BRPI0510319A - inibidores da enzima integrase de hiv - Google Patents
inibidores da enzima integrase de hivInfo
- Publication number
- BRPI0510319A BRPI0510319A BRPI0510319-3A BRPI0510319A BRPI0510319A BR PI0510319 A BRPI0510319 A BR PI0510319A BR PI0510319 A BRPI0510319 A BR PI0510319A BR PI0510319 A BRPI0510319 A BR PI0510319A
- Authority
- BR
- Brazil
- Prior art keywords
- integrase enzyme
- enzyme inhibitors
- hiv integrase
- hiv
- inhibitors
- Prior art date
Links
- 108010002459 HIV Integrase Proteins 0.000 title abstract 2
- 239000002532 enzyme inhibitor Substances 0.000 title abstract 2
- 241000725303 Human immunodeficiency virus Species 0.000 abstract 2
- 102100034343 Integrase Human genes 0.000 abstract 1
- 108010061833 Integrases Proteins 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Immunology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Virology (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
INIBIDORES DA ENZIMA INTEGRASE DE HIV. A presente invenção refere-se a compostos de fórmula (I), e sais e solvatos farmaceuticamente aceitáveis dos mesmos, sua síntese e seu uso como moduladores ou inibidores da enzima integrase do vírus da imunodeficiência humana ("HIV").
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56570504P | 2004-04-26 | 2004-04-26 | |
| US66050205P | 2005-03-09 | 2005-03-09 | |
| PCT/IB2005/001029 WO2005103003A2 (en) | 2004-04-26 | 2005-04-14 | Pyrrolopyridine derivatives and their use as hiv-integrase inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0510319A true BRPI0510319A (pt) | 2007-10-16 |
Family
ID=35033770
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0510319-3A BRPI0510319A (pt) | 2004-04-26 | 2005-04-14 | inibidores da enzima integrase de hiv |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7468375B2 (pt) |
| EP (1) | EP1756103A2 (pt) |
| JP (1) | JP2007534739A (pt) |
| BR (1) | BRPI0510319A (pt) |
| CA (1) | CA2564356A1 (pt) |
| MX (1) | MXPA06012449A (pt) |
| WO (1) | WO2005103003A2 (pt) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PA8586801A1 (es) | 2002-10-31 | 2005-02-04 | Pfizer | Inhibidores de hiv-integrasa, composiciones farmaceuticas y metodos para su uso |
| WO2005103003A2 (en) | 2004-04-26 | 2005-11-03 | Pfizer Inc. | Pyrrolopyridine derivatives and their use as hiv-integrase inhibitors |
| BRPI0510306A (pt) | 2004-04-26 | 2007-09-04 | Pfizer | inibidores da enzima de hiv integrase,composição farmacêutica contendo os referidos inibidores bem como seu uso |
| CA2578841A1 (en) * | 2004-09-07 | 2006-03-16 | Pfizer Inc. | Inhibitors of the hiv integrase enzyme |
| WO2007039802A1 (en) * | 2005-10-03 | 2007-04-12 | Pfizer Products Inc. | Inhibitors of the hiv integrase enzyme |
| WO2008095276A1 (en) * | 2007-02-06 | 2008-08-14 | Cymcorp International, Inc. | Novel non-toxic composition and method of using such for treating a degenerative or an immune system-related disease |
| WO2009146555A1 (en) | 2008-06-04 | 2009-12-10 | Ambrilia Biopharma Inc. | Hiv integrase inhibitors from pyridoxine |
| US8568659B2 (en) * | 2008-09-11 | 2013-10-29 | Mabgen, Llc | Fiber optic device |
| US8993808B2 (en) | 2009-01-21 | 2015-03-31 | Oryzon Genomics, S.A. | Phenylcyclopropylamine derivatives and their medical use |
| US8859555B2 (en) | 2009-09-25 | 2014-10-14 | Oryzon Genomics S.A. | Lysine Specific Demethylase-1 inhibitors and their use |
| US8946296B2 (en) | 2009-10-09 | 2015-02-03 | Oryzon Genomics S.A. | Substituted heteroaryl- and aryl-cyclopropylamine acetamides and their use |
| US8962627B2 (en) | 2009-10-30 | 2015-02-24 | Prestwick Chemical, Inc. | Oxime derivatives and their use as allosteric modulators of metabotropic glutamate receptors |
| CN102060855B (zh) * | 2009-11-12 | 2014-04-16 | 上海药明康德新药开发有限公司 | 一种八氢-吡喏-并[3,4-c]吡啶-衍生物的制备方法 |
| US9186337B2 (en) | 2010-02-24 | 2015-11-17 | Oryzon Genomics S.A. | Lysine demethylase inhibitors for diseases and disorders associated with Hepadnaviridae |
| WO2011106105A2 (en) | 2010-02-24 | 2011-09-01 | Oryzon Genomics, S.A. | Inhibitors for antiviral use |
| RU2599248C2 (ru) | 2010-04-19 | 2016-10-10 | Оризон Дженомикс С.А. | Лизинспецифические ингибиторы деметилазы-1 и их применение |
| US9006449B2 (en) | 2010-07-29 | 2015-04-14 | Oryzon Genomics, S.A. | Cyclopropylamine derivatives useful as LSD1 inhibitors |
| ME03085B (me) | 2010-07-29 | 2019-01-20 | Oryzon Genomics Sa | Demetilaza inhibitori lsd1 zasnovani na arilciklopropilaminu i njihova medicinska primjena |
| US9061966B2 (en) | 2010-10-08 | 2015-06-23 | Oryzon Genomics S.A. | Cyclopropylamine inhibitors of oxidases |
| WO2012072713A2 (en) | 2010-11-30 | 2012-06-07 | Oryzon Genomics, S.A. | Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae |
| EP3981395A1 (en) | 2011-02-08 | 2022-04-13 | Oryzon Genomics, S.A. | Lysine demethylase inhibitors for myeloproliferative disorders |
| BR112014009238B1 (pt) | 2011-10-20 | 2022-08-09 | Oryzon Genomics S.A. | Compostos de (hetero)aril ciclopropilamina, seus usos e composições farmacêuticas |
| BR112014009306B1 (pt) | 2011-10-20 | 2021-07-20 | Oryzon Genomics S.A. | Compostos de (hetero)aril ciclopropilamina como inibidores de lsd1 |
| EP2781519B1 (en) * | 2011-11-15 | 2019-10-30 | ST Pharm Co., Ltd. | Novel antiviral pyrrolopyridine derivative and a production method for same |
| TWI627173B (zh) | 2013-09-26 | 2018-06-21 | 比利時商健生藥品公司 | 作為NIK抑制劑的新穎3-(1H-吡唑-4-基)-1H-吡咯并[2,3-c]吡啶衍生物 |
| TWI704146B (zh) | 2013-09-26 | 2020-09-11 | 比利時商健生藥品公司 | 用作NIK抑制劑之新的1-(4-嘧啶基)-1H-吡唑並[3,2-c]吡啶衍生物 |
| GB201321735D0 (en) | 2013-12-09 | 2014-01-22 | Ucb Pharma Sa | Therapeutic Agents |
| ME03654B (me) * | 2014-02-13 | 2020-07-20 | Incyte Corp | Ciklopropilamini kao lsd1 inhibitori |
| PT3105226T (pt) * | 2014-02-13 | 2019-11-06 | Incyte Corp | Ciclopropilaminas como inibidores de lsd1 |
| JP6616412B2 (ja) | 2014-10-23 | 2019-12-04 | ヤンセン ファーマシューティカ エヌ.ベー. | Nik阻害剤としての新規のピラゾロピリミジン誘導体 |
| AU2015334914B2 (en) | 2014-10-23 | 2019-09-19 | Janssen Pharmaceutica Nv | New thienopyrimidine derivatives as NIK inhibitors |
| MX371153B (es) * | 2014-10-23 | 2020-01-20 | Janssen Pharmaceutica Nv | Nuevos compuestos como inhibidores de la cinasa inductora de nf-kb (nik). |
| US9981962B2 (en) | 2014-10-23 | 2018-05-29 | Janssen Pharmaceutica Nv | Pyrazole derivatives as NIK inhibitors |
| EP3241830A1 (de) | 2016-05-04 | 2017-11-08 | Bayer CropScience Aktiengesellschaft | Kondensierte bicyclische heterocyclen-derivate als schädlingsbekämpfungsmittel |
| US11352322B2 (en) * | 2016-05-09 | 2022-06-07 | Jubilant Epicore LLC | Cyclopropyl-amide compounds as dual LSD1/HDAC inhibitors |
| KR102435080B1 (ko) | 2016-07-19 | 2022-08-22 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 해충 방제제로서의 축합 바이시클릭 헤테로사이클 유도체 |
| MX2019001918A (es) | 2016-08-15 | 2019-09-06 | Bayer Cropscience Ag | Derivados del heterociclo biciclico condensado como agentes de control de plagas. |
| KR102148294B1 (ko) * | 2017-03-24 | 2020-08-26 | 에스티팜 주식회사 | 신규한 피롤로피리딘 유도체, 이의 제조방법 및 용도 |
| KR20220023187A (ko) * | 2020-08-20 | 2022-03-02 | 에스티팜 주식회사 | 피롤로피리딘 유도체 및 이들의 용도 |
| CA3262084A1 (en) * | 2022-08-05 | 2024-02-08 | The Governing Council Of The University Of Toronto | HISTONE DEACETYLASE INHIBITORS AND THEIR USE |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ194747A (en) * | 1979-08-29 | 1988-11-29 | Schering Ag | 9h-pyrido(3,4-b)indol-3-ylcarboxylic acid derivatives |
| GB8720125D0 (en) | 1987-08-26 | 1987-09-30 | Roussel Lab Ltd | Chemical compounds |
| US5616609A (en) | 1991-08-08 | 1997-04-01 | Ikekawa; Tetsuro | Carcinostatic compound and production thereof |
| GB2271566A (en) | 1992-10-14 | 1994-04-20 | Merck & Co Inc | HIV integrase inhibitors |
| US5726203A (en) | 1993-07-19 | 1998-03-10 | Li; Zelin | Qinghaosu derivatives against AIDS |
| GB2306476A (en) | 1995-10-27 | 1997-05-07 | Merck & Co Inc | Hiv integrase inhibitors |
| US6057297A (en) * | 1996-08-06 | 2000-05-02 | Polifarma S.P.A. | Inhibitor compounds of zinc-dependent metalloproteinases associated with pathological conditions, and therapeutic use thereof |
| FR2754262B1 (fr) * | 1996-10-08 | 1998-10-30 | Synthelabo | Derives de 1h-pyrido[3,4-b]indole-4-carboxamide, leur preparation et leur application en therapeutique |
| AU4917397A (en) | 1996-10-31 | 1998-05-22 | Merck & Co., Inc. | Benzodiazepine hydrazide derivatives as inhibitors of hiv integrase |
| GB2327674A (en) | 1997-07-29 | 1999-02-03 | Merck & Co Inc | HIV integrase inhibitors |
| US6403347B1 (en) * | 1998-02-03 | 2002-06-11 | Merck & Co., Inc. | HIV integrase inhibitors |
| ES2188184T3 (es) | 1998-06-12 | 2003-06-16 | Sod Conseils Rech Applic | Compuestos de beta-carbolinas. |
| CA2372791A1 (en) | 1999-05-12 | 2000-11-16 | Nouri Neamati | Thiazepine and oxazepine inhibitors of hiv-1 integrase |
| US6245806B1 (en) | 1999-08-03 | 2001-06-12 | Merck & Co., Inc. | HIV integrase inhibitors |
| WO2001027309A1 (en) * | 1999-10-13 | 2001-04-19 | Merck & Co., Inc. | Hiv integrase inhibitors |
| EP1209158A1 (en) | 2000-11-18 | 2002-05-29 | Aventis Pharma Deutschland GmbH | Substituted beta-carbolines |
| AU2001269895B2 (en) * | 2000-06-16 | 2005-10-20 | Bristol-Myers Squibb Company | Hiv integrase inhibitors |
| WO2002002516A2 (en) | 2000-06-30 | 2002-01-10 | Thomas Jefferson University | Inhibitors of hiv integrase |
| MXPA03007765A (es) * | 2001-03-01 | 2003-12-08 | Shionogi & Co | Compuestos heteroarilo que contienen nitrogeno, que tienen actividad inhibitoria contra virus de inmunodeficiencia humana integrasa. |
| WO2002070491A1 (en) | 2001-03-01 | 2002-09-12 | Shionogi & Co., Ltd. | Nitrogenous heteroaromatic ring derivative having hiv integrase inhibitory activity |
| JP2003171381A (ja) | 2001-09-25 | 2003-06-20 | Takeda Chem Ind Ltd | エントリー阻害剤 |
| JP2003119137A (ja) | 2001-10-10 | 2003-04-23 | Japan Tobacco Inc | Hiv阻害剤 |
| DE60216952T2 (de) | 2001-10-19 | 2007-07-05 | Transtech Pharma Inc. | Beta-carbolin-derivate als ptp-inhibitoren |
| DE60218511T2 (de) * | 2001-10-26 | 2007-10-25 | Istituto Di Richerche Di Biologia Molecolare P. Angeletti S.P.A. | Dihydroxypyrimidin-carbonsäueramid-hemmer der hiv-integrase |
| JP4497347B2 (ja) | 2001-12-05 | 2010-07-07 | 塩野義製薬株式会社 | Hivインテグラーゼ阻害活性を有する誘導体 |
| CA2469592C (en) | 2001-12-12 | 2005-08-23 | Bristol-Myers Squibb Company | Hiv integrase inhibitors |
| DE60315796T2 (de) | 2002-01-17 | 2008-06-05 | Merck & Co., Inc. | Hydroxynaphthyridinoncarbonsäureamide, die sich als inhibitoren der hiv-integrase eignen |
| AU2003220170B2 (en) * | 2002-03-15 | 2008-12-11 | Merck Sharp & Dohme Corp. | N-(Substituted benzyl)-8-hydroxy-1,6-naphthyridine-7- carboxamides useful as HIV integrase inhibitors |
| WO2003082881A2 (en) | 2002-03-28 | 2003-10-09 | Procyon Biopharma Inc. | Pyridoxal-5-phosphate derivatives as hiv integrase inhibitors |
| US20050165000A1 (en) | 2002-04-10 | 2005-07-28 | Robertson Sandra K. | Pharmaceutical compositions containing an hiv integrase inhibitor and a nonionic surfactant |
| AU2002335027A1 (en) | 2002-10-15 | 2004-05-04 | Chiron Corporation | Treatment of tnf-alpha-mediated disorders with casein kinase i epsilon inhibitors |
| PA8586801A1 (es) | 2002-10-31 | 2005-02-04 | Pfizer | Inhibidores de hiv-integrasa, composiciones farmaceuticas y metodos para su uso |
| CA2513141A1 (en) | 2003-01-27 | 2004-08-12 | Pfizer Inc. | Hiv-integrase inhibitors, pharmaceutical compositions, and methods for their use |
| WO2005103003A2 (en) | 2004-04-26 | 2005-11-03 | Pfizer Inc. | Pyrrolopyridine derivatives and their use as hiv-integrase inhibitors |
| BRPI0510306A (pt) | 2004-04-26 | 2007-09-04 | Pfizer | inibidores da enzima de hiv integrase,composição farmacêutica contendo os referidos inibidores bem como seu uso |
| CA2578841A1 (en) | 2004-09-07 | 2006-03-16 | Pfizer Inc. | Inhibitors of the hiv integrase enzyme |
-
2005
- 2005-04-14 WO PCT/IB2005/001029 patent/WO2005103003A2/en not_active Ceased
- 2005-04-14 MX MXPA06012449A patent/MXPA06012449A/es not_active Application Discontinuation
- 2005-04-14 BR BRPI0510319-3A patent/BRPI0510319A/pt not_active IP Right Cessation
- 2005-04-14 CA CA002564356A patent/CA2564356A1/en not_active Abandoned
- 2005-04-14 JP JP2007510140A patent/JP2007534739A/ja not_active Abandoned
- 2005-04-14 EP EP05718474A patent/EP1756103A2/en not_active Withdrawn
- 2005-04-25 US US11/115,003 patent/US7468375B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA06012449A (es) | 2007-01-17 |
| US7468375B2 (en) | 2008-12-23 |
| WO2005103003A2 (en) | 2005-11-03 |
| US20050277662A1 (en) | 2005-12-15 |
| JP2007534739A (ja) | 2007-11-29 |
| WO2005103003A3 (en) | 2006-03-16 |
| EP1756103A2 (en) | 2007-02-28 |
| CA2564356A1 (en) | 2005-11-03 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE AS 4A, 5A, 6A E 7A ANUIDADES. |
|
| B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2158 DE 15/05/2012. |