BRPI9915552B8 - pirimidinas inibidoras da reprodução do hiv - Google Patents
pirimidinas inibidoras da reprodução do hivInfo
- Publication number
- BRPI9915552B8 BRPI9915552B8 BRPI9915552A BR9915552A BRPI9915552B8 BR PI9915552 B8 BRPI9915552 B8 BR PI9915552B8 BR PI9915552 A BRPI9915552 A BR PI9915552A BR 9915552 A BR9915552 A BR 9915552A BR PI9915552 B8 BRPI9915552 B8 BR PI9915552B8
- Authority
- BR
- Brazil
- Prior art keywords
- alkyl
- optionally substituted
- nhc
- amino
- alkyloxycarbonyl
- Prior art date
Links
- 230000002401 inhibitory effect Effects 0.000 title abstract 2
- 150000003230 pyrimidines Chemical class 0.000 title abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000001475 halogen functional group Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 2
- 241000725303 Human immunodeficiency virus Species 0.000 abstract 2
- -1 cyano, nitro, amino Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 2
- 125000002098 pyridazinyl group Chemical group 0.000 abstract 2
- 125000004076 pyridyl group Chemical group 0.000 abstract 2
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
Classifications
-
- 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
- C07D403/12—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 chain containing hetero atoms as chain links
-
- 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
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
-
- 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
- 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
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/80—Oxygen atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
patente de invenção: <b>"pirimidinas inibidoras da reprodução do hiv"<d>. esta invenção trata do uso de compostos da fórmula (i), os n-óxidos, os sais de adição farmaceuticamente aceitáveis, aminas qua-ternárias e a sua forma estereoquimicamente isoméricas, onde a^ 1^=a^ 2^=a^ 3^=a^ 4^-forma um fenila, piridinila, pirimidinila, piridazinila ou pirazinila com o grupo vinila agregado; n é 0 a 4; e onde possível 5; r^ 1^ é hidrogênio, arila, formila, c~ 1-6~alquilcarbonila, c~ 1-6~alquila, c~ 1-6~alquiloxicarbonila, c~ 1-6~ alquila substituída ou c~ 1-6~alquilóxic~ 1-6~ alquilcarbonila substituída; cada r3 independentemente é hidróxi, halo, opcionalmente substituído c~ 1-6~ alquila, c~ 2-6~alquenila ou c~ 2-6~-alquinila, c~ 3-7~cicloalquila, c~ 1-6~alquilóxi, c~ 1-6~alquiloxicarbonila, carboxila, ciano, nitro, amino, mono- ou di(c~ 1-6~alquila)amino, polihalometila, polihalo-metilóxi, polihalometiltio, -s(=o)~ p~r^ 6^, -nh-s(=o)~ p~r^ 6^, - c(=o)r^ 6^, -nhc(=o)h, -c(=o)nhnh~ 2~, -nhc(=o)r^ 6^, -c(=nh)r^ 6^ ou um anel heterocíclico de 5 membros; p é 1 ou 2; l é opcionalmente substituído c~ 1-10~ alquila, c~ 2-10~ alquenila ou c~ 3-7~ cicloalquila; ou l é -x-r^ 3^ onde r^ 3^ é fenila, piridinila, pirimidinila, pirazinila ou piridazinila, opcionalmente substituída x é -nr^ 1^-, -nh-nh-, -n=n, -o-, c(=o)-choh-, -s-, -s(=o)- ou -s(=o)~ 2~-; q é hidrogênio, c~ 1-6~alquila, halo, polihalo-c~ 1-6~alquila ou um grupo opcionalmente substituído; y representa hidróxi, halo c~ 3-7~cicloalquila, c~ 1-6~alquila, c~ 2-6~ alquenila ou c~ 2-6~ alquila, opcionalmente substituída, c~ 1-6~alquilóxi, c~ 1-6~ alquiloxicarbonila, carbonila, ciano, nitro, amino, mono-ou di(c~ 1-6~ alquila)amino, polihalo-metila, polihalometilóxi, polihalometitio, -s(=o)~ p~r^ 6^, -nh-s(=o)~ p~r^ 6^, -c(=o)r^ 6^, -nhc(=o)h, -c(=o)nhnh~ 2~, -nhc(=o)r^ 6^, -c(=nh)r^ 6^ ou arila; arila é fenila opcionalmente substituído; het é um radical heterocíclico opcionalmente substituída; para a fabricação de um medicamento para o tratamento de doentes sofrendo da infecção do hiv (vírus da imunodeficiência humana).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10779298P | 1998-11-10 | 1998-11-10 | |
| US14396299P | 1999-07-15 | 1999-07-15 | |
| PCT/EP1999/007417 WO2000027825A1 (en) | 1998-11-10 | 1999-09-24 | Hiv replication inhibiting pyrimidines |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| BR9915552A BR9915552A (pt) | 2001-08-14 |
| BR9915552B1 BR9915552B1 (pt) | 2013-11-19 |
| BRPI9915552B8 true BRPI9915552B8 (pt) | 2021-05-25 |
Family
ID=26805159
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI9915552A BRPI9915552B8 (pt) | 1998-11-10 | 1999-09-24 | pirimidinas inibidoras da reprodução do hiv |
Country Status (41)
| Country | Link |
|---|---|
| US (5) | US6878717B2 (pt) |
| EP (2) | EP1002795B1 (pt) |
| JP (1) | JP3635238B2 (pt) |
| KR (1) | KR100658489B1 (pt) |
| CN (1) | CN1214013C (pt) |
| AP (1) | AP1683A (pt) |
| AR (1) | AR024227A1 (pt) |
| AT (2) | ATE233740T1 (pt) |
| AU (2) | AU762523C (pt) |
| BG (1) | BG65103B1 (pt) |
| BR (1) | BRPI9915552B8 (pt) |
| CA (1) | CA2350801C (pt) |
| CY (1) | CY2008021I2 (pt) |
| CZ (1) | CZ301367B6 (pt) |
| DE (3) | DE122009000003I1 (pt) |
| DK (1) | DK1002795T3 (pt) |
| EA (1) | EA004049B1 (pt) |
| EE (1) | EE05086B1 (pt) |
| ES (2) | ES2338760T3 (pt) |
| FR (1) | FR09C0004I2 (pt) |
| HK (1) | HK1048817B (pt) |
| HR (2) | HRP20010161B9 (pt) |
| HU (2) | HU230394B1 (pt) |
| ID (1) | ID28376A (pt) |
| IL (2) | IL143023A0 (pt) |
| LT (1) | LTC1002795I2 (pt) |
| LU (1) | LU91528I2 (pt) |
| MY (1) | MY121108A (pt) |
| NL (1) | NL300373I2 (pt) |
| NO (3) | NO318801B1 (pt) |
| NZ (1) | NZ511116A (pt) |
| OA (1) | OA11674A (pt) |
| PL (1) | PL204427B1 (pt) |
| PT (1) | PT1002795E (pt) |
| SI (1) | SI1002795T1 (pt) |
| SK (2) | SK287270B6 (pt) |
| TR (1) | TR200101306T2 (pt) |
| TW (1) | TWI238161B (pt) |
| UA (1) | UA70966C2 (pt) |
| WO (1) | WO2000027825A1 (pt) |
| ZA (1) | ZA200103769B (pt) |
Families Citing this family (129)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI9915552B8 (pt) * | 1998-11-10 | 2021-05-25 | Janssen Pharmaceutica Nv | pirimidinas inibidoras da reprodução do hiv |
| GB9914258D0 (en) * | 1999-06-18 | 1999-08-18 | Celltech Therapeutics Ltd | Chemical compounds |
| SI1225874T1 (sl) | 1999-09-24 | 2006-06-30 | Janssen Pharmaceutica Nv | Protivirusne trdne disperzije |
| DE19945982A1 (de) | 1999-09-24 | 2001-03-29 | Knoll Ag | Geschwindigkeitsbestimmte Partikel |
| MXPA02003436A (es) | 1999-10-07 | 2002-08-20 | Amgen Inc | Inhibidores de triazina cinasa. |
| AU2001237041B9 (en) | 2000-02-17 | 2005-07-28 | Amgen Inc. | Kinase inhibitors |
| WO2001085700A2 (en) | 2000-05-08 | 2001-11-15 | Janssen Pharmaceutica N.V. | Hiv replication inhibiting pyrimidines and triazines |
| ES2559273T3 (es) | 2000-05-08 | 2016-02-11 | Janssen Pharmaceutica Nv | Profármacos de pirimidinas que inhiben la replicación del VIH |
| CN1302418C (zh) * | 2000-11-01 | 2007-02-28 | 斯雷普内姆斯·Com公司 | 集成注册机构的互联网域名获取系统 |
| JP4291135B2 (ja) | 2001-05-29 | 2009-07-08 | バイエル・シエーリング・ファーマ アクチエンゲゼルシャフト | Cdk阻害性ピリミジン、それらの製造および薬剤としての使用 |
| US6958211B2 (en) | 2001-08-08 | 2005-10-25 | Tibotech Bvba | Methods of assessing HIV integrase inhibitor therapy |
| US8101629B2 (en) | 2001-08-13 | 2012-01-24 | Janssen Pharmaceutica N.V. | Salt of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino]benzonitrile |
| JO3429B1 (ar) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
| US7638522B2 (en) | 2001-08-13 | 2009-12-29 | Janssen Pharmaceutica N.V. | Salt of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino] benzonitrile |
| US7115617B2 (en) | 2001-08-22 | 2006-10-03 | Amgen Inc. | Amino-substituted pyrimidinyl derivatives and methods of use |
| US6939874B2 (en) | 2001-08-22 | 2005-09-06 | Amgen Inc. | Substituted pyrimidinyl derivatives and methods of use |
| EP1453516A2 (de) | 2001-10-17 | 2004-09-08 | Boehringer Ingelheim Pharma GmbH & Co.KG | 5-substituierte 4-amino-2-phenylamino-pyrimdinderivate und ihre verwendung als beta-amyloid modulatoren |
| EP1438053B1 (de) | 2001-10-17 | 2008-09-10 | Boehringer Ingelheim Pharma GmbH & Co.KG | Pyrimidinderivate, arzneimittel enthaltend diese verbindungen, deren verwendung und verfahren zu ihrer herstellung |
| HUP0402330A3 (en) | 2001-11-01 | 2010-03-29 | Janssen Pharmaceutica Nv | Amide derivatives as glycogen synthase kinase 3-beta inhibitors, process for producing them, pharmaceutical compositions containing them and use thereof |
| US7514445B2 (en) | 2001-11-01 | 2009-04-07 | Janssen Pharmaceutica N.V. | Heteroaryl amines as glycogen synthase kinase 3β inhibitors (GSK3 inhibitors) |
| SE0104140D0 (sv) | 2001-12-07 | 2001-12-07 | Astrazeneca Ab | Novel Compounds |
| TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| MY140390A (en) | 2002-03-13 | 2009-12-31 | Janssen Pharmaceutica Nv | Sulfonylamino-derivatives as novel inhibitors of histone deacetylase |
| PL212089B1 (pl) | 2002-03-13 | 2012-08-31 | Janssen Pharmaceutica Nv | Związki heterocykliczne jako inhibitory deacetylazy histonowej, kompozycja farmaceutyczna je zawierająca, ich zastosowanie, sposób wytwarzania, sposób wykrywania lub identyfikacji HDAC oraz kompozycja |
| GB0206215D0 (en) | 2002-03-15 | 2002-05-01 | Novartis Ag | Organic compounds |
| AU2003222310B2 (en) * | 2002-05-03 | 2009-04-09 | Janssen Pharmaceutica N.V. | Polymeric microemulsions |
| AR039540A1 (es) * | 2002-05-13 | 2005-02-23 | Tibotec Pharm Ltd | Compuestos microbicidas con contenido de pirimidina o triazina |
| TW200409629A (en) | 2002-06-27 | 2004-06-16 | Bristol Myers Squibb Co | 2,4-disubstituted-pyridine N-oxides useful as HIV reverse transcriptase inhibitors |
| JP2006514989A (ja) | 2002-07-29 | 2006-05-18 | ライジェル ファーマシューティカルズ | 2,4−ピリミジンジアミン化合物による自己免疫疾患の治療および予防方法 |
| CA2686429C (en) | 2002-08-09 | 2010-11-16 | Janssen Pharmaceutica N.V. | Processes for the preparation of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl]amino]benzonitrile |
| US7815934B2 (en) * | 2002-09-20 | 2010-10-19 | Alpharma Pharmaceuticals, Llc | Sequestering subunit and related compositions and methods |
| MXPA05005547A (es) * | 2002-11-28 | 2005-07-26 | Schering Ag | Pirimidinas inhibidoras de chk, pdk y akt, su produccion y uso como agentes farmaceuticos. |
| GEP20084540B (en) | 2003-01-14 | 2008-11-25 | Arena Pharm Inc | 1,2,3-trisubstituted aryl and heteroaryl derivatives as modulators of metabolism and the prpphylaxis and treatment of disorders related thereto such as diabetes and hyperglycemia |
| HRP20050688B1 (hr) | 2003-02-07 | 2017-03-24 | Janssen Pharmaceutica N.V. | Derivati pirimidina za sprječavanje hiv infekcije |
| WO2004074266A1 (en) * | 2003-02-07 | 2004-09-02 | Janssen Pharmaceutica N.V. | Hiv inhibiting 1,2,4-triazines |
| CL2004000306A1 (es) | 2003-02-20 | 2005-04-08 | Tibotec Pharm Ltd | Compuestos derivados de pirimidina sustituidas con indano; proceso para su preparacion; composicion farmaceutica que lo comprende; combinacion farmaceutica; y su uso para el tratamiento o profilaxis de una enfermedad infecciosa. |
| ATE433447T1 (de) * | 2003-02-20 | 2009-06-15 | Smithkline Beecham Corp | Pyrimiidinverbindungen |
| AR045047A1 (es) | 2003-07-11 | 2005-10-12 | Arena Pharm Inc | Derivados arilo y heteroarilo trisustituidos como moduladores del metabolismo y de la profilaxis y tratamiento de desordenes relacionados con los mismos |
| EP1648467B1 (en) | 2003-07-17 | 2018-03-21 | Janssen Sciences Ireland UC | Process for preparing particles containing an antiviral |
| ES2421139T3 (es) | 2003-07-30 | 2013-08-29 | Rigel Pharmaceuticals, Inc. | Compuestos de 2,4-pirimidindiamina para su uso en el tratamiento o la prevención de enfermedades autoinmunitarias |
| CN100475815C (zh) * | 2003-09-25 | 2009-04-08 | 詹森药业有限公司 | 抑制hiv复制的嘌呤衍生物 |
| EP1728186A2 (en) | 2004-03-02 | 2006-12-06 | Virco Bvba | Estimation of clinical cut-offs |
| EP1598343A1 (de) | 2004-05-19 | 2005-11-23 | Boehringer Ingelheim International GmbH | 2-Arylaminopyrimidine als PLK Inhibitoren |
| SG156687A1 (en) | 2004-07-28 | 2009-11-26 | Janssen Pharmaceutica Nv | Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase |
| CA2575002C (en) | 2004-08-10 | 2015-01-20 | Janssen Pharmaceutica N.V. | Hiv inhibiting 1,2,4-triazin-6-one derivatives |
| US8946248B2 (en) * | 2004-09-30 | 2015-02-03 | Janssen R&D Ireland | HIV inhibiting 5-substituted pyrimidines |
| CA2577467C (en) * | 2004-09-30 | 2013-05-28 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 5-heterocyclyl pyrimidines |
| BRPI0515935B8 (pt) * | 2004-09-30 | 2021-05-25 | Janssen Sciences Ireland Uc | pirimidinas heterociclil- ou 5-carbo substituídas para inibição de hiv, e composição farmacêutica |
| CN101048410B (zh) | 2004-10-29 | 2010-06-23 | 泰博特克药品有限公司 | 抑制hiv的双环嘧啶衍生物 |
| EP1812069A2 (en) * | 2004-11-08 | 2007-08-01 | Boehringer Ingelheim International GmbH | Method for treating hiv infection through co-administration of tipranavir and etravirine |
| DK1814878T3 (da) | 2004-11-24 | 2012-05-07 | Rigel Pharmaceuticals Inc | Spiro-2, 4-pyrimidindiamin-forbindelser og anvendelser deraf |
| PL1856135T3 (pl) | 2005-01-19 | 2010-05-31 | Rigel Pharmaceuticals Inc | Proleki związków 2,4-pirymidynodiaminy i ich zastosowanie |
| WO2006079656A1 (en) * | 2005-01-27 | 2006-08-03 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 2-( 4-cyanophenylamino) pyrimidine derivatives |
| ATE398613T1 (de) | 2005-02-16 | 2008-07-15 | Astrazeneca Ab | Chemische verbindungen |
| CN101119976B (zh) * | 2005-02-18 | 2010-12-22 | 泰博特克药品有限公司 | 抑制hiv的2-(4-氰基苯氨基)嘧啶氧化物衍生物 |
| ES2347815T3 (es) * | 2005-03-04 | 2010-11-04 | Tibotec Pharmaceuticals | 2-(4-cianofenil)-6-hidroxilaminopirimidinas inhibidoras de hiv. |
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