PE20081753A1 - Compuestos y composiciones como inhibidores de la proteasa activadora de canal - Google Patents
Compuestos y composiciones como inhibidores de la proteasa activadora de canalInfo
- Publication number
- PE20081753A1 PE20081753A1 PE2008000284A PE2008000284A PE20081753A1 PE 20081753 A1 PE20081753 A1 PE 20081753A1 PE 2008000284 A PE2008000284 A PE 2008000284A PE 2008000284 A PE2008000284 A PE 2008000284A PE 20081753 A1 PE20081753 A1 PE 20081753A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- compounds
- inhibitors
- compositions
- activating protease
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 108091005804 Peptidases Proteins 0.000 title abstract 2
- 239000004365 Protease Substances 0.000 title abstract 2
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 title abstract 2
- 230000003213 activating effect Effects 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title 1
- -1 4-PIPERIDINYL Chemical class 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000000241 respiratory effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06086—Dipeptides with the first amino acid being basic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- A61P35/00—Antineoplastic agents
-
- 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
- A61P37/08—Antiallergic 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
- 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
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06191—Dipeptides containing heteroatoms different from O, S, or N
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Abstract
SE REFIERE A UN COMPUESTO DE FORMULA I, DONDE B ES DE PREFERENCIA 3-(4-PIPERIDINIL)-1N-METILSULFONILAMIDA; Y ES -SO2-, -NHCO-, -CO-, ENTRE OTROS; J ES BENZOXAZOLILO, 1,2,3-OXADIAZOL-2-ILO, OXAZOLO-[4,5-b]-PIRIDIN-2-ILO, ENTRE OTROS; R1 ES H, ALQUILO C1-C6, OPCIONALMENTE HALOGENADO, ALQUENILO C2-C6, ENTRE OTROS; R2 ES ALQUILO C1-C6, ALQUENILO C2-C6, ENTRE OTROS; R3 ES ALQUILO C1-C6, ALQUENILO C2-C6, ALQUINILO C2-C6, ENTRE OTROS; R4 ES ALQUILO C1-C6, ALQUENILO C2-C6, ANILLO HETEROCICLICO, ENTRE OTROS; R5 ES ANILLO CARBOCICLICO DE 5-12 MIEMBROS OPCIONALMENTE SUSTITUIDO, ANILLO HETEROCICLICO, ENTRE OTROS; k, m Y n SON CADA UNO 1-6. SON COMPUESTOS PREFERIDOS: A, B, ENTRE OTROS. REFERIDA TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PROTEASA ACTIVADORA DE CANAL (CAP) UTILES EN EL TRATAMIENTO DE ENFERMEDADES RESPIRATORIAS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US88900807P | 2007-02-09 | 2007-02-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20081753A1 true PE20081753A1 (es) | 2009-01-22 |
Family
ID=39322557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008000284A PE20081753A1 (es) | 2007-02-09 | 2008-02-08 | Compuestos y composiciones como inhibidores de la proteasa activadora de canal |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20100239551A1 (es) |
| EP (1) | EP2117541A1 (es) |
| JP (1) | JP2010518097A (es) |
| CN (1) | CN101646437A (es) |
| AR (1) | AR065266A1 (es) |
| AU (1) | AU2008214214B2 (es) |
| BR (1) | BRPI0806970A2 (es) |
| CA (1) | CA2677485A1 (es) |
| CL (1) | CL2008000408A1 (es) |
| EA (1) | EA200901082A1 (es) |
| MX (1) | MX2009008493A (es) |
| PE (1) | PE20081753A1 (es) |
| TW (1) | TW200845982A (es) |
| WO (1) | WO2008097673A1 (es) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8003617B2 (en) | 2004-11-10 | 2011-08-23 | Genzyme Corporation | Methods of treating diabetes mellitus |
| SI2032134T1 (sl) | 2006-05-09 | 2015-10-30 | Genzyme Corporation | Postopki zdravljenja bolezni zamaščenih jeter, ki obsegajo inhibicijo sintezo glukosfingolipida |
| RU2419626C2 (ru) | 2006-05-23 | 2011-05-27 | Айрм Ллк | Соединения и композиции в качестве ингибиторов протеазы, активирующей каналы |
| CA2677487A1 (en) * | 2007-02-09 | 2008-08-14 | Irm Llc | Compounds and compositions as channel activating protease inhibitors |
| US8304447B2 (en) | 2007-05-31 | 2012-11-06 | Genzyme Corporation | 2-acylaminopropoanol-type glucosylceramide synthase inhibitors |
| KR20160085917A (ko) | 2007-10-05 | 2016-07-18 | 젠자임 코포레이션 | 세라마이드 유도체로 다낭성 신장질환을 치료하는 방법 |
| EP2320886B1 (en) | 2008-07-28 | 2017-06-28 | Genzyme Corporation | Glucosylceramide synthase inhibition for the treatment of collapsing glomerulopathy and other glomerular disease |
| KR101687039B1 (ko) | 2008-10-03 | 2016-12-15 | 젠자임 코포레이션 | 2-아실아미노프로판올형 글루코실세라미드 합성효소 억제제 |
| AR076880A1 (es) | 2009-05-18 | 2011-07-13 | Orion Corp | Inhibidores de proteasa, composiciones farmaceuticas que los contienen y su uso. |
| DE102009022794A1 (de) * | 2009-05-27 | 2010-12-02 | Philipps-Universität Marburg | Verwendung von Hemmstoffen der HAT und TMPRSS2 als Arzneimittel |
| US8729061B2 (en) * | 2011-11-25 | 2014-05-20 | Hoffmann-La Roche Inc. | Pyrrolidine derivatives |
| NZ704666A (en) | 2012-08-23 | 2018-05-25 | Alios Biopharma Inc | Compounds for the treatment of paramoxyvirus viral infections |
| HRP20181197T1 (hr) * | 2013-10-29 | 2018-11-30 | Biomarin Pharmaceutical Inc. | Derivati n-(1-hidroksi-3-(pirolidinil)propan-2-il)pirolidin-3-karboksamida kao inhibitori glukozilceramid sintaze |
| CN107153117B (zh) * | 2016-03-04 | 2019-02-19 | 中国人民解放军军事医学科学院生物工程研究所 | 一种用于判断靶向单克隆抗体治疗肿瘤疗效的预测分子 |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6235216A (ja) | 1985-08-09 | 1987-02-16 | Noritoshi Nakabachi | 不均質物質層の層厚非破壊測定方法および装置 |
| WO1993018007A1 (fr) | 1992-03-13 | 1993-09-16 | Tokyo Tanabe Company Limited | Nouveau derive de carbostyrile |
| US6150334A (en) * | 1994-11-21 | 2000-11-21 | Cortech, Inc. | Serine protease inhibitors-tripeptoid analogs |
| US5618792A (en) * | 1994-11-21 | 1997-04-08 | Cortech, Inc. | Substituted heterocyclic compounds useful as inhibitors of (serine proteases) human neutrophil elastase |
| US5523308A (en) * | 1995-06-07 | 1996-06-04 | Costanzo; Michael J. | Peptidyl heterocycles useful in the treatment of thrombin related disorders |
| TW523513B (en) * | 1996-03-01 | 2003-03-11 | Akzo Nobel Nv | Serine protease inhibitors |
| EP1114822A3 (en) * | 1998-06-03 | 2002-11-13 | Cortech Inc. | Indoles and tetrahydroisoquinolines containing alpha-keto oxadiazoles as serine protease inhibitors |
| KR20010078724A (ko) * | 1998-06-03 | 2001-08-21 | 존 더블류. 갈루치 2세 | 세린 프로테아제 저해제로서의 인돌 및테트라히드로이소퀴놀린을 함유하는 α-케토 옥사디아졸 |
| US6362371B1 (en) | 1998-06-08 | 2002-03-26 | Advanced Medicine, Inc. | β2- adrenergic receptor agonists |
| EP1147097A1 (en) * | 1999-01-27 | 2001-10-24 | Ortho-Mcneil Pharmaceutical, Inc. | Peptidyl heterocyclic ketones useful as tryptase inhibitors |
| JP2000256396A (ja) * | 1999-03-03 | 2000-09-19 | Dainippon Pharmaceut Co Ltd | 複素環式化合物およびその中間体ならびにエラスターゼ阻害剤 |
| GB9913083D0 (en) | 1999-06-04 | 1999-08-04 | Novartis Ag | Organic compounds |
| US6683115B2 (en) | 1999-06-02 | 2004-01-27 | Theravance, Inc. | β2-adrenergic receptor agonists |
| OA11558A (en) | 1999-12-08 | 2004-06-03 | Advanced Medicine Inc | Beta 2-adrenergic receptor agonists. |
| JP2003533448A (ja) | 2000-04-27 | 2003-11-11 | ベーリンガー インゲルハイム ファルマ ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディトゲゼルシャフト | 新規持続性ベータ擬似剤、その製造方法及びその医薬としての使用 |
| GB0015876D0 (en) | 2000-06-28 | 2000-08-23 | Novartis Ag | Organic compounds |
| ES2523930T3 (es) | 2000-08-05 | 2014-12-02 | Glaxo Group Limited | Éster s-fluorometílico del ácido 6-alfa,9-alfa-difluoro-17-alfa-[(2-furanilcarbonil)oxi]-11-beta-hidroxi-16-alfa-metil-3-oxo-androst-1,4-dien-17-carbotioico como agente antiinflamatorio |
| GB0103630D0 (en) | 2001-02-14 | 2001-03-28 | Glaxo Group Ltd | Chemical compounds |
| ES2288543T3 (es) | 2001-03-08 | 2008-01-16 | Glaxo Group Limited | Agonistas de beta-adrenorreceptores. |
| ES2296923T3 (es) | 2001-03-22 | 2008-05-01 | Glaxo Group Limited | Derivados formanilidas como agonistas del adrenorreceptor beta2. |
| PT1383786E (pt) | 2001-04-30 | 2008-12-30 | Glaxo Group Ltd | Derivados anti-inflamatórios de éster 17.beta-carbotioato de androstano com um grupo éster ciclíco na posição 17.alfa |
| US20040248867A1 (en) | 2001-06-12 | 2004-12-09 | Keith Biggadike | Novel anti-inflammatory 17.alpha.-heterocyclic-esters of 17.beta.carbothioate androstane derivatives |
| DK1425001T3 (da) | 2001-09-14 | 2009-04-14 | Glaxo Group Ltd | Phenethanolaminderivater til behandling af respiratoriske sygdomme |
| US6653323B2 (en) | 2001-11-13 | 2003-11-25 | Theravance, Inc. | Aryl aniline β2 adrenergic receptor agonists |
| TWI249515B (en) | 2001-11-13 | 2006-02-21 | Theravance Inc | Aryl aniline beta2 adrenergic receptor agonists |
| GB0204719D0 (en) | 2002-02-28 | 2002-04-17 | Glaxo Group Ltd | Medicinal compounds |
| ATE381535T1 (de) | 2002-04-25 | 2008-01-15 | Glaxo Group Ltd | Phenethanolaminderivate |
| JP2005527618A (ja) | 2002-05-28 | 2005-09-15 | セラヴァンス インコーポレーテッド | アルコキシアリールβ2アドレナリン作動性レセプターアゴニスト |
| GB0217225D0 (en) | 2002-07-25 | 2002-09-04 | Glaxo Group Ltd | Medicinal compounds |
| AR040962A1 (es) | 2002-08-09 | 2005-04-27 | Novartis Ag | Compuestos derivados de tiazol 1,3-2-ona, composicion farmaceutica y proceso de preparacion del compuesto |
| GB0220730D0 (en) | 2002-09-06 | 2002-10-16 | Glaxo Group Ltd | Medicinal compounds |
| DE10246374A1 (de) | 2002-10-04 | 2004-04-15 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Betamimetika mit verlängerter Wirkungsdauer, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel |
| EP1440966A1 (en) | 2003-01-10 | 2004-07-28 | Pfizer Limited | Indole derivatives useful for the treatment of diseases |
| ATE392206T1 (de) | 2002-10-11 | 2008-05-15 | Pfizer | Indolderivate als beta-2 agonisten |
| PL2019837T3 (pl) * | 2006-05-23 | 2011-09-30 | Irm Llc | Związki i kompozycje jako inhibitory proteazy aktywującej kanały |
| RU2419626C2 (ru) * | 2006-05-23 | 2011-05-27 | Айрм Ллк | Соединения и композиции в качестве ингибиторов протеазы, активирующей каналы |
-
2008
- 2008-01-04 EA EA200901082A patent/EA200901082A1/ru unknown
- 2008-01-04 MX MX2009008493A patent/MX2009008493A/es active IP Right Grant
- 2008-01-04 JP JP2009549148A patent/JP2010518097A/ja active Pending
- 2008-01-04 US US12/525,991 patent/US20100239551A1/en not_active Abandoned
- 2008-01-04 CA CA002677485A patent/CA2677485A1/en not_active Abandoned
- 2008-01-04 AU AU2008214214A patent/AU2008214214B2/en not_active Ceased
- 2008-01-04 CN CN200880004423A patent/CN101646437A/zh active Pending
- 2008-01-04 BR BRPI0806970-0A2A patent/BRPI0806970A2/pt not_active IP Right Cessation
- 2008-01-04 WO PCT/US2008/050289 patent/WO2008097673A1/en not_active Ceased
- 2008-01-04 EP EP08713564A patent/EP2117541A1/en not_active Withdrawn
- 2008-02-05 TW TW097104668A patent/TW200845982A/zh unknown
- 2008-02-08 PE PE2008000284A patent/PE20081753A1/es not_active Application Discontinuation
- 2008-02-08 AR ARP080100549A patent/AR065266A1/es unknown
- 2008-02-08 CL CL200800408A patent/CL2008000408A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2677485A1 (en) | 2008-08-14 |
| EP2117541A1 (en) | 2009-11-18 |
| AU2008214214A1 (en) | 2008-08-14 |
| TW200845982A (en) | 2008-12-01 |
| AR065266A1 (es) | 2009-05-27 |
| BRPI0806970A2 (pt) | 2014-04-08 |
| AU2008214214B2 (en) | 2011-09-15 |
| WO2008097673A1 (en) | 2008-08-14 |
| JP2010518097A (ja) | 2010-05-27 |
| CN101646437A (zh) | 2010-02-10 |
| EA200901082A1 (ru) | 2010-02-26 |
| CL2008000408A1 (es) | 2008-08-29 |
| US20100239551A1 (en) | 2010-09-23 |
| MX2009008493A (es) | 2009-08-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |