Kikuchi O, Eguchi T, Kakinuma K, Koezuka Y, Shindo K, Otake N
Department of Chemistry, Tokyo Institute of Technology, Japan.
J Antibiot (Tokyo). 1993 Jun;46(6):985-91. doi: 10.7164/antibiotics.46.985.
Gilvocarcin V was chemically transformed to alter its biological activities as well as its solubility by mainly focusing on the vinyl side chain. The oxirane and oxime derivatives showed slightly decreased in vivo antitumor activity, while the aminoethylmorpholine derivative turned out to be soluble in some organic solvents.
通过主要关注乙烯基侧链,对吉尔vocarcin V进行化学转化,以改变其生物活性和溶解度。环氧乙烷和肟衍生物的体内抗肿瘤活性略有下降,而氨乙基吗啉衍生物在某些有机溶剂中可溶。