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Merck
CN

D8174

9,11-二脱氧基-11α,9α-亚甲基环氧前列腺素 F

≥98% (HPLC), solution, thromboxane A2 agonist

别名:

U-46619, U46619

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关于此项目

经验公式(希尔记法):
C21H34O4
化学文摘社编号:
分子量:
350.49
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352211
MDL number:
Beilstein/REAXYS Number:
4267334
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产品名称

9,11-二脱氧基-11α,9α-亚甲基环氧前列腺素 F, solution, 10 mg/mL in methyl acetate

InChI

1S/C21H34O4/c1-2-3-6-9-17(22)12-13-19-18(16-14-20(19)25-15-16)10-7-4-5-8-11-21(23)24/h4,7,12-13,16-20,22H,2-3,5-6,8-11,14-15H2,1H3,(H,23,24)/b7-4-,13-12+/t16?,17-,18-,19+,20?/m0/s1

SMILES string

CCCCC[C@H](O)\C=C\[C@H]1C2CC(CO2)[C@@H]1C\C=C/CCCC(O)=O

InChI key

LQANGKSBLPMBTJ-REGKDVDGSA-N

form

solution

concentration

10 mg/mL in methyl acetate

shipped in

dry ice

storage temp.

−20°C

Quality Level

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Application

9,11-双脱氧-11α,9α-环氧基甲烷前列腺素F2α已用于:
  • 诱导肌球蛋白轻链9(Myl9)基因缺失的小鼠的主动脉平滑肌(SM)收缩
  • 诱导收缩作为小鼠主动脉血管反应性实验的一部分
  • 作为血栓素/前列腺激动剂,以研究二硫苏糖醇(DTT)对小鼠动脉血管活性的影响

Biochem/physiol Actions

9,11-双脱氧-11α,9α-环氧基甲烷前列腺素F2α是一种血栓素A2激动剂。它可在体外实验中诱导血小板的形状变化、凝集、分泌、磷酸肌醇水解和蛋白质磷酸化。它还会引起胞质Ca++水平的升高,轻微影响环磷酸腺苷(cAMP)的形成。它可用作血管细胞粘附分子-1(VCAM-1)的有效刺激因子,以介导白细胞粘附至内皮细胞。

Features and Benefits

《受体分类和信号转导》手册的 前列腺素类受体 页面有该化合物的介绍。想要浏览手册的其他页面, 请单击此处

General description

9,11-双脱氧-11α,9α-环氧基甲烷前列腺素F2α是一种内过氧化物/血栓素类似物。

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

target_organs

Central nervous system

supp_hazards

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

14.0 °F

flash_point_c

-10 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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