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479-13-0

中文名稱 考邁斯托醇
英文名稱 COUMESTROL
CAS 479-13-0
EINECS 編號 207-525-6
分子式 C15H8O5
MDL 編號 MFCD00016885
分子量 268.22
MOL 文件 479-13-0.mol
更新日期 2025/02/19 15:12:40
479-13-0 結構式 479-13-0 結構式

基本信息

中文別名
考邁斯托醇
擬雌內(nèi)酯
香豆雌酚
英文別名
[2-(2,4-DIHYDROXYPHENYL)-6-HYDROXY-3-BENZOFURAN-CARBOXYLIC ACID ALPHA-LACTONE]
2-(2,4-DIHYDROXYPHENYL)-6-HYDROXY-3-BENZOFURANCARBOXYLIC ACID DELTA-LACTONE
2-(2 4-DIHYDROXYPHENYL)-6-HYDROXY-3-BENZOFURANCARBOXYLIC ACID D-LACTONE
3,9-DIHYDROXY-6H-BENZOFURO[3,2-C]-[1]BENZOPYRAN-6-ONE
7,12-DIHYDROXYCOUMESTAN
7,12-DIHYDROXYCOUMESTANE
7(1), 6-DIHYDROXYCOUMARINO(3(1), 4(1), 3,2)COUMARONE
COUMESTROL
2-(2,4-dihydroxyphenyl)-6-hydroxy-3-benzofurancarboxylicacidelta-lacton
2-c)(1)benzopyran-6-one,3,9-dihydroxy-6h-benzofuro(
2-c][1]benzopyran-6-one,3,9-dihydroxy-6h-benzofuro[
cumoesterol
Coumesterol
COUMESTROL(P)
COUMOESTROL
7 12-DIHYDROXYCOUMESTAN 98%
2-(2 4-DIHYDROXYPHENYL)-6-HYDROXY-3-BENZOFURANCARBOXYLIC ACID D-LACTONE 98%
所屬類別
天然產(chǎn)物:香豆素

物理化學性質

熔點≥350 °C(lit.)
沸點331.39°C (rough estimate)
密度1.2586 (rough estimate)
折射率1.7680 (estimate)
儲存條件Refrigerator
溶解度DMSO: soluble
酸度系數(shù)(pKa)8.25±0.20(Predicted)
形態(tài)淺米色固體。
顏色淡黃色至深棕色
BRN266702
LogP2.940 (est)
CAS 數(shù)據(jù)庫479-13-0(CAS DataBase Reference)
EPA化學物質信息Coumestrol (479-13-0)

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H302-H315-H319-H335
危險品標志Xn
危險類別碼R22-R36/37/38
安全說明S26-S36
WGK Germany3
RTECS號DF8077000

知名試劑公司產(chǎn)品信息

考邁斯托醇價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2025/02/08HY-N2335考邁斯托醇
Coumestrol
479-13-01 mg419元
2025/02/08HY-N2335考邁斯托醇
Coumestrol
479-13-05mg950元
2025/02/08HY-N2335考邁斯托醇
Coumestrol
479-13-010 mM * 1 mLin DMSO1045元

常見問題列表

生物活性
Coumestrol是大豆產(chǎn)品中存在的植物雌激素。可用于癌癥,神經(jīng)障礙和自身免疫疾病的研究。抑制ES2細胞增殖的IC50值為50 μM。
靶點

IC50: 50 μM

體外研究

Coumestrol exerts chemotherapeutic effects via PI3K and ERK1/2 MAPK pathways. Coumestrol inhibits viability and invasion, and induces apoptosis of ES2 (clear cell-/serous carcinoma origin) cells. In addition, immunoreactive PCNA and ERBB2, markers of proliferation of ovarian carcinoma, are attenuated in their expression in coumestrol-induced death of ES2 cells. Phosphorylation of AKT, p70S6K, ERK1/2, JNK1/2 and p90RSK is inactivated by coumestrol treatment in a dose- and time-dependent manner. Coumestrol inhibits proliferation and induces apoptosis in MCF-7 cells, which is prevented by copper chelator neocuproine and ROS scavengers. Coumestrol treatment induces ROS generation coupled to DNA fragmentation, up-regulation of p53/p21, cell cycle arrest at G1/S phase, mitochondrial membrane depolarization and caspases 9/3 activation.

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