KR20110059875A - C형 간염의 치료를 위한 화합물 - Google Patents
C형 간염의 치료를 위한 화합물 Download PDFInfo
- Publication number
- KR20110059875A KR20110059875A KR1020117008085A KR20117008085A KR20110059875A KR 20110059875 A KR20110059875 A KR 20110059875A KR 1020117008085 A KR1020117008085 A KR 1020117008085A KR 20117008085 A KR20117008085 A KR 20117008085A KR 20110059875 A KR20110059875 A KR 20110059875A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- solvent
- phenyl
- amino
- 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.)
- Ceased
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- 0 CC*C(C)(*)N Chemical compound CC*C(C)(*)N 0.000 description 4
- NVNHBPOLPPDKRC-UHFFFAOYSA-N C(C1)C2C3C1C2CC3 Chemical compound C(C1)C2C3C1C2CC3 NVNHBPOLPPDKRC-UHFFFAOYSA-N 0.000 description 1
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- IHIQMDRCORRRKP-UHFFFAOYSA-N CC(C)CNC(c(cc1-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)ccc1OCC1NCCC1)=O Chemical compound CC(C)CNC(c(cc1-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)ccc1OCC1NCCC1)=O IHIQMDRCORRRKP-UHFFFAOYSA-N 0.000 description 1
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- BHIGYNBMRJUONV-UHFFFAOYSA-N CC(C)CNC(c1cc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)ccc1-c1ccccc1OC)=O Chemical compound CC(C)CNC(c1cc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)ccc1-c1ccccc1OC)=O BHIGYNBMRJUONV-UHFFFAOYSA-N 0.000 description 1
- SNIFPAOWYDKABB-UHFFFAOYSA-N CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)cc(OCCC2CCNCC2)c1)=O Chemical compound CC(C)CNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)cc(OCCC2CCNCC2)c1)=O SNIFPAOWYDKABB-UHFFFAOYSA-N 0.000 description 1
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- VMORANHZINEZAS-UHFFFAOYSA-N CCC(CC)(c1ccccc1)NC(c(cc1)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1Cl)=O Chemical compound CCC(CC)(c1ccccc1)NC(c(cc1)cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2)c1Cl)=O VMORANHZINEZAS-UHFFFAOYSA-N 0.000 description 1
- OTQYYXHPVWYMHH-UHFFFAOYSA-N CCC(c1ccccc1)NC(c(cc1-c(cc2c(C(NC)=O)c(-c(cc3)ccc3F)[o]c2c2)c2NS(C)(=O)=O)ccc1F)=O Chemical compound CCC(c1ccccc1)NC(c(cc1-c(cc2c(C(NC)=O)c(-c(cc3)ccc3F)[o]c2c2)c2NS(C)(=O)=O)ccc1F)=O OTQYYXHPVWYMHH-UHFFFAOYSA-N 0.000 description 1
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- OHVCRBIYETYGPA-UHFFFAOYSA-N CCNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2F)c(C)cc1OC)=O Chemical compound CCNC(c1cc(-c2ccc3[o]c(-c(cc4)ccc4F)c(C(NC)=O)c3c2F)c(C)cc1OC)=O OHVCRBIYETYGPA-UHFFFAOYSA-N 0.000 description 1
- HEXZNOJVVVNIOV-UHFFFAOYSA-N CCOc1cc(C(NCC(C)C)=O)cc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)c1 Chemical compound CCOc1cc(C(NCC(C)C)=O)cc(-c(cc2)cc3c2[o]c(-c(cc2)ccc2F)c3C(NC)=O)c1 HEXZNOJVVVNIOV-UHFFFAOYSA-N 0.000 description 1
- DSMFZNYMBWVYOE-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1cc(N(CCO)S(C)(=O)=O)c2-c1cccc(C(NC2(CC2)c2ccccn2)=O)c1)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1cc(N(CCO)S(C)(=O)=O)c2-c1cccc(C(NC2(CC2)c2ccccn2)=O)c1)=O DSMFZNYMBWVYOE-UHFFFAOYSA-N 0.000 description 1
- JWLAIYBPTJSFJI-UHFFFAOYSA-N CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c(cc(cc1)C(NC2(CC2)c2ccccn2)=O)c1OCCN)=O Chemical compound CNC(c(c1c2)c(-c(cc3)ccc3F)[o]c1ccc2-c(cc(cc1)C(NC2(CC2)c2ccccn2)=O)c1OCCN)=O JWLAIYBPTJSFJI-UHFFFAOYSA-N 0.000 description 1
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- LZAUGCMVNLZVJV-UHFFFAOYSA-N Cc(c(-c(ccc1c2c(C(NC)=O)c(-c(cc3)ccc3F)[o]1)c2F)c1)ccc1C(NC1(CC1)c1ncccn1)=O Chemical compound Cc(c(-c(ccc1c2c(C(NC)=O)c(-c(cc3)ccc3F)[o]1)c2F)c1)ccc1C(NC1(CC1)c1ncccn1)=O LZAUGCMVNLZVJV-UHFFFAOYSA-N 0.000 description 1
- GCPTXARPKLFJAL-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)cc(-c2ccccc2Cl)c1C(OC)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)cc(-c2ccccc2Cl)c1C(OC)=O GCPTXARPKLFJAL-UHFFFAOYSA-N 0.000 description 1
- DIDNPWXWHTUCSB-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)cc(OC)c1C(NC1(CC1)C(NO)=N)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)cc(OC)c1C(NC1(CC1)C(NO)=N)=O DIDNPWXWHTUCSB-UHFFFAOYSA-N 0.000 description 1
- CFWXKDOVALSOLA-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC#C)CC1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC#C)CC1)=O CFWXKDOVALSOLA-UHFFFAOYSA-N 0.000 description 1
- NCCRXFSIWURJAR-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)C(NN)=O)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)C(NN)=O)=O NCCRXFSIWURJAR-UHFFFAOYSA-N 0.000 description 1
- DITJBPJLGLTIOY-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c(cc1)ccc1F)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c(cc1)ccc1F)=O DITJBPJLGLTIOY-UHFFFAOYSA-N 0.000 description 1
- UCBDIOKDLDLARK-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1cncnc1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1cncnc1)=O UCBDIOKDLDLARK-UHFFFAOYSA-N 0.000 description 1
- XYSVTMJUTXGIGZ-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nc(-c2ncccc2)n[o]1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nc(-c2ncccc2)n[o]1)=O XYSVTMJUTXGIGZ-UHFFFAOYSA-N 0.000 description 1
- KCWQOCLBLVNNLJ-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1ncccc1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1ncccc1)=O KCWQOCLBLVNNLJ-UHFFFAOYSA-N 0.000 description 1
- GNXIYUQMCFGQHP-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nnc(-c(cc2)ccc2Cl)[nH]1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nnc(-c(cc2)ccc2Cl)[nH]1)=O GNXIYUQMCFGQHP-UHFFFAOYSA-N 0.000 description 1
- GZZOXXYWQBNESD-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nnc(-c2ccccc2)[nH]1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nnc(-c2ccccc2)[nH]1)=O GZZOXXYWQBNESD-UHFFFAOYSA-N 0.000 description 1
- XDRVWQKGDRXTTO-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nnc(-c2ccncc2)[nH]1)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)c1)ccc1C(NC1(CC1)c1nnc(-c2ccncc2)[nH]1)=O XDRVWQKGDRXTTO-UHFFFAOYSA-N 0.000 description 1
- IGUDKPSFDSIFKP-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)cc(C(NC1(CC1)c1ncccc1)=O)c1)c1OCc1ccccc1 Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1)cc(C(NC1(CC1)c1ncccc1)=O)c1)c1OCc1ccccc1 IGUDKPSFDSIFKP-UHFFFAOYSA-N 0.000 description 1
- ZOKLTPBWPHADTF-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1F)c1)cc(OC)c1C(OC)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1F)c1)cc(OC)c1C(OC)=O ZOKLTPBWPHADTF-UHFFFAOYSA-N 0.000 description 1
- ZAYQIBAADVPTHC-UHFFFAOYSA-N Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1F)c1)ccc1C(O)=O Chemical compound Cc(c(-c1ccc2[o]c(-c(cc3)ccc3F)c(C(NC)=O)c2c1F)c1)ccc1C(O)=O ZAYQIBAADVPTHC-UHFFFAOYSA-N 0.000 description 1
- PCNNOOGFYLVQSM-UHFFFAOYSA-N Cc(ccc(C(NC1(CC1)c1nnc(C2CC2)[nH]1)=O)c1)c1-c(cc1)cc2c1[o]c(-c(cc1)ccc1F)c2C(NC)=O Chemical compound Cc(ccc(C(NC1(CC1)c1nnc(C2CC2)[nH]1)=O)c1)c1-c(cc1)cc2c1[o]c(-c(cc1)ccc1F)c2C(NC)=O PCNNOOGFYLVQSM-UHFFFAOYSA-N 0.000 description 1
- OGSRNIZJAGWQSF-UHFFFAOYSA-N Cc1ccc(C(OC)=O)c(F)c1-c(cc1)cc2c1[o]c(-c(cc1)ccc1F)c2C(NC)=O Chemical compound Cc1ccc(C(OC)=O)c(F)c1-c(cc1)cc2c1[o]c(-c(cc1)ccc1F)c2C(NC)=O OGSRNIZJAGWQSF-UHFFFAOYSA-N 0.000 description 1
- JXYCXMPXYPIJBO-UHFFFAOYSA-N Cc1cnc(C2(CC2)NC(c(cc(c(C)c2)-c3ccc4[o]c(-c(cc5)ccc5F)c(C(NC)=O)c4c3)c2OC)=O)[s]1 Chemical compound Cc1cnc(C2(CC2)NC(c(cc(c(C)c2)-c3ccc4[o]c(-c(cc5)ccc5F)c(C(NC)=O)c4c3)c2OC)=O)[s]1 JXYCXMPXYPIJBO-UHFFFAOYSA-N 0.000 description 1
- DMTAIGQTCPTJRW-UHFFFAOYSA-N Cc1nnc(-c2cc(-c3ccc4[o]c(-c(cc5)ccc5F)c(C(NC)=O)c4c3)ccc2)[o]1 Chemical compound Cc1nnc(-c2cc(-c3ccc4[o]c(-c(cc5)ccc5F)c(C(NC)=O)c4c3)ccc2)[o]1 DMTAIGQTCPTJRW-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/82—Benzo [b] furans; Hydrogenated benzo [b] furans 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 carbon atoms of the hetero ring
- C07D307/84—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/04—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 two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D405/02—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 two hetero rings
- C07D405/10—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 two hetero rings linked by a carbon chain containing aromatic rings
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- C07D405/02—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 two hetero rings
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- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D417/10—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 aromatic rings
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- 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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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
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- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
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| US9600508P | 2008-09-11 | 2008-09-11 | |
| US61/096,005 | 2008-09-11 |
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| US7994171B2 (en) * | 2008-09-11 | 2011-08-09 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US8198449B2 (en) * | 2008-09-11 | 2012-06-12 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| EP2361242B1 (en) | 2008-10-17 | 2018-08-01 | Oryzon Genomics, S.A. | Oxidase inhibitors and their use |
| US8399494B2 (en) * | 2008-10-30 | 2013-03-19 | Merck Sharp & Dohme Corp. | 2,5-disubstituted phenyl carboxamide orexin receptor antagonists |
| WO2010084160A1 (en) | 2009-01-21 | 2010-07-29 | Oryzon Genomics S.A. | Phenylcyclopropylamine derivatives and their medical use |
| CN102574778B (zh) * | 2009-06-22 | 2015-01-07 | 弗·哈夫曼-拉罗切有限公司 | 新的联苯基和苯基-吡啶酰胺类化合物 |
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| EP2545042A1 (en) * | 2010-03-11 | 2013-01-16 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis c |
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| RS55348B1 (sr) | 2010-04-19 | 2017-03-31 | Oryzon Gnomics S A | Inhibitori lizin specifične demetilaze-1 i njihova upotreba |
| AR082453A1 (es) | 2010-04-21 | 2012-12-12 | Novartis Ag | Compuestos de furopiridina, composiciones farmaceuticas que los contienen y usos de los mismos |
| WO2011140333A1 (en) | 2010-05-07 | 2011-11-10 | The Board Of Trustees Of The Leland Stanford Junior University | Identification of stabilizers of multimeric proteins |
| US8445497B2 (en) * | 2010-06-30 | 2013-05-21 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| EP2598480B1 (en) | 2010-07-29 | 2019-04-24 | Oryzon Genomics, S.A. | Cyclopropylamine derivatives useful as lsd1 inhibitors |
| WO2012013728A1 (en) | 2010-07-29 | 2012-02-02 | Oryzon Genomics S.A. | Arylcyclopropylamine based demethylase inhibitors of lsd1 and their medical use |
| BR112013004520A2 (pt) | 2010-08-26 | 2016-06-07 | Univ Emory | inibidores potentes e seletivos do virus da hepatite c |
| US9061966B2 (en) | 2010-10-08 | 2015-06-23 | Oryzon Genomics S.A. | Cyclopropylamine inhibitors of oxidases |
| MX2013004655A (es) | 2010-10-26 | 2013-08-27 | Presidio Pharmaceuticals Inc | Inhibidores del virus de la hepatitis c. |
| WO2012072713A2 (en) * | 2010-11-30 | 2012-06-07 | Oryzon Genomics, S.A. | Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae |
| US8507683B2 (en) * | 2010-12-09 | 2013-08-13 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| CA2822357A1 (en) | 2010-12-22 | 2012-06-28 | Abbvie Inc. | Hepatitis c inhibitors and uses thereof |
| WO2012107498A1 (en) | 2011-02-08 | 2012-08-16 | Oryzon Genomics S.A. | Lysine demethylase inhibitors for myeloproliferative disorders |
| WO2013033900A1 (en) * | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds and methods of use thereof for the treatment of viral diseases |
| WO2013033901A1 (en) * | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Heterocyclic-substituted benzofuran derivatives and methods of use thereof for the treatment of viral diseases |
| WO2013033899A1 (en) * | 2011-09-08 | 2013-03-14 | Merck Sharp & Dohme Corp. | Substituted benzofuran compounds and methods of use thereof for the treatment of viral diseases |
| MX356344B (es) | 2011-10-20 | 2018-05-23 | Oryzon Genomics Sa | Compuestos de (hetero)arilciclopropilamina como inhibidores de lsd1. |
| RU2668952C2 (ru) | 2011-10-20 | 2018-10-05 | Оризон Дженомикс, С.А. | (гетеро)арилциклопропиламины в качестве ингибиторов lsd1 |
| US9303020B2 (en) | 2012-02-08 | 2016-04-05 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| EP2831066B1 (en) | 2012-03-27 | 2016-10-05 | Bristol-Myers Squibb Company | Benzofuran derivatives for the treatment of hepatitis c |
| WO2013163466A1 (en) * | 2012-04-25 | 2013-10-31 | Presidio Pharmaceuticals, Inc. | Inhibitors of hepatitis c virus |
| US9169214B2 (en) | 2012-12-21 | 2015-10-27 | The Board Of Trustees Of The Leland Stanford Junior University | Compounds and compositions that bind and stabilize transthyretin and their use for inhibiting transthyretin amyloidosis and protein-protein interactions |
| JP2016505011A (ja) * | 2013-01-10 | 2016-02-18 | ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company | C型肝炎の治療用の大環状ベンゾフランおよびアザベンゾフラン化合物 |
| WO2014121416A1 (en) * | 2013-02-07 | 2014-08-14 | Merck Sharp & Dohme Corp. | Tetracyclic heterocycle compounds and methods of use thereof for the treatment of hepatitis c |
| US8962651B2 (en) | 2013-03-13 | 2015-02-24 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
| US9738653B2 (en) | 2013-03-14 | 2017-08-22 | Bristol-Myers Squibb Company | Fused furans for the treatment of hepatitis C |
| WO2014205593A1 (en) | 2013-06-24 | 2014-12-31 | Merck Sharp & Dohme Corp. | Substituted benzofuran compounds and methods of use thereof for treatment of viral diseases |
| WO2015088958A1 (en) * | 2013-12-13 | 2015-06-18 | Bristol-Myers Squibb Company | A novel compound for the treatment of hepatitis c |
| WO2015143256A1 (en) * | 2014-03-21 | 2015-09-24 | Bristol-Myers Squibb Company | Cyanoamino (aza)benzofuran compounds for the treatment of hepatitis c |
| SG11201607750PA (en) * | 2014-03-21 | 2016-10-28 | Bristol Myers Squibb Co | Cyano containing azabenzofuran compounds for the treatment of hepatitis c |
| US20160045609A1 (en) | 2014-08-14 | 2016-02-18 | Mamoun M. Alhamadsheh | Conjugation of pharmaceutically active agents with transthyretin ligands through adjustable linkers to increase serum half-life |
| US10087167B2 (en) | 2015-02-19 | 2018-10-02 | Bristol-Myers Squibb Company | Benzofurans substituted with secondary benzamide as HCV inhibitors |
| US10570108B2 (en) | 2015-02-19 | 2020-02-25 | Bristol-Myers Squibb Company | Substituted benzofuran compounds for the treatment of hepatitis C |
| WO2016133961A1 (en) * | 2015-02-19 | 2016-08-25 | Bristol-Myers Squibb Company | Benzofurans substituted with bicyclic secondary benzamide as hcv inhibitors |
| US10131645B2 (en) | 2015-02-19 | 2018-11-20 | Bristol-Myers Squibb Company | Benzofurans substituted with primary benzamide as HCV inhibitors |
| WO2016137832A1 (en) * | 2015-02-23 | 2016-09-01 | Bristol-Myers Squibb Company | Novel compounds for the treatment of hepatitis c |
| US11161837B2 (en) | 2016-03-21 | 2021-11-02 | Bristol-Myers Squibb Company | Benzofuran derivatives for the treatment of hepatitis C |
| KR102874295B1 (ko) | 2017-02-17 | 2025-10-20 | 에이도스 테라퓨틱스, 인코포레이티드 | Ag-10, 이의 중간체, 및 이의 염을 제조하는 방법 |
| KR102512548B1 (ko) | 2017-12-22 | 2023-03-22 | 삼성디스플레이 주식회사 | 유기 전계 발광 소자 및 유기 전계 발광 소자용 함질소 화합물 |
| US11058668B2 (en) | 2018-03-23 | 2021-07-13 | Eidos Therapeutics, Inc. | Methods of treating TTR amyloidosis using AG10 |
| IL325404A (en) | 2018-08-17 | 2026-02-01 | Eidos Therapeutics Inc | Spice formulations containing 3-(3-(5,3-dimethyl-1h-pyrazol-4-yl)propoxy)-4-fluorobenzoic acid |
| WO2020113094A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| CN114174283B (zh) * | 2019-07-18 | 2023-05-12 | 石药集团中奇制药技术(石家庄)有限公司 | 作为nmt抑制剂的化合物及其应用 |
| WO2025147320A1 (en) * | 2024-01-03 | 2025-07-10 | Kymera Therapeutics, Inc. | Stat6 inhibitors and uses thereof |
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| JPS57123181A (en) | 1981-01-23 | 1982-07-31 | Mitsubishi Paper Mills Ltd | Preparation of pyrazolo (1,5-a) pyridine derivative |
| PE20020506A1 (es) | 2000-08-22 | 2002-07-09 | Glaxo Group Ltd | Derivados de pirazol fusionados como inhibidores de la proteina cinasa |
| WO2002078701A1 (en) | 2001-03-30 | 2002-10-10 | Smithkline Beecham Corporation | Use of pyrazolopyridines as therapeutic compounds |
| CN1731993A (zh) * | 2002-11-01 | 2006-02-08 | 维洛药品公司 | 苯并呋喃化合物、组合物以及治疗和预防丙型肝炎病毒感染及相关疾病的方法 |
| US7868037B2 (en) * | 2004-07-14 | 2011-01-11 | Ptc Therapeutics, Inc. | Methods for treating hepatitis C |
| TW200815384A (en) * | 2006-08-25 | 2008-04-01 | Viropharma Inc | Combination therapy method for treating hepatitis C virus infection and pharmaceutical compositions for use therein |
| CN101687789A (zh) * | 2007-02-12 | 2010-03-31 | 因特蒙公司 | C型肝炎病毒复制的新颖抑制剂 |
| GB0707000D0 (en) | 2007-04-12 | 2007-05-30 | Istituto Di Ricerche D Biolog | Antiviral agents |
| EP2245023B1 (en) | 2008-02-14 | 2011-12-28 | F. Hoffmann-La Roche AG | Heterocyclic antiviral compounds |
| WO2009137500A1 (en) | 2008-05-05 | 2009-11-12 | Wyeth | 6-substituted benzofuran compounds to treat infection with hepatitis c virus |
| WO2009137493A1 (en) | 2008-05-05 | 2009-11-12 | Wyeth | 2-substituted benzofuran compounds to treat infection with hepatitis c virus |
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| CN102209717B (zh) | 2015-02-18 |
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| AR073740A1 (es) | 2010-12-01 |
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| ZA201105720B (en) | 2012-08-29 |
| AU2009291966B2 (en) | 2014-08-28 |
| EP2326633A1 (en) | 2011-06-01 |
| TW201014836A (en) | 2010-04-16 |
| PE20110806A1 (es) | 2011-10-31 |
| EA019185B1 (ru) | 2014-01-30 |
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