Levina E V, Kalinovskiĭ A I, Andriiashchenko P V, Menzorova N I, Dmitrenok P S
Bioorg Khim. 2007 May-Jun;33(3):357-64.
Three new polar steroids identified as trofoside A, (20R,24S)-24-O-(3-O-methyl-beta-D-xylopyranosyl)-3beta,6alpha,8,15beta,24-pentahydroxy-5alpha-cholestane, its 22(23)-dehydro derivative (trofoside B), and 15-sulfoxy-(20R,24S)-5alpha-cholestane-3beta,6beta,8,15alpha,24-pentaol sodium salt, were isolated from Trofodiscus uber starfish extracts collected in the Sea of Okhotsk. Two known compounds, trofoside A aglycone, (20R,24S)-3beta,6alpha,8,15beta,24-pentahydroxy-5alpha-cholestane, and triseramide, (20R,24R,25S,22E)-24-methyl-3beta,6alpha,8,15beta-tetrahydroxy-5alpha-cholest-22-en-27-oic acid (2-sulfoethyl)amide sodium salt, were also found. The structures of the isolated polyoxysteroids were established from their spectra. Minimal concentrations causing degradation of unfertilized egg-cells of the sea-urchin Strongylocentrotus intermedius (C(min)) and terminating the cell division at the stage of the first division (C(min) embr.), as well as the concentrations causing 50% immobilization of sperm cells (ImC50) and inhibiting their ability to fertilize egg-cells by 50% (IC50) were determined for the isolated compounds. Of three compounds highly toxic in embryos and sea-urchin sperm cells, the polyol with a sulfo group in the steroid core was the most active; two glycosides with monosaccharide chains located at C3 and C24 atoms were less toxic. Note that all the compounds with the spermiotoxic activities differently affected the embryo development. The positions of monosaccharide residues in the core considerably influence the compound activity. For example, both mono- and double chained glycosides with the monosaccharide fragment at C3 and C24 atoms are active against sea-urchin sperm cells and embryos, whereas the C24 glycosylated trofoside A does not affect embryos and displays a poor spermiotoxicity.
从鄂霍次克海采集的超大型海星(Trofodiscus uber)提取物中分离出三种新的极性甾体化合物,分别鉴定为trofoside A,即(20R,24S)-24-O-(3-O-甲基-β-D-吡喃木糖基)-3β,6α,8,15β,24-五羟基-5α-胆甾烷;其22(23)-脱氢衍生物(trofoside B);以及15-亚磺氧基-(20R,24S)-5α-胆甾烷-3β,6β,8,15α,24-五醇钠盐。还发现了两种已知化合物,trofoside A苷元,即(20R,24S)-3β,6α,8,15β,24-五羟基-5α-胆甾烷,以及triseramide,即(20R,24R,25S,22E)-24-甲基-3β,6α,8,15β-四羟基-5α-胆甾-22-烯-27-酸(2-磺基乙基)酰胺钠盐。通过光谱确定了分离出的多氧甾体化合物的结构。测定了分离出的化合物对中间球海胆(Strongylocentrotus intermedius)未受精卵细胞降解的最小浓度(C(min))以及在第一次分裂阶段终止细胞分裂的最小浓度(C(min) embr.),以及导致50%精子细胞固定的浓度(ImC50)和抑制其使卵细胞受精能力50%的浓度(IC50)。在对胚胎和海胆精子细胞具有高毒性的三种化合物中,甾体核心带有磺基的多元醇活性最高;在C3和C24原子处带有单糖链的两种糖苷毒性较小。请注意,所有具有精子毒性活性的化合物对胚胎发育的影响各不相同。核心中糖残基的位置对化合物活性有很大影响。例如,在C3和C24原子处带有单糖片段的单链和双链糖苷对海胆精子细胞和胚胎均有活性,而C24糖基化的trofoside A对胚胎无影响且精子毒性较差。