CN104159887A - 酰基-腙和噁二唑化合物、含有它们的药物组合物及其用途 - Google Patents

酰基-腙和噁二唑化合物、含有它们的药物组合物及其用途 Download PDF

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Publication number
CN104159887A
CN104159887A CN201280063518.9A CN201280063518A CN104159887A CN 104159887 A CN104159887 A CN 104159887A CN 201280063518 A CN201280063518 A CN 201280063518A CN 104159887 A CN104159887 A CN 104159887A
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China
Prior art keywords
phenyl
compounds
och
compound
leukemia
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CN201280063518.9A
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English (en)
Chinese (zh)
Inventor
R·J·尼内丝
A·马斯卡雷洛
R·A·尤尼斯
T·R·斯顿夫
P·C·莱亚尔
J·A·尤尼斯
C·佩雷拉·德·索萨·梅洛
R·R·卡内瓦罗洛
L·多梅内吉尼·基亚拉迪亚
A·博尔托利尼·西尔韦拉
A·B·A·拉兰热拉
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Universidade Federal de Santa Catarina
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Universidade Federal de Santa Catarina
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Publication of CN104159887A publication Critical patent/CN104159887A/zh
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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
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/166Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/22Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/38Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/381Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/41641,3-Diazoles
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4245Oxadiazoles
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C243/00Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
    • C07C243/24Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
    • C07C243/38Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C251/00Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C251/72Hydrazones
    • C07C251/86Hydrazones having doubly-bound carbon atoms of hydrazone groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D271/00Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
    • C07D271/02Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/101,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
    • C07D271/1071,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with two aryl or substituted aryl radicals attached in positions 2 and 5
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30Hetero atoms other than halogen
    • C07D333/36Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/42Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms with nitro or nitroso radicals directly attached to ring carbon atoms

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (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)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Oncology (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)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
CN201280063518.9A 2011-11-25 2012-11-26 酰基-腙和噁二唑化合物、含有它们的药物组合物及其用途 Pending CN104159887A (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
BRPI1107312-8A BRPI1107312B1 (pt) 2011-11-25 2011-11-25 Composto de acil-hidrazona
BRPI1107312-8 2011-11-25
PCT/BR2012/000480 WO2013075199A1 (pt) 2011-11-25 2012-11-26 "compostos acil-hidrazonas e oxadiazóis, composições farmacêuticas compreendendo os mesmos e seus usos

Publications (1)

Publication Number Publication Date
CN104159887A true CN104159887A (zh) 2014-11-19

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CN201280063518.9A Pending CN104159887A (zh) 2011-11-25 2012-11-26 酰基-腙和噁二唑化合物、含有它们的药物组合物及其用途

Country Status (9)

Country Link
US (1) US20150191445A1 (enExample)
EP (1) EP2784061B1 (enExample)
JP (1) JP2015504432A (enExample)
KR (1) KR102189562B1 (enExample)
CN (1) CN104159887A (enExample)
BR (2) BRPI1107312B1 (enExample)
CA (1) CA2869807C (enExample)
RU (1) RU2664327C2 (enExample)
WO (1) WO2013075199A1 (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110498809A (zh) * 2018-05-17 2019-11-26 香港科技大学深圳研究院 基于酰腙配体类的有机硼化合物及其制备方法和应用
CN113336729A (zh) * 2021-05-31 2021-09-03 四川大学华西医院 硝呋齐特类衍生物及其制备方法和用途

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101719541B1 (ko) 2015-08-13 2017-03-24 연세대학교 산학협력단 항암용 약학 조성물 및 ano1 활성억제제
KR20170141542A (ko) * 2016-06-15 2017-12-26 국립암센터 위암을 예방 및 치료하는 rhoa 억제제의 약학적 조성물
KR102131331B1 (ko) 2018-09-19 2020-07-07 연세대학교 산학협력단 항암용 신규 약학 조성물 및 ano1 활성억제제

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4760021A (en) * 1983-11-14 1988-07-26 Director-General Of Agency Of Industrial Science & Technology Biological response modifier having cell differentiation-induction activity and process for production thereof
EP0400464A1 (en) * 1989-06-01 1990-12-05 Health Research, Inc. Monoclonal antibody reactive to a unique antigen widely present on various human leukemia and lymphoma cells and methods of using same for diagnosis and treatment
CN1081909A (zh) * 1992-04-15 1994-02-16 安姆根有限公司 在减少副作用的条件下用干扰素治疗疾病的方法和制剂
CN1159324A (zh) * 1995-12-20 1997-09-17 日本脏器制药株式会社 活性氧、自由基去除剂

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2400996A1 (en) 2002-09-03 2004-03-03 Lisa Mckerracher 1,4-substituted cyclohexane derivatives
KR101155883B1 (ko) 2003-12-23 2012-06-20 아제닉스 유에스에이 인코포레이티드 사이클린 의존적 키나제 저해제, 그 조성물 및 그의 용도
DE102004010207A1 (de) 2004-03-02 2005-09-15 Aventis Pharma S.A. Neue 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate
WO2005097763A2 (en) * 2004-04-01 2005-10-20 Aventis Pharmaceuticals Inc. 1,3,4-oxadiazol-2-ones as ppar delta
AR052559A1 (es) 2005-01-21 2007-03-21 Astex Therapeutics Ltd Derivados de pirazol para inhibir cdk's y gsk's
WO2006101937A1 (en) 2005-03-18 2006-09-28 Janssen Pharmaceutica N.V. Acylhydrazones as kinase modulators
CN1824657A (zh) * 2006-04-05 2006-08-30 贵州大学 3-取代-2-芳基取代-5-(3,4,5-三烷氧基苯基)-1,3,4-噁二唑衍生物及制备方法和用途
US20110189306A1 (en) * 2010-01-13 2011-08-04 Norbert Kartner COMPOUNDS, COMPOSITIONS AND TREATMENTS FOR V-ATPase RELATED DISEASES

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4760021A (en) * 1983-11-14 1988-07-26 Director-General Of Agency Of Industrial Science & Technology Biological response modifier having cell differentiation-induction activity and process for production thereof
EP0400464A1 (en) * 1989-06-01 1990-12-05 Health Research, Inc. Monoclonal antibody reactive to a unique antigen widely present on various human leukemia and lymphoma cells and methods of using same for diagnosis and treatment
CN1081909A (zh) * 1992-04-15 1994-02-16 安姆根有限公司 在减少副作用的条件下用干扰素治疗疾病的方法和制剂
CN1159324A (zh) * 1995-12-20 1997-09-17 日本脏器制药株式会社 活性氧、自由基去除剂

Non-Patent Citations (10)

* Cited by examiner, † Cited by third party
Title
DEISE M.BORCHHARDT等: "Biochemical Evaluation of a Series of Synthetic Chalcone and Hydrazide Derivatives as Novel Inhibitors of Cruzain from Trypanosoma cruzi", 《J.BRAZ.CHEM.SOC.》 *
LAUREN LEE等: "Design, Synthesis, and Biological Evaluations of 2,5-diaryl-2,3-dihydro-1,3,4-oxadiazoline analogs of combretastatin-A4", 《JOURNAL OF MEDICINAL CHEMISTRY》 *
LINHONG JIN等: "Synthesis, structure, and bioactivity of N´-substituted benzylidene-3,4,5-trimethoxybenzohydrazide and 3-acetyl-2-substituted phenyl-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazole derivatives", 《BIOORGANIC & MEDICINAL CHEMISTRY LETTERS》 *
LINHONG JIN等: "Synthesis, structure, and bioactivity of N´-substituted benzylidene-3,4,5-trimethoxybenzohydrazide and 3-acetyl-2-substituted phenyl-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazole derivatives", 《BIOORGANIC & MEDICINAL CHEMISTRY LETTERS》, vol. 16, 31 December 2006 (2006-12-31), pages 5037 - 1 *
MAZZONE,G.;ARRIGO REINA,R.: "3,4,5-Trimethoxybenzoyl hydrazides and their anti-MAO [monoamine oxidase] activity", 《BOLLETTINO DELLE SEDUTE DELLA ACCADEMIA GIOENIA DI SCIENZE NATURALI IN CATANIA》 *
MAZZONE,G.等: "2,5-diaryl-substituted 1,3,4-oxadiazoles: synthesis and preliminary pharmacological research", 《FARMACO》 *
SHEHATA,I.A.等: "Synthesis and biological testing of certain 1,3,4-oxadiazole and 1,2,4-triazole derivatives as potential antimicrobial agents", 《SCIENTIA PHARMACEUTICA》 *
THAÍS MOREIRA OSÓRIO等: "Antibacterial activity of chalcones, hydrazones and oxadiazoles against methicillin-resistant Staphylococcus aureus", 《BIOORGANIC & MEDICINAL CHEMISTRY LETTERS》 *
XIU-FANG CAO等: "Synthesis and Biological Activity of a Series of Novel N-Substituted β-Lactams Derived from Natural Gallic Acid", 《JOURNAL OF THE CHINESE CHEMICAL SOCIETY》 *
ZHAO WANG等: "Identifying Novel Molecular Structures for Advanced Melanoma by Ligand-Based Virtual Screening", 《J.CHEM.INF.MODEL.》 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110498809A (zh) * 2018-05-17 2019-11-26 香港科技大学深圳研究院 基于酰腙配体类的有机硼化合物及其制备方法和应用
CN110498809B (zh) * 2018-05-17 2022-04-05 香港科技大学深圳研究院 基于酰腙配体类的有机硼化合物及其制备方法和应用
CN113336729A (zh) * 2021-05-31 2021-09-03 四川大学华西医院 硝呋齐特类衍生物及其制备方法和用途
CN113336729B (zh) * 2021-05-31 2022-05-27 四川大学华西医院 硝呋齐特类衍生物及其制备方法和用途

Also Published As

Publication number Publication date
US20150191445A1 (en) 2015-07-09
RU2014125519A (ru) 2015-12-27
BRPI1107312B1 (pt) 2021-09-08
CA2869807A1 (en) 2013-05-30
CA2869807C (en) 2021-03-09
JP2015504432A (ja) 2015-02-12
EP2784061A4 (en) 2015-05-27
KR102189562B1 (ko) 2020-12-14
BRPI1107312A2 (pt) 2016-09-20
RU2664327C2 (ru) 2018-08-16
EP2784061A1 (en) 2014-10-01
EP2784061B1 (en) 2018-11-07
KR20140112489A (ko) 2014-09-23
BR112014012582A2 (pt) 2017-06-06
WO2013075199A1 (pt) 2013-05-30

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Application publication date: 20141119