JP2006507235A5 - - Google Patents
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- Publication number
- JP2006507235A5 JP2006507235A5 JP2004526388A JP2004526388A JP2006507235A5 JP 2006507235 A5 JP2006507235 A5 JP 2006507235A5 JP 2004526388 A JP2004526388 A JP 2004526388A JP 2004526388 A JP2004526388 A JP 2004526388A JP 2006507235 A5 JP2006507235 A5 JP 2006507235A5
- Authority
- JP
- Japan
- Prior art keywords
- lower alkyl
- independently hydrogen
- hydrogen
- aryl
- alkenyl
- 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.)
- Pending
Links
- 125000000217 alkyl group Chemical group 0.000 claims 154
- 229910052739 hydrogen Inorganic materials 0.000 claims 154
- 239000001257 hydrogen Substances 0.000 claims 154
- 150000002431 hydrogen Chemical class 0.000 claims 116
- 125000003342 alkenyl group Chemical group 0.000 claims 59
- 125000003118 aryl group Chemical group 0.000 claims 59
- 229910052794 bromium Inorganic materials 0.000 claims 57
- 229910052801 chlorine Inorganic materials 0.000 claims 57
- 229910052731 fluorine Inorganic materials 0.000 claims 57
- 229910052736 halogen Inorganic materials 0.000 claims 57
- 150000002367 halogens Chemical class 0.000 claims 57
- 229910052740 iodine Inorganic materials 0.000 claims 57
- 125000003710 aryl alkyl group Chemical group 0.000 claims 50
- 125000000539 amino acid group Chemical group 0.000 claims 47
- 125000002947 alkylene group Chemical group 0.000 claims 40
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 38
- 125000003545 alkoxy group Chemical group 0.000 claims 38
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 38
- 125000002577 pseudohalo group Chemical group 0.000 claims 38
- 125000001072 heteroaryl group Chemical group 0.000 claims 31
- 125000000623 heterocyclic group Chemical group 0.000 claims 31
- 150000001875 compounds Chemical class 0.000 claims 30
- 229910052760 oxygen Inorganic materials 0.000 claims 28
- 150000003839 salts Chemical class 0.000 claims 28
- 229910052717 sulfur Inorganic materials 0.000 claims 25
- 239000003937 drug carrier Substances 0.000 claims 24
- 239000008194 pharmaceutical composition Substances 0.000 claims 22
- 125000002252 acyl group Chemical group 0.000 claims 19
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 19
- 125000000753 cycloalkyl group Chemical group 0.000 claims 19
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 19
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 19
- 208000015181 infectious disease Diseases 0.000 claims 18
- 229910052711 selenium Inorganic materials 0.000 claims 16
- -1 carbocycle Chemical group 0.000 claims 15
- 108010050904 Interferons Proteins 0.000 claims 12
- 102000014150 Interferons Human genes 0.000 claims 12
- 125000004103 aminoalkyl group Chemical group 0.000 claims 12
- 125000005001 aminoaryl group Chemical group 0.000 claims 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 12
- 229940079322 interferon Drugs 0.000 claims 12
- 239000001301 oxygen Substances 0.000 claims 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 9
- 239000003814 drug Substances 0.000 claims 9
- 239000011593 sulfur Substances 0.000 claims 9
- 125000005842 heteroatom Chemical group 0.000 claims 8
- 229940124597 therapeutic agent Drugs 0.000 claims 8
- SCVHJVCATBPIHN-SJCJKPOMSA-N (3s)-3-[[(2s)-2-[[2-(2-tert-butylanilino)-2-oxoacetyl]amino]propanoyl]amino]-4-oxo-5-(2,3,5,6-tetrafluorophenoxy)pentanoic acid Chemical compound N([C@@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)COC=1C(=C(F)C=C(F)C=1F)F)C(=O)C(=O)NC1=CC=CC=C1C(C)(C)C SCVHJVCATBPIHN-SJCJKPOMSA-N 0.000 claims 6
- 108010005716 Interferon beta-1a Proteins 0.000 claims 6
- 108010078233 Thymalfasin Proteins 0.000 claims 6
- DKNWSYNQZKUICI-UHFFFAOYSA-N amantadine Chemical compound C1C(C2)CC3CC2CC1(N)C3 DKNWSYNQZKUICI-UHFFFAOYSA-N 0.000 claims 6
- 239000003443 antiviral agent Substances 0.000 claims 6
- 229950000234 emricasan Drugs 0.000 claims 6
- PPZMYIBUHIPZOS-UHFFFAOYSA-N histamine dihydrochloride Chemical compound Cl.Cl.NCCC1=CN=CN1 PPZMYIBUHIPZOS-UHFFFAOYSA-N 0.000 claims 6
- NZVYCXVTEHPMHE-ZSUJOUNUSA-N thymalfasin Chemical compound CC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O NZVYCXVTEHPMHE-ZSUJOUNUSA-N 0.000 claims 6
- 229960004231 thymalfasin Drugs 0.000 claims 6
- 229960004295 valine Drugs 0.000 claims 6
- 108010010648 interferon alfacon-1 Proteins 0.000 claims 4
- IWUCXVSUMQZMFG-RGDLXGNYSA-N 1-[(2s,3s,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,4-triazole-3-carboxamide Chemical compound N1=C(C(=O)N)N=CN1[C@@H]1[C@@H](O)[C@@H](O)[C@H](CO)O1 IWUCXVSUMQZMFG-RGDLXGNYSA-N 0.000 claims 3
- ABEXEQSGABRUHS-UHFFFAOYSA-N 16-methylheptadecyl 16-methylheptadecanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C ABEXEQSGABRUHS-UHFFFAOYSA-N 0.000 claims 3
- 108010078049 Interferon alpha-2 Proteins 0.000 claims 3
- 108010047761 Interferon-alpha Proteins 0.000 claims 3
- 102000006992 Interferon-alpha Human genes 0.000 claims 3
- 102000003814 Interleukin-10 Human genes 0.000 claims 3
- 108090000174 Interleukin-10 Proteins 0.000 claims 3
- 241000764238 Isis Species 0.000 claims 3
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-Valine Natural products CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 3
- 125000003580 L-valyl group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(C([H])([H])[H])(C([H])([H])[H])[H] 0.000 claims 3
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical group 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 3
- 102400000800 Thymosin alpha-1 Human genes 0.000 claims 3
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 claims 3
- 229960003805 amantadine Drugs 0.000 claims 3
- 125000002619 bicyclic group Chemical group 0.000 claims 3
- 229960001340 histamine Drugs 0.000 claims 3
- 229960004931 histamine dihydrochloride Drugs 0.000 claims 3
- 102000011749 human hepatitis C immune globulin Human genes 0.000 claims 3
- 108010062138 human hepatitis C immune globulin Proteins 0.000 claims 3
- 238000005417 image-selected in vivo spectroscopy Methods 0.000 claims 3
- 238000012739 integrated shape imaging system Methods 0.000 claims 3
- 229960003521 interferon alfa-2a Drugs 0.000 claims 3
- 229960003358 interferon alfacon-1 Drugs 0.000 claims 3
- 229960004461 interferon beta-1a Drugs 0.000 claims 3
- 229940076144 interleukin-10 Drugs 0.000 claims 3
- 229940002988 pegasys Drugs 0.000 claims 3
- 108010092853 peginterferon alfa-2a Proteins 0.000 claims 3
- 229940038850 rebif Drugs 0.000 claims 3
- 229960000329 ribavirin Drugs 0.000 claims 3
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 claims 3
- NHKZSTHOYNWEEZ-AFCXAGJDSA-N taribavirin Chemical compound N1=C(C(=N)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 NHKZSTHOYNWEEZ-AFCXAGJDSA-N 0.000 claims 3
- 229950006081 taribavirin Drugs 0.000 claims 3
- 239000004474 valine Substances 0.000 claims 3
- 125000002987 valine group Chemical group [H]N([H])C([H])(C(*)=O)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 3
- 229940090438 infergen Drugs 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 0 C[C@@](C([C@@](*)(C1)O2)OC2=S)OCC1[n]1nnc(C(N2)=O)c1NC2=O Chemical compound C[C@@](C([C@@](*)(C1)O2)OC2=S)OCC1[n]1nnc(C(N2)=O)c1NC2=O 0.000 description 5
- VQJNXQICGCPJNJ-YUMJJMQISA-N CC(C)(CC12)OC1C(C[n]1n[n-]c(C(N3)=S)c11)O[C@H]2N1C3=O Chemical compound CC(C)(CC12)OC1C(C[n]1n[n-]c(C(N3)=S)c11)O[C@H]2N1C3=O VQJNXQICGCPJNJ-YUMJJMQISA-N 0.000 description 1
- KQRSVWIORINOKB-ACJOCUEISA-N CN(C(c(nn[n]1C2)c1N1[C@@H](C3O)O[C@H]2[C@@H]3O)=O)C1=O Chemical compound CN(C(c(nn[n]1C2)c1N1[C@@H](C3O)O[C@H]2[C@@H]3O)=O)C1=O KQRSVWIORINOKB-ACJOCUEISA-N 0.000 description 1
- WLJKCZVHEMOUFK-CSWMIUAYSA-N CN(C)C(C([N-][NH+](N1C[C@@H](C2)[C@@H]3O)/[O]=C(\C=C4)/N5c6c4nn[n]6C[C@H]4O[C@@H]5CC4=O)=C1N1[C@H]2C3O)=NC1=O Chemical compound CN(C)C(C([N-][NH+](N1C[C@@H](C2)[C@@H]3O)/[O]=C(\C=C4)/N5c6c4nn[n]6C[C@H]4O[C@@H]5CC4=O)=C1N1[C@H]2C3O)=NC1=O WLJKCZVHEMOUFK-CSWMIUAYSA-N 0.000 description 1
- YRGGJVPXWDISKE-RKBOWSCOSA-N O=C(C=C1)N2c3c1nn[n]3C[C@H]([C@@H]1O3)O[C@@H]2[C@H]1OC3=S Chemical compound O=C(C=C1)N2c3c1nn[n]3C[C@H]([C@@H]1O3)O[C@@H]2[C@H]1OC3=S YRGGJVPXWDISKE-RKBOWSCOSA-N 0.000 description 1
- XWHZXQKXLMRJDA-UKPFUCPKSA-N OC([C@@H](C[n]1nnc(C(N2)=S)c11)O[C@H]3N1C2=O)[C@@H]3O Chemical compound OC([C@@H](C[n]1nnc(C(N2)=S)c11)O[C@H]3N1C2=O)[C@@H]3O XWHZXQKXLMRJDA-UKPFUCPKSA-N 0.000 description 1
- BQGPSQMCORFWQS-ACJOCUEISA-N O[C@@H]([C@@H](C[n]1c2c(C(N3)=O)nc1)O[C@H]1N2C3=O)C1O Chemical compound O[C@@H]([C@@H](C[n]1c2c(C(N3)=O)nc1)O[C@H]1N2C3=O)C1O BQGPSQMCORFWQS-ACJOCUEISA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45371602P | 2002-08-01 | 2002-08-01 | |
| US60/453,716 | 2002-08-01 | ||
| PCT/US2003/024324 WO2004013300A2 (en) | 2002-08-01 | 2003-08-01 | Compounds with the bicyclo[4.2.1]nonane system for the treatment of flaviviridae infections |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006507235A JP2006507235A (ja) | 2006-03-02 |
| JP2006507235A5 true JP2006507235A5 (enExample) | 2006-09-28 |
Family
ID=31496098
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004526388A Pending JP2006507235A (ja) | 2002-08-01 | 2003-08-01 | フラビウイルス科ウイルス感染治療のためのビシクロ[4.2.1]ノナン系を有する化合物 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US8093380B2 (enExample) |
| EP (1) | EP1545545A4 (enExample) |
| JP (1) | JP2006507235A (enExample) |
| KR (1) | KR20050040912A (enExample) |
| AU (1) | AU2003257157C1 (enExample) |
| BR (1) | BR0313164A (enExample) |
| CA (1) | CA2494340C (enExample) |
| IL (1) | IL166640A0 (enExample) |
| MX (1) | MXPA05001298A (enExample) |
| SG (1) | SG174624A1 (enExample) |
| WO (1) | WO2004013300A2 (enExample) |
Families Citing this family (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IN183120B (enExample) | 1996-10-18 | 1999-09-11 | Vertex Pharma | |
| SV2003000617A (es) | 2000-08-31 | 2003-01-13 | Lilly Co Eli | Inhibidores de la proteasa peptidomimetica ref. x-14912m |
| RU2005133093A (ru) * | 2003-03-28 | 2006-07-27 | Фармассет, Инк. (Us) | Соединения для лечения флавивирусных инфекций |
| KR100883703B1 (ko) | 2003-05-30 | 2009-02-12 | 파마셋 인코포레이티드 | 변형 불소화 뉴클레오시드 유사체 |
| KR20060084845A (ko) * | 2003-07-25 | 2006-07-25 | 이데닉스 (케이만) 리미티드 | C형 간염을 포함하는 플라비비리다에를 치료하기 위한퓨린 뉴클레오시드 유사체 |
| WO2005018330A1 (en) * | 2003-08-18 | 2005-03-03 | Pharmasset, Inc. | Dosing regimen for flaviviridae therapy |
| UY28500A1 (es) | 2003-09-05 | 2005-04-29 | Vertex Pharma | Inhibidores de proteasas de serina, en particular proteasa ns3-ns4a del vhc. |
| US20050182252A1 (en) | 2004-02-13 | 2005-08-18 | Reddy K. R. | Novel 2'-C-methyl nucleoside derivatives |
| US7534767B2 (en) | 2004-06-15 | 2009-05-19 | Merck & Co., Inc. | C-purine nucleoside analogs as inhibitors of RNA-dependent RNA viral polymerase |
| RU2007102281A (ru) * | 2004-06-23 | 2008-07-27 | Айденикс (Кайман) Лимитед (Ky) | 5-аза-7-деазапуриновые производные для лечения заболеваний, связанных с flaviviridae |
| US20070265222A1 (en) | 2004-06-24 | 2007-11-15 | Maccoss Malcolm | Nucleoside Aryl Phosphoramidates for the Treatment of Rna-Dependent Rna Viral Infection |
| TW200621233A (en) | 2004-10-01 | 2006-07-01 | Vertex Pharma | HCV NS3-NS4A protease inhibition |
| MY141025A (en) | 2004-10-29 | 2010-02-25 | Vertex Pharma | Dose forms |
| US7879797B2 (en) | 2005-05-02 | 2011-02-01 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| WO2006130553A2 (en) * | 2005-06-02 | 2006-12-07 | Schering Corporation | Hcv protease inhibitors |
| US7470664B2 (en) | 2005-07-20 | 2008-12-30 | Merck & Co., Inc. | HCV NS3 protease inhibitors |
| AU2006275605B2 (en) | 2005-08-01 | 2011-01-06 | Merck Sharp & Dohme Corp. | Macrocyclic peptides as HCV NS3 protease inhibitors |
| WO2007016589A2 (en) * | 2005-08-02 | 2007-02-08 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
| US7964624B1 (en) * | 2005-08-26 | 2011-06-21 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
| AR055395A1 (es) * | 2005-08-26 | 2007-08-22 | Vertex Pharma | Compuestos inhibidores de la actividad de la serina proteasa ns3-ns4a del virus de la hepatitis c |
| US20100087388A1 (en) | 2005-10-03 | 2010-04-08 | Kotra Lakshmi P | Odcase inhibitors as anti-virals and antibiotics |
| EP2340836A1 (en) | 2006-02-27 | 2011-07-06 | Vertex Pharmceuticals Incorporated | Co-crystals comprising VX-950 and their pharmaceutical compositions |
| NZ571280A (en) | 2006-03-16 | 2011-10-28 | Vertex Pharma | Deuterated hepatitis C protease inhibitors |
| GB0609492D0 (en) | 2006-05-15 | 2006-06-21 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| GB0612423D0 (en) | 2006-06-23 | 2006-08-02 | Angeletti P Ist Richerche Bio | Therapeutic agents |
| CA2667165A1 (en) | 2006-10-24 | 2008-05-02 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
| JP5345941B2 (ja) | 2006-10-24 | 2013-11-20 | メルク・シャープ・アンド・ドーム・コーポレーション | Hcvns3プロテアーゼ阻害剤 |
| CA2667146C (en) | 2006-10-24 | 2016-01-19 | Merck & Co., Inc. | Hcv ns3 protease inhibitors |
| US20100099695A1 (en) | 2006-10-27 | 2010-04-22 | Liverton Nigel J | HCV NS3 Protease Inhibitors |
| ES2444575T3 (es) | 2006-10-27 | 2014-02-25 | Merck Sharp & Dohme Corp. | Inhibidores de la proteasa NS3 del VHC |
| ES2348687T3 (es) * | 2006-12-11 | 2010-12-10 | F. Hoffmann-La Roche Ag | Procedimiento para la preparaciã“n de derivados de 4'-azidocitidina. |
| JP2010513450A (ja) | 2006-12-20 | 2010-04-30 | イステイチユート・デイ・リチエルケ・デイ・ビオロジア・モレコラーレ・ピ・アンジエレツテイ・エツセ・ピー・アー | 抗ウイルス性インドール |
| GB0625345D0 (en) | 2006-12-20 | 2007-01-31 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| GB0625349D0 (en) | 2006-12-20 | 2007-01-31 | Angeletti P Ist Richerche Bio | Therapeutic compounds |
| CA2673649A1 (en) | 2007-01-05 | 2008-07-17 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Nucleoside aryl phosphoramidates for the treatment of rna-dependent rna viral infection |
| AU2008219704A1 (en) * | 2007-02-27 | 2008-09-04 | Vertex Pharmaceuticals Incorporated | Inhibitors of serine proteases |
| EP2463284A1 (en) * | 2007-02-27 | 2012-06-13 | Vertex Pharmceuticals Incorporated | Co-crystals and pharmaceutical compositions comprising the same |
| CN101754970B (zh) | 2007-07-17 | 2013-07-10 | P.安杰莱蒂分子生物学研究所 | 用于治疗丙型肝炎的大环吲哚衍生物 |
| WO2009010804A1 (en) | 2007-07-19 | 2009-01-22 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Macrocyclic compounds as antiviral agents |
| AU2008297015B2 (en) * | 2007-08-30 | 2013-08-22 | Vertex Pharmaceuticals Incorporated | Co-crystals and pharmaceutical compositions comprising the same |
| US8461107B2 (en) | 2008-04-28 | 2013-06-11 | Merck Sharp & Dohme Corp. | HCV NS3 protease inhibitors |
| SI2310095T1 (sl) | 2008-07-22 | 2013-01-31 | Merck Sharp & Dohme Corp. | Makrocikliäśne kuinoksalinske spojine kot hcv ns3 proteazni inhibitorji |
| WO2010082050A1 (en) | 2009-01-16 | 2010-07-22 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Macrocyclic and 7-aminoalkyl-substituted benzoxazocines for treatment of hepatitis c infections |
| GB0900914D0 (en) | 2009-01-20 | 2009-03-04 | Angeletti P Ist Richerche Bio | Antiviral agents |
| JP2012517478A (ja) | 2009-02-12 | 2012-08-02 | バーテックス ファーマシューティカルズ インコーポレイテッド | ペグ化インターフェロン、リバビリンおよびテラプレビルを含む、hcv組合せ治療剤 |
| US8828930B2 (en) | 2009-07-30 | 2014-09-09 | Merck Sharp & Dohme Corp. | Hepatitis C virus NS3 protease inhibitors |
| EP2459211A1 (en) | 2009-07-31 | 2012-06-06 | Medtronic, Inc. | Continuous subcutaneous administration of interferon- to hepatitis c infected patients |
| WO2011094489A1 (en) | 2010-01-29 | 2011-08-04 | Vertex Pharmaceuticals Incorporated | Therapies for treating hepatitis c virus infection |
| WO2011156545A1 (en) | 2010-06-09 | 2011-12-15 | Vertex Pharmaceuticals Incorporated | Viral dynamic model for hcv combination therapy |
| TW201208704A (en) | 2010-07-14 | 2012-03-01 | Vertex Pharma | Palatable pharmaceutical composition |
| WO2012109646A1 (en) | 2011-02-11 | 2012-08-16 | Vertex Pharmaceuticals Incorporated | Treatment of hcv in hiv infection patients |
| WO2013074386A2 (en) | 2011-11-15 | 2013-05-23 | Merck Sharp & Dohme Corp. | Hcv ns3 protease inhibitors |
| WO2013116339A1 (en) | 2012-01-31 | 2013-08-08 | Vertex Pharmaceuticals Incorporated | High potency formulations of vx-950 |
| EP2814816A2 (en) | 2012-02-14 | 2014-12-24 | University Of Georgia Research Foundation, Inc. | Spiro [2.4]heptanes for treatment of flaviviridae infections |
| WO2014121418A1 (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 |
| WO2014121417A1 (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 |
| CN107427530B (zh) | 2015-03-06 | 2020-09-08 | 阿堤亚制药公司 | 用于HCV治疗的β-D-2’-脱氧-2’α-氟-2’-β-C-取代的-2-改性的-N6-取代的嘌呤核苷酸 |
| WO2018013937A1 (en) | 2016-07-14 | 2018-01-18 | Atea Pharmaceuticals, Inc. | Beta-d-2'-deoxy-2'-alpha-fluoro-2'-beta-c-substituted-4'-fluoro-n6-substituted-6-amino-2-substituted purine nucleotides for the treatment of hepatitis c virus infection |
| AU2017324939B2 (en) | 2016-09-07 | 2021-10-14 | Atea Pharmaceuticals, Inc. | 2'-substituted-N6-substituted purine nucleotides for RNA virus treatment |
| US10519186B2 (en) | 2017-02-01 | 2019-12-31 | Atea Pharmaceuticals, Inc. | Nucleotide hemi-sulfate salt for the treatment of hepatitis C virus |
| KR20200140865A (ko) | 2018-04-10 | 2020-12-16 | 아테아 파마슈티컬즈, 인크. | 간경변증을 갖는 hcv 감염 환자의 치료 |
| US10874687B1 (en) | 2020-02-27 | 2020-12-29 | Atea Pharmaceuticals, Inc. | Highly active compounds against COVID-19 |
| CN117500494A (zh) | 2021-06-17 | 2024-02-02 | 阿堤亚制药公司 | 有利的抗hcv联合疗法 |
| CN116059363B (zh) * | 2021-11-01 | 2025-07-08 | 上海居知园生物技术有限公司 | 一种能有效防止sn三键结构化合物失活增靶向活性的药物组合物及其制备方法 |
Family Cites Families (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5506215A (en) * | 1987-11-03 | 1996-04-09 | Medivir Ab | 1-(3'-fluoro-2',3'-dideoxy-β-D-ribofuranosyl)-5-substituted pyrimidine nucleosides |
| US5026687A (en) | 1990-01-03 | 1991-06-25 | The United States Of America As Represented By The Department Of Health And Human Services | Treatment of human retroviral infections with 2',3'-dideoxyinosine alone and in combination with other antiviral compounds |
| FR2662165B1 (fr) | 1990-05-18 | 1992-09-11 | Univ Paris Curie | Derives nucleosidiques branches, leur procede de preparation et leur utilisation a titre de medicament. |
| JPH05140179A (ja) | 1991-11-25 | 1993-06-08 | Yamasa Shoyu Co Ltd | 9,5′‐シクロヌクレオシド誘導体および該誘導体を製造するための合成中間体 |
| ZA931934B (en) | 1992-03-18 | 1993-03-18 | Us Bioscience | Compostitions of N-(phosphonoacetyl)-L-aspartic acid and methods of their use as broad spectrum antivirals |
| DE69419244T2 (de) | 1993-02-24 | 1999-10-14 | Wang | Zusammensetzungen und methoden zur anwendung von reaktiven antiviralen polymeren |
| EP0702556B1 (en) | 1993-06-10 | 2002-10-23 | Wake Forest University | (phospho)lipids for combatting hepatitis b virus infection |
| WO1995003056A1 (en) | 1993-07-19 | 1995-02-02 | Tokyo Tanabe Company Limited | Hepatitis c virus proliferation inhibitor |
| DE4415539C2 (de) | 1994-05-03 | 1996-08-01 | Osama Dr Dr Med Omer | Pflanzen mit virustatischer und antiviraler Wirkung |
| US5830905A (en) | 1996-03-29 | 1998-11-03 | Viropharma Incorporated | Compounds, compositions and methods for treatment of hepatitis C |
| US5633388A (en) | 1996-03-29 | 1997-05-27 | Viropharma Incorporated | Compounds, compositions and methods for treatment of hepatitis C |
| US5891874A (en) | 1996-06-05 | 1999-04-06 | Eli Lilly And Company | Anti-viral compound |
| US5837257A (en) | 1996-07-09 | 1998-11-17 | Sage R&D | Use of plant extracts for treatment of HIV, HCV and HBV infections |
| US5858389A (en) | 1996-08-28 | 1999-01-12 | Shaker H. Elsherbini | Squalene is an antiviral compound for treating hepatitis C virus carriers |
| US5922757A (en) | 1996-09-30 | 1999-07-13 | The Regents Of The University Of California | Treatment and prevention of hepatic disorders |
| CA2266889A1 (en) | 1996-10-16 | 1998-04-23 | Guangyi Wang | Purine l-nucleosides, analogs and uses thereof |
| CA2267279A1 (en) | 1996-10-16 | 1998-04-23 | Devron Averett | Monocyclic l-nucleosides, analogs and uses thereof |
| IL119833A (en) | 1996-12-15 | 2001-01-11 | Lavie David | Hypericum perforatum extracts for the preparation of pharmaceutical compositions for the treatment of hepatitis |
| US5849800A (en) | 1997-03-28 | 1998-12-15 | The Penn State Research Foundation | Use of amantadine for treatment of Hepatitis C |
| AU724974B2 (en) | 1997-06-30 | 2000-10-05 | Merz Pharma Gmbh & Co. Kgaa | 1-amino-alkylcyclohexane NMDA receptor antagonists |
| FR2766189A1 (fr) * | 1997-07-17 | 1999-01-22 | Univ Picardie | Synthese regiospecifique de 5-aminoimidazol et 5-aminotriazol-1-yl desoxyglucofuranose et de leurs derives 1,5'-cyclo-5-(5'-desoxy-b-d-glucofuranosylamino), produits obtenus et leurs applications |
| US6348587B1 (en) | 1998-02-25 | 2002-02-19 | Emory University | 2′-Fluoronucleosides |
| US6833361B2 (en) | 1998-05-26 | 2004-12-21 | Ribapharm, Inc. | Nucleosides having bicyclic sugar moiety |
| CA2389745C (en) | 1999-11-04 | 2010-03-23 | Shire Biochem Inc. | Method for the treatment or prevention of flaviviridae viral infection using nucleoside analogues |
| US6495677B1 (en) | 2000-02-15 | 2002-12-17 | Kanda S. Ramasamy | Nucleoside compounds |
| AU2001235278A1 (en) | 2000-02-18 | 2001-08-27 | Shire Biochem Inc | Method for the treatment or prevention of flavivirus infections using nucleoside analogues |
| KR100974917B1 (ko) | 2000-04-13 | 2010-08-09 | 파마셋 인코포레이티드 | 간염 바이러스 감염 치료를 위한 3'- 또는2'-하이드록시메틸 치환된 뉴클레오시드 유도체 |
| MY164523A (en) | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
| AU2001272923A1 (en) | 2000-05-26 | 2001-12-11 | Idenix (Cayman) Limited | Methods and compositions for treating flaviviruses and pestiviruses |
| UA72612C2 (en) | 2000-07-06 | 2005-03-15 | Pyrido[2.3-d]pyrimidine and pyrimido[4.5-d]pyrimidine nucleoside analogues, prodrugs and method for inhibiting growth of neoplastic cells | |
| US20030008841A1 (en) | 2000-08-30 | 2003-01-09 | Rene Devos | Anti-HCV nucleoside derivatives |
| EP1411954B1 (en) | 2000-10-18 | 2010-12-15 | Pharmasset, Inc. | Modified nucleosides for treatment of viral infections and abnormal cellular proliferation |
| WO2002048165A2 (en) | 2000-12-15 | 2002-06-20 | Pharmasset Ltd. | Antiviral agents for treatment of flaviviridae infections |
| JP2004532184A (ja) | 2001-01-22 | 2004-10-21 | メルク エンド カムパニー インコーポレーテッド | Rna依存性rnaウィルスポリメラーゼ阻害薬としてのヌクレオシド誘導体 |
| EP1363927A2 (en) | 2001-03-01 | 2003-11-26 | Pharmasset Limited | Method for the synthesis of 2',3'-dideoxy-2',3'-didehydronucleosides |
| GB0112617D0 (en) | 2001-05-23 | 2001-07-18 | Hoffmann La Roche | Antiviral nucleoside derivatives |
| GB0114286D0 (en) | 2001-06-12 | 2001-08-01 | Hoffmann La Roche | Nucleoside Derivatives |
| EP1435974A4 (en) | 2001-09-28 | 2006-09-06 | Idenix Cayman Ltd | METHODS AND COMPOSITIONS FOR THE TREATMENT OF HEPATITIS C VIRUS USING 4 'MODIFIED NUCLEOSIDES |
| EP1438054A4 (en) | 2001-09-28 | 2006-07-26 | Idenix Cayman Ltd | METHODS AND COMPOSITIONS FOR TREATING FLAVIVIRUS AND PESTIVIRUS USING MODIFIED NUCLEOSIDE AT 4 'POSITION |
| CN100560073C (zh) | 2001-12-14 | 2009-11-18 | 法玛塞特公司 | 用于治疗病毒感染的n4-酰基胞嘧啶核苷 |
| WO2003051899A1 (en) | 2001-12-17 | 2003-06-26 | Ribapharm Inc. | Deazapurine nucleoside libraries and compounds |
| WO2003062256A1 (en) | 2002-01-17 | 2003-07-31 | Ribapharm Inc. | 2'-beta-modified-6-substituted adenosine analogs and their use as antiviral agents |
| EP1572705A2 (en) | 2002-01-17 | 2005-09-14 | Ribapharm, Inc. | Sugar modified nucleosides as viral replication inhibitors |
| WO2003061385A1 (en) | 2002-01-17 | 2003-07-31 | Ribapharm Inc. | Tricyclic nucleoside library compounds, synthesis, and use as antiviral agents |
| EP1480982A4 (en) | 2002-02-14 | 2007-08-01 | Pharmasset Inc | MODIFIED FLUORINATED NUCLEOSIDE ANALOGUES |
| AU2003217863B9 (en) | 2002-02-28 | 2009-10-29 | Biota Scientific Management Pty Ltd | Nucleotide mimics and their prodrugs |
| CA2484921A1 (en) | 2002-05-06 | 2003-11-13 | Genelabs Technologies, Inc. | Nucleoside derivatives for treating hepatitis c virus infection |
-
2003
- 2003-08-01 WO PCT/US2003/024324 patent/WO2004013300A2/en not_active Ceased
- 2003-08-01 BR BRPI0313164-5A patent/BR0313164A/pt not_active IP Right Cessation
- 2003-08-01 JP JP2004526388A patent/JP2006507235A/ja active Pending
- 2003-08-01 US US10/632,997 patent/US8093380B2/en not_active Expired - Fee Related
- 2003-08-01 SG SG2007015332A patent/SG174624A1/en unknown
- 2003-08-01 KR KR1020057001868A patent/KR20050040912A/ko not_active Ceased
- 2003-08-01 EP EP03767138A patent/EP1545545A4/en not_active Withdrawn
- 2003-08-01 IL IL16664003A patent/IL166640A0/xx unknown
- 2003-08-01 AU AU2003257157A patent/AU2003257157C1/en not_active Ceased
- 2003-08-01 CA CA2494340A patent/CA2494340C/en not_active Expired - Fee Related
- 2003-08-01 MX MXPA05001298A patent/MXPA05001298A/es active IP Right Grant
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