ES2799408T3 - Derivados de pirimidina inhibidores del VIH - Google Patents
Derivados de pirimidina inhibidores del VIH Download PDFInfo
- Publication number
- ES2799408T3 ES2799408T3 ES10178189T ES10178189T ES2799408T3 ES 2799408 T3 ES2799408 T3 ES 2799408T3 ES 10178189 T ES10178189 T ES 10178189T ES 10178189 T ES10178189 T ES 10178189T ES 2799408 T3 ES2799408 T3 ES 2799408T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- formula
- cyano
- compound
- substituted
- 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.)
- Expired - Lifetime
Links
- 0 C*C1N(C)C(NC)NCC1C Chemical compound C*C1N(C)C(NC)NCC1C 0.000 description 7
- CPMJKKCHPLJCRY-UHFFFAOYSA-N Cc(ccc([I](C)C)c1C)c1Nc1ccnc(Nc(cc2)ccc2NC)n1 Chemical compound Cc(ccc([I](C)C)c1C)c1Nc1ccnc(Nc(cc2)ccc2NC)n1 CPMJKKCHPLJCRY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07D239/48—Two nitrogen atoms
-
- 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
- C07D401/12—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 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
- A61K31/495—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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
- C07C255/42—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being further bound to other hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/10—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
- C07C257/12—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to hydrogen atoms
-
- 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
- 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
- C07D401/14—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 three or more hetero rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D413/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
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)
- Epidemiology (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Tropical Medicine & Parasitology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01203090 | 2001-08-13 | ||
EP02077748 | 2002-06-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2799408T3 true ES2799408T3 (es) | 2020-12-17 |
Family
ID=26076978
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES10178189T Expired - Lifetime ES2799408T3 (es) | 2001-08-13 | 2002-08-09 | Derivados de pirimidina inhibidores del VIH |
ES20165399T Expired - Lifetime ES2923581T3 (es) | 2001-08-13 | 2002-08-09 | Pirimidinas inhibidoras de la replicación del VIH |
ES02764839T Expired - Lifetime ES2368996T3 (es) | 2001-08-13 | 2002-08-09 | Derivados de pirimidinas inhibidores del hiv |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES20165399T Expired - Lifetime ES2923581T3 (es) | 2001-08-13 | 2002-08-09 | Pirimidinas inhibidoras de la replicación del VIH |
ES02764839T Expired - Lifetime ES2368996T3 (es) | 2001-08-13 | 2002-08-09 | Derivados de pirimidinas inhibidores del hiv |
Country Status (37)
Families Citing this family (152)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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 |
JO3429B1 (ar) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
MY169670A (en) * | 2003-09-03 | 2019-05-08 | Tibotec Pharm Ltd | Combinations of a pyrimidine containing nnrti with rt inhibitors |
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 |
TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
IL164006A0 (en) | 2002-03-13 | 2005-12-18 | Janssen Pharmaceutica Nv | Inhibitors of histone deacetylase |
AR039540A1 (es) * | 2002-05-13 | 2005-02-23 | Tibotec Pharm Ltd | Compuestos microbicidas con contenido de pirimidina o triazina |
IL166241A (en) | 2002-07-29 | 2011-12-29 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds for use in the treatment of autoimmune diseases |
CN101481356B (zh) * | 2002-08-09 | 2012-07-11 | 詹森药业有限公司 | 制备4-[[4-[[4-(2-氰基乙烯基)-2,6-二甲基苯基]氨基]-2-嘧啶基]氨基]苄腈的方法 |
JP2006508997A (ja) * | 2002-11-28 | 2006-03-16 | シエーリング アクチエンゲゼルシャフト | Chk−、Pdk−およびAkt−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 |
US7585861B2 (en) * | 2003-02-07 | 2009-09-08 | Janssen Pharmaceutica, N.V. | HIV inhibiting 1,2,4-triazines |
US20070021449A1 (en) * | 2003-02-07 | 2007-01-25 | Jan Heeres | Pyrimidine derivatives for the prevention of hiv infection |
CL2004000303A1 (es) | 2003-02-20 | 2005-04-08 | Tibotec Pharm Ltd | Compuestos derivados de pirimidinas y triazinas; proceso de preparacion; composicion farmaceutica; y su uso para inhibir la replicacion del vih. |
ES2667668T3 (es) | 2003-07-17 | 2018-05-14 | Janssen Sciences Ireland Uc | Procedimiento para preparar partículas que contienen un antiviral |
US7122542B2 (en) | 2003-07-30 | 2006-10-17 | Rigel Pharmaceuticals, Inc. | Methods of treating or preventing autoimmune diseases with 2,4-pyrimidinediamine compounds |
NZ585188A (en) * | 2003-08-15 | 2011-09-30 | Novartis Ag | 2,4-Pyrimidinediamines useful in the treatment of neoplastic diseases, inflammatory and immune system disorders |
TWI365744B (en) * | 2003-09-03 | 2012-06-11 | Tibotec Pharm Ltd | Combinations of a pyrimidine containing nnrti with rt inhibitors |
WO2005028479A2 (en) * | 2003-09-25 | 2005-03-31 | Janssen Pharmaceutica N.V. | Hiv replication inhibiting purine derivatives |
US7456176B2 (en) | 2004-04-08 | 2008-11-25 | Targegen, Inc. | Benzotriazine inhibitors of kinases |
SG156687A1 (en) | 2004-07-28 | 2009-11-26 | Janssen Pharmaceutica Nv | Substituted indolyl alkyl amino derivatives as novel inhibitors of histone deacetylase |
JP5031564B2 (ja) | 2004-08-10 | 2012-09-19 | 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 | Hiv抑制1,2,4−トリアジン−6−オン誘導体 |
US7947721B2 (en) | 2004-08-25 | 2011-05-24 | Ardes Biosciences Inc. | S-triazolyl α-mercaptoacetanilides as inhibitors of HIV reverse transcriptase |
WO2007050087A1 (en) | 2004-08-25 | 2007-05-03 | Ardea Biosciences, Inc. | N[S(4-aryl-triazol-3-yl)α -mercaptoacetyl]-p-amino benozoic acids AS HIV REVERSE TRANSCRIPTASE INHIBITORS |
RS51923B2 (sr) * | 2004-09-02 | 2022-05-31 | Janssen Pharmaceutica Nv | So 4[[4-[[4-(2-cijanoetenil)-2,6-dimetilfenil]amino]-2- pirimidinil]amino]benzonitrila |
WO2006024668A1 (en) * | 2004-09-02 | 2006-03-09 | Janssen Pharmaceutica N.V. | Hydrochloride of 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2-pyrimidinyl] amino]benzonitrile |
ATE550074T1 (de) * | 2004-09-02 | 2012-04-15 | Janssen Pharmaceutica Nv | Fumarat aus 4-((4-((4-(2-cyanoethenyl)-2,6- dimethylphenyl amino -2-pyrimidinyl amino benzonitril |
WO2006024667A1 (en) * | 2004-09-02 | 2006-03-09 | Janssen Pharmaceutica N.V. | Furamate of 4-( (4-( (4- (2-cyanoethenyl) -2,6-dimethylphenyl)amino)-2-pyrimidinyl)amino)benzonitrile |
UA92467C2 (ru) * | 2004-09-02 | 2010-11-10 | Янссен Фармацевтика Н.В. | Гидрохлорид 4-[[4-[[4-(2-цианоэтенил)-2,6-диметилфенил]амино]-2-пиримидинил]амино]бензонитрила |
WO2006034338A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as mediators of stearoyl-coa desaturase |
TW200624427A (en) | 2004-09-20 | 2006-07-16 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as therapeutic agents |
TW200626154A (en) | 2004-09-20 | 2006-08-01 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as therapeutic agents |
AR051094A1 (es) | 2004-09-20 | 2006-12-20 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores de la estearoil-coa desaturasa |
MX2007003321A (es) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como agentes terapeuticos. |
EP1804799B1 (en) | 2004-09-20 | 2013-08-21 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
TW200626592A (en) | 2004-09-20 | 2006-08-01 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as therapeutic agents |
ATE520672T1 (de) * | 2004-09-30 | 2011-09-15 | Tibotec Pharm Ltd | Hiv-hemmende 5-carbo- oder heterozyklisch substituierte pyrimidine |
BRPI0516748B8 (pt) * | 2004-09-30 | 2021-05-25 | Janssen Sciences Ireland Uc | pirimidinas 5-substituídas inibidoras de hiv e composição farmacêutica que as compreende |
ES2371923T3 (es) | 2004-09-30 | 2012-01-11 | Tibotec Pharmaceuticals | 5-heterociclil-pirimidinas que inhiben el vih. |
SI1814878T1 (sl) | 2004-11-24 | 2012-06-29 | Rigel Pharmaceuticals Inc | Spojine spiro-2,4-pirimidindiamina in njihova uporaba |
SI1856135T1 (sl) | 2005-01-19 | 2010-04-30 | Rigel Pharmaceuticals Inc | Predzdravila 2,4-pirimidindiaminskih spojin in njihove uporabe |
US7906511B2 (en) | 2005-03-31 | 2011-03-15 | Santen Pharmaceutical Co., Ltd. | Cyclic compound having pyrimidinylalkylthio group |
TW201414495A (zh) | 2005-04-04 | 2014-04-16 | Tibotec Pharm Ltd | Hiv-感染之預防 |
WO2006122003A2 (en) | 2005-05-05 | 2006-11-16 | Ardea Biosciences, Inc. | Diaryl-purine, azapurines and -deazapurines as non-nucleoside reverse transcriptase inhibitors for treatment of hiv |
RU2458056C2 (ru) * | 2005-05-26 | 2012-08-10 | Тиботек Фармасьютикалз Лтд | Способ получения 4-(1,6-дигидро-6-оксо-2-пиримидинил)амино-бензонитрила |
US8541457B2 (en) | 2005-06-03 | 2013-09-24 | Xenon Pharmaceuticals Inc. | Aminothiazole derivatives as human stearoyl-CoA desaturase inhibitors |
NZ563454A (en) | 2005-06-08 | 2011-03-31 | Rigel Pharmaceuticals Inc | 2,4-diaminopyrimidine derivatives for inhibition of the JAK pathway |
US20070203161A1 (en) | 2006-02-24 | 2007-08-30 | Rigel Pharmaceuticals, Inc. | Compositions and methods for inhibition of the jak pathway |
RU2597364C2 (ru) | 2005-11-01 | 2016-09-10 | Таргеджен, Инк. | Би-арил-мета-пиримидиновые ингибиторы киназ |
CN101370790B (zh) | 2006-01-19 | 2015-10-21 | 詹森药业有限公司 | 作为组蛋白去乙酰化酶抑制剂的吡啶和嘧啶衍生物 |
UA96436C2 (ru) * | 2006-01-20 | 2011-11-10 | Тиботек Фармасьютикелз Лтд. | Долгосрочное лечение вич-инфекции |
MX2008012577A (es) | 2006-03-30 | 2008-10-10 | Tibotec Pharm Ltd | Pirimidinas sustituidas con 5-(hidroximetileno y aminometileno) que inhiben el virus de inmunodeficiencia humana. |
WO2007113254A1 (en) | 2006-03-30 | 2007-10-11 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 5-amido substituted pyrimidines |
AU2016219555B2 (en) * | 2006-06-23 | 2017-08-10 | Janssen Sciences Ireland Uc | Aqueous suspensions of TMC278 |
CN101478950B (zh) * | 2006-06-23 | 2013-02-06 | 泰博特克药品有限公司 | Tmc278的水性悬浮液 |
AU2014200819B2 (en) * | 2006-06-23 | 2016-05-26 | Janssen Sciences Ireland Uc | Aqueous suspensions of TMC278 |
WO2008058285A2 (en) | 2006-11-09 | 2008-05-15 | Ardea Biosciences, Inc. | 4-cyanophenylamino-substituted bicyclic heterocyclic compounds as hiv inhibitors |
BRPI0722384A2 (pt) | 2006-12-08 | 2012-06-12 | Irm Llc | compostos inibidores de proteÍna quinase, composiÇÕes contendo os mesmos bem como seus usos |
ES2550152T3 (es) | 2006-12-13 | 2015-11-04 | F. Hoffmann-La Roche Ag | Derivados de 2-(piperidin-4-il)-4-fenoxi-o fenilamino-pirimidina como inhibidores no nucleósidos de transcriptasa inversa |
CA2674185C (en) | 2006-12-29 | 2017-02-28 | Tibotec Pharmaceuticals Ltd. | Hiv inhibiting 5,6-substituted pyrimidines |
KR20090094073A (ko) | 2006-12-29 | 2009-09-03 | 티보텍 파마슈티칼즈 리미티드 | Hiv를 억제하는 6-치환된 피리미딘 |
AU2008210455A1 (en) | 2007-01-31 | 2008-08-07 | Vertex Pharmaceuticals Incorporated | 2-aminopyridine derivatives useful as kinase inhibitors |
TWI494133B (zh) | 2007-03-14 | 2015-08-01 | Tibotec Pharm Ltd | 重組用粉末 |
BRPI0810411B8 (pt) | 2007-04-18 | 2021-05-25 | Pfizer Prod Inc | derivados de sulfonil amida para o tratamento de crescimento celular anormal, seu sos, bem como composição farmacêutica |
ES2542153T3 (es) | 2007-05-30 | 2015-07-31 | F. Hoffmann-La Roche Ag | Inhibidores no nucleósidos de la transcriptasa inversa |
KR101294731B1 (ko) * | 2007-06-04 | 2013-08-16 | 삼성디스플레이 주식회사 | 어레이 기판, 이를 갖는 표시패널 및 이의 제조방법 |
WO2009007441A2 (en) * | 2007-07-12 | 2009-01-15 | Tibotec Pharmaceuticals Ltd. | Crystalline form of (e) 4-[[4-[[4-(2-cyanoethenyl)-2,6-dimethylphenyl]amino]-2 pyrimidinyl]amino]benzonitrile |
CN101407476B (zh) * | 2007-10-12 | 2012-07-18 | 中国人民解放军军事医学科学院毒物药物研究所 | 作为非核苷类hiv逆转录酶抑制剂的间二芳烃-多取代苯胺类化合物、其制备方法及用途 |
CN103058944B (zh) | 2007-11-27 | 2015-08-05 | 亚德生化公司 | 调节血液尿酸水平的化合物 |
CA2709176C (en) | 2007-12-14 | 2013-02-05 | Ardea Biosciences, Inc. | Reverse transcriptase inhibitors |
US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
US11351168B1 (en) | 2008-06-27 | 2022-06-07 | Celgene Car Llc | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
NZ603525A (en) | 2008-06-27 | 2015-02-27 | Celgene Avilomics Res Inc | Pyrimidine based compound and uses thereof |
NZ590784A (en) | 2008-07-23 | 2012-12-21 | Vertex Pharma | Pyrazolopyridine kinase inhibitors |
AU2009274023A1 (en) | 2008-07-23 | 2010-01-28 | Vertex Pharmaceuticals Incorporated | Tri-cyclic pyrazolopyridine kinase inhibitors |
US8569337B2 (en) | 2008-07-23 | 2013-10-29 | Vertex Pharmaceuticals Incorporated | Tri-cyclic pyrazolopyridine kinase inhibitors |
EP2313372B1 (en) * | 2008-08-06 | 2013-04-10 | Vertex Pharmaceuticals Incorporated | Aminopyridine kinase inhibitors |
CN101717364B (zh) * | 2008-10-09 | 2014-08-13 | 中国人民解放军军事医学科学院毒物药物研究所 | 作为hiv逆转录酶抑制剂的吡啶类化合物及其制备方法和用途 |
US8933106B2 (en) | 2008-10-09 | 2015-01-13 | Institute Of Pharmacology And Toxicology Academy Of Military Medical Sciences P.L.A. China | 2-(4-substituted phenylamino) polysubstituted pyridine compounds as inhibitors of non-nucleoside HIV reverse transcriptase, preparation methods and uses thereof |
EP2181991A1 (en) | 2008-10-28 | 2010-05-05 | LEK Pharmaceuticals D.D. | Novel salts of sunitinib |
EP2186809A1 (en) * | 2008-11-13 | 2010-05-19 | LEK Pharmaceuticals D.D. | New crystal form of sunitinib malate |
US20110256206A1 (en) | 2008-12-24 | 2011-10-20 | Schachter Deborah M | Implantable devices for treating hiv |
JP5918693B2 (ja) | 2009-05-05 | 2016-05-18 | ダナ ファーバー キャンサー インスティテュート インコーポレイテッド | Egfr阻害剤及び疾患の治療方法 |
CA2760705A1 (en) | 2009-05-06 | 2010-11-11 | Vertex Pharmaceuticals Incorporated | Pyrazolopyridines |
AU2011209726A1 (en) | 2010-01-27 | 2012-08-09 | Vertex Pharmaceuticals Incorporated | Pyrazolopyridine kinase inhibitors |
CN102869663A (zh) | 2010-01-27 | 2013-01-09 | 沃泰克斯药物股份有限公司 | 吡唑并吡嗪激酶抑制剂 |
KR101964923B1 (ko) | 2010-01-27 | 2019-04-02 | 비이브 헬쓰케어 컴퍼니 | 항바이러스 치료 |
JP2013518114A (ja) | 2010-01-27 | 2013-05-20 | バーテックス ファーマシューティカルズ インコーポレイテッド | ピラゾロピリミジンキナーゼ阻害剤 |
US20140018379A1 (en) * | 2010-02-18 | 2014-01-16 | Concert Pharmaceuticals Inc. | Pyrimidine derivatives |
US8367315B2 (en) * | 2010-03-05 | 2013-02-05 | Adan Rios | Inactivation of reverse transcriptases by azido-diarylpyrimidines |
AU2011289604C1 (en) | 2010-08-10 | 2016-04-21 | Celgene Avilomics Research, Inc. | Besylate salt of a BTK inhibitor |
JP5956999B2 (ja) | 2010-11-01 | 2016-07-27 | セルジーン アヴィロミクス リサーチ, インコーポレイテッド | ヘテロアリール化合物およびその使用 |
NZ609957A (en) | 2010-11-01 | 2015-08-28 | Celgene Avilomics Res Inc | Heterocyclic compounds and uses thereof |
CA2816957A1 (en) | 2010-11-07 | 2012-05-10 | Targegen, Inc. | Compositions and methods for treating myelofibrosis |
ES2665013T3 (es) | 2010-11-10 | 2018-04-24 | Celgene Car Llc | Inhibidores de EGFR selectivos de mutante y usos de los mismos |
PE20211657A1 (es) | 2010-11-19 | 2021-08-24 | Gilead Sciences Inc | Composiciones terapeuticas que comprenden rilpivirina hcl y tenofovir disoproxil fumarato |
WO2012125993A1 (en) | 2011-03-17 | 2012-09-20 | Teva Pharmaceutical Industries Ltd. | Solid state forms of rilpivirine base, and rilipivirine salts |
WO2012147091A2 (en) | 2011-04-25 | 2012-11-01 | Hetero Research Foundation | Process for rilpivirine |
JP6038151B2 (ja) | 2011-08-30 | 2016-12-07 | シーエイチディーアイ ファウンデーション,インコーポレーテッド | キヌレニン−3−モノオキシゲナーゼインヒビターおよびその医薬組成物ならびにこれらの使用方法 |
US9233935B2 (en) * | 2011-09-16 | 2016-01-12 | Hetero Research Foundation | Rilpivirine hydrochloride |
US9364476B2 (en) | 2011-10-28 | 2016-06-14 | Celgene Avilomics Research, Inc. | Methods of treating a Bruton's Tyrosine Kinase disease or disorder |
EP2628732A1 (en) | 2012-02-20 | 2013-08-21 | Sandoz AG | Novel crystalline form of rilpivirine hydrochloride |
EP2604593A1 (en) | 2011-12-14 | 2013-06-19 | Sandoz AG | Polymorph of Rilpivirine hydrochloride and its use as antiviral |
WO2013087794A1 (en) | 2011-12-14 | 2013-06-20 | Sandoz Ag | Polymorph of rilpivirine hydrochloride and its use as antiviral |
CA2866857C (en) | 2012-03-15 | 2021-03-09 | Celgene Avilomics Research, Inc. | Salts of an epidermal growth factor receptor kinase inhibitor |
CN108658873B (zh) | 2012-03-15 | 2021-09-14 | 西建卡尔有限责任公司 | 表皮生长因子受体激酶抑制剂的固体形式 |
WO2013153162A1 (en) | 2012-04-11 | 2013-10-17 | Sandoz Ag | Polymorph of rilpivirine hydrochloride |
WO2013153161A2 (en) | 2012-04-11 | 2013-10-17 | Sandoz Ag | Novel polymorph of rilpivirine hydrochloride |
WO2013179105A1 (en) * | 2012-06-01 | 2013-12-05 | Laurus Labs Private Limited | Improved process for preparation of rilpivirine and pharmaceutically acceptable salts thereof |
US9139535B2 (en) * | 2012-07-12 | 2015-09-22 | Hetero Research Foundation | Process for rilpivirine using novel intermediate |
WO2014072419A1 (en) | 2012-11-08 | 2014-05-15 | Universiteit Antwerpen | Novel anti-hiv compounds |
WO2014100748A1 (en) | 2012-12-21 | 2014-06-26 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
WO2014124230A2 (en) | 2013-02-08 | 2014-08-14 | Celgene Avilomics Research, Inc. | Erk inhibitors and uses thereof |
US9914709B2 (en) | 2013-06-21 | 2018-03-13 | Yale University | Compositions and methods of treating HIV-1 infections using same |
US9492471B2 (en) | 2013-08-27 | 2016-11-15 | Celgene Avilomics Research, Inc. | Methods of treating a disease or disorder associated with Bruton'S Tyrosine Kinase |
US9415049B2 (en) | 2013-12-20 | 2016-08-16 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
WO2016011316A1 (en) | 2014-07-17 | 2016-01-21 | Chdi Foundation, Inc. | Methods and compositions for treating hiv-related disorders |
ES2741785T3 (es) | 2014-08-13 | 2020-02-12 | Celgene Car Llc | Formas y composiciones de un inhibidor de ERK |
SG11201702379TA (en) | 2014-09-26 | 2017-04-27 | Glaxosmithkline Ip No 2 Ltd | Long acting pharmaceutical compositions |
CZ201532A3 (cs) | 2015-01-21 | 2015-02-25 | Zentiva, K.S. | Způsob výroby vysoce čistého Rilpivirinu a jeho solí |
CN104926829A (zh) * | 2015-06-08 | 2015-09-23 | 山东大学 | 一种噻吩并嘧啶类衍生物及其制备方法和应用 |
ES2925246T3 (es) | 2015-06-30 | 2022-10-14 | Gilead Sciences Inc | Formulaciones farmacéuticas que comprenden tenofovir y emtricitabina |
CZ2015579A3 (cs) | 2015-08-27 | 2017-03-08 | Zentiva, K.S. | Krystalická forma A Rilpivirin Adipátu a způsob její přípravy |
CN106187916B (zh) * | 2016-07-04 | 2018-08-21 | 宜昌人福药业有限责任公司 | 一种有效去除利匹韦林异构体的方法 |
US11065198B2 (en) | 2016-10-24 | 2021-07-20 | Janssen Sciences Ireland Unlimited Company | Dispersible compositions |
CN106749203B (zh) * | 2016-11-28 | 2020-04-10 | 洛阳聚慧医药科技有限公司 | 一种嘧啶类杂环化合物、嘧啶类杂环化合物盐以及制备方法和应用 |
CN106588696B (zh) * | 2016-12-08 | 2018-12-25 | 西北师范大学 | 一种反式α,β-不饱和腈类化合物的制备方法 |
CN106905244B (zh) * | 2017-02-27 | 2019-08-16 | 武汉工程大学 | 二芳基嘧啶-二酮酸类杂合型hiv-1抑制剂及其制备方法 |
KR102722927B1 (ko) | 2017-06-30 | 2024-10-28 | 비이브 헬쓰케어 컴퍼니 | 조합물 및 이의 용도 및 치료 |
CR20210175A (es) | 2018-09-18 | 2021-06-01 | Nikang Therapeutics Inc | Derivados de anillo tricíclico condensado como inhibidores de la fosfatasa de homología a src 2 (shp2) |
CN109293581B (zh) * | 2018-09-21 | 2020-03-27 | 宜昌人福药业有限责任公司 | 一种制备盐酸利匹韦林异构体z和杂质x的方法及杂质x作为杀虫剂在农业中的应用 |
WO2020084142A1 (en) | 2018-10-25 | 2020-04-30 | Minakem | Process for the preparation of rilpivirine |
US20210000823A1 (en) * | 2019-07-03 | 2021-01-07 | Janssen Sciences Ireland Unlimited Company | Methods of treating hiv |
CN110526873B (zh) * | 2019-08-15 | 2022-09-16 | 复旦大学 | 氰乙烯基取代的苯并二芳基嘧啶类化合物及其制备方法和用途 |
JP2023503403A (ja) | 2019-11-29 | 2023-01-30 | シピオ ライフ サイエンシズ リミテッド | リルピビリンを含む組成物及び腫瘍又は癌を治療するためのその使用 |
CN111004215B (zh) * | 2019-12-22 | 2022-08-09 | 华北理工大学 | 2,4-取代嘧啶类衍生物及其制备方法和在制备抗肿瘤药物中的应用 |
CN111217833B (zh) * | 2020-02-21 | 2021-03-16 | 山东大学 | 噻吩并[2,3-d]嘧啶类HIV-1非核苷类逆转录酶抑制剂及其制备方法和应用 |
WO2022000019A1 (en) * | 2020-06-30 | 2022-01-06 | University Of South Australia | New therapeutic use of rilpivirine |
CN112028836B (zh) * | 2020-09-09 | 2021-12-07 | 山东大学 | 一种含有六元氮杂环的二芳基嘧啶类衍生物及其制备方法与应用 |
CN112010810B (zh) * | 2020-09-09 | 2024-01-30 | 瑞阳制药股份有限公司 | 一锅法制备高纯度利匹韦林中间体的方法 |
WO2022079739A1 (en) | 2020-10-14 | 2022-04-21 | Cipla Limited | Fixed dose compositions of cabotegravir and rilpivirine |
TW202233192A (zh) | 2020-11-17 | 2022-09-01 | 愛爾蘭商健生科學愛爾蘭無限公司 | Hiv感染之治療或預防 |
CN112546969B (zh) * | 2020-12-07 | 2022-12-23 | 安徽贝克制药股份有限公司 | 催化加氢连续生产装置和利托那韦中间体的制备方法 |
CN112778214A (zh) * | 2021-01-13 | 2021-05-11 | 安徽贝克联合制药有限公司 | 用于合成利匹韦林的中间体、其合成方法和利匹韦林的合成方法 |
CN113105394A (zh) * | 2021-03-08 | 2021-07-13 | 复旦大学 | 一种含芳杂环结构的联苯二芳基嘧啶类衍生物及其制备方法和应用 |
CN113461666A (zh) * | 2021-05-06 | 2021-10-01 | 复旦大学 | 含芳杂环结构的联苯二芳基甲基嘧啶衍生物及其制备方法 |
CN113845515A (zh) * | 2021-09-03 | 2021-12-28 | 复旦大学 | 一种含芳杂环结构的二甲基联苯二芳基嘧啶类衍生物及其制备方法和应用 |
EP4433026A1 (en) | 2021-11-17 | 2024-09-25 | Janssen Sciences Ireland Unlimited Company | Dissolution test |
TW202408580A (zh) | 2022-04-22 | 2024-03-01 | 愛爾蘭商健生科學愛爾蘭無限公司 | 冷凍乾燥組成物(二) |
US20250268896A1 (en) | 2022-04-22 | 2025-08-28 | Janssen Sciences Ireland Unlimited Company | Liquid compositions |
TW202408527A (zh) | 2022-05-17 | 2024-03-01 | 愛爾蘭商健生科學愛爾蘭無限公司 | 治療或預防hiv感染(二) |
TW202408526A (zh) | 2022-05-17 | 2024-03-01 | 愛爾蘭商健生科學愛爾蘭無限公司 | 治療或預防hiv感染(一) |
CN115490642B (zh) * | 2022-09-21 | 2024-11-15 | 山东大学 | 一种含醚键的二芳基嘧啶类化合物及其制备方法与应用 |
Family Cites Families (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3459731A (en) | 1966-12-16 | 1969-08-05 | Corn Products Co | Cyclodextrin polyethers and their production |
US3953398A (en) * | 1970-07-20 | 1976-04-27 | The Goodyear Tire & Rubber Company | Age resistant polymeric compositions |
JPS63159316A (ja) * | 1977-11-28 | 1988-07-02 | アルキユサル インコーポレーテツド ピーテイワイ リミテツド | 中性銅結合体を含む抗炎症組成物 |
EP0002341B1 (en) * | 1977-11-28 | 1982-01-20 | Barry Boettcher | Complexes of bivalent copper, methods of preparation thereof and compositions containing said complexes |
JPS5879920A (ja) * | 1981-11-09 | 1983-05-13 | Kanegafuchi Chem Ind Co Ltd | 血小板凝集阻害剤 |
GB9012592D0 (en) | 1990-06-06 | 1990-07-25 | Smithkline Beecham Intercredit | Compounds |
US5318780A (en) * | 1991-10-30 | 1994-06-07 | Mediventures Inc. | Medical uses of in situ formed gels |
US5691364A (en) | 1995-03-10 | 1997-11-25 | Berlex Laboratories, Inc. | Benzamidine derivatives and their use as anti-coagulants |
GB9523675D0 (en) * | 1995-11-20 | 1996-01-24 | Celltech Therapeutics Ltd | Chemical compounds |
NZ322907A (en) | 1995-11-23 | 1998-12-23 | Janssen Pharmaceutica Nv | Solid mixtures of cyclodextrins prepared via melt-extrusion |
TW429256B (en) | 1995-12-27 | 2001-04-11 | Janssen Pharmaceutica Nv | 1-(1,2-disubstituted piperidinyl)-4-(benzimidazolyl- and imidazopyridinyl)-piperidine derivatives |
GB9705361D0 (en) | 1997-03-14 | 1997-04-30 | Celltech Therapeutics Ltd | Chemical compounds |
JP3990808B2 (ja) * | 1998-03-26 | 2007-10-17 | Tdk株式会社 | 非水電解質電池用電極の製造方法 |
DE69943247D1 (de) * | 1998-03-27 | 2011-04-14 | Janssen Pharmaceutica Nv | HIV hemmende Pyrimidin Derivate |
EP0945447A1 (en) * | 1998-03-27 | 1999-09-29 | Janssen Pharmaceutica N.V. | Trisubstituted 1,3,5-triazine derivatives for treatment of HIV infections |
TR200002760T2 (tr) * | 1998-03-27 | 2000-12-21 | Janssen Pharmaceutica N.V. | HIV engelleyici pirimidin türevleri |
JP2000035628A (ja) * | 1998-07-16 | 2000-02-02 | Konica Corp | ハロゲン化銀写真感光材料 |
EP1107957B1 (en) * | 1998-08-29 | 2006-10-18 | AstraZeneca AB | Pyrimidine compounds |
WO2000027825A1 (en) * | 1998-11-10 | 2000-05-18 | Janssen Pharmaceutica N.V. | Hiv replication inhibiting pyrimidines |
PL350651A1 (en) | 1999-03-09 | 2003-01-27 | Upjohn Co | 4-oxo-4,7-dihydro-thieno[2,3-b]pyridine-5-carboxamides as antiviral agents |
RU2260592C9 (ru) | 1999-04-15 | 2017-04-07 | Бристол-Маерс Сквибб Ко. | Циклические ингибиторы протеинтирозинкиназ |
GB9914258D0 (en) | 1999-06-18 | 1999-08-18 | Celltech Therapeutics Ltd | Chemical compounds |
DE19945982A1 (de) | 1999-09-24 | 2001-03-29 | Knoll Ag | Geschwindigkeitsbestimmte Partikel |
PL207590B1 (pl) * | 1999-09-24 | 2011-01-31 | Janssen Pharmaceutica Nv | Cząstka stanowiąca dyspersję stałą oraz postać dawkowania, sposób ich otrzymywania i zastosowanie |
HUP0301117A3 (en) * | 2000-02-17 | 2004-01-28 | Amgen Inc Thousand Oaks | Imidazole derivatives kinase inhibitors, their use, process for their preparation and pharmaceutical compositions containing them |
GB0004888D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
GB0004887D0 (en) * | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
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 |
US6596729B2 (en) | 2000-07-20 | 2003-07-22 | Bristol-Myers Squibb Company | Tricyclic-2-pyridone compounds useful as HIV reverse transcriptase inhibitors |
MXPA03007883A (es) * | 2001-03-02 | 2003-12-04 | Smithkline Beecham Corp | Benzofenonas como inhibidores de transcriptasa inversa. |
US6949544B2 (en) * | 2001-03-29 | 2005-09-27 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-Jun N-terminal kinases (JNK) and other protein kinases |
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 |
MY169670A (en) | 2003-09-03 | 2019-05-08 | Tibotec Pharm Ltd | Combinations of a pyrimidine containing nnrti with rt inhibitors |
CA2457526A1 (en) * | 2001-08-29 | 2003-03-13 | Umd, Inc. | Vaginal delivery of chemotherapeutic agents and inhibitors of membrane efflux systems for cancer therapy |
TWI329105B (en) * | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
MXPA04010778A (es) * | 2002-05-03 | 2005-03-07 | Janssen Pharmaceutica Nv | Microemulsiones polimericas. |
CN101481356B (zh) | 2002-08-09 | 2012-07-11 | 詹森药业有限公司 | 制备4-[[4-[[4-(2-氰基乙烯基)-2,6-二甲基苯基]氨基]-2-嘧啶基]氨基]苄腈的方法 |
WO2004050068A1 (en) | 2002-11-29 | 2004-06-17 | Janssen Pharmaceutica N.V. | Pharmaceutical compositions comprising a basic respectively acidic drug compound, a surfactant and a physiologically tolerable water-soluble acid respectively base |
US20070021449A1 (en) | 2003-02-07 | 2007-01-25 | Jan Heeres | Pyrimidine derivatives for the prevention of hiv infection |
WO2011103559A1 (en) * | 2010-02-22 | 2011-08-25 | Nektar Therapeutics | Oligomer modified diaromatic substituted compounds |
-
2002
- 2002-07-16 JO JOP/2002/0074A patent/JO3429B1/ar active
- 2002-08-09 PT PT02764839T patent/PT1419152E/pt unknown
- 2002-08-09 NZ NZ530951A patent/NZ530951A/en not_active IP Right Cessation
- 2002-08-09 HU HU1900370A patent/HU231274B1/hu active Protection Beyond IP Right Term
- 2002-08-09 KR KR1020077022611A patent/KR100969273B1/ko not_active Expired - Lifetime
- 2002-08-09 EP EP20165399.5A patent/EP3808743B1/en not_active Expired - Lifetime
- 2002-08-09 CN CN200910145401.5A patent/CN101816658B/zh not_active Expired - Lifetime
- 2002-08-09 OA OA1200400047A patent/OA12652A/en unknown
- 2002-08-09 US US10/485,636 patent/US7125879B2/en active Active
- 2002-08-09 CN CNB028159209A patent/CN100509801C/zh not_active Expired - Lifetime
- 2002-08-09 IL IL16032802A patent/IL160328A0/xx active IP Right Grant
- 2002-08-09 BR BR122015032641-9A patent/BR122015032641B1/pt not_active IP Right Cessation
- 2002-08-09 SI SI200231101T patent/SI3808743T1/sl unknown
- 2002-08-09 DK DK02764839.3T patent/DK1419152T3/da active
- 2002-08-09 ES ES10178189T patent/ES2799408T3/es not_active Expired - Lifetime
- 2002-08-09 HR HRP20120265A patent/HRP20120265B1/hr not_active IP Right Cessation
- 2002-08-09 EA EA200400304A patent/EA006656B1/ru active IP Right Maintenance
- 2002-08-09 ES ES20165399T patent/ES2923581T3/es not_active Expired - Lifetime
- 2002-08-09 KR KR1020047000372A patent/KR100817453B1/ko not_active Expired - Lifetime
- 2002-08-09 AP APAP/P/2004/002993A patent/AP1610A/en active
- 2002-08-09 BR BR122015023612A patent/BR122015023612B8/pt not_active IP Right Cessation
- 2002-08-09 PL PL368270A patent/PL216398B1/pl unknown
- 2002-08-09 WO PCT/EP2002/008953 patent/WO2003016306A1/en active Application Filing
- 2002-08-09 LT LTEP20165399.5T patent/LT3808743T/lt unknown
- 2002-08-09 HR HRP20192051AA patent/HRP20192051B1/hr not_active IP Right Cessation
- 2002-08-09 ES ES02764839T patent/ES2368996T3/es not_active Expired - Lifetime
- 2002-08-09 DK DK20165399.5T patent/DK3808743T3/da active
- 2002-08-09 EP EP10178189.6A patent/EP2298761B1/en not_active Expired - Lifetime
- 2002-08-09 BR BRPI0211909-9 patent/BRPI0211909B8/pt active IP Right Grant
- 2002-08-09 HR HRP20040096AA patent/HRP20040096B1/hr not_active IP Right Cessation
- 2002-08-09 MY MYPI20071005A patent/MY189572A/en unknown
- 2002-08-09 SI SI200230963T patent/SI1419152T1/sl unknown
- 2002-08-09 EP EP02764839A patent/EP1419152B1/en not_active Expired - Lifetime
- 2002-08-09 JP JP2003521229A patent/JP2005507380A/ja not_active Withdrawn
- 2002-08-09 AU AU2002329238A patent/AU2002329238C1/en active Active
- 2002-08-09 HU HU0401346A patent/HU230192B1/hu active Protection Beyond IP Right Term
- 2002-08-09 PL PL402388A patent/PL402388A1/pl unknown
- 2002-08-09 CA CA002452217A patent/CA2452217C/en not_active Expired - Lifetime
- 2002-08-09 AT AT02764839T patent/ATE517891T1/de active
- 2002-08-09 MX MXPA04001401A patent/MXPA04001401A/es active IP Right Grant
- 2002-08-10 EG EG2002080892A patent/EG24684A/xx active
- 2002-08-12 AR ARP020103034A patent/AR036387A1/es active IP Right Grant
- 2002-08-12 PA PA20028552901A patent/PA8552901A1/es unknown
- 2002-09-08 UA UA2004031903A patent/UA78221C2/uk unknown
-
2004
- 2004-02-11 IL IL160328A patent/IL160328A/en active Protection Beyond IP Right Term
- 2004-02-12 NO NO20040633A patent/NO327639B1/no not_active IP Right Cessation
- 2004-02-12 ZA ZA2004/01159A patent/ZA200401159B/en unknown
-
2006
- 2006-06-26 US US11/474,855 patent/US8080551B2/en not_active Expired - Fee Related
-
2008
- 2008-09-02 NO NO20083770A patent/NO337142B1/no not_active IP Right Cessation
-
2009
- 2009-11-12 JP JP2009259107A patent/JP5247661B2/ja not_active Expired - Lifetime
-
2011
- 2011-06-16 JP JP2011134088A patent/JP4838396B2/ja not_active Expired - Lifetime
- 2011-06-17 JP JP2011135468A patent/JP5539927B2/ja not_active Expired - Lifetime
- 2011-09-30 US US13/249,796 patent/US20120076835A1/en not_active Abandoned
- 2011-10-26 CY CY20111101014T patent/CY1112331T1/el unknown
-
2012
- 2012-05-08 BE BE2012C020C patent/BE2012C020I2/nl unknown
- 2012-05-16 LU LU92001C patent/LU92001I2/fr unknown
- 2012-05-18 CY CY2012012C patent/CY2012012I1/el unknown
- 2012-05-22 FR FR12C0035C patent/FR12C0035I2/fr active Active
- 2012-05-23 NO NO2012010C patent/NO2012010I2/no unknown
- 2012-05-24 BE BE2012C022C patent/BE2012C022I2/nl unknown
- 2012-05-24 LU LU92008C patent/LU92008I2/fr unknown
- 2012-05-25 CY CY2012013C patent/CY2012013I2/el unknown
- 2012-05-25 FR FR12C0036C patent/FR12C0036I2/fr active Active
- 2012-05-25 DE DE201212000038 patent/DE122012000038I1/de active Pending
-
2014
- 2014-08-05 US US14/451,761 patent/US9580392B2/en not_active Expired - Fee Related
-
2015
- 2015-10-20 HU HUS1500051C patent/HUS1500051I1/hu unknown
-
2016
- 2016-02-03 HU HUS1500055C patent/HUS1500055I1/hu unknown
-
2017
- 2017-01-16 US US15/406,918 patent/US20170121292A1/en not_active Abandoned
- 2017-07-20 US US15/655,570 patent/US9981919B2/en not_active Expired - Lifetime
-
2018
- 2018-04-26 US US15/963,352 patent/US10370340B2/en not_active Expired - Fee Related
-
2019
- 2019-07-02 US US16/460,898 patent/US10611732B2/en not_active Expired - Fee Related
-
2022
- 2022-07-27 FR FR22C1036C patent/FR22C1036I1/fr active Active
- 2022-07-28 BE BE2022C531C patent/BE2022C531I2/nl unknown
- 2022-08-01 CY CY2022024C patent/CY2022024I2/el unknown
- 2022-08-02 LT LTPA2022515C patent/LTC3808743I2/lt unknown
- 2022-08-02 HU HUS2200038C patent/HUS2200038I1/hu unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES2799408T3 (es) | Derivados de pirimidina inhibidores del VIH | |
ES2361835T3 (es) | Derivados de purina inhibidores de la replicación del hiv. | |
ES2508766T3 (es) | Derivados de pirimidina bicíclicos que inhiben el VIH | |
ES2442857T3 (es) | Derivados de 1,2,4-triazin-6-ona inhibidores de VIH | |
ES2598404T3 (es) | Derivados de pirimidina para la prevención de infección por el VIH | |
AU2002329238A1 (en) | HIV inhibiting pyrimidines derivatives | |
ES2365015T3 (es) | Pirimidinas sustituidas con indano que inhiben la replicación del vih. |