321309-33-5Relevant articles and documents
Dimer of 5-methyl-3-isoxazolyl isothiocyanate
Proshin,Pushin,Makarov
, p. 1483 - 1484 (2007)
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4-Chlorocolchicine derivatives bearing a thiourea side chain at the C-7 position as potent anticancer agents
Nishiyama, Hiroyuki,Ono, Masahiro,Sugimoto, Takuya,Sasai, Toshio,Asakawa, Naoyuki,Ueno, Satoshi,Tominaga, Yoshitaka,Yaegashi, Takashi,Nagaoka, Masato,Matsuzaki, Takeshi,Kogure, Noriyuki,Kitajima, Mariko,Takayama, Hiromitsu
supporting information, p. 452 - 458 (2014/04/17)
A series of 4-substituted colchicine derivatives were synthesized and evaluated with an eye toward developing new anticancer agents. As a result, 4-chlorocolchicine derivatives bearing a thioureide side chain at the C-7 position were found to exhibit significant cytotoxicities to three human cancer cell lines (A549, HT-29, and HCT116). In particular, compound 26 having an ethylthioureide group at the C-7 had high antitumor activity in vivo and a broad effective dosage range. Furthermore, compound 58, which has a (5-methylpyrazol-3-yl)thioureide group at the C-7 side chain, exhibited strong cytotoxicity and desirable metabolic stability in vitro.
Novel 1,2,4-thiadiazole derivatives as potent neuroprotectors: Approach to creation of bioavailable drugs
Perlovich, German L.,Proshin, Alexey N.,Volkova, Tatyana V.,Petrova, Ludmila N.,Bachurin, Sergey O.
experimental part, p. 2156 - 2167 (2012/10/08)
Novel 1,2,4-thiadiazole derivatives as potent neuroprotectors were synthesized and identified. Their ability to inhibit the glutamate stimulated Ca uptake was measured. Permeation experiments on the phospholipid membranes were conducted, and the apparent