WO2002088108A1 - Triazole compounds useful in treating diseases associated with unwanted cytokine activity - Google Patents
Triazole compounds useful in treating diseases associated with unwanted cytokine activity Download PDFInfo
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- WO2002088108A1 WO2002088108A1 PCT/US2002/013074 US0213074W WO02088108A1 WO 2002088108 A1 WO2002088108 A1 WO 2002088108A1 US 0213074 W US0213074 W US 0213074W WO 02088108 A1 WO02088108 A1 WO 02088108A1
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- triazole
- fluorophenyl
- pyridin
- ethoxymethyl
- pyrimidin
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- GIUKJOXZIFLOOD-UHFFFAOYSA-N Fc(cc1)ccc1-c1c(-c2ccncc2)[nH]nn1 Chemical compound Fc(cc1)ccc1-c1c(-c2ccncc2)[nH]nn1 GIUKJOXZIFLOOD-UHFFFAOYSA-N 0.000 description 2
- BSDGZUDFPKIYQG-UHFFFAOYSA-N Brc1ccncc1 Chemical compound Brc1ccncc1 BSDGZUDFPKIYQG-UHFFFAOYSA-N 0.000 description 1
- GWVMLCQWXVFZCN-UHFFFAOYSA-N C1NCc2ccccc12 Chemical compound C1NCc2ccccc12 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 description 1
- NNAORCAPXBDCBZ-UHFFFAOYSA-N CCOC[n]1nnc(-c(cc2)ccc2F)c1-c1nc(SC)ncc1 Chemical compound CCOC[n]1nnc(-c(cc2)ccc2F)c1-c1nc(SC)ncc1 NNAORCAPXBDCBZ-UHFFFAOYSA-N 0.000 description 1
- UPRHDGKORMLJJH-UHFFFAOYSA-N CCOC[n]1nnc(-c2nc(SC)ncc2)c1-c(cc1)ccc1F Chemical compound CCOC[n]1nnc(-c2nc(SC)ncc2)c1-c(cc1)ccc1F UPRHDGKORMLJJH-UHFFFAOYSA-N 0.000 description 1
- 0 C[n]1c(C#Cc(cc2)ccc2F)cnc1* Chemical compound C[n]1c(C#Cc(cc2)ccc2F)cnc1* 0.000 description 1
- FLLQAXOVIQIYMX-UHFFFAOYSA-N C[n]1c(Sc2ccccc2)ncc1C#Cc(cc1)ccc1F Chemical compound C[n]1c(Sc2ccccc2)ncc1C#Cc(cc1)ccc1F FLLQAXOVIQIYMX-UHFFFAOYSA-N 0.000 description 1
- YXBSWORWIQOCFT-UHFFFAOYSA-N Fc(cc1)ccc1-c1c(-c2ccncc2)[n](-c2ccccc2)nn1 Chemical compound Fc(cc1)ccc1-c1c(-c2ccncc2)[n](-c2ccccc2)nn1 YXBSWORWIQOCFT-UHFFFAOYSA-N 0.000 description 1
- TXCDCPKCNAJMEE-UHFFFAOYSA-N c(cc1)cc2c1[o]c1c2cccc1 Chemical compound c(cc1)cc2c1[o]c1c2cccc1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N c(cc1)cc2c1nn[nH]2 Chemical compound c(cc1)cc2c1nn[nH]2 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- FYADHXFMURLYQI-UHFFFAOYSA-N c1cnncn1 Chemical compound c1cnncn1 FYADHXFMURLYQI-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N c1cnnnc1 Chemical compound c1cnnnc1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- HTJMXYRLEDBSLT-UHFFFAOYSA-N c1nncnn1 Chemical compound c1nncnn1 HTJMXYRLEDBSLT-UHFFFAOYSA-N 0.000 description 1
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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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
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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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Definitions
- the present invention is directed to certain triazole compounds that inhibit the release of inflammatory cytokines such as interleukin-1 (E -l) and tumor necrosis factor (TNF) from cells.
- E -l interleukin-1
- TNF tumor necrosis factor
- cytokine-mediated diseases and conditions are associated with excessive or unregulated production or activity of one or more cytokines such as interleukin 1 (LL-1), tumor necrosis factor (TNF), interleukin 6 (IL-6) and interleukin 8 (LL-8).
- IL-1 and TNF are important proinflammatory cytokines, which along with several other related molecules, mediate inflammatory cellular response in a wide variety of diseases and conditions.
- Proinflammatory cytokines such as LL-1 and TNF stimulate other inflammatory mediators such as nitric oxide, cyclooxygenase-2, matrix metalloproteinases. The inhibition of these cytokines is consequently both directly and indirectly beneficial in controlling, reducing and alleviating many of these disease states.
- Elevated levels of proinflammatory cytokines are implicated in many disease states, including rheumatoid arthritis (Dinarello, C. A., et al. 1984, Rev. Infect. Disease 6:51; Maini, R.E. 1999, The Lancet 354:1932; Weinblatt, M. E. 1999, New Eng. J. Med. 340:253), osteoarthritis (Pelletier and Pelletier 1989, J. Rheum. 16:19; Pelletier, et al. 1993, Am. J. Path. 142:95; Farahat, et al. 1993, Ann. Rheum. Dis. 52:870; Til u, et al. 1992, Cell Immunol.
- the invention provides compounds which are potent cytokine inhibitors and which are effective in treating conditions characterized by excess activity of these enzymes.
- the present invention is directed to compounds having a structure according to Formula (I):
- the invention also includes optical isomers, diasteriomers, and enantiomers of the structure above, and pharmaceutically-acceptable salts thereof.
- the compounds of the present invention are useful for the treatment of diseases and conditions which are characterized by unwanted cytokine activity. Accordingly, the invention further provides pharmaceutical compositions comprising these compounds. The invention still further provides methods of treatment for diseases associated with unwanted cytokine activity using these compounds or the compositions comprising them.
- the invention is directed to a novel group of compounds which are potent inhibitors of cytokines and which are effective in treating conditions characterized by excess activity of these enzymes.
- Alkenyl is a monovalent hydrocarbon chain having 2 to 18 carbon atoms, preferably 2 to 12, more preferably 2 to 6 carbon atoms and at least one (preferably only one) carbon-carbon double bond. Alkenyl groups may be straight or branched. Preferred branched alkenyl groups have one or two branches, preferably one branch. Alkenyl groups may be unsubstituted or substituted with from 1 to 4 substituents. Preferred substituted alkenyl groups have 1 to 3 substituents unless otherwise specified.
- Alkenyl group substituents include halo, OH, alkoxy, aryloxy (e.g., phenoxy), aryl (e.g., phenyl), heteroaryl, cycloalkyl, heterocycloalkyl, thioalkoxy, thioaryloxy, amino, keto, thioketo, nitro, and cyano.
- Preferred alkenyl group substituents include halo, OH, alkoxy, aryloxy (e.g., phenoxy), aryl (e.g., phenyl), heteroaryl, heterocycloalkyl, amino, and keto.
- the term "lower alkenyl” refers to an alkenyl group having from 2 to 6, preferably from 2 to 4, carbon atoms.
- Alkyl is a monovalent saturated hydrocarbon chain having 1 to 18 carbon atoms, preferably 1 to 12, more preferably 1 to 6 carbon atoms. Alkyl groups may be straight or branched. Preferred branched alkyl groups have one or two branches, preferably one branch. Alkyl groups may be unsubstituted or substituted with from 1 to 4 substituents. Preferred substituted alkyl groups have 1 to 3 substituents unless otherwise specified.
- Alkyl group substituents include halo, OH, alkoxy, aryloxy (e.g., phenoxy), aryl (e.g., phenyl), heteroaryl, cycloalkyl, heterocycloalkyl, thioalkoxy, thioaryloxy, amino, keto, thioketo, nitro, and cyano.
- Preferred alkyl group substituents include halo, OH, alkoxy, aryloxy (e.g., phenoxy), aryl (e.g., phenyl), heteroaryl, heterocycloalkyl, amino, and keto.
- the term "lower alkyl” refers to an alkyl group having from 1 to 6, preferably from 1 to 4, carbon atoms.
- Alkoxy refers to the group -OR where R is alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, cycloalkyl, cycloalkenyl, or heterocycloalkyl.
- Preferred alkoxy groups include methoxy, ethoxy, and tso-propoxy.
- Alkynyl is a monovalent hydrocarbon chain having 2 to 18 carbon atoms, preferably 2 to 12, more preferably 2 to 6 carbon atoms and at least one (preferably only one) carbon-carbon triple bond. Alkynyl groups may be straight or branched. Preferred branched alkynyl groups have one or two branches, preferably one branch. Alkynyl groups may be unsubstituted or substituted with from 1 to 4 substituents. Preferred substituted alkynyl groups have 1 to 3 substituents unless otherwise specified.
- Alkynyl group substituents include halo, OH, alkoxy, aryloxy (e.g., phenoxy), aryl (e.g., phenyl), heteroaryl, cycloalkyl, heterocycloalkyl, thioalkoxy, thioaryloxy, amino, keto, thioketo, nitro, and cyano.
- Preferred alkynyl group substituents include halo, OH, alkoxy, aryloxy (e.g., phenoxy), aryl (e.g., phenyl), heteroaryl, heterocycloalkyl, amino, and keto.
- the term "lower alkynyl" refers to an alkynyl group having from 2 to 6, preferably from 2 to 4, carbon atoms.
- Amino refers to the group -N(R) 2 where each R is independently chosen from the group consisting of: hydrogen, alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, aryl and heteroaryl.
- Preferred amino groups include NH 2 , NHCH 3 , and NHC(O)CH 3 .
- Aryl is an aromatic hydrocarbon ring system.
- Aryl rings are either monocyclic ring systems or fused bicyclic ring systems.
- Monocyclic aryl rings contain 6 carbon atoms in the ring.
- Monocyclic aryl rings are also referred to as phenyl rings.
- Bicyclic aryl rings contain from 8 to 12 carbon atoms, preferably 8 to 10 carbon atoms, more preferably 10 carbon atoms, in the ring.
- Bicyclic aryl rings include ring systems wherein both rings are aromatic or only one ring is aromatic.
- Preferred bicyclic aryl rings comprise 5-, 6- or 7-membered rings fused to 5-, 6-, or 7-membered rings.
- Preferred aryl rings include naphthyl, tolyl, xylyl, and phenyl.
- the most preferred aryl ring is phenyl.
- Aryl rings may be unsubstituted or substituted with from 1 to 5, preferably from 1 to 3, more preferably from 1 to 2 substituents on the ring.
- Preferred aryl rings are unsubstituted or substituted with 1 or 2 substituents.
- Aryl rings may be substituted with halo, cyano, nitro, hydroxy, amino, alkyl, lower alkenyl, lower alkynyl, heteroalkyl, aryloxy, alkoxy, methylenedioxy [which refers to the group (-OCH 2 O-)], thioalkoxy, thioaryloxy, or any combination thereof.
- Preferred aryl ring substituents include halo, cyano, amino, alkyl, heteroalkyl, aryloxy, alkoxy, methylenedioxy, thioalkoxy, thioaryloxy.
- Aryloxy refers to the group -OR where R is aryl or heteroaryl. Preferred aryloxy groups include phenoxy and pyridinyloxy.
- Cyano refers to the group -CN.
- Cycloalkyl is a saturated hydrocarbon ring. Cycloalkyl rings are monocyclic, or are fused, spiro, or bridged bicyclic ring systems. Preferred cycloalkyl rings are monocyclic. Monocyclic cycloalkyl rings contain from 3 to 10 carbon atoms, preferably from 3 to 7 carbon atoms, more preferably 3, 5, or 6 carbon atoms in the ring. Bicyclic cycloalkyl rings contain from 7 to 17 carbon atoms, preferably from 7 to 12 carbon atoms, in the ring. Preferred bicyclic cycloalkyl rings comprise 5-, 6- or 7-membered rings fused to 5-, 6-, or 7-membered rings.
- Preferred cycloalkyl rings include cyclopropyl, cyclopentyl, and cyclohexyl. Cycloalkyl rings may be unsubstituted or substituted with from 1 to 4 substituents on the ring. Cycloalkyl group substituents include alkyl, aryl (e.g., phenyl), alkoxy, aryloxy (e.g., phenoxy), thioalkoxy, thioaryloxy, heteroaryl, heterocycloalkyl, halo, hydroxy, amino, keto, thioketo, nitro, and cyano.
- aryl e.g., phenyl
- alkoxy aryloxy (e.g., phenoxy)
- thioalkoxy thioaryloxy
- heteroaryl heterocycloalkyl
- halo hydroxy, amino, keto, thioketo, nitro, and cyano.
- Preferred cycloalkyl group substituents include halo, hydroxy, alkyl, aryl (e.g., phenyl), alkoxy, aryloxy (e.g., phenoxy), heteroaryl, heterocycloalkyl, amino, and keto. More preferred cycloalkyl group substituents include hydroxy, alkyl, and alkoxy.
- Cycloalkenyl is an unsaturated hydrocarbon ring. Cycloalkenyl rings are not aromatic and contain at least one (preferably only one) carbon-carbon double bond. Cycloalkenyl rings are monocyclic, or are fused, spiro, or bridged bicyclic ring systems. Preferred cycloalkenyl rings are monocyclic. Monocyclic cycloalkenyl rings contain from 5 to 10 carbon atoms, preferably from 5 to 7 carbon atoms, more preferably 5 or 6 carbon atoms in the ring. Bicyclic cycloalkenyl rings contain from 8 to 12 carbon atoms in the ring.
- Preferred bicyclic cycloalkenyl rings comprise 5-, 6- or 7-membered rings fused to 5-, 6-, or 7-membered rings.
- Cycloalkenyl rings may be unsubstituted or substituted with from 1 to 4 substituents on the ring.
- Cycloalkenyl group substituents include alkyl, aryl (e.g., phenyl), alkoxy, aryloxy (e.g., phenoxy), thioalkoxy, thioaryloxy, heteroaryl, heterocycloalkyl, halo, hydroxy, amino, keto, thioketo, nitro, and cyano.
- Preferred cycloalkenyl group substituents include halo, hydroxy, alkyl, alkoxy, aryloxy (e.g., phenoxy), aryl (e.g., phenyl), heteroaryl, heterocycloalkyl, amino, and keto. More preferred cycloalkyl group substituents include OH, alkyl, alkoxy, and keto.
- Halo or "halogen” is fluoro, chloro, bromo or iodo. Preferred halo are fluoro, chloro and bromo. More preferred halo are chloro and fluoro, especially fluoro.
- Heteroalkenyl is a monovalent chain having 3 to 18 member atoms (carbon and heteroatoms) in the chain, preferably 3 to 12, more preferably 3 to 6 member atoms and at least one (preferably only one) carbon-carbon double bond. Heteroalkenyl chains have at least one heteroatom member atom. Heteroalkenyl groups may be straight or branched. Preferred branched heteroalkenyl groups have one or two branches, preferably one branch. Heteroalkenyl groups may be unsubstituted or substituted with from 1 to 4 substituents. Preferred substituted heteroalkenyl groups have 1 to 3 substituents unless otherwise specified.
- Heteroalkenyl group substituents include halo, hydroxy, alkyl, alkoxy, aryloxy (e.g., phenoxy), thioalkoxy, thioaryloxy, aryl (e.g., phenyl), heteroaryl, cycloalkyl, heterocycloalkyl, amino, keto, thioketo, nitro, and cyano.
- Preferred heteroalkenyl group substituents include halo, hydroxy, alkyl, alkoxy, aryloxy (e.g., phenoxy), aryl (e.g., phenyl), heteroaryl, heterocycloalkyl, amino, and keto.
- the term "lower heteroalkenyl” refers to a heteroalkenyl group having from 3 to 6, preferably from 3 to 4, member atoms.
- Heteroalkyl is a monovalent saturated chain having from 2 to 18 member atoms (carbon and heteroatoms) in the chain, preferably 2 to 12, more preferably 2 to 6. Heteroalkyl chains have at least one heteroatom member atom. Heteroalkyl groups may be straight or branched. Preferred branched heteroalkyl have one or two branches, preferably one branch. Heteroalkyl chains may be unsubstituted or substituted with from 1 to 4 substituents. Preferred substituted heteroalkyl groups have 1 to 3 substituents unless otherwise specified.
- Heteroalkyl group substituents include aryl (e.g., phenyl), alkoxy, aryloxy (e.g., phenoxy), thioalkoxy, thioaryloxy, heteroaryl, cycloalkyl, heterocycloalkyl, halo, hydroxy, amino, keto, thioketo, nitro, and cyano.
- Preferred heteroalkyl group substituents include aryl (e.g., phenyl), alkoxy, aryloxy (e.g., phenoxy), heteroaryl, heterocycloalkyl, halo, hydroxy, amino, and keto.
- the term "lower heteroalkyl” refers to a heteroalkyl group having from 2 to 6, preferably from 2 to 4, member atoms.
- Heteroalkynyl is a monovalent chain having 3 to 18 member atoms (carbon and heteroatoms) in the chain, preferably 3 to 12, more preferably 3 to 6 member atoms and at least one (preferably only one) carbon-carbon triple bond. Heteroalkynyl chains have at least one heteroatom member atom. Heteroalkynyl groups may be straight or branched. Preferred branched heteroalkynyl groups have one or two branches, preferably one branch. Heteroalkynyl groups may be unsubstituted or substituted with from 1 to 4 substituents. Preferred substituted heteroalkynyl groups have 1 to 3 substituents unless otherwise specified.
- Heteroalkynyl group substituents include alkyl, aryl (e.g., phenyl), alkoxy, aryloxy (e.g., phenoxy), heteroaryl, cycloalkyl, heterocycloalkyl, halo, hydroxy, amino, keto, thioketo, nitro, and cyano.
- Preferred heteroalkynyl group substituents include alkyl, aryl (e.g., phenyl), alkoxy, aryloxy (e.g., phenoxy), heteroaryl, heterocycloalkyl, halo, hydroxy, amino, and keto.
- the term "lower heteroalkynyl” refers to a heteroalkynyl group having from 3 to 6, preferably from 3 to 4, member atoms.
- Heteroaryl is an aromatic ring containing carbon atoms and from 1 to 6 heteroatoms in the ring. Heteroaryl rings are monocyclic or fused polycychc ring systems. Monocyclic heteroaryl rings contain from 5 to 9 member atoms (carbon and heteroatoms), preferably 5 or 6 member atoms, in the ring. Polycychc heteroaryl rings contain 8 to 17 member atoms, preferably 8 to 12 member atoms, in the ring. Polycychc heteroaryl rings include ring systems wherein at least one ring is heteroaryl (the second ring may be aryl, heteroaryl, cycloalkyl, cycloalkenyl, or heterocycloalkyl). Preferred bicyclic heteroaryl ring systems comprise 5-, 6- or 7-membered rings fused to 5-, 6-, or 7- membered rings. Preferred heteroaryl rings include, but are not limited to, the following rings:
- Heteroaryl rings may be unsubstituted or substituted with from 1 to 4, preferably from 1 to 3, more preferably from 1 to 2, substituents on the ring. Preferred heteroaryl rings are unsubstituted or substituted with 1 or 2 substituents. Heteroaryl rings may be substituted with halo, cyano, nitro, hydroxy, amino, alkyl, lower alkenyl, lower alkynyl, heteroalkyl, aryloxy, alkoxy, methylenedioxy, thioalkoxy, thioaryloxy, or any combination thereof.
- heteroaryl ring substituents include halo, cyano, amino, alkyl, heteroalkyl, aryloxy, alkoxy, methylenedioxy, thioalkoxy, thioaryloxy.
- Heteroatom refers to a nitrogen, sulfur, or oxygen atom. Groups containing more than one heteroatom may contain different heteroatoms.
- Heterocycloalkyl is a saturated ring containing carbon atoms and from 1 to 4, preferably 1 to 3, heteroatoms in the ring. Heterocycloalkyl rings are not aromatic. Heterocycloalkyl rings are monocyclic, or are fused, bridged, or spiro polycychc ring systems. Monocyclic heterocycloalkyl rings contain from 3 to 9 member atoms (carbon and heteroatoms), preferably from 5 to 7 member atoms, in the ring. Polycychc heterocycloalkyl rings contain from 7 to 17 member atoms, preferably 7 to 12 member atoms, in the ring. Preferred polycychc heterocycloalkyl rings comprise 5-, 6- or 7- membered rings fused to 5-, 6-, or 7-membered rings. Preferred heterocycloalkyl rings include but are not limited to the following:
- Oxirane Aziridine Oxetane Azetidine Tetrahydrofuran Pyrrolidine 3H-Indole
- Heterocycloalkyl rings may be unsubstituted or substituted with from 1 to 4 substituents on the ring.
- Heterocycloalkyl group substituents include alkyl, aryl (e.g., phenyl), alkoxy, aryloxy (e.g., phenoxy), thioalkoxy, thioaryloxy, heteroaryl, cycloalkyl, halo, hydroxy, amino, keto, thioketo, nitro, and cyano.
- Preferred heterocycloalkyl group substituents include alkyl, aryl (e.g., phenyl), alkoxy, aryloxy (e.g., phenoxy), heteroaryl, halo, hydroxy, amino, and keto.
- Niro refers to the group -NO .
- Optical isomer "stereoisomer”, and “diastereomer” as referred to herein have the standard art recognized meanings (see, e.g., Hawlev's Condensed Chemical Dictionary, 11th Ed.).
- the illustration of derivatives of the compounds of the instant invention is not intended to be limiting.
- the application of useful protecting groups, salt forms, etc. is within the ability of the skilled artisan.
- a "pharmaceutically-acceptable salt” is a cationic salt formed at any acidic (e.g., carboxylic acid) group, or an anionic salt formed at any basic (e.g., amino) group.
- Preferred cationic salts include the alkali metal salts (such as sodium and potassium), and alkaline earth metal salts (such as magnesium and calcium) and organic salts.
- Preferred anionic salts include the halides (such as chloride salts), sulfonates, carboxylates, phosphates, and the like.
- addition salts that may provide an optical center where once there is none.
- a chiral tartrate salt may be prepared from the compounds of the invention, and this definition includes such chiral salts.
- Such salts are well understood by the skilled artisan, and the skilled artisan is able to prepare any number of salts given the knowledge in the art. Furthermore, it is recognized that the skilled artisan may prefer one salt over another for reasons of solubility, stability, formulation ease and the like. Determination and optimization of such salts is within the purview of the skilled artisan's practice.
- Thioalkoxy refers to the group -S(O) 0-2 R where R is alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, cycloalkyl, cycloalkenyl, or heterocycloalkyl.
- Preferred thioalkoxy groups include methanesulfonyl.
- Thioaryloxy refers to the group -S(O) 0 - 2 R where R is aryl or heteroaryl.
- Preferred thioaryloxy groups include phenylsulfide, benzenesulfonyl and pyridinesulfonyl.
- the invention is directed to compounds of Formula (I):
- each R 1 is independently selected from the group consisting of: lower alkyl, lower alkenyl, lower alkynyl, lower heteroalkyl, lower heteroalkenyl, lower heteroalkynyl, heterocycloalkyl, heteroaryl, halo, CN, OR 4 , SR 4 , S(O)R 4 , S(O) 2 R 4 , and NR 4 R 5 .
- Preferred R 1 is lower alkyl, halo, CN, OR 4 , and NR 4 R 5 . More preferred R 1 is lower alkyl, halo, and CN.
- m is an integer from 0 to 5.
- Preferred m is 0 to 3. More preferred m is 1 or 2.
- Q is selected from the group consisting of
- Each R 2 is independently selected from the group consisting of: H, alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, heterocycloalkyl, heteroaryl, halo, OH, CN, OR 4 , SR 4 , S(O)R 4 , S(O) 2 R 4 , and NR 4 R 5 .
- Preferred R 2 is H, and halo. More preferred R is H.
- R 2 is not NR 4 R 5 when both Y is CR 2 and R 3 is H.
- R 3 is selected from the group consisting of: H, alkyl, alkenyl, alkynyl, heteroalkyl, heteroalkenyl, heteroalkynyl, heterocycloalkyl, heteroaryl, halo, OH, CN, OR 4 , SR 4 , S(O)R 4 , and S(O) 2 R 4 .
- Preferred R 3 is H, alkyl, halo, OR 4 , SR 4 , S(O)R 4 , S(O) 2 R 4 . More preferred R 3 is H and OR 4 .
- X is selected from the group consisting of: CR 2 and N. Preferred X is CR 2 . The most preferred X is CH.
- Y is selected from the group consisting of: CR 2 and N.
- Preferred Y is CH and N.
- Z is selected from the group consisting of CR 2 , NR 4 , O, and S.
- A is selected from the group consisting of: nil, H, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroalkyl, heteroalkenyl, heteroalkynyl, heterocycloalkyl, heteroaryl, OR 4 , and S(O) 2 R 4 .
- Preferred A is alkyl, alkynyl, aryl, heteroalkyl, heteroalkynyl, heterocycloaUcyl, heteroaryl, OR 4 , S(O) 2 R 4 . More preferred A is substituted alkyl (wherein the preferred substituents are keto, alkoxy, aryloxy, amino, heteroaryl, heterocycloaUcyl) and aryl.
- a is single bond or double bond, provided that when A is nil a is double bond and when A is other than nil a is single bond.
- B is selected from the group consisting of: nil, H, alkyl, alkenyl, aUcynyl, cycloalkyl, cycloalkenyl, aryl, heteroaUcyl, heteroalkenyl, heteroalkynyl, heterocycloalkyl, heteroaryl, OR 4 , and S(O) R 4 .
- Preferred B is aUcyl, alkynyl, aryl, heteroalkyl, heteroaUcynyl, heterocycloalkyl, heteroaryl, OR 4 , S(O) 2 R 4 . More preferred B is substituted alkyl (wherein the preferred substituents are keto, alkoxy, aryloxy, amino, heteroaryl, heterocycloaUcyl) and aryl.
- b is single bond or double bond, provided that when B is nil b is double bond and when B is other than nil b is single bond.
- one and only one of A and B is nil.
- Each R 4 is independently selected from H, lower alkyl, lower alkenyl, lower alkynyl, cycloalkyl, cycloalkenyl, aryl, heteroalkyl, heteroalkenyl, heteroalkynyl, heterocycloalkyl, heterocycloalkenyl, and heteroaryl.
- Preferred R 4 is H, lower alkyl, heteroalkyl, aryl, and heteroaryl.
- Each R 5 is independently selected from H, lower aUcyl, lower aUcenyl, lower aUcynyl, cycloalkyl, cycloalkenyl, aryl, heteroaUcyl, heteroaUcenyl, heteroalkynyl, heterocycloalkyl, heterocycloaUcenyl, heteroaryl, OR 4 , and S(O) 2 R 4 .
- Preferred R 5 is H, lower aUcyl, and S(O) 2 R 4 .
- the compounds of the invention can be prepared using conventional organic syntheses. Particularly preferred syntheses are carried out according to the following general reaction schemes, Schemes 1, 2 and 3. Schemes 1 and 2 describe general reaction schemes for making compounds of the invention wherein the "Q" substituent is a six-membered heterocyclic ring. Scheme 3 describes a general reaction scheme for making compounds of the invention wherein the "Q" substituent is a five-membered heterocyclic ring.
- R 1 , R 2 , R 3 , m, X, Y, A, B, and Q are as defined above.
- Alkynes of type Sla and substituted heterocycles of type Sib are either commercially available as starting material or are made from commercially available starting materials using methods known to one of ordinary skill in the art. Coupling of Sla with Sib to form aUcyne Sic is accomplished using the method described by Mangalagiu, I. et al. (Acta Chem. Scand. 1996, 50, 914-917).
- alkynes of type Sic can be obtained from a wide variety of commercially available substituted arylhalides and substituted 4- ethynyl-heterocycles, which in turn can be made by known methods.
- 3+2 Cycloaddition of aUcyne Sic to give triazole Sid is performed according to a known method, but under slightly modified conditions using sodium azide to give directly the disubstituted triazole (See, Caliendo, et al. Eur. J. Med. Chem. 1999, 34, 719-727).
- Elaboration of triazole Sid is accomplished under a variety conditions to provide access to a wide variety of functionalized triazoles of type Sle and Slf.
- acylation of Sid with acyl halides and tertiary amine base gives amides.
- Reaction of Sid with isocyanates or carbamoyl chlorides gives ureas.
- pretreatment of Sid with phosgene or a phosgene equivalent e.g., triphosgene, carbonyl diimidazole
- Copper-mediated coupling of Sid with aryl boronic acids gives aryl amines.
- Reaction of Sid with sulfonyl chlorides and tertiary amine base gives sulfonamides.
- R 1 , R 2 , R 3 , m, X, Y, A, B, and Q are as defined above.
- R' and R" are each appropriate functional groups which enable the skilled artisan to functionalize the six-membered heterocycle to ultimately form a compound according to the invention.
- R' and R" on S2d may be exchanged for a wide variety of functional groups (R and R ).
- two approaches are used. In the first approach, triazoles of type S2d are substituted at the triazole nitrogen position as described in Scheme 1 to give S2e.
- triazole S2d is oxidized specifically to either the corresponding sulfoxide or the sulphone (not shown) with several different commonly-used reagents (e.g., peracetic acid, 3-chloroperbenzoic acid, or potassium peroxymonosulfate). Either the sulfoxide or the corresponding sulphone is then displaced under nucleophilic conditions to give compounds of type S2f.
- S2d (where R' and/or R' ' is -SMe) is first oxidized specifically to either the sulfoxide or the sulphone.
- R' and/or R" may be -SMe, halo, or some other substituent capable of being displaced by R 2 or R 3 .
- halo for Z' and/or Z" precludes the additional step of oxidizing R' and/or R" to a better leaving group.
- R 1 , R 3 , m, X, Z, A, B, and Q are as defined above.
- R' and R" are defined above.
- Alkynes of type S3a and substituted heterocycles of type S3b are either commercially available as starting material or are made from commercially available starting materials using methods known to one of ordinary skill in the art. Several substituted heterocycles of type S3b have been previously disclosed in the literature (Blass, B. E. et al. Bio. Med. Chem. Lett. 2000, 10, 1543-1545). Coupling of S3a with S3b to form aUcyne S3c is accomplished as described in Scheme 1.
- alkynes of type S3c are obtained from a wide variety of commercially available substituted arylhalides and substituted 4-ethynyl-heterocycles, which in turn can be made by known methods.
- Oxidation to the sulphone using literature procedure is followed by 3+2 cycloaddition with sodium azide to give triazole S3d as described in Schemes 1 and 2.
- Functionalization of both heterocyclic rings proceeds as described in Schemes 1 and 2 to give the desired final compounds.
- Schemes 1, 2 and 3 the steps may be varied to increase the yield of the desired product.
- the skilled artisan will recognize the judicious choice of reactants, solvents, and temperatures is an important component in any successful synthesis.
- the compounds of the invention may have one or more chiral centers.
- one optical isomer including diastereomer and enantiomer
- another optical starting materials for example by chiral starting materials, catalysts or solvents
- both stereoisomers or both optical isomers including diastereomers and enantiomers at once (a racemic mixture).
- the compounds of the invention may exist as racemic mixtures, mixtures of optical isomers, including diastereomers and enantiomers, or stereoisomers may be separated using known methods, such as chiral salts, chiral chromatography and the like.
- optical isomer including diastereomer and enantiomer, or stereoisomer may have favorable properties over the other.
- optical isomers including diastereomers and enantiomers, or stereoisomers substantially free of the other are disclosed and claimed as well.
- Ph phenyl cone: concentrated
- Examples 2-39 are prepared using substantially the same procedures as those described in Example 1, substituting the appropriate starting materials.
- the skilled artisan may change temperature, pressure, atmosphere, solvents, or the order of reactions as appropriate. Additionally, the skilled artisan may use protecting groups to block side reactions or to increase yields as appropriate. All such modifications can be readily carried out by the skilled artisan in organic chemistry, and thus are within the scope fo the invention.
- [l,2,3]triazole a) 4-(4-Fluorophenyl)-5-pyridin-4-yl-l-chlorocarbonyl-[l,2,3]triazole and 5-(4-Fluorophenyl)-4-pyridin-4-yl-l-chlorocarbonyl-[l,2,3]triazole
- compounds of type 40b can also be made by reaction of an appropriate amine (e.g. aniline) with phosgene, followed by subsequent reaction with triazole lb to give urea products (e.g. 40b).
- an appropriate amine e.g. aniline
- triazole lb e.g. 40b
- Examples 41-54 are prepared using substantially the same procedures as those described in Example 40, substituting the appropriate starting materials.
- the skilled artisan may change temperature, pressure, atmosphere, solvents, or the order of reactions as appropriate. Additionally, the skilled artisan may use protecting groups to block side reactions or to increase yields as appropriate. All such modifications can be readily carried out by the skilled artisan in organic chemistry, and thus are within the scope fo the invention.
- Examples 41-54 are illustrated by Formula 4b and Table 3 below:
- Example 55 4-(4-Fluorophenyl)-5-pyridm-4-yl-l-(iV-methyl-iV- phenylaminocarbonyl)-[l,2,3]triazole
- Examples 58-61 are prepared using substantially the same procedures as those described in Example 57, substituting the appropriate starting materials.
- the skilled artisan may change temperature, pressure, atmosphere, solvents, or the order of reactions as appropriate. Additionally, the skilled artisan may use protecting groups to block side reactions or to increase yields as appropriate. All such modifications can be readily carried out by the skilled artisan in organic chemistry, and thus are within the scope fo the invention.
- Examples 58-61 are illustrated by Formula 4a and Table 4 below:
- Examples 87-116 are prepared using substantially the same procedures as those described in Example 86, substituting the appropriate starting materials.
- the slcilled artisan may change temperature, pressure, atmosphere, solvents, or the order of reactions as appropriate. Additionally, the slcilled artisan may use protecting groups to block side reactions or to increase yields as appropriate. All such modifications can be readily carried out by the slcilled artisan in organic chemistry, and thus are within the scope fo the invention.
- Examples 87-116 are illustrated by Formula 4c and Table 6 below:
- Examples 119-142 are prepared using substantially the same procedures as those described in Example 118, substituting the appropriate starting materials.
- the slcilled artisan may change temperature, pressure, atmosphere, solvents, or the order of reactions as appropriate. Additionally, the slcilled artisan may use protecting groups to block side reactions or to increase yields as appropriate. All such modifications can be readily carried out by the skilled artisan in organic chemistry, and thus are within the scope fo the invention.
- Example 143 4-(4-FluorophenyI)-5-[3-methyl-2-phenoxyimidazo-4-yl]-l- ethoxymethyl- [1 ,2,3] triazole
- alkyne 143a (2.70 g, 8.7 mmol) in CH 2 C1 2 (70 ml) is added MCPBA (5.82 g 70 %, 20.7 mmol). After 24 hours, the reaction is poured into 200 ml EtOAc, washed with Na 2 CO 3 (3x50 ml), dried over MgSO , filtered and stripped to a solid. Chromatography with 3/1 hexane/EtOAc yields aUcyne 143b as a white solid.
- Alkyne 143b is reacted with sodium azide as described for Example 86a to give the crude product as an oil. Chromatography with 1:1 hexane:EtOAc yields triazole 143c as a pale yellow solid.
- Triazole 143c is reacted with chloroethoxy methyl ether as described for Example 86b to give the crude product as an oil. Chromatography with 2:1 hexane:EtOAc yields the desired separable regioisomers as pale white solids.
- Triazole 143d is reacted with sodium phenoxide as described for Example 86e to give the crude product as an oil. Chromatography with 60:40:0.8 hexane:EtOAc:MeOH provides 143e as a colorless oil.
- Examples 144-146 are prepared using substantially the same procedures as those described in Example 143, substituting the appropriate starting materials.
- the slcilled artisan may change temperature, pressure, atmosphere, solvents, or the order of reactions as appropriate. Additionally, the slcilled artisan may use protecting groups to block side reactions or to increase yields as appropriate. All such modifications can be readily carried out by the skilled artisan in organic chemistry, and thus are within the scope fo the invention.
- the compounds of the present invention are potent cytokine inhibitors. Accordingly, the compounds of Formula (I) or a pharmaceutically acceptable salt thereof can be used for the prophylactic or therapeutic treatment of diseases in humans or mammals that is associated with unwanted cytokine activity.
- Cytokine refers to any secreted protein secreted by many different cell types involved in cell-to-cell communication and modulates interactions between cells in the inflammatory, immune or hematopoietic response.
- a cytokine includes, but is not limited to, monokines and lymphokines.
- cytokines include, but are not limited to, Interleukin- 1 (IL-1), Tumor Necrosis Factor alpha and beta referred to collectively herein as (TNF), h ⁇ terleukin-8 (IL-8) and Interleukin-6 (IL-6).
- IL-1 Interleukin- 1
- TNF Tumor Necrosis Factor alpha and beta referred to collectively herein as
- IL-8 h ⁇ terleukin-8
- IL-6 Interleukin-6
- Cytokine inhibition refers to: (i) a decrease of excessive in vivo levels of cytokines such as but not limited to IL-1, TNF, IL-6 and IL-8 to normal or sub-normal levels by inhibition of the in vivo release of the cytokines by all cells; (ii) a down regulation of the excessive expression of cytokine rnRNA in vivo in a human to normal or sub-normal levels; (iii) a down regulation by inhibition of the direct synthesis of the cytokines such as but not limited to IL-1, TNF, IL-6 and IL-8 as a posttranslational event; or (iv) a down regulation, at the translational level, of excessive in vivo levels of cytokines such as but not limited to IL-1, TNF, IL-6 and IL-8 in a human to normal or sub-normal levels.
- Compounds of Formula (I) are capable of inhibiting cytokines such as but not limited to IL-1, TNF, IL-6 and IL-8. These as well as other cytokines are important mediators of inflammation in a wide variety of diseases. The inhibition of these inflammatory cytokines is of benefit in treating many of these disease states.
- the invention also provides a method of treating a proteinase mediated disease in humans or mammals, wherein the production of the proteinase is affected by cytokines.
- proteinases include but are not limited to the matrix metalloproteinases and disintegrin metalloproteases (ADAMs).
- LPS lipopolysaccharide
- TNF-1 lipopolysaccharide stimulated human monocytic cells
- the compounds of Formula (I) are administered in a amount sufficient to inhibit cytokines such as but not limited to IL-1, TNF, IL-6 and IL-8, so that it is regulated to normal or subnormal levels, so as to prevent the disease state.
- the amount of cytolcine considered abnormal for the present invention constitute; levels of free cytokines such as but not limited to IL-1, TNF, IL-6 and IL-8 greater than or equal to 1 picogram per ml; any cell associated cytokines or; the presence of cytokine mRNA above basal levels in cells or tissues.
- these compounds are useful therapeutic agents for the treatment of diseases associated with unwanted cytolcine activity including, osteoarthritis, rheumatoid arthritis, septic arthritis, psoriatic arthritis, rheumatic fever, gout, Reiter's syndrome, osteoperosis, diabetes, inflammatory bowel diseases including Crohn's disease and ulcerative colitis, pancreatitis, diverticulitis, sepsis, septic shock, toxic shock syndrome, respiratory diseases including asthma, chronic obstructive pulmonary disease (COPD), bronchitis, emphysema, cystic fibrosis, acute respiratory distress, fibrotic diseases of the lung and liver, diseases of the central nervous system such as Alzheimer's disease, amyotrophic lateral sclerosis (ALS), muscular dystrophy and multiple sclerosis, cachexia secondary to infection or malignancy and cachexia secondary to acquired immune deficiency syndrome.
- diseases associated with unwanted cytolcine activity including, osteoarthritis, rheumatoid
- the compounds of this invention are useful in preventing prosthesis loosening. It is known in the art that over time protheses loosen, become painful, and may result in further bone injury, thus requiring replacement.
- the need for replacement of such protheses includes those such as in, joint replacements (for example hip, knee and shoulder replacements), dental prosthesis, including dentures, bridges and prothesis secured to the maxilla and/ mandible.
- Cytokines and proteinases are also active in remodeling in the cardiovascular system. It has been suggested that one of the reasons angioplasty has a higher than expected long term failure rate (reclosure over time) is that cytokine and proteinase activity is not desired or is elevated in response to what may be recognized by the body as "injury' to the basement membrane of the vessel. Similarly restenosis of surgical cardiovascular stents is thought to be mediated by cytolcine induced proteinase production in response to "injury" induced by placement of the stent.
- Compounds of this invention are also useful for the treatment of diseases which are caused by excessive or inappropriate angiogenesis.
- diseases, conditions or disorders include but are not limited to, various ocular diseases, such as macular degeneration and diabetic retinopathy, tumor growth and metastasis, atherosclerosis and rheumatoid arthritis.
- cytokines are implicated in the remodeling or "'turnover' of skin.
- the regulation of cytokines improves treatment of skin conditions including but not limited to, wrinkle repair, regulation, prevention and repair of ultraviolet induced skin damage.
- a treatment includes prophylactic treatment or treatment before the physiological manifestations are obvious.
- the cytolcine inhibitor may be applied as a preexposure treatment to prevent ultraviolet damage and / or during or after exposure to prevent or minimize post-exposure damage.
- cytokines are implicated in skin disorders and diseases related to abnormal tissues that result from abnormal turnover such as epidermolysis bullosa, psoriasis, sclerodenna and atopic dermatitis.
- the compounds of this invention are also useful for treating the consequences of "normal" injury to the skin including scarring or "contraction" of tissue for example, following bums and perhaps the regulation of hair growth.
- Inhibition of cytokines are also thought to be useful for the treatment of ocular disorders (especially corneal ulceration, lack of corneal healing, macular degeneration and pterygium) gum disease (especially periodontal disease and gingivitis).
- ocular disorders especially corneal ulceration, lack of corneal healing, macular degeneration and pterygium
- gum disease especially periodontal disease and gingivitis.
- Compounds preferred for, but not limited to, the treatment of ocular disorders, gum disease, and skin diseases may be administered topically.
- compositions of the invention comprise:
- cytokine activity As discussed above, numerous diseases are known to be mediated by excess or undesired cytokine activity. For example, these include osteoarthritis, rheumatoid arthritis, diabetes, HIN/AIDS, inflammatory bowel disease, chronic heart failure, hypertension, periodontitis and the like.
- the compounds of the invention are useful in the treatment or prevention of conditions involving this unwanted activity.
- the invention compounds can therefore be formulated into pharmaceutical compositions for use in treatment or prophylaxis of these conditions.
- Standard pharmaceutical formulation techniques are used, such as those disclosed in Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa., latest edition.
- a "safe and effective amount" of a Formula (I) compound is an amount that is effective, to inhibit cytokines at the site(s) of activity, in an animal, preferably a mammal, more preferably a human subject, without undue adverse side effects (such as toxicity, irritation, or allergic response), commensurate with a reasonable benefit/risk ratio when used in the manner of this invention.
- the specific "safe and effective amount” will, obviously, vary with such factors as the particular condition being treated, the physical condition of the patient, the duration of treatment, the nature of concurrent therapy (if any), the specific dosage form to be used, the carrier employed, the solubility of the Formula (I) compound therein, and the dosage regimen desired for the composition.
- compositions of the subject invention contain a pharmaceutically-acceptable ca ier.
- pharmaceutically-acceptable carrier means one or more compatible solid or liquid filler diluents or encapsulating substances which are suitable for admimstration to an animal, preferably a mammal, more preferably a human.
- compatible means that the components of the composition are capable of being commingled with the subject compound, and with each other, in a manner such that there is no interaction which would substantially reduce the pharmaceutical efficacy of the composition under ordinary use situations.
- Pharmaceutically-acceptable carriers must, of course, be of sufficiently high purity and sufficiently low toxicity to render them suitable for administration to the animal, preferably a mammal, more preferably a human being treated.
- substances which can serve as pharmaceutically-acceptable carriers or components thereof are sugars, such as lactose, glucose and sucrose; starches, such as com starch and potato starch; cellulose and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose, and methyl cellulose; powdered tragacanth; malt; gelatin; talc; solid lubricants, such as stearic acid and magnesium stearate; calcium sulfate; vegetable oils, such as peanut oil, cottonseed oil, sesame oil, olive oil, com oil and oil of theobroma; polyols such as propylene glycol, glycerine, sorbitol, mannitol, and polyethylene glycol; alginic acid; emulsifiers, such as the Tweens®; wetting agents, such sodium lauryl sulfate; coloring agents; flavoring agents; tableting agents, stabilizers; antioxidants; preservatives; pyrogen
- a pharmaceutically-acceptable carrier to be used in conjunction with the subject compound is basically determined by the way the compound is to be administered.
- the preferred pharmaceutically- acceptable carrier is sterile, physiological saline, with blood-compatible suspending agent, the pH of which has been adjusted to about 7.4.
- pharmaceutically-acceptable carriers for systemic administration include sugars, starches, cellulose and its derivatives, malt, gelatin, talc, calcium sulfate, vegetable oils, synthetic oils, polyols, alginic acid, phosphate buffer solutions, emulsifiers, isotonic saline, and pyrogen-free water.
- Preferred carriers for parenteral administration include propylene glycol, ethyl oleate, pyrrolidone, ethanol, and sesame oil.
- the pharmaceutically-acceptable carrier, in compositions for parenteral administration comprises at least about 90% by weight of the total composition.
- compositions of this invention are preferably provided in unit dosage form.
- a "unit dosage form” is a composition of this invention containing an amount of a Formula (I) compound that is suitable for administration to an animal, preferably a mammal, more preferably a human subject, in a single dose, according to good medical practice.
- These compositions preferably contain from about 5 mg (milligrams) to about 1000 mg, more preferably from about 10 mg to about 500 mg, more preferably from about 10 mg to about 300 mg, of a Formula (I) compound.
- compositions of this invention may be in any of a variety of forms, suitable (for example) for oral, rectal, topical, nasal, ocular or parenteral administration.
- a variety of pharmaceutically-acceptable carriers well-known in the art may be used. These include solid or liquid fillers, diluents, hydrotropes, surface-active agents, and encapsulating substances.
- Optional pharmaceutically-active materials may be included, which do not substantially interfere with the inhibitory activity of the Formula (I) compound.
- the amount of carrier employed in conjunction with the Formula (I) compound is sufficient to provide a practical quantity of material for administration per unit dose of the Formula (I) compound.
- oral dosage fonns can be used, including such solid forms as tablets, capsules, granules and bulk powders. These oral fonns comprise a safe and effective amount, usually at least about 5%, and preferably from about 25% to about 50%>, of the Formula (I) compound. Tablets can be compressed, tablet triturates, enteric- coated, sugar-coated, film-coated, or multiple-compressed, containing suitable binders, lubricants, diluents, disintegrating agents, coloring agents, flavoring agents, flow-inducing agents, and melting agents.
- Liquid oral dosage forms include aqueous solutions, emulsions, suspensions, solutions and/or suspensions reconstituted from non-effervescent granules, and effervescent preparations reconstituted from effervescent granules, containing suitable solvents, preservatives, emulsifying agents, suspending agents, diluents, sweeteners, melting agents, coloring agents and flavoring agents.
- the pharmaceutically-acceptable carrier suitable for the preparation of unit dosage forms for peroral administration are well-known in the art.
- Tablets typically comprise conventional pharmaceutically-compatible adjuvants as inert diluents, such as calcium carbonate, sodium carbonate, mannitol, lactose and cellulose; binders such as starch, gelatin and sucrose; disintegrants such as starch, alginic acid and croscarmelose; lubricants such as magnesium stearate, stearic acid and talc.
- Glidants such as silicon dioxide can be used to improve flow characteristics of the powder mixture.
- Coloring agents such as the FD&C dyes, can be added for appearance.
- Sweeteners and flavoring agents such as aspartame, saccharin, menthol, peppermint, and fruit flavors, are useful adjuvants for chewable tablets.
- Capsules typically comprise one or more solid diluents disclosed above. The selection of canier components depends on secondary considerations like taste, cost, and shelf stability, which are not critical for the purposes of the subject invention, and can be readily made by a person slcilled in the art.
- Peroral compositions also include liquid solutions, emulsions, suspensions, and the like.
- the pharmaceutically-acceptable carriers suitable for preparation of such compositions are well known in the art.
- Typical components of carriers for syrups, elixirs, emulsions and suspensions include ethanol, glycerol, propylene glycol, polyethylene glycol, liquid sucrose, sorbitol and water.
- typical suspending agents include methyl cellulose, sodium carboxymethyl cellulose, Avicel RC- 591, tragacanth and sodium alginate; typical wetting agents include lecithin and polysorbate 80; and typical preservatives include methyl paraben and sodium benzoate.
- Peroral liquid compositions may also contain one or more components such as sweeteners, flavoring agents and colorants disclosed above.
- compositions may also be coated by conventional methods, typically with pH or time-dependent coatings, such that the subject compound is released in the gastrointestinal tract in the vicinity of the desired topical application, or at various times to extend the desired action.
- dosage forms typically include, but are not limited to, one or more of cellulose acetate phthalate, polyvinylacetate phthalate, hydroxypropyl methyl cellulose phthalate, ethyl cellulose, Eudragit coatings, waxes and shellac.
- compositions of the subject invention may optionally include other drug actives.
- compositions useful for attaining systemic delivery of the subject compounds include sublingual, buccal and nasal dosage forms.
- Such compositions typically comprise one or more of soluble filler substances such as sucrose, sorbitol and mannitol; and binders such as acacia, microcrystalline cellulose, carboxymethyl cellulose and hydroxypropyl methyl cellulose. Glidants, lubricants, sweeteners, colorants, antioxidants and flavoring agents disclosed above may also be included.
- compositions of this invention can also be administered topically to a subject, e.g., by the direct laying on or spreading of the composition on the epidem al or epithelial tissue of the subject, or transdermally via a "patch".
- Such compositions include, for example, lotions, creams, solutions, gels and solids.
- These topical compositions preferably comprise a safe and effective amount, usually at least about 0.1%), and preferably from about 1% to about 5%, of the Formula (I) compound.
- Suitable carriers for topical administration preferably remain in place on the skin as a continuous film, and resist being removed by perspiration or immersion in water.
- the carrier is organic in nature and capable of having dispersed or dissolved therein the Formula (I) compound.
- the carrier may include pharmaceutically-acceptable emollients, emulsifiers, thickening agents, solvents and the like.
- This invention also provides methods of treating or preventing disorders associated with excess or undesired cytolcine activity in a human or other animal subject, by administering a safe and effective amount of a Formula (I) compound to said subject.
- the methods of the invention are useful in treating or preventing disorders described above.
- compositions of this invention can be administered topically or systemically.
- Systemic application includes any method of introducing Formula (I) compound into the tissues of the body, e.g., intra-articular (especially in treatment of rheumatoid arthritis), intrathecal, epidural, intramuscular, transdennal, intravenous, intraperitoneal, subcutaneous, sublingual, rectal, and oral administration.
- the Formula (I) compounds of the present invention are preferably administered orally.
- the specific dosage of inhibitor to be administered, as well as the duration of treatment, and whether the treatment is topical or systemic are interdependent.
- the dosage and treatment regimen will also depend upon such factors as the specific Formula (I) compound used, the treatment indication, the ability of the Formula (I) compound to reach minimum inhibitory concentrations at the site of the metalloprotease to be inhibited, the personal attributes of the subject (such as weight), compliance with the treatment regimen, and the presence and severity of any side effects of the treatment.
- a preferred method of administration for treatment of rheumatoid arthritis is oral or parenterally via intra-articular injection.
- all formulations for parenteral administration must be sterile.
- individual doses of from about 10 mg to about 1000 mg are preferred.
- a preferred method of systemic administration is oral. Individual doses of from about 10 mg to about 1000 mg, preferably from about 10 mg to about 300 mg are preferred.
- Topical administration can be used to deliver the Formula (I) compound systemically, or to treat a subject locally.
- the amounts of Formula (I) compound to be topically administered depends upon such factors as skin sensitivity, type and location of the tissue to be treated, the composition and carrier (if any) to be administered, the particular Formula (I) compound to be administered, as well as the particular disorder to be treated and the extent to which systemic (as distinguished from local) effects are desired.
- the inhibitors of the invention can be targeted to specific locations where the cytokine is accumulated by using targeting ligands.
- the inhibitor is conjugated to an antibody or fragment thereof which is immunoreactive with a cellular marker as is generally understood in the preparation of immunotoxins in general.
- the targeting ligand can also be a ligand suitable for a receptor which is present on the target cell. Any targeting ligand which specifically reacts with a marker for the intended target tissue can be used.
- Methods for coupling the invention compound to the targeting ligand are well known and are similar to those described below for coupling to carrier.
- the conjugates are formulated and administered as described above.
- topical administration is preferred.
- direct application to the affected eye may employ a formulation as eyedrops or aerosol.
- the compounds of the invention can also be fonnulated as gels, drops or ointments, or can be incorporated into collagen or a hydrophilic polymer shield.
- the materials can also be inserted as a contact lens or reservoir or as a subconjunctival formulation.
- the compound is applied locally and topically, in a gel, paste, salve or ointment.
- the compound may be applied locally in a gel, paste, mouth wash, or implant.
- the mode of treatment thus reflects the nature of the condition and suitable formulations for any selected route are available in the art.
- the compounds of the invention can be administered alone or as mixtures, and the compositions may further include additional drugs or excipients as appropriate for the indication.
Abstract
Description
Claims
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AU2002305226A AU2002305226B2 (en) | 2001-04-30 | 2002-04-25 | Triazole compounds useful in treating diseases associated with unwanted cytokine activity |
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EP02734036A EP1383759A1 (en) | 2001-04-30 | 2002-04-25 | Triazole compounds useful in treating diseases associated with unwanted cytokine activity |
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1684756A1 (en) * | 2003-10-30 | 2006-08-02 | Celgene Corporation | Cytokine inhibitory drugs for treatment of macular degeneration |
US7745630B2 (en) | 2003-12-22 | 2010-06-29 | Justin Stephen Bryans | Triazolyl piperidine arginine vasopressin receptor modulators |
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- 2002-04-24 US US10/133,044 patent/US6727364B2/en not_active Expired - Fee Related
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- 2002-04-25 CN CNA028090780A patent/CN1505625A/en active Pending
- 2002-04-25 CA CA002444499A patent/CA2444499A1/en not_active Abandoned
- 2002-04-25 EP EP02734036A patent/EP1383759A1/en not_active Withdrawn
- 2002-04-25 WO PCT/US2002/013074 patent/WO2002088108A1/en not_active Application Discontinuation
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US7807832B2 (en) | 2005-07-28 | 2010-10-05 | Janssen Pharmaceutica Nv | Synthesis of 4/5-pyrimidinylimidazoles via sequential functionalization of 2,4-dichloropyrimidine |
US8242273B2 (en) | 2005-07-28 | 2012-08-14 | Janssen Pharmaceutica, Nv | Synthesis of 4/5-pyrimidinylimidazoles via sequential functionalization of 2,4-dichloropyrimidine |
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AU2009330821B2 (en) * | 2008-12-24 | 2015-06-11 | Bial - Portela & Ca, S.A. | Pharmaceutical compounds |
CN103275023A (en) * | 2013-06-08 | 2013-09-04 | 浙江工业大学 | 1- aryl-1, 2, 3-triazole compound, as well as preparation method and application thereof |
CN103275023B (en) * | 2013-06-08 | 2015-10-07 | 浙江工业大学 | 1-aryl-1,2,3-triazole compound and Synthesis and applications thereof |
WO2014199164A1 (en) * | 2013-06-12 | 2014-12-18 | Ampla Pharmaceuticals, Inc. | Diaryl substituted heteroaromatic compounds |
EP3590342A4 (en) * | 2017-03-03 | 2020-12-30 | The University of Tokyo | Strigolactone receptor inhibitor, agricultural composition and use thereof, striga seed germination inhibitor, and triazole urea compound |
RU2781643C2 (en) * | 2018-01-25 | 2022-10-17 | Фудзимото Ко., Лтд. | Thiophene derivative and its use |
Also Published As
Publication number | Publication date |
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US20030013712A1 (en) | 2003-01-16 |
CA2444499A1 (en) | 2002-11-07 |
AU2002305226B2 (en) | 2006-02-02 |
JP2004528351A (en) | 2004-09-16 |
PE20021089A1 (en) | 2003-02-18 |
US6727364B2 (en) | 2004-04-27 |
EP1383759A1 (en) | 2004-01-28 |
CN1505625A (en) | 2004-06-16 |
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