About: 7-Deacetyl-10-alkylthiocolchicine derivatives - new compounds with potent anticancer and fungicidal activity

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scientific article published on 16 August 2018

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2018 (fr) im Oktober 2018 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'agostu de 2018 (ast) наукова стаття, опублікована в жовтні 2018 (uk) scientific article published on 16 August 2018 (en)
publication date	wds:Q62652625-096DAB45-F0E7-42E2-965A-CA7685C42AA8
publication date	2018-08-16 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q62652625-EEBDFC1A-CFDC-40F5-8F7F-7471F0C2DA30
language of work or name	English
cites work	wds:Q62652625-0A727077-C0E5-4740-A379-AE68546F5422 wds:Q62652625-247AFB74-D89E-4176-BCD7-2F459D8A3DA0 wds:Q62652625-2B4E65B0-8AF4-49D5-90C8-DF7B373FFD3B wds:Q62652625-3C211CC1-C381-435D-A805-06F6F9AD318E wds:Q62652625-3D5EC030-6CAA-442A-8F7A-7216FC557957 wds:Q62652625-4026B5AE-7D45-4BC6-B86B-591D1B3B3D36 wds:Q62652625-7DD65389-76AB-43D9-A18E-36262E51A636 wds:Q62652625-84083488-F19E-4448-9EB0-33266BC89ED1 wds:Q62652625-909F059A-9FC1-496D-998C-34CFD89E7DDD wds:Q62652625-962D2179-B0A7-4932-B6F6-7B7F163DAC6E wds:Q62652625-982D0692-7688-425E-96DD-AB0075C457FE wds:Q62652625-AE6385AC-E761-43F6-A635-010E99CCD164 wds:Q62652625-BAA48066-4F6D-47D4-9CCF-99A8B50602D5 wds:Q62652625-C14ACB1C-4663-4846-899A-16BAD1325133 wds:Q62652625-C28F7699-4F2E-460F-B9F8-EC6E70A3D2BC wds:Q62652625-C554165E-F714-45C9-8417-3D4F134A1030 wds:Q62652625-D18EFE91-D72A-47CC-9116-6A9FC783F4B7 wds:Q62652625-D9A8D5A0-0678-467F-ADAC-513DC62181F1 wds:Q62652625-DD1911D5-698D-4D49-92A2-A97277BDB8E3 wds:Q62652625-F03F0818-35D4-476E-93BD-E251813D1095 wds:Q62652625-FD0362E6-9AF8-428D-BBB3-1EB498CD03C4
cites work	Inhibitors of tubulin polymerization: synthesis and biological evaluation of hybrids of vindoline, anhydrovinblastine and vinorelbine with thiocolchicine, podophyllotoxin and baccatin III. Colchicine and its analogues: recent findings Antitumor agents. 199. Three-dimensional quantitative structure-activity relationship study of the colchicine binding site ligands using comparative molecular field analysis Exploring QSAR and QAAR for inhibitors of cytochrome P450 2A6 and 2A5 enzymes using GFA and G/PLS techniques Alfred Burger award address. Bioactive alkaloids. 4. Results of recent investigations with colchicine and physostigmine Antitumor agents. 272. Structure-activity relationships and in vivo selective anti-breast cancer activity of novel neo-tanshinlactone analogues. Antitumor agents. 172. Synthesis and biological evaluation of novel deacetamidothiocolchicin-7-ols and ester analogs as antitubulin agents Population biology of Aureobasidium pullulans on apple leaf surfaces Genome sequencing of four Aureobasidium pullulans varieties: biotechnological potential, stress tolerance, and description of new species Characterization of the colchicine binding site on avian tubulin isotype betaVI. Antitubulin effects of derivatives of 3-demethylthiocolchicine, methylthio ethers of natural colchicinoids, and thioketones derived from thiocolchicine. Comparison with colchicinoids Synthesis and biological effects of novel thiocolchicines. 3. Evaluation of N-acyldeacetylthiocolchicines, N-(alkoxycarbonyl) deacetylthiocolchicines, and O-ethyldemethylthiocolchicines. New synthesis of thiodemecolcine and antileukemic effects of 2 Antitumor agents--CLXXV. Anti-tubulin action of (+)-thiocolchicine prepared by partial synthesis Antitumor agents. Part 236: Synthesis of water-soluble colchicine derivatives Effects of thiocolchicine on axonal cytoskeleton of the rat peroneus nerve 3-demethoxy-3-glycosylaminothiocolchicines: Synthesis of a new class of putative muscle relaxant compounds. Antitumor agents 273. Design and synthesis of N-alkyl-thiocolchicinoids as potential antitumor agents New synthetic thiocolchicine derivatives as lowtoxic anticancer agents Derivatives of thiocolchicine and its applications to CEM cells treatment using 19F magnetic resonance ex vivo. N-Deacetyl-N-aminoacylthiocolchicine Derivatives: Synthesis and Biological Evaluation on MDR-Positive and MDR-Negative Human Cancer Cell Lines Antitumor agents. 141. Synthesis and biological evaluation of novel thiocolchicine analogs: N-acyl-, N-aroyl-, and N-(substituted benzyl)deacetylthiocolchicines as potent cytotoxic and antimitotic compounds
author name string	wds:Q62652625-2E0AAD11-7FF1-4185-96F4-3DBB757E071B wds:Q62652625-92BBFD1D-D85D-4DA6-BBB1-909195806B4C
author name string	Krzysztof Myszkowski Grzegorz Cofta
rdfs:label	7-Deacetyl-10-alkylthiocolchicine derivatives - new compounds with potent anticancer and fungicidal activity (en) 7-Deacetyl-10-alkylthiocolchicine derivatives - new compounds with potent anticancer and fungicidal activity (nl)
skos:prefLabel	7-Deacetyl-10-alkylthiocolchicine derivatives - new compounds with potent anticancer and fungicidal activity (en) 7-Deacetyl-10-alkylthiocolchicine derivatives - new compounds with potent anticancer and fungicidal activity (nl)
name	7-Deacetyl-10-alkylthiocolchicine derivatives - new compounds with potent anticancer and fungicidal activity (en) 7-Deacetyl-10-alkylthiocolchicine derivatives - new compounds with potent anticancer and fungicidal activity (nl)
author	wds:Q62652625-17C947FF-E462-4677-9B45-75C0981C52C1 wds:Q62652625-2E5252B1-BADA-4521-9397-3A0874D60FB4 wds:Q62652625-4A0A3D6B-B92E-426F-9E37-C3B61CFD6FF6 wds:Q62652625-6D8E21F0-F49A-4C5F-8789-CAA82D5579DB wds:Q62652625-7388B6F9-E55F-4206-8B39-5F30557E2DC8 wds:Q62652625-7A7D1222-D69A-4AF1-96AC-03A774C3F8A6 wds:Q62652625-83918D44-D997-4248-A498-9791DFE062A5 wds:Q62652625-E2D811F8-9479-432B-9242-C1A0A34321B7 wds:Q62652625-E35EBD08-0369-4B1A-B74B-40AF8879724C
author	Piotr Barczyński Rafał Kurczab Marek Murias Beata Jasiewicz Joanna Kurek Patrycja Kwaśniewska-Sip Krzysztof Myszkowski Grzegorz Cofta
title	wds:Q62652625-9E93B97F-833F-4542-9ABB-CB9FAF738133
title	7-Deacetyl-10-alkylthiocolchicine derivatives - new compounds with potent anticancer and fungicidal activity (en)
page(s)	wds:Q62652625-D4BA1B81-7E9E-4BD7-92F2-ECC7608E5DB0
page(s)	1708-1714
instance of	wds:Q62652625-8E5A02A9-9155-4112-978E-91210E0B332A
instance of	scholarly article
PubMed ID	wds:Q62652625-634B4AD2-0502-4CDF-95CD-3930C5CDCC3A
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30429975
PubMed ID	30429975
published in	wds:Q62652625-533EA180-3C7C-40AC-8FA8-28A46CF602DA
published in	MedChemComm
issue	wds:Q62652625-CE5CC090-C6F8-461C-8DD7-19DBDB4F9B8D
volume	wds:Q62652625-DA9CCDF9-4E3E-4E70-89B6-26F08F1BA136
issue	10
volume	9
DOI	wds:Q62652625-2373D2F1-4E6E-46C9-8509-E696E5895295
DOI	http://dx.doi.org/10.1039/C8MD00352A
DOI	10.1039/C8MD00352A
PMCID	wds:Q62652625-24B39D66-D784-4903-83DD-83FC07D2F9A7
PMCID	6195099

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