JP2007504255A - Atp結合カセットトランスポーターの調節因子 - Google Patents
Atp結合カセットトランスポーターの調節因子 Download PDFInfo
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- JP2007504255A JP2007504255A JP2006525534A JP2006525534A JP2007504255A JP 2007504255 A JP2007504255 A JP 2007504255A JP 2006525534 A JP2006525534 A JP 2006525534A JP 2006525534 A JP2006525534 A JP 2006525534A JP 2007504255 A JP2007504255 A JP 2007504255A
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- Prior art keywords
- ring
- aliphatic
- optionally substituted
- phenyl
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 0 C***(C)C(C)NC Chemical compound C***(C)C(C)NC 0.000 description 17
- USWISHAKGUSBMI-UHFFFAOYSA-N CCC(C(Nc1ncc(Cc(cccc2)c2Cl)[s]1)=O)Br Chemical compound CCC(C(Nc1ncc(Cc(cccc2)c2Cl)[s]1)=O)Br USWISHAKGUSBMI-UHFFFAOYSA-N 0.000 description 2
- NQUVCRCCRXRJCK-UHFFFAOYSA-N Cc(cc1)ccc1C(Cl)=O Chemical compound Cc(cc1)ccc1C(Cl)=O NQUVCRCCRXRJCK-UHFFFAOYSA-N 0.000 description 2
- XDWGEGZDMFHZBL-UHFFFAOYSA-N Nc1nc(-c2ccccc2)c(-c2ccccc2)[s]1 Chemical compound Nc1nc(-c2ccccc2)c(-c2ccccc2)[s]1 XDWGEGZDMFHZBL-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N C1CCCCC1 Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-N C1CCNCC1 Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 1
- BSGAIIGQYTVPHR-UHFFFAOYSA-N CC(CBr)c1ccccc1Cl Chemical compound CC(CBr)c1ccccc1Cl BSGAIIGQYTVPHR-UHFFFAOYSA-N 0.000 description 1
- ZDOYHCIRUPHUHN-UHFFFAOYSA-N CC(c1ccccc1Cl)=O Chemical compound CC(c1ccccc1Cl)=O ZDOYHCIRUPHUHN-UHFFFAOYSA-N 0.000 description 1
- QXPYGNFIESNXJV-UHFFFAOYSA-N CC1C(c2c(-c3ccccc3)nc(NC(c(cc3)ccc3OC)=O)[s]2)=CC=CC1 Chemical compound CC1C(c2c(-c3ccccc3)nc(NC(c(cc3)ccc3OC)=O)[s]2)=CC=CC1 QXPYGNFIESNXJV-UHFFFAOYSA-N 0.000 description 1
- SILRNKZBMNSABG-UHFFFAOYSA-N CC1N=C(N)SC1 Chemical compound CC1N=C(N)SC1 SILRNKZBMNSABG-UHFFFAOYSA-N 0.000 description 1
- ZVEJRZRAUYJYCO-UHFFFAOYSA-N CC1c(cccc2)c2-c2c1cccc2 Chemical compound CC1c(cccc2)c2-c2c1cccc2 ZVEJRZRAUYJYCO-UHFFFAOYSA-N 0.000 description 1
- YAQLSKVCTLCIIE-UHFFFAOYSA-N CCC(C(O)=O)Br Chemical compound CCC(C(O)=O)Br YAQLSKVCTLCIIE-UHFFFAOYSA-N 0.000 description 1
- JWCCWGJFEPOBEU-UHFFFAOYSA-O CCOC(CC(N)=CSC(C)[NH3+])=O Chemical compound CCOC(CC(N)=CSC(C)[NH3+])=O JWCCWGJFEPOBEU-UHFFFAOYSA-O 0.000 description 1
- AASAQQFBLTWENE-UHFFFAOYSA-N CCOC(Cc1c[s]c(NC(C(c2ccccc2)c2ccccc2)=O)n1)=O Chemical compound CCOC(Cc1c[s]c(NC(C(c2ccccc2)c2ccccc2)=O)n1)=O AASAQQFBLTWENE-UHFFFAOYSA-N 0.000 description 1
- BVHGYJSKAPKOIP-UHFFFAOYSA-N CCOC(c1c[s]c(NC(C(c2ccccc2)c2ccccc2)=O)n1)=O Chemical compound CCOC(c1c[s]c(NC(C(c2ccccc2)c2ccccc2)=O)n1)=O BVHGYJSKAPKOIP-UHFFFAOYSA-N 0.000 description 1
- XHFUVBWCMLLKOZ-UHFFFAOYSA-O CCOC(c1c[s]c([NH3+])n1)=O Chemical compound CCOC(c1c[s]c([NH3+])n1)=O XHFUVBWCMLLKOZ-UHFFFAOYSA-O 0.000 description 1
- ZSXGLVDWWRXATF-UHFFFAOYSA-N CN(C)C(OC)OC Chemical compound CN(C)C(OC)OC ZSXGLVDWWRXATF-UHFFFAOYSA-N 0.000 description 1
- DDUCBJHZOCRWLR-UHFFFAOYSA-N CN(C)CNc1ncc(C(c2ccccc2Cl)=O)[s]1 Chemical compound CN(C)CNc1ncc(C(c2ccccc2Cl)=O)[s]1 DDUCBJHZOCRWLR-UHFFFAOYSA-N 0.000 description 1
- MXMOTZIXVICDSD-UHFFFAOYSA-N COc(cc1)ccc1C(Cl)=O Chemical compound COc(cc1)ccc1C(Cl)=O MXMOTZIXVICDSD-UHFFFAOYSA-N 0.000 description 1
- KASSWCYNWATCNS-UHFFFAOYSA-N COc1ncccc1Cc1cnc(N)[s]1 Chemical compound COc1ncccc1Cc1cnc(N)[s]1 KASSWCYNWATCNS-UHFFFAOYSA-N 0.000 description 1
- ARLHWYFAPHJCJT-UHFFFAOYSA-N Cc(cc1)ccc1-c1c[s]c(N)n1 Chemical compound Cc(cc1)ccc1-c1c[s]c(N)n1 ARLHWYFAPHJCJT-UHFFFAOYSA-N 0.000 description 1
- YMUIWYBAUJKUEL-UHFFFAOYSA-N Cc(cc1)ccc1C(Nc1nc(-c2ccc(C)cc2)c[s]1)=O Chemical compound Cc(cc1)ccc1C(Nc1nc(-c2ccc(C)cc2)c[s]1)=O YMUIWYBAUJKUEL-UHFFFAOYSA-N 0.000 description 1
- GUABFMPMKJGSBQ-UHFFFAOYSA-N Cc1cnc(N)[s]1 Chemical compound Cc1cnc(N)[s]1 GUABFMPMKJGSBQ-UHFFFAOYSA-N 0.000 description 1
- ZPGDCLFUACUTRF-UHFFFAOYSA-N Cc1cnc(NC(c2ccc(C)cc2)=O)[s]1 Chemical compound Cc1cnc(NC(c2ccc(C)cc2)=O)[s]1 ZPGDCLFUACUTRF-UHFFFAOYSA-N 0.000 description 1
- PYSJLPAOBIGQPK-UHFFFAOYSA-N Nc1nc(-c2ccccc2)c[s]1 Chemical compound Nc1nc(-c2ccccc2)c[s]1 PYSJLPAOBIGQPK-UHFFFAOYSA-N 0.000 description 1
- OKSWEXUXMSNDEZ-UHFFFAOYSA-N Nc1ncc(Cc(cccc2)c2C#N)[s]1 Chemical compound Nc1ncc(Cc(cccc2)c2C#N)[s]1 OKSWEXUXMSNDEZ-UHFFFAOYSA-N 0.000 description 1
- LIGACIXOYTUXAW-UHFFFAOYSA-N O=C(CBr)c1ccccc1 Chemical compound O=C(CBr)c1ccccc1 LIGACIXOYTUXAW-UHFFFAOYSA-N 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N O=C(c1ccccc1)Cl Chemical compound O=C(c1ccccc1)Cl PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- JQHAHDXKCUBZBX-UHFFFAOYSA-N O=C(c1ccccc1)Nc1nc(-c2ccccc2)c(-c2ccccc2)[s]1 Chemical compound O=C(c1ccccc1)Nc1nc(-c2ccccc2)c(-c2ccccc2)[s]1 JQHAHDXKCUBZBX-UHFFFAOYSA-N 0.000 description 1
- PYHXGXCGESYPCW-UHFFFAOYSA-N OC(C(c1ccccc1)c1ccccc1)=O Chemical compound OC(C(c1ccccc1)c1ccccc1)=O PYHXGXCGESYPCW-UHFFFAOYSA-N 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N c1cc2ccccc2cc1 Chemical compound c1cc2ccccc2cc1 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/426—1,3-Thiazoles
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- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
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- C07D277/68—Benzothiazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/145—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/15—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
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- 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
- C07D417/02—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 two hetero rings
- C07D417/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
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- 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
- C07D417/02—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 two hetero rings
- C07D417/06—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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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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
- C07D417/02—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 two hetero rings
- C07D417/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
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- G—PHYSICS
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- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
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- G01N33/5076—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics involving cell organelles, e.g. Golgi complex, endoplasmic reticulum
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| US50044403P | 2003-09-06 | 2003-09-06 | |
| PCT/US2004/029206 WO2005026137A2 (en) | 2003-09-06 | 2004-09-07 | Modulators of atp-binding cassette transporters |
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| JP2007504255A true JP2007504255A (ja) | 2007-03-01 |
| JP2007504255A5 JP2007504255A5 (enExample) | 2007-11-08 |
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| AU (1) | AU2004272599A1 (enExample) |
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| IL (1) | IL174128A0 (enExample) |
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| RU (1) | RU2006111093A (enExample) |
| WO (1) | WO2005026137A2 (enExample) |
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| JP2023500408A (ja) * | 2019-11-12 | 2023-01-05 | ジェンザイム・コーポレーション | Cftr活性の欠損が介在する状態を治療するための5員ヘテロアリールアミノスルホンアミド |
| JP7721517B2 (ja) | 2019-11-12 | 2025-08-12 | ジェンザイム・コーポレーション | Cftr活性の欠損が介在する状態を治療するための5員ヘテロアリールアミノスルホンアミド |
Also Published As
| Publication number | Publication date |
|---|---|
| IL174128A0 (en) | 2006-08-01 |
| US7973169B2 (en) | 2011-07-05 |
| CA2537841A1 (en) | 2005-03-24 |
| NO20061543L (no) | 2006-06-06 |
| US20130252333A1 (en) | 2013-09-26 |
| WO2005026137A2 (en) | 2005-03-24 |
| KR20060088537A (ko) | 2006-08-04 |
| US8431605B2 (en) | 2013-04-30 |
| US8853415B2 (en) | 2014-10-07 |
| WO2005026137A3 (en) | 2005-07-21 |
| CN1898221A (zh) | 2007-01-17 |
| US8741939B2 (en) | 2014-06-03 |
| US20150025076A1 (en) | 2015-01-22 |
| US9249131B2 (en) | 2016-02-02 |
| MXPA06002567A (es) | 2006-09-04 |
| US20160228414A1 (en) | 2016-08-11 |
| US20140072995A1 (en) | 2014-03-13 |
| AU2004272599A1 (en) | 2005-03-24 |
| EP1664006A2 (en) | 2006-06-07 |
| US20120004216A1 (en) | 2012-01-05 |
| US20050176789A1 (en) | 2005-08-11 |
| ZA200602755B (en) | 2007-06-27 |
| RU2006111093A (ru) | 2007-10-27 |
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