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MX2012008212A - Uso de un agente modificador de hormonas suprarrenales. - Google Patents

Uso de un agente modificador de hormonas suprarrenales.

Info

Publication number
MX2012008212A
MX2012008212A MX2012008212A MX2012008212A MX2012008212A MX 2012008212 A MX2012008212 A MX 2012008212A MX 2012008212 A MX2012008212 A MX 2012008212A MX 2012008212 A MX2012008212 A MX 2012008212A MX 2012008212 A MX2012008212 A MX 2012008212A
Authority
MX
Mexico
Prior art keywords
sub
hydrogen
aryl
modifying agent
halogen
Prior art date
Application number
MX2012008212A
Other languages
English (en)
Inventor
Erik Meredith
Lauren G Monovich
Julien Papillon
Qi-Ying Hu
Christoph Schumacher
Gary Ksander
Original Assignee
Novartis Ag
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=43735742&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MX2012008212(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of MX2012008212A publication Critical patent/MX2012008212A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • C07F9/6503Five-membered rings
    • C07F9/6506Five-membered rings having the nitrogen atoms in positions 1 and 3
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • A61K31/41881,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Endocrinology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Steroid Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La presente invención se refiere a un método para el tratamiento de una enfermedad o trastorno caracterizado por un aumento en los niveles de hormonas de estrés y/o por una disminución en los niveles de hormonas de andrógenos en un sujeto, el cual comprende administrar al sujeto, una cantidad terapéuticamente efectiva de un compuesto representado por la fórmula (I): (Ver Formula) en donde n es 1 ó 3; R es hidrógeno o --C(O)N(Ra)-(Rb), en donde Ra y Rb son independientemente --alquilo (de 1 a 4 átomos de carbono), o --alquilo (de 1 a 4 átomos de carbono)-arilo (de 5 a 7 átomos de carbono), en donde cada uno de Ra y Rb está opcionalmente sustituido por --alcoxilo (de 1 a 4 átomos de carbono); R1, R2, y R3, son independientemente hidrógeno, halógeno, ciano o --arilo (de 6 a 10 átomos de carbono), en donde este --arilo (de 6 a 10 átomos de carbono) está opcionalmente sustituido por halógeno, con la condición de que no más de uno de R1, R2, y R3 es hidrógeno; y R4 y R5 son hidrógeno; o de una sal farmacéuticamente aceptable del mismo.
MX2012008212A 2010-01-14 2011-01-13 Uso de un agente modificador de hormonas suprarrenales. MX2012008212A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US29498010P 2010-01-14 2010-01-14
PCT/US2011/021100 WO2011088188A1 (en) 2010-01-14 2011-01-13 Use of an adrenal hormone-modifying agent

Publications (1)

Publication Number Publication Date
MX2012008212A true MX2012008212A (es) 2012-08-03

Family

ID=43735742

Family Applications (2)

Application Number Title Priority Date Filing Date
MX2014011700A MX354022B (es) 2010-01-14 2011-01-13 Uso de un agente modificador de hormonas suprarrenales.
MX2012008212A MX2012008212A (es) 2010-01-14 2011-01-13 Uso de un agente modificador de hormonas suprarrenales.

Family Applications Before (1)

Application Number Title Priority Date Filing Date
MX2014011700A MX354022B (es) 2010-01-14 2011-01-13 Uso de un agente modificador de hormonas suprarrenales.

Country Status (34)

Country Link
US (2) US8609862B2 (es)
EP (2) EP2523731B1 (es)
JP (4) JP5602250B2 (es)
KR (1) KR101412206B1 (es)
CN (2) CN105440038A (es)
AU (1) AU2011205290C1 (es)
BR (1) BR112012017458B1 (es)
CA (1) CA2786443C (es)
CL (1) CL2012001961A1 (es)
CY (2) CY1121320T1 (es)
DK (1) DK2523731T3 (es)
ES (1) ES2707596T3 (es)
HR (1) HRP20190064T1 (es)
HU (2) HUE041967T2 (es)
IL (1) IL220804A0 (es)
LT (2) LT2523731T (es)
LU (1) LUC00159I2 (es)
MA (1) MA33904B1 (es)
ME (1) ME03371B (es)
MX (2) MX354022B (es)
NL (1) NL301043I2 (es)
NO (1) NO2020012I1 (es)
NZ (1) NZ601077A (es)
PH (1) PH12012501422B1 (es)
PL (1) PL2523731T3 (es)
PT (1) PT2523731T (es)
RS (1) RS58234B1 (es)
RU (1) RU2598708C2 (es)
SG (1) SG182393A1 (es)
SI (1) SI2523731T1 (es)
TN (1) TN2012000352A1 (es)
TR (1) TR201900515T4 (es)
WO (1) WO2011088188A1 (es)
ZA (1) ZA201205058B (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HRP20190064T1 (hr) * 2010-01-14 2019-03-08 Novartis Ag Uporaba sredstva za modifikaciju adrenalnog hormona
KR20130135820A (ko) 2010-06-16 2013-12-11 엠베라 뉴로 테라퓨틱스 인코포레이티드 중독,정신 장애 및 신경퇴행성 질환 치료용 조성물 및 방법
TWI518073B (zh) 2011-06-14 2016-01-21 美國禮來大藥廠 醛固酮合成酶抑制劑
WO2013043520A1 (en) 2011-09-22 2013-03-28 Merck Sharp & Dohme Corp. Triazolopyridyl compounds as aldosterone synthase inhibitors
US20140235667A1 (en) 2011-09-22 2014-08-21 Merck Sharp & Dohme Corp. Imidazopyridyl compounds as aldosterone synthase inhibitors
US9351973B2 (en) 2011-09-22 2016-05-31 Merck Sharp & Dohme Corp. Pyrazolopyridyl compounds as aldosterone synthase inhibitors
PE20142358A1 (es) * 2012-01-17 2015-01-30 Novartis Ag Nuevas formas y sales de un dihidropirrolo[1,2-c]imidazolilo, inhibidor de la aldosterona sintasa o aromatasa
IN2014DN09240A (es) 2012-04-12 2015-07-10 Novartis Ag
CA2886117C (en) 2012-10-05 2022-05-31 Merck Sharp & Dohme Corp. Indoline compounds and their use as aldosterone synthase inhibitors
JP2015093832A (ja) * 2013-11-08 2015-05-18 日本メジフィジックス株式会社 放射性ハロゲン標識化合物又はその塩、これを含む医薬
MX2016017315A (es) * 2014-07-07 2017-04-27 Novartis Ag Formas de dosificacion farmaceutica.
WO2016048984A1 (en) * 2014-09-25 2016-03-31 Cortendo Ab (Publ) Methods and compositions for the treatment of cushing's syndrome using 2s, 4r ketoconazole
AU2016210899B2 (en) * 2015-01-29 2019-03-07 Recordati Ag Process for the production of condensed imidazolo Derivatives
US20160287565A1 (en) 2015-04-06 2016-10-06 Millendo Therapeutics, Inc. Combination therapy for treating disorders associated with excess cortisol production
CA2990413A1 (en) * 2015-06-22 2016-12-29 Embera Neurotherapeutics, Inc. Compositions and methods for the treatment of substance use disorders, addiction, and psychiatric disorders
AU2018230521B2 (en) 2017-03-10 2022-02-03 Embera Neurotherapeutics, Inc. Pharmaceutical compositions and uses thereof

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4889861A (en) * 1982-12-21 1989-12-26 Ciba-Geigy Corp. Substituted imidazo[1,5-a]pyridine derivatives and other substituted bicyclic derivatives and their use as aromatase inhibitors
US4814333A (en) 1987-07-28 1989-03-21 The Trustees Of Dartmouth College Method for treatment of hypercortisolemic, depressed patients
US5503843A (en) 1994-04-22 1996-04-02 Flora Inc. Transdermal delivery of alpha adrenoceptor blocking agents
US5658881A (en) 1994-10-14 1997-08-19 Twk, Inc. Method for topical inhibition of the metabolic activity of cytochrome P450
DE19814087A1 (de) * 1998-03-30 1999-10-14 Lohmann Therapie Syst Lts Feuchtigkeitsaktivierbares therapeutisches System
US7417038B1 (en) 1998-10-15 2008-08-26 Imperial Innovations Limited Methods of treating cachexia
ES2275853T3 (es) 2001-02-16 2007-06-16 Aventis Pharmaceuticals Inc. Derivados heterociclicos de urea y su uso como ligandos de receptores de dopamina d3.
TWI263640B (en) 2001-12-19 2006-10-11 Bristol Myers Squibb Co Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
GB0212412D0 (en) * 2002-05-29 2002-07-10 Novartis Ag Combination of organic compounds
JP5138875B2 (ja) 2005-07-19 2013-02-06 株式会社デンソー センサ装置
GT200600381A (es) * 2005-08-25 2007-03-28 Compuestos organicos
AR056888A1 (es) 2005-12-09 2007-10-31 Speedel Experimenta Ag Derivados de heterociclil imidazol
CA2645678A1 (en) 2006-03-16 2007-09-20 Yeda Research And Development Co. Ltd. Method and composition for protecting neuronal tissue from damage induced by elevated glutamate levels
US20100240641A1 (en) * 2006-05-26 2010-09-23 Julien Papillon Aldosterone Synthase and/or 11B-hydroxylase Inhibitors
EP1886695A1 (en) 2006-06-27 2008-02-13 Speedel Experimenta AG Pharmaceutical combination of an aldosterone synthase inhibitor and a glucocorticoid receptor antagonist or a cortisol synthesis inhibitor or a corticotropin releasing factor antagonist
AU2007290695A1 (en) * 2006-08-25 2008-03-06 Novartis Ag Fused imidazole derivatives for the treatment of disorders mediated by aldosterone synthase and/or 11-beta-hydroxylase and/or aromatase
EP2121652A1 (en) * 2006-12-18 2009-11-25 Novartis AG 4-imidazolyl-1,2,3,4-tetrahydroquinoline derivatives and their use as aldosterone/11-beta-hydroxylase inhibitors
EP2095819A1 (en) * 2008-02-28 2009-09-02 Maastricht University N-benzyl imidazole derivatives and their use as aldosterone synthase inhibitors
AR072297A1 (es) 2008-06-27 2010-08-18 Novartis Ag Derivados de indol-2-il-piridin-3-ilo, composicion farmaceutica que los comprende y su uso en medicamentos para el tratamiento de enfermedades mediadas por la sintasa aldosterona.
HRP20190064T1 (hr) * 2010-01-14 2019-03-08 Novartis Ag Uporaba sredstva za modifikaciju adrenalnog hormona
PE20142358A1 (es) * 2012-01-17 2015-01-30 Novartis Ag Nuevas formas y sales de un dihidropirrolo[1,2-c]imidazolilo, inhibidor de la aldosterona sintasa o aromatasa
IN2014DN09240A (es) * 2012-04-12 2015-07-10 Novartis Ag

Also Published As

Publication number Publication date
US8609862B2 (en) 2013-12-17
NL301043I2 (nl) 2020-07-06
NO2020012I1 (no) 2020-06-09
AU2011205290C1 (en) 2014-11-06
US20140171392A1 (en) 2014-06-19
TN2012000352A1 (en) 2014-01-30
RS58234B1 (sr) 2019-03-29
US20120295888A1 (en) 2012-11-22
JP6181610B2 (ja) 2017-08-16
CA2786443A1 (en) 2011-07-21
EP2523731B1 (en) 2018-10-24
SI2523731T1 (sl) 2019-02-28
HUS2000018I1 (hu) 2020-07-28
CA2786443C (en) 2018-12-11
EP3527208A1 (en) 2019-08-21
DK2523731T3 (en) 2019-02-04
JP2018150326A (ja) 2018-09-27
PH12012501422B1 (en) 2018-09-12
LTPA2020512I1 (lt) 2020-07-27
CN105440038A (zh) 2016-03-30
AU2011205290A1 (en) 2012-08-02
LUC00159I1 (es) 2020-06-16
NZ601077A (en) 2014-07-25
MA33904B1 (fr) 2013-01-02
CY1121320T1 (el) 2020-05-29
PT2523731T (pt) 2019-01-21
CY2020018I1 (el) 2020-11-25
JP2013517280A (ja) 2013-05-16
JP2017002063A (ja) 2017-01-05
HUS000508I2 (hu) 2021-03-29
CN102711916B (zh) 2015-09-02
CY2020018I2 (el) 2020-11-25
KR101412206B1 (ko) 2014-06-25
IL220804A0 (en) 2012-08-30
JP2015013859A (ja) 2015-01-22
ME03371B (me) 2020-01-20
LT2523731T (lt) 2019-02-11
JP5602250B2 (ja) 2014-10-08
BR112012017458A2 (pt) 2017-12-19
JP6425688B2 (ja) 2018-11-21
ES2707596T3 (es) 2019-04-04
CL2012001961A1 (es) 2013-03-22
CN102711916A (zh) 2012-10-03
BR112012017458B1 (pt) 2020-10-20
NL301043I1 (nl) 2020-06-17
TR201900515T4 (tr) 2019-02-21
RU2012134510A (ru) 2014-02-20
MX354022B (es) 2018-02-08
LTC2523731I2 (lt) 2022-05-10
ZA201205058B (en) 2014-04-30
PL2523731T3 (pl) 2019-04-30
LUC00159I2 (es) 2021-07-06
HRP20190064T1 (hr) 2019-03-08
PH12012501422A1 (en) 2012-10-22
KR20120116482A (ko) 2012-10-22
HUE041967T2 (hu) 2019-06-28
WO2011088188A1 (en) 2011-07-21
AU2011205290B2 (en) 2014-06-26
EP2523731A1 (en) 2012-11-21
US9434754B2 (en) 2016-09-06
SG182393A1 (en) 2012-08-30
RU2598708C2 (ru) 2016-09-27

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