KR101444486B1 - 인돌 화합물 - Google Patents
인돌 화합물 Download PDFInfo
- Publication number
- KR101444486B1 KR101444486B1 KR1020097010151A KR20097010151A KR101444486B1 KR 101444486 B1 KR101444486 B1 KR 101444486B1 KR 1020097010151 A KR1020097010151 A KR 1020097010151A KR 20097010151 A KR20097010151 A KR 20097010151A KR 101444486 B1 KR101444486 B1 KR 101444486B1
- Authority
- KR
- South Korea
- Prior art keywords
- group
- substituted
- alkyl
- compound
- optionally substituted
- 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.)
- Expired - Fee Related
Links
- 0 CC(CCCCCC*C(C)C(*)CCCC=*CC=*)N Chemical compound CC(CCCCCC*C(C)C(*)CCCC=*CC=*)N 0.000 description 24
- JLSBFQZTOFAFSS-UHFFFAOYSA-N CC(C)(C)C(Oc(cc1[N+]([O-])=O)cc2c1[nH]c(C(NCC(C(OC)OC)SCc1ccccc1)=O)c2)=O Chemical compound CC(C)(C)C(Oc(cc1[N+]([O-])=O)cc2c1[nH]c(C(NCC(C(OC)OC)SCc1ccccc1)=O)c2)=O JLSBFQZTOFAFSS-UHFFFAOYSA-N 0.000 description 1
- IVTWTMMWSNXMKG-HYXAFXHYSA-N CC(C)=C/C=C\N Chemical compound CC(C)=C/C=C\N IVTWTMMWSNXMKG-HYXAFXHYSA-N 0.000 description 1
- PENXHWWLNWCYSL-UHFFFAOYSA-N CC(CC1SC(c2cc(cccc3NS(c4ccc[s]4)(=O)=O)c3[nH]2)=NC1)=O Chemical compound CC(CC1SC(c2cc(cccc3NS(c4ccc[s]4)(=O)=O)c3[nH]2)=NC1)=O PENXHWWLNWCYSL-UHFFFAOYSA-N 0.000 description 1
- NYFBJSZBUPANPP-UHFFFAOYSA-N CC(CNCCNCc1cnc(-c2cc(cccc3N(C)S(c4cccs4)(=O)=O)c3[nH]2)[s]1)=O Chemical compound CC(CNCCNCc1cnc(-c2cc(cccc3N(C)S(c4cccs4)(=O)=O)c3[nH]2)[s]1)=O NYFBJSZBUPANPP-UHFFFAOYSA-N 0.000 description 1
- OAIZYKNYKLAWJO-HCGXMYGOSA-N CC/C=C(\SC)/S(N(C)c1cccc2c1[nH]c(-c1ncc(CN(CC3)CC3c3ncccn3)[s]1)c2)(O)=O Chemical compound CC/C=C(\SC)/S(N(C)c1cccc2c1[nH]c(-c1ncc(CN(CC3)CC3c3ncccn3)[s]1)c2)(O)=O OAIZYKNYKLAWJO-HCGXMYGOSA-N 0.000 description 1
- LKAGTMGRWMSKHY-UHFFFAOYSA-N CC1c2cccc(N(C)S(c3ccc[s]3)(=O)=O)c2CCC1C1(C)SC(CN(C)CCC2=NCCC=C2)=CN1 Chemical compound CC1c2cccc(N(C)S(c3ccc[s]3)(=O)=O)c2CCC1C1(C)SC(CN(C)CCC2=NCCC=C2)=CN1 LKAGTMGRWMSKHY-UHFFFAOYSA-N 0.000 description 1
- GZPRHKQRRRVCMV-UHFFFAOYSA-N CCN(CC)C(C1SC(c2cc(cccc3N(C)S(c4ccc[s]4)(=O)=O)c3[nH]2)=NC1)=O Chemical compound CCN(CC)C(C1SC(c2cc(cccc3N(C)S(c4ccc[s]4)(=O)=O)c3[nH]2)=NC1)=O GZPRHKQRRRVCMV-UHFFFAOYSA-N 0.000 description 1
- LPXFGSHIFWPFIS-UHFFFAOYSA-N CCN(c1cccc2c1[nH]c(C1=NCC(CC(O)=O)S1)c2)S(c1ccc[s]1)(=O)=O Chemical compound CCN(c1cccc2c1[nH]c(C1=NCC(CC(O)=O)S1)c2)S(c1ccc[s]1)(=O)=O LPXFGSHIFWPFIS-UHFFFAOYSA-N 0.000 description 1
- FWXGOKWQPCLBRA-NTUHNPAUSA-N CCOC(/C(/C)=N/Nc(ccc(Br)c1)c1[N+]([O-])=O)=O Chemical compound CCOC(/C(/C)=N/Nc(ccc(Br)c1)c1[N+]([O-])=O)=O FWXGOKWQPCLBRA-NTUHNPAUSA-N 0.000 description 1
- LZIRLVYSGBBWQI-UHFFFAOYSA-N CCOC(C(Cc1cc(OCCOC)c2)N(C(OC(C)(C)C)=O)c1c2N)=O Chemical compound CCOC(C(Cc1cc(OCCOC)c2)N(C(OC(C)(C)C)=O)c1c2N)=O LZIRLVYSGBBWQI-UHFFFAOYSA-N 0.000 description 1
- DPQGBMMPZFVSRY-UHFFFAOYSA-N CCOC(CC1SC(c2cc(cc(c(-c3cccnc3S)c3N)OCCOC)c3[nH]2)=NC1)=O Chemical compound CCOC(CC1SC(c2cc(cc(c(-c3cccnc3S)c3N)OCCOC)c3[nH]2)=NC1)=O DPQGBMMPZFVSRY-UHFFFAOYSA-N 0.000 description 1
- HNYPLZYKEBXARA-UHFFFAOYSA-N CCOC(c1cc(cccc2N(C)S(c3ncc[n]3C)(=O)=O)c2[nH]1)=O Chemical compound CCOC(c1cc(cccc2N(C)S(c3ncc[n]3C)(=O)=O)c2[nH]1)=O HNYPLZYKEBXARA-UHFFFAOYSA-N 0.000 description 1
- IOJRUDLLTPHSBB-UHFFFAOYSA-N CCOCCN(c1cccc2c1[nH]c(-c1ncc(CN(CC3)CCC3OC3N=CC=CN3)[s]1)c2)S(c1ccc[s]1)(=O)=O Chemical compound CCOCCN(c1cccc2c1[nH]c(-c1ncc(CN(CC3)CCC3OC3N=CC=CN3)[s]1)c2)S(c1ccc[s]1)(=O)=O IOJRUDLLTPHSBB-UHFFFAOYSA-N 0.000 description 1
- JZSMCVDKFSIBHQ-UHFFFAOYSA-N CN(C1C=CC=C2C=C(C3=NCC(CC(N(CC4)CCS4(=O)=O)=O)S3)NC12)S(c1ccc[s]1)(=O)=O Chemical compound CN(C1C=CC=C2C=C(C3=NCC(CC(N(CC4)CCS4(=O)=O)=O)S3)NC12)S(c1ccc[s]1)(=O)=O JZSMCVDKFSIBHQ-UHFFFAOYSA-N 0.000 description 1
- KUZZKPRTWXEPSP-UHFFFAOYSA-N CN(c1c2[nH]c(C3=NCC4(CCN(CC(O)=O)CC4)S3)cc2ccc1)S(c1ccc[s]1)(=O)=O Chemical compound CN(c1c2[nH]c(C3=NCC4(CCN(CC(O)=O)CC4)S3)cc2ccc1)S(c1ccc[s]1)(=O)=O KUZZKPRTWXEPSP-UHFFFAOYSA-N 0.000 description 1
- ZTHYGEGFPKVUNY-UHFFFAOYSA-N CN(c1cc(OCCOC)cc2c1[nH]c(C1=NCC(CN(C3)CC3O)S1)c2)[S+](c1ncccc1)O Chemical compound CN(c1cc(OCCOC)cc2c1[nH]c(C1=NCC(CN(C3)CC3O)S1)c2)[S+](c1ncccc1)O ZTHYGEGFPKVUNY-UHFFFAOYSA-N 0.000 description 1
- VJDAHJLMGXNCOU-UHFFFAOYSA-O CN(c1cccc2c1[NH2+]C(C1=NCC3(CCN(Cc4ccc[o]4)CC3)S1)=C2)S(c1ccc[s]1)(=O)=O Chemical compound CN(c1cccc2c1[NH2+]C(C1=NCC3(CCN(Cc4ccc[o]4)CC3)S1)=C2)S(c1ccc[s]1)(=O)=O VJDAHJLMGXNCOU-UHFFFAOYSA-O 0.000 description 1
- AZYPCVSNUOATEC-UHFFFAOYSA-N CN(c1cccc2c1[nH]c(C1=NCC(CC(N)=O)S1)c2F)S(c1ccc[s]1)=O Chemical compound CN(c1cccc2c1[nH]c(C1=NCC(CC(N)=O)S1)c2F)S(c1ccc[s]1)=O AZYPCVSNUOATEC-UHFFFAOYSA-N 0.000 description 1
- ULUYMXODQBCOKS-UHFFFAOYSA-N CN(c1cccc2c1[nH]c(C1=NCC(CC(NC3CCOCC3)=O)S1)c2)S(c1ccc[s]1)(=O)=O Chemical compound CN(c1cccc2c1[nH]c(C1=NCC(CC(NC3CCOCC3)=O)S1)c2)S(c1ccc[s]1)(=O)=O ULUYMXODQBCOKS-UHFFFAOYSA-N 0.000 description 1
- SBSASQSPINOSPF-UHFFFAOYSA-N CN(c1cccc2c1[nH]c(C1=NCC(CC3)(CCC3=O)S1)c2)S(c1ccc[s]1)(=O)=O Chemical compound CN(c1cccc2c1[nH]c(C1=NCC(CC3)(CCC3=O)S1)c2)S(c1ccc[s]1)(=O)=O SBSASQSPINOSPF-UHFFFAOYSA-N 0.000 description 1
- SKJBJUCZMURIEE-UHFFFAOYSA-N CN(c1cccc2c1[nH]c(C1=NCC(CCO)S1)c2)S(c1ccc[o]1)(=O)=O Chemical compound CN(c1cccc2c1[nH]c(C1=NCC(CCO)S1)c2)S(c1ccc[o]1)(=O)=O SKJBJUCZMURIEE-UHFFFAOYSA-N 0.000 description 1
- MZSKTQYWKHTRRT-UHFFFAOYSA-N CN(c1cccc2c1[nH]c(C1=NCC(CCSCC(O)=O)S1)c2)S(c1ccc[s]1)(=O)=O Chemical compound CN(c1cccc2c1[nH]c(C1=NCC(CCSCC(O)=O)S1)c2)S(c1ccc[s]1)(=O)=O MZSKTQYWKHTRRT-UHFFFAOYSA-N 0.000 description 1
- IFFORHGXUXGKIK-UHFFFAOYSA-N CN(c1cccc2c1[nH]c(C1=NCC(CN3C=CNC3CO)S1)c2)[Tc](C)c1ccccn1 Chemical compound CN(c1cccc2c1[nH]c(C1=NCC(CN3C=CNC3CO)S1)c2)[Tc](C)c1ccccn1 IFFORHGXUXGKIK-UHFFFAOYSA-N 0.000 description 1
- ZMJZZBWGKFOYFX-UHFFFAOYSA-N CNc1c(-c2c(S)[s]cc2)c(OCCOC)cc2c1[nH]c(C1=NCC(CC(N)=O)S1)c2 Chemical compound CNc1c(-c2c(S)[s]cc2)c(OCCOC)cc2c1[nH]c(C1=NCC(CC(N)=O)S1)c2 ZMJZZBWGKFOYFX-UHFFFAOYSA-N 0.000 description 1
- SAQKNGSOQBILRR-UHFFFAOYSA-O CNc1c(-c2cccnc2[SH2+])c(OC)cc2c1[nH]c(C(S1)=NCC1=C(OC)OC)c2 Chemical compound CNc1c(-c2cccnc2[SH2+])c(OC)cc2c1[nH]c(C(S1)=NCC1=C(OC)OC)c2 SAQKNGSOQBILRR-UHFFFAOYSA-O 0.000 description 1
- NTLFVUGAPKPGCY-UHFFFAOYSA-N COC(C1SC(c2cc(cccc3N)c3[nH]2)=NC1)OC Chemical compound COC(C1SC(c2cc(cccc3N)c3[nH]2)=NC1)OC NTLFVUGAPKPGCY-UHFFFAOYSA-N 0.000 description 1
- MMIVORFGZDFBBE-UHFFFAOYSA-N COCCOc(cc1NSc2ccc[s]2)cc2c1[nH]c(C1=NCC(CC(O)=O)S1)c2 Chemical compound COCCOc(cc1NSc2ccc[s]2)cc2c1[nH]c(C1=NCC(CC(O)=O)S1)c2 MMIVORFGZDFBBE-UHFFFAOYSA-N 0.000 description 1
- CQADLWLAJDCRLA-UHFFFAOYSA-N Cc(c1c2[nH]c(C3=NCC(CN)S3)c1)ccc2N(C)S(c1ccc[s]1)(=O)=O Chemical compound Cc(c1c2[nH]c(C3=NCC(CN)S3)c1)ccc2N(C)S(c1ccc[s]1)(=O)=O CQADLWLAJDCRLA-UHFFFAOYSA-N 0.000 description 1
- LKNOQFJHOWMUQH-UHFFFAOYSA-O Cc(cc1N(C)S(c2ccc[s]2)[OH2+])cc2c1[nH]c(C1=NCC(CCO)S1)c2 Chemical compound Cc(cc1N(C)S(c2ccc[s]2)[OH2+])cc2c1[nH]c(C1=NCC(CCO)S1)c2 LKNOQFJHOWMUQH-UHFFFAOYSA-O 0.000 description 1
- KMARFKPJOVAIPP-UHFFFAOYSA-N Cc1cc(N(C)Sc2ccc[s]2)c2[nH]c(C(NCC(C3N=C3)SCc3ccccc3)O)cc2c1 Chemical compound Cc1cc(N(C)Sc2ccc[s]2)c2[nH]c(C(NCC(C3N=C3)SCc3ccccc3)O)cc2c1 KMARFKPJOVAIPP-UHFFFAOYSA-N 0.000 description 1
- BSWYYBCETNYCPA-UHFFFAOYSA-N Nc1c2[nH]c(C(NCC(CN3CCSCC3)SCC3C(C4)C4C=CC3)=O)cc2cc(OC(CO)c2cc(S)ncc2)c1 Chemical compound Nc1c2[nH]c(C(NCC(CN3CCSCC3)SCC3C(C4)C4C=CC3)=O)cc2cc(OC(CO)c2cc(S)ncc2)c1 BSWYYBCETNYCPA-UHFFFAOYSA-N 0.000 description 1
- SWKVQJQPSGTEBD-UHFFFAOYSA-N O=C1OCC2N1CCNC2 Chemical compound O=C1OCC2N1CCNC2 SWKVQJQPSGTEBD-UHFFFAOYSA-N 0.000 description 1
- OPBPHPUJWRNFOB-UHFFFAOYSA-N OCCC1SC(c2cc(cccc3NS(c4ccc[s]4)(=O)=O)c3[nH]2)=NC1 Chemical compound OCCC1SC(c2cc(cccc3NS(c4ccc[s]4)(=O)=O)c3[nH]2)=NC1 OPBPHPUJWRNFOB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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
- A61K31/433—Thidiazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Epidemiology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JPJP-P-2006-285551 | 2006-10-19 | ||
| JP2006285551 | 2006-10-19 | ||
| PCT/JP2007/070772 WO2008050821A1 (en) | 2006-10-19 | 2007-10-18 | Indole compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20090068292A KR20090068292A (ko) | 2009-06-25 |
| KR101444486B1 true KR101444486B1 (ko) | 2014-09-24 |
Family
ID=39010108
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020097010151A Expired - Fee Related KR101444486B1 (ko) | 2006-10-19 | 2007-10-18 | 인돌 화합물 |
Country Status (26)
| Country | Link |
|---|---|
| US (4) | US7652133B2 (enExample) |
| EP (2) | EP2508524A3 (enExample) |
| JP (1) | JP5260507B2 (enExample) |
| KR (1) | KR101444486B1 (enExample) |
| CN (1) | CN101573357B (enExample) |
| AU (1) | AU2007310064B2 (enExample) |
| BR (1) | BRPI0717722A2 (enExample) |
| CA (1) | CA2666973C (enExample) |
| CL (1) | CL2008001017A1 (enExample) |
| CR (1) | CR10748A (enExample) |
| EC (1) | ECSP099330A (enExample) |
| GE (1) | GEP20115241B (enExample) |
| IL (1) | IL198154A (enExample) |
| MA (1) | MA30890B1 (enExample) |
| ME (1) | MEP11809A (enExample) |
| MX (1) | MX2009003972A (enExample) |
| MY (1) | MY158052A (enExample) |
| NO (1) | NO20091948L (enExample) |
| NZ (1) | NZ576570A (enExample) |
| PE (1) | PE20090884A1 (enExample) |
| RU (1) | RU2454415C9 (enExample) |
| TN (1) | TN2009000129A1 (enExample) |
| TW (1) | TWI460176B (enExample) |
| UA (1) | UA97257C2 (enExample) |
| WO (1) | WO2008050821A1 (enExample) |
| ZA (1) | ZA200902585B (enExample) |
Families Citing this family (89)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101511074B1 (ko) * | 2007-04-16 | 2015-04-13 | 애브비 인코포레이티드 | 7-치환된 인돌 Mcl-1 억제제 |
| JPWO2008136428A1 (ja) | 2007-04-27 | 2010-07-29 | 武田薬品工業株式会社 | 含窒素5員複素環化合物 |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EP2178870B1 (en) * | 2007-08-17 | 2018-09-19 | LG Chem, Ltd. | Indole and indazole compounds as an inhibitor of cellular necrosis |
| RU2450001C2 (ru) * | 2007-12-20 | 2012-05-10 | Эл Джи Лайф Сайенсиз Лтд. | Активаторы глюкокиназы и фармацевтические композиции, содержащие их в качестве активного ингредиента |
| KR101098583B1 (ko) * | 2008-01-04 | 2011-12-26 | 주식회사 엘지생명과학 | 세포, 조직 및 장기 보존 효과를 갖는 인돌 및 인다졸 유도체 |
| WO2009097995A1 (de) * | 2008-02-07 | 2009-08-13 | Sanofi-Aventis | Neue phenyl-substituierte imidazolidine, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| CA2720686A1 (en) | 2008-04-10 | 2009-10-15 | Takeda Pharmaceutical Company Limited | Fused ring compounds and use thereof |
| WO2009128481A1 (ja) * | 2008-04-16 | 2009-10-22 | 武田薬品工業株式会社 | 含窒素5員複素環化合物 |
| AR072297A1 (es) * | 2008-06-27 | 2010-08-18 | Novartis Ag | Derivados de indol-2-il-piridin-3-ilo, composicion farmaceutica que los comprende y su uso en medicamentos para el tratamiento de enfermedades mediadas por la sintasa aldosterona. |
| WO2010021686A1 (en) * | 2008-08-18 | 2010-02-25 | Promega Corporation | Luminogenic compounds and methods to detect cytochrome p450 3a enzymes |
| TW201014850A (en) | 2008-09-25 | 2010-04-16 | Takeda Pharmaceutical | Solid pharmaceutical composition |
| JP5535931B2 (ja) | 2008-10-27 | 2014-07-02 | 武田薬品工業株式会社 | 二環性化合物 |
| US8557805B2 (en) | 2008-12-29 | 2013-10-15 | Takeda Pharmaceutical Company Limited | Fused ring compound and use thereof |
| WO2010117085A1 (en) * | 2009-04-09 | 2010-10-14 | Banyu Pharmaceutical Co.,Ltd. | Aryl indole derivatives |
| US20120172351A1 (en) | 2009-06-09 | 2012-07-05 | Nobuyuki Negoro | Novel fused cyclic compound and use thereof |
| CN102548556A (zh) | 2009-07-28 | 2012-07-04 | 武田药品工业株式会社 | 片剂 |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| UY33354A (es) | 2010-04-27 | 2011-12-01 | Takeda Pharmaceutical | Compuesto biciclico como inhibidor acc |
| CN103068816B (zh) | 2010-06-16 | 2015-01-07 | 武田药品工业株式会社 | 酰胺化合物的结晶 |
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