-10-14 | 2016-07-19 | Bristol-Myers Squibb Company | Substituted 1,2,3,4-tetrahydro-2,6-naphthyridines as factor XIa inhibitors |
US8697715B2 (en) | 2012-03-01 | 2014-04-15 | Array Biopharma, Inc. | Serine/threonine kinase inhibitors |
EP3321262A1 (en) * | 2012-03-01 | 2018-05-16 | Array Biopharma, Inc. | Serine/threonine kinase inhibitors |
WO2013130976A1 (en) * | 2012-03-01 | 2013-09-06 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
CN104507926A (en) * | 2012-03-01 | 2015-04-08 | 阵列生物制药公司 | Serine/threonine kinase inhibitors |
US9259470B2 (en) | 2012-03-01 | 2016-02-16 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
AU2013225737B2 (en) * | 2012-03-01 | 2018-03-01 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
US9708290B2 (en) | 2012-03-01 | 2017-07-18 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
CN104507926B (en) * | 2012-03-01 | 2016-08-31 | 阵列生物制药公司 | Serine/threonine kinase inhibitor |
US10519126B2 (en) | 2012-03-01 | 2019-12-31 | Array Biopharma Inc. | Serine/threonine kinase inhibitors |
US9376444B2 (en) | 2012-08-03 | 2016-06-28 | Bristol-Myers Squibb Company | Dihydropyridone P1 as factor XIa inhibitors |
US9951071B2 (en) | 2012-08-03 | 2018-04-24 | Bristol-Myers Squibb Company | Dihydropyridone P1 as factor XIa inhibitors |
US9409908B2 (en) | 2012-08-03 | 2016-08-09 | Bristol-Myers Squibb Company | Dihydropyridone p1 as factor XIa inhibitors |
US9388171B2 (en) | 2012-08-27 | 2016-07-12 | Genetech, Inc. | Serine/threonine kinase inhibitors |
US9315519B2 (en) | 2012-10-12 | 2016-04-19 | Bristol-Myers Squibb Company | Guanidine substituted tetrahydroisoquinoline compounds as factor XIa inhibitors |
US9403774B2 (en) | 2012-10-12 | 2016-08-02 | Bristol-Myers Squibb Company | Guanidine and amine substituted tetrahydroisoquinoline compounds as factor xia inhibitors |
US9920034B2 (en) | 2012-10-12 | 2018-03-20 | Bristol-Myers Squibb Company | Crystalline forms of a factor XIa inhibitor |
US9834513B2 (en) | 2013-01-08 | 2017-12-05 | Kalvista Pharmceuticals Limited | Benzylamine derivatives |
US9670157B2 (en) | 2013-01-08 | 2017-06-06 | Kalvista Pharmaceuticals Limited | Benzylamine derivatives |
US9849100B2 (en) | 2013-01-09 | 2017-12-26 | Kalvista Pharmaceuticals Limited | Pharmaceutical compositions suitable for parenteral administration comprising aqueous suspensions of benzylamine derivatives having low solubilities |
US10478409B2 (en) | 2013-01-09 | 2019-11-19 | Kalvista Pharmaceuticals Limited | Pharmaceutical compositions |
US9738655B2 (en) | 2013-03-25 | 2017-08-22 | Bristol-Myers Squibb Company | Tetrahydroisoquinolines containing substituted azoles as factor XIa inhibitors |
US9533987B2 (en) | 2013-05-23 | 2017-01-03 | Kalvista Pharmaceuticals Limited | Heterocyclic derivates |
RU2712621C2 (en) * | 2013-05-23 | 2020-01-30 | Калвиста Фармасьютикалз Лимитед | Nitrogen-containing heterocyclic derivatives useful as plasma kallikrein inhibitor |
KR20160029749A (en) * | 2013-05-23 | 2016-03-15 | 칼비스타 파마슈티컬즈 리미티드 | Heterocyclic derivates |
EP3305778A1 (en) | 2013-05-23 | 2018-04-11 | Kalvista Pharmaceuticals Limited | Inhibitors of plasma kallikrein |
WO2014188211A1 (en) * | 2013-05-23 | 2014-11-27 | Kalvista Pharmaceuticals Limited | Heterocyclic derivates |
KR102276700B1 (en) | 2013-05-23 | 2021-07-12 | 칼비스타 파마슈티컬즈 리미티드 | Heterocyclic derivates |
WO2015022546A1 (en) * | 2013-08-14 | 2015-02-19 | Kalvista Pharmaceuticals Limited | Inhibitors of plasma kallikrein |
CN105683179A (en) * | 2013-08-14 | 2016-06-15 | 卡尔维斯塔制药有限公司 | Inhibitors of plasma kallikrein |
US9738641B2 (en) | 2013-08-14 | 2017-08-22 | Kalvista Pharmaceuticals Limited | Bicyclic inhibitors |
US10221161B2 (en) | 2013-08-14 | 2019-03-05 | Kalvista Pharmaceuticals Limited | Inhibitors of plasma kallikrein |
US11242333B2 (en) | 2013-08-14 | 2022-02-08 | Kalvista Pharmaceuticals Limited | Inhibitors of plasma kallikrein |
CN105683179B (en) * | 2013-08-14 | 2018-10-26 | 卡尔维斯塔制药有限公司 | The inhibitor of plasma kallikrein |
US10273236B2 (en) | 2014-01-31 | 2019-04-30 | Bristol-Myers Squibb | Macrocyclic factor XIa inhibitors bearing heterocyclic groups |
US9777001B2 (en) | 2014-01-31 | 2017-10-03 | Bristol-Myers Squibb Company | Macrocycles with aromatic P2′ groups as factor xia inhibitors |
WO2015123093A1 (en) | 2014-02-11 | 2015-08-20 | Merck Sharp & Dohme Corp. | Factor xia inhibitors |
WO2015123091A1 (en) | 2014-02-11 | 2015-08-20 | Merck Sharp & Dohme Corp. | Factor xia inhibitors |
US10202353B2 (en) | 2014-02-28 | 2019-02-12 | Gilead Sciences, Inc. | Therapeutic compounds |
WO2015164308A1 (en) | 2014-04-22 | 2015-10-29 | Merck Sharp & Dohme Corp. | FACTOR XIa INHIBITORS |
WO2016015593A1 (en) | 2014-07-28 | 2016-02-04 | Merck Sharp & Dohme Corp. | FACTOR XIa INHIBITORS |
US10081623B2 (en) | 2014-09-04 | 2018-09-25 | Bristol-Myers Squibb Company | Diamide macrocycles that are FXIa inhibitors |
US9453018B2 (en) | 2014-10-01 | 2016-09-27 | Bristol-Myers Squibb Company | Pyrimidinones as factor XIa inhibitors |
US10336754B2 (en) | 2014-10-01 | 2019-07-02 | Bristol-Myers Squibb Company | Pyrimidinones as factor XIa inhibitors |
US11053247B2 (en) | 2014-10-01 | 2021-07-06 | Bristol-Myers Squibb Company | Pyrimidinones as factor XIA inhibitors |
US10364238B2 (en) | 2014-11-27 | 2019-07-30 | Kalvista Pharmaceuticals Limited | N-((het) arylmethyl)-heteroaryl-carboxamides compounds as plasma kallikrein inhibitors |
EP4039681A1 (en) | 2014-11-27 | 2022-08-10 | Kalvista Pharmaceuticals Limited | N-((het)arylmethyl)-heteroaryl-carboxamides compounds as plasma kallikrein inhibitors |
EP3556752A1 (en) | 2014-11-27 | 2019-10-23 | Kalvista Pharmaceuticals Limited | N-((het)arylmethyl)-heteroaryl-carboxamides compounds as plasma kallikrein inhibitors |
WO2016083816A1 (en) | 2014-11-27 | 2016-06-02 | Kalvista Pharmaceuticals Limited | N-((heteroarylmethyl)-heteroaryl-carboxamide derivatives as plasma kallikrein inhibitors |
EP3567037A1 (en) | 2014-11-27 | 2019-11-13 | Kalvista Pharmaceuticals Limited | N-((het)arylmethyl)-heteroaryl-carboxamides compounds as plasma kallikrein inhibitors |
US11001578B2 (en) | 2014-11-27 | 2021-05-11 | Kalvista Pharmaceuticals Limited | N-((HET)arylmethyl)-heteroaryl-carboxamides compounds as plasma kallikrein inhibitors |
US11198691B2 (en) | 2014-11-27 | 2021-12-14 | Kalvista Pharmaceuticals Limited | N-((het)arylmethyl)-heteroaryl-carboxamides compounds as kallikrein inhibitors |
US10781181B2 (en) | 2014-11-27 | 2020-09-22 | Kalvista Pharmaceuticals Limited | N-((het) arylmethyl)-heteroaryl-carboxamides compounds as plasma kallikrein inhibitors |
US11084809B2 (en) | 2014-11-27 | 2021-08-10 | Kalvista Pharmaceuticals Limited | N-((HET)arylmethyl)-heteroaryl-carboxamides compounds as kallikrein inhibitors |
US10611758B2 (en) | 2014-11-27 | 2020-04-07 | Kalvista Pharmaceuticals Limited | N-((het)arylmethyl)-heteroaryl-carboxamides compounds as kallikrein inhibitors |
US9980945B2 (en) | 2015-01-13 | 2018-05-29 | Vanderbilt University | Benzoisoxazole-substituted compounds as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
US10526323B2 (en) | 2015-01-30 | 2020-01-07 | Vanderbilt University | Indazole and azaindazole substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
US10160750B2 (en) | 2015-06-19 | 2018-12-25 | Bristol-Myers Squibb Company | Diamide macrocycles as factor XIa inhibitors |
US10676477B2 (en) | 2015-07-29 | 2020-06-09 | Bristol-Myers Squibb Company | Factor XIa macrocycle inhibitors bearing a non-aromatic P2' group |
US10287288B2 (en) | 2015-07-29 | 2019-05-14 | Bristol-Myers Squibb | Factor XIa macrocyclic inhibitors bearing alkyl or cycloalkyl P2' moieties |
WO2017074832A1 (en) | 2015-10-29 | 2017-05-04 | Merck Sharp & Dohme Corp. | FACTOR XIa INHIBITORS |
WO2017074833A1 (en) | 2015-10-29 | 2017-05-04 | Merck Sharp & Dohme Corp. | Macrocyclic spirocarbamate derivatives as factor xia inhibitors, pharmaceutically acceptable compositions and their use |
US10472344B2 (en) | 2015-12-02 | 2019-11-12 | Merck Sharp & Dohme Corp. | Factor XIa inhibitors |
EP3383847A4 (en) * | 2015-12-02 | 2019-05-08 | Merck Sharp & Dohme Corp. | FACTOR XIa INHIBITORS |
US11180484B2 (en) | 2016-05-31 | 2021-11-23 | Kalvista Pharmaceuticals Limited | Pyrazole derivatives as plasma kallikrein inhibitors |
EP3760622A1 (en) | 2016-05-31 | 2021-01-06 | Kalvista Pharmaceuticals Limited | Pyrazole derivatives as plasma kallikrein inhibitors |
US11739068B2 (en) | 2016-06-01 | 2023-08-29 | Kalvista Pharmaceuticals Limited | Polymorphs of N-[(3-fluoro-4-methoxypyridin-2-yl)methyl]-3-(methoxymethyl)-1-({4-[(2-oxopyridin-1-yl)methyl]phenyl}methyl)pyrazole-4-carboxamide and salts thereof |
EP4151630A1 (en) | 2016-06-01 | 2023-03-22 | Kalvista Pharmaceuticals Limited | Polymorphs of n-[(3-fluoro-4-methoxypyridin-2-yl)methyl]-3-(methoxymethyl)-1-({4-[2-oxopyridin-1-yl)methyl]phenyl}methyl)pyrazole-4-carboxamide as kallikrein inhibitors |
US10752607B2 (en) | 2016-06-01 | 2020-08-25 | Kalvista Pharmaceuticals Limited | Polymorphs of N-[(6-cyano-2-fluoro)-3-methoxyphenyl)methyl]-3-(methoxymethyl)-1-({4-[(2-oxopyridin-1-yl)methyl]phenyl}methyl)pyrazole-4-carboxamide as kallikrein inhibitors |
US11230537B2 (en) | 2016-06-01 | 2022-01-25 | Kalvista Pharmaceuticals Limited | Polymorphs of n-[(3-fluoro-4-methoxypyridin-2-yl)methyl]-3-(methoxymethyl)-1-({4-[2-oxopyridin-1-yl)methyl]phenyl} methyl)pyrazole-4-carboxamide as iallikrein inhibitors |
US11993583B2 (en) | 2016-08-19 | 2024-05-28 | Gilead Sciences, Inc. | Therapeutic compounds |
US10654827B2 (en) | 2016-08-19 | 2020-05-19 | Gilead Sciences, Inc. | Therapeutic compounds |
WO2018039094A1 (en) | 2016-08-22 | 2018-03-01 | Merck Sharp & Dohme Corp. | Pyridine-1-oxide derivatives and their use as factor xia inhibitors |
CN108203433A (en) * | 2016-12-16 | 2018-06-26 | 成都先导药物开发有限公司 | A kind of ROCK inhibitor and its application |
US11833143B2 (en) | 2017-08-17 | 2023-12-05 | Gilead Sciences, Inc. | Choline salt forms of an HIV capsid inhibitor |
US11266638B2 (en) | 2017-08-17 | 2022-03-08 | Gilead Sciences, Inc. | Choline salt forms of an HIV capsid inhibitor |
US10849892B2 (en) | 2017-08-17 | 2020-12-01 | Gilead Sciences, Inc. | Choline salt forms of an HIV capsid inhibitor |
US11267799B2 (en) | 2017-08-17 | 2022-03-08 | Gilead Sciences, Inc. | Solid forms of an HIV capsid inhibitor |
WO2019037640A1 (en) * | 2017-08-22 | 2019-02-28 | Js Innopharm (Shanghai) Ltd | Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof |
US11242334B2 (en) | 2017-08-22 | 2022-02-08 | Js Innopharm (Shanghai) Ltd. | Heterocyclic compounds as kinase inhibitors, compositions comprising the heterocyclic compound, and methods of use thereof |
US11234939B2 (en) | 2017-11-29 | 2022-02-01 | Kalvista Pharmaceuticals Limited | Dosage forms comprising a plasma kallikrein inhibitor |
US11584735B2 (en) | 2017-11-29 | 2023-02-21 | Kalvista Pharmaceuticals Limited | Solid forms of a plasma kallikrein inhibitor and salts thereof |
US11753399B2 (en) | 2018-02-15 | 2023-09-12 | Gilead Sciences, Inc. | Therapeutic compounds |
US10836746B2 (en) | 2018-02-15 | 2020-11-17 | Gilead Sciences, Inc. | Therapeutic compounds |
US11267801B2 (en) | 2018-02-15 | 2022-03-08 | Gilead Sciences, Inc. | Therapeutic compounds |
US11117886B2 (en) | 2018-02-16 | 2021-09-14 | Gilead Sciences, Inc. | Methods and intermediates for preparing therapeutic compounds |
US10696657B2 (en) | 2018-02-16 | 2020-06-30 | Gilead Sciences, Inc. | Methods and intermediates for preparing therapeutic compounds |
US11760746B2 (en) | 2018-02-16 | 2023-09-19 | Gilead Sciences, Inc. | Methods and intermediates for preparing therapeutic compounds |
US11884660B2 (en) | 2018-04-10 | 2024-01-30 | Bayer Pharma Aktiengesellschaft | Substituted oxopyridine derivative |
WO2019197244A1 (en) | 2018-04-10 | 2019-10-17 | Bayer Pharma Aktiengesellschaft | A substituted oxopyridine derivative |
US11944611B2 (en) | 2018-07-16 | 2024-04-02 | Gilead Sciences, Inc. | Capsid inhibitors for the treatment of HIV |
WO2020249979A1 (en) | 2019-06-14 | 2020-12-17 | Kalvista Pharmaceuticals Limited | Treatments of angioedema |
WO2020249977A1 (en) | 2019-06-14 | 2020-12-17 | Kalvista Pharmaceuticals Limited | Treatments of hereditary angioedema |
EP4282474A2 (en) | 2019-06-14 | 2023-11-29 | Kalvista Pharmaceuticals Limited | Treatments of hereditary angioedema |
WO2021028645A1 (en) | 2019-08-09 | 2021-02-18 | Kalvista Pharmaceuticals Limited | Plasma kallikrein inhibitors |
US11613527B2 (en) | 2019-08-09 | 2023-03-28 | Kalvista Pharmaceuticals Limited | Enzyme inhibitors |
WO2021028649A1 (en) | 2019-08-09 | 2021-02-18 | Kalvista Pharmaceuticals Limited | Plasma kallikrein inhibitors |
US11807625B2 (en) | 2019-11-26 | 2023-11-07 | Gilead Sciences, Inc. | Capsid inhibitors for the prevention of HIV |
WO2021116679A1 (en) | 2019-12-09 | 2021-06-17 | Kalvista Pharmaceuticals Limited | Treatments of diabetic macular edema and impaired visual acuity |
GB2591730A (en) | 2019-12-09 | 2021-08-11 | Kalvista Pharmaceuticals Ltd | New polymorphs |
US11680064B2 (en) | 2020-06-25 | 2023-06-20 | Gilead Sciences, Inc. | Capsid inhibitors for the treatment of HIV |
WO2022079446A1 (en) | 2020-10-15 | 2022-04-21 | Kalvista Pharmaceuticals Limited | Treatments of angioedema |
WO2022084693A1 (en) | 2020-10-23 | 2022-04-28 | Kalvista Pharmaceuticals Limited | Treatments of angioedema |
WO2022172006A1 (en) | 2021-02-09 | 2022-08-18 | Kalvista Pharmaceuticals Limited | Treatments of hereditary angioedema |
WO2023002219A1 (en) | 2021-07-23 | 2023-01-26 | Kalvista Pharmaceuticals Limited | Treatments of hereditary angioedema |
US11787825B2 (en) | 2021-12-03 | 2023-10-17 | Gilead Sciences, Inc. | Therapeutic compounds for HIV virus infection |
WO2023209381A1 (en) | 2022-04-27 | 2023-11-02 | Kalvista Pharmaceuticals Limited | Formulations of a plasma kallikrein inhibitor |
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US20060009455A1 (en) | 2006-01-12 |
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