NO20090835L - Nye HIV-reverstranskriptaseinhibitorer - Google Patents
Nye HIV-reverstranskriptaseinhibitorerInfo
- Publication number
- NO20090835L NO20090835L NO20090835A NO20090835A NO20090835L NO 20090835 L NO20090835 L NO 20090835L NO 20090835 A NO20090835 A NO 20090835A NO 20090835 A NO20090835 A NO 20090835A NO 20090835 L NO20090835 L NO 20090835L
- Authority
- NO
- Norway
- Prior art keywords
- reverse transcriptase
- transcriptase inhibitors
- hiv reverse
- new hiv
- compounds
- Prior art date
Links
- 108010078851 HIV Reverse Transcriptase Proteins 0.000 title 1
- 239000003419 rna directed dna polymerase inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000002148 esters Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
-
- 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
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83280606P | 2006-07-24 | 2006-07-24 | |
| PCT/US2007/016703 WO2008016522A2 (fr) | 2006-07-24 | 2007-07-24 | Inhibiteurs inédits de la transcriptase inverse du vih |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20090835L true NO20090835L (no) | 2009-04-23 |
Family
ID=38997642
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20090835A NO20090835L (no) | 2006-07-24 | 2009-02-23 | Nye HIV-reverstranskriptaseinhibitorer |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US8106064B2 (fr) |
| EP (1) | EP2044037A2 (fr) |
| JP (1) | JP2009544710A (fr) |
| KR (2) | KR20110089463A (fr) |
| CN (1) | CN101495461A (fr) |
| AP (1) | AP2514A (fr) |
| AU (1) | AU2007281604A1 (fr) |
| BR (1) | BRPI0714880A2 (fr) |
| CA (1) | CA2658479A1 (fr) |
| EA (1) | EA200900213A1 (fr) |
| HR (1) | HRP20090114A2 (fr) |
| IL (1) | IL196675A0 (fr) |
| MX (1) | MX2009000871A (fr) |
| NO (1) | NO20090835L (fr) |
| NZ (1) | NZ573793A (fr) |
| SG (1) | SG174016A1 (fr) |
| UA (1) | UA95955C2 (fr) |
| WO (1) | WO2008016522A2 (fr) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009544710A (ja) | 2006-07-24 | 2009-12-17 | ギリアード サイエンシーズ， インコーポレイテッド | Ｈｉｖ逆転写酵素インヒビター |
| KR20100041798A (ko) * | 2007-06-29 | 2010-04-22 | 한국화학연구원 | 신규 ｈｉｖ 역전사효소 억제제 |
| CN101784532B (zh) * | 2007-06-29 | 2014-10-22 | 韩国化学研究院 | Hiv逆转录酶抑制剂 |
| WO2009085797A1 (fr) | 2007-12-21 | 2009-07-09 | Gilead Sciences, Inc. | Procédés de préparation d'inhibiteurs de la transcriptase inverse du vih |
| MX2010013275A (es) * | 2008-06-03 | 2011-03-15 | Taiho Pharmaceutical Co Ltd | Compuesto novedoso de uracilo o su sal que tiene actividad inhibidora de desoxiuridin trifosfatasa de humano. |
| WO2010068899A1 (fr) * | 2008-12-12 | 2010-06-17 | Creighton University | Nanoparticules comprenant des combinaisons d'agents antirétroviraux, et utilisations de celles-ci |
| US8921415B2 (en) | 2009-01-29 | 2014-12-30 | Mapi Pharma Ltd. | Polymorphs of darunavir |
| MX2011008362A (es) | 2009-02-13 | 2011-08-24 | Shionogi & Co | Derivado novedoso de triazina y composicion farmaceutica que comprende el mismo. |
| GB0908394D0 (en) | 2009-05-15 | 2009-06-24 | Univ Leuven Kath | Novel viral replication inhibitors |
| EP2342186B1 (fr) * | 2009-06-22 | 2014-09-17 | Emcure Pharmaceuticals Limited | Procédé pour la synthèse d'etravirine |
| GB0913636D0 (en) | 2009-08-05 | 2009-09-16 | Univ Leuven Kath | Novel viral replication inhibitors |
| PL2528923T3 (pl) | 2010-01-28 | 2015-01-30 | Mapi Pharma Ltd | Sposób wytwarzania darunawiru i pochodnych darunawiru |
| WO2011133802A1 (fr) | 2010-04-21 | 2011-10-27 | Helix Therapeutics, Inc. | Compositions et méthodes de traitement de troubles de stockage lysosomial |
| WO2011133803A1 (fr) | 2010-04-21 | 2011-10-27 | Helix Therapeutics, Inc. | Compositions et méthodes d'inactivation ciblée de récepteurs de surface cellulaire de vih |
| DK2604595T3 (en) | 2010-08-10 | 2016-05-23 | Shionogi & Co | TRIAZINE DERIVATIVES AND PHARMACEUTICAL RELATIONSHIP CONTAINING THIS AND PROVIDING ANALGETIC ACTIVITY |
| EP2604260B1 (fr) * | 2010-08-10 | 2017-05-10 | Shionogi&Co., Ltd. | Nouveaux dérivés hétérocycliques, et composition pharmaceutique comprenant ceux-ci |
| MY158809A (en) * | 2010-09-22 | 2016-11-15 | Craun Res Sdn Bhd | Pharmaceutical compositions for calanolides, their derivatives and analogues, and process for producing the same |
| JP2013542243A (ja) | 2010-11-15 | 2013-11-21 | カトリーケ ウニヴェルシテイト ルーヴェン | 新規な抗ウイルス性化合物 |
| EP4556010A3 (fr) | 2011-11-30 | 2025-07-23 | Emory University | Inhibiteurs jak destinées à la prévention ou au traitement d'une maladie causé par une coronaviridée |
| CA2863632C (fr) | 2012-01-19 | 2017-07-11 | The Johns Hopkins University | Formulations de nanoparticules presentant une penetration amelioree dans les muqueuses |
| WO2013118855A1 (fr) | 2012-02-09 | 2013-08-15 | 塩野義製薬株式会社 | Noyau hétérocyclique et dérivé carbocyclique |
| SI3333173T1 (sl) | 2012-10-03 | 2019-08-30 | Gilead Sciences, Inc. | Postopki za pripravo analogov protivirusnega nukleotida |
| EP2941423B1 (fr) | 2013-01-07 | 2021-06-09 | University of Southern California | Inhibiteurs de la désoxyuridine triphosphatase |
| WO2014124006A1 (fr) | 2013-02-05 | 2014-08-14 | The Johns Hopkins University | Nanoparticules pour le suivi de l'imagerie par résonance magnétique et procédés de fabrication et d'utilisation associés |
| TWI637949B (zh) | 2013-06-14 | 2018-10-11 | 塩野義製藥股份有限公司 | 胺基三衍生物及含有其等之醫藥組合物 |
| US9790214B2 (en) | 2014-01-03 | 2017-10-17 | University Of Southern California | Heteroatom containing deoxyuridine triphosphatase inhibitors |
| WO2015127368A1 (fr) | 2014-02-23 | 2015-08-27 | The Johns Hopkins University | Formulations microbicides hypotoniques et leurs méthodes d'utilisation |
| DK3236972T3 (en) | 2014-12-26 | 2021-10-04 | Univ Emory | Antivirale N4-hydroxycytidin-derivativer |
| CN107635545A (zh) | 2015-01-27 | 2018-01-26 | 约翰霍普金斯大学 | 用于增强粘膜表面处活性剂的输送的低渗水凝胶制剂 |
| WO2017006283A1 (fr) | 2015-07-08 | 2017-01-12 | Cv6 Therapeutics (Ni) Limited | Inhibiteurs de désoxyuridine triphosphatase contenant une liaison cyclopropano |
| SI3319939T1 (sl) | 2015-07-08 | 2025-04-30 | Cv6 Therapeutics (Ni) Limited | Zaviralci deoksiuridin trifosfataze, ki vsebujejo hidantoin |
| WO2017006271A1 (fr) | 2015-07-08 | 2017-01-12 | University Of Southern California | Inhibiteurs de désoxyuridine triphosphatase contenant une liaison sulfonyle aminée |
| US10577321B2 (en) | 2015-07-08 | 2020-03-03 | University Of Southern California | Deoxyuridine triphosphatase inhibitors |
| WO2018098207A1 (fr) | 2016-11-23 | 2018-05-31 | Cv6 Therapeutics (Ni) Limited | Hydantoïne contenant des inhibiteurs de la désoxyuridine triphosphatase |
| US10858344B2 (en) | 2016-11-23 | 2020-12-08 | Cv6 Therapeutics (Ni) Limited | Hydantoin containing deoxyuridine triphosphatase inhibitors |
| WO2018098208A1 (fr) | 2016-11-23 | 2018-05-31 | Cv6 Therapeutics (Ni) Limited | Inhibiteurs de désoxyuridine triphosphatase liés à un cycle azote |
| WO2018098204A1 (fr) | 2016-11-23 | 2018-05-31 | Cv6 Therapeutics (Ni) Limited | Isostères d'uracile à 6 chaînons |
| US11168059B2 (en) | 2016-11-23 | 2021-11-09 | Cv6 Therapeutics (Ni) Limited | Amino sulfonyl compounds |
| WO2018128720A1 (fr) | 2017-01-05 | 2018-07-12 | Cv6 Therapeutics (Ni) Limited | Composés contenant de l'uracile |
| US12156523B2 (en) * | 2017-03-17 | 2024-12-03 | Mmag Co., Ltd. | Plant disease control agent |
| JP6804790B1 (ja) | 2017-12-07 | 2020-12-23 | エモリー ユニバーシティー | Ｎ４−ヒドロキシシチジンおよび誘導体ならびにそれらに関連する抗ウイルス用途 |
| US12496279B2 (en) | 2019-04-11 | 2025-12-16 | The Johns Hopkins University | Nanoparticles for drug delivery to brain |
| JPWO2023195529A1 (fr) | 2022-04-08 | 2023-10-12 | ||
| CN115536596A (zh) * | 2022-11-08 | 2022-12-30 | 巨鑫生物制药股份有限公司 | 一种acc007中间体的制备方法 |
| CN117209435A (zh) * | 2023-08-04 | 2023-12-12 | 浙江海昇药业股份有限公司 | 一种微通道制备2,6-二甲氧基-4-氨基嘧啶的方法 |
| CN117304118A (zh) * | 2023-09-15 | 2023-12-29 | 江苏艾迪药业股份有限公司 | 抗艾滋病药物艾诺韦林的合成方法 |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4656209A (en) | 1982-05-26 | 1987-04-07 | Ciba-Geigy Corporation | Chlorinated thermoplastics stabilized with aminouracils |
| KR0155168B1 (ko) | 1989-09-29 | 1998-11-16 | 미우라 아끼라 | 6-치환된 아시클로피리미딘 뉴클레오시드 유도체 및 이를 활성성분으로 함유하는 항비루스제 |
| US5162326A (en) | 1990-02-15 | 1992-11-10 | Takeda Chemical Industries, Ltd. | Pyrimidinedione derivatives, their production and use |
| IL99731A0 (en) * | 1990-10-18 | 1992-08-18 | Merck & Co Inc | Hydroxylated pyridine derivatives,their preparation and pharmaceutical compositions containing them |
| EP0748316B1 (fr) | 1994-02-28 | 2002-05-08 | Sunkyong Industries Co., Ltd. | Derives acyclonucleosides pyrimidiques |
| JPH083143A (ja) | 1994-06-21 | 1996-01-09 | Mitsubishi Chem Corp | ６−アラルキル置換ピリミジン誘導体の製造方法 |
| US6174998B1 (en) | 1996-03-12 | 2001-01-16 | Roche Diagnostics Gmbh | C-nucleoside derivatives and their use in the detection of nucleic acids |
| DE69628750T2 (de) | 1996-02-22 | 2004-04-29 | Samjin Pharm, Co., Ltd. | Neue antivirale, homocarbozklische nukleosidderivate von substituierten pyrimidindionen, verfahren zu ihrer herstellung und zusammensetzungen, die diese als aktiven bestandteil enthalten |
| KR100219922B1 (ko) | 1996-05-16 | 1999-09-01 | 이서봉 | 신규한 항바이러스성 6-아릴옥시 및 6-아릴카르보닐 2,4-피리미딘디온 유도체 및 그의 제조 방법 |
| JPH10130244A (ja) | 1996-09-06 | 1998-05-19 | Mitsubishi Chem Corp | アシクロヌクレオシドの製造方法 |
| JPH10130245A (ja) | 1996-09-06 | 1998-05-19 | Mitsubishi Chem Corp | アシクロヌクレオシドの製造方法 |
| DE69724630T2 (de) | 1996-10-02 | 2004-07-29 | Bristol-Myers Squibb Pharma Co. | 4,4-disubstituierte 1,4-dihydro-2h-3,1-benzoxazin-2-one die anwendbar sind als hiv-reverstranskriptase-inhibitoren, zwischenprodukte und verfahren zu ihrer herstellung |
| JPH10168068A (ja) | 1996-12-05 | 1998-06-23 | Mitsubishi Chem Corp | アシクロヌクレオシドの製造方法 |
| US5998411A (en) | 1998-03-17 | 1999-12-07 | Hughes Institute | Heterocyclic nonnucleoside inhibitors of reverse transcriptase |
| AU3199099A (en) * | 1998-03-27 | 1999-10-18 | Du Pont Pharmaceuticals Company | 4,4-disubstituted-3,4-dihydro-2(1h)-quinazolinthione derivatives, their preparation and their use as hiv reverse transcriptase inhibitors |
| FR2779721A1 (fr) | 1998-06-15 | 1999-12-17 | Expansia Sa | Substitution d'une 1,5-dialkyl uracile en position 6 |
| FR2779722A1 (fr) | 1998-06-15 | 1999-12-17 | Expansia Sa | Hydrogenation de 6-alpha-alkylcarboxy methylaryl-1,5-dialkyl uracile |
| WO2000051990A1 (fr) * | 1999-03-04 | 2000-09-08 | Korea Research Institute Of Chemical Technology | Derives de 2,4-pyrimidinedione antiviraux et leur procede de preparation |
| KR20000065885A (ko) | 1999-04-10 | 2000-11-15 | 최승주 | 항바이러스성 피리미딘다이온 유도체 및 그 제조방법 |
| AU7450300A (en) | 1999-09-29 | 2001-04-30 | Sankyo Company Limited | Sulfonamide derivatives |
| JP2001114767A (ja) | 1999-10-15 | 2001-04-24 | Sumika Fine Chemicals Co Ltd | ピリミジン化合物の製造方法、およびその中間体の製造方法 |
| JP2004525914A (ja) * | 2001-03-02 | 2004-08-26 | スミスクライン ビーチャム コーポレーション | 逆転写酵素阻害剤としてのベンゾフェノン類 |
| JP2002284686A (ja) | 2001-03-28 | 2002-10-03 | Sankyo Co Ltd | スルホンアミド化合物を含有する医薬組成物 |
| WO2003029226A1 (fr) | 2001-09-26 | 2003-04-10 | Basf Aktiengesellschaft | Phenoxyalkyl-, phenylthioalkyl-, phenylaminoalkyl- et phenylalkyl-sulfamoylcarboxamides a substitution heterocyclyle |
| AU2003205536A1 (en) | 2002-01-11 | 2003-07-24 | Statens Serum Institut | Anti-retroviral 5,6-disubstituted acyclopyrimidine nucleoside derivatives |
| CN1625579A (zh) | 2002-01-31 | 2005-06-08 | 西巴特殊化学品控股有限公司 | 与加氯水永久接触的聚烯烃的稳定化 |
| MXPA05002070A (es) * | 2002-08-23 | 2005-07-05 | Ribapharm Inc | Inhibidores no nucleosidicos de la transcriptasa inversa. |
| WO2006070292A2 (fr) | 2004-10-12 | 2006-07-06 | Queen's University At Kingston | Composes de pyrimidine en tant qu'agents anti-ictogeniques et/ou agents anti-epileptogeniques |
| US7250421B2 (en) | 2005-01-31 | 2007-07-31 | University Of Georgia Research Foundation, Inc. | Diketo acids with nucleobase scaffolds: anti-HIV replication inhibitors targeted at HIV integrase |
| US20060223834A1 (en) | 2005-04-04 | 2006-10-05 | Vasu Nair | Diketo acids on nucleobase scaffolds as inhibitors of Flaviviridae |
| CN103396398A (zh) * | 2005-12-29 | 2013-11-20 | 詹森药业有限公司 | 激肽原1受体拮抗剂 |
| EP1976528A2 (fr) * | 2005-12-29 | 2008-10-08 | Janssen Pharmaceutica, N.V. | Antagonistes du recepteur de la prokineticine 2 |
| WO2007106450A2 (fr) | 2006-03-10 | 2007-09-20 | University Of Georgia Research Foundation, Inc. | Acides diceto a squelettes nucleobase : inhibiteurs de replication anti-vih cibles au niveau de l'integrase du vih en therapie de combinaison |
| JP2009544710A (ja) | 2006-07-24 | 2009-12-17 | ギリアード サイエンシーズ， インコーポレイテッド | Ｈｉｖ逆転写酵素インヒビター |
| CN101784532B (zh) * | 2007-06-29 | 2014-10-22 | 韩国化学研究院 | Hiv逆转录酶抑制剂 |
-
2007
- 2007-07-24 JP JP2009521814A patent/JP2009544710A/ja active Pending
- 2007-07-24 HR HR20090114A patent/HRP20090114A2/hr not_active Application Discontinuation
- 2007-07-24 KR KR1020117017501A patent/KR20110089463A/ko not_active Ceased
- 2007-07-24 CN CNA2007800280617A patent/CN101495461A/zh active Pending
- 2007-07-24 EA EA200900213A patent/EA200900213A1/ru unknown
- 2007-07-24 KR KR1020097003836A patent/KR20090040449A/ko not_active Ceased
- 2007-07-24 WO PCT/US2007/016703 patent/WO2008016522A2/fr not_active Ceased
- 2007-07-24 US US11/880,854 patent/US8106064B2/en not_active Expired - Fee Related
- 2007-07-24 EP EP07836229A patent/EP2044037A2/fr not_active Withdrawn
- 2007-07-24 SG SG2011054681A patent/SG174016A1/en unknown
- 2007-07-24 CA CA002658479A patent/CA2658479A1/fr not_active Abandoned
- 2007-07-24 MX MX2009000871A patent/MX2009000871A/es not_active Application Discontinuation
- 2007-07-24 US US12/373,237 patent/US20100034827A1/en not_active Abandoned
- 2007-07-24 BR BRPI0714880-1A patent/BRPI0714880A2/pt not_active IP Right Cessation
- 2007-07-24 AU AU2007281604A patent/AU2007281604A1/en not_active Abandoned
- 2007-07-24 NZ NZ573793A patent/NZ573793A/en not_active IP Right Cessation
- 2007-07-24 AP AP2009004759A patent/AP2514A/xx active
- 2007-07-24 UA UAA200814467A patent/UA95955C2/ru unknown
-
2009
- 2009-01-22 IL IL196675A patent/IL196675A0/en unknown
- 2009-02-23 NO NO20090835A patent/NO20090835L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| CA2658479A1 (fr) | 2008-02-07 |
| WO2008016522A2 (fr) | 2008-02-07 |
| NZ573793A (en) | 2012-01-12 |
| AP2009004759A0 (en) | 2009-02-28 |
| KR20110089463A (ko) | 2011-08-08 |
| US20100034827A1 (en) | 2010-02-11 |
| IL196675A0 (en) | 2009-11-18 |
| US20080070920A1 (en) | 2008-03-20 |
| SG174016A1 (en) | 2011-09-29 |
| WO2008016522A3 (fr) | 2008-12-11 |
| CN101495461A (zh) | 2009-07-29 |
| KR20090040449A (ko) | 2009-04-24 |
| US8106064B2 (en) | 2012-01-31 |
| EA200900213A1 (ru) | 2009-06-30 |
| BRPI0714880A2 (pt) | 2013-05-21 |
| AU2007281604A1 (en) | 2008-02-07 |
| JP2009544710A (ja) | 2009-12-17 |
| UA95955C2 (ru) | 2011-09-26 |
| HRP20090114A2 (hr) | 2010-03-31 |
| AP2514A (en) | 2012-11-23 |
| MX2009000871A (es) | 2009-05-08 |
| EP2044037A2 (fr) | 2009-04-08 |
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