格尔德霉素

Geldanamycin from Streptomyces hygroscopicus (订货以英文为准)

编号:G102383
CAS号:30562-34-6
分子式:C29H40N2O9
分子量:560.64
货号 品牌 包装 目录价 您的价格 库存 数量 购买
G102383-10mg 阿拉丁 10mg ¥985.90
G102383-50mg 阿拉丁 50mg ¥3015.90
G102383-250mg 阿拉丁 250mg ¥6117.90
产品名称 Geldanamycin from Streptomyces hygroscopicus
中文名称 格尔德霉素
CAS号 30562-34-6
MDL编码 MFCD00274570
分子式(M.F.) C29H40N2O9
分子量(M.W.) 560.64
储存条件 -20°C储存
熔点255°C
敏感性对热敏感
溶解性Soluble in dimethyl sulfoxide at 100 mg/mL.
存贮条件储存温度:-20℃
密度1.2300
产品介绍λmax 305(MeOH)(Lit.) A benzoquinoid antibiotic that inhibits p60c-src tyrosine kinase and c-myc gene expression in murine lymphoblastoma cells. Geldanamycin has antiproliferative and antitumor effects. Rapidly depletes p185c-erbB2 protein tyrosine kinase in breast carcinoma cells. Binds to HSP90 and disrupts Raf1-HSP90 complex leading to destabilization of Raf1. Inhibits basal and hypoxia-induced expression of c-Jun (IC50 = 75 nM) and abolishes hypoxia-induced increase in c-Jun N-terminal kinase activity. Also known to selectively destabilize mutated p53 protein from a number of breast, leukemia, and prostate cell lines.A benzoquinoid antibiotic that is a potent inhibitor of pp60src tyrosine kinase. Geldanamycin has antiproliferative and antitumor effects. Inhibits basal and hypoxia-induced expression of c-Jun (IC50 = 75 nM) and abolishes hypoxia-induced increase in c-Jun N-terminal Kinase activity. Binds to HSP90 and disrupts raf1-HSP90 complex leading to destabilizing of Raf1. Also destabilizes mutant p53 protein from a number of breast, leukemic, and prostate cell lines. Inhibits c-myc expression in murine lymphoblastoma cells. Approximately ten-fold more potent than herbimycin A
生化机理格尔德霉素是一种强效的抗肿瘤抗生素。在纳摩尔浓度级对60个细胞系具有活性。特异性结合热休克蛋白Hsp90和它的内质网同源物GP96,从而干扰了蛋白质的构象和细胞应激反应。此外,它是一种强效的核激素受体家族抑制剂。
别名格尔德霉素;Streptomyces hygroscopicus - CAS 30562-34-6 - Calbiochem;NSC 122750 U-29135
Reaxys-RN4627629
WGK德国3
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