SI2004641T1 - HIV inhibirajoči 5-(hidroksimetilen in aminometilen) substituirani pirimidini - Google Patents
HIV inhibirajoči 5-(hidroksimetilen in aminometilen) substituirani pirimidiniInfo
- Publication number
- SI2004641T1 SI2004641T1 SI200730458T SI200730458T SI2004641T1 SI 2004641 T1 SI2004641 T1 SI 2004641T1 SI 200730458 T SI200730458 T SI 200730458T SI 200730458 T SI200730458 T SI 200730458T SI 2004641 T1 SI2004641 T1 SI 2004641T1
- Authority
- SI
- Slovenia
- Prior art keywords
- aminomethylene
- hydroxymethylene
- substituted pyrimidines
- hiv inhibiting
- hiv
- Prior art date
Links
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
-
- 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
- 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
- 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
-
- 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
- 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
- C07D417/06—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 carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D417/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06112045 | 2006-03-30 | ||
| PCT/EP2007/053113 WO2007113256A1 (en) | 2006-03-30 | 2007-03-30 | Hiv inhibiting 5-(hydroxymethylene and aminomethylene) substituted pyrimidines |
| EP07727585A EP2004641B1 (en) | 2006-03-30 | 2007-03-30 | Hiv inhibiting 5-(hydroxymethylene and aminomethylene) substituted pyrimidines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SI2004641T1 true SI2004641T1 (sl) | 2011-02-28 |
Family
ID=36808784
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI200730458T SI2004641T1 (sl) | 2006-03-30 | 2007-03-30 | HIV inhibirajoči 5-(hidroksimetilen in aminometilen) substituirani pirimidini |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US8163745B2 (sl) |
| EP (1) | EP2004641B1 (sl) |
| JP (1) | JP5070278B2 (sl) |
| KR (1) | KR20080104040A (sl) |
| CN (1) | CN101410394B (sl) |
| AT (1) | ATE482953T1 (sl) |
| AU (1) | AU2007233739B2 (sl) |
| BR (1) | BRPI0709266B8 (sl) |
| CA (1) | CA2645959C (sl) |
| DE (1) | DE602007009508D1 (sl) |
| DK (1) | DK2004641T3 (sl) |
| ES (1) | ES2353725T3 (sl) |
| HR (1) | HRP20100696T1 (sl) |
| IL (1) | IL193725A (sl) |
| MX (1) | MX2008012577A (sl) |
| RU (1) | RU2452737C2 (sl) |
| SI (1) | SI2004641T1 (sl) |
| WO (1) | WO2007113256A1 (sl) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2007010051A (es) * | 2005-02-18 | 2007-09-21 | Tibotec Pharm Ltd | Derivados de oxido de 2-(4-cianofenilamino)pirimidina que inhiben el virus de inmunodeficiencia humana. |
| DK2114901T3 (da) * | 2006-12-29 | 2014-06-30 | Janssen R & D Ireland | Hiv-inhiberende 6-substituerede pyrimidiner |
| US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
| EP3210609A1 (en) | 2008-05-21 | 2017-08-30 | Ariad Pharmaceuticals, Inc. | Phosphorous derivatives as kinase inhibitors |
| US11351168B1 (en) | 2008-06-27 | 2022-06-07 | Celgene Car Llc | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
| CA2986640C (en) | 2008-06-27 | 2019-03-26 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| CA2760794C (en) | 2009-05-05 | 2017-07-25 | Dana Farber Cancer Institute | Egfr inhibitors and methods of treating disorders |
| KR20130099040A (ko) | 2010-08-10 | 2013-09-05 | 셀진 아빌로믹스 리서치, 인코포레이티드 | Ｂｔｋ 억제제의 베실레이트 염 |
| US8975249B2 (en) | 2010-11-01 | 2015-03-10 | Celgene Avilomics Research, Inc. | Heterocyclic compounds and uses thereof |
| EP2635285B1 (en) | 2010-11-01 | 2017-05-03 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| US8796255B2 (en) | 2010-11-10 | 2014-08-05 | Celgene Avilomics Research, Inc | Mutant-selective EGFR inhibitors and uses thereof |
| BR112013027734A2 (pt) | 2011-05-04 | 2017-08-08 | Ariad Pharma Inc | compostos para a inibição de proliferação celular em cânceres impulsionados pelo egfr, método e composição farmacêutica |
| CN102260215A (zh) * | 2011-05-13 | 2011-11-30 | 复旦大学 | 一种二芳基嘧啶类衍生物及其制备方法和用途 |
| CA2853498A1 (en) | 2011-10-28 | 2013-05-02 | Celgene Avilomics Research, Inc. | Methods of treating a bruton's tyrosine kinase disease or disorder |
| RS57901B1 (sr) | 2012-03-15 | 2019-01-31 | Celgene Car Llc | Soli inhibitora kinaze receptora epidermalnog faktora rasta |
| EP2825041B1 (en) | 2012-03-15 | 2021-04-21 | Celgene CAR LLC | Solid forms of an epidermal growth factor receptor kinase inhibitor |
| JP6469567B2 (ja) | 2012-05-05 | 2019-02-13 | アリアド・ファーマシューティカルズ・インコーポレイテッド | Ｅｇｆｒ発動性がんの細胞増殖阻害用化合物 |
| EP2935226A4 (en) | 2012-12-21 | 2016-11-02 | Celgene Avilomics Res Inc | HETEROARYL COMPOUNDS AND USES THEREOF |
| PE20151274A1 (es) | 2013-02-08 | 2015-09-12 | Celgene Avilomics Res Inc | Inhibidores de erk y sus usos |
| US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
| 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 |
| CN103483272B (zh) * | 2013-09-29 | 2015-10-21 | 山东大学 | 间二芳烃-多取代嘧啶类衍生物及其制备方法与应用 |
| RU2547844C1 (ru) * | 2013-10-29 | 2015-04-10 | Федеральное государственное бюджетное учреждение науки Институт органического синтеза им. И.Я. Постовского Уральского отделения Российской академии наук | Способ получения 5-(гет)арил-4-(2-тиенил)-2-(тио)морфолилпиримидина |
| US9415049B2 (en) | 2013-12-20 | 2016-08-16 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| ES2741785T3 (es) | 2014-08-13 | 2020-02-12 | Celgene Car Llc | Formas y composiciones de un inhibidor de ERK |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3459731A (en) * | 1966-12-16 | 1969-08-05 | Corn Products Co | Cyclodextrin polyethers and their production |
| HUP9900730A3 (en) | 1995-11-23 | 2001-04-28 | Janssen Pharmaceutica Nv | Solid mixtures of cyclodextrins prepared via melt-extrusion |
| DE69905306T2 (de) * | 1998-03-27 | 2003-11-27 | Janssen Pharmaceutica Nv | HIV hemmende Pyrimidin Derivate |
| NZ511116A (en) | 1998-11-10 | 2003-08-29 | Janssen Pharmaceutica Nv | HIV replication inhibiting pyrimidines |
| WO2001085700A2 (en) * | 2000-05-08 | 2001-11-15 | Janssen Pharmaceutica N.V. | Hiv replication inhibiting pyrimidines and triazines |
| JO3429B1 (ar) | 2001-08-13 | 2019-10-20 | Janssen Pharmaceutica Nv | مشتقات برميدينات مثبطة فيروس الايدز |
| DE602004021558D1 (de) * | 2003-01-17 | 2009-07-30 | Warner Lambert Co | 2-aminopyridin-substituierteheterocyclen als inhibitoren der zellulären proliferation |
| PL227577B1 (pl) * | 2003-02-07 | 2017-12-29 | Janssen Pharmaceutica Nv | Zastosowanie pochodnych pirymidyny do wytwarzania leku do zapobiegania zakażeniu wirusem HIV oraz kompozycja farmaceutyczna |
| MX2007003798A (es) * | 2004-09-30 | 2007-04-23 | Tibotec Pharm Ltd | Pirimidinas 5-sustituidas con carbociclos o heterociclos inhibidoras del vih. |
-
2007
- 2007-03-30 JP JP2009502114A patent/JP5070278B2/ja active Active
- 2007-03-30 CA CA2645959A patent/CA2645959C/en active Active
- 2007-03-30 RU RU2008143018/04A patent/RU2452737C2/ru active
- 2007-03-30 CN CN2007800110048A patent/CN101410394B/zh active Active
- 2007-03-30 DK DK07727585.7T patent/DK2004641T3/da active
- 2007-03-30 BR BRPI0709266A patent/BRPI0709266B8/pt not_active IP Right Cessation
- 2007-03-30 MX MX2008012577A patent/MX2008012577A/es active IP Right Grant
- 2007-03-30 ES ES07727585T patent/ES2353725T3/es active Active
- 2007-03-30 WO PCT/EP2007/053113 patent/WO2007113256A1/en active Application Filing
- 2007-03-30 DE DE602007009508T patent/DE602007009508D1/de active Active
- 2007-03-30 US US12/294,725 patent/US8163745B2/en active Active
- 2007-03-30 KR KR1020087023894A patent/KR20080104040A/ko not_active Application Discontinuation
- 2007-03-30 AU AU2007233739A patent/AU2007233739B2/en not_active Ceased
- 2007-03-30 EP EP07727585A patent/EP2004641B1/en active Active
- 2007-03-30 AT AT07727585T patent/ATE482953T1/de not_active IP Right Cessation
- 2007-03-30 SI SI200730458T patent/SI2004641T1/sl unknown
-
2008
- 2008-08-27 IL IL193725A patent/IL193725A/en active IP Right Grant
-
2010
- 2010-12-17 HR HR20100696T patent/HRP20100696T1/hr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| RU2452737C2 (ru) | 2012-06-10 |
| HRP20100696T1 (hr) | 2011-01-31 |
| CN101410394A (zh) | 2009-04-15 |
| CN101410394B (zh) | 2012-02-08 |
| DK2004641T3 (da) | 2011-01-24 |
| MX2008012577A (es) | 2008-10-10 |
| WO2007113256A1 (en) | 2007-10-11 |
| CA2645959C (en) | 2016-05-17 |
| BRPI0709266A2 (pt) | 2011-06-28 |
| ATE482953T1 (de) | 2010-10-15 |
| AU2007233739A1 (en) | 2007-10-11 |
| KR20080104040A (ko) | 2008-11-28 |
| IL193725A0 (en) | 2009-05-04 |
| JP2009531395A (ja) | 2009-09-03 |
| US20100234375A1 (en) | 2010-09-16 |
| IL193725A (en) | 2014-11-30 |
| ES2353725T3 (es) | 2011-03-04 |
| BRPI0709266B8 (pt) | 2021-05-25 |
| AU2007233739B2 (en) | 2013-01-17 |
| JP5070278B2 (ja) | 2012-11-07 |
| DE602007009508D1 (de) | 2010-11-11 |
| CA2645959A1 (en) | 2007-10-11 |
| RU2008143018A (ru) | 2010-05-10 |
| BRPI0709266B1 (pt) | 2020-09-29 |
| EP2004641A1 (en) | 2008-12-24 |
| US8163745B2 (en) | 2012-04-24 |
| EP2004641B1 (en) | 2010-09-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IL193725A0 (en) | Hiv inhibiting 5-(hydroxymethylene and aminomethylene) substituted pyrimidines | |
| MX2008012576A (es) | Pirimidinas 5-amido sustituidas inhibidoras del virus de inmunodeficiencia humana. | |
| WO2008127364A3 (en) | Antiviral compounds and use thereof | |
| WO2008031556A3 (en) | 2 amino-pyrimidine derivatives as h4 receptor antagonists, processes for preparing them and their use in pharmaceutical compositions | |
| EA201000777A1 (ru) | Ингибиторы репликации вируса иммунодефицита человека | |
| GEP20125701B (en) | Application of 2-[6-(3-amino-piperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydro-2h-pyrimidin-1-ylmethyl]-4-fluoro-benzonitrile | |
| MY148634A (en) | Pyridazinone derivatives | |
| MX2009005363A (es) | Pirimidinas y su uso como antagonistas del receptor cxcr2. | |
| WO2007067506A3 (en) | 2-pyrimidinyl pyrazolopyridine erbb kinase inhibitors | |
| HK1128471A1 (en) | Heterocyclic non-nucleoside compounds, their preparation, pharmaceutical composition and their use as antiviral agents | |
| TW200800968A (en) | Sulfoximine-substituted pyrimidines, processes for production thereof and use thereof as drugs | |
| WO2008089105A3 (en) | Antiviral nucleoside analogs | |
| WO2007044565A3 (en) | Composition and synthesis of new reagents for inhibition of hiv replication | |
| MX2010004576A (es) | Derivados de pirimidina novedosos. | |
| MXPA05008368A (es) | 1,2,4-triazinas inhibidoras del virus de inmunodeficiencia humana. | |
| WO2007014352A3 (en) | Antiviral phosphonate conjugates for inhibition of hiv | |
| WO2007065595A3 (en) | Xanthine derivatives, processes for preparing them and their uses | |
| UA93599C2 (en) | powder valgancyclovir preparation | |
| MX2009008495A (es) | Novedosos analogos de nucleosidos para el tratamiento de infecciones virales. | |
| WO2009013545A3 (en) | Chemical compounds | |
| WO2006097617A3 (fr) | Nouveaux derives dihydropyrimidines et leur utilisation comme agents anti-cancereux | |
| MX2009009952A (es) | Sal clorhidrato de 5-[3-(3-hidroxifenoxi)azetidin-1-il]-5-metil-2, 2-difenilhexanamida. | |
| EP2131849A4 (en) | COMPOSITIONS AND METHODS OF DISTRIBUTING AGENTS AGAINST CANCER | |
| TW200621260A (en) | Selected fused heterocyclics and uses thereof | |
| HK1135329A1 (en) | Stable aqueous g-csf formulations |