PE20020509A1 - Aza y poliaza-naftalenil carboxamidas utiles como inhibidores de la integrasa del vih - Google Patents
Aza y poliaza-naftalenil carboxamidas utiles como inhibidores de la integrasa del vihInfo
- Publication number
- PE20020509A1 PE20020509A1 PE2001001008A PE2001001008A PE20020509A1 PE 20020509 A1 PE20020509 A1 PE 20020509A1 PE 2001001008 A PE2001001008 A PE 2001001008A PE 2001001008 A PE2001001008 A PE 2001001008A PE 20020509 A1 PE20020509 A1 PE 20020509A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- fluoroalkyl
- poliaza
- aza
- inhibitors
- Prior art date
Links
- 108010002459 HIV Integrase Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000003857 carboxamides Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 4-FLUOROBENZYL Chemical class 0.000 abstract 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 2
- 208000030507 AIDS Diseases 0.000 abstract 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002265 prevention Effects 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
-
- 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
-
- 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
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Animal Behavior & Ethology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
SE REFIERE A COMPUESTOS AZA Y POLIAZA-NAFTALENIL CARBOXAMIDAS DE FORMULA I DONDE A ES GRUPO AROMATICO, GRUPOS BICICLICOS; L ES UNA SOLA UNION, -(CH2)1-3, -(CH2)1-2OH, ENTRE OTROS; Q2 ES H, ALQUILO C1-C4, FLUOROALQUILO C1-C4, ENTRE OTROS; Q4 ES H, ALQUILO C1-C4, FLUOROALQUILO C1-C4, -O- ALQUILO C1-C4, ENTRE OTROS; R1 Y R2 SON H, ALQUILO C1-C4, FLUOROALQUILO C1-C4, -O-ALQUILO C1-C4, OH, ENTRE OTROS; R3 Y R4 SON H, HALO, CN, OH, ALQUILO C1-C4, FLUOROALQUILO C1-C4, ENTRE OTROS; R5 ES H, ALQUILO C1-C4, FENILO, ALQUILO C1-C4 SUSTITUIDO CON FENILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS N-1-(7-{[(4-FLUOROBENCIL)AMINO]CARBONIL}-8-HIDROXI-1,6-NAFTIRIDIN-5-IL)-N-1-,N-2,N-2-TRIMETILETANDIAMIDA, 5-(1,1-DIOXIDO-1,2-TIACINAN-2-IL)-N-(4-FLUOROBENCIL)-8-HIDROXI-1,6-NAFTIRIDIN-7-CARBOXAMIDA, N-(4-FLUOROBENCIL)-5-(1,1,-DIOXIDO-1,2,5-TIADIACEPAN-2-IL)-8-HIDROXI-[1,6]NAFTIRIDIN-7-CARBOXAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. LOS COMPUESTOS MENCIONADOS SON UTILES COMO INHIBIDORES DE LA INTEGRASA DEL VIH UTIL PARA LA PREVENCION Y TRATAMIENTO DEL INICIO DE SIDA
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23970700P | 2000-10-12 | 2000-10-12 | |
| US28165601P | 2001-04-05 | 2001-04-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20020509A1 true PE20020509A1 (es) | 2002-06-20 |
Family
ID=26932782
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2001001008A PE20020509A1 (es) | 2000-10-12 | 2001-10-11 | Aza y poliaza-naftalenil carboxamidas utiles como inhibidores de la integrasa del vih |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US6921759B2 (es) |
| EP (1) | EP1326865B1 (es) |
| JP (1) | JP4252797B2 (es) |
| KR (1) | KR20030036922A (es) |
| CN (1) | CN1469878A (es) |
| AR (1) | AR033845A1 (es) |
| AT (1) | ATE430745T1 (es) |
| AU (3) | AU2002211527B2 (es) |
| BG (1) | BG107677A (es) |
| BR (1) | BR0114610A (es) |
| CA (1) | CA2425440C (es) |
| CZ (1) | CZ20031028A3 (es) |
| DE (1) | DE60138635D1 (es) |
| EA (1) | EA200300449A1 (es) |
| EE (1) | EE200300145A (es) |
| HU (1) | HUP0302367A2 (es) |
| IL (1) | IL155089A0 (es) |
| IS (1) | IS6760A (es) |
| MX (1) | MXPA03003263A (es) |
| NO (1) | NO20031672L (es) |
| NZ (1) | NZ525088A (es) |
| PE (1) | PE20020509A1 (es) |
| PL (1) | PL360944A1 (es) |
| SK (1) | SK4322003A3 (es) |
| WO (2) | WO2002030931A2 (es) |
| YU (1) | YU27903A (es) |
Families Citing this family (93)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002030931A2 (en) * | 2000-10-12 | 2002-04-18 | Merck & Co., Inc. | Aza- and polyaza-naphthalenyl carboxamides useful as hiv integrase inhibitors |
| TWI243164B (en) | 2001-02-13 | 2005-11-11 | Aventis Pharma Gmbh | Acylated indanyl amines and their use as pharmaceuticals |
| WO2002070486A1 (en) | 2001-03-01 | 2002-09-12 | Shionogi & Co., Ltd. | Nitrogen-containing heteroaryl compounds having hiv integrase inhibitory activity |
| EP2181985B1 (en) | 2001-08-10 | 2011-10-26 | Shionogi & Co., Ltd. | Antiviral Agent |
| WO2003016294A1 (en) * | 2001-08-17 | 2003-02-27 | Merck & Co., Inc. | Process for preparing sultams |
| US20050014780A1 (en) * | 2001-08-17 | 2005-01-20 | Maligres Peter E. | Process for preparing 5-sulfonamido-8-hydroxy-1,6-naphthyridine-7-carboxamides |
| AR036256A1 (es) * | 2001-08-17 | 2004-08-25 | Merck & Co Inc | Sal sodica de un inhibidor de integrasa del vih, procesos para su preparacion, composiciones farmaceuticas que lo contienen y su uso para la manufactura de un medicamento |
| CA2463976C (en) * | 2001-10-26 | 2007-02-13 | Benedetta Crescenzi | N-substituted hydroxypyrimidinone carboxamide inhibitors of hiv integrase |
| DK1441734T3 (da) * | 2001-10-26 | 2007-06-11 | Angeletti P Ist Richerche Bio | Dihydroxypyrimidin-carboxamid-inhibitorer a HIV-integrase |
| DE10155075A1 (de) * | 2001-11-09 | 2003-05-22 | Merck Patent Gmbh | Cyclische Sulfonamide |
| US7279487B2 (en) | 2002-01-17 | 2007-10-09 | Merck & Co., Inc. | Hydroxynaphthyridinone carboxamides useful as HIV integrase inhibitors |
| US7323460B2 (en) | 2002-03-15 | 2008-01-29 | Merck & Co., Inc. | N-(substituted benzyl)-8-hydroxy-1,6-naphthyridine-7-carboxamides useful as HIV integrase inhibitors |
| WO2003086319A2 (en) * | 2002-04-10 | 2003-10-23 | Merck & Co., Inc. | Pharmaceutical compositions containing an hiv integrase inhibitor and a nonionic surfactant |
| US7109233B2 (en) * | 2002-05-22 | 2006-09-19 | Smithkline Beecham Corporation | Protease inhibitors |
| EP1388535A1 (en) * | 2002-08-07 | 2004-02-11 | Aventis Pharma Deutschland GmbH | Acylated arylcycloalkylamines and their use as pharmaceuticals |
| AU2003257822A1 (en) | 2002-08-13 | 2004-04-30 | Shionogi And Co., Ltd. | Heterocyclic compound having hiv integrase inhibitory activity |
| US7399763B2 (en) | 2002-09-11 | 2008-07-15 | Merck & Co., Inc. | 8-hydroxy-1-oxo-tetrahydropyrrolopyrazine compounds useful as HIV integrase inhibitors |
| JP2006506352A (ja) | 2002-09-11 | 2006-02-23 | メルク エンド カムパニー インコーポレーテッド | Hivインテグラーゼ阻害剤として有用なジヒドロキシピリドピラジン−1,6−ジオン化合物 |
| KR101122782B1 (ko) | 2002-10-04 | 2012-04-12 | 프라나 바이오테크놀로지 리미티드 | 신경 활성 화합물 |
| US7074810B2 (en) | 2002-10-07 | 2006-07-11 | Bristol-Myers Squibb Company | Triazolone and triazolethione derivatives as inhibitors of matrix metalloproteinases and/or TNF-α converting enzyme |
| WO2004035577A2 (en) * | 2002-10-16 | 2004-04-29 | Gilead Sciences, Inc. | Pre-organized tricyclic integrase inhibitor compounds |
| KR20050087865A (ko) | 2002-12-27 | 2005-08-31 | 이스티투토 디 리세르쉐 디 비올로지아 몰레콜라레 피. 안젤레티에스.피.에이. | HIV 인테그라제 억제제로서 유용한테트라하이드로-4H-피리도[1,2-a]피리미딘 및 관련화합물 |
| US20040220273A1 (en) * | 2003-03-12 | 2004-11-04 | Jaemoon Lee | Preparation of 2-aminomethyl-5-fluorobenzamides |
| WO2004080402A2 (en) * | 2003-03-12 | 2004-09-23 | Merck & Co. Inc. | Potassium salt of an hiv integrase inhibitor |
| EP1622615A4 (en) | 2003-05-13 | 2009-02-18 | Smithkline Beecham Corp | INHIBITORS OF THE INTEGRASE OF NAPHTHYRIDINE |
| US20060173046A1 (en) * | 2003-07-15 | 2006-08-03 | Bell Ian M | Hydroxypyridine cgrp receptor antagonists |
| TW200510425A (en) | 2003-08-13 | 2005-03-16 | Japan Tobacco Inc | Nitrogen-containing fused ring compound and use thereof as HIV integrase inhibitor |
| WO2005028478A1 (en) | 2003-09-19 | 2005-03-31 | Gilead Sciences, Inc. | Aza-quinolinol phosphonate integrase inhibitor compounds |
| WO2005041664A1 (en) | 2003-10-20 | 2005-05-12 | Merck & Co., Inc. | Hydroxy pyridopyrrolopyrazine dione compounds useful as hiv integrase inhibitors |
| TW200533357A (en) | 2004-01-08 | 2005-10-16 | Millennium Pharm Inc | 2-(amino-substituted)-4-aryl pyrimidines and related compounds useful for treating inflammatory diseases |
| CN101014571A (zh) * | 2004-01-30 | 2007-08-08 | 默克公司 | 用作hiv整合酶抑制剂的n-苄基-3,4-二羟基吡啶-2-羧酰胺类和n-苄基-2,3-二羟基吡啶-4-羧酰胺类化合物 |
| US7919623B2 (en) | 2004-02-04 | 2011-04-05 | Shionogi & Co., Ltd. | Naphthyridine derivatives having inhibitory activity against HIV integrase |
| JP4859676B2 (ja) | 2004-02-11 | 2012-01-25 | スミスクライン ビーチャム コーポレーション | Hivインテグラーゼ阻害剤 |
| EP1725102A4 (en) * | 2004-03-09 | 2009-04-29 | Merck & Co Inc | HIV integrase |
| CN101014574A (zh) * | 2004-03-09 | 2007-08-08 | 默克公司 | Hiv整合酶抑制剂 |
| CA2557926A1 (en) * | 2004-03-09 | 2005-09-22 | Monica Donghi | Hiv integrase inhibitors |
| NZ549449A (en) * | 2004-03-09 | 2009-05-31 | Merck & Co Inc | HIV Integrase inhibitors |
| CN1964975B (zh) * | 2004-05-07 | 2011-11-30 | 默沙东公司 | Hiv整合酶抑制剂 |
| CA2568389A1 (en) * | 2004-06-09 | 2005-12-22 | Merck & Co., Inc. | Hiv integrase inhibitors |
| KR20070085702A (ko) * | 2004-12-03 | 2007-08-27 | 머크 앤드 캄파니 인코포레이티드 | Ugt1a1에 의해 대사된 약물의 약력학을 개선시키기위한 아타자나비르의 용도 |
| UA87884C2 (uk) | 2004-12-03 | 2009-08-25 | Мерк Энд Ко., Инк. | Безводна кристалічна калієва сіль інгібітора віл-інтегрази |
| EP1852434B1 (en) * | 2005-02-21 | 2011-07-13 | Shionogi Co., Ltd. | Bicyclic carbamoylpyridone derivative having hiv integrase inhibiting activity |
| CN101146811B (zh) * | 2005-03-31 | 2012-01-11 | P.安杰莱蒂分子生物学研究所 | Hiv整合酶抑制剂 |
| WO2006121831A2 (en) | 2005-05-10 | 2006-11-16 | Merck & Co., Inc. | Hiv integrase inhibitors |
| WO2006125048A2 (en) * | 2005-05-16 | 2006-11-23 | Gilead Sciences, Inc. | Hiv-integrase inhibitor compounds |
| WO2007019098A2 (en) * | 2005-08-04 | 2007-02-15 | Smithkline Beecham Corporation | Hiv integrase inhibitors |
| WO2007019130A2 (en) * | 2005-08-04 | 2007-02-15 | Smithkline Beecham Corporation | Hiv integrase inhibitors |
| EP1910355A4 (en) * | 2005-08-04 | 2010-11-24 | Glaxosmithkline Llc | HIV integrase |
| EP1910356A4 (en) * | 2005-08-04 | 2009-10-21 | Smithkline Beecham Corp | HIV integrase |
| EP1937678B1 (en) * | 2005-10-04 | 2011-07-27 | Istituto Di Ricerche Di Biologia Molecolare P. Angeletti S.P.A. | Hiv integrase inhibitors |
| AU2006306355A1 (en) * | 2005-10-27 | 2007-05-03 | Merck & Co., Inc. | HIV integrase inhibitors |
| JP5131689B2 (ja) | 2005-10-27 | 2013-01-30 | 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多環性カルバモイルピリドン誘導体 |
| EP1979349B1 (en) * | 2005-12-21 | 2010-07-28 | Abbott Laboratories | Anti-viral compounds |
| NZ572367A (en) * | 2006-05-16 | 2011-09-30 | Gilead Sciences Inc | Fused cyclic compounds as integrase inhibitors |
| US20100056516A1 (en) * | 2006-07-17 | 2010-03-04 | Williams Peter D | 1-hydroxy naphthyridine compounds as anti-hiv agents |
| AU2007280984A1 (en) * | 2006-07-25 | 2008-02-07 | Envivo Pharmaceutical Inc. | Quinoline derivatives |
| AU2007292387A1 (en) * | 2006-09-05 | 2008-03-13 | Bipar Sciences, Inc. | Treatment of cancer |
| ES2488922T3 (es) | 2006-09-29 | 2014-09-01 | Idenix Pharmaceuticals, Inc. | Fosfoindoles enantiómeramente puros como inhibidores del HIV |
| US20100216834A1 (en) * | 2006-10-18 | 2010-08-26 | Isaacs Richard C A | Hiv integrase inhibitors |
| US20090291921A1 (en) * | 2007-11-20 | 2009-11-26 | Gilead Sciences, Inc. | Integrase inhibitors |
| MX2010008148A (es) | 2008-01-25 | 2010-10-20 | Chimerix Inc | Métodos de tratamiento de infecciones virales. |
| EP2318406B1 (en) | 2008-07-17 | 2016-01-27 | Critical Outcome Technologies, Inc. | Thiosemicarbazone inhibitor compounds and cancer treatment methods |
| EP2379076B1 (en) | 2008-12-23 | 2014-11-12 | The Trustees of Columbia University in the City of New York | Phosphodiesterase inhibitors and uses thereof |
| CA2762582A1 (en) | 2009-05-27 | 2010-12-02 | Merck Sharp & Dohme Corp. | Hiv protease inhibitors |
| EA019558B1 (ru) * | 2009-10-13 | 2014-04-30 | Эланко Энимал Хэлс Аиэлэнд Лимитед | Макроциклические ингибиторы интегразы |
| EP3970702A1 (en) | 2009-10-26 | 2022-03-23 | Merck Sharp & Dohme Corp. | Solid pharmaceutical compositions containing an integrase inhibitor |
| EP2345642A1 (en) | 2009-12-29 | 2011-07-20 | Polichem S.A. | Secondary 8-hydroxyquinoline-7-carboxamide derivatives for use as antifungal agents |
| EP2345641A1 (en) | 2009-12-29 | 2011-07-20 | Polichem S.A. | New secondary 8-hydroxyquinoline-7-carboxamide derivatives |
| EP2345643A1 (en) | 2009-12-29 | 2011-07-20 | Polichem S.A. | New tertiary 8-hydroxyquinoline-7-carboxamide derivatives and uses thereof |
| WO2011100698A2 (en) | 2010-02-12 | 2011-08-18 | Chimerix, Inc. | Methods of treating viral infection |
| CA2999435A1 (en) | 2010-04-01 | 2011-10-06 | Critical Outcome Technologies Inc. | Compounds and method for treatment of hiv |
| RU2567385C2 (ru) | 2010-04-02 | 2015-11-10 | ЯНССЕН Ар ЭНД Ди АЙРЛЭНД | Макроциклические ингибиторы интегразы |
| WO2012055031A1 (en) | 2010-10-28 | 2012-05-03 | Merck Canada Inc. | Hiv protease inhibitors |
| WO2012087872A1 (en) * | 2010-12-23 | 2012-06-28 | Merck Sharp & Dohme Corp. | Quinolines and aza-quinolines as crth2 receptor modulators |
| CN103702985B (zh) | 2010-12-23 | 2016-02-17 | 默沙东公司 | 作为crth2受体调节剂的喹喔啉和氮杂喹喔啉 |
| EP2487176A1 (en) * | 2011-02-14 | 2012-08-15 | Elanco Animal Health Ireland Limited | Macrocyclic integrase inhibitors for use in the treatment of feline immunodeficiency virus |
| US8865741B2 (en) | 2011-02-18 | 2014-10-21 | Asana Biosciences, Llc | Aminoindane compounds and use thereof in treating pain |
| EP2771332B1 (en) | 2011-10-26 | 2016-06-29 | Merck Canada Inc. | Thiophen and thiazol sulfonamid derivatives as HIV protease inhibitors for the treatment of AIDS |
| WO2014028675A1 (en) | 2012-08-15 | 2014-02-20 | Endo Pharmaceuticals Inc. | Use of aminoindane compounds in treating overactive bladder and interstitial cystitis |
| CA2882831A1 (en) | 2012-09-11 | 2014-03-20 | Merck Sharp & Dohme Corp. | Hiv protease inhibitors |
| CN103709162B (zh) * | 2012-09-29 | 2016-12-07 | 中国科学院上海药物研究所 | 三取代咪唑并二氮杂萘酮化合物及其制备方法和用途 |
| CN104003986B (zh) * | 2013-02-22 | 2016-06-08 | 中国科学院上海药物研究所 | 吡啶骈环类化合物及其制备方法、其药物组合物和用途 |
| WO2015013835A1 (en) | 2013-07-31 | 2015-02-05 | Merck Sharp & Dohme Corp. | Piperazine derivatives as hiv protease inhibitors |
| US9737545B2 (en) | 2013-12-19 | 2017-08-22 | Merck Sharp & Dohme Corp. | HIV protease inhibitors |
| US9834526B2 (en) | 2013-12-19 | 2017-12-05 | Merck Sharp & Dohme Corp. | HIV protease inhibitors |
| US9994587B2 (en) | 2014-03-06 | 2018-06-12 | Merck Sharp & Dohme Corp. | HIV protease inhibitors |
| WO2015138220A1 (en) | 2014-03-10 | 2015-09-17 | Merck Sharp & Dohme Corp. | Piperazine derivatives as hiv protease inhibitors |
| AU2017225769B2 (en) | 2016-03-02 | 2023-01-05 | The Board Of Regents Of The University Of Texas System | Sting activating nanovaccine for immunotherapy |
| CN106588922B (zh) * | 2017-01-17 | 2018-04-27 | 北京工业大学 | 二取代八氢-1,6-萘啶类化合物及其制备方法和应用 |
| EP3655401B1 (en) * | 2017-07-18 | 2023-09-06 | Merck Patent GmbH | Tlr7/8 antagonists and uses thereof |
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| CN115710249B (zh) * | 2022-11-14 | 2024-11-19 | 广东工业大学 | 一种多取代异喹啉和1,6-萘啶化合物的制备方法及光电材料常见分子骨架 |
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Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5751837B2 (es) | 1973-04-05 | 1982-11-04 | ||
| US4416884A (en) | 1978-04-12 | 1983-11-22 | Otsuka Pharmaceutical Co., Ltd. | Piperazinylbenzoheterocyclic compounds |
| FR2632639B1 (fr) | 1988-06-09 | 1990-10-05 | Sanofi Sa | Derives d'amino-4 carboxy-3 naphtyridines, leur preparation et compositions pharmaceutiques qui les contiennent |
| IL101860A0 (en) | 1991-05-31 | 1992-12-30 | Ici Plc | Heterocyclic derivatives |
| US5681832A (en) * | 1995-02-17 | 1997-10-28 | The United States Of America As Represented By The Department Of Health And Human Services | Aroylaniline compounds, pharmaceutical compositions, and methods of using same to inhibit viral activity |
| US5633362A (en) | 1995-05-12 | 1997-05-27 | E. I. Du Pont De Nemours And Company | Production of 1,3-propanediol from glycerol by recombinant bacteria expressing recombinant diol dehydratase |
| ATE258437T1 (de) | 1995-08-02 | 2004-02-15 | Darwin Discovery Ltd | Chinolone und deren therapeutische verwendung |
| US5945431A (en) | 1996-03-15 | 1999-08-31 | Biochem Therapeutics Incorporated | Cytomegalovirus inhibiting compounds |
| AU4172197A (en) | 1996-09-10 | 1998-04-02 | Pharmacia & Upjohn Company | 8-hydroxy-7-substituted quinolines as anti-viral agents |
| US6809097B1 (en) | 1996-09-25 | 2004-10-26 | Zeneca Limited | Quinoline derivatives inhibiting the effect of growth factors such as VEGF |
| US5766944A (en) | 1996-12-31 | 1998-06-16 | Ruiz; Margaret Eileen | T cell differentiation of CD34+ stem cells in cultured thymic epithelial fragments |
| WO1999000388A1 (en) | 1997-06-30 | 1999-01-07 | Nippon Kayaku Kabushiki Kaisha | Novel naphthyridine derivatives or salts thereof |
| YU10500A (sh) | 1997-08-25 | 2002-10-18 | Neurogen Corporation | Supstituisani 4-okso-naptiridin-3-karboksamidi kao gaba moždani receptorski liganidi |
| GB9720052D0 (en) | 1997-09-19 | 1997-11-19 | Smithkline Beecham Plc | Novel compounds |
| ATE314347T1 (de) | 1997-09-30 | 2006-01-15 | Daiichi Seiyaku Co | Sulfonylderivate |
| JP2001526265A (ja) | 1997-12-22 | 2001-12-18 | ファルマシア・アンド・アップジョン・カンパニー | 抗ウイルス剤としての4−ヒドロキシキノリン−3−カルボキサミドおよびヒドラジド |
| US6262055B1 (en) | 1998-06-03 | 2001-07-17 | Merck & Co., Inc. | HIV integrase inhibitors |
| US6380249B1 (en) | 1998-06-03 | 2002-04-30 | Merck & Co., Inc. | HIV integrase inhibitors |
| US6306891B1 (en) | 1998-06-03 | 2001-10-23 | Merck & Co., Inc. | HIV integrase inhibitors |
| SE9802550D0 (sv) | 1998-07-15 | 1998-07-15 | Active Biotech Ab | Quinoline derivatives |
| AU5880600A (en) | 1999-06-25 | 2001-01-31 | Merck & Co., Inc. | 1-(aromatic- or heteroaromatic-substituted)-3-(heteroaromatic substituted)-1,3-propanediones and uses thereof |
| US6730682B2 (en) | 2000-07-12 | 2004-05-04 | Pharmacia & Upjohn Company | Heterocycle carboxamides as antiviral agents |
| GB0017676D0 (en) | 2000-07-19 | 2000-09-06 | Angeletti P Ist Richerche Bio | Inhibitors of viral polymerase |
| WO2002030931A2 (en) * | 2000-10-12 | 2002-04-18 | Merck & Co., Inc. | Aza- and polyaza-naphthalenyl carboxamides useful as hiv integrase inhibitors |
| CN1336363A (zh) | 2001-07-25 | 2002-02-20 | 张元宾 | 乙酰磺胺酸钾的合成制备方法 |
| US20050014780A1 (en) | 2001-08-17 | 2005-01-20 | Maligres Peter E. | Process for preparing 5-sulfonamido-8-hydroxy-1,6-naphthyridine-7-carboxamides |
| AR036256A1 (es) * | 2001-08-17 | 2004-08-25 | Merck & Co Inc | Sal sodica de un inhibidor de integrasa del vih, procesos para su preparacion, composiciones farmaceuticas que lo contienen y su uso para la manufactura de un medicamento |
| DK1441734T3 (da) | 2001-10-26 | 2007-06-11 | Angeletti P Ist Richerche Bio | Dihydroxypyrimidin-carboxamid-inhibitorer a HIV-integrase |
| CA2463976C (en) | 2001-10-26 | 2007-02-13 | Benedetta Crescenzi | N-substituted hydroxypyrimidinone carboxamide inhibitors of hiv integrase |
| WO2003086319A2 (en) * | 2002-04-10 | 2003-10-23 | Merck & Co., Inc. | Pharmaceutical compositions containing an hiv integrase inhibitor and a nonionic surfactant |
-
2001
- 2001-10-09 WO PCT/US2001/042564 patent/WO2002030931A2/en not_active Ceased
- 2001-10-09 WO PCT/US2001/031456 patent/WO2002030930A2/en not_active Ceased
- 2001-10-09 AT AT01979582T patent/ATE430745T1/de not_active IP Right Cessation
- 2001-10-09 CN CNA018172970A patent/CN1469878A/zh active Pending
- 2001-10-09 NZ NZ525088A patent/NZ525088A/en unknown
- 2001-10-09 AU AU2002211527A patent/AU2002211527B2/en not_active Ceased
- 2001-10-09 EA EA200300449A patent/EA200300449A1/ru unknown
- 2001-10-09 MX MXPA03003263A patent/MXPA03003263A/es unknown
- 2001-10-09 DE DE60138635T patent/DE60138635D1/de not_active Expired - Lifetime
- 2001-10-09 CZ CZ20031028A patent/CZ20031028A3/cs unknown
- 2001-10-09 EP EP01979582A patent/EP1326865B1/en not_active Expired - Lifetime
- 2001-10-09 SK SK432-2003A patent/SK4322003A3/sk unknown
- 2001-10-09 IL IL15508901A patent/IL155089A0/xx unknown
- 2001-10-09 AU AU1152702A patent/AU1152702A/xx active Pending
- 2001-10-09 KR KR10-2003-7005140A patent/KR20030036922A/ko not_active Withdrawn
- 2001-10-09 HU HU0302367A patent/HUP0302367A2/hu unknown
- 2001-10-09 JP JP2002534317A patent/JP4252797B2/ja not_active Expired - Fee Related
- 2001-10-09 EE EEP200300145A patent/EE200300145A/xx unknown
- 2001-10-09 CA CA2425440A patent/CA2425440C/en not_active Expired - Fee Related
- 2001-10-09 AU AU2002211874A patent/AU2002211874A1/en not_active Abandoned
- 2001-10-09 BR BR0114610-6A patent/BR0114610A/pt not_active IP Right Cessation
- 2001-10-09 PL PL01360944A patent/PL360944A1/xx not_active Application Discontinuation
- 2001-10-09 YU YU27903A patent/YU27903A/sh unknown
- 2001-10-10 US US09/973,853 patent/US6921759B2/en not_active Expired - Fee Related
- 2001-10-11 AR ARP010104777A patent/AR033845A1/es not_active Application Discontinuation
- 2001-10-11 PE PE2001001008A patent/PE20020509A1/es not_active Application Discontinuation
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2003
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- 2003-03-27 IS IS6760A patent/IS6760A/is unknown
- 2003-04-11 NO NO20031672A patent/NO20031672L/no not_active Application Discontinuation
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2005
- 2005-02-11 US US11/056,412 patent/US20050176718A1/en not_active Abandoned
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