MA37650A1 - Forme amorphe d'un composé pyrimidinyl-cyclopentane inhibiteur de akt, compositions et procédés de celle-ci - Google Patents

Forme amorphe d'un composé pyrimidinyl-cyclopentane inhibiteur de akt, compositions et procédés de celle-ci

Info

Publication number
MA37650A1
MA37650A1 MA37650A MA37650A MA37650A1 MA 37650 A1 MA37650 A1 MA 37650A1 MA 37650 A MA37650 A MA 37650A MA 37650 A MA37650 A MA 37650A MA 37650 A1 MA37650 A1 MA 37650A1
Authority
MA
Morocco
Prior art keywords
akt
compositions
methods
amorphous form
cyclopentane compound
Prior art date
Application number
MA37650A
Other languages
English (en)
Inventor
Francis Gosselin
Scott J Savage
Jeffrey Stults
Paroma Chakravarty
Sanjeev Kothari
Original Assignee
Genentech Inc
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=48539412&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA37650(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Genentech Inc filed Critical Genentech Inc
Publication of MA37650A1 publication Critical patent/MA37650A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Inorganic Chemistry (AREA)

Abstract

La présente invention concerne le monochlorhydrate de (
MA37650A 2012-05-17 2014-12-12 Forme amorphe d'un composé pyrimidinyl-cyclopentane inhibiteur de akt, compositions et procédés de celle-ci MA37650A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261648536P 2012-05-17 2012-05-17
PCT/US2013/041728 WO2013173811A1 (fr) 2012-05-17 2013-05-17 Forme amorphe d'un composé pyrimidinyl-cyclopentane inhibiteur de akt, compositions et procédés de celle-ci

Publications (1)

Publication Number Publication Date
MA37650A1 true MA37650A1 (fr) 2016-11-30

Family

ID=48539412

Family Applications (1)

Application Number Title Priority Date Filing Date
MA37650A MA37650A1 (fr) 2012-05-17 2014-12-12 Forme amorphe d'un composé pyrimidinyl-cyclopentane inhibiteur de akt, compositions et procédés de celle-ci

Country Status (31)

Country Link
US (2) US9290458B2 (fr)
EP (2) EP3719014A1 (fr)
JP (2) JP6283663B2 (fr)
KR (5) KR20200074252A (fr)
CN (1) CN104470912B (fr)
AU (2) AU2013262548B2 (fr)
BR (1) BR112014028593A2 (fr)
CA (1) CA2873663C (fr)
CL (1) CL2014003115A1 (fr)
CO (1) CO7151489A2 (fr)
CR (1) CR20140560A (fr)
DK (1) DK2858989T3 (fr)
ES (1) ES2799512T3 (fr)
HK (1) HK1208462A1 (fr)
HR (1) HRP20200992T1 (fr)
HU (1) HUE051254T2 (fr)
IL (2) IL235712B (fr)
LT (1) LT2858989T (fr)
MA (1) MA37650A1 (fr)
MX (1) MX353041B (fr)
MY (1) MY170086A (fr)
NZ (1) NZ702513A (fr)
PE (1) PE20150725A1 (fr)
PH (1) PH12014502538A1 (fr)
PL (1) PL2858989T3 (fr)
PT (1) PT2858989T (fr)
RS (1) RS60417B9 (fr)
RU (1) RU2650511C2 (fr)
SG (1) SG11201407618VA (fr)
SI (1) SI2858989T1 (fr)
WO (1) WO2013173811A1 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR112014028593A2 (pt) 2012-05-17 2017-12-19 Genentech Inc forma amorfa de um composto de pirimidinil-ciclopentano inibidor de akt, composições e métodos dos mesmos"
CA2873654C (fr) 2012-05-17 2021-06-22 Array Biopharma Inc. Procede de fabrication de composes de cyclopentylpyrimidine hydroxylee
ES2765511T3 (es) * 2013-11-15 2020-06-09 Hoffmann La Roche Procesos para la preparación de compuestos de pirimidinilciclopentano
SI2946774T1 (sl) 2014-05-19 2020-07-31 Tillotts Pharma Ag Obložene kapsule s prirejenim sproščanjem
CN115350192A (zh) * 2016-08-10 2022-11-18 豪夫迈·罗氏有限公司 包含Akt蛋白激酶抑制剂的药物组合物
TW202120096A (zh) * 2019-08-12 2021-06-01 美商建南德克公司 使用包含atp競爭性akt抑制劑、cdk4/6抑制劑及氟維司群之組合療法治療乳癌
JP2024520798A (ja) * 2021-06-09 2024-05-24 ロンザ・ベンド・インコーポレーテッド 非晶質固体分散体の調製のための噴霧乾燥のための混合溶媒
WO2023043869A1 (fr) * 2021-09-15 2023-03-23 Teva Pharmaceuticals International Gmbh Formes à l'état solide de citrate d'ipatasertib

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BR9408197A (pt) 1993-12-12 1997-08-26 Agrogene Ltd Método para proteger plantas contra doenças fúngicas
JP2001524079A (ja) 1997-04-07 2001-11-27 メルク エンド カンパニー インコーポレーテッド ガンの治療方法
US6201023B1 (en) 1997-06-10 2001-03-13 Agrogene Ltd. Methods and compositions to protect crops against plant parasitic nematodes
ES2137137B1 (es) 1998-05-25 2000-08-16 Medichem Sa Nuevo polimorfo de gabapentina no hidratada, su procedimiento de obtencion y su utilizacion para la obtencion de gabapentina de calidad farmaceutica.
EP0982300A3 (fr) 1998-07-29 2000-03-08 Societe Civile Bioprojet Non-imidazole alkylamines comme antagonistes du recepteur histamine H3 et leur application thérapeutique
US6376496B1 (en) 1999-03-03 2002-04-23 Merck & Co., Inc. Inhibitors of prenyl-protein transferase
AU7715300A (en) 1999-09-27 2001-04-30 Merck & Co., Inc. Method of preventing osteoporosis
WO2003063822A2 (fr) 2002-02-01 2003-08-07 Pfizer Products Inc. Procede de fabrication de dispersions medicamenteuses amorphes solides homogenes sechees par pulverisation au moyen d'un appareil de sechage par pulverisation modifie
JP4550811B2 (ja) 2003-06-09 2010-09-22 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング パピローマウイルスのインヒビター
CN1882347A (zh) 2003-11-21 2006-12-20 阿雷生物药品公司 Akt蛋白激酶抑制剂
MY139645A (en) * 2004-02-11 2009-10-30 Amgen Inc Vanilloid receptor ligands and their use in treatments
US8927546B2 (en) 2006-02-28 2015-01-06 Dart Neuroscience (Cayman) Ltd. Therapeutic piperazines
US8063050B2 (en) 2006-07-06 2011-11-22 Array Biopharma Inc. Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors
UA95641C2 (en) * 2006-07-06 2011-08-25 Эррей Биофарма Инк. Hydroxylated cyclopenta [d] pyrimidines as akt protein kinase inhibitors
AU2008272830B8 (en) 2007-07-05 2013-12-12 Array Biopharma Inc. Pyrimidyl cyclopentanes as AKT protein kinase inhibitors
US20100298289A1 (en) 2007-10-09 2010-11-25 Ucb Pharma, S.A. Heterobicyclic compounds as histamine h4-receptor antagonists
NZ586346A (en) * 2008-01-09 2012-02-24 Array Biopharma Inc Hydroxylated pyrimidyl cyclopentanes as akt protein kinase inhibitors
RU2541571C2 (ru) 2009-04-15 2015-02-20 Эббви Инк. Противовирусные соединения
EP2491032B1 (fr) 2009-10-23 2014-04-16 Eli Lilly and Company Inhibiteurs d'akt
RU2012148699A (ru) * 2010-04-16 2014-05-27 Дженентек, Инк. Foxo3a как прогностический биомаркер для эффективности ингибитора пути киназы pi3k/акт
US9050334B2 (en) 2010-07-16 2015-06-09 Innov88 Llc MIF inhibitors and their uses
WO2012177925A1 (fr) 2011-06-21 2012-12-27 The Board Institute, Inc. Inhibiteurs akt pour le traitement d'un cancer exprimant un gène de fusion magi3 - akt3
BR112014028593A2 (pt) 2012-05-17 2017-12-19 Genentech Inc forma amorfa de um composto de pirimidinil-ciclopentano inibidor de akt, composições e métodos dos mesmos"
CA2873654C (fr) 2012-05-17 2021-06-22 Array Biopharma Inc. Procede de fabrication de composes de cyclopentylpyrimidine hydroxylee
MA37647A1 (fr) 2012-05-17 2016-03-31 Genentech Inc Procédé de fabrication de composés de cyclopentapyrimidine hydroxylée et sels de ceux-ci
CN104487430B (zh) 2012-05-17 2016-08-24 阵列生物制药公司 用于制造羟基化的环戊基嘧啶化合物的方法
CA2873658C (fr) 2012-05-17 2021-01-26 Genentech, Inc. Procede de preparation de composes d'acides amines
CA2889855A1 (fr) 2012-11-01 2014-05-08 Robert S. Katz Methodes de traitement de la fibromyalgie
JP2016513112A (ja) 2013-02-18 2016-05-12 ザ スクリプス リサーチ インスティテュート 治療的潜在能力を有するバソプレッシン受容体のモジュレーター
US10131637B2 (en) 2013-03-15 2018-11-20 Shifa Biomedical Corporation Anti-PCSK9 compounds and methods for the treatment and/or prevention of cardiovascular diseases

Also Published As

Publication number Publication date
CR20140560A (es) 2015-01-12
IL235712A0 (en) 2015-02-01
NZ702513A (en) 2016-09-30
HK1208462A1 (en) 2016-03-04
HUE051254T2 (hu) 2021-03-01
RU2650511C2 (ru) 2018-04-16
PH12014502538B1 (en) 2015-01-21
HRP20200992T1 (hr) 2020-10-16
CL2014003115A1 (es) 2015-07-03
EP3719014A1 (fr) 2020-10-07
DK2858989T3 (da) 2020-06-02
PT2858989T (pt) 2020-06-25
WO2013173811A1 (fr) 2013-11-21
LT2858989T (lt) 2020-08-10
ES2799512T3 (es) 2020-12-18
EP2858989B1 (fr) 2020-05-06
SI2858989T1 (sl) 2020-08-31
PL2858989T3 (pl) 2020-11-16
JP6518352B2 (ja) 2019-05-22
EP2858989B9 (fr) 2021-04-14
KR102125588B1 (ko) 2020-06-22
AU2017279607B2 (en) 2018-11-22
US20150274677A1 (en) 2015-10-01
CA2873663C (fr) 2020-01-14
IL235712B (en) 2020-01-30
EP2858989A1 (fr) 2015-04-15
AU2017279607A1 (en) 2018-01-18
IL272037B (en) 2020-10-29
AU2013262548A1 (en) 2015-01-15
JP2015517533A (ja) 2015-06-22
KR20150020200A (ko) 2015-02-25
CN104470912B (zh) 2017-11-14
RU2014151016A (ru) 2016-07-10
AU2017279607C1 (en) 2019-05-16
PE20150725A1 (es) 2015-05-17
RS60417B9 (sr) 2021-07-30
PH12014502538A1 (en) 2015-01-21
CA2873663A1 (fr) 2013-11-21
KR102678074B1 (ko) 2024-06-26
US20160152575A1 (en) 2016-06-02
US9290458B2 (en) 2016-03-22
RS60417B1 (sr) 2020-07-31
MY170086A (en) 2019-07-04
BR112014028593A2 (pt) 2017-12-19
JP2018062536A (ja) 2018-04-19
MX2014013856A (es) 2015-02-18
IL272037A (en) 2020-02-27
KR20200074252A (ko) 2020-06-24
CO7151489A2 (es) 2014-12-29
KR20210095238A (ko) 2021-07-30
MX353041B (es) 2017-12-18
AU2013262548B2 (en) 2017-09-21
CN104470912A (zh) 2015-03-25
KR20240066293A (ko) 2024-05-14
KR20220143143A (ko) 2022-10-24
JP6283663B2 (ja) 2018-02-21
US9505725B2 (en) 2016-11-29
SG11201407618VA (en) 2015-01-29

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