CN102863432B - Cftr调节剂 - Google Patents
Cftr调节剂 Download PDFInfo
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- CN102863432B CN102863432B CN201210355068.2A CN201210355068A CN102863432B CN 102863432 B CN102863432 B CN 102863432B CN 201210355068 A CN201210355068 A CN 201210355068A CN 102863432 B CN102863432 B CN 102863432B
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- base
- methyl
- dioxole
- compound
- disease
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- 0 C*C1C(C)C=C*1 Chemical compound C*C1C(C)C=C*1 0.000 description 17
- YPEFNKQILHGHDL-WAYWQWQTSA-N C/C(/C=C)=C/N=C Chemical compound C/C(/C=C)=C/N=C YPEFNKQILHGHDL-WAYWQWQTSA-N 0.000 description 1
- KVXOOBUVBFFPJY-UHFFFAOYSA-N CC(C)(C(C)(C)O1)OB1P1OC(C)(C)C(C)(C)O1 Chemical compound CC(C)(C(C)(C)O1)OB1P1OC(C)(C)C(C)(C)O1 KVXOOBUVBFFPJY-UHFFFAOYSA-N 0.000 description 1
- AYSMVZYHJIVTAZ-WPMHFGGOSA-N CC(C)/C(/C1(CC1)C(NCC1=NC(C(C(C)=C2)=CNC2=O)=CC(C)=CC1)=O)=C\C(O1)=C(C)[U]C1(CF)F Chemical compound CC(C)/C(/C1(CC1)C(NCC1=NC(C(C(C)=C2)=CNC2=O)=CC(C)=CC1)=O)=C\C(O1)=C(C)[U]C1(CF)F AYSMVZYHJIVTAZ-WPMHFGGOSA-N 0.000 description 1
- YPNDLAZAJARUFB-WUXMJOGZSA-N CC(C)N/C(/NC(CC1(CC1)C(C)=C)=O)=C\C Chemical compound CC(C)N/C(/NC(CC1(CC1)C(C)=C)=O)=C\C YPNDLAZAJARUFB-WUXMJOGZSA-N 0.000 description 1
- BZSKMPQHCWDSOR-UHFFFAOYSA-N CC(C=CC1)NC=C1C1=C(C)C=CC(N)N1 Chemical compound CC(C=CC1)NC=C1C1=C(C)C=CC(N)N1 BZSKMPQHCWDSOR-UHFFFAOYSA-N 0.000 description 1
- MPAYRQKBQNNUGX-JTQLQIEISA-N CC(C[C@@H](C=N1)c2nc(N)ccc2C)=C1OC Chemical compound CC(C[C@@H](C=N1)c2nc(N)ccc2C)=C1OC MPAYRQKBQNNUGX-JTQLQIEISA-N 0.000 description 1
- ADKVUCJOBDNETB-UHFFFAOYSA-N CC1(C2(CC2)C(Nc2cc(C)c(C)c(C(C=CN3)=CC3=O)n2)=O)C=CC(OCC2)=C2C1 Chemical compound CC1(C2(CC2)C(Nc2cc(C)c(C)c(C(C=CN3)=CC3=O)n2)=O)C=CC(OCC2)=C2C1 ADKVUCJOBDNETB-UHFFFAOYSA-N 0.000 description 1
- AOJQMFVCBDIPCM-UHFFFAOYSA-N CC1(Oc2ccc(C3(CC3)C(Nc3nc(C)cc(C)c3)=O)cc2N1)F Chemical compound CC1(Oc2ccc(C3(CC3)C(Nc3nc(C)cc(C)c3)=O)cc2N1)F AOJQMFVCBDIPCM-UHFFFAOYSA-N 0.000 description 1
- LWJHQBIQXKOKRJ-SOFGYWHQSA-N COC(CN(/C=C(\C#C)/Br)C(CC#N)=O)=O Chemical compound COC(CN(/C=C(\C#C)/Br)C(CC#N)=O)=O LWJHQBIQXKOKRJ-SOFGYWHQSA-N 0.000 description 1
- IJNNWPMZHGIFOW-UHFFFAOYSA-N COc1ccc(C2(CC2)C(O)=O)cc1Cl Chemical compound COc1ccc(C2(CC2)C(O)=O)cc1Cl IJNNWPMZHGIFOW-UHFFFAOYSA-N 0.000 description 1
- ZEUQFPQKGFFHKK-UHFFFAOYSA-N COc1ncc(B(O)[O]#C)cc1 Chemical compound COc1ncc(B(O)[O]#C)cc1 ZEUQFPQKGFFHKK-UHFFFAOYSA-N 0.000 description 1
- MPKRSQTWJWEDNS-HHULDZLWSA-N C[C@@H](C(C)(C)/C(/C)=C/N(CC(OC)=C)C(C=C)=N)/C=C\C(N)=N Chemical compound C[C@@H](C(C)(C)/C(/C)=C/N(CC(OC)=C)C(C=C)=N)/C=C\C(N)=N MPKRSQTWJWEDNS-HHULDZLWSA-N 0.000 description 1
- HVJOHMMPNGYFKU-UHFFFAOYSA-N Cc(ccc(NC(C1(CC1)c(cc1)cc2c1OCC2)=O)n1)c1[I]1CC1 Chemical compound Cc(ccc(NC(C1(CC1)c(cc1)cc2c1OCC2)=O)n1)c1[I]1CC1 HVJOHMMPNGYFKU-UHFFFAOYSA-N 0.000 description 1
- FXZZSHICIXUGPZ-UHFFFAOYSA-N Cc1ccc(N)nc1-c(cn1)cc(C)c1OC Chemical compound Cc1ccc(N)nc1-c(cn1)cc(C)c1OC FXZZSHICIXUGPZ-UHFFFAOYSA-N 0.000 description 1
- JEQMIWKGYIYSRE-UHFFFAOYSA-N Cc1ccc(NC(C2(CC2)c(cc2)cc(O3)c2OC3(F)F)=O)nc1C(C=C1)=CN(C)C1O Chemical compound Cc1ccc(NC(C2(CC2)c(cc2)cc(O3)c2OC3(F)F)=O)nc1C(C=C1)=CN(C)C1O JEQMIWKGYIYSRE-UHFFFAOYSA-N 0.000 description 1
- PGIPMCQBPWOKLX-UHFFFAOYSA-N Cc1ccc(NC(C2(CC2)c(cc2C)ccc2OC)=O)nc1-c(cc1C)cnc1OC Chemical compound Cc1ccc(NC(C2(CC2)c(cc2C)ccc2OC)=O)nc1-c(cc1C)cnc1OC PGIPMCQBPWOKLX-UHFFFAOYSA-N 0.000 description 1
- KPZRCZMNXPBHEH-UHFFFAOYSA-O Cc1ccc([NH3+])nc1Cl Chemical compound Cc1ccc([NH3+])nc1Cl KPZRCZMNXPBHEH-UHFFFAOYSA-O 0.000 description 1
- CVUZRMUCKVDRRQ-UHFFFAOYSA-N ClCc1ccc(CCC2)c2c1 Chemical compound ClCc1ccc(CCC2)c2c1 CVUZRMUCKVDRRQ-UHFFFAOYSA-N 0.000 description 1
- XPXFMBWUSVZTMV-UHFFFAOYSA-N N#CC1(CC1)c1cc(CCC2)c2cc1 Chemical compound N#CC1(CC1)c1cc(CCC2)c2cc1 XPXFMBWUSVZTMV-UHFFFAOYSA-N 0.000 description 1
- CDYRKUBOLVGYNF-UHFFFAOYSA-N N#CC1=CC(Br)=CCNCC1=O Chemical compound N#CC1=CC(Br)=CCNCC1=O CDYRKUBOLVGYNF-UHFFFAOYSA-N 0.000 description 1
- FZSXXUAESILITC-UHFFFAOYSA-N N#CCc1ccc(CCC2)c2c1 Chemical compound N#CCc1ccc(CCC2)c2c1 FZSXXUAESILITC-UHFFFAOYSA-N 0.000 description 1
- SJKGAFDWIVOCSE-UHFFFAOYSA-N OCc1cc(CCC2)c2cc1 Chemical compound OCc1cc(CCC2)c2cc1 SJKGAFDWIVOCSE-UHFFFAOYSA-N 0.000 description 1
Classifications
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
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- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
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- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Neurology (AREA)
- Immunology (AREA)
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- Psychology (AREA)
- Oncology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pulmonology (AREA)
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- Pathology (AREA)
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- Biochemistry (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US92833407P | 2007-05-09 | 2007-05-09 | |
| US60/928,334 | 2007-05-09 | ||
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| JP6662885B2 (ja) | 2015-01-26 | 2020-03-11 | ライジェル ファーマシューティカルズ, インコーポレイテッド | カルボン酸生物学的等価体としてのテトラゾロン |
| UY36680A (es) | 2015-05-19 | 2016-12-30 | Glaxosmithkline Ip Dev Ltd | Amidas heterocíclicas como inhibidores de quinasa |
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- 2008-05-09 EP EP14168373.0A patent/EP2789606B1/en active Active
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- 2008-05-09 CN CN201410752029.5A patent/CN104447716A/zh active Pending
- 2008-05-09 CA CA2686838A patent/CA2686838C/en active Active
- 2008-05-09 JP JP2010507681A patent/JP5497633B2/ja active Active
- 2008-05-09 CN CN201210355068.2A patent/CN102863432B/zh active Active
- 2008-05-09 US US12/117,941 patent/US8969386B2/en active Active
- 2008-05-09 WO PCT/US2008/063144 patent/WO2008141119A2/en not_active Ceased
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| EP2164840A2 (en) | 2010-03-24 |
| AU2008251504A1 (en) | 2008-11-20 |
| CN104447716A (zh) | 2015-03-25 |
| CN101687842B (zh) | 2013-03-06 |
| HK1138586A1 (en) | 2010-08-27 |
| EP2789606B1 (en) | 2017-11-15 |
| NZ581259A (en) | 2012-07-27 |
| JP2013245219A (ja) | 2013-12-09 |
| CA2686838A1 (en) | 2008-11-20 |
| US20150031708A1 (en) | 2015-01-29 |
| JP5951674B2 (ja) | 2016-07-13 |
| CN102863432A (zh) | 2013-01-09 |
| US9725440B2 (en) | 2017-08-08 |
| CA2686838C (en) | 2017-03-14 |
| JP2016033162A (ja) | 2016-03-10 |
| US20150166516A1 (en) | 2015-06-18 |
| WO2008141119A3 (en) | 2009-04-30 |
| AU2008251504B2 (en) | 2013-07-18 |
| US8969386B2 (en) | 2015-03-03 |
| CN101687842A (zh) | 2010-03-31 |
| JP2014133757A (ja) | 2014-07-24 |
| EP2789606A1 (en) | 2014-10-15 |
| JP5497633B2 (ja) | 2014-05-21 |
| JP2010526831A (ja) | 2010-08-05 |
| WO2008141119A2 (en) | 2008-11-20 |
| JP5706485B2 (ja) | 2015-04-22 |
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