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MX2021008645A - Forma cristalina de un inhibidor de cinasa ciclinodependiente (cdk). - Google Patents

Forma cristalina de un inhibidor de cinasa ciclinodependiente (cdk).

Info

Publication number
MX2021008645A
MX2021008645A MX2021008645A MX2021008645A MX2021008645A MX 2021008645 A MX2021008645 A MX 2021008645A MX 2021008645 A MX2021008645 A MX 2021008645A MX 2021008645 A MX2021008645 A MX 2021008645A MX 2021008645 A MX2021008645 A MX 2021008645A
Authority
MX
Mexico
Prior art keywords
crystalline form
cdk inhibitor
relates
compositions
methylcyclopentyl
Prior art date
Application number
MX2021008645A
Other languages
English (en)
Inventor
Douglas Carl Behenna
Martha Alicia Ornelas
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of MX2021008645A publication Critical patent/MX2021008645A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Esta invención se refiere a una forma cristalina de la base libre de 6-(difluorometil)-8- [(1R,2R)-2-hidroxi-2-metilciclopentil]-2-{ [1-(metilsulfonil)piperidin-4-il]amino}pirido[2,3-d]pirimidin-7(8 H)-ona (PF-06873600) (Forma 1); la invención también se refiere a composiciones farmacéuticas que comprenden esta forma cristalina, y a métodos de uso de la forma cristalina y dichas composiciones para el tratamiento de crecimiento celular anormal, tal como el cáncer, en un mamífero.
MX2021008645A 2019-01-17 2020-01-13 Forma cristalina de un inhibidor de cinasa ciclinodependiente (cdk). MX2021008645A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962793516P 2019-01-17 2019-01-17
US201962949990P 2019-12-18 2019-12-18
PCT/IB2020/050240 WO2020148635A1 (en) 2019-01-17 2020-01-13 Crystalline form of a cdk inhibitor

Publications (1)

Publication Number Publication Date
MX2021008645A true MX2021008645A (es) 2021-08-19

Family

ID=69326588

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2021008645A MX2021008645A (es) 2019-01-17 2020-01-13 Forma cristalina de un inhibidor de cinasa ciclinodependiente (cdk).

Country Status (12)

Country Link
US (1) US20220127262A1 (es)
EP (1) EP3911650A1 (es)
JP (2) JP7036846B2 (es)
KR (1) KR20210114996A (es)
CN (1) CN113260617A (es)
AU (1) AU2020209500B2 (es)
BR (1) BR112021013050A2 (es)
CA (1) CA3126788A1 (es)
MX (1) MX2021008645A (es)
SG (1) SG11202107225SA (es)
TW (1) TWI745831B (es)
WO (1) WO2020148635A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2023281413A1 (en) 2021-07-09 2023-01-12 Pfizer Inc. Methods and dosing regimens comprising pf-06873600 for the treatment of cancer
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
WO2025034702A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Rmc-6291 for use in the treatment of ras protein-related disease or disorder
US20250154171A1 (en) 2023-10-12 2025-05-15 Revolution Medicines, Inc. Ras inhibitors

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2619944C2 (ru) * 2013-02-21 2017-05-22 Пфайзер Инк. Твердые формы селективного ингибитора CDK4/6
MX382600B (es) * 2015-07-31 2025-03-13 Pfizer Forma cristalina de base libre de lorlatinib.
LT3497103T (lt) 2016-08-15 2021-07-26 Pfizer Inc. Piridopirimidinono cdk2/4/6 inhibitoriai

Also Published As

Publication number Publication date
AU2020209500B2 (en) 2022-08-25
KR20210114996A (ko) 2021-09-24
EP3911650A1 (en) 2021-11-24
JP7036846B2 (ja) 2022-03-15
TWI745831B (zh) 2021-11-11
CN113260617A (zh) 2021-08-13
JP2021193151A (ja) 2021-12-23
TW202043224A (zh) 2020-12-01
CA3126788A1 (en) 2020-07-23
SG11202107225SA (en) 2021-08-30
JP2020114808A (ja) 2020-07-30
AU2020209500A1 (en) 2021-07-29
US20220127262A1 (en) 2022-04-28
BR112021013050A2 (pt) 2021-09-21
WO2020148635A1 (en) 2020-07-23

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