JP2013537905A5 - - Google Patents
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- Publication number
- JP2013537905A5 JP2013537905A5 JP2013530121A JP2013530121A JP2013537905A5 JP 2013537905 A5 JP2013537905 A5 JP 2013537905A5 JP 2013530121 A JP2013530121 A JP 2013530121A JP 2013530121 A JP2013530121 A JP 2013530121A JP 2013537905 A5 JP2013537905 A5 JP 2013537905A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- pharmaceutically acceptable
- acceptable salt
- interleukin
- additional
- 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.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 4
- 239000011780 sodium chloride Substances 0.000 claims 4
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 201000009910 diseases by infectious agent Diseases 0.000 claims 2
- 229920000160 (ribonucleotides)n+m Polymers 0.000 claims 1
- DKNWSYNQZKUICI-UHFFFAOYSA-N Amantadine Chemical compound C1C(C2)CC3CC2CC1(N)C3 DKNWSYNQZKUICI-UHFFFAOYSA-N 0.000 claims 1
- 229960003805 Amantadine Drugs 0.000 claims 1
- 108020005544 Antisense RNA Proteins 0.000 claims 1
- DOUYETYNHWVLEO-UHFFFAOYSA-N Imiquimod Chemical compound C1=CC=CC2=C3N(CC(C)C)C=NC3=C(N)N=C21 DOUYETYNHWVLEO-UHFFFAOYSA-N 0.000 claims 1
- HAEJPQIATWHALX-KQYNXXCUSA-N Inosine triphosphate Chemical compound O[C@@H]1[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O[C@H]1N1C(N=CNC2=O)=C2N=C1 HAEJPQIATWHALX-KQYNXXCUSA-N 0.000 claims 1
- 102000014150 Interferons Human genes 0.000 claims 1
- 108010050904 Interferons Proteins 0.000 claims 1
- 102000013462 Interleukin-12 Human genes 0.000 claims 1
- 108010065805 Interleukin-12 Proteins 0.000 claims 1
- 229940117681 Interleukin-12 Drugs 0.000 claims 1
- 102000000588 Interleukin-2 Human genes 0.000 claims 1
- 108010002350 Interleukin-2 Proteins 0.000 claims 1
- 229940100601 Interleukin-6 Drugs 0.000 claims 1
- 102000004889 Interleukin-6 Human genes 0.000 claims 1
- 108090001005 Interleukin-6 Proteins 0.000 claims 1
- 102000004316 Oxidoreductases Human genes 0.000 claims 1
- 108090000854 Oxidoreductases Proteins 0.000 claims 1
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical compound N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 claims 1
- 229960000329 Ribavirin Drugs 0.000 claims 1
- UBCHPRBFMUDMNC-UHFFFAOYSA-N Rimantadine Chemical compound C1C(C2)CC3CC2CC1(C(N)C)C3 UBCHPRBFMUDMNC-UHFFFAOYSA-N 0.000 claims 1
- 210000003283 T-Lymphocytes, Helper-Inducer Anatomy 0.000 claims 1
- 229920002847 antisense RNA Polymers 0.000 claims 1
- 239000003184 complementary RNA Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 230000002708 enhancing Effects 0.000 claims 1
- 210000002443 helper T lymphocyte Anatomy 0.000 claims 1
- 229960002751 imiquimod Drugs 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 230000002401 inhibitory effect Effects 0.000 claims 1
- 230000002452 interceptive Effects 0.000 claims 1
- 229940079322 interferon Drugs 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 229960000888 rimantadine Drugs 0.000 claims 1
- 0 C*C(N[C@@](C1CCOCC1)C(N([C@]1[C@](C2)[C@]1C)[C@@]2c1cnc(-c(cc2)ccc2C#Cc(cc2)ccc2-c2ncc([C@](C[C@@]3[C@@]4[C@]3C)N4C([C@](C3CCOCC3)NC(O)=O)=O)[n]2)[n]1)=O)=O Chemical compound C*C(N[C@@](C1CCOCC1)C(N([C@]1[C@](C2)[C@]1C)[C@@]2c1cnc(-c(cc2)ccc2C#Cc(cc2)ccc2-c2ncc([C@](C[C@@]3[C@@]4[C@]3C)N4C([C@](C3CCOCC3)NC(O)=O)=O)[n]2)[n]1)=O)=O 0.000 description 2
- MNKIODQOJLMNMB-LKOLDZRLSA-N C[C@H]([C@@H]1C2)[C@H]1N[C@@H]2c1cnc(-c(cc2)ccc2C#Cc(cc2)ccc2-c2ncc([C@H]3N[C@@H](C4)[C@]4(C)C3)[nH]2)[nH]1 Chemical compound C[C@H]([C@@H]1C2)[C@H]1N[C@@H]2c1cnc(-c(cc2)ccc2C#Cc(cc2)ccc2-c2ncc([C@H]3N[C@@H](C4)[C@]4(C)C3)[nH]2)[nH]1 MNKIODQOJLMNMB-LKOLDZRLSA-N 0.000 description 1
- HCDZFGVDKDJPSH-ZTRUCFIOSA-N C[C@H]([C@@H]1C[C@H]2c3cnc(-c(cc4)ccc4C#Cc(cc4)ccc4-c4ncc([C@H]5N[C@@H](C6)[C@@]6(C)C5)[nH]4)[nH]3)[C@H]1N2C(OC(C)(C)C)=O Chemical compound C[C@H]([C@@H]1C[C@H]2c3cnc(-c(cc4)ccc4C#Cc(cc4)ccc4-c4ncc([C@H]5N[C@@H](C6)[C@@]6(C)C5)[nH]4)[nH]3)[C@H]1N2C(OC(C)(C)C)=O HCDZFGVDKDJPSH-ZTRUCFIOSA-N 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2010/050138 WO2012039717A1 (en) | 2010-09-24 | 2010-09-24 | Hepatitis c virus inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013537905A JP2013537905A (ja) | 2013-10-07 |
| JP2013537905A5 true JP2013537905A5 (de) | 2013-11-14 |
| JP5619289B2 JP5619289B2 (ja) | 2014-11-05 |
Family
ID=43037168
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013530121A Expired - Fee Related JP5619289B2 (ja) | 2010-09-24 | 2010-09-24 | Ｃ型肝炎ウイルス阻害剤 |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP2619195A1 (de) |
| JP (1) | JP5619289B2 (de) |
| CN (1) | CN103249730A (de) |
| BR (1) | BR112013008148A2 (de) |
| CA (1) | CA2812699A1 (de) |
| EA (1) | EA201370078A1 (de) |
| MX (1) | MX2013002927A (de) |
| WO (1) | WO2012039717A1 (de) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2737601C (en) | 2009-06-11 | 2014-10-21 | Abbott Laboratories | Anti-viral compounds |
| US8937150B2 (en) | 2009-06-11 | 2015-01-20 | Abbvie Inc. | Anti-viral compounds |
| CA2767887A1 (en) | 2009-07-16 | 2011-01-20 | Vertex Pharmaceuticals Incorporated | Benzimidazole analogues for the treatment or prevention of flavivirus infections |
| EP2550267A1 (de) | 2010-03-24 | 2013-01-30 | Vertex Pharmaceuticals Incorporated | Analoga zur behandlung oder vorbeugung von flavivirus-infektionen |
| NZ605440A (en) | 2010-06-10 | 2014-05-30 | Abbvie Bahamas Ltd | Solid compositions comprising an hcv inhibitor |
| EP2616461A4 (de) | 2010-08-26 | 2014-03-26 | Rfs Pharma Llc | Potente und selektive inhibitoren des hepatitis-c-virus |
| US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
| WO2013030750A1 (en) | 2011-09-01 | 2013-03-07 | Lupin Limited | Antiviral compounds |
| US9034832B2 (en) | 2011-12-29 | 2015-05-19 | Abbvie Inc. | Solid compositions |
| US9073943B2 (en) | 2012-02-10 | 2015-07-07 | Lupin Limited | Antiviral compounds with a dibenzooxaheterocycle moiety |
| DK2855453T3 (en) | 2012-06-04 | 2017-02-06 | Actelion Pharmaceuticals Ltd | Benzimidazol-proline derivatives |
| BR112015007516A2 (pt) | 2012-10-10 | 2017-07-04 | Actelion Pharmaceuticals Ltd | antagonistas do receptor de orexina que são derivados de [orto bi-(hetero-)aril]-[2-(meta bi-(hetero-)aril)- pirrolidin-1-il]-metanona |
| EP2970241A1 (de) | 2013-03-12 | 2016-01-20 | Actelion Pharmaceuticals Ltd. | Azetidinamidderivate als orexinrezeptor-antagonisten |
| US11484534B2 (en) | 2013-03-14 | 2022-11-01 | Abbvie Inc. | Methods for treating HCV |
| KR102330133B1 (ko) | 2013-12-04 | 2021-11-23 | 이도르시아 파마슈티컬스 리미티드 | 벤즈이미다졸-프롤린 유도체의 용도 |
| WO2015103490A1 (en) | 2014-01-03 | 2015-07-09 | Abbvie, Inc. | Solid antiviral dosage forms |
| JP7146797B2 (ja) | 2017-03-31 | 2022-10-04 | シンジェンタ パーティシペーションズ アーゲー | 殺菌性組成物 |
| GB201803342D0 (en) | 2018-03-01 | 2018-04-18 | Medimmune Ltd | Methods |
| GB201806022D0 (en) | 2018-04-12 | 2018-05-30 | Medimmune Ltd | Pyrrolobenzodiazepines and conjugates thereof |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
| WO2004014852A2 (en) | 2002-08-12 | 2004-02-19 | Bristol-Myers Squibb Company | Iminothiazolidinones as inhibitors of hcv replication |
| US7420079B2 (en) | 2002-12-09 | 2008-09-02 | Bristol-Myers Squibb Company | Methods and compounds for producing dipeptidyl peptidase IV inhibitors and intermediates thereof |
| US7135462B2 (en) | 2003-11-20 | 2006-11-14 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| DE102004036971B4 (de) | 2004-07-30 | 2009-07-30 | Advanced Micro Devices, Inc., Sunnyvale | Technik zur Bewertung lokaler elektrischer Eigenschaften in Halbleiterbauelementen |
| US8303944B2 (en) | 2006-08-11 | 2012-11-06 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8329159B2 (en) * | 2006-08-11 | 2012-12-11 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| JP2010034721A (ja) * | 2008-07-28 | 2010-02-12 | Fujitsu Ltd | パケットキャプチャ装置，パケットキャプチャ方法およびパケットキャプチャプログラム |
| CA2745119A1 (en) * | 2008-12-03 | 2010-06-10 | Presidio Pharmaceuticals, Inc. | Inhibitors of hcv ns5a |
| US8796466B2 (en) * | 2009-03-30 | 2014-08-05 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
| US8138215B2 (en) * | 2009-05-29 | 2012-03-20 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
-
2010
- 2010-09-24 CN CN2010800703399A patent/CN103249730A/zh active Pending
- 2010-09-24 JP JP2013530121A patent/JP5619289B2/ja not_active Expired - Fee Related
- 2010-09-24 EA EA201370078A patent/EA201370078A1/ru unknown
- 2010-09-24 MX MX2013002927A patent/MX2013002927A/es not_active Application Discontinuation
- 2010-09-24 EP EP10761101.4A patent/EP2619195A1/de not_active Withdrawn
- 2010-09-24 CA CA2812699A patent/CA2812699A1/en not_active Abandoned
- 2010-09-24 BR BR112013008148A patent/BR112013008148A2/pt not_active IP Right Cessation
- 2010-09-24 WO PCT/US2010/050138 patent/WO2012039717A1/en active Application Filing
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