JP2011518835A5 - - Google Patents
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- JP2011518835A5 JP2011518835A5 JP2011506429A JP2011506429A JP2011518835A5 JP 2011518835 A5 JP2011518835 A5 JP 2011518835A5 JP 2011506429 A JP2011506429 A JP 2011506429A JP 2011506429 A JP2011506429 A JP 2011506429A JP 2011518835 A5 JP2011518835 A5 JP 2011518835A5
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- alkyl
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- 150000001875 compounds Chemical class 0.000 claims description 46
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 24
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 14
- 239000003814 drug Substances 0.000 claims description 14
- 239000003112 inhibitor Substances 0.000 claims description 14
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 229910052736 halogen Inorganic materials 0.000 claims description 10
- 150000002367 halogens Chemical class 0.000 claims description 10
- 229910052717 sulfur Inorganic materials 0.000 claims description 10
- 241000700605 Viruses Species 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 150000001721 carbon Chemical group 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 8
- 229940124597 therapeutic agent Drugs 0.000 claims description 8
- 230000009385 viral infection Effects 0.000 claims description 8
- 208000036142 Viral infection Diseases 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 125000005884 carbocyclylalkyl group Chemical group 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 6
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 6
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 6
- 125000003107 substituted aryl group Chemical group 0.000 claims description 6
- 101001023866 Arabidopsis thaliana Mannosyl-oligosaccharide glucosidase GCS1 Proteins 0.000 claims description 4
- 241000710780 Bovine viral diarrhea virus 1 Species 0.000 claims description 4
- 241000725619 Dengue virus Species 0.000 claims description 4
- 241000711549 Hepacivirus C Species 0.000 claims description 4
- 102000014150 Interferons Human genes 0.000 claims description 4
- 108010050904 Interferons Proteins 0.000 claims description 4
- 241000710842 Japanese encephalitis virus Species 0.000 claims description 4
- 241000710912 Kunjin virus Species 0.000 claims description 4
- 241000710908 Murray Valley encephalitis virus Species 0.000 claims description 4
- 241000725177 Omsk hemorrhagic fever virus Species 0.000 claims description 4
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical class 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 description 4
- 101800001838 Serine protease/helicase NS3 Proteins 0.000 claims description 4
- 241000710888 St. Louis encephalitis virus Species 0.000 claims description 4
- 241000710771 Tick-borne encephalitis virus Species 0.000 claims description 4
- 241000710886 West Nile virus Species 0.000 claims description 4
- 241000710772 Yellow fever virus Species 0.000 claims description 4
- 241000907316 Zika virus Species 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000000134 cyclophilin inhibitor Substances 0.000 claims description 4
- 229940079593 drug Drugs 0.000 claims description 4
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 4
- 125000001072 heteroaryl group Chemical group 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 239000002777 nucleoside Substances 0.000 claims description 4
- 150000003833 nucleoside derivatives Chemical class 0.000 claims description 4
- 239000000137 peptide hydrolase inhibitor Substances 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 229940051021 yellow-fever virus Drugs 0.000 claims description 4
- -1 —C (═O) OR 11 Chemical compound 0.000 claims description 4
- 241000710781 Flaviviridae Species 0.000 claims description 3
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229940122806 Cyclophilin inhibitor Drugs 0.000 claims description 2
- FWKQNCXZGNBPFD-UHFFFAOYSA-N Guaiazulene Chemical compound CC(C)C1=CC=C(C)C2=CC=C(C)C2=C1 FWKQNCXZGNBPFD-UHFFFAOYSA-N 0.000 claims description 2
- 208000005176 Hepatitis C Diseases 0.000 claims description 2
- 229940123066 Polymerase inhibitor Drugs 0.000 claims description 2
- 229940124158 Protease/peptidase inhibitor Drugs 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000002837 carbocyclic group Chemical group 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims description 2
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
- 230000002401 inhibitory effect Effects 0.000 claims description 2
- 229940079322 interferon Drugs 0.000 claims description 2
- 229940047124 interferons Drugs 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 9
- 238000002560 therapeutic procedure Methods 0.000 claims 2
- 0 C[C@@]1([C@](c2cnc3[n]2ncnc3N)O*(CO)[C@@]1O)O Chemical compound C[C@@]1([C@](c2cnc3[n]2ncnc3N)O*(CO)[C@@]1O)O 0.000 description 2
- 241000124008 Mammalia Species 0.000 description 2
- 108060004795 Methyltransferase Proteins 0.000 description 2
- 150000007523 nucleic acids Chemical class 0.000 description 2
- 102000039446 nucleic acids Human genes 0.000 description 2
- 108020004707 nucleic acids Proteins 0.000 description 2
- CXWJHESCXVNONN-ZQSATUNPSA-O CC(C)OC([C@H](C)NP(OC[C@H]([C@H]([C@@]1(C)O)O)O[C@H]1c1ncc(C(NC(N)=[NH2+])=O)[nH]1)(Oc(cc1)ccc1Cl)=O)=O Chemical compound CC(C)OC([C@H](C)NP(OC[C@H]([C@H]([C@@]1(C)O)O)O[C@H]1c1ncc(C(NC(N)=[NH2+])=O)[nH]1)(Oc(cc1)ccc1Cl)=O)=O CXWJHESCXVNONN-ZQSATUNPSA-O 0.000 description 1
- YBMVANKKUWKANX-MTZIDLBNSA-N C[C@@]1([C@H](C2=NNC3N2N=C(N)NC3=O)O[C@H](CO)[C@H]1O)O Chemical compound C[C@@]1([C@H](C2=NNC3N2N=C(N)NC3=O)O[C@H](CO)[C@H]1O)O YBMVANKKUWKANX-MTZIDLBNSA-N 0.000 description 1
- WQYSRGOXWKFONQ-FHZUQPTBSA-N C[C@@]1([C@H](c2cnc3[n]2nc(N)nc3N)O[C@H](CO)[C@H]1O)O Chemical compound C[C@@]1([C@H](c2cnc3[n]2nc(N)nc3N)O[C@H](CO)[C@H]1O)O WQYSRGOXWKFONQ-FHZUQPTBSA-N 0.000 description 1
- JBHVJPXLXOQTCM-FHZUQPTBSA-N C[C@@]1([C@H](c2ncc3[n]2N=C(N)NC3=O)O[C@H](CO)[C@H]1O)O Chemical compound C[C@@]1([C@H](c2ncc3[n]2N=C(N)NC3=O)O[C@H](CO)[C@H]1O)O JBHVJPXLXOQTCM-FHZUQPTBSA-N 0.000 description 1
- TXFFMYZKEICLPT-XTWHOAMZSA-N C[C@@]1([C@H](c2nnc3[n]2ncnc3N)O[C@H](CO)[C@H]1O)O Chemical compound C[C@@]1([C@H](c2nnc3[n]2ncnc3N)O[C@H](CO)[C@H]1O)O TXFFMYZKEICLPT-XTWHOAMZSA-N 0.000 description 1
- 208000004576 Flaviviridae Infections Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4726308P | 2008-04-23 | 2008-04-23 | |
| US61/047,263 | 2008-04-23 | ||
| US13944908P | 2008-12-19 | 2008-12-19 | |
| US61/139,449 | 2008-12-19 | ||
| PCT/US2009/041432 WO2009132123A1 (en) | 2008-04-23 | 2009-04-22 | Carba-nucleoside analogs for antiviral treatment |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013218139A Division JP2014012739A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のためのカルバ−ヌクレオシドアナログ |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011518835A JP2011518835A (ja) | 2011-06-30 |
| JP2011518835A5 true JP2011518835A5 (OSRAM) | 2013-03-21 |
| JP5425186B2 JP5425186B2 (ja) | 2014-02-26 |
Family
ID=40887058
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011506435A Active JP5425187B2 (ja) | 2008-04-23 | 2009-04-22 | 抗ウイルス処置のための１’−置換カルバ−ヌクレオシドアナログ |
| JP2011506429A Active JP5425186B2 (ja) | 2008-04-23 | 2009-04-22 | 抗ウイルス処置のためのカルバ−ヌクレオシドアナログ |
| JP2013218139A Withdrawn JP2014012739A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のためのカルバ−ヌクレオシドアナログ |
| JP2013218129A Withdrawn JP2014040471A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のための１’−置換カルバ−ヌクレオシドアナログ |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011506435A Active JP5425187B2 (ja) | 2008-04-23 | 2009-04-22 | 抗ウイルス処置のための１’−置換カルバ−ヌクレオシドアナログ |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013218139A Withdrawn JP2014012739A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のためのカルバ−ヌクレオシドアナログ |
| JP2013218129A Withdrawn JP2014040471A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のための１’−置換カルバ−ヌクレオシドアナログ |
Country Status (32)
| Country | Link |
|---|---|
| US (5) | US8008264B2 (OSRAM) |
| EP (3) | EP2268642B1 (OSRAM) |
| JP (4) | JP5425187B2 (OSRAM) |
| KR (3) | KR101681559B1 (OSRAM) |
| CN (3) | CN102015714B (OSRAM) |
| AP (2) | AP3237A (OSRAM) |
| AR (1) | AR071395A1 (OSRAM) |
| AU (2) | AU2009240642B2 (OSRAM) |
| BR (2) | BRPI0910455B8 (OSRAM) |
| CA (2) | CA2722084C (OSRAM) |
| CO (2) | CO6321235A2 (OSRAM) |
| CY (4) | CY1113647T1 (OSRAM) |
| DK (3) | DK2268642T3 (OSRAM) |
| EA (2) | EA019883B1 (OSRAM) |
| EC (2) | ECSP10010609A (OSRAM) |
| ES (3) | ES2398684T3 (OSRAM) |
| HR (3) | HRP20130048T1 (OSRAM) |
| HU (3) | HUE025528T2 (OSRAM) |
| IL (2) | IL208515A (OSRAM) |
| LT (2) | LT2937350T (OSRAM) |
| LU (1) | LUC00193I2 (OSRAM) |
| ME (1) | ME03089B (OSRAM) |
| MX (2) | MX2010011659A (OSRAM) |
| NO (1) | NO2937350T3 (OSRAM) |
| NZ (2) | NZ588670A (OSRAM) |
| PL (3) | PL2268642T3 (OSRAM) |
| PT (3) | PT2937350T (OSRAM) |
| RS (2) | RS57092B1 (OSRAM) |
| SI (3) | SI2268642T1 (OSRAM) |
| TW (2) | TW201334784A (OSRAM) |
| WO (2) | WO2009132135A1 (OSRAM) |
| ZA (2) | ZA201007713B (OSRAM) |
Families Citing this family (187)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY164523A (en) | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
| CA2410579C (en) | 2000-05-26 | 2010-04-20 | Jean-Pierre Sommadossi | Methods and compositions for treating flaviviruses and pestiviruses |
| JP2006519753A (ja) | 2002-11-15 | 2006-08-31 | イデニクス（ケイマン）リミテツド | ２’−分枝ヌクレオシドおよびフラビウイルス科ウイルス突然変異 |
| CN102015714B (zh) | 2008-04-23 | 2014-09-24 | 吉里德科学公司 | 用于抗病毒治疗的1’-取代的carba-核苷类似物 |
| US8173621B2 (en) | 2008-06-11 | 2012-05-08 | Gilead Pharmasset Llc | Nucleoside cyclicphosphates |
| WO2010002877A2 (en) * | 2008-07-03 | 2010-01-07 | Biota Scientific Management | Bycyclic nucleosides and nucleotides as therapeutic agents |
| CA2745295C (en) | 2008-12-09 | 2017-01-10 | Gilead Sciences, Inc. | Modulators of toll-like receptors |
| CL2009002207A1 (es) | 2008-12-23 | 2011-02-18 | Gilead Pharmasset Llc | Compuestos derivados de 3-hidroxi-5-(9h-purin-9-il)tetrahidrofuran-2-il, inhibidor de la replicacion de arn viral dependiente de arn; composicion farmaceutica; uso para el tratamiento de hepatitis c. |
| CL2009002208A1 (es) | 2008-12-23 | 2010-10-29 | Gilead Pharmasset Llc | Un compuesto (2s)-2-((((2r,3r,4r,5r)-5-(2-amino-6-etoxi-9h-purin-9-il)-4-fluoro-3-hidroxi-4-metiltetrahidrofuran-2-il)metoxi)(hidroxi)fosforilamino)propanoico, inhibidores de la replicacion de arn viral; composicion farmaceutica; y su uso en el tratamiento de infeccion por hepatitis c, virus del nilo occidental, entre otras. |
| KR20110104074A (ko) | 2008-12-23 | 2011-09-21 | 파마셋 인코포레이티드 | 퓨린 뉴클레오시드의 합성 |
| US8618076B2 (en) | 2009-05-20 | 2013-12-31 | Gilead Pharmasset Llc | Nucleoside phosphoramidates |
| TWI583692B (zh) | 2009-05-20 | 2017-05-21 | 基利法瑪席特有限責任公司 | 核苷磷醯胺 |
| US7973013B2 (en) | 2009-09-21 | 2011-07-05 | Gilead Sciences, Inc. | 2'-fluoro substituted carba-nucleoside analogs for antiviral treatment |
| US8455451B2 (en) * | 2009-09-21 | 2013-06-04 | Gilead Sciences, Inc. | 2'-fluoro substituted carba-nucleoside analogs for antiviral treatment |
| BR112012006180A2 (pt) | 2009-09-21 | 2015-09-08 | Gilead Sciences Inc | processos e intermediários para a preparação de análogos de 1'-substituido carba-nucleosídeo |
| SMT201700091T1 (it) * | 2009-09-21 | 2017-03-08 | Gilead Sciences Inc | ANALOGHI CARBA-NUCLEOSIDlCI2'-FLUORO SOSTITUITI PER TRATTAMENTO ANTIVIRALE |
| EA020847B1 (ru) | 2009-10-30 | 2015-02-27 | Янссен Фармацевтика Нв | ПРОИЗВОДНЫЕ ИМИДАЗО[1,2-b]ПИРИДАЗИНА И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ ИНГИБИТОРОВ PDE10 |
| AR080754A1 (es) | 2010-03-09 | 2012-05-09 | Janssen Pharmaceutica Nv | Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10 |
| MX2012011171A (es) * | 2010-03-31 | 2013-02-01 | Gilead Pharmasset Llc | Fosforamidatos de nucleosido. |
| TW201201815A (en) * | 2010-05-28 | 2012-01-16 | Gilead Sciences Inc | 1'-substituted-carba-nucleoside prodrugs for antiviral treatment |
| PT2596004E (pt) | 2010-07-19 | 2014-11-28 | Gilead Sciences Inc | Métodos para a preparação de pró-fármacos de fosforamidato diastereomericamente puros |
| SG186830A1 (en) * | 2010-07-22 | 2013-02-28 | Gilead Sciences Inc | Methods and compounds for treating paramyxoviridae virus infections |
| TW201305185A (zh) | 2010-09-13 | 2013-02-01 | Gilead Sciences Inc | 用於抗病毒治療之２’－氟取代之碳－核苷類似物 |
| PH12013500311B1 (en) * | 2010-09-20 | 2017-11-08 | Gilead Sciences Inc | 2' -fluoro substituted carba-nucleoside analogs for antiviral treatment |
| CA2812962C (en) | 2010-09-22 | 2020-03-31 | Alios Biopharma, Inc. | Azido nucleosides and nucleotide analogs |
| AU2011336632B2 (en) | 2010-11-30 | 2015-09-03 | Gilead Pharmasset Llc | Compounds |
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| US8877744B2 (en) * | 2011-04-04 | 2014-11-04 | Hoffmann-La Roche Inc. | 1,4-Oxazepines as BACE1 and/or BACE2 inhibitors |
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