JP2004500352A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2004500352A5 JP2004500352A5 JP2001541459A JP2001541459A JP2004500352A5 JP 2004500352 A5 JP2004500352 A5 JP 2004500352A5 JP 2001541459 A JP2001541459 A JP 2001541459A JP 2001541459 A JP2001541459 A JP 2001541459A JP 2004500352 A5 JP2004500352 A5 JP 2004500352A5
- Authority
- JP
- Japan
- Prior art keywords
- phosphonate
- alkyl
- alkenyl
- acyl
- phosphonate compound
- 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
- -1 phosphonate compound Chemical class 0.000 description 17
- 125000002252 acyl group Chemical group 0.000 description 12
- 125000003342 alkenyl group Chemical group 0.000 description 12
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 7
- 125000006701 (C1-C7) alkyl group Chemical group 0.000 description 6
- 241000124008 Mammalia Species 0.000 description 4
- 229940122361 Bisphosphonate Drugs 0.000 description 3
- 150000004663 bisphosphonates Chemical class 0.000 description 3
- 125000006686 (C1-C24) alkyl group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000001588 bifunctional effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229960000961 floxuridine Drugs 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000002777 nucleoside Substances 0.000 description 2
- 150000003833 nucleoside derivatives Chemical class 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 2
- 0 **OC(*)(*)*C(*)(*)N Chemical compound **OC(*)(*)*C(*)(*)N 0.000 description 1
- CFOQUIOWNVKBIC-FJFJXFQQSA-N 2-amino-1-[(2r,3s,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-7h-purin-6-one Chemical compound NC1=NC=2N=CNC=2C(=O)N1[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O CFOQUIOWNVKBIC-FJFJXFQQSA-N 0.000 description 1
- YXQUGSXUDFTPLL-LURJTMIESA-N 4-amino-1-[[(5s)-2-hydroxy-2-oxo-1,4,2$l^{5}-dioxaphosphinan-5-yl]methyl]pyrimidin-2-one Chemical compound O=C1N=C(N)C=CN1C[C@@H]1OCP(O)(=O)OC1 YXQUGSXUDFTPLL-LURJTMIESA-N 0.000 description 1
- OGSPWJRAVKPPFI-UHFFFAOYSA-N Alendronic Acid Chemical compound NCCCC(O)(P(O)(O)=O)P(O)(O)=O OGSPWJRAVKPPFI-UHFFFAOYSA-N 0.000 description 1
- VWFCHDSQECPREK-LURJTMIESA-N Cidofovir Chemical compound NC=1C=CN(C[C@@H](CO)OCP(O)(O)=O)C(=O)N=1 VWFCHDSQECPREK-LURJTMIESA-N 0.000 description 1
- PTOAARAWEBMLNO-KVQBGUIXSA-N Cladribine Chemical compound C1=NC=2C(N)=NC(Cl)=NC=2N1[C@H]1C[C@H](O)[C@@H](CO)O1 PTOAARAWEBMLNO-KVQBGUIXSA-N 0.000 description 1
- UHDGCWIWMRVCDJ-CCXZUQQUSA-N Cytarabine Chemical class O=C1N=C(N)C=CN1[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O1 UHDGCWIWMRVCDJ-CCXZUQQUSA-N 0.000 description 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- MPBVHIBUJCELCL-UHFFFAOYSA-N Ibandronate Chemical compound CCCCCN(C)CCC(O)(P(O)(O)=O)P(O)(O)=O MPBVHIBUJCELCL-UHFFFAOYSA-N 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 208000001132 Osteoporosis Diseases 0.000 description 1
- IIDJRNMFWXDHID-UHFFFAOYSA-N Risedronic acid Chemical compound OP(=O)(O)C(P(O)(O)=O)(O)CC1=CC=CN=C1 IIDJRNMFWXDHID-UHFFFAOYSA-N 0.000 description 1
- DKJJVAGXPKPDRL-UHFFFAOYSA-N Tiludronic acid Chemical compound OP(O)(=O)C(P(O)(O)=O)SC1=CC=C(Cl)C=C1 DKJJVAGXPKPDRL-UHFFFAOYSA-N 0.000 description 1
- 208000036142 Viral infection Diseases 0.000 description 1
- UGEPSJNLORCRBO-UHFFFAOYSA-N [3-(dimethylamino)-1-hydroxy-1-phosphonopropyl]phosphonic acid Chemical compound CN(C)CCC(O)(P(O)(O)=O)P(O)(O)=O UGEPSJNLORCRBO-UHFFFAOYSA-N 0.000 description 1
- 229960001997 adefovir Drugs 0.000 description 1
- WOZSCQDILHKSGG-UHFFFAOYSA-N adefovir depivoxil Chemical group N1=CN=C2N(CCOCP(=O)(OCOC(=O)C(C)(C)C)OCOC(=O)C(C)(C)C)C=NC2=C1N WOZSCQDILHKSGG-UHFFFAOYSA-N 0.000 description 1
- 229940062527 alendronate Drugs 0.000 description 1
- 230000000118 anti-neoplastic effect Effects 0.000 description 1
- 230000000840 anti-viral effect Effects 0.000 description 1
- 230000006907 apoptotic process Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 210000002449 bone cell Anatomy 0.000 description 1
- 230000004663 cell proliferation Effects 0.000 description 1
- 229960000724 cidofovir Drugs 0.000 description 1
- ACSIXWWBWUQEHA-UHFFFAOYSA-N clodronic acid Chemical compound OP(O)(=O)C(Cl)(Cl)P(O)(O)=O ACSIXWWBWUQEHA-UHFFFAOYSA-N 0.000 description 1
- 229960002286 clodronic acid Drugs 0.000 description 1
- IWLDTXOHXPDPQG-UHFFFAOYSA-L disodium;hydroxy-[1-hydroxy-1-[hydroxy(oxido)phosphoryl]-3-pyrrolidin-1-ylpropyl]phosphinate Chemical compound [Na+].[Na+].OP(=O)(O)C(P([O-])([O-])=O)(O)CCN1CCCC1 IWLDTXOHXPDPQG-UHFFFAOYSA-L 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 229940009626 etidronate Drugs 0.000 description 1
- ODKNJVUHOIMIIZ-RRKCRQDMSA-N floxuridine Chemical compound C1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=O)C(F)=C1 ODKNJVUHOIMIIZ-RRKCRQDMSA-N 0.000 description 1
- 229960000390 fludarabine Drugs 0.000 description 1
- GIUYCYHIANZCFB-FJFJXFQQSA-N fludarabine phosphate Chemical compound C1=NC=2C(N)=NC(F)=NC=2N1[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@@H]1O GIUYCYHIANZCFB-FJFJXFQQSA-N 0.000 description 1
- SDUQYLNIPVEERB-QPPQHZFASA-N gemcitabine Chemical compound O=C1N=C(N)C=CN1[C@H]1C(F)(F)[C@H](O)[C@@H](CO)O1 SDUQYLNIPVEERB-QPPQHZFASA-N 0.000 description 1
- 229960005277 gemcitabine Drugs 0.000 description 1
- 229940015872 ibandronate Drugs 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 210000000963 osteoblast Anatomy 0.000 description 1
- WRUUGTRCQOWXEG-UHFFFAOYSA-N pamidronate Chemical compound NCCC(O)(P(O)(O)=O)P(O)(O)=O WRUUGTRCQOWXEG-UHFFFAOYSA-N 0.000 description 1
- 229940046231 pamidronate Drugs 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229940089617 risedronate Drugs 0.000 description 1
- 229960004556 tenofovir Drugs 0.000 description 1
- VCMJCVGFSROFHV-WZGZYPNHSA-N tenofovir disoproxil fumarate Chemical compound OC(=O)\C=C\C(O)=O.N1=CN=C2N(C[C@@H](C)OCP(=O)(OCOC(=O)OC(C)C)OCOC(=O)OC(C)C)C=NC2=C1N VCMJCVGFSROFHV-WZGZYPNHSA-N 0.000 description 1
- 229940019375 tiludronate Drugs 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
- HBOMLICNUCNMMY-XLPZGREQSA-N zidovudine Chemical class O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](N=[N+]=[N-])C1 HBOMLICNUCNMMY-XLPZGREQSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16881399P | 1999-12-03 | 1999-12-03 | |
| US60/168,813 | 1999-12-03 | ||
| US20571900P | 2000-05-19 | 2000-05-19 | |
| US60/205,719 | 2000-05-19 | ||
| PCT/US2000/033079 WO2001039724A2 (en) | 1999-12-03 | 2000-12-04 | Phosphonate compounds |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011153911A Division JP2011246475A (ja) | 1999-12-03 | 2011-07-12 | ホスホネート化合物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004500352A JP2004500352A (ja) | 2004-01-08 |
| JP2004500352A5 true JP2004500352A5 (enExample) | 2011-09-01 |
| JP4993649B2 JP4993649B2 (ja) | 2012-08-08 |
Family
ID=26864475
Family Applications (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001541459A Expired - Lifetime JP4993649B2 (ja) | 1999-12-03 | 2000-12-04 | ホスホネート化合物 |
| JP2011153911A Withdrawn JP2011246475A (ja) | 1999-12-03 | 2011-07-12 | ホスホネート化合物 |
| JP2014002881A Expired - Lifetime JP5963787B2 (ja) | 1999-12-03 | 2014-01-10 | ホスホネート化合物 |
| JP2015006124A Expired - Lifetime JP5963894B2 (ja) | 1999-12-03 | 2015-01-15 | ホスホネート化合物 |
Family Applications After (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011153911A Withdrawn JP2011246475A (ja) | 1999-12-03 | 2011-07-12 | ホスホネート化合物 |
| JP2014002881A Expired - Lifetime JP5963787B2 (ja) | 1999-12-03 | 2014-01-10 | ホスホネート化合物 |
| JP2015006124A Expired - Lifetime JP5963894B2 (ja) | 1999-12-03 | 2015-01-15 | ホスホネート化合物 |
Country Status (18)
| Country | Link |
|---|---|
| US (14) | US6716825B2 (enExample) |
| EP (1) | EP1233770B1 (enExample) |
| JP (4) | JP4993649B2 (enExample) |
| KR (1) | KR20020073342A (enExample) |
| CN (1) | CN1414854B (enExample) |
| AT (1) | ATE385797T1 (enExample) |
| AU (3) | AU785355B2 (enExample) |
| BR (1) | BR0016058A (enExample) |
| CA (2) | CA2747954C (enExample) |
| CY (1) | CY1107927T1 (enExample) |
| DE (1) | DE60038038T2 (enExample) |
| DK (2) | DK1233770T3 (enExample) |
| ES (2) | ES2300281T3 (enExample) |
| HK (1) | HK1050627B (enExample) |
| MX (1) | MXPA02005490A (enExample) |
| PT (2) | PT1914237E (enExample) |
| RU (1) | RU2258707C2 (enExample) |
| WO (1) | WO2001039724A2 (enExample) |
Families Citing this family (83)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7205404B1 (en) | 1999-03-05 | 2007-04-17 | Metabasis Therapeutics, Inc. | Phosphorus-containing prodrugs |
| US6716825B2 (en) | 1999-12-03 | 2004-04-06 | The Regents Of The University Of California | Phosphonate compounds |
| WO2002102813A1 (en) * | 2001-06-20 | 2002-12-27 | Merck Frosst Canada & Co. | Aryldifluoromethylphosphonic acids for treatment of diabetes |
| FR2837490B1 (fr) * | 2002-03-21 | 2009-04-17 | Univ Paris 13 | Nouveaux derives de bisphosphonates, leurs preparations et utilisations |
| ES2336312T3 (es) * | 2001-07-16 | 2010-04-12 | Universite Paris 13 | Procedimiento de preparacion de derivados de bisfosfonatos. |
| WO2003075884A1 (en) * | 2002-03-06 | 2003-09-18 | Lifizz, Inc. | Effervescent compositions comprising bisphosphonates and methods related thereto |
| US7488496B2 (en) | 2002-03-06 | 2009-02-10 | Christer Rosen | Effervescent compositions comprising bisphosphonates and methods related thereto |
| EP1509537B9 (en) * | 2002-04-26 | 2007-11-14 | Gilead Sciences, Inc. | Cellular accumulation of phosphonate analogs of hiv protease inhibitor compounds and the compounds as such |
| RU2309747C2 (ru) * | 2002-09-18 | 2007-11-10 | Михаил Владимирович Кутушов | Применение 2-хлорэтилфосфоновой кислоты и ее солей в качестве противоопухолевого средства |
| AU2003901813A0 (en) * | 2003-04-15 | 2003-05-01 | Vital Health Sciences Pty Ltd | Pharmaceutical derivatives |
| US7470724B2 (en) | 2003-04-25 | 2008-12-30 | Gilead Sciences, Inc. | Phosphonate compounds having immuno-modulatory activity |
| WO2005002626A2 (en) | 2003-04-25 | 2005-01-13 | Gilead Sciences, Inc. | Therapeutic phosphonate compounds |
| US7432261B2 (en) | 2003-04-25 | 2008-10-07 | Gilead Sciences, Inc. | Anti-inflammatory phosphonate compounds |
| US7452901B2 (en) | 2003-04-25 | 2008-11-18 | Gilead Sciences, Inc. | Anti-cancer phosphonate analogs |
| US7427636B2 (en) | 2003-04-25 | 2008-09-23 | Gilead Sciences, Inc. | Inosine monophosphate dehydrogenase inhibitory phosphonate compounds |
| US7300924B2 (en) | 2003-04-25 | 2007-11-27 | Gilead Sciences, Inc. | Anti-infective phosphonate analogs |
| US7407965B2 (en) | 2003-04-25 | 2008-08-05 | Gilead Sciences, Inc. | Phosphonate analogs for treating metabolic diseases |
| JP5069463B2 (ja) | 2003-04-25 | 2012-11-07 | ギリアード サイエンシーズ， インコーポレイテッド | 抗ウイルス性ホスホネート類似物 |
| KR20060022647A (ko) | 2003-04-25 | 2006-03-10 | 길리애드 사이언시즈, 인코포레이티드 | 키나아제 억제 포스포네이트 유사체 |
| US7432273B2 (en) | 2003-10-24 | 2008-10-07 | Gilead Sciences, Inc. | Phosphonate analogs of antimetabolites |
| EP1678322A2 (en) | 2003-10-24 | 2006-07-12 | Gilead Sciences, Inc. | Methods and compositions for identifying therapeutic compounds |
| WO2005044279A1 (en) | 2003-10-24 | 2005-05-19 | Gilead Sciences, Inc. | Purine nucleoside phosphonate conjugates |
| WO2005056019A1 (ja) * | 2003-12-12 | 2005-06-23 | Astellas Pharma Inc. | 悪性黒色腫治療剤 |
| EP1706405B1 (en) | 2003-12-22 | 2009-03-04 | Gilead Sciences, Inc. | 4'-substituted carbovir- and abacavir-derivatives as well as related compounds with hiv and hcv antiviral activity |
| WO2005090370A1 (en) | 2004-02-05 | 2005-09-29 | The Regents Of The University Of California | Pharmacologically active agents containing esterified phosphonates and methods for use thereof |
| WO2006076015A2 (en) * | 2004-04-30 | 2006-07-20 | The Regents Of The University Of California | 1-[2-(phosphonomethoxy)ethyl]-cytosine and analogs thereof |
| ES2720618T3 (es) | 2004-07-27 | 2019-07-23 | Gilead Sciences Inc | Análogos de fosfonato de compuestos de inhibidores de VIH |
| WO2006055525A2 (en) * | 2004-11-15 | 2006-05-26 | Ceptyr, Inc. | Protein tyrosine phosphatase inhibitors and methods of use thereof |
| US8101745B2 (en) | 2004-12-16 | 2012-01-24 | The Regents Of The University Of California | Lung-targeted drugs |
| US8071574B2 (en) * | 2005-02-22 | 2011-12-06 | John Dennis Bobyn | Implant improving local bone formation |
| US20060219637A1 (en) * | 2005-03-29 | 2006-10-05 | Killeen Kevin P | Devices, systems and methods for liquid chromatography |
| US20090156545A1 (en) * | 2005-04-01 | 2009-06-18 | Hostetler Karl Y | Substituted Phosphate Esters of Nucleoside Phosphonates |
| WO2006110655A2 (en) * | 2005-04-08 | 2006-10-19 | Chimerix, Inc. | Compounds, compositions and methods for the treatment of poxvirus infections |
| EP1865967A4 (en) * | 2005-04-08 | 2011-02-09 | Chimerix Inc | COMPOUNDS, COMPOSITIONS AND METHODS FOR TREATING VIRAL INFECTIONS AND OTHER DISEASES |
| CA2606399A1 (en) * | 2005-04-25 | 2006-11-02 | Institute Of Organic Chemistry And Biochemistry Of The Academy Of Scienc Es Of The Czech Republic | Use of compounds to enhance processivity of telomerase |
| US7914810B2 (en) * | 2005-05-06 | 2011-03-29 | Synthes Usa, Llc | Methods for the in situ treatment of bone cancer |
| US8114843B2 (en) | 2005-11-18 | 2012-02-14 | The Regents Of The University Of California | Photoreactive regulator of protein function and methods of use thereof |
| EP2012799B1 (en) * | 2006-05-03 | 2016-08-24 | Chimerix, Inc. | Metabolically stable alkoxyalkyl esters of antiviral or antiproliferative phosphonates, nucleoside phosphonates and nucleoside phosphates |
| CN101678122A (zh) * | 2007-04-27 | 2010-03-24 | 奇默里克斯公司 | 在核苷给药的受体中降低肾中毒性的方法 |
| JP2011508740A (ja) * | 2007-12-27 | 2011-03-17 | エピファニー バイオサイエンシズ， インク． | 抗ウイルス化合物 |
| EP3085377A1 (en) | 2008-01-25 | 2016-10-26 | Chimerix, Inc. | Methods of treating viral infections |
| NZ590075A (en) | 2008-07-08 | 2012-12-21 | Gilead Sciences Inc | citrate, malonate and succinate salts of the HIV inhibitor ethyl N-[(S)({ [(2R,5R)-5-(6-amino-9H-purin-9-yl)-4-fluoro-2,5-dihydrofuran-2-yl]oxy} methyl)phenoxyphosphinoyl]-L-alaninate |
| US8628812B2 (en) | 2008-12-30 | 2014-01-14 | Pepsico, Inc. | Preservative system for acidic beverages based on sequestrants |
| EP2270021A1 (en) * | 2009-06-18 | 2011-01-05 | Centre National de la Recherche Scientifique | Phosphonates synthons for the synthesis of phosphonates derivatives showing better bioavailability |
| WO2011005510A2 (en) * | 2009-06-22 | 2011-01-13 | Cerapedics, Inc. | Peptide conjugates and uses thereof |
| WO2011011519A1 (en) | 2009-07-21 | 2011-01-27 | Chimerix, Inc. | Compounds, compositions and methods for treating ocular conditions |
| AU2010279678B2 (en) | 2009-08-03 | 2015-09-10 | Emergent Biodefense Operations Lansing Llc | Composition and methods of treating viral infections and viral induced tumors |
| EP2483283B1 (en) * | 2009-10-02 | 2015-01-07 | Straitmark Holding AG | Method for the manufacture of aminohydroxy diphosphonic acids |
| HUE032860T2 (en) | 2010-02-12 | 2017-11-28 | Chimerix Inc | A method for treating a virus infection |
| CN102939291B (zh) | 2010-04-14 | 2016-09-07 | 加利福尼亚大学董事会 | 用于病毒感染治疗的具有降低的毒性的膦酸酯 |
| US9278135B2 (en) | 2010-04-26 | 2016-03-08 | Chimerix Inc. | Methods of treating retroviral infections and related dosage regimes |
| AU2015201895B2 (en) * | 2010-08-31 | 2016-11-17 | Emergent Biodefence Operations Lansing Llc | Phosphonate ester derivatives and methods of synthesis thereof |
| BR112013004925B1 (pt) | 2010-08-31 | 2020-09-29 | Chimerix, Inc | Formas mórficas do éster [[(s)-2-(4-amino-2-oxo-1(2h)-pirimidinil) -1-(hidroximetil)etóxi]metil] mono[3-(hexadecilóxi) propílico] do ácido fosfônico, composições farmacêuticas das mesmas, método para síntese e uso de uma forma mórfica b |
| US8884027B2 (en) | 2010-10-22 | 2014-11-11 | University Of Rochester | Melampomagnolide B derivatives as antileukemic and cytotoxic agents |
| CN103945869A (zh) * | 2011-08-31 | 2014-07-23 | 马林克罗特有限公司 | 使用h-膦酸酯-烯/-炔的氢膦酸酯化反应进行的靶向纳米颗粒的远程组装 |
| ES2734495T3 (es) | 2011-12-22 | 2019-12-10 | Geron Corp | Análogos de guanina como sustratos de telomerasa y afectores de la longitud de los telómeros |
| WO2014035945A1 (en) * | 2012-08-28 | 2014-03-06 | Glaxosmithkline Llc | Pharmaceutical compositions |
| SI2970346T1 (sl) * | 2013-03-15 | 2018-12-31 | The Regents Of The University Of California | Aciklični diestri nukleozid fosfonata |
| IL302520A (en) | 2013-11-15 | 2023-07-01 | Chimerix Inc | Morphic forms of hexadecyloxypropyl-phosphonate esters |
| EP3623364A1 (en) | 2014-02-13 | 2020-03-18 | Ligand Pharmaceuticals, Inc. | Prodrug compounds and their uses |
| KR102448455B1 (ko) | 2014-03-14 | 2022-09-28 | 올텍 법인회사 | 셀레노유기 화합물의 조성물 및 이의 사용 방법 |
| CN106687118A (zh) | 2014-07-02 | 2017-05-17 | 配体药物公司 | 前药化合物及其用途 |
| PT3194411T (pt) | 2014-09-15 | 2022-06-06 | Univ California | Análogos de nucleótidos |
| US10160778B2 (en) | 2014-10-27 | 2018-12-25 | Concert Pharmaceuticals, Inc. | Pyrimidine phosphonic acid esters |
| 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 |
| AU2016255725B2 (en) * | 2015-04-27 | 2021-09-23 | The Medical Research, Infrastructure and Health Services Fund of the Tel Aviv Medical Center | EGR1 targeting molecules for the treatment of inflammatory and hyperproliferative conditions |
| EP3875462A1 (en) | 2015-09-15 | 2021-09-08 | The Regents of The University of California | Nucleotide analogs |
| WO2017048252A1 (en) | 2015-09-15 | 2017-03-23 | Alltech, Inc. | Compositions of selenoorganic compounds and methods of use thereof |
| JP6878473B2 (ja) | 2016-06-28 | 2021-05-26 | キメリックス インコーポレイテッド | ブリンシドフォビルの製剤 |
| RU2628456C1 (ru) * | 2016-06-29 | 2017-08-17 | Федеральное Государственное Бюджетное Учреждение Науки Институт Молекулярной Биологии Им. В.А. Энгельгардта Российской Академии Наук (Имб Ран) | Новые пиримидиновые ингибиторы репликации аденовируса человека |
| 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 |
| PT3661937T (pt) | 2017-08-01 | 2021-09-24 | Gilead Sciences Inc | Formas cristalinas de ((s)-((((2r,5r)-5-(6-amino-9h-purin-9-il)-4-fluoro-2,5-dihidrofurano-2-il)oxi)metil)(fenoxi)fosforil)-l-alaninato de etil (gs-9131) para tratamento de infeções virais |
| RU2670204C1 (ru) * | 2017-12-01 | 2018-10-19 | федеральное государственное бюджетное учреждение "Национальный исследовательский центр эпидемиологии и микробиологии имени почетного академика Н.Ф. Гамалеи" Министерства здравоохранения Российской Федерации | Производные 2-тиоурацила, обладающие противоаденовирусной активностью |
| US11447512B2 (en) * | 2017-12-21 | 2022-09-20 | Shenzhen Targetrx, Inc. | Antiviral nucleoside reverse transcriptase inhibitor |
| US11970482B2 (en) | 2018-01-09 | 2024-04-30 | Ligand Pharmaceuticals Inc. | Acetal compounds and therapeutic uses thereof |
| US12049474B2 (en) | 2019-08-22 | 2024-07-30 | Emory University | Nucleoside prodrugs and uses related thereto |
| US10874687B1 (en) | 2020-02-27 | 2020-12-29 | Atea Pharmaceuticals, Inc. | Highly active compounds against COVID-19 |
| WO2021173713A1 (en) | 2020-02-27 | 2021-09-02 | Atea Pharmaceuticals, Inc. | Highly active compounds against covid-19 |
| JP7559223B2 (ja) | 2020-08-24 | 2024-10-01 | ギリアード サイエンシーズ， インコーポレイテッド | リン脂質化合物及びその使用 |
| TW202344257A (zh) | 2020-10-16 | 2023-11-16 | 美商基利科學股份有限公司 | 磷脂化合物及其用途 |
| CN117285566A (zh) * | 2022-06-24 | 2023-12-26 | 润佳（苏州）医药科技有限公司 | 一种膦酸酯类化合物及其医药用途 |
| WO2024020127A1 (en) | 2022-07-21 | 2024-01-25 | Antiva Biosciences, Inc. | Compositions and dosage forms for treatment of hpv infection and hpv-induced neoplasia |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1944530A (en) * | 1929-04-08 | 1934-01-23 | Ig Farbenindustrie Ag | Phosphoric acid esters |
| DE2009341C3 (de) * | 1970-02-27 | 1979-06-21 | Max-Planck-Gesellschaft Zur Foerderung Der Wissenschaften E.V., 3400 Goettingen | 3-Octadecyloxy-propanol-(l)-phosphorsäure-monocholinester und Verfahren zu dessen Herstellung |
| US5223263A (en) * | 1988-07-07 | 1993-06-29 | Vical, Inc. | Liponucleotide-containing liposomes |
| FR2586685B1 (fr) * | 1985-09-03 | 1987-12-11 | Protex Manuf Prod Chimiq | Procede de preparation de nouveaux agents dispersants cationiques |
| SU1594953A1 (ru) * | 1988-12-30 | 1991-05-15 | Институт Молекулярной Биологии Им.В.А.Энгельгардта | Аммонийна соль 9-(4-гидрофосфорил-2-оксабутил)гуанина, обладающа избирательной активностью против вируса простого герпеса |
| FI83421C (fi) * | 1989-06-21 | 1991-07-10 | Huhtamaeki Oy | Foerfarande foer framstaellning av farmakologiskt anvaendbara metylenbisfosfonsyraderivat. |
| US5411947A (en) * | 1989-06-28 | 1995-05-02 | Vestar, Inc. | Method of converting a drug to an orally available form by covalently bonding a lipid to the drug |
| US5463092A (en) * | 1989-11-22 | 1995-10-31 | Vestar, Inc. | Lipid derivatives of phosphonacids for liposomal incorporation and method of use |
| ES2118069T3 (es) | 1990-09-14 | 1998-09-16 | Acad Of Science Czech Republic | Profarmacos de fosfonatos. |
| EP0477454A1 (en) * | 1990-09-28 | 1992-04-01 | Merrell Dow Pharmaceuticals Inc. | Novel phosphonate derivatives of certain nucleosides |
| US5672697A (en) * | 1991-02-08 | 1997-09-30 | Gilead Sciences, Inc. | Nucleoside 5'-methylene phosphonates |
| JPH05339280A (ja) * | 1991-04-26 | 1993-12-21 | Japan Tobacco Inc | （ｎ−二環置換）アミノメチレンビスフォスフォン酸誘導体 |
| JP3341303B2 (ja) * | 1991-07-11 | 2002-11-05 | 東レ株式会社 | メチレンジホスホン酸誘導体、その製造方法およびその医薬用途 |
| US5879700A (en) * | 1991-10-15 | 1999-03-09 | Hostetler; Karl Y. | Nucleoside analogue phosphates for topical use |
| US5618804A (en) | 1992-07-10 | 1997-04-08 | Toray Industries, Inc. | Methanediphosphonic acid derivative, process for production thereof and use for pharmaceuticals |
| JP3580377B2 (ja) * | 1993-06-29 | 2004-10-20 | 三菱化学株式会社 | ホスホナートヌクレオチドエステル誘導体 |
| ATE199906T1 (de) | 1993-06-29 | 2001-04-15 | Mitsubishi Chem Corp | Phosphonat-nukleotid ester-derivate |
| US5627185A (en) * | 1994-11-23 | 1997-05-06 | Gosselin; Gilles | Acyclovir derivatives as antiviral agents |
| CH690163A5 (fr) * | 1995-07-28 | 2000-05-31 | Symphar Sa | Dérivés gem-diphosphonates substitués utiles en tant qu'agents anti-cancers. |
| US5922695A (en) * | 1996-07-26 | 1999-07-13 | Gilead Sciences, Inc. | Antiviral phosphonomethyoxy nucleotide analogs having increased oral bioavarilability |
| WO1998026749A1 (en) * | 1996-12-19 | 1998-06-25 | Kao Corporation | Coating composition for teeth |
| US6686462B2 (en) * | 1997-02-28 | 2004-02-03 | The Regents Of The University Of California | Antiviral compounds and methods of administration |
| IL134619A0 (en) * | 1997-08-18 | 2001-04-30 | Univ Kingston | Phosphono-carboxylate compounds for treating amyloidosis |
| FR2781228B1 (fr) * | 1998-07-16 | 2000-09-29 | Pf Medicament | Phosphonates insatures derives d'indole |
| US6716825B2 (en) * | 1999-12-03 | 2004-04-06 | The Regents Of The University Of California | Phosphonate compounds |
-
2000
- 2000-12-04 US US10/148,374 patent/US6716825B2/en not_active Expired - Lifetime
- 2000-12-04 HK HK03101480.2A patent/HK1050627B/en not_active IP Right Cessation
- 2000-12-04 PT PT80014087T patent/PT1914237E/pt unknown
- 2000-12-04 DK DK00982468T patent/DK1233770T3/da active
- 2000-12-04 CA CA2747954A patent/CA2747954C/en not_active Expired - Lifetime
- 2000-12-04 JP JP2001541459A patent/JP4993649B2/ja not_active Expired - Lifetime
- 2000-12-04 ES ES00982468T patent/ES2300281T3/es not_active Expired - Lifetime
- 2000-12-04 PT PT00982468T patent/PT1233770E/pt unknown
- 2000-12-04 CA CA2393410A patent/CA2393410C/en not_active Expired - Lifetime
- 2000-12-04 BR BR0016058-0A patent/BR0016058A/pt not_active Application Discontinuation
- 2000-12-04 RU RU2002118327/04A patent/RU2258707C2/ru active
- 2000-12-04 AU AU19497/01A patent/AU785355B2/en not_active Ceased
- 2000-12-04 DE DE60038038T patent/DE60038038T2/de not_active Expired - Lifetime
- 2000-12-04 MX MXPA02005490A patent/MXPA02005490A/es active IP Right Grant
- 2000-12-04 DK DK08001408.7T patent/DK1914237T3/da active
- 2000-12-04 WO PCT/US2000/033079 patent/WO2001039724A2/en not_active Ceased
- 2000-12-04 AT AT00982468T patent/ATE385797T1/de active
- 2000-12-04 EP EP00982468A patent/EP1233770B1/en not_active Expired - Lifetime
- 2000-12-04 KR KR1020027007074A patent/KR20020073342A/ko not_active Ceased
- 2000-12-04 CN CN00818111.XA patent/CN1414854B/zh not_active Expired - Lifetime
- 2000-12-04 ES ES08001408.7T patent/ES2498046T3/es not_active Expired - Lifetime
-
2004
- 2004-01-15 US US10/759,345 patent/US7034014B2/en not_active Expired - Lifetime
-
2005
- 2005-04-06 US US11/100,882 patent/US7094772B2/en not_active Expired - Lifetime
- 2005-04-06 US US11/101,259 patent/US7098197B2/en not_active Expired - Lifetime
-
2006
- 2006-08-17 US US11/506,292 patent/US7452898B2/en not_active Expired - Lifetime
- 2006-12-15 AU AU2006252074A patent/AU2006252074B2/en not_active Ceased
-
2007
- 2007-03-07 US US11/715,604 patent/US7790703B2/en not_active Expired - Fee Related
- 2007-10-26 US US11/925,309 patent/US7687480B2/en not_active Expired - Fee Related
-
2008
- 2008-04-30 CY CY20081100465T patent/CY1107927T1/el unknown
-
2010
- 2010-02-05 US US12/701,410 patent/US8008308B2/en not_active Expired - Fee Related
- 2010-12-20 AU AU2010257309A patent/AU2010257309B2/en not_active Ceased
-
2011
- 2011-07-12 JP JP2011153911A patent/JP2011246475A/ja not_active Withdrawn
- 2011-08-29 US US13/220,548 patent/US8309565B2/en not_active Expired - Fee Related
-
2012
- 2012-10-04 US US13/645,105 patent/US8710030B2/en not_active Expired - Fee Related
-
2013
- 2013-10-21 US US14/059,365 patent/US8889658B2/en not_active Expired - Fee Related
-
2014
- 2014-01-10 JP JP2014002881A patent/JP5963787B2/ja not_active Expired - Lifetime
- 2014-10-29 US US14/527,156 patent/US9206208B2/en not_active Expired - Fee Related
-
2015
- 2015-01-15 JP JP2015006124A patent/JP5963894B2/ja not_active Expired - Lifetime
- 2015-11-16 US US14/942,926 patent/US9649321B2/en not_active Expired - Fee Related
-
2017
- 2017-05-15 US US15/595,496 patent/US10071110B2/en not_active Expired - Fee Related
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2004500352A5 (enExample) | ||
| RU2002118327A (ru) | Фосфонатные соединения | |
| CA2393410A1 (en) | Phosphonate compounds | |
| AU649466B2 (en) | Targeted drug delivery via phosphonate derivatives | |
| US10046055B2 (en) | Bone targeted therapeutics and methods of making and using the same | |
| JP2009538829A5 (enExample) | ||
| CY1106482T1 (el) | Φαρμακευτικη παρεντepικη συνθεση πepιεχοντας ενα διφωσφονικο | |
| JP2002505333A5 (enExample) | ||
| KR20060008297A (ko) | 2'-데옥시-β-Ｌ-뉴클레오시드의 제조방법 | |
| WO1992017185A1 (en) | Targeted drug delivery via mixed phosphate derivatives | |
| US8110676B2 (en) | Prodrugs activated by RNA-dependent DNA-polymerases | |
| EP1914237A2 (en) | Phosphonate ester antiviral compounds | |
| AU668506C (en) | Targeted drug delivery via mixed phosphate derivatives | |
| JP2001335593A5 (enExample) | ||
| JP2006524186A5 (enExample) | ||
| ZA200204194B (en) | Phosphonate compounds. |