MX2024005429A - Inhibidores de las fosfatidilinositol 3-cinasas-alfa (pi3k-alfa) y metodos para su produccion y uso. - Google Patents

Inhibidores de las fosfatidilinositol 3-cinasas-alfa (pi3k-alfa) y metodos para su produccion y uso.

Info

Publication number
MX2024005429A
MX2024005429A MX2024005429A MX2024005429A MX2024005429A MX 2024005429 A MX2024005429 A MX 2024005429A MX 2024005429 A MX2024005429 A MX 2024005429A MX 2024005429 A MX2024005429 A MX 2024005429A MX 2024005429 A MX2024005429 A MX 2024005429A
Authority
MX
Mexico
Prior art keywords
making
methods
pi3k
same
alpha inhibitors
Prior art date
Application number
MX2024005429A
Other languages
English (en)
Spanish (es)
Inventor
Surendra P Singh
Wei Gu
Alessandro Boezio
Yuan Lin
Siyi Jiang
André Lescarbeau
Min Lu
Jiahui Chen
Hongyan He
Qinglin Che
Qiuxiang Zhou
Jiajia Zhou
Yunfei Zhou
Xijian Gong
Xiaohong Wang
Changbo Yin
Original Assignee
Relay Therapeutics 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 Relay Therapeutics Inc filed Critical Relay Therapeutics Inc
Publication of MX2024005429A publication Critical patent/MX2024005429A/es

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/4353—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01—Sulfonic acids
    • C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
    • C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C309/04—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing only one sulfo group
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01—Sulfonic acids
    • C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/29—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of non-condensed six-membered aromatic rings
    • C07C309/30—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of non-condensed six-membered aromatic rings of six-membered aromatic rings substituted by alkyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01—Sulfonic acids
    • C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/33—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of six-membered aromatic rings being part of condensed ring systems
    • C07C309/34—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of six-membered aromatic rings being part of condensed ring systems formed by two rings
    • C07C309/35—Naphthalene sulfonic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
MX2024005429A 2021-11-03 2022-11-03 Inhibidores de las fosfatidilinositol 3-cinasas-alfa (pi3k-alfa) y metodos para su produccion y uso. MX2024005429A (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202163263474P 2021-11-03 2021-11-03
CN2021128533 2021-11-03
PCT/US2022/079221 WO2023081757A1 (en) 2021-11-03 2022-11-03 Pi3k-alpha inhibitors and methods of making and using the same

Publications (1)

Publication Number Publication Date
MX2024005429A true MX2024005429A (es) 2024-05-21

Family

ID=86242193

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2024005429A MX2024005429A (es) 2021-11-03 2022-11-03 Inhibidores de las fosfatidilinositol 3-cinasas-alfa (pi3k-alfa) y metodos para su produccion y uso.

Country Status (13)

Country Link
US (1) US20260125374A1 (enExample)
EP (1) EP4426314A4 (enExample)
JP (1) JP2024540303A (enExample)
KR (1) KR20240112283A (enExample)
CN (1) CN118401245A (enExample)
AU (1) AU2022381187A1 (enExample)
CA (1) CA3236861A1 (enExample)
CL (1) CL2024001364A1 (enExample)
IL (1) IL312466A (enExample)
MX (1) MX2024005429A (enExample)
PE (1) PE20250676A1 (enExample)
TW (1) TW202334136A (enExample)
WO (1) WO2023081757A1 (enExample)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2021263914B2 (en) 2020-04-29 2026-07-23 D.E. Shaw Research, Llc PI3K-α inhibitors and methods of use thereof
WO2024055992A1 (zh) * 2022-09-14 2024-03-21 南京再明医药有限公司 三环化合物及其应用
JP2025538147A (ja) 2022-11-02 2025-11-26 ペトラ・ファーマ・コーポレイション 疾患の治療のためのホスホイノシチド3-キナーゼ(pi3k)のアロステリックポケット及びオルソステリックポケットの標的化
WO2024233256A1 (en) 2023-05-05 2024-11-14 Eli Lilly And Company Imlunestrant or salts thereof for use in treating and preventing central nervous system (cns) metastases in subjects having er+ breast cancer

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010007100A1 (en) * 2008-07-15 2010-01-21 Cellzome Ltd 7-substituted amino triazoles as pi3k inhibitors
JP6472803B2 (ja) * 2013-09-05 2019-02-20 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft トリアゾロピリジン化合物、その組成物及び使用方法
WO2017000277A1 (en) * 2015-07-01 2017-01-05 Merck Sharp & Dohme Corp. Substituted triazolo bicycliccompounds as pde2 inhibitors
EP3931188B1 (en) * 2019-02-26 2023-08-30 Boehringer Ingelheim International GmbH New isoindolinone substituted indoles and derivatives as ras inhibitors
AU2021263914B2 (en) * 2020-04-29 2026-07-23 D.E. Shaw Research, Llc PI3K-α inhibitors and methods of use thereof

Also Published As

Publication number Publication date
CL2024001364A1 (es) 2024-10-25
KR20240112283A (ko) 2024-07-18
EP4426314A1 (en) 2024-09-11
IL312466A (en) 2024-06-01
CN118401245A (zh) 2024-07-26
JP2024540303A (ja) 2024-10-31
EP4426314A4 (en) 2025-10-01
US20260125374A1 (en) 2026-05-07
PE20250676A1 (es) 2025-03-04
CA3236861A1 (en) 2023-05-11
AU2022381187A1 (en) 2024-05-16
TW202334136A (zh) 2023-09-01
WO2023081757A1 (en) 2023-05-11

Similar Documents

Publication Publication Date Title
MX2022008103A (es) Formulaciones de inhibidores de la cinasa amorfa y metodos de estas.
PH12020550703A1 (en) Sulfonamide compounds and use thereof
JOP20180113A1 (ar) مركبات ,تركيبات وطرق
NZ736709A (en) Benzimidazole and imidazopyridine carboximidamide compounds having activity as inhibitors of indoleamine 2,3-dioxygenase
MX2017007884A (es) Derivados de tiadiazol amida como inhibidores de la nadph oxidasa.
PH12022550843A1 (en) Thienopyrimidones as trpa1 inhibitors
NZ726608A (en) Phosphatidylinositol 3-kinase inhibitors
PH12021551873A1 (en) Hydroxypyridoxazepines as nrf2 activators
MX2016016530A (es) Inhibidores de fosfatidilinositol 3-quinasa.
MX2016016528A (es) Inhibidores de fosfatidilinositol 3-quinasa.
PH12021550382A1 (en) Tetrahydropyridopyrimidine derivatives as ahr modulators
MX2022010944A (es) Inhibidores del factor de iniciacion de traduccion eucariotica 4e (eif4e) y sus usos.
PH12022551241A1 (en) Egfr inhibitors
PH12021550857A1 (en) Compounds, compositions, and methods for modulating cdk9 activity
MX2021015656A (es) Formas amorfas y cristalinas de inhibidores de indolamina 2,3-dioxigenasa (ido).
MX2016002764A (es) Compuestos de triazolopiridina, composiciones y metodos de uso de los mismos.
ZA202107777B (en) Voruciclib polymorphs and methods of making and using thereof
PH12021552133A1 (en) Aromatic derivatives, preparation methods, and medical uses thereof
PH12022550846A1 (en) Thienopyrimidones as trpa1 inhibitors
PH12019502462A1 (en) Substituted bicyclic heterocyclic compounds as nadph oxidase inhibitors
MX2025003568A (es) Compuestos y composiciones útiles como inhibidores de las proteínas inhibidoras de la apoptosis (iap)
MX2021001904A (es) Formas solidas de benzoxaborol sustituido y composiciones de las mismas.
IL290625A (en) Crystalline forms of quinoline analogs and their salts, compositions, and methods of their use
MX2023010566A (es) Inhibidores de proteina transportadora vesicular monoaminotransportadora-2 (vmat2) y metodos de uso.
MX2025001201A (es) Sales y cristales novedosos