SI3494115T1 - Derivati N-(fenilsulfonil)benzamida kot BCL-2 inhibitorji - Google Patents

Derivati N-(fenilsulfonil)benzamida kot BCL-2 inhibitorji

Info

Publication number
SI3494115T1
SI3494115T1 SI201730535T SI201730535T SI3494115T1 SI 3494115 T1 SI3494115 T1 SI 3494115T1 SI 201730535 T SI201730535 T SI 201730535T SI 201730535 T SI201730535 T SI 201730535T SI 3494115 T1 SI3494115 T1 SI 3494115T1
Authority
SI
Slovenia
Prior art keywords
phenylsulfonyl
bcl
inhibitors
benzamide derivatives
benzamide
Prior art date
Application number
SI201730535T
Other languages
English (en)
Slovenian (sl)
Inventor
Shaomeng Wang
Jianyong Chen
Original Assignee
The Regents Of The University Of Michigan Office Of Technology Transfer
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 The Regents Of The University Of Michigan Office Of Technology Transfer filed Critical The Regents Of The University Of Michigan Office Of Technology Transfer
Publication of SI3494115T1 publication Critical patent/SI3494115T1/sl

Links

Classifications

    • 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

Landscapes

  • 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)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (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)
SI201730535T 2016-08-05 2017-08-04 Derivati N-(fenilsulfonil)benzamida kot BCL-2 inhibitorji SI3494115T1 (sl)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201662371504P 2016-08-05 2016-08-05
US201762454101P 2017-02-03 2017-02-03
EP17754889.8A EP3494115B1 (en) 2016-08-05 2017-08-04 N-(phenylsulfonyl)benzamide derivatives as bcl-2 inhibitors
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
SI3494115T1 true SI3494115T1 (sl) 2021-02-26

Family

ID=59677319

Family Applications (1)

Application Number Title Priority Date Filing Date
SI201730535T SI3494115T1 (sl) 2016-08-05 2017-08-04 Derivati N-(fenilsulfonil)benzamida kot BCL-2 inhibitorji

Country Status (27)

Country Link
US (3) US10829488B2 (enExample)
EP (3) EP4129999A1 (enExample)
JP (2) JP6651180B2 (enExample)
KR (2) KR102429704B1 (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) SG11201900135YA (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
US11001582B2 (en) * 2016-03-10 2021-05-11 Assia Chemical Industries Ltd. Solid state forms of Venetoclax and processes for preparation of Venetoclax
RU2744358C2 (ru) * 2016-08-05 2021-03-05 Дзе Риджентс Оф Дзе Юниверсити Оф Мичиган N-(фенилсульфонил) бензамиды и родственные соединения в качестве ингибиторов bcl-2
WO2018127130A1 (en) 2017-01-07 2018-07-12 Shanghai Fochon Pharmaceutical Co., Ltd. Compounds as bcl-2-selective apoptosis-inducing agents
MX391501B (es) 2017-04-18 2025-03-21 Fochon Pharmaceuticals Ltd Agentes inductores de apoptosis
CN112437772B (zh) 2018-04-29 2023-11-21 百济神州有限公司 Bcl-2抑制剂
EA202091963A1 (ru) 2018-07-31 2021-05-13 Эсентейдж Фарма (Сучжоу) Ко., Лтд. СИНЕРГИЧЕСКИЙ ПРОТИВООПУХОЛЕВЫЙ ЭФФЕКТ ИНГИБИТОРА Bcl-2 В СОЧЕТАНИИ С РИТУКСИМАБОМ И/ИЛИ БЕНДАМУСТИНОМ ИЛИ ИНГИБИТОРА Bcl-2 В СОЧЕТАНИИ С CHOP
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
CN114522167A (zh) 2018-07-31 2022-05-24 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
TWI752335B (zh) * 2018-07-31 2022-01-11 大陸商蘇州亞盛藥業有限公司 Bcl-2抑制劑與MDM2抑制劑的組合產品及其在預防及/或治療疾病中的用途
TWI732353B (zh) * 2018-11-23 2021-07-01 大陸商蘇州亞盛藥業有限公司 藥物組成物及其用途
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
WO2021000899A1 (en) * 2019-07-02 2021-01-07 Ascentage Pharma (Suzhou) Co., Ltd. A PHARMACEUTICAL COMBINATION CONTAINING mTOR INHIBITOR AND USE THEREOF
TW202114664A (zh) * 2019-07-31 2021-04-16 大陸商蘇州亞盛藥業有限公司 Bcl-2/Bcl-xL抑制劑與化療藥的組合產品及其在預防和/或治療疾病中的用途
CN114929689B (zh) 2019-10-28 2024-08-27 百济神州有限公司 Bcl-2抑制剂
US12287338B2 (en) 2019-11-27 2025-04-29 Ascentage Pharma (Suzhou) Co., Ltd. Method and compositions for predicting anti-cancer efficacy of compounds targeting apoptosis pathway
CN119097631A (zh) * 2019-12-03 2024-12-10 苏州亚盛药业有限公司 作为bcl-2抑制剂的n-(苯基磺酰基)苯甲酰胺及相关化合物
TWI777321B (zh) * 2019-12-04 2022-09-11 大陸商蘇州亞盛藥業有限公司 藥物組合及其用途
JP7142173B2 (ja) 2019-12-06 2022-09-26 ロクソ オンコロジー, インコーポレイテッド ブルトン型チロシンキナーゼ阻害剤の投薬
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
CN115244051B (zh) * 2020-03-12 2024-10-18 南京明德新药研发有限公司 苯并五元环类化合物
US12286430B2 (en) 2020-04-15 2025-04-29 Beigene, Ltd. Bcl-2 inhibitor
WO2021227763A1 (en) * 2020-05-14 2021-11-18 Ascentage Pharma (Suzhou) Co., Ltd. Hplc analysis method for n- (phenylsulfonyl) benzamide compound
US20230159524A1 (en) * 2020-07-01 2023-05-25 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
AU2021306781A1 (en) 2020-07-10 2023-03-02 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
US20230301989A1 (en) * 2020-08-21 2023-09-28 Ascentage Pharma (Suzhou) Co., Ltd. Compositions and methods for treating systemic lupus erythematosus
JP2023551056A (ja) * 2020-11-25 2023-12-06 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 固体分散体、医薬製剤、その製造方法及び応用
CN114681458B (zh) * 2020-12-28 2023-07-18 苏州亚盛药业有限公司 治疗多发性硬化症的方法
WO2022161496A1 (en) * 2021-02-01 2022-08-04 Ascentage Pharma (Suzhou) Co., Ltd. Sulfonyl benzamide derivatives as bcl-2 inhibitors
WO2022216942A1 (en) 2021-04-07 2022-10-13 Dana-Farber Cancer Institute, Inc. Compositions and methods for the treatment of cancer
WO2023011488A1 (zh) 2021-08-02 2023-02-09 苏州亚盛药业有限公司 一种药物组合及其用途
WO2023104043A1 (zh) * 2021-12-06 2023-06-15 杭州和正医药有限公司 一种抗凋亡蛋白bcl-2抑制剂、药物组合物及其应用
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
WO2005049593A2 (en) 2003-11-13 2005-06-02 Abbott Laboratories N-acylsulfonamide apoptosis promoters
US7767684B2 (en) * 2003-11-13 2010-08-03 Abbott Laboratories Apoptosis promoters
US8624027B2 (en) 2005-05-12 2014-01-07 Abbvie Inc. Combination therapy for treating cancer and diagnostic assays for use therein
CN101534904B (zh) 2006-09-05 2013-11-06 Abbvie公司 治疗血小板过量的bcl抑制剂
KR20090087491A (ko) 2006-12-04 2009-08-17 아보트 러보러터리즈 암 치료요법을 위한 동반 진단 검정
UA108193C2 (uk) * 2008-12-04 2015-04-10 Апоптозіндукуючий засіб для лікування раку і імунних і аутоімунних захворювань
DK2376480T3 (en) 2008-12-05 2016-09-12 Abbvie Inc Sulfonamide derivatives AS BCL-2-selective apoptosis inducing agents for the treatment of cancer and immune diseases
NZ593594A (en) 2009-01-19 2013-08-30 Abbvie Inc Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
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
CA2929347A1 (en) * 2009-05-26 2010-12-02 Milan Bruncko (hetero)aryl substituted sulfonyl-2-(1h-pyrrolo[2,3-b]pyridine-5-oxy)benzamide compounds and their use as apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US8546399B2 (en) * 2009-05-26 2013-10-01 Abbvie Inc. Apoptosis inducing agents for the treatment of cancer and immune and autoimmune diseases
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
SG10201801794WA (en) 2010-10-29 2018-04-27 Abbvie Inc Solid dispersions containing an apoptosis-inducing agent
KR101923364B1 (ko) 2010-11-23 2018-11-30 애브비 인코포레이티드 아폽토시스­유도제의 염 및 결정형
MY165884A (en) 2010-11-23 2018-05-18 Abbvie Ireland Unlimited Co Methods of treatment using selective bcl-2 inhibitors
US10362975B2 (en) 2015-12-30 2019-07-30 Dexcom, Inc. System and method for factory calibration or reduced calibration of an indwelling sensor based on sensitivity profile and baseline model of sensors
RU2744358C2 (ru) * 2016-08-05 2021-03-05 Дзе Риджентс Оф Дзе Юниверсити Оф Мичиган N-(фенилсульфонил) бензамиды и родственные соединения в качестве ингибиторов bcl-2

Also Published As

Publication number Publication date
JP2019527705A (ja) 2019-10-03
US10221174B2 (en) 2019-03-05
MX2020013014A (es) 2021-02-22
EP4129999A1 (en) 2023-02-08
SA519401020B1 (ar) 2022-03-16
CN109311871A (zh) 2019-02-05
RS61821B1 (sr) 2021-06-30
IL282099A (en) 2021-05-31
CN110483501A (zh) 2019-11-22
US11718613B2 (en) 2023-08-08
EP3494115B1 (en) 2020-10-21
MX381588B (es) 2025-03-12
ES2849959T3 (es) 2021-08-24
US10829488B2 (en) 2020-11-10
AU2017305508A1 (en) 2019-02-07
RU2020114660A3 (enExample) 2020-09-15
HRP20202073T1 (hr) 2021-02-19
JP7205903B2 (ja) 2023-01-17
SMT202100025T1 (it) 2021-03-15
SG11201900135YA (en) 2019-02-27
ZA201908466B (en) 2020-05-27
RU2020134802A (ru) 2022-04-25
KR20190035710A (ko) 2019-04-03
RU2020114660A (ru) 2020-06-19
PE20190711A1 (es) 2019-05-17
PT3494115T (pt) 2021-01-15
KR102429704B1 (ko) 2022-08-04
RU2744358C2 (ru) 2021-03-05
ZA201900240B (en) 2020-05-27
AU2021202113B2 (en) 2022-08-18
MY199409A (en) 2023-10-25
HUE053414T2 (hu) 2021-06-28
KR102376764B1 (ko) 2022-03-18
BR112019001666A2 (pt) 2019-05-28
EP3569601A3 (en) 2019-11-27
EP3494115A1 (en) 2019-06-12
JP2020007311A (ja) 2020-01-16
JP6651180B2 (ja) 2020-02-19
PH12019500231A1 (en) 2019-07-29
WO2018027097A1 (en) 2018-02-08
CN109311871B (zh) 2020-02-28
LT3494115T (lt) 2021-01-25
AU2017305508B2 (en) 2021-01-07
DK3494115T3 (da) 2021-01-18
CN110483501B (zh) 2022-07-01
CA3031419C (en) 2021-08-24
IL282099B (en) 2022-03-01
CY1123859T1 (el) 2022-05-27
IL264059A (en) 2019-01-31
EP3569601B1 (en) 2022-06-22
MX2019001391A (es) 2019-06-06
US20180354950A1 (en) 2018-12-13
KR20210107170A (ko) 2021-08-31
EP3569601A2 (en) 2019-11-20
AU2021202113A1 (en) 2021-05-06
CA3031419A1 (en) 2018-02-08
SG10201913643YA (en) 2020-03-30
RU2722560C1 (ru) 2020-06-01
IL264059B (en) 2021-05-31
NZ750100A (en) 2021-01-29
US20190315739A1 (en) 2019-10-17
US20210002277A1 (en) 2021-01-07

Similar Documents

Publication Publication Date Title
IL282099B (en) N-(phenylsulfonyl)benzamides and related compounds as bcl–2 inhibitors
IL272910A (en) Ectonucleotide pyrophosphate-phosphodiesterase 1 (ENPP-1) inhibitors and their uses
LT3788042T (lt) Bcl-2 inhibitoriai
DK3298002T3 (da) Heterocykliske amider som kinasehæmmere
IL263739B (en) History of n-(converted-phenyl)-sulfonamide as kinase inhibitors
DK3672976T3 (da) Bcl-2-hæmmere
DK3328849T3 (da) 1,1,1-trifluor-3-hydroxypropan-2-yl-carbamat-derivater og 1,1,1-trifluor-4-hydroxybutan-2-yl-carbamat-derivater som magl-inhibitorer
DK3442947T3 (da) Aminsubstituerede aryl- eller heteroarylforbindelser som ehmt1- og ehmt2-hæmmere
DK3440076T3 (da) Heterocykliske amider, der kan anvendes som proteinmodulatorer
DK3277681T3 (da) Imidazolonylquinoliner og deres anvendelse som atm-kinaseinhibitorer
DK3455204T3 (da) Cyklopropyl-amid-forbindelser som dobbelte lsd1/hdac-hæmmere
HUE058009T2 (hu) 1,3-Tiazol-2-il szubsztituált benzamid-származékok
DK3105218T3 (da) Cyclopropylaminer som lsd1-inhibitorer
DK3105226T3 (da) Cyclopropylaminer som lsd1-inhibitorer
IL252089B (en) 2-amino-6-(difluoromethyl)- 5,5-difluoro-6-phenyl-3,4,5,6-tetrahydropyridines as bace1 inhibitors
ZA201900606B (en) Novel pyrazole derivative as alk5 inhibitor and uses thereof
IL304547A (en) 3-substituted benzamide derivatives as kinase inhibitors
DK3724196T3 (da) Substituerede azetidindihydrothienopyridiner og anvendelse deraf som phosphodiesterasehæmmere
DK3126354T3 (da) Halogenerede quinazolin-thf-aminer som pde1-inhibitorer
DK3319970T3 (da) Pyrido-oxazinonderivater som tnap-hæmmere
DK3712162T3 (da) Smac-mimetica anvendt som iap-inhibitorer og anvendelse deraf
DK3277682T3 (da) 6-morpholinyl-2-pyrazolyl-9h-purinderivater og anvendelse heraf som pi3k- hæmmere
DK3551634T3 (da) Substituerede pyrazoloazepin-8-oner og anvendelse deraf som phosphodiesterasehæmmere
DK3551633T3 (da) Substituerede pyrazoloazepin-4-oner og anvendelse deraf som phosphodiesterasehæmmere
ZA202002786B (en) Indole (sulfomyl) n-hydroxy benzamide derivatives as selective hdac inhibitors