[go: up one dir, main page]

MD4349C1 - Соединение N-(3-метоксифенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамид - ингибитор пролиферации клеток MeW-164 меланомы человека - Google Patents

Соединение N-(3-метоксифенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамид - ингибитор пролиферации клеток MeW-164 меланомы человека Download PDF

Info

Publication number
MD4349C1
MD4349C1 MDA20140062A MD20140062A MD4349C1 MD 4349 C1 MD4349 C1 MD 4349C1 MD A20140062 A MDA20140062 A MD A20140062A MD 20140062 A MD20140062 A MD 20140062A MD 4349 C1 MD4349 C1 MD 4349C1
Authority
MD
Moldova
Prior art keywords
human melanoma
ylmethylene
mew
methoxyphenyl
compound
Prior art date
Application number
MDA20140062A
Other languages
English (en)
Romanian (ro)
Other versions
MD4349B1 (ru
Inventor
Аурелиан ГУЛЯ
Анджей ЛИПКОВСКИЙ
Ольга ГАРБУЗ
Джоанна МАТАЛИНСКА
Виктор ЦАПКОВ
Original Assignee
Государственный Университет Молд0
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 Государственный Университет Молд0 filed Critical Государственный Университет Молд0
Priority to MDA20140062A priority Critical patent/MD4349C1/ru
Publication of MD4349B1 publication Critical patent/MD4349B1/ru
Publication of MD4349C1 publication Critical patent/MD4349C1/ru

Links

Landscapes

  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

Изобретение относится к химии и медицине, а именно к органическому соединению класса тиоамидов, который может найти применение в медицине в качестве цитостатика для профилактики и лечения меланомы человека.Сущность изобретения заключается в синтезе соединения N-(3-метоксифенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамида формулы:,который проявляет свойство ингибирования пролиферации клеток MeW-164меланомы человека.
MDA20140062A 2014-06-23 2014-06-23 Соединение N-(3-метоксифенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамид - ингибитор пролиферации клеток MeW-164 меланомы человека MD4349C1 (ru)

Priority Applications (1)

Application Number Priority Date Filing Date Title
MDA20140062A MD4349C1 (ru) 2014-06-23 2014-06-23 Соединение N-(3-метоксифенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамид - ингибитор пролиферации клеток MeW-164 меланомы человека

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
MDA20140062A MD4349C1 (ru) 2014-06-23 2014-06-23 Соединение N-(3-метоксифенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамид - ингибитор пролиферации клеток MeW-164 меланомы человека

Publications (2)

Publication Number Publication Date
MD4349B1 MD4349B1 (ru) 2015-05-31
MD4349C1 true MD4349C1 (ru) 2015-12-31

Family

ID=53190461

Family Applications (1)

Application Number Title Priority Date Filing Date
MDA20140062A MD4349C1 (ru) 2014-06-23 2014-06-23 Соединение N-(3-метоксифенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамид - ингибитор пролиферации клеток MeW-164 меланомы человека

Country Status (1)

Country Link
MD (1) MD4349C1 (ru)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MD4520C1 (ru) * 2016-12-16 2018-05-31 Государственный Университет Молд0 N-(4-бутоксифенил)-2-(пиридин-2-илметилиден)гидразинкарботиоамид в качестве ингибитора роста клеток T-47D рака молочной железы

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5281715A (en) * 1992-05-13 1994-01-25 Yale University 2-formylpyridine thiosemicarbazone compounds
CN101260121A (zh) * 2007-03-07 2008-09-10 卡南吉医药科技(上海)有限公司 杂芳环缩氨基硫脲与过渡金属的络合物及其在制备抗肿瘤药物中的应用
MD3655G2 (ru) * 2007-09-03 2009-02-28 Государственный Университет Молд0 Ингибитор миелоидной лейкемии человека на основе бис(2-гидрокси-8-фенил-трицикло/7.3.1.0.2,7/-тридекан-13-он-тиосемикарбазонато)меди
MD3771G2 (ru) * 2008-04-30 2009-07-31 Государственный Университет Молд0 Ингибиторы энзима 17β-HSD, стимулирующего размножение клеток рака простаты
MD3995B1 (en) * 2009-05-11 2009-12-31 Universitatea De Stat Din Moldova Use of di(Á-Ophenoxy)-di{[2-(4-aminobenzenesulfamido)-5-ethyl-1,3,4-thiadiazole]-3,5-dibromosalicylidenethiosemicarbazonato(-1)-copper} as inhibitor of mammary cancer T-47D cell proliferation
MD3890G2 (ru) * 2008-09-08 2009-12-31 Государственный Университет Молд0 Ингибиторы миелоидной лейкемии человека на основе координационных соединений меди(II) с салицилидентиокарбазидами
MD3996B1 (en) * 2009-05-25 2009-12-31 Universitatea De Stat Din Moldova Perchlorates of 5-R-salicylidene-4-phenylthiosemicarbazonato(1-)-aquacopper(II) possessing properties of inhibitors of 17Beta-HSD enzyme activity (type 1)
WO2010006438A1 (en) * 2008-07-17 2010-01-21 Critical Outcome Technologies Inc. Thiosemicarbazone inhibitor compounds and cancer treatment methods
CN102210698A (zh) * 2004-01-02 2011-10-12 维奥恩药品公司 包含3-氨基吡啶-2-甲醛缩氨基硫脲的癌症治疗
MD4190B1 (en) * 2011-06-16 2012-12-31 Univ De Stat Din Moldova Inhibitor of human myeloid leukemia based on {bis¢2-(3,5-dibrom-2-hydroxyphenyl)-2-oxoethyl-piperidin-1-carbodithioato(1-)-O,O′]copper}
MD4215B1 (en) * 2012-07-09 2013-04-30 Univ De Stat Din Moldova Inhibitor of human myeloid leukemia based on N-(4-(5-(pyridin-2-yl)-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-2-(pyridin-2-ylmethylen)-hydrazinecarbothioamide

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5281715A (en) * 1992-05-13 1994-01-25 Yale University 2-formylpyridine thiosemicarbazone compounds
US5721259A (en) * 1992-05-13 1998-02-24 Yale University Method of using 2-formylpyridine thiosemicarbazone compounds
CN102210698A (zh) * 2004-01-02 2011-10-12 维奥恩药品公司 包含3-氨基吡啶-2-甲醛缩氨基硫脲的癌症治疗
CN101260121A (zh) * 2007-03-07 2008-09-10 卡南吉医药科技(上海)有限公司 杂芳环缩氨基硫脲与过渡金属的络合物及其在制备抗肿瘤药物中的应用
MD3655G2 (ru) * 2007-09-03 2009-02-28 Государственный Университет Молд0 Ингибитор миелоидной лейкемии человека на основе бис(2-гидрокси-8-фенил-трицикло/7.3.1.0.2,7/-тридекан-13-он-тиосемикарбазонато)меди
MD3771G2 (ru) * 2008-04-30 2009-07-31 Государственный Университет Молд0 Ингибиторы энзима 17β-HSD, стимулирующего размножение клеток рака простаты
WO2010006438A1 (en) * 2008-07-17 2010-01-21 Critical Outcome Technologies Inc. Thiosemicarbazone inhibitor compounds and cancer treatment methods
MD3890G2 (ru) * 2008-09-08 2009-12-31 Государственный Университет Молд0 Ингибиторы миелоидной лейкемии человека на основе координационных соединений меди(II) с салицилидентиокарбазидами
MD3995B1 (en) * 2009-05-11 2009-12-31 Universitatea De Stat Din Moldova Use of di(Á-Ophenoxy)-di{[2-(4-aminobenzenesulfamido)-5-ethyl-1,3,4-thiadiazole]-3,5-dibromosalicylidenethiosemicarbazonato(-1)-copper} as inhibitor of mammary cancer T-47D cell proliferation
MD3996B1 (en) * 2009-05-25 2009-12-31 Universitatea De Stat Din Moldova Perchlorates of 5-R-salicylidene-4-phenylthiosemicarbazonato(1-)-aquacopper(II) possessing properties of inhibitors of 17Beta-HSD enzyme activity (type 1)
MD4190B1 (en) * 2011-06-16 2012-12-31 Univ De Stat Din Moldova Inhibitor of human myeloid leukemia based on {bis¢2-(3,5-dibrom-2-hydroxyphenyl)-2-oxoethyl-piperidin-1-carbodithioato(1-)-O,O′]copper}
MD4215B1 (en) * 2012-07-09 2013-04-30 Univ De Stat Din Moldova Inhibitor of human myeloid leukemia based on N-(4-(5-(pyridin-2-yl)-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-2-(pyridin-2-ylmethylen)-hydrazinecarbothioamide

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
Anuszewska E., Chlopkiewicz B., Gruber B., Marczewska J., Priebe W., Skurzak H. Estimation of DNA damage and cytotoxicity of anthracycline analogs in human melanoma cells on early and late passages. Acta Poloniae Pharmaceutica - Drug Research, 2006, vol. 63, nr. 4, p. 321-324 *
Douglas West, Jack Ingram, Nicole Kozub, Gordon Bain, Anthony Liberta. Copper(II) complexes of 2-formyl-, 2-acetyl- and 2-benzoyl-pyridine N(4)-phenyl-, N(4)-o-methoxyphenyl-, N(4)-p-methoxy-phenyl- and N(4)-p-nitrophenylthiosemicarbazones. Transition Metal Chemistry, June 1996, vol. 21, issue 3, p. 213-218 (regăsit în Internet la 2015.02.10 URL:<http://link.springer.com/content/pdf/10.1007/BF00165969.pdf#>) *
Douglas X. West et al. Copper(II) complexes of 2- formyl-, 6-methyl-2-formyl- and 2- benzoylpyridine N(4)-(2-methylpyridinyl)-, N(4)- (2-ethylpyridinyl)- and N(4)-methyl(2- ethylpyridinyl)thiosemicarbazones. Transition Metal Chemistry, 1996, 21, 289-295; (regăsit în Internet la 2015.02.11 URL: <http://www.springerlink.com/content/g90np851733v87lk/>) *
Giorgio Pelosi. Thiosemicarbazone Metal Complexes: from structure to activity. The Open Crystallography Journal, 2010, 3, pag. 16-28, (regăsit în Internet la 2015.02.10 URL: < <http://benthamopen.com/contents/pdf/TOCRYJ/TOCRYJ-3-16.pdf>>) *

Also Published As

Publication number Publication date
MD4349B1 (ru) 2015-05-31

Similar Documents

Publication Publication Date Title
Gul et al. New copper complexes inducing bimodal death through apoptosis and autophagy in A549 cancer cells
Mendes et al. Gallium (III) complexes of 2-pyridineformamide thiosemicarbazones: cytotoxic activity against malignant glioblastoma
Zhang et al. Synthesis, molecular modeling and biological evaluation of chalcone thiosemicarbazide derivatives as novel anticancer agents
Vyas et al. Effect of ligand substitution in pyrazolone based binary and ternary Cu (II) complexes on DNA binding, protein binding and anti-cancer activity on A549 lung carcinoma cell lines
Utreja et al. Schiff bases and their metal complexes as anti-cancer agents: A review
Akocak et al. Synthesis and biological evaluation of novel aromatic and heterocyclic bis-sulfonamide Schiff bases as carbonic anhydrase I, II, VII and IX inhibitors
Chen et al. Ruthenium (II) salicylate complexes inducing ROS-mediated apoptosis by targeting thioredoxin reductase
Maia et al. Organometallic gold (III) complexes with hybrid SNS-donating thiosemicarbazone ligands: cytotoxicity and anti-Trypanosoma cruzi activity
Zafar et al. Synthesis, characterization and anti-cancer properties of water-soluble bis (PYE) pro-ligands and derived palladium (II) complexes
Bjelogrlić et al. Synthesis, structure and characterization of novel Cd (II) and Zn (II) complexes with the condensation product of 2-formylpyridine and selenosemicarbazide: antiproliferative activity of the synthesized complexes and related selenosemicarbazone complexes
Van Le et al. Highly cytotoxic gold (i)-phosphane dithiocarbamate complexes trigger an ER stress-dependent immune response in ovarian cancer cells
Božić et al. Quinoline based mono-and bis-(thio) carbohydrazones: synthesis, anticancer activity in 2D and 3D cancer and cancer stem cell models
Mal et al. Nuclease activity and anti-proliferative effect on human cancerous cells of a newly synthesized and characterized mononuclear copper (ii) complex [Cu II (L)(fu) 2][L= 2-(2-pyridyl) benzimidazole, fu= furoate]
Kaya et al. Iron (III) and nickel (II) complexes with S-alkyl (n-C1-6)-thiosemicarbazidato ligands: Synthesis, structural characterization, and antioxidant features
Steiner et al. Discovery of ‘click’1, 2, 3-triazolium salts as potential anticancer drugs
Scarpa et al. Natural and synthetic avenanthramides activate caspases 2, 8, 3 and downregulate hTERT, MDR1 and COX-2 genes in CaCo-2 and Hep3B cancer cells
Todorović et al. (Chalcogen) semicarbazones and their cobalt complexes differentiate HL-60 myeloid leukaemia cells and are cytotoxic towards tumor cell lines
Peerzada et al. Identification of morpholine based hydroxylamine analogues: selective inhibitors of MARK4/Par-1d causing cancer cell death through apoptosis
CN106496052B (zh) 一种査尔酮类化合物及其制备方法和应用
Chohan et al. Metal‐based isatin‐bearing sulfonamides: their synthesis, characterization and biological properties
Ikhtiarudin et al. Microwave-assisted synthesis, molecular docking study and in vitro evaluation of halogen substituted flavonols against P388 murine leukemia cells
Ol'ga et al. Cytotoxicity of new alkylamino-and phenylamino-containing polyfluorinated derivatives of 1, 4-naphthoquinone
Ali et al. New Mn (III)/Fe (III) complexes with thiohydantoin-supported imidazolium ionic liquids for breast cancer therapy
MD4349C1 (ru) Соединение N-(3-метоксифенил)-2-(пиридин-2-илметилен)-гидразинкарботиоамид - ингибитор пролиферации клеток MeW-164 меланомы человека
Hadi et al. SYNTHESIS AND CHARACTERIZATION OF NOVEL METAL COMPLEXES WITH NEW SCHIFF BASE LIGAND DERIVED FROM 6-AMINO PENCILLIC ACID AND TOXICOLOGICAL STUDIES OF ITS COMPLEX WITH AU (III) ON HUMAN CELLS FOR COLON CANCER LS-174.

Legal Events

Date Code Title Description
FG4A Patent for invention issued
KA4A Patent for invention lapsed due to non-payment of fees (with right of restoration)
MM4A Patent for invention definitely lapsed due to non-payment of fees