AR042602A1 - Compuestos de 1,2,4-triazol - Google Patents
Compuestos de 1,2,4-triazolInfo
- Publication number
- AR042602A1 AR042602A1 ARP020104915A ARP020104915A AR042602A1 AR 042602 A1 AR042602 A1 AR 042602A1 AR P020104915 A ARP020104915 A AR P020104915A AR P020104915 A ARP020104915 A AR P020104915A AR 042602 A1 AR042602 A1 AR 042602A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- substituted
- pyridyl
- unsubstituted
- cyano
- Prior art date
Links
Classifications
-
- 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
- C07D413/10—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 carbon chain containing aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
- C07D311/08—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring
- C07D311/16—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring substituted in position 7
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un nuevo compuesto de 1,2,4-triazol es útil como agente terapéutico para la hiperuricemia y la gota provocada por hiperuricemia. Un compuesto se representa por la fórmula general (1). También se provee un proceso para la producción de un compuesto haciendo reaccionar un nitrilo y una hidracina, y un agente terapéutico, particularmente un inhibidor de xantina oxidasa. Reivindicación 1: Un compuesto de 1,2,4-triazol caracterizado porque se representa mediante la fórmula general (1), donde R2 representa un grupo piridilo no sustituido o un grupo piridilo sustituido con un grupo ciano, alquilo inferior, halógeno, alcoxi inferior o alquiltio inferior como sustituyente, R1 representa un grupo piridilo no sustituido o sustituido que puede estar sustituido con un halógeno, grupo ciano o fenilo como sustituyente, un grupo piridina-N-óxido correspondiente a dichos grupos piridilo, un grupo fenilo sustituido con un grupo ciano o nitro o un grupo fenilo sustituido con, además de un grupo ciano o nitro como sustituyente, un grupo alcoxi inferior sustituido o no sustituido, un grupo N-alquilo inferior-piperazino, un grupo alquiltio inferior, un grupo feniltio, o un grupo alquilamino inferior, siempre y cuando R1 no sea un grupo piridilo no sustituido, un grupo piridilo sustituido con un grupo alquilo inferior o un grupo piridina-N-óxido correspondiente a dichos grupos piridilo en el caso donde R2 sea un grupo piridilo no sustituido, o un grupo piridilo sustituido con un grupo inferior, y R3 representa hidrógeno o un grupo alquilo inferior sustituido con un grupo pivaloiloxi y en cada caso R3 se une a uno de lo átomos de nitrógeno en el anillo 1,2,4-triazol representado por la fórmula general (1), o un hidrato o una sal del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002017825 | 2002-01-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR042602A1 true AR042602A1 (es) | 2005-06-29 |
Family
ID=27653386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP020104915A AR042602A1 (es) | 2002-01-28 | 2002-12-17 | Compuestos de 1,2,4-triazol |
Country Status (22)
Country | Link |
---|---|
US (1) | US7074816B2 (es) |
EP (1) | EP1471065B1 (es) |
JP (1) | JP3600832B2 (es) |
CN (1) | CN1561340B (es) |
AR (1) | AR042602A1 (es) |
AT (1) | ATE387438T1 (es) |
AU (1) | AU2002349754B2 (es) |
BR (1) | BRPI0212775B8 (es) |
CA (1) | CA2462132C (es) |
DE (1) | DE60225341T2 (es) |
DK (1) | DK1471065T3 (es) |
ES (1) | ES2300486T3 (es) |
HK (1) | HK1067132A1 (es) |
MX (1) | MXPA04004037A (es) |
NO (1) | NO326941B1 (es) |
NZ (1) | NZ531673A (es) |
PL (1) | PL208260B1 (es) |
PT (1) | PT1471065E (es) |
RU (1) | RU2293733C2 (es) |
TW (1) | TWI257926B (es) |
WO (1) | WO2003064410A1 (es) |
ZA (1) | ZA200401777B (es) |
Families Citing this family (48)
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KR20060037373A (ko) * | 2003-07-24 | 2006-05-03 | 가부시키가이샤 후지야쿠힝 | 1,2,4-트리아졸 화합물의 제조 방법 및 그 중간체 |
US20060189811A1 (en) * | 2004-07-23 | 2006-08-24 | Fujiyakuhin Co., Ltd. | Process for producing 1,2,4-triazole compound and intermediate therefor |
WO2006121995A2 (en) | 2005-05-09 | 2006-11-16 | Tap Pharmaceutical Products, Inc. | Methods for treating nephrolithiasis |
EP1940397A4 (en) * | 2005-08-03 | 2010-01-20 | Takeda Pharmaceuticals North A | METHOD FOR TREATING HYPERTONIA |
KR20080066938A (ko) * | 2005-10-07 | 2008-07-17 | 깃세이 야쿠힌 고교 가부시키가이샤 | 질소 함유 복소환 화합물 및 그것을 함유하는 의약 조성물 |
KR20140037954A (ko) * | 2006-06-22 | 2014-03-27 | 닛뽕 케미파 가부시키가이샤 | 항암제 내성 극복제 |
JP5110536B2 (ja) * | 2006-07-19 | 2012-12-26 | 学校法人日本医科大学 | 筋萎縮性側索硬化症治療薬 |
KR20160031040A (ko) * | 2006-11-13 | 2016-03-21 | 다케다 파마슈티칼스 유에스에이, 인코포레이티드 | 크산틴 옥시도리덕타아제 억제제를 사용하여 신장 기능을 보존하는 방법 |
US20090124623A1 (en) * | 2006-11-13 | 2009-05-14 | Christopher Lademacher | Methods for preserving and/or increasing renal function using xanthine oxidoreductase inhibitors |
JP2010516691A (ja) * | 2007-01-19 | 2010-05-20 | タケダ ファーマシーティカルズ ノース アメリカ,アイエヌシー. | 抗炎症剤及びキサンチン酸化還元酵素阻害剤を用いて痛風の突発を抑え、又はその数を減少させる方法 |
JO2784B1 (en) * | 2007-10-18 | 2014-03-15 | شركة جانسين فارماسوتيكا ان. في | 5,3,1 - Triazole substitute derivative |
DK2217577T3 (da) | 2007-11-27 | 2014-10-20 | Ardea Biosciences Inc | Hidtil ukendte forbindelser og præparater og fremgangsmåder til anvendelse deraf |
EP2165705A1 (en) | 2008-09-18 | 2010-03-24 | Centre National de la Recherche Scientifique (CNRS) | Use of a compound capable of reducing the uric acid level for the prevention and/or the treatment of lung inflammation and fibrosis |
US20100311756A1 (en) * | 2009-01-22 | 2010-12-09 | Takeda Pharmaceuticals North America, Inc. | Methods for delaying the progression of at least one of cardiac hypertrophy, cardiac remodeling or left ventricular function or the onset of heart failure in subjects in need of treatment thereof |
RU2013109380A (ru) | 2010-09-10 | 2014-10-20 | Такеда Фармасьютикалс Ю.С.А.,Инк. | Способ сопутствующей терапии с применением теофиллина и фебуксостата |
WO2012060308A1 (ja) * | 2010-11-01 | 2012-05-10 | 株式会社 三和化学研究所 | 腎機能障害の予防又は治療に用いる医薬 |
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WO2012118485A1 (en) | 2011-03-01 | 2012-09-07 | Empire Technology Development Llc | Temperature controlled variable reflectivity coatings |
RU2476428C1 (ru) * | 2011-09-01 | 2013-02-27 | Государственное образовательное учреждение высшего профессионального образования "Южно-Российский государственный технический университет (Новочеркасский политехнический институт)" | Способ получения дигидрохлорида 5-амино-3-аминометил-1,2,4-триазола |
ES2690315T3 (es) | 2012-06-15 | 2018-11-20 | Mitsubishi Tanabe Pharma Corporation | Compuestos de imidazol y triazol como inhibidores de DGAT-1 |
CN104411700B (zh) * | 2012-07-25 | 2016-06-15 | 株式会社富士药品 | 4-[5-(吡啶-4-基)-1h-1,2,4-三唑-3-基]吡啶-2-腈的多晶型及其制造方法 |
BR112014032229B1 (pt) * | 2012-07-25 | 2021-02-09 | Fujiyakuhin Co., Ltd. | método para produzir 4-[5-(piridin-4-il)-1h-1,2,4-triazol-3- il]piridina-2-carbonitrila |
CN103724329B (zh) * | 2013-12-23 | 2015-02-18 | 济南百诺医药科技开发有限公司 | 4-[5-(吡啶-4-基)-1h-[1,2,4]三唑-3-基]吡啶-2-甲腈的制备方法 |
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CN104151297B (zh) * | 2014-08-27 | 2016-03-16 | 王庆本 | 4-[5-(吡啶-4-基)-1h-[1,2,4]三唑-3-基]吡啶-2-甲腈的制备方法 |
JP6684264B2 (ja) * | 2015-02-17 | 2020-04-22 | 株式会社三和化学研究所 | 心不全の予防又は治療のための医薬 |
JP6891108B2 (ja) | 2015-02-24 | 2021-06-18 | 国立大学法人鳥取大学 | 認知症の予防及び/又は治療のための医薬 |
CN107531677A (zh) * | 2015-02-25 | 2018-01-02 | 法尔玛赞公司 | 用于制备托匹司他及其中间体的方法 |
CN105693699B (zh) * | 2015-03-30 | 2019-06-18 | 苏州晶云药物科技股份有限公司 | 托吡司他的晶型及其制备方法 |
CN104910068B (zh) * | 2015-04-24 | 2017-07-14 | 南京医科大学 | 一种2‑氰基异烟酸酰肼1.5对甲苯磺酸盐的合成方法 |
CN106279111A (zh) * | 2015-05-12 | 2017-01-04 | 北京济美堂医药研究有限公司 | 一种精制托吡司他的新方法 |
CN104961730B (zh) * | 2015-06-18 | 2017-05-17 | 山东金城医药化工股份有限公司 | 托吡司他新晶型及其制备方法 |
CN105130958B (zh) * | 2015-08-31 | 2017-10-31 | 济南康和医药科技有限公司 | 5‑(2‑氰基4‑吡啶基)‑3‑(4‑吡啶基)‑1,2,4‑三唑的制备工艺 |
CN105294656A (zh) * | 2015-10-10 | 2016-02-03 | 大道隆达(北京)医药科技发展有限公司 | 一种托匹司他的制备工艺和方法 |
CN106336399A (zh) * | 2015-11-03 | 2017-01-18 | 江苏悦兴药业有限公司 | 托匹司他工艺杂质的制备方法 |
CN105294584A (zh) * | 2015-11-30 | 2016-02-03 | 中国医科大学 | 1-取代苯基-1h-1,2,3-三唑类化合物、制备方法及其用途 |
CN105399732A (zh) * | 2015-12-07 | 2016-03-16 | 青岛正大海尔制药有限公司 | 一种托匹司他的制备方法 |
CN106008465A (zh) * | 2016-03-16 | 2016-10-12 | 江苏悦兴药业有限公司 | 一种托匹司他杂质的合成方法 |
CN108250183A (zh) * | 2016-12-29 | 2018-07-06 | 北京诚济制药有限公司 | 一种高纯度的托匹司他的制备方法 |
CN109721586B (zh) * | 2017-10-27 | 2021-03-02 | 中国医科大学 | 一种5-苄基-3-吡啶基-1h-1,2,4-三唑类化合物及其制备方法和用途 |
CN107652271B (zh) * | 2017-11-06 | 2020-06-16 | 上海中拓医药科技有限公司 | 一种托匹司他晶型i的制备方法 |
CN108017619B (zh) * | 2017-12-06 | 2020-08-11 | 成都惟邦药业有限公司 | 一种托匹司他杂质及其制备方法 |
CN113354616B (zh) * | 2020-03-05 | 2024-03-26 | 中国医学科学院药物研究所 | 二芳基-1,2,4-三唑类化合物及其制法和药物用途 |
CN113666909B (zh) * | 2020-05-14 | 2024-07-02 | 鲁南制药集团股份有限公司 | 一种托匹司他的制备方法 |
CN114773262B (zh) * | 2022-05-19 | 2024-05-07 | 兄弟科技股份有限公司 | 2-氰基-4-吡啶羧酸甲酯的合成方法 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL7112373A (es) * | 1970-09-25 | 1972-03-28 | ||
US3947577A (en) * | 1973-05-21 | 1976-03-30 | Merck & Co., Inc. | Anti-hyperuricemia composition |
US3963731A (en) * | 1973-05-21 | 1976-06-15 | Merck & Co., Inc. | Pyridyl containing 1-benzenesulfonyl triazoles |
US3928361A (en) * | 1973-05-21 | 1975-12-23 | Merck & Co Inc | 1-(Sulfamoylphenylalkyl)-3,5-dipyridyl-1,2,4 triazoles |
US3984558A (en) * | 1973-05-21 | 1976-10-05 | Merck & Co., Inc. | 1,3,5-Trisubstituted-1,2,4-triazole compounds used as bronchodilators |
US3882134A (en) * | 1973-05-21 | 1975-05-06 | Merck & Co Inc | 1-Substituted-3,5-dipyridyl-1,2,4-triazoles |
US4104393A (en) * | 1976-04-02 | 1978-08-01 | Merck & Co., Inc. | 1,3,5-Trisubstituted-1,2,4-triazole compounds |
ES2133312T3 (es) * | 1991-12-05 | 1999-09-16 | Wallac Oy | Quelatos de lantanidos luminiscentes. |
WO2000024735A1 (en) * | 1998-10-23 | 2000-05-04 | Dow Agrosciences Llc | Insecticidal 1-(substituted pyridyl)-1,2,4-triazoles |
EP1379525B1 (en) * | 2001-02-21 | 2007-10-10 | Nps Pharmaceuticals, Inc. | Heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists |
-
2002
- 2002-12-03 EP EP02781876A patent/EP1471065B1/en not_active Expired - Lifetime
- 2002-12-03 PT PT02781876T patent/PT1471065E/pt unknown
- 2002-12-03 WO PCT/JP2002/012662 patent/WO2003064410A1/ja active IP Right Grant
- 2002-12-03 AU AU2002349754A patent/AU2002349754B2/en not_active Ceased
- 2002-12-03 US US10/495,322 patent/US7074816B2/en not_active Expired - Lifetime
- 2002-12-03 BR BRPI0212775A patent/BRPI0212775B8/pt not_active IP Right Cessation
- 2002-12-03 DE DE60225341T patent/DE60225341T2/de not_active Expired - Lifetime
- 2002-12-03 NZ NZ531673A patent/NZ531673A/en not_active IP Right Cessation
- 2002-12-03 CA CA2462132A patent/CA2462132C/en not_active Expired - Lifetime
- 2002-12-03 MX MXPA04004037A patent/MXPA04004037A/es active IP Right Grant
- 2002-12-03 ES ES02781876T patent/ES2300486T3/es not_active Expired - Lifetime
- 2002-12-03 CN CN028192761A patent/CN1561340B/zh not_active Expired - Lifetime
- 2002-12-03 DK DK02781876T patent/DK1471065T3/da active
- 2002-12-03 JP JP2003564033A patent/JP3600832B2/ja not_active Expired - Lifetime
- 2002-12-03 PL PL368672A patent/PL208260B1/pl unknown
- 2002-12-03 AT AT02781876T patent/ATE387438T1/de active
- 2002-12-03 RU RU2004106554/04A patent/RU2293733C2/ru active
- 2002-12-09 TW TW091135529A patent/TWI257926B/zh not_active IP Right Cessation
- 2002-12-17 AR ARP020104915A patent/AR042602A1/es not_active Application Discontinuation
-
2004
- 2004-03-04 ZA ZA2004/01777A patent/ZA200401777B/en unknown
- 2004-03-15 NO NO20041075A patent/NO326941B1/no not_active IP Right Cessation
-
2005
- 2005-01-25 HK HK05100651.5A patent/HK1067132A1/xx not_active IP Right Cessation
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