101932-71-2
中文名称
蛋白磷酸酯酶抑制剂
英文名称
CALYCULIN A
CAS
101932-71-2
分子式
C50H81N4O15P
分子量
1009.17
MOL 文件
101932-71-2.mol
更新日期
2023/03/20 15:41:23
101932-71-2 结构式
基本信息
中文别名
花萼海绵诱癌素蛋白磷酸酯酶抑制剂
PP2A催化亚基抑制剂(CALYCULIN A)
英文别名
C05370CALYCULIN A
(-)-CALYCULIN A
Calyculin A ((-)-Calyculin A)
CALYCULIN A, DISCODERMIA CALYX
calyculin A from discodermia calyx
CALYCULIN A FROM DISCODERMIA CALYX, 10 U G
Calyculin A, Discodermia calyx - CAS 101932-71-2 - Calbiochem
InSolution Calyculin A, Discodermia calyx - CAS 101932-71-2 - Calbiochem
N-[(3S)-[4-(1E)-3-[(2R,3R,4R,7S,8S,9R)-2-[(1S,3S,4S,5R,7E,9E,11E,13Z)-14-Cyano-3,5-dihydroxy-1-methoxy-4,6,8,9,13-pentam
物理化学性质
熔点247-249°
比旋光度D -60° (c = 0.1 in ethanol)
密度1.25±0.1 g/cm3(Predicted)
储存条件-20°C
溶解度DMSO: soluble
溶解度可溶于DMSO
酸度系数(pKa)1.81±0.10(Predicted)
形态solid
颜色white
水溶解性Soluble in DMSO (50 mM), ethanol (1 mg/ml), methanol, acetone, acetonitrile, chloroform, methylene chloride, and benzene. Insoluble in water.
Merck13,1731
BRN4903216
安全数据
警示词危险
危险性描述H301+H311+H331-H315
危险品标志T
危险类别码23/24/25-38
安全说明36/37/39-45
危险品运输编号UN 3462 6.1/PG 3
危险品运输编号UN 3462 6.1/PG 3
WGK Germany3
WGK Germany3
F8-10
危险等级6.1(a)
包装类别II
海关编码2934999090
蛋白磷酸酯酶抑制剂价格(试剂级)
| 报价日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
| 2024/04/30 | HY-18983 | 蛋白磷酸酯酶抑制剂 Calyculin A | 101932-71-2 | 10μg(0.5mM * 20μL in DMSO) | 1200元 |
| 2024/04/30 | HY-18983 | 蛋白磷酸酯酶抑制剂 Calyculin A | 101932-71-2 | 25μg(0.5mM * 50μL in DMSO) | 2050元 |
| 2024/04/30 | HY-18983 | 蛋白磷酸酯酶抑制剂 Calyculin A | 101932-71-2 | 100μg(0.5mM * 200μL in DMSO) | 5530元 |
常见问题列表
生物活性
Calyculin A ((-)-Calyculin A) 是有效，可渗透细胞的蛋白磷酸酶 1 (PP1) 和蛋白磷酸酶 2A (PP2A) 抑制剂，其 IC50 值分别为 2 nM 和 0.5-1 nM。靶点
IC50: 2 nM (PP1); 0.5-1 nM (PP2A)
体外研究
Calyculin A (1-10 nM; 24 hours) induces cytotoxicity in MG63 cells in a dose-dependent manner up to 10 nM in MG63 cells.
Cell Cytotoxicity Assay
| Cell Line: | Human osteosarcoma MG63 cells |
| Concentration: | 0, 1, 2, 5, 10 nM |
| Incubation Time: | 24 hours |
| Result: | Treatment with 0.1 nM for 24 h had a minimal effect on MG63 cell survival. Cell rounding and shrinking were obvious in the cultures treated for 24 h with 5 nM. The level of the cell viability treated with 10 nM was 27% that of the control cultures. |