DK3494115T3 - N-(phenylsulfonyl)benzamidderivater som bcl-2-hæmmere - Google Patents

N-(phenylsulfonyl)benzamidderivater som bcl-2-hæmmere Download PDF

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Publication number
DK3494115T3
DK3494115T3 DK17754889.8T DK17754889T DK3494115T3 DK 3494115 T3 DK3494115 T3 DK 3494115T3 DK 17754889 T DK17754889 T DK 17754889T DK 3494115 T3 DK3494115 T3 DK 3494115T3
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Prior art keywords
phenylsulphonyl
bcl
inhibitors
benzamide derivatives
benzamide
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DK17754889.8T
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Danish (da)
English (en)
Inventor
Jianyong Chen
Shaomeng Wang
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Univ Michigan Regents
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Publication of DK3494115T3 publication Critical patent/DK3494115T3/da

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    • 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
    • A61K31/4353Heterocyclic 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
    • A61K31/437Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)
DK17754889.8T 2016-08-05 2017-08-04 N-(phenylsulfonyl)benzamidderivater som bcl-2-hæmmere DK3494115T3 (da)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662371504P 2016-08-05 2016-08-05
US201762454101P 2017-02-03 2017-02-03
PCT/US2017/045428 WO2018027097A1 (en) 2016-08-05 2017-08-04 N-(phenylsulfonyl)benzamides and related compounds as bcl-2 inhibitors

Publications (1)

Publication Number Publication Date
DK3494115T3 true DK3494115T3 (da) 2021-01-18

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DK17754889.8T DK3494115T3 (da) 2016-08-05 2017-08-04 N-(phenylsulfonyl)benzamidderivater som bcl-2-hæmmere

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US (3) US10829488B2 (enExample)
EP (3) EP3569601B1 (enExample)
JP (2) JP6651180B2 (enExample)
KR (2) KR102376764B1 (enExample)
CN (2) CN109311871B (enExample)
AU (2) AU2017305508B2 (enExample)
CA (1) CA3031419C (enExample)
CY (1) CY1123859T1 (enExample)
DK (1) DK3494115T3 (enExample)
ES (1) ES2849959T3 (enExample)
HR (1) HRP20202073T1 (enExample)
HU (1) HUE053414T2 (enExample)
IL (2) IL264059B (enExample)
LT (1) LT3494115T (enExample)
MX (2) MX381588B (enExample)
MY (1) MY199409A (enExample)
PE (1) PE20190711A1 (enExample)
PH (1) PH12019500231A1 (enExample)
PT (1) PT3494115T (enExample)
RS (1) RS61821B1 (enExample)
RU (2) RU2744358C2 (enExample)
SA (1) SA519401020B1 (enExample)
SG (2) SG10201913643YA (enExample)
SI (1) SI3494115T1 (enExample)
SM (1) SMT202100025T1 (enExample)
WO (1) WO2018027097A1 (enExample)
ZA (2) ZA201900240B (enExample)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017156398A1 (en) * 2016-03-10 2017-09-14 Assia Chemical Industries Ltd. Solid state forms of venetoclax and processes for preparation of venetoclax
JP6651180B2 (ja) * 2016-08-05 2020-02-19 ザ・リージェンツ・オブ・ザ・ユニバーシティ・オブ・ミシガンThe Regents Of The University Of Michigan Bcl−2阻害剤としてのn−(フェニルスルホニル)ベンズアミドおよび関連化合物
US11053239B2 (en) 2017-01-07 2021-07-06 Fochon Pharmaceuticals, Ltd. Compounds as BLC-2-selective apoptosis-inducing agents
AU2018255621B2 (en) 2017-04-18 2022-03-10 Fochon Pharmaceuticals, Ltd. Apoptosis-inducing agents
JP2021521138A (ja) 2018-04-29 2021-08-26 ベイジーン リミテッド Bcl−2阻害剤
KR20200139139A (ko) 2018-07-31 2020-12-11 어센테지 파마 (쑤저우) 컴퍼니 리미티드 리툭시맙 및/또는 벤다무스틴과 병용된 Bcl-2 억제제 또는 CHOP와 병용된 Bcl-2 억제제의 시너지적 항종양 효과
TWI725488B (zh) * 2018-07-31 2021-04-21 大陸商蘇州亞盛藥業有限公司 Bcl-2抑制劑與化療藥的組合產品及其在預防及/或治療疾病中的用途
CN110772521A (zh) 2018-07-31 2020-02-11 苏州亚盛药业有限公司 Bcl-2抑制剂或Bcl-2/Bcl-xL抑制剂与BTK抑制剂的组合产品及其用途
US11478469B2 (en) 2018-07-31 2022-10-25 Ascentage Pharma (Suzhou) Co., Ltd. Combination product of BCL-2 inhibitor and MDM2 inhibitor and use thereof in the prevention and/or treatment of diseases
AU2019385458A1 (en) * 2018-11-23 2021-01-07 Ascentage Pharma (Suzhou) Co., Ltd. Pharmaceutical composition and use thereof
TWI770503B (zh) * 2019-05-13 2022-07-11 大陸商蘇州亞盛藥業有限公司 用於預測bcl-2/bcl-xl抑制劑對癌症的功效的方法和組合物
TW202114692A (zh) * 2019-07-02 2021-04-16 大陸商蘇州亞盛藥業有限公司 一種含有mTOR抑制劑的藥物組合及其應用
JP2021535129A (ja) * 2019-07-31 2021-12-16 アセンテージ ファーマ(スーチョウ)カンパニー,リミティド Bcl−2/Bcl−xL阻害剤及び化学療法剤の組み合わせ製品、並びに疾患の予防及び/又は治療におけるその使用
WO2021083135A1 (en) 2019-10-28 2021-05-06 Beigene, Ltd. Bcl-2 INHIBITORS
TWI885019B (zh) 2019-11-27 2025-06-01 大陸商蘇州亞盛藥業有限公司 用於預測靶向細胞凋亡途徑的化合物的抗癌功效的方法和組合物
US12343352B2 (en) 2019-12-03 2025-07-01 Ascentage Pharma (Suzhou) Co., Ltd. N-(phenylsulfonyl)benzamides and related compounds as Bcl-2 inhibitors
US12514863B2 (en) 2019-12-04 2026-01-06 Ascentage Pharma (Suzhou) Co., Ltd. Pharmaceutical combination and use thereof
WO2021113497A1 (en) 2019-12-06 2021-06-10 Loxo Oncology, Inc. Dosing of a bruton's tyrosine kinase inhibitor
CN113354636B (zh) * 2020-03-06 2022-08-09 苏州亚盛药业有限公司 N-(苯基磺酰基)苯甲酰胺类化合物或其盐、溶剂合物的结晶形式或无定形形式
WO2021180040A1 (zh) * 2020-03-12 2021-09-16 南京明德新药研发有限公司 苯并五元环类化合物
BR112022019525A2 (pt) 2020-04-15 2023-11-14 Beigene Ltd Composto, composição farmacêutica e método para tratar doenças apoptóticas desreguladas
WO2021227763A1 (en) * 2020-05-14 2021-11-18 Ascentage Pharma (Suzhou) Co., Ltd. Hplc analysis method for n- (phenylsulfonyl) benzamide compound
WO2022002178A1 (en) * 2020-07-01 2022-01-06 Ascentage Pharma (Suzhou) Co., Ltd. Methods for synthesizing n-(phenylsulfonyl)benzamide compounds and intermediates thereof
CN111537654B (zh) * 2020-07-07 2020-11-10 上海亚盛医药科技有限公司 N-(苯基磺酰基)苯甲酰胺化合物的hplc分析方法
US20230250077A1 (en) * 2020-07-10 2023-08-10 Jiangsu Hengrui Pharmaceuticals Co., Ltd. Sulfonylbenzamide derivative and conjugate thereof, preparation method therefor and use thereof
CN114057728A (zh) * 2020-08-06 2022-02-18 北京诺诚健华医药科技有限公司 作为bcl-2抑制剂的杂环化合物
CN114073703B (zh) * 2020-08-21 2022-12-30 苏州亚盛药业有限公司 用于治疗非酒精性脂肪肝炎的组合物和方法
JP2023539114A (ja) * 2020-08-21 2023-09-13 アセンテージ ファーマ(スーチョウ)カンパニー,リミティド 全身性エリテマトーデスを治療する組成物及び方法
WO2022111558A1 (en) * 2020-11-25 2022-06-02 Ascentage Pharma (Suzhou) Co., Ltd. Solid dispersion, pharmaceutical preparations, preparation method, and application thereof
US20240316069A1 (en) * 2020-12-28 2024-09-26 Ascentage Pharma (Suzhou) Co., Ltd. Methods of treating multiple sclerosis
EP4298098A4 (en) * 2021-02-01 2025-06-25 Ascentage Pharma (Suzhou) Co., Ltd. SULFONYL BENZAMIDE DERIVATIVES AS BCL-2 INHIBITORS
EP4319800A1 (en) 2021-04-07 2024-02-14 Dana-Farber Cancer Institute, Inc. Compositions and methods for the treatment of cancer
US20250099440A1 (en) 2021-08-02 2025-03-27 Ascentage Pharma (Suzhou) Co., Ltd. A pharmaceutical combination and use thereof
JP7765790B2 (ja) * 2021-12-06 2025-11-07 杭州和正医薬有限公司 抗アポトーシスタンパク質bcl-2阻害剤、医薬組成物及びその使用
CN115260191B (zh) * 2022-09-29 2022-12-27 上海睿跃生物科技有限公司 哌啶类化合物及其制备方法和应用
EP4421075A1 (en) * 2023-02-27 2024-08-28 KRKA, d.d., Novo mesto Process for the preparation of venetoclax and intermediates used therein
WO2024184233A1 (en) 2023-03-03 2024-09-12 Ionctura Sa Combination of roginolisib and bcl-2 inhibitor in the treatment of haematological malignancy

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1021343A (en) 1912-01-17 1912-03-26 M A N Mfg Company Locking-clamp.
US5093330A (en) 1987-06-15 1992-03-03 Ciba-Geigy Corporation Staurosporine derivatives substituted at methylamino nitrogen
US7767684B2 (en) * 2003-11-13 2010-08-03 Abbott Laboratories Apoptosis promoters
WO2005049593A2 (en) 2003-11-13 2005-06-02 Abbott Laboratories N-acylsulfonamide apoptosis promoters
US8624027B2 (en) 2005-05-12 2014-01-07 Abbvie Inc. Combination therapy for treating cancer and diagnostic assays for use therein
US7842681B2 (en) 2006-09-05 2010-11-30 Abbott Laboratories Treatment of myeoproliferative diseases
RU2009125575A (ru) 2006-12-04 2011-01-20 Эбботт Лэборетриз (Us) Комплексные диагностические анализы для терапии рака
UA108193C2 (uk) * 2008-12-04 2015-04-10 Апоптозіндукуючий засіб для лікування раку і імунних і аутоімунних захворювань
CN106008322B (zh) 2008-12-05 2018-09-04 Abbvie 公司 作为用于治疗癌症和免疫疾病的bcl-2-选择性诱发细胞凋亡药剂的磺酰胺衍生物
BRPI1006115A8 (pt) 2009-01-19 2017-09-26 Abbott Lab "agentes indutores de apoptose para o tratamento de câncer e doenças autoimunes".
US9045800B2 (en) 2009-02-11 2015-06-02 Abbvie Inc. Methods and compositions for identifying, classifying and monitoring subject having Bcl-2 family inhibitor-resistant tumors and cancers
US8546399B2 (en) * 2009-05-26 2013-10-01 Abbvie Inc. Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases
CN102448959B (zh) * 2009-05-26 2015-06-17 艾伯维巴哈马有限公司 用于治疗癌症和免疫和自身免疫疾病的细胞程序死亡诱导药剂
TWI520960B (zh) * 2010-05-26 2016-02-11 艾伯維有限公司 用於治療癌症及免疫及自體免疫疾病之細胞凋亡誘導劑
MX349533B (es) 2010-10-29 2017-08-02 Abbvie Inc Dispersiones solidas que contienen un agente inductor de apoptosis.
AR083946A1 (es) * 2010-11-23 2013-04-10 Abbott Lab Metodos de tratamiento con inhibidores selectivos de bcl-2
RU2628560C2 (ru) 2010-11-23 2017-08-18 Эббви Инк. Соли и кристаллические формы индуцирующего апоптоз агента
EP3397164B1 (en) 2015-12-30 2023-05-17 Dexcom, Inc. System and method for factory calibration or reduced calibration of an indwelling sensor based on sensitivity profile
JP6651180B2 (ja) 2016-08-05 2020-02-19 ザ・リージェンツ・オブ・ザ・ユニバーシティ・オブ・ミシガンThe Regents Of The University Of Michigan Bcl−2阻害剤としてのn−(フェニルスルホニル)ベンズアミドおよび関連化合物

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JP2020007311A (ja) 2020-01-16
SMT202100025T1 (it) 2021-03-15
EP3494115B1 (en) 2020-10-21
SG10201913643YA (en) 2020-03-30
HUE053414T2 (hu) 2021-06-28
AU2017305508A1 (en) 2019-02-07
KR102376764B1 (ko) 2022-03-18
CN109311871A (zh) 2019-02-05
US10221174B2 (en) 2019-03-05
BR112019001666A2 (pt) 2019-05-28
EP3569601A2 (en) 2019-11-20
CN110483501B (zh) 2022-07-01
AU2021202113B2 (en) 2022-08-18
CY1123859T1 (el) 2022-05-27
CN110483501A (zh) 2019-11-22
KR20190035710A (ko) 2019-04-03
KR20210107170A (ko) 2021-08-31
SA519401020B1 (ar) 2022-03-16
IL282099B (en) 2022-03-01
EP4129999A1 (en) 2023-02-08
CN109311871B (zh) 2020-02-28
US20190315739A1 (en) 2019-10-17
MX381588B (es) 2025-03-12
MX2019001391A (es) 2019-06-06
SI3494115T1 (sl) 2021-02-26
US20210002277A1 (en) 2021-01-07
PE20190711A1 (es) 2019-05-17
PH12019500231A1 (en) 2019-07-29
RU2020114660A (ru) 2020-06-19
JP2019527705A (ja) 2019-10-03
LT3494115T (lt) 2021-01-25
JP7205903B2 (ja) 2023-01-17
RU2722560C1 (ru) 2020-06-01
MY199409A (en) 2023-10-25
EP3569601A3 (en) 2019-11-27
RS61821B1 (sr) 2021-06-30
CA3031419A1 (en) 2018-02-08
AU2021202113A1 (en) 2021-05-06
WO2018027097A1 (en) 2018-02-08
RU2020114660A3 (enExample) 2020-09-15
AU2017305508B2 (en) 2021-01-07
RU2744358C2 (ru) 2021-03-05
KR102429704B1 (ko) 2022-08-04
JP6651180B2 (ja) 2020-02-19
RU2020134802A (ru) 2022-04-25
US20180354950A1 (en) 2018-12-13
CA3031419C (en) 2021-08-24
US10829488B2 (en) 2020-11-10
NZ750100A (en) 2021-01-29
IL264059A (en) 2019-01-31
IL264059B (en) 2021-05-31
ES2849959T3 (es) 2021-08-24
SG11201900135YA (en) 2019-02-27
MX2020013014A (es) 2021-02-22
ZA201908466B (en) 2020-05-27
IL282099A (en) 2021-05-31
EP3569601B1 (en) 2022-06-22
PT3494115T (pt) 2021-01-15
HRP20202073T1 (hr) 2021-02-19
ZA201900240B (en) 2020-05-27
US11718613B2 (en) 2023-08-08
EP3494115A1 (en) 2019-06-12

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