| 中文名 | 杯苋甾酮 |
|---|---|
| 英文名 | cyasterone |
| 中文别名 |
杯觅甾酮对照品
杯苋甾酮(Cyasterone) 杯苋甾酮(杯觅甾酮) 杯苋甾酮(标准品) 杯苋甾酮, 来源于川牛膝 (3S,4S,5R)-4-((2R,3R)-2,3-二羟基-3-((2S,3R,5R,9R,10R,13R,17S)-2,3,14-三羟基- 10,13-二甲基-6-氧代-2,3,4,5,6,9,10,11,12,13,14,15,16,17-十四氢-1H-环戊二烯并[A]菲-17-丁基)-5-羟基-3-甲基四氢-2H-吡喃-2-酮 杯觅甾酮标准品 杯苋甾酮(对照品) 杯苋甾酮|||CYASTERON CYASTERONE 杯苋甾酮 环阿屯酮 杯苋甾酮(Cyasterone) 环甾酮 杯觅甾酮 |
| 英文别名 |
Cyasterone(AS)
Cyasterone from Cyathula officinalis K.C. Kuan (2β,3β,5β,23R,24ξ,25S,28R)-2,3,14,20,23-Pentahydroxy-26,28-epoxystigmast-7-ene-6,26-dione Cyasterone, from Cyathula officinalis K.C. Kuan cyasteron 7,(5BETA)-CHOLESTEN-26-CBOXYLIC ACID-24BETA-(1-HYDROXYETHYL)-2BETA, 3BETA, 14ALPHA,20BETA, 22R-PENTOL-6-ONE GAMMA-LACTONE (2β,3β,5β,22R,24S,25S,28R)-2,3,14,20,22-Pentahydroxy-26,28-epoxystigmast-7-ene-6,26-dione Cyasteron Cyasterone CYASTERONE (3S,4S,5R)-4-[(2R,3R)-2,3-Dihydroxy-3-[(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]butyl]-3,5-dimethyloxolan-2-one 2-beta,3-beta,14,20,22,28-hexahydroxy-6-oxo-5-beta-stigmast-7-en-26-oicaci 5β-Stigmast-7-en-26-oic acid, 2β,3β,14,20,22,28-hexahydroxy-6-oxo-, γ-lactone, (22R,24S,25S,28R)-Stigmast-7-en-26-oic acid, 2,3,14,20,22,28-hexahydroxy-6-oxo-, γ-lactone, (2β,3β,5β,22R,24S,25S,28R)-(22r,24s,25s,28r)-gamma-lactoncyasteron (3S,4S,5R)-4-((2R,3R)-2,3-Dihydroxy-3-((2S,3R,5R,9R,10R,13R,17S)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)butyl)-5-hydroxy-3-methyltetrahydro-2H-pyran-2-one Stigmast-7-en-26-oic acid, 2,3,14,20,22,28-hexahydroxy-6-oxo-, γ-lactone, (2β,3β,5β,22R,24S,25S,28R) (22R,24S,25S,28R)-2β,3β,14,20,22,28-Hexahydroxy-6-oxo(C)-5β-stigmasta-7-ene-26-oic acid γ-lactone (22r,24s,25s,28r)-gamma-lacton Cup amanth steroid |
| 描述 | Cyasterone,一种天然的 EGFR 抑制剂,主要分离自 Ajuga decumbens Thunb (Labiatae)。Cyasterone 通过诱导细胞凋亡 (apoptosis) 和细胞周期阻滞表现出抗增殖作用。 Cyasterone 可作为抗人类肿瘤的临床治疗性药物。 |
|---|---|
| 相关类别 | |
| 体外研究 | 半胱氨酸(0-100μM; 24小时)以浓度和时间依赖性方式抑制细胞生长,A549和MGC823细胞中IC50值分别为38.50 mg/mL,32.96 mg/mL [1]。细胞活力测定[1]细胞系:A549,HCT116,MGC823细胞浓度:0-100μM培养时间:24小时结果:抑制3种人癌细胞系A549,HCT116,MGC823细胞的生长。 |
| 参考文献 |
| 密度 | 1.3±0.1 g/cm3 |
|---|---|
| 沸点 | 742.8±60.0 °C at 760 mmHg |
| 分子式 | C29H44O8 |
| 分子量 | 520.655 |
| 闪点 | 242.0±26.4 °C |
| 精确质量 | 520.303589 |
| PSA | 144.52000 |
| LogP | -0.25 |
| 蒸汽压 | 0.0±5.6 mmHg at 25°C |
| 折射率 | 1.600 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATAMUTATION DATA
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| 安全声明 (欧洲) | 24/25 |
|---|---|
| 危险品运输编码 | NONH for all modes of transport |
| RTECS号 | WJ2510000 |