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
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)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Oppfinnelsen vedrører forbindelser med formel (I), (II) eller (III): eller farmasøytisk akseptabelt salt, solvat, ester og/eller fosfonat derav, preparater som inneholder slike forbindelser, og terapeutiske fremgangsmåter som inkluderer administreringen av slike forbindelser.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US83280606P | 2006-07-24 | 2006-07-24 | |
PCT/US2007/016703 WO2008016522A2 (en) | 2006-07-24 | 2007-07-24 | Hiv reverse transcriptase inhibitors |
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 (no) |
EP (1) | EP2044037A2 (no) |
JP (1) | JP2009544710A (no) |
KR (2) | KR20110089463A (no) |
CN (1) | CN101495461A (no) |
AP (1) | AP2514A (no) |
AU (1) | AU2007281604A1 (no) |
BR (1) | BRPI0714880A2 (no) |
CA (1) | CA2658479A1 (no) |
EA (1) | EA200900213A1 (no) |
HR (1) | HRP20090114A2 (no) |
IL (1) | IL196675A0 (no) |
MX (1) | MX2009000871A (no) |
NO (1) | NO20090835L (no) |
NZ (1) | NZ573793A (no) |
SG (1) | SG174016A1 (no) |
UA (1) | UA95955C2 (no) |
WO (1) | WO2008016522A2 (no) |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101495461A (zh) | 2006-07-24 | 2009-07-29 | 吉里德科学公司 | 新的hiv逆转录酶抑制剂 |
US8354421B2 (en) * | 2007-06-29 | 2013-01-15 | Korea Research Insitute Of Chemical Technology | HIV reverse transcriptase inhibitors |
TW200918507A (en) * | 2007-06-29 | 2009-05-01 | Gilead Sciences Inc | Novel HIV reverse transcriptase inhibitors |
US8119800B2 (en) | 2007-12-21 | 2012-02-21 | Korea Research Institute Of Chemical Technology | Processes for preparing HIV reverse transcriptase inhibitors |
MY149180A (en) | 2008-06-03 | 2013-07-31 | Taiho Pharmaceutical Co Ltd | Uracil compound having inhibitor activity on human deoxyuridine triphosphatase or salt thereof |
WO2010068899A1 (en) * | 2008-12-12 | 2010-06-17 | Creighton University | Nanoparticles comprising combinations of antiretroviral agents and use thereof |
US8921415B2 (en) | 2009-01-29 | 2014-12-30 | Mapi Pharma Ltd. | Polymorphs of darunavir |
SG173647A1 (en) | 2009-02-13 | 2011-10-28 | Shionogi & Co | Novel triazine derivative and pharmaceutical composition containing same |
GB0908394D0 (en) | 2009-05-15 | 2009-06-24 | Univ Leuven Kath | Novel viral replication inhibitors |
WO2010150279A2 (en) * | 2009-06-22 | 2010-12-29 | Emcure Pharmaceuticals Limited | Process for synthesis of diarylpyrimidine non-nucleoside reverse transcriptase inhibitor |
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 |
WO2011133803A1 (en) | 2010-04-21 | 2011-10-27 | Helix Therapeutics, Inc. | Compositions and methods for targeted inactivation of hiv cell surface receptors |
WO2011133802A1 (en) | 2010-04-21 | 2011-10-27 | Helix Therapeutics, Inc. | Compositions and methods for treatment of lysosomal storage disorders |
BR112013002984B1 (pt) | 2010-08-10 | 2021-10-26 | Shionogi & Co., Ltd | Compostos derivados de triazina e composições farmacêuticas que os compreendem |
US9212130B2 (en) | 2010-08-10 | 2015-12-15 | Shionogi & Co., Ltd. | Heterocyclic derivative and pharmaceutical composition comprising the same |
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 |
KR20140003438A (ko) | 2010-11-15 | 2014-01-09 | 카톨리에케 유니버시테이트 루벤 | 항바이러스성 축합 헤테로사이클릭 화합물 |
PT3333173T (pt) | 2011-10-07 | 2019-09-10 | Gilead Sciences Inc | Métodos de preparação de análogos de nucleótidos antivirais |
EP2785184B1 (en) | 2011-11-30 | 2020-06-10 | Emory University | Compositions comprising jak inhibitors and haart drugs for use in the prevention or treatment of hiv |
CN104936620B (zh) | 2012-01-19 | 2019-08-09 | 约翰霍普金斯大学 | 增强粘膜渗透的纳米粒子调配物 |
WO2013118855A1 (ja) | 2012-02-09 | 2013-08-15 | 塩野義製薬株式会社 | 複素環および炭素環誘導体 |
CN105189478B (zh) | 2013-01-07 | 2019-10-22 | 南加州大学 | 脱氧尿苷三磷酸酶抑制剂 |
WO2014124006A1 (en) | 2013-02-05 | 2014-08-14 | The Johns Hopkins University | Nanoparticles for magnetic resonance imaging tracking and methods of making and using thereof |
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 |
WO2015127389A1 (en) | 2014-02-23 | 2015-08-27 | The Johns Hopkins University | Hypotonic enema formulations and methods of use |
BR112017013858A2 (pt) | 2014-12-26 | 2018-02-27 | Univ Emory | n4-hidroxicitidina e derivados e usos antivirais relacionados aos mesmos |
KR20170106460A (ko) | 2015-01-27 | 2017-09-20 | 더 존스 홉킨스 유니버시티 | 점막표면에서 활성제의 향상된 수송을 위한 저장성 하이드로겔 제제 |
WO2017006270A1 (en) | 2015-07-08 | 2017-01-12 | University Of Southern California | Deoxyuridine triphosphatase inhibitors |
US10570100B2 (en) | 2015-07-08 | 2020-02-25 | University Of Southern California | Deoxyuridine triphosphatase inhibitors containing amino sulfonyl linkage |
US10544105B2 (en) | 2015-07-08 | 2020-01-28 | Cv6 Therapeutics (Ni) Limited | Deoxyuridine triphosphatase inhibitors containing cyclopropano linkage |
EA037990B1 (ru) | 2015-07-08 | 2021-06-21 | Св6 Терапьютикс (Най) Лимитед | Ингибиторы дезоксиуридинтрифосфатазы, содержащие гидантоин |
US11168059B2 (en) | 2016-11-23 | 2021-11-09 | Cv6 Therapeutics (Ni) Limited | Amino sulfonyl compounds |
WO2018098206A1 (en) | 2016-11-23 | 2018-05-31 | Cv6 Therapeutics (Ni) Limited | Hydantoin containing deoxyuridine triphosphatase inhibitors |
US10829457B2 (en) | 2016-11-23 | 2020-11-10 | Cv6 Therapeutics (Ni) Limited | Nitrogen ring linked deoxyuridine triphosphatase inhibitors |
WO2018098207A1 (en) | 2016-11-23 | 2018-05-31 | Cv6 Therapeutics (Ni) Limited | Hydantoin containing deoxyuridine triphosphatase inhibitors |
WO2018098204A1 (en) | 2016-11-23 | 2018-05-31 | Cv6 Therapeutics (Ni) Limited | 6-membered uracil isosteres |
US11247984B2 (en) | 2017-01-05 | 2022-02-15 | Cv6 Therapeutics (Ni) Limited | Uracil containing compounds |
TWI775823B (zh) * | 2017-03-17 | 2022-09-01 | 日商Mmag股份有限公司 | 植物病害防治劑 |
MX2020005392A (es) | 2017-12-07 | 2020-12-07 | Univ Emory | N4-hidroxicitidina y derivados y usos antivirales relacionados con los mismos. |
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 |
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 |
CA2159817C (en) * | 1994-02-28 | 2000-09-12 | Dae Kee Kim | Pyrimidine acyclonucleoside derivatives |
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 |
CA2217026C (en) * | 1996-02-22 | 2001-11-20 | Samjin Pharmaceutical Co., Ltd. | New antiviral substituted pyrimidinedione homocarbocyclic nucleoside derivatives and methods for the preparation thereof and compositions containing the same as active ingredients |
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 |
AU4802797A (en) | 1996-10-02 | 1998-04-24 | Du Pont Pharmaceuticals Company | 4,4-disubstituted-1,4-dihydro-2h-3,1-benzoxazin-2-ones useful as hiv rever se transcriptase inhibitors and intermediates and processes for making the same |
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 |
JP2002509922A (ja) * | 1998-03-27 | 2002-04-02 | デュポン ファーマシューティカルズ カンパニー | 4,4−二置換−3,4−ジヒドロ−2(1h)−キナゾリンチオン誘導体、それらの調製法、およびhiv逆転写酵素阻害剤としてのそれらの使用 |
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 |
EP1159271B1 (en) * | 1999-03-04 | 2004-08-25 | Korea Research Institute of Chemical Technology | Antiviral 2,4-pyrimidinedione derivatives and process for the preparation thereof |
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 |
AU2002254056C1 (en) * | 2001-03-02 | 2006-04-13 | Smithkline Beecham Corporation | Benzophenones as inhibitors of reverse transcriptase |
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 (en) | 2001-09-26 | 2003-04-10 | Basf Aktiengesellschaft | Heterocyclyl substituted phenoxyalkyl-, phenylthioalkyl-, phenylaminoalkyl- and phenylalkyl-sulfamoylcarboxamides |
AU2003205536A1 (en) | 2002-01-11 | 2003-07-24 | Statens Serum Institut | Anti-retroviral 5,6-disubstituted acyclopyrimidine nucleoside derivatives |
ATE345364T1 (de) | 2002-01-31 | 2006-12-15 | Ciba Sc Holding Ag | Stabilisierung von polyolefinen, die in permanentem kontakt mit chloriertem wasser stehen |
ATE504294T1 (de) * | 2002-08-23 | 2011-04-15 | Ardea Biosciences Inc | Nichtnukleosidische reverse-transkriptase-hemmer |
WO2006070292A2 (en) | 2004-10-12 | 2006-07-06 | Queen's University At Kingston | Pyrimidine compounds as anti-ictogenic and/or anti-epileptogenic agents |
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 |
EP1976528A2 (en) * | 2005-12-29 | 2008-10-08 | Janssen Pharmaceutica, N.V. | Prokineticin 2 receptor antagonists |
CA2635842C (en) * | 2005-12-29 | 2015-02-17 | Janssen Pharmaceutica N.V. | Prokineticin 1 receptor antagonists |
WO2007106450A2 (en) | 2006-03-10 | 2007-09-20 | University Of Georgia Research Foundation, Inc. | Diketo acids with nucleobase scaffolds: anti-hiv replication inhibitors targeted at hiv integrase in combination therapy |
CN101495461A (zh) * | 2006-07-24 | 2009-07-29 | 吉里德科学公司 | 新的hiv逆转录酶抑制剂 |
TW200918507A (en) * | 2007-06-29 | 2009-05-01 | Gilead Sciences Inc | Novel HIV reverse transcriptase inhibitors |
-
2007
- 2007-07-24 CN CNA2007800280617A patent/CN101495461A/zh active Pending
- 2007-07-24 UA UAA200814467A patent/UA95955C2/ru unknown
- 2007-07-24 EP EP07836229A patent/EP2044037A2/en not_active Withdrawn
- 2007-07-24 BR BRPI0714880-1A patent/BRPI0714880A2/pt not_active IP Right Cessation
- 2007-07-24 CA CA002658479A patent/CA2658479A1/en not_active Abandoned
- 2007-07-24 KR KR1020117017501A patent/KR20110089463A/ko not_active Application Discontinuation
- 2007-07-24 JP JP2009521814A patent/JP2009544710A/ja active Pending
- 2007-07-24 EA EA200900213A patent/EA200900213A1/ru unknown
- 2007-07-24 MX MX2009000871A patent/MX2009000871A/es not_active Application Discontinuation
- 2007-07-24 SG SG2011054681A patent/SG174016A1/en unknown
- 2007-07-24 KR KR1020097003836A patent/KR20090040449A/ko not_active Application Discontinuation
- 2007-07-24 NZ NZ573793A patent/NZ573793A/en not_active IP Right Cessation
- 2007-07-24 AU AU2007281604A patent/AU2007281604A1/en not_active Abandoned
- 2007-07-24 US US11/880,854 patent/US8106064B2/en not_active Expired - Fee Related
- 2007-07-24 AP AP2009004759A patent/AP2514A/xx active
- 2007-07-24 US US12/373,237 patent/US20100034827A1/en not_active Abandoned
- 2007-07-24 WO PCT/US2007/016703 patent/WO2008016522A2/en active Application Filing
-
2009
- 2009-01-22 IL IL196675A patent/IL196675A0/en unknown
- 2009-02-23 NO NO20090835A patent/NO20090835L/no not_active Application Discontinuation
- 2009-02-24 HR HR20090114A patent/HRP20090114A2/hr not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
IL196675A0 (en) | 2009-11-18 |
SG174016A1 (en) | 2011-09-29 |
WO2008016522A2 (en) | 2008-02-07 |
CA2658479A1 (en) | 2008-02-07 |
UA95955C2 (ru) | 2011-09-26 |
EP2044037A2 (en) | 2009-04-08 |
KR20110089463A (ko) | 2011-08-08 |
AP2514A (en) | 2012-11-23 |
US8106064B2 (en) | 2012-01-31 |
NZ573793A (en) | 2012-01-12 |
WO2008016522A3 (en) | 2008-12-11 |
MX2009000871A (es) | 2009-05-08 |
US20100034827A1 (en) | 2010-02-11 |
AU2007281604A1 (en) | 2008-02-07 |
EA200900213A1 (ru) | 2009-06-30 |
US20080070920A1 (en) | 2008-03-20 |
KR20090040449A (ko) | 2009-04-24 |
CN101495461A (zh) | 2009-07-29 |
AP2009004759A0 (en) | 2009-02-28 |
HRP20090114A2 (hr) | 2010-03-31 |
JP2009544710A (ja) | 2009-12-17 |
BRPI0714880A2 (pt) | 2013-05-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
NO20090835L (no) | Nye HIV-reverstranskriptaseinhibitorer | |
EA200971115A1 (ru) | Новые ингибиторы обратной транскриптазы вич | |
NO20080865L (no) | Spirokromanonderivater som acetyl-koenzym-A-karboksylase(ACC)inhibitorer | |
NO20072978L (no) | Nye betuinderivater, preparat derav og anvendelse derav | |
SE0400284D0 (sv) | Novel compounds | |
EA200970156A1 (ru) | Пиридизиноновые производные | |
WO2008086226A3 (en) | Factor xa inhibitors | |
DE602004008098D1 (de) | Substituierte 2h-ä1,2,4ütriazoloä4,3-aüpyrazine als gsk-3-inhibitoren | |
EA200802288A1 (ru) | Замещенные имидазолы, композиция на их основе, способ профилактики или лечения нежелательного тромбообразования с их помощью и способ ингибирования коагуляции образцов крови | |
EA200900135A1 (ru) | Производные пиразола в качестве ингибиторов цитохрома р450 | |
NO20091553L (no) | Fenylderivater og deres anvendelse som immunmodulatorer | |
NO20084418L (no) | Azolopyridin-3-on derivater som inhibitorer av endoteliallipase | |
NO20082090L (no) | Pyridopyrimidinoninhibitorer av P13K alfa | |
NO20072371L (no) | Kinuklidinderivater og deres anvendelse som muskarine M3-reseptorantagonister | |
NO20070224L (no) | 2-karbamid-4-fenyltiazolderivater, fremstilling og terapeutisk anvendelse derav | |
PH12014501283A1 (en) | 4`-azido, 3``-fluoro substituted nucleoside derivatives as inhibitors of hcv rna replication | |
NO20092723L (no) | Indazolylester og amidderivater for behandling av gluccocorticoid reseptormedierte sykdommer | |
NO20055568L (no) | Substituerte 1,4-diazepiner og anvendelser derav | |
NO20092286L (no) | Nitrogenhaldige heterosykliske forbindelser og anvendelse derav | |
NO20063449L (no) | Substituerte heterocykler og deres anvendelse | |
NO20071617L (no) | Indozolonderivater som 11B-HSD1-inhibitorer | |
NO20072963L (no) | 5-substituerte kinolin- og isokinolinderivater, fremgangsmate for deres fremstilling og deres anvendelse som betennelseshemmere | |
NO20085212L (no) | Nye pyridinanaloger | |
EA201291217A1 (ru) | ФАРМАЦЕВТИЧЕСКИЕ КОМПОЗИЦИИ, СОДЕРЖАЩИЕ ПРОИЗВОДНЫЕ 1-(β-D-ГЛЮКОПИРАНОЗИЛ)-2-ТИЕНИЛМЕТИЛБЕНЗОЛА КАК ИНГИБИТОРЫ НЗПГ | |
WO2008011117A3 (en) | Antiviral protease inhibitors |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC2A | Withdrawal, rejection or dismissal of laid open patent application |