MX2009006730A - Derivados de n-(5, 6, 7, 8-tetrahidronaftalen-1-il) urea y compuestos relacionados como antagonistas de receptor vaniloide trpv1 par el tratamiento de dolor. - Google Patents

Derivados de n-(5, 6, 7, 8-tetrahidronaftalen-1-il) urea y compuestos relacionados como antagonistas de receptor vaniloide trpv1 par el tratamiento de dolor.

Info

Publication number
MX2009006730A
MX2009006730A MX2009006730A MX2009006730A MX2009006730A MX 2009006730 A MX2009006730 A MX 2009006730A MX 2009006730 A MX2009006730 A MX 2009006730A MX 2009006730 A MX2009006730 A MX 2009006730A MX 2009006730 A MX2009006730 A MX 2009006730A
Authority
MX
Mexico
Prior art keywords
antagonists
trpv1 receptor
trpv1
antagonictc
exacerbated
Prior art date
Application number
MX2009006730A
Other languages
English (en)
Inventor
Erol K Bayburt
Chih-Hung Lee
Robert G Schmidt
Arthur R Gomtsyan
Jerome F Daanen
Steven P Latshaw
Original Assignee
Abbott Lab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Abbott Lab filed Critical Abbott Lab
Publication of MX2009006730A publication Critical patent/MX2009006730A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C275/32Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/10Drugs for disorders of the urinary system of the bladder
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/12Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/38Nitrogen atoms
    • C07D215/42Nitrogen atoms attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D215/54Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic 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
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic 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
    • C07D311/74Benzo[b]pyrans, hydrogenated in the carbocyclic ring

Abstract

La presente solicitud se dirige a compuestos que son antagonistas TRPV1 y que tienen la fórmula: (I); en donde las variables Ar1, L1, R1, R2, R3, R4, R5, Y1, Y2 y Y3 son tal como se definen en la descripción, las cuales son útiles para tratar transtornos originados o exacerbados por la actividad de receptor vaniloide.
MX2009006730A 2006-12-20 2007-12-12 Derivados de n-(5, 6, 7, 8-tetrahidronaftalen-1-il) urea y compuestos relacionados como antagonistas de receptor vaniloide trpv1 par el tratamiento de dolor. MX2009006730A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US87589006P 2006-12-20 2006-12-20
PCT/US2007/087163 WO2008079683A2 (en) 2006-12-20 2007-12-12 N- (5, 6, 7, 8-tetrahydronaphthalen-1-yl) urea derivatives and related compounds as trpv1 vanilloid receptor antagonists for the treatment of pain

Publications (1)

Publication Number Publication Date
MX2009006730A true MX2009006730A (es) 2009-06-30

Family

ID=39102978

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009006730A MX2009006730A (es) 2006-12-20 2007-12-12 Derivados de n-(5, 6, 7, 8-tetrahidronaftalen-1-il) urea y compuestos relacionados como antagonistas de receptor vaniloide trpv1 par el tratamiento de dolor.

Country Status (7)

Country Link
US (3) US8030504B2 (es)
EP (2) EP2134678A2 (es)
JP (1) JP2010513557A (es)
CN (1) CN101563318A (es)
CA (1) CA2672196A1 (es)
MX (1) MX2009006730A (es)
WO (1) WO2008079683A2 (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009037707A2 (en) 2007-09-20 2009-03-26 Ramot At Tel Aviv University Ltd. N-phenyl anthranilic acid derivatives and uses thereof
WO2010023512A1 (en) * 2008-08-28 2010-03-04 Matrix Laboratories Ltd. Novel vanilloid receptor modulators, process for their preparation and pharmaceutical compositions containing them
WO2010045402A1 (en) * 2008-10-17 2010-04-22 Abbott Laboratories Trpv1 antagonists
TW201020236A (en) * 2008-10-17 2010-06-01 Abbott Lab TRPV1 antagonists
US9012651B2 (en) 2011-03-24 2015-04-21 Abbvie Inc. TRPV3 modulators
WO2012134943A1 (en) * 2011-03-25 2012-10-04 Abbott Laboratories Trpv1 antagonists
US8969325B2 (en) 2011-12-19 2015-03-03 Abbvie Inc. TRPV1 antagonists
US8859584B2 (en) 2011-12-19 2014-10-14 Abbvie, Inc. TRPV1 antagonists
US8796328B2 (en) 2012-06-20 2014-08-05 Abbvie Inc. TRPV1 antagonists
EP2700431A1 (en) 2012-08-24 2014-02-26 AnalytiCon Discovery GmbH Plant extracts for modulating TRPV1 function
US11849727B2 (en) 2013-11-13 2023-12-26 Bedoukian Research, Inc. Synergistic formulations for control and repellency of biting arthropods
JP7441042B2 (ja) 2016-12-02 2024-02-29 シムライズ アーゲー 化粧品ブレンド
EP3401307A1 (en) * 2017-05-11 2018-11-14 Antalgenics, S.L. Trpv1 modulator compounds
CN111548313A (zh) * 2019-02-11 2020-08-18 绍兴从零医药科技有限公司 预防和治疗慢性疼痛药物的胍类化合物

Family Cites Families (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1344579A (fr) 1961-11-23 1963-11-29 Sandoz Sa Nouveaux dérivés de l'indole et leur préparation
US3647819A (en) * 1969-09-19 1972-03-07 Sterling Drug Inc Indazolylphenylureas and indazolyl-phenylthioureas
US3647910A (en) * 1970-03-20 1972-03-07 Standard Oil Co Ohio Dehydrogenation of hydrocarbons employing a catalyst of iron oxide-containing activated carbon
US3711610A (en) * 1971-06-01 1973-01-16 Sterling Drug Inc Anticoccidiosis method and compositions involving indazolylphenylureas and indazolylphenylthioureas
US3814711A (en) * 1971-07-26 1974-06-04 Mallinckrodt Chemical Works 10-acetamido-s-triazolo-(3,4-a)-isoquinolines
NL7902993A (nl) 1978-04-24 1979-10-26 Rhone Poulenc Ind Nieuwe isochinolinederivaten, de bereiding ervan en farmaceutische preparaten, die de nieuwe isochinoline- derivaten bevatten.
DE3586123D1 (de) * 1984-08-15 1992-07-02 Schering Ag Neue dopamin-derivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel.
MX22406A (es) 1989-09-15 1994-01-31 Pfizer Nuevos derivados de n-aril y n-heteroarilamidas y urea como inhibidores de acil coenzima a: acil transferasa del colesterol (acat).
EP0518961A1 (fr) 1990-03-07 1992-12-23 Aventis Pharma S.A. Derives de glycinamide, leur preparation et les medicaments les contenant
JPH04178363A (ja) * 1990-11-13 1992-06-25 Tosoh Corp 尿素誘導体及びそれを含有する有害生物防除剤
JPH04178362A (ja) 1990-11-13 1992-06-25 Tosoh Corp 尿素誘導体およびそれを含有する有害生物防除剤
US5362878A (en) 1991-03-21 1994-11-08 Pfizer Inc. Intermediates for making N-aryl and N-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme A: cholesterol acyl transferase (ACAT)
US5444038A (en) * 1992-03-09 1995-08-22 Zeneca Limited Arylindazoles and their use as herbicides
EP0642498A1 (en) * 1992-05-28 1995-03-15 Pfizer Inc. NEW $i(N)-ARYL AND $i(N)-HETEROARYLUREA DERIVATIVES AS INHIBITORS OF ACYL COENZYME A:CHOLESTEROL ACYL TRANSFERASE (ACAT)
US5374643A (en) 1992-09-11 1994-12-20 E. R. Squibb & Sons, Inc. Aryl urea (thiourea) and cyanoguanidine derivatives
CA2107196A1 (en) * 1992-09-29 1994-03-30 Mitsubishi Chemical Corporation Carboxamide derivatives
FI98337C (fi) * 1992-11-30 1997-06-10 Risto Juhani Ilmoniemi Menetelmä ja laite aivojen herätevasteiden ja spontaanitoiminnan sekä sydämestä mitattujen signaalien eri komponenttien erottelemiseksi toisistaan
GB9307833D0 (en) * 1993-04-15 1993-06-02 Glaxo Inc Modulators of cholecystokinin and gastrin
CN1209803A (zh) 1996-01-16 1999-03-03 布里斯托尔-迈尔斯斯奎布公司 微粒体甘油三酯转移蛋白的构象限制性芳族抑制剂及方法
US5760246A (en) * 1996-12-17 1998-06-02 Biller; Scott A. Conformationally restricted aromatic inhibitors of microsomal triglyceride transfer protein and method
WO1998050347A1 (en) 1997-05-05 1998-11-12 The Regents Of The University Of California Naphthols useful in antiviral methods
AU2804400A (en) * 1999-02-12 2000-08-29 Smithkline Beecham Plc Phenyl urea and phenyl thiourea derivatives as orexin receptor antagonists
JP3727851B2 (ja) 1999-02-22 2005-12-21 アモレパシフィック コーポレーション 強力なバニロイド受容体アゴニストおよび鎮痛剤としてのレジニフェラトキシンファーマコフォアを含むバニロイド同類体、その組成物およびその用途
DE60023128T2 (de) * 1999-05-12 2006-07-06 Ortho-Mcneil Pharmaceutical, Inc. Pyrazolcarboxamide zur behandlung von fettleibigkeit und anderen erkrankungen
US6858577B1 (en) * 1999-06-29 2005-02-22 Ortho-Mcneil Pharmaceutical, Inc. Indole peptidomimetics as thrombin receptor antagonists
YU54202A (sh) * 2000-01-18 2006-01-16 Agouron Pharmaceuticals Inc. Jedinjenja indazola, farmaceutske smeše i postupci za stimulisanje i inhibiranje ćelijske proliferacije
US7217722B2 (en) 2000-02-01 2007-05-15 Kirin Beer Kabushiki Kaisha Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same
US6723730B2 (en) 2000-07-20 2004-04-20 Neurogen Corporation Capsaicin receptor ligands
EP1403255A4 (en) 2001-06-12 2005-04-06 Sumitomo Pharma INHIBITORS OF RHO KINASE
US20040259875A1 (en) 2001-07-31 2004-12-23 Takeshi Yura Amine derivatives
PE20030417A1 (es) 2001-09-13 2003-08-06 Smithkline Beecham Plc Derivados de urea como antagonistas del receptor vainilloide
JP4178362B2 (ja) 2001-09-27 2008-11-12 株式会社三洋物産 遊技機
SE0104248D0 (sv) * 2001-12-14 2001-12-14 Astrazeneca Ab Method of treatment
SE0104250D0 (sv) * 2001-12-14 2001-12-14 Astrazeneca Ab Heterocyclic compounds
DE10163439A1 (de) 2001-12-21 2003-07-10 Bosch Gmbh Robert Koffer, insbesondere Werkzeugmaschinenkoffer
CA2469967A1 (en) 2001-12-26 2003-07-10 Bayer Healthcare Ag Urea derivatives as vr1- antagonists
JP2003192587A (ja) * 2001-12-26 2003-07-09 Bayer Ag 尿素誘導体
ES2319886T3 (es) 2002-02-20 2009-05-14 Abbott Laboratories Compuestos azabiciclicos condensados que inhiben el sutipo 1 del receptor valinoide (vr1).
GB0206876D0 (en) 2002-03-22 2002-05-01 Merck Sharp & Dohme Therapeutic agents
NZ536418A (en) * 2002-05-08 2006-04-28 Bayer Healthcare Ag Hydroxy tetrahydro-naphthalenylurea derivatives having vanilloid receptor (VR) antagonistic activity
CA2486092A1 (en) 2002-05-17 2003-11-27 Janssen Pharmaceutica N.V. Aminotetralin-derived urea modulators of vanilloid vr1 receptor
US7035841B2 (en) * 2002-07-18 2006-04-25 Xerox Corporation Method for automatic wrapper repair
DE60315704T2 (de) * 2002-12-06 2008-06-05 Xention Ltd. Iconix Park Tetrahydronaphalin-derivate
US7544716B2 (en) * 2002-12-09 2009-06-09 Xention Limited Tetrahydro-naphthalene derivatives as vanilloid receptor antagonists
US6933311B2 (en) * 2003-02-11 2005-08-23 Abbott Laboratories Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor
EP1493438A1 (en) * 2003-07-03 2005-01-05 Bayer HealthCare AG Vanilloid receptor (VR) inhibitors for treatment of Human Immunodeficiency Virus (HIV)-mediated pain states
US20080045546A1 (en) * 2003-10-15 2008-02-21 Axel Bouchon Tetradydro-Naphthalene And Urea Derivatives
EP2527339A1 (en) * 2004-11-24 2012-11-28 Abbott Laboratories Chromanylurea compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor and uses thereof
CA2599778A1 (en) * 2005-03-05 2006-09-14 Bayer Healthcare Ag Use of hydroxy tetrahydro-naphtalene derivates for the treatment of respiratory diseases

Also Published As

Publication number Publication date
CA2672196A1 (en) 2008-07-03
WO2008079683A3 (en) 2008-08-28
US20080153871A1 (en) 2008-06-26
US8030504B2 (en) 2011-10-04
US20130165479A1 (en) 2013-06-27
JP2010513557A (ja) 2010-04-30
EP2450346A1 (en) 2012-05-09
US20120022103A1 (en) 2012-01-26
EP2134678A2 (en) 2009-12-23
WO2008079683A2 (en) 2008-07-03
CN101563318A (zh) 2009-10-21
US8350083B2 (en) 2013-01-08

Similar Documents

Publication Publication Date Title
MX2009006730A (es) Derivados de n-(5, 6, 7, 8-tetrahidronaftalen-1-il) urea y compuestos relacionados como antagonistas de receptor vaniloide trpv1 par el tratamiento de dolor.
MX2009011205A (es) Derivados de 2-iminoisotiazol como ligandos del receptor canabinoide.
EP1861399A4 (en) CGRP RECEPTOR ANTAGONISTS
IL182317A0 (en) Cgrp receptor antagonists
EP1804919A4 (en) CGRP RECEPTOR ANTAGONISTS
DE602008005771D1 (de) Disubstituierte alkyl-8-azabicycloä3.2.1üoktan-verbindungen als mu-opioid-rezeptorantagonisten
TW200716584A (en) Dihydrobenzofuran derivatives and uses thereof
MX2007011023A (es) 2-(4-oxo-4h-quinazolin-3-il) acetamidas y su uso como antagonistas de vasopresin v3.
JO2910B1 (en) Organic compounds
MXPA06014721A (es) Derivados de alquinilo como moduladores de los receptores de glutamato metabotropico.
IL187208A0 (en) Antagonists of the vanilloid receptor subtype 1 (vr1) and uses thereof
UA83311C2 (en) 3-aminocyclopentanecarboxamides as modulators of chemokine receptors
ATE553093T1 (de) Indazolderivate zur hemmung von trpv1 und verwendungen davon
MX2009012374A (es) Compuestos novedosos como ligandos del receptor de canabinoides.
MX2010004498A (es) Derivados de ciclohexenoamida y su uso como antagonistas de trpv1.
RS20080246A (en) 3-aminocyclopentanecarboxamides as modulators of chemokine receptors
WO2008063781A3 (en) Chemical compounds as cannabinoid receptor ligands
TW200800958A (en) N-substituted-azacyclylamines as histamine-3 antagonists
MX2009003645A (es) Azaciclilaminas n-sustituidas como antagonistas de histamina-3.
MX2010001486A (es) Derivados de tetrahidropiridin carboxamida como antagonistas de trpvl.
MX2008002805A (es) Derivados de carboxamida como antagonistas del receptor muscarinico.
GB0513886D0 (en) Novel compounds
EP1802372A4 (en) CGRP RECEPTOR ANTAGONISTS)
MX2010004495A (es) Derivados de 2-aminooxazol como antagonistas de vanilloide-1 de receptor potencial transitorio (trpv1) utiles para tratar dolor.
MY149973A (en) 3-carboxypropyl-aminotetralin derivatives as mu opioid receptor antagonists

Legal Events

Date Code Title Description
FG Grant or registration
GB Transfer or rights