AU2009333433B2 - Compounds useful for inhibiting Chk1 - Google Patents

Compounds useful for inhibiting Chk1 Download PDF

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Publication number
AU2009333433B2
AU2009333433B2 AU2009333433A AU2009333433A AU2009333433B2 AU 2009333433 B2 AU2009333433 B2 AU 2009333433B2 AU 2009333433 A AU2009333433 A AU 2009333433A AU 2009333433 A AU2009333433 A AU 2009333433A AU 2009333433 B2 AU2009333433 B2 AU 2009333433B2
Authority
AU
Australia
Prior art keywords
cancer
compound
salt
pyrazol
ylamino
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
AU2009333433A
Other languages
English (en)
Other versions
AU2009333433A1 (en
Inventor
Francine S. Farouz
Ryan Coatsworth Holcomb
Ramesh Kasar
Steven Scott Myers
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.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
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 Eli Lilly and Co filed Critical Eli Lilly and Co
Publication of AU2009333433A1 publication Critical patent/AU2009333433A1/en
Application granted granted Critical
Publication of AU2009333433B2 publication Critical patent/AU2009333433B2/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
    • 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
    • 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
    • A61K31/4965—Non-condensed pyrazines
    • A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/10—Drugs for disorders of the urinary system of the bladder
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (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)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Urology & Nephrology (AREA)
  • Dermatology (AREA)
  • Pulmonology (AREA)
  • Endocrinology (AREA)
  • Reproductive Health (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
AU2009333433A 2008-12-17 2009-12-10 Compounds useful for inhibiting Chk1 Ceased AU2009333433B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US13817608P 2008-12-17 2008-12-17
US61/138,176 2008-12-17
PCT/US2009/067437 WO2010077758A1 (en) 2008-12-17 2009-12-10 Compounds useful for inhibiting chk1

Publications (2)

Publication Number Publication Date
AU2009333433A1 AU2009333433A1 (en) 2011-06-30
AU2009333433B2 true AU2009333433B2 (en) 2012-06-14

Family

ID=42079067

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2009333433A Ceased AU2009333433B2 (en) 2008-12-17 2009-12-10 Compounds useful for inhibiting Chk1

Country Status (37)

Country Link
EP (1) EP2379532B1 (OSRAM)
JP (1) JP5705743B2 (OSRAM)
KR (1) KR101301777B1 (OSRAM)
CN (1) CN102245597B (OSRAM)
AR (1) AR074471A1 (OSRAM)
AU (1) AU2009333433B2 (OSRAM)
BR (1) BRPI0922468A2 (OSRAM)
CA (1) CA2746423C (OSRAM)
CL (1) CL2011001463A1 (OSRAM)
CO (1) CO6382122A2 (OSRAM)
CR (1) CR20110339A (OSRAM)
CY (1) CY1113930T1 (OSRAM)
DK (1) DK2379532T3 (OSRAM)
DO (1) DOP2011000185A (OSRAM)
EA (1) EA018118B1 (OSRAM)
EC (1) ECSP11011136A (OSRAM)
ES (1) ES2401558T3 (OSRAM)
HN (1) HN2011001446A (OSRAM)
HR (1) HRP20130167T1 (OSRAM)
IL (1) IL213160A (OSRAM)
JO (1) JO2886B1 (OSRAM)
MA (1) MA32901B1 (OSRAM)
MX (1) MX2011006603A (OSRAM)
MY (1) MY156998A (OSRAM)
NZ (1) NZ593440A (OSRAM)
PA (1) PA8850801A1 (OSRAM)
PE (1) PE20120077A1 (OSRAM)
PL (1) PL2379532T3 (OSRAM)
PT (1) PT2379532E (OSRAM)
RS (1) RS52739B (OSRAM)
SG (1) SG172222A1 (OSRAM)
SI (1) SI2379532T1 (OSRAM)
TN (1) TN2011000298A1 (OSRAM)
TW (1) TWI436996B (OSRAM)
UA (1) UA101998C2 (OSRAM)
WO (1) WO2010077758A1 (OSRAM)
ZA (1) ZA201103946B (OSRAM)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8314108B2 (en) * 2008-12-17 2012-11-20 Eli Lilly And Company 5-(5-(2-(3-aminopropoxy)-6-methoxyphenyl)-1H-pyrazol-3-ylamino)pyrazine-2-carbonitrile, pharmaceutically acceptable salts thereof, or solvate of salts
JO3145B1 (ar) * 2010-11-08 2017-09-20 Lilly Co Eli مركبات مفيدة لتثبيط chk1
GB201402277D0 (en) * 2014-02-10 2014-03-26 Sentinel Oncology Ltd Pharmaceutical compounds
TWI725041B (zh) * 2015-07-23 2021-04-21 美商美國禮來大藥廠 用於治療神經母細胞瘤及/或軟組織肉瘤之chk1/2抑制劑
AR106772A1 (es) * 2015-12-07 2018-02-14 Lilly Co Eli Sales de (s)-lactato
US20180228795A1 (en) * 2015-12-15 2018-08-16 Eli Lilly And Company Combination therapy for cancer
CN108601781B (zh) * 2016-02-04 2019-11-22 广州必贝特医药技术有限公司 作为检测点激酶1(chk1)抑制剂的3,5-二取代吡唑及其制备及应用
US20200108074A1 (en) 2017-03-31 2020-04-09 Seattle Genetics, Inc. Combinations of chk1- and wee1- inhibitors
EP3461480A1 (en) 2017-09-27 2019-04-03 Onxeo Combination of a dna damage response cell cycle checkpoint inhibitors and belinostat for treating cancer
CN112457306A (zh) 2019-09-06 2021-03-09 上海瑛派药业有限公司 3,5-二取代吡唑化合物作为激酶抑制剂及其应用
CN114746413B (zh) * 2019-11-29 2024-02-23 南京明德新药研发有限公司 二氮杂吲哚类衍生物及其作为Chk1抑制剂的应用
WO2021119236A1 (en) 2019-12-10 2021-06-17 Seagen Inc. Preparation of a chk1 inhibitor compound
MX2023006364A (es) 2020-11-30 2023-06-13 Sumitomo Pharma Co Ltd Derivado de 5-heteroaril-1h-pirazol-3-amina.
US11564920B2 (en) 2020-11-30 2023-01-31 Sumitomo Pharma Co., Ltd. 5-heteroaryl-1H-pyrazol-3-amine derivative
JP2024520481A (ja) * 2021-05-27 2024-05-24 バウンドレス バイオ，インク． チェックポイントキナーゼ１（ｃｈｋ１）阻害剤およびその使用
GB202107932D0 (en) 2021-06-03 2021-07-21 Sentinel Oncology Ltd Preparation of a CHK1 Inhibitor Compound
GB202107924D0 (en) 2021-06-03 2021-07-21 Sentinel Oncology Ltd A pharmaceutical salt
EP4455134A4 (en) 2021-12-24 2025-10-08 Sumitomo Pharma Co Ltd 1H-PYRAZOLE-3-AMINE DERIVATIVE HAVING A BICYCLIC SKELETON
CN119403571A (zh) * 2022-05-27 2025-02-07 住友制药株式会社 对免疫检查点抑制剂示出治疗抗性的癌症的治疗药
JP7546104B2 (ja) * 2022-05-27 2024-09-05 住友ファーマ株式会社 ５－ヘテロアリール－１ｈ－ピラゾール－３－アミン誘導体からなる医薬
GB202213792D0 (en) 2022-09-21 2022-11-02 Benevolentai Bio Ltd New compounds and method
GB202403910D0 (en) 2024-03-19 2024-05-01 Benovental Cambridge Ltd New processes and intermediates for pharmaceutical products

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005009435A1 (en) * 2003-07-25 2005-02-03 Pfizer Inc. Aminopyrazole compounds and use as chk1 inhibitors
WO2008117050A1 (en) * 2007-03-27 2008-10-02 Astrazeneca Ab Pyrazolyl-amino-substituted pyrazines and their use for the treatment of cancer

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040034038A1 (en) * 2002-08-13 2004-02-19 Goaquan Li Urea kinase inhibitors
US20090270418A1 (en) * 2008-01-09 2009-10-29 Marianne Sloss Pyrazole pyrazine amine compounds as kinase inhibitors, compositions thereof and methods of treatment therewith

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005009435A1 (en) * 2003-07-25 2005-02-03 Pfizer Inc. Aminopyrazole compounds and use as chk1 inhibitors
WO2008117050A1 (en) * 2007-03-27 2008-10-02 Astrazeneca Ab Pyrazolyl-amino-substituted pyrazines and their use for the treatment of cancer

Also Published As

Publication number Publication date
JO2886B1 (en) 2015-03-15
KR101301777B1 (ko) 2013-08-30
MA32901B1 (fr) 2011-12-01
DK2379532T3 (da) 2013-03-18
MY156998A (en) 2016-04-15
CL2011001463A1 (es) 2012-01-20
DOP2011000185A (es) 2017-12-15
CA2746423A1 (en) 2010-07-08
PL2379532T3 (pl) 2013-07-31
HRP20130167T1 (hr) 2013-03-31
CO6382122A2 (es) 2012-02-15
IL213160A (en) 2013-12-31
CA2746423C (en) 2014-01-14
EA018118B1 (ru) 2013-05-30
PE20120077A1 (es) 2012-02-06
EP2379532B1 (en) 2013-02-20
UA101998C2 (ru) 2013-05-27
RS52739B (sr) 2013-08-30
NZ593440A (en) 2013-02-22
TN2011000298A1 (en) 2012-12-17
ES2401558T3 (es) 2013-04-22
HK1160110A1 (en) 2012-08-10
EP2379532A1 (en) 2011-10-26
SI2379532T1 (sl) 2013-05-31
PT2379532E (pt) 2013-03-25
AU2009333433A1 (en) 2011-06-30
JP5705743B2 (ja) 2015-04-22
EA201170834A1 (ru) 2011-12-30
ECSP11011136A (es) 2011-07-29
JP2012512249A (ja) 2012-05-31
CY1113930T1 (el) 2016-07-27
MX2011006603A (es) 2011-09-27
CN102245597A (zh) 2011-11-16
AR074471A1 (es) 2011-01-19
BRPI0922468A2 (pt) 2020-08-04
ZA201103946B (en) 2012-10-31
KR20110084539A (ko) 2011-07-25
HN2011001446A (es) 2013-08-05
TW201029994A (en) 2010-08-16
CR20110339A (es) 2011-09-14
WO2010077758A1 (en) 2010-07-08
SG172222A1 (en) 2011-07-28
TWI436996B (zh) 2014-05-11
CN102245597B (zh) 2014-04-16
PA8850801A1 (es) 2010-07-27
IL213160A0 (en) 2011-07-31

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Legal Events

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