MX2023004799A - Formas de estado solido de inhibidor de hdac. - Google Patents

Formas de estado solido de inhibidor de hdac.

Info

Publication number
MX2023004799A
MX2023004799A MX2023004799A MX2023004799A MX2023004799A MX 2023004799 A MX2023004799 A MX 2023004799A MX 2023004799 A MX2023004799 A MX 2023004799A MX 2023004799 A MX2023004799 A MX 2023004799A MX 2023004799 A MX2023004799 A MX 2023004799A
Authority
MX
Mexico
Prior art keywords
solid state
hdac inhibitor
state forms
inhibitor solid
quinolin
Prior art date
Application number
MX2023004799A
Other languages
English (en)
Inventor
Xiaohu Deng
Wanping Mai
Robert C Mcrae
Biljana Nadjsombati
Original Assignee
Viracta Subsidiary 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
Application filed by Viracta Subsidiary Inc filed Critical Viracta Subsidiary Inc
Publication of MX2023004799A publication Critical patent/MX2023004799A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • 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
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • A61K31/52Purines, e.g. adenine
    • A61K31/522Purines, e.g. adenine having oxo groups directly attached to the heterocyclic ring, e.g. hypoxanthine, guanine, acyclovir
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/02Sulfonic acids having sulfo groups bound to acyclic carbon atoms
    • C07C309/03Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C309/04Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing only one sulfo group
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/18Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente descripción se refiere a la sal de Forma 1 de mesilato cristalino N-hidroxi 2-{6-[(6-fluoro-quinolin-2-ilmetil)- amino]-3-aza-biciclo[3.1.0]hex-3-il}pirimidina-5-carboxamida y métodos para fabricar la misma. La sal de Forma 1 de mesilato cristalino N-hidroxi 2-{6-[(6-fluoro-quinolin-2-ilmetil)-amino]-3- aza-biciclo[3.1.0]hex-3-il}pirimidina-5-carboxamida es útil en la preparación de composiciones farmacéuticas y formas de dosificación para el tratamiento de cáncer, trastornos inmunitarios e inflamación.
MX2023004799A 2020-10-28 2021-10-28 Formas de estado solido de inhibidor de hdac. MX2023004799A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US202063106811P 2020-10-28 2020-10-28
PCT/US2021/057106 WO2022094122A1 (en) 2020-10-28 2021-10-28 Hdac inhibitor solid state forms

Publications (1)

Publication Number Publication Date
MX2023004799A true MX2023004799A (es) 2023-05-10

Family

ID=81384331

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2023004799A MX2023004799A (es) 2020-10-28 2021-10-28 Formas de estado solido de inhibidor de hdac.

Country Status (11)

Country Link
US (3) US20230382888A1 (es)
EP (1) EP4237409A4 (es)
JP (1) JP2024503180A (es)
KR (1) KR20230097098A (es)
CN (1) CN116648449A (es)
AU (1) AU2021368107A1 (es)
CA (1) CA3196385A1 (es)
IL (1) IL302289A (es)
MX (1) MX2023004799A (es)
TW (1) TW202233595A (es)
WO (1) WO2022094122A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021113694A1 (en) 2019-12-05 2021-06-10 Viracta Therapeutics, Inc. Hdac inhibitor solid state forms
KR20230097098A (ko) 2020-10-28 2023-06-30 비락타 서브시디어리 인크. Hdac 억제제 고체 상태 형태

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0510204D0 (en) * 2005-05-19 2005-06-22 Chroma Therapeutics Ltd Enzyme inhibitors
US20110245154A1 (en) 2010-03-11 2011-10-06 Hemaquest Pharmaceuticals, Inc. Methods and Compositions for Treating Viral or Virally-Induced Conditions
WO2018013975A1 (en) * 2016-07-15 2018-01-18 Viracta Therapeutics, Inc. Hdac inhibitors for use with nk cell based therapies
US20200368280A1 (en) 2018-01-12 2020-11-26 Viracta Therapeutics, Inc. Epigenetic modifiers for use in cellular immunotherapy
TWI813666B (zh) 2018-04-20 2023-09-01 大陸商四川科倫博泰生物醫藥股份有限公司 一種多功能化合物、其製備方法及其在醫藥上的應用
WO2020243326A1 (en) 2019-05-31 2020-12-03 Viracta Therapeutics, Inc. Methods of treating virally associated cancers with histone deacetylase inhibitors
WO2021071809A1 (en) 2019-10-07 2021-04-15 Viracta Therapeutics, Inc. Dosages for hdac treatment with reduced side effects
WO2021113694A1 (en) 2019-12-05 2021-06-10 Viracta Therapeutics, Inc. Hdac inhibitor solid state forms
KR20230097098A (ko) 2020-10-28 2023-06-30 비락타 서브시디어리 인크. Hdac 억제제 고체 상태 형태
EP4373525A1 (en) 2021-07-21 2024-05-29 Viracta Subsidiary, Inc. Cancer treatment combinations

Also Published As

Publication number Publication date
US11760748B2 (en) 2023-09-19
CA3196385A1 (en) 2022-05-05
US20230159499A1 (en) 2023-05-25
JP2024503180A (ja) 2024-01-25
EP4237409A4 (en) 2024-08-28
WO2022094122A1 (en) 2022-05-05
US20240166628A1 (en) 2024-05-23
AU2021368107A1 (en) 2023-06-22
KR20230097098A (ko) 2023-06-30
TW202233595A (zh) 2022-09-01
IL302289A (en) 2023-06-01
AU2021368107A9 (en) 2024-10-03
EP4237409A1 (en) 2023-09-06
US20230382888A1 (en) 2023-11-30
US12012396B2 (en) 2024-06-18
CN116648449A (zh) 2023-08-25

Similar Documents

Publication Publication Date Title
MX2023004799A (es) Formas de estado solido de inhibidor de hdac.
MX2016006901A (es) Forma cristalina i de ibrutinib.
PH12020550216A1 (en) Pyridine, pyrazine, and triazine compounds as allosteric shp2 inhibitors
MX2020009957A (es) Compuestos para el tratamiento de enfermedad de hungtinton.
EP4230623A3 (en) Pyridine compounds as allosteric shp2 inhibitors
PH12019502033A1 (en) Pharmaceutical composition comprising selexipag
MX2024001201A (es) Combinaciones de agonistas de receptores de hormona tiroidea (tr-\03b2) con agonistas de glp-1 para usarse en tratar enfermedades del higado graso.
BR112012021337A8 (pt) formulações de apixaban.
EA201691242A1 (ru) Фармацевтические композиции, содержащие azd9291
TN2012000316A1 (en) Fused heteroaromatic pyrrolidinones as syk inhibitors
MY192354A (en) 4-imidazopyridazin-1-yl-benzamides and 4-imidazotriazin-1-yl-benzamides as btk-inhibitors
PH12015502630A1 (en) Substituted tetrahydrocarbazole and carbazole carboxamide compounds useful as kinase inhibitors
MX2022006741A (es) Formas de estado solido del inhibidor de hdac.
MX2021006619A (es) Inhibidores de la tirosina quinasa, composiciones y sus metodos.
MX2024007058A (es) Derivados de 5,6,7,8-tetrahidro-2,6-naftiridina como terapeuticos contra el cancer.
MX2024005429A (es) Inhibidores de las fosfatidilinositol 3-cinasas-alfa (pi3k-alfa) y metodos para su produccion y uso.
MX2021012248A (es) Polimorfos de voruciclib y metodos de elaboracion y uso de los mismos.
MX2015015200A (es) Inhibidores de nicotamida fosforibosiltransferasa, composiciones, productos y usos de los mismos.
MX2023000198A (es) Inhibidores de atr y usos de estos.
SG11201902588PA (en) N3-Cyclically Substituted Thienouracils And Use Thereof
MX2022012404A (es) Composiciones que comprenden 15-hepe para tratar o prevenir trastornos hematológicos y/o enfermedades relacionadas.
EA201990129A1 (ru) Таблетированный состав с улучшенным профилем растворения для лечения болезни паркинсона
MX2020001199A (es) Compuestos y composiciones farmaceuticas de los mismos para usarse en el tratamiento de enfermedades fibroticas.
MX2023006086A (es) Métodos para prevenir, retrasar o aliviar enfermedades atópicas.
MX2022009851A (es) Compuestos útiles para inhibir la cetohexocinasa y métodos para elaborarlos y utilizarlos.