GT200400020A - USEFUL TRIAZOL COMPOUNDS IN THERAPY - Google Patents

USEFUL TRIAZOL COMPOUNDS IN THERAPY

Info

Publication number
GT200400020A
GT200400020A GT200400020A GT200400020A GT200400020A GT 200400020 A GT200400020 A GT 200400020A GT 200400020 A GT200400020 A GT 200400020A GT 200400020 A GT200400020 A GT 200400020A GT 200400020 A GT200400020 A GT 200400020A
Authority
GT
Guatemala
Prior art keywords
useful
therapy
compounds
triazol compounds
triazol
Prior art date
Application number
GT200400020A
Other languages
Spanish (es)
Inventor
Justin Stephen Bryans
Patrick Stephen Johns
Thomas Ryckmans
Alan Stobie
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 filed Critical
Publication of GT200400020A publication Critical patent/GT200400020A/en

Links

Classifications

    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • 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
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

Abstract

LA PRESENTE INVENCION SE REFIERE A COMPUESTOS DE FORMULA GENERAL I EN LA QUE A,B,X,Y,Z,W,V, SON GRUPOS FUNCIONALES DESCRITOS EN EL EXPEDIENTE. POR SUS CARACTERISTICAS ESPECIALES, ESTOS COMPUESTOS SON DE UTILIDAD EN UNA AMPLIA VARIEDAD DE PATOLOGIAS TALES COMO ANSIEDAD, ANOREXIA NERVIOSA, HIPERTENSION, EDEMA, ENTRE OTRAS MUCHAS DESCRITAS EN LA INVENCION.THE PRESENT INVENTION REFERS TO COMPOUNDS OF GENERAL FORMULA I IN WHICH A, B, X, Y, Z, W, V, ARE FUNCTIONAL GROUPS DESCRIBED IN THE RECORD. BY THEIR SPECIAL CHARACTERISTICS, THESE COMPOUNDS ARE USEFUL IN A WIDE VARIETY OF SUCH PATHOLOGIES AS ANXIETY, NERVOUS ANOREXY, HYPERTENSION, EDEMA, BETWEEN MANY DESCRIBED IN THE INVENTION.

GT200400020A 2003-02-19 2004-02-18 USEFUL TRIAZOL COMPOUNDS IN THERAPY GT200400020A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0303852.8A GB0303852D0 (en) 2003-02-19 2003-02-19 Triazole compounds useful in therapy

Publications (1)

Publication Number Publication Date
GT200400020A true GT200400020A (en) 2004-09-21

Family

ID=9953327

Family Applications (1)

Application Number Title Priority Date Filing Date
GT200400020A GT200400020A (en) 2003-02-19 2004-02-18 USEFUL TRIAZOL COMPOUNDS IN THERAPY

Country Status (11)

Country Link
CN (1) CN1751047A (en)
AR (1) AR043210A1 (en)
CL (1) CL2004000293A1 (en)
GB (1) GB0303852D0 (en)
GT (1) GT200400020A (en)
NL (1) NL1025527C2 (en)
PA (1) PA8596101A1 (en)
PE (1) PE20050222A1 (en)
TW (1) TW200500367A (en)
UY (1) UY28201A1 (en)
WO (1) WO2004074291A1 (en)

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DE102004001871A1 (en) * 2004-01-14 2005-09-01 Bayer Healthcare Ag Tricyclic benzazepine derivatives and their use
US7456170B2 (en) 2004-08-25 2008-11-25 Pfizer Inc. Triazolobenzodiazepines and their use as vasopressin antagonists
WO2006114706A1 (en) * 2005-04-26 2006-11-02 Pfizer Limited Triazole derivatives as vasopressin antagonists
KR101348499B1 (en) 2008-11-13 2014-01-06 에프. 호프만-라 로슈 아게 Spiro-5,6-dihydro-4h-2,3,5,10b-tetraaza-benzo[e]azulenes
PL2358714T3 (en) 2008-11-18 2012-12-31 Hoffmann La Roche Alkylcyclohexylethers of dihydrotetraazabenzoazulenes
UA103504C2 (en) 2008-11-28 2013-10-25 Ф. Хоффманн-Ля Рош Аг Arylcyclohexylethers of dihydrotetraazabenzoazulenes for use as vasopressin via receptor antagonists
CA2756871A1 (en) 2009-03-31 2010-10-07 Arqule, Inc. Substituted heterocyclic compounds
CA2779088A1 (en) * 2009-11-16 2011-05-19 Mellitech [1,5]-diazocin derivatives
US8420633B2 (en) * 2010-03-31 2013-04-16 Hoffmann-La Roche Inc. Aryl-cyclohexyl-tetraazabenzo[e]azulenes
US8461151B2 (en) * 2010-04-13 2013-06-11 Hoffmann-La Roche Inc. Aryl-/heteroaryl-cyclohexenyl-tetraazabenzo[e]azulenes
US8492376B2 (en) 2010-04-21 2013-07-23 Hoffmann-La Roche Inc. Heteroaryl-cyclohexyl-tetraazabenzo[e]azulenes
US8481528B2 (en) * 2010-04-26 2013-07-09 Hoffmann-La Roche Inc. Heterobiaryl-cyclohexyl-tetraazabenzo[e]azulenes
US8513238B2 (en) * 2010-05-10 2013-08-20 Hoffmann-La Roche Inc. Heteroaryl-cyclohexyl-tetraazabenzo[E]azulenes
US9006450B2 (en) * 2010-07-01 2015-04-14 Boehringer Ingelheim International Gmbh Compounds, pharmaceutical compositions and uses thereof
AR083313A1 (en) 2010-10-07 2013-02-13 Takeda Pharmaceutical DERIVATIVES OF 1,4-OXAZEPAN USEFUL AS INHIBITORS OF THE RECOVERY OF SUPERIOR MONOAMINE
RU2011122942A (en) 2011-06-08 2012-12-20 Общество С Ограниченной Ответственностью "Асинэкс Медхим" NEW KINAZ INHIBITORS
US8828989B2 (en) * 2011-09-26 2014-09-09 Hoffmann-La Roche Inc. Oxy-cyclohexyl-4H,6H-5-oxa-2,3,10b-triaza-benzo[E]azulenes as V1A antagonists
RU2014117471A (en) * 2011-10-05 2015-11-10 Ф. Хоффманн-Ля Рош Аг CYCLOGEXYL-4H, 6H-5-OXA-2,3,10B-TRIAZABENZO [e] ASULENES AS V1A RECEPTOR ANTAGONISTS
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CN102766674A (en) * 2012-07-25 2012-11-07 辉源生物科技（上海）有限公司 Establishment of screening platform for cynomolgus monkey antidiuretic hormone receptor V1A antagonist
IN2015DN00960A (en) 2012-09-25 2015-06-12 Hoffmann La Roche
AR095079A1 (en) 2013-03-12 2015-09-16 Hoffmann La Roche DERIVATIVES OF OCTAHIDRO-PIRROLO [3,4-C] -PIRROL AND PIRIDINA-FENILO
CN105492010B (en) * 2013-08-19 2020-01-03 豪夫迈·罗氏有限公司 V1a antagonists for the treatment of phase shift sleep disorders
PL3074400T3 (en) 2013-11-26 2018-03-30 F.Hoffmann-La Roche Ag Octahydro-cyclobuta [1,2-c;3,4-c']dipyrrole derivatives as autotaxin inhibitors
CA3142754C (en) 2013-12-05 2024-01-02 F. Hoffmann-La Roche Ag Synthesis of trans-8-chloro-5-methyl- 1-[4-(pyridin-2-yloxy)-cyclohexyl]-5,6-dihydro-4h-2,3,5,10b-tetraaza-benzo[e]azulene and crystalline forms thereof
MA50635A (en) 2014-03-26 2020-08-12 Hoffmann La Roche NEW BICYCLIC COMPOUNDS AS INHIBITORS OF AUTOTAXIN (ATX) AND LYSOPHOSPHATIDIC ACID PRODUCTION
UA119347C2 (en) 2014-03-26 2019-06-10 Ф. Хоффманн-Ля Рош Аг Condensed [1,4]diazepine compounds as autotaxin (atx) and lysophosphatidic acid (lpa) production inhibitors
MA41898A (en) 2015-04-10 2018-02-13 Hoffmann La Roche BICYCLIC QUINAZOLINONE DERIVATIVES
PE20180479A1 (en) 2015-09-04 2018-03-07 Hoffmann La Roche NEW DERIVATIVES OF PHENOXYMETHYL
RU2724899C2 (en) 2015-09-24 2020-06-26 Ф. Хоффманн-Ля Рош Аг New bicyclic compounds as dual inhibitors of atx/ca
CA2983782A1 (en) 2015-09-24 2017-03-30 F. Hoffmann-La Roche Ag Bicyclic compounds as atx inhibitors
CA2991615A1 (en) 2015-09-24 2017-03-30 F. Hoffmann-La Roche Ag Bicyclic compounds as atx inhibitors
CA2984585A1 (en) 2015-09-24 2017-03-30 F. Hoffmann-La Roche Ag New bicyclic compounds as dual atx/ca inhibitors
JP7090099B2 (en) 2017-03-16 2022-06-23 エフ．ホフマン－ラ ロシュ アーゲー A novel bicyclic compound as an ATX inhibitor
CN110392679B (en) 2017-03-16 2023-04-07 豪夫迈·罗氏有限公司 Heterocyclic compounds useful as dual ATX/CA inhibitors
EP3634963B8 (en) 2017-06-05 2023-03-29 Blackthorn Therapeutics, Inc. 1-(2-azaspiro[3.3]heptan-6-yl)-5,6-dihydro-4h-benzo[f][1,2,4]triazolo[4,3-a][1,4]diazepine derivatives as v1a receptor antagonists for treating neuropsychological disorders
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Also Published As

Publication number Publication date
CN1751047A (en) 2006-03-22
PE20050222A1 (en) 2005-04-13
GB0303852D0 (en) 2003-03-26
AR043210A1 (en) 2005-07-20
PA8596101A1 (en) 2005-08-04
UY28201A1 (en) 2004-09-30
TW200500367A (en) 2005-01-01
NL1025527C2 (en) 2005-03-14
WO2004074291A1 (en) 2004-09-02
CL2004000293A1 (en) 2005-01-07
NL1025527A1 (en) 2004-08-23

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