MX2023001689A - Inhibidores de bcl-2. - Google Patents

Inhibidores de bcl-2.

Info

Publication number
MX2023001689A
MX2023001689A MX2023001689A MX2023001689A MX2023001689A MX 2023001689 A MX2023001689 A MX 2023001689A MX 2023001689 A MX2023001689 A MX 2023001689A MX 2023001689 A MX2023001689 A MX 2023001689A MX 2023001689 A MX2023001689 A MX 2023001689A
Authority
MX
Mexico
Prior art keywords
bcl
treating
inhibitors
disclosed
undesirable
Prior art date
Application number
MX2023001689A
Other languages
English (en)
Inventor
Yunhang Guo
Zhiwei Wang
Hai Xue
Hanzi Sun
Original Assignee
Beigene Ltd
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 Beigene Ltd filed Critical Beigene Ltd
Publication of MX2023001689A publication Critical patent/MX2023001689A/es

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Classifications

    • 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
    • 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
    • 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
    • A61K31/495—Heterocyclic 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
    • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
    • C07D207/09—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic 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
    • C07D403/12—Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • 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
    • C07D471/12—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 three hetero rings
    • C07D471/14—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

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)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyrrole Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Se describe en este documento un compuesto de fórmula (I) para inhibir Bcl-2 y tratar enfermedades asociadas con actividad indeseable de bcl-2 (enfermedades relacionadas con Bcl-2), un método para usar los compuestos descritos en este documento para tratar enfermedades apoptóticas desreguladas, incluidos cánceres, y tratamiento de enfermedad autoinmune, y una composición farmacéutica que la comprende.
MX2023001689A 2018-04-29 2020-10-29 Inhibidores de bcl-2. MX2023001689A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN2018085217 2018-04-29
CN2018107134 2018-09-21

Publications (1)

Publication Number Publication Date
MX2023001689A true MX2023001689A (es) 2023-02-22

Family

ID=68386968

Family Applications (2)

Application Number Title Priority Date Filing Date
MX2020011495A MX2020011495A (es) 2018-04-29 2019-04-29 Inhibidores de bcl-2.
MX2023001689A MX2023001689A (es) 2018-04-29 2020-10-29 Inhibidores de bcl-2.

Family Applications Before (1)

Application Number Title Priority Date Filing Date
MX2020011495A MX2020011495A (es) 2018-04-29 2019-04-29 Inhibidores de bcl-2.

Country Status (11)

Country Link
US (2) US11420968B2 (es)
EP (1) EP3788042A4 (es)
JP (2) JP2021521138A (es)
KR (1) KR20210005677A (es)
CN (3) CN117683029A (es)
AU (1) AU2019264475B2 (es)
BR (1) BR112020022092A2 (es)
CA (1) CA3098348A1 (es)
MX (2) MX2020011495A (es)
SG (1) SG11202009933WA (es)
WO (1) WO2019210828A1 (es)

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AU2019207608B2 (en) 2018-01-10 2024-03-28 Recurium Ip Holdings, Llc Benzamide compounds
CA3098348A1 (en) 2018-04-29 2019-11-07 Beigene, Ltd. Bcl-2 inhibitors
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EP4051676A4 (en) * 2019-10-28 2023-11-22 BeiGene, Ltd. BCL-2 INHIBITORS
WO2021110102A1 (en) * 2019-12-02 2021-06-10 Beigene, Ltd. Methods of cancer treatment using bcl-2 inhibitor
KR20230127372A (ko) 2019-12-06 2023-08-31 록쏘 온콜로지, 인코포레이티드 브루톤 티로신 키나제 억제제의 투여
WO2021133817A1 (en) 2019-12-27 2021-07-01 Guangzhou Lupeng Pharmaceutical Company Ltd. 1h-pyrrolo[2,3-b]pyridine derivatives as bcl-2 inhibitors for the treatment of neoplastic and autoimmune diseases
TW202200574A (zh) * 2020-04-15 2022-01-01 英屬開曼群島商百濟神州有限公司 Bcl-2抑制劑
CN115843297A (zh) * 2020-05-08 2023-03-24 重庆复创医药研究有限公司 作为bcl-2抑制剂的化合物
CN114478520A (zh) * 2020-10-28 2022-05-13 杭州和正医药有限公司 Bcl-2蛋白凋亡诱导剂及应用
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WO2024017354A1 (en) * 2022-07-21 2024-01-25 Beigene, Ltd. Methods of treating multiple myeloma using bcl-2 inhibitor
WO2024140692A1 (en) * 2022-12-27 2024-07-04 Beigene (Suzhou) Co., Ltd. Salts and solid forms of sonrotoclax intermediate
WO2024140678A1 (en) * 2022-12-27 2024-07-04 Beigene (Suzhou) Co., Ltd. A ketal protected intermediate for sonrotoclax and preparation method thereof
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Also Published As

Publication number Publication date
US20220402915A1 (en) 2022-12-22
JP2024119916A (ja) 2024-09-03
TW202043217A (zh) 2020-12-01
JP2021521138A (ja) 2021-08-26
CN112437772A (zh) 2021-03-02
US12077536B2 (en) 2024-09-03
CN117430601A (zh) 2024-01-23
US20210269433A1 (en) 2021-09-02
KR20210005677A (ko) 2021-01-14
EP3788042A4 (en) 2022-01-26
CN117683029A (zh) 2024-03-12
SG11202009933WA (en) 2020-11-27
WO2019210828A1 (en) 2019-11-07
AU2019264475B2 (en) 2024-09-26
BR112020022092A2 (pt) 2021-02-02
AU2019264475A1 (en) 2020-11-12
JP7540113B1 (ja) 2024-08-26
EP3788042A1 (en) 2021-03-10
CA3098348A1 (en) 2019-11-07
CN112437772B (zh) 2023-11-21
US11420968B2 (en) 2022-08-23
MX2020011495A (es) 2021-01-15

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