CU20210035A7 - Compuestos de azalactam como inhibidores de hpk 1 - Google Patents

Compuestos de azalactam como inhibidores de hpk 1

Info

Publication number
CU20210035A7
CU20210035A7 CU2021000035A CU20210035A CU20210035A7 CU 20210035 A7 CU20210035 A7 CU 20210035A7 CU 2021000035 A CU2021000035 A CU 2021000035A CU 20210035 A CU20210035 A CU 20210035A CU 20210035 A7 CU20210035 A7 CU 20210035A7
Authority
CU
Cuba
Prior art keywords
sup
compounds
azalactam
hpk
inhibitors
Prior art date
Application number
CU2021000035A
Other languages
English (en)
Inventor
Omar Khaled Ahmad
Bel Matthew L Del
Rebecca Anne Gallego
Mingying He
Mehran Jalaie
Ted William Johnson
Robert Steven Kania
Michele Ann Mctigue
Sajiv Krishnan Nair
Anne-Marie Dechert Schmitt
Jamison Bryce Tuttle
Dahui Zhou
Ru Zhou
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 CU20210035A7 publication Critical patent/CU20210035A7/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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

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

Abstract

<p>La presente invención se refiere a compuestos de la fórmula general (I)</p> <p>Espacio para la fórmula:</p> <p>y sales de estos aceptables desde el punto de vista farmacéutico, en donde R<sup>1</sup>, R<sup>1</sup><sup>a</sup>, R<sup>2</sup>, R<sup>3</sup>, R<sup>4</sup>, y (R<sup>5</sup>)<sub>a</sub> son como se definen en la presente, útiles para el tratamiento del crecimiento anormal de células, que incluye cáncer.</p>
CU2021000035A 2018-11-15 2019-11-12 Compuestos de azalactam como inhibidores de hpk 1 CU20210035A7 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862767602P 2018-11-15 2018-11-15
US201962909970P 2019-10-03 2019-10-03
PCT/IB2019/059702 WO2020100027A1 (en) 2018-11-15 2019-11-12 2,3-dihydro-1h-pyrrolo[3,4-c]pyridin-1-one derivatives as hpk1 inhibitors for the treatment of cancer

Publications (1)

Publication Number Publication Date
CU20210035A7 true CU20210035A7 (es) 2021-12-08

Family

ID=68771726

Family Applications (1)

Application Number Title Priority Date Filing Date
CU2021000035A CU20210035A7 (es) 2018-11-15 2019-11-12 Compuestos de azalactam como inhibidores de hpk 1

Country Status (36)

Country Link
US (1) US11142525B2 (es)
EP (1) EP3880676B1 (es)
JP (1) JP7118267B2 (es)
KR (1) KR20210090675A (es)
CN (1) CN113316576A (es)
AU (1) AU2019378184B2 (es)
BR (1) BR112021008991A2 (es)
CA (1) CA3061392A1 (es)
CL (1) CL2021001190A1 (es)
CO (1) CO2021006114A2 (es)
CR (1) CR20210251A (es)
CU (1) CU20210035A7 (es)
DK (1) DK3880676T3 (es)
DO (1) DOP2021000088A (es)
EC (1) ECSP21034668A (es)
ES (1) ES2958948T3 (es)
FI (1) FI3880676T3 (es)
GE (1) GEP20227434B (es)
HR (1) HRP20231089T1 (es)
HU (1) HUE063367T2 (es)
IL (1) IL283149A (es)
LT (1) LT3880676T (es)
MD (1) MD3880676T2 (es)
MX (1) MX2021005754A (es)
PE (1) PE20211868A1 (es)
PH (1) PH12021551117A1 (es)
PL (1) PL3880676T3 (es)
PT (1) PT3880676T (es)
RS (1) RS64655B1 (es)
SG (1) SG11202104394XA (es)
SI (1) SI3880676T1 (es)
TW (1) TWI718758B (es)
UA (1) UA127426C2 (es)
UY (1) UY38471A (es)
WO (1) WO2020100027A1 (es)
ZA (1) ZA202103099B (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3116347A1 (en) 2018-10-31 2020-05-07 Gilead Sciences, Inc. Substituted 6-azabenzimidazole compounds having hpk1 inhibitory activity
IL282535B2 (en) 2018-10-31 2024-05-01 Gilead Sciences Inc Transformed 6-azabanzimidazole compounds as HPK1 inhibitors
US11453681B2 (en) 2019-05-23 2022-09-27 Gilead Sciences, Inc. Substituted eneoxindoles and uses thereof
MX2022013401A (es) * 2020-05-01 2022-11-14 Pfizer Compuestos de azalactama como inhibidores de hpk1.
CN112409268A (zh) * 2020-12-03 2021-02-26 西南交通大学 靶向Fam20C抑制剂的制备及其抗三阴性乳腺癌作用
CN117460732A (zh) * 2021-06-11 2024-01-26 杭州中美华东制药有限公司 吡咯并吡啶酮类化合物及其制备方法和用途
CN117693503A (zh) 2021-07-20 2024-03-12 阿斯利康(瑞典)有限公司 作为hpk1抑制剂用于治疗癌症的经取代的吡嗪-2-甲酰胺
WO2023023942A1 (en) * 2021-08-24 2023-03-02 Biofront Ltd (Cayman) Hpk1 inhibitors, compositions comprising hpk1 inhibitor, and methods of using the same
WO2023030478A1 (zh) * 2021-09-03 2023-03-09 浙江海正药业股份有限公司 吡啶并内酰胺类衍生物及其制备方法和用途
WO2023057883A1 (en) * 2021-10-05 2023-04-13 Pfizer Inc. Crystalline form of azalactam compound

Family Cites Families (12)

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Publication number Priority date Publication date Assignee Title
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
US5376645A (en) 1990-01-23 1994-12-27 University Of Kansas Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof
US5243049A (en) * 1992-01-22 1993-09-07 Neurogen Corporation Certain pyrroloquinolinones: a new class of GABA brain receptor ligands
GB9518953D0 (en) 1995-09-15 1995-11-15 Pfizer Ltd Pharmaceutical formulations
WO2000035296A1 (en) 1996-11-27 2000-06-22 Wm. Wrigley Jr. Company Improved release of medicament active agents from a chewing gum coating
GB9711643D0 (en) 1997-06-05 1997-07-30 Janssen Pharmaceutica Nv Glass thermoplastic systems
WO2008063888A2 (en) 2006-11-22 2008-05-29 Plexxikon, Inc. Compounds modulating c-fms and/or c-kit activity and uses therefor
CA2693967A1 (en) * 2007-07-19 2009-01-29 Schering Corporation Heterocyclic amide compounds as protein kinase inhibitors
WO2018049324A1 (en) 2016-09-12 2018-03-15 Numerate, Inc. Monocyclic compounds useful as gpr120 modulators
WO2018167147A1 (en) 2017-03-15 2018-09-20 F. Hoffmann-La Roche Ag Azaindoles as inhibitors of hpk1
WO2019015559A1 (zh) 2017-07-18 2019-01-24 南京圣和药业股份有限公司 作为ask抑制剂的杂环化合物及其应用
EP3743063A4 (en) 2018-01-26 2021-10-20 Nurix Therapeutics, Inc. CBL-B INHIBITORS AND METHOD OF USING THEREOF

Also Published As

Publication number Publication date
SG11202104394XA (en) 2021-05-28
TW202031657A (zh) 2020-09-01
WO2020100027A1 (en) 2020-05-22
HRP20231089T1 (hr) 2023-12-22
ZA202103099B (en) 2023-11-29
KR20210090675A (ko) 2021-07-20
CN113316576A (zh) 2021-08-27
LT3880676T (lt) 2023-09-25
CA3061392A1 (en) 2020-05-15
PT3880676T (pt) 2023-10-04
TWI718758B (zh) 2021-02-11
PH12021551117A1 (en) 2021-11-22
HUE063367T2 (hu) 2024-01-28
ES2958948T3 (es) 2024-02-16
US20200172539A1 (en) 2020-06-04
SI3880676T1 (sl) 2023-10-30
PL3880676T3 (pl) 2023-12-11
US11142525B2 (en) 2021-10-12
CO2021006114A2 (es) 2021-05-31
EP3880676B1 (en) 2023-08-02
MX2021005754A (es) 2021-08-11
JP7118267B2 (ja) 2022-08-15
PE20211868A1 (es) 2021-09-21
CL2021001190A1 (es) 2021-12-24
DK3880676T3 (da) 2023-09-04
UY38471A (es) 2020-06-30
MD3880676T2 (ro) 2023-12-31
DOP2021000088A (es) 2021-06-30
UA127426C2 (uk) 2023-08-16
AU2019378184A1 (en) 2021-05-27
IL283149A (en) 2021-06-30
CR20210251A (es) 2021-07-14
BR112021008991A2 (pt) 2021-08-10
EP3880676A1 (en) 2021-09-22
RS64655B1 (sr) 2023-10-31
GEP20227434B (en) 2022-10-25
ECSP21034668A (es) 2021-06-30
JP2022507231A (ja) 2022-01-18
AU2019378184B2 (en) 2022-09-15
FI3880676T3 (fi) 2023-09-15

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