NO20090135L - Polymorfer av N-hydroksy-3-[4-[[[-(2-metyl-1H-indol-3-yl)etyl]amino]metyl]fenyl]2E-2-propenamid - Google Patents

Polymorfer av N-hydroksy-3-[4-[[[-(2-metyl-1H-indol-3-yl)etyl]amino]metyl]fenyl]2E-2-propenamid

Info

Publication number
NO20090135L
NO20090135L NO20090135A NO20090135A NO20090135L NO 20090135 L NO20090135 L NO 20090135L NO 20090135 A NO20090135 A NO 20090135A NO 20090135 A NO20090135 A NO 20090135A NO 20090135 L NO20090135 L NO 20090135L
Authority
NO
Norway
Prior art keywords
methyl
indol
hydroxy
phenyl
ethyl
Prior art date
Application number
NO20090135A
Other languages
English (en)
Norwegian (no)
Inventor
Joel Slade
Piotr Karpinski
Dimitris Papoutsakis
Joginder S Bajwa
Frank Stowasser
Murat Acemoglu
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=38832679&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO20090135(L) "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 NO20090135L publication Critical patent/NO20090135L/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/20—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
    • C07D209/16—Tryptamines
    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
    • C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D209/20—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals substituted additionally by nitrogen atoms, e.g. tryptophane

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Indole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Epidemiology (AREA)
NO20090135A 2006-06-12 2009-01-09 Polymorfer av N-hydroksy-3-[4-[[[-(2-metyl-1H-indol-3-yl)etyl]amino]metyl]fenyl]2E-2-propenamid NO20090135L (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US80451706P 2006-06-12 2006-06-12
US88322407P 2007-01-03 2007-01-03
PCT/US2007/070561 WO2007146716A2 (fr) 2006-06-12 2007-06-07 Polymorphes de n-hydroxy-3-[4-[[[2-(2-méthyl-1h-indol-3-yl)éthyl]amino]méthyl]phényl]-2e-2-propénamide

Publications (1)

Publication Number Publication Date
NO20090135L true NO20090135L (no) 2009-03-12

Family

ID=38832679

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20090135A NO20090135L (no) 2006-06-12 2009-01-09 Polymorfer av N-hydroksy-3-[4-[[[-(2-metyl-1H-indol-3-yl)etyl]amino]metyl]fenyl]2E-2-propenamid

Country Status (29)

Country Link
US (1) US7989494B2 (fr)
EP (2) EP2086930A2 (fr)
JP (3) JP2009540006A (fr)
KR (4) KR20140142335A (fr)
CN (1) CN102584673B (fr)
AR (1) AR061297A1 (fr)
AU (1) AU2007257881B2 (fr)
BR (1) BRPI0712993A2 (fr)
CA (1) CA2650263A1 (fr)
CL (1) CL2007001689A1 (fr)
CR (1) CR10440A (fr)
EA (1) EA017984B1 (fr)
EC (1) ECSP088976A (fr)
GE (1) GEP20115175B (fr)
GT (1) GT200800280A (fr)
IL (1) IL195015A (fr)
MA (1) MA30511B1 (fr)
ME (1) ME00529B (fr)
MX (1) MX2008015900A (fr)
MY (1) MY149337A (fr)
NI (1) NI200800306A (fr)
NO (1) NO20090135L (fr)
PE (1) PE20080852A1 (fr)
PH (2) PH12012501724A1 (fr)
SM (1) SMP200900001B (fr)
TN (1) TNSN08495A1 (fr)
TW (2) TWI453196B (fr)
UY (1) UY30406A1 (fr)
WO (1) WO2007146716A2 (fr)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GEP20105125B (en) * 2006-06-12 2010-11-25 Novartis Ag Salts of n-hydroxy-3-[4-[[[2-(2-methyl-1h-indol-3-yl) ethyl] amino] methyl] phenyl]-2e-2-propenamide
EP2117598A2 (fr) * 2007-01-10 2009-11-18 Novartis AG Formulations d'inhibiteurs de la déacétylase
WO2017032281A1 (fr) * 2015-08-21 2017-03-02 苏州晶云药物科技有限公司 Nouvelles formes cristallines de lactate de panobinostat
CN106866491B (zh) * 2015-12-10 2021-12-10 江苏豪森药业集团有限公司 帕比司他乳酸盐晶型ⅰ及其制备方法和用途
CN106866492B (zh) * 2015-12-10 2021-11-26 江苏豪森药业集团有限公司 帕比司他乳酸盐晶型ii及其制备方法和用途
WO2018092151A1 (fr) * 2016-11-21 2018-05-24 Msn Laboratories Private Limited, R&D Center Procédé de préparation de l'acide 2- (e)-n-hydroxy-3-[4- [[ [2- (2-méthyl -1 h-indol-3-yl) éthyl] amino] méthyl] phényl]-2-propénamide 2-hydroxypropanoïque (1 : 1) et ses polymorphes
WO2018163114A1 (fr) * 2017-03-10 2018-09-13 Shilpa Medicare Limited Panobinostat amorphe et son sel de lactate
US10537585B2 (en) 2017-12-18 2020-01-21 Dexcel Pharma Technologies Ltd. Compositions comprising dexamethasone
CN114302873A (zh) * 2019-08-20 2022-04-08 小野药品工业株式会社 具有s1p5受体激动活性的化合物的盐和晶形
GB201913122D0 (en) 2019-09-11 2019-10-23 Seald As Compositions and methods for treatment of cholangiocarcinoma
GB201913124D0 (en) 2019-09-11 2019-10-23 Seald As Compositions and methods for treatment of cholangiocarcinoma
GB201913121D0 (en) 2019-09-11 2019-10-23 Seald As Compositions and methods for treatment of cholangiocarcinoma
TW202233595A (zh) * 2020-10-28 2022-09-01 美商維拉克塔股份有限公司 Ｈｄａｃ抑制劑固態形式

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20020354A1 (es) * 2000-09-01 2002-06-12 Novartis Ag Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda)
ATE352319T1 (de) 2001-11-06 2007-02-15 Novartis Pharma Gmbh Kombination cyclooxygenase-2 inhibitor/ histone deacetylase inhibitor
JP2005511062A (ja) 2001-12-07 2005-04-28 ノバルティス アクチエンゲゼルシャフト タンパク質脱アセチル化酵素阻害剤についての生物マーカーとしてのアルファ−チューブリンアセチル化レベルの使用
WO2004103358A2 (fr) 2003-05-21 2004-12-02 Novartis Ag Combinaison d'inhibiteurs d'histone deacetylase avec des agents chimiotherapeutiques
US20060270730A1 (en) 2003-08-07 2006-11-30 Andreas Katopodis Histone deacetylase inhibitors as immunosuppressants
EP1682181A2 (fr) 2003-09-23 2006-07-26 Novartis AG Polytherapie combinant un inhibiteur des recepteurs du facteur vegf avec un agent chimiotherapeutique
GEP20105125B (en) 2006-06-12 2010-11-25 Novartis Ag Salts of n-hydroxy-3-[4-[[[2-(2-methyl-1h-indol-3-yl) ethyl] amino] methyl] phenyl]-2e-2-propenamide

Also Published As

Publication number Publication date
AR061297A1 (es) 2008-08-20
JP2015164968A (ja) 2015-09-17
PE20080852A1 (es) 2008-08-19
EP2086930A2 (fr) 2009-08-12
IL195015A0 (en) 2009-08-03
JP2013139476A (ja) 2013-07-18
KR20160032264A (ko) 2016-03-23
CL2007001689A1 (es) 2008-05-16
TW200815344A (en) 2008-04-01
UY30406A1 (es) 2008-01-31
EP2409967A1 (fr) 2012-01-25
TNSN08495A1 (en) 2010-04-14
TWI515179B (zh) 2016-01-01
CN102584673B (zh) 2014-08-06
TW201441190A (zh) 2014-11-01
BRPI0712993A2 (pt) 2012-04-17
CR10440A (es) 2011-08-22
CN102584673A (zh) 2012-07-18
TWI453196B (zh) 2014-09-21
CA2650263A1 (fr) 2007-12-21
AU2007257881A1 (en) 2007-12-21
AU2007257881B2 (en) 2011-06-16
KR20140142335A (ko) 2014-12-11
EA017984B1 (ru) 2013-04-30
US7989494B2 (en) 2011-08-02
GEP20115175B (en) 2011-03-10
SMAP200900001A (it) 2009-01-14
SMP200900001B (it) 2010-03-01
PH12012501724A1 (en) 2014-05-12
KR20090015968A (ko) 2009-02-12
NI200800306A (es) 2012-02-01
ME00529B (fr) 2011-10-10
WO2007146716A3 (fr) 2009-07-30
JP2009540006A (ja) 2009-11-19
PH12012501725A1 (en) 2015-07-06
MX2008015900A (es) 2009-03-06
MY149337A (en) 2013-08-30
GT200800280A (es) 2015-11-24
WO2007146716A2 (fr) 2007-12-21
MA30511B1 (fr) 2009-06-01
KR20150082690A (ko) 2015-07-15
IL195015A (en) 2014-03-31
EA200802383A1 (ru) 2010-02-26
ECSP088976A (es) 2009-01-30
US20090192210A1 (en) 2009-07-30

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Legal Events

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FC2A Withdrawal, rejection or dismissal of laid open patent application