Thiocolchicine
WebApr 25, 2024 · A series of colchicine and thiocolchicine derivatives bearing a Michael acceptor moiety in ring A were synthesized. Some of these compounds exhibit cytotox … WebIt was shown, that cultured ex vivo human T-Lymphoblastoid (CEM) cells respond to synthesized thiocolchicine and fluorine thiocolchicine derivatives. The preparation of derivatives with substitution at C-3 and C-7 is described. All compounds were used at concentration from 1 nM to 1000 nM. Inhibitor …
Thiocolchicine
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WebTHIOCOLCHICINE 2-GLUCOSIDE ANALOG [MI] THIOCOLCHICOSIDE [INN] THIOCOLCHICOSIDE [MART.] THIOCOLCHICOSIDE [WHO-DD] Resources. Common Chemistry. i. Inxight Drugs. i. NCATS GSRS Full Record. i. NCI Thesaurus. i. PubChem. i. Note. UNIIs are generated based on scientific identity characteristics using ISO 11238 … WebNov 15, 2024 · In a previously conducted study, the structurally related benzyl analogs of thiocolchicine were found potent against various tumor cell lines. 37 Thus, we decided to …
WebThiocolchicine (10-Demethoxy-10-(methylthio)colchicine );≥97% HPLC; Thiocolchicine is an antimitotic alkaloid and apoptosis inducer; Thiocolchicine is an antimitotic alkaloid and … WebTwo colchicine analogs with modifications only in the C ring are better inhibitors than colchicine of cell growth and tubulin polymerization. Radiolabeled thiocolchicine (with a thiomethyl instead of a methoxy group at position C-10) and N-acetylcolchinol O-methyl ether (NCME) (with a methoxy-substituted benzenoid instead of the methoxy-substituted …
Webm.cnreagent.com 扫一扫,直接在手机上打开 Web394 rows · Thiocolchicoside. Thiocolchicoside is a semi-synthetic colchicine derivative …
WebFeb 6, 2024 · Thiocolchicine 31 is a colchicine 1 derivative used in the therapy of some diseases and extensively studied in the field of oncological research as antimitotic agent … brake pads 2200WebJan 1, 2010 · Thiocolchicine homodimers exhibited a much greater ability to disrupt tubulin polymerization in vitro than dimers containing podophyllotoxin, but this was not directly reflected in their in vivo activity, with compounds based on both parent molecules (particularly compounds 12, 13, 18 and 20) acting as potent disruptors of the microtubule ... sv 07 nauheim restaurantWebApr 25, 2024 · A series of colchicine and thiocolchicine derivatives bearing a Michael acceptor moiety in ring A were synthesized. Some of these compounds exhibit cytotoxic activity in the nanomolar range, efficiently disrupt the mitotic spindle, and cause the accumulation of G2/M-phase cells resulting in the development of apoptosis. These … brake pads 2206025WebIt was shown, that cultured ex vivo human T-Lymphoblastoid (CEM) cells respond to synthesized thiocolchicine and fluorine thiocolchicine derivatives. The preparation of … brake pads 2018 subaru foresterWebIn this paper we report on the design, synthesis and in vitro evaluation of a group of thiocolchicine derivatives, modified at ring-B, labelled here compounds 4-14. These compounds have been obtained in a simple reaction of 7-deacetyl-10-thiocolchicine 3 with eleven different alcohols in the presence of triphosgene. sv0xmksuWebThiocolchicine was bound 2-4 times as rapidly as colchicine, but the activation energies of the reactions were nearly identical (18 kcal/mol for colchicine, 20 kcal/mol for … brake pads 2018 dodge ram 1500WebKR102512597B1 KR1020247033500A KR20247033500A KR102512597B1 KR 102512597 B1 KR102512597 B1 KR 102512597B1 KR 1020247033500 A KR1020247033500 A KR 1020247033500A KR 20247033500 A KR20247033500 A KR 20247033500A KR 102512597 B1 KR102512597 B1 KR 102512597B1 Authority KR South Korea Prior art keywords cmet … brake pads 211 8rzr s