AU2010294292B2 - Sulfonamides as inhibitors of Bcl-2 family proteins for the treatment of cancer - Google Patents

Sulfonamides as inhibitors of Bcl-2 family proteins for the treatment of cancer Download PDF

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Publication number
AU2010294292B2
AU2010294292B2 AU2010294292A AU2010294292A AU2010294292B2 AU 2010294292 B2 AU2010294292 B2 AU 2010294292B2 AU 2010294292 A AU2010294292 A AU 2010294292A AU 2010294292 A AU2010294292 A AU 2010294292A AU 2010294292 B2 AU2010294292 B2 AU 2010294292B2
Authority
AU
Australia
Prior art keywords
alkyl
benzenesulfonamide
methyl
butan
pharmaceutically acceptable
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
AU2010294292A
Other languages
English (en)
Other versions
AU2010294292A1 (en
Inventor
Karen Miller-Moslin
Bakary-Barry Toure
Michael Scott Visser
Naeem Yusuff
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Novartis AG
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 Novartis AG filed Critical Novartis AG
Publication of AU2010294292A1 publication Critical patent/AU2010294292A1/en
Application granted granted Critical
Publication of AU2010294292B2 publication Critical patent/AU2010294292B2/en
Ceased legal-status Critical Current
Anticipated expiration legal-status Critical

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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
    • A61K31/495—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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (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)
  • Pyridine Compounds (AREA)
AU2010294292A 2009-09-10 2010-09-08 Sulfonamides as inhibitors of Bcl-2 family proteins for the treatment of cancer Ceased AU2010294292B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US24125109P 2009-09-10 2009-09-10
US61/241,251 2009-09-10
PCT/EP2010/063169 WO2011029842A1 (en) 2009-09-10 2010-09-08 Sulfonamides as inhibitors of bcl-2 family proteins for the treatment of cancer

Publications (2)

Publication Number Publication Date
AU2010294292A1 AU2010294292A1 (en) 2012-03-01
AU2010294292B2 true AU2010294292B2 (en) 2013-07-18

Family

ID=43016684

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2010294292A Ceased AU2010294292B2 (en) 2009-09-10 2010-09-08 Sulfonamides as inhibitors of Bcl-2 family proteins for the treatment of cancer

Country Status (12)

Country Link
US (1) US8809352B2 (enExample)
EP (1) EP2475661B1 (enExample)
JP (1) JP2013504536A (enExample)
KR (1) KR20120078715A (enExample)
CN (1) CN102498111A (enExample)
AU (1) AU2010294292B2 (enExample)
BR (1) BR112012005343A2 (enExample)
CA (1) CA2772989A1 (enExample)
EA (1) EA020586B1 (enExample)
ES (1) ES2443845T3 (enExample)
MX (1) MX2012003007A (enExample)
WO (1) WO2011029842A1 (enExample)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101762724B1 (ko) * 2011-01-25 2017-07-28 더 리젠츠 오브 더 유니버시티 오브 미시건 Bcl-2/bcl-xl 억제제 및 이를 이용한 치료 방법
EA201491264A1 (ru) 2011-12-23 2014-11-28 Новартис Аг Соединения для ингибирования взаимодействия bcl-2 с партнерами по связыванию
AU2012355613A1 (en) 2011-12-23 2014-07-17 Novartis Ag Compounds for inhibiting the interaction of BCL2 with binding partners
LT6064B (lt) 2012-10-15 2014-08-25 Vilniaus Universitetas Fluorinti benzensulfonamidai kaip karboanhidrazės inhibitoriai
CA2920791C (en) 2013-10-14 2021-11-16 Eisai R&D Management Co., Ltd. Selectively substituted quinoline compounds
RS59911B1 (sr) 2013-10-14 2020-03-31 Eisai R&D Man Co Ltd Selektivno supstituisana jedinjenja hinolina
US10195213B2 (en) 2015-03-13 2019-02-05 Unity Biotechnology, Inc. Chemical entities that kill senescent cells for use in treating age-related disease
JP2018529649A (ja) * 2015-08-12 2018-10-11 メモリアル スローン ケタリング キャンサー センター フェニルスルホンアミド−ベンゾフラン誘導体およびその使用
CN108697811B (zh) 2016-01-11 2023-04-07 梅里麦克制药股份有限公司 抑制共济失调毛细血管扩张和Rad3相关蛋白(ATR)
JP2019501225A (ja) * 2016-01-11 2019-01-17 メリマック ファーマシューティカルズ インコーポレーティッド Ｂ細胞リンパ腫２（ｂｃｌ−２）及び関連タンパク質の阻害
SI3788042T1 (sl) 2018-04-29 2025-06-30 Beigene Switzerland Gmbh Zaviralci BCL-2
SG11202110742TA (en) 2019-04-02 2021-10-28 Aligos Therapeutics Inc Compounds targeting prmt5
WO2021208963A1 (en) 2020-04-15 2021-10-21 Beigene, Ltd. Bcl-2 inhibitor
US20250333409A1 (en) * 2022-06-10 2025-10-30 Hitgen Inc. Compound and use thereof in preparation of BCL-XL inhibitor

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008061208A2 (en) * 2006-11-15 2008-05-22 Genentech, Inc. Arylsulfonamide compounds

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MXPA04009141A (es) * 2002-03-21 2004-11-26 Abbott Lab Promotores de apoptosis, de n-sulfonilurea.
US20040157836A1 (en) * 2002-10-08 2004-08-12 Comess Kenneth M. Sulfonamides having antiangiogenic and anticancer activity
CA2514733A1 (en) 2003-02-28 2004-09-16 Transform Pharmaceuticals, Inc. Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothiazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen
EP1778206A4 (en) * 2004-08-20 2009-08-05 Univ Michigan SMALL MOLECULE INHIBITORS FROM MEMBERS OF THE ANTIOPTOTIC BCL-2 FAMILY AND USES THEREOF
FR2912145B1 (fr) * 2007-02-02 2009-03-06 Servier Lab Nouveaux derives tricycliques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008061208A2 (en) * 2006-11-15 2008-05-22 Genentech, Inc. Arylsulfonamide compounds

Also Published As

Publication number Publication date
CA2772989A1 (en) 2011-03-17
US8809352B2 (en) 2014-08-19
MX2012003007A (es) 2012-04-11
EP2475661A1 (en) 2012-07-18
AU2010294292A1 (en) 2012-03-01
ES2443845T3 (es) 2014-02-20
EA020586B1 (ru) 2014-12-30
US20120165298A1 (en) 2012-06-28
EP2475661B1 (en) 2013-10-23
JP2013504536A (ja) 2013-02-07
BR112012005343A2 (pt) 2016-03-22
EA201200472A1 (ru) 2012-10-30
WO2011029842A1 (en) 2011-03-17
KR20120078715A (ko) 2012-07-10
CN102498111A (zh) 2012-06-13

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Date Code Title Description
FGA Letters patent sealed or granted (standard patent)
MK14 Patent ceased section 143(a) (annual fees not paid) or expired