[go: up one dir, main page]

UA95955C2 - Ингибиторы обратной транскриптазы вич - Google Patents

Ингибиторы обратной транскриптазы вич

Info

Publication number
UA95955C2
UA95955C2 UAA200814467A UAA200814467A UA95955C2 UA 95955 C2 UA95955 C2 UA 95955C2 UA A200814467 A UAA200814467 A UA A200814467A UA A200814467 A UAA200814467 A UA A200814467A UA 95955 C2 UA95955 C2 UA 95955C2
Authority
UA
Ukraine
Prior art keywords
reverse transcriptase
transcriptase inhibitors
hiv reverse
compounds
hiv
Prior art date
Application number
UAA200814467A
Other languages
English (en)
Ukrainian (uk)
Inventor
Хонгйян Гуо
Чоунг У. Ким
Илл Йонг Ли
Майкл Л. Митчелл
Йонг Чан Сан
Лианхонг Ксу
Торстен А. Киршберг
Original Assignee
Кореа Ресерч Инститьют Оф Кемикал Текнолоджи
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Кореа Ресерч Инститьют Оф Кемикал Текнолоджи filed Critical Кореа Ресерч Инститьют Оф Кемикал Текнолоджи
Publication of UA95955C2 publication Critical patent/UA95955C2/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/06Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/06Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic 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
    • C07D413/06Heterocyclic 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)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Virology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (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)

Abstract

Изобретение касается соединений Формулы (I), (II) или (III) или их фармацевтически приемлемых солей, сольватов, сложных эфиров и/или фосфонатов, композиций, которые содержат такие соединения, и терапевтических способов, которые включают применение таких соединений.
UAA200814467A 2006-07-24 2007-07-24 Ингибиторы обратной транскриптазы вич UA95955C2 (ru)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US83280606P 2006-07-24 2006-07-24

Publications (1)

Publication Number Publication Date
UA95955C2 true UA95955C2 (ru) 2011-09-26

Family

ID=38997642

Family Applications (1)

Application Number Title Priority Date Filing Date
UAA200814467A UA95955C2 (ru) 2006-07-24 2007-07-24 Ингибиторы обратной транскриптазы вич

Country Status (18)

Country Link
US (2) US20100034827A1 (ru)
EP (1) EP2044037A2 (ru)
JP (1) JP2009544710A (ru)
KR (2) KR20090040449A (ru)
CN (1) CN101495461A (ru)
AP (1) AP2514A (ru)
AU (1) AU2007281604A1 (ru)
BR (1) BRPI0714880A2 (ru)
CA (1) CA2658479A1 (ru)
EA (1) EA200900213A1 (ru)
HR (1) HRP20090114A2 (ru)
IL (1) IL196675A0 (ru)
MX (1) MX2009000871A (ru)
NO (1) NO20090835L (ru)
NZ (1) NZ573793A (ru)
SG (1) SG174016A1 (ru)
UA (1) UA95955C2 (ru)
WO (1) WO2008016522A2 (ru)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20090040449A (ko) 2006-07-24 2009-04-24 길리애드 사이언시즈, 인코포레이티드 신규 hiv 역전사 효소 억제제
US8354421B2 (en) * 2007-06-29 2013-01-15 Korea Research Insitute Of Chemical Technology HIV reverse transcriptase inhibitors
CA2692460A1 (en) * 2007-06-29 2009-01-08 Korea Research Institute Of Chemical Technology Hiv reverse transcriptase inhibitors
KR20100092960A (ko) 2007-12-21 2010-08-23 한국화학연구원 Hiv 역전사 효소 억제제의 제조 방법
PL2295414T3 (pl) * 2008-06-03 2013-02-28 Taiho Pharmaceutical Co Ltd Związek uracylu o aktywności hamującej ludzką trifosfatazę deoksyurydyny lub jego sól
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
PL2399910T3 (pl) 2009-02-13 2014-09-30 Shionogi & Co Pochodne triazyny jako antagoniści receptora p2x3 i/albo p2x2/3 i kompozycja farmaceutyczna zawierająca je
GB0908394D0 (en) 2009-05-15 2009-06-24 Univ Leuven Kath Novel viral replication inhibitors
US20110196156A1 (en) * 2009-06-22 2011-08-11 Mukund Keshav Gurjar 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
ES2516916T3 (es) 2010-01-28 2014-10-31 Mapi Pharma Limited Procedimiento para la preparación de darunavir e intermedios de darunavir
US20110262406A1 (en) 2010-04-21 2011-10-27 Yale University 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
BR112013011737A2 (pt) 2010-11-15 2016-08-09 Univ Leuven Kath composto, uso de um composto composição farmacêutica, e, método de tratamento ou prevenção de uma infecção por hiv
CN107266498B (zh) * 2011-10-07 2023-10-03 吉利德科学公司 制备抗病毒核苷酸类似物的方法
CA3131037A1 (en) 2011-11-30 2013-06-06 Emory University Antiviral jak inhibitors useful in treating or preventing retroviral and other viral infections
CA2863632C (en) 2012-01-19 2017-07-11 The Johns Hopkins University Nanoparticle formulations with enhanced mucosal penetration
US9550763B2 (en) 2012-02-09 2017-01-24 Shionogi & Co., Ltd. Heterocyclic ring and carbocyclic derivative
WO2014107622A1 (en) 2013-01-07 2014-07-10 University Of Southern California Deoxyuridine triphosphatase inhibitors
US10568975B2 (en) 2013-02-05 2020-02-25 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
JP7381190B2 (ja) 2014-12-26 2023-11-15 エモリー・ユニバーシテイ N4-ヒドロキシシチジン及び誘導体並びにそれに関連する抗ウイルス用途
EP3250184B1 (en) 2015-01-27 2024-12-18 The Johns Hopkins University Hypotonic hydrogel formulations for enhanced transport of active agents at mucosal surfaces
US10570100B2 (en) 2015-07-08 2020-02-25 University Of Southern California Deoxyuridine triphosphatase inhibitors containing amino sulfonyl linkage
WO2017006283A1 (en) 2015-07-08 2017-01-12 Cv6 Therapeutics (Ni) Limited Deoxyuridine triphosphatase inhibitors containing cyclopropano linkage
AU2016290987C1 (en) 2015-07-08 2023-07-20 Cv6 Therapeutics (Ni) Limited Hydantoin containing deoxyuridine triphosphatase inhibitors
WO2017006270A1 (en) 2015-07-08 2017-01-12 University Of Southern California Deoxyuridine triphosphatase inhibitors
WO2018098204A1 (en) 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited 6-membered uracil isosteres
WO2018098208A1 (en) 2016-11-23 2018-05-31 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
US10858344B2 (en) 2016-11-23 2020-12-08 Cv6 Therapeutics (Ni) Limited Hydantoin containing deoxyuridine triphosphatase inhibitors
WO2018098209A1 (en) 2016-11-23 2018-05-31 Cv6 Therapeutics (Ni) Limited Amino sulfonyl compounds
US11247984B2 (en) 2017-01-05 2022-02-15 Cv6 Therapeutics (Ni) Limited Uracil containing compounds
WO2018169038A1 (ja) * 2017-03-17 2018-09-20 Meiji Seikaファルマ株式会社 植物病害防除剤
KR102626210B1 (ko) 2017-12-07 2024-01-18 에모리 유니버시티 N4-하이드록시사이티딘 및 유도체 및 이와 관련된 항-바이러스 용도
WO2020210805A1 (en) 2019-04-11 2020-10-15 The Johns Hopkins University Nanoparticles for drug delivery to brain
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)

* Cited by examiner, † Cited by third party
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
WO1995023138A1 (en) 1994-02-28 1995-08-31 Sunkyong Industries Co., Ltd. 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
RU2138487C1 (ru) 1996-02-22 1999-09-27 Самдзин Фармасьютикал Ко., Лтд. Новые противовирусные гомокарбоциклические нуклеозидные производные замещенных пиримидиндионов, способ их получения и композиция, содержащая их в качестве активных ингредиентов
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
EP1068189A1 (en) * 1998-03-27 2001-01-17 Bristol-Myers Squibb Pharma 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
AU2946300A (en) * 1999-03-04 2000-09-21 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
WO2001023363A1 (en) 1999-09-29 2001-04-05 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
KR100638954B1 (ko) * 2001-03-02 2006-10-25 스미스클라인 비참 코포레이션 역전사 효소 억제제로서의 벤조페논
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
AU2003215542A1 (en) 2002-01-31 2003-09-02 Ciba Specialty Chemicals Holding Inc. Stabilization of polyolefins in permanent contact with chlorinated water
AU2003295324B2 (en) * 2002-08-23 2008-08-28 Ardea Biosciences,Inc. Non-nucleoside reverse transcriptase inhibitors
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
JP5452934B2 (ja) * 2005-12-29 2014-03-26 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ プロキネチシン1受容体アンタゴニスト
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
KR20090040449A (ko) * 2006-07-24 2009-04-24 길리애드 사이언시즈, 인코포레이티드 신규 hiv 역전사 효소 억제제
CA2692460A1 (en) * 2007-06-29 2009-01-08 Korea Research Institute Of Chemical Technology Hiv reverse transcriptase inhibitors

Also Published As

Publication number Publication date
CN101495461A (zh) 2009-07-29
AP2009004759A0 (en) 2009-02-28
WO2008016522A3 (en) 2008-12-11
IL196675A0 (en) 2009-11-18
HRP20090114A2 (hr) 2010-03-31
SG174016A1 (en) 2011-09-29
EA200900213A1 (ru) 2009-06-30
CA2658479A1 (en) 2008-02-07
NZ573793A (en) 2012-01-12
NO20090835L (no) 2009-04-23
BRPI0714880A2 (pt) 2013-05-21
MX2009000871A (es) 2009-05-08
US20100034827A1 (en) 2010-02-11
KR20110089463A (ko) 2011-08-08
KR20090040449A (ko) 2009-04-24
EP2044037A2 (en) 2009-04-08
US8106064B2 (en) 2012-01-31
AU2007281604A1 (en) 2008-02-07
WO2008016522A2 (en) 2008-02-07
US20080070920A1 (en) 2008-03-20
JP2009544710A (ja) 2009-12-17
AP2514A (en) 2012-11-23

Similar Documents

Publication Publication Date Title
UA95955C2 (ru) Ингибиторы обратной транскриптазы вич
MX2009013804A (es) Inhibidores novedosos de transcriptasa inversa de vih.
WO2008011116A3 (en) Aza-peptide protease inhibitors
WO2008011117A3 (en) Antiviral protease inhibitors
MX2009009920A (es) Inhibidores no nucleosidos de transcriptasa inversa.
TN2009000049A1 (en) A pyrrolopyrazin as syk-kinase inhibitor
GEP20115320B (en) Non-nucleoside reverse transcriptase inhibitors
SG179418A1 (en) Inhibitors of the hedgehog pathway
PT1940839E (pt) Inibidores de piridopirimidinona pi3k alfa
WO2008086226A3 (en) Factor xa inhibitors
UA94606C2 (ru) Производные тиоксантина, композиция, которая их содержит, и их применение в терапии
TW200618804A (en) Phosphonate analogs of HIV inhibitor compounds
EA200900135A1 (ru) Производные пиразола в качестве ингибиторов цитохрома р450
WO2009155121A3 (en) Inhibitors of pi3 kinase
TW200833370A (en) Pharmaceutical composition containing low substituted hydroxypropylcellulose
GEP20125459B (en) Compounds for inhibiting mitotic progression
MX2009005691A (es) Inhibidores de la enzima de diacilglicerol o-acilotransferasa tipo i.
SE0400284D0 (sv) Novel compounds
MY149512A (en) Pyrazolylaminopyridine derivatives useful as kinase inhibitors
IL193252A0 (en) N-hydroxyacrylamide compounds
TN2010000038A1 (en) Organic compounds
TW200616979A (en) Non-nucleoside reverse transcriptase inhibitors
UA103329C2 (ru) Соли соединений-ингибиторов вич
MX2009010932A (es) Inhibidores no nucleosidos de transcriptasa inversa.
MX2009012704A (es) Inhibidores de transcriptasa inversa de no nucleosidos.