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120373-36-6

中文名稱 烏諾前列酮
英文名稱 UNOPROSTONE
CAS 120373-36-6
分子式 C22H38O5
分子量 382.53
MOL 文件 120373-36-6.mol
120373-36-6 結(jié)構(gòu)式 120373-36-6 結(jié)構(gòu)式

基本信息

中文別名
烏諾前列酮 1KG
英文別名
UNOPROSTONE
Unii-6X4F561V3w
Unoprostone [inn]
13,14-DIHYDRO-15-KETO-20-ETHYL PROSTAGLANDIN F2ALPHA
9ALPHA, 11ALPHA-DIHYDROXY-15-OXO-20A,20B-DIHOMOPROST-5-EN-1-OIC ACID
(E)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-(3-oxodecyl)cyclopentyl]-5-heptenoic acid
5-Heptenoic acid, 7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-(3-oxodecyl)cyclopentyl]-, (5Z)-

物理化學(xué)性質(zhì)

沸點(diǎn)562.9±40.0 °C(Predicted)
密度1.069±0.06 g/cm3(Predicted)
儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMF: 25 mg/ml; DMSO: 17 mg/ml; Ethanol: 12 mg/ml; PBS (7.2): 90 μg/ml
酸度系數(shù)(pKa)4.76±0.10(Predicted)

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS08
警示詞危險(xiǎn)
危險(xiǎn)性描述H360

常見(jiàn)問(wèn)題列表

生物活性
Unoprostone 是一種前列腺素 F2α 類似物 (PGAs),可通過(guò)激活 BK 通道來(lái)減少氧化應(yīng)激和光誘導(dǎo)的視網(wǎng)膜細(xì)胞死亡以及吞噬功能障礙。Unoprostone 可以降低眼內(nèi)壓,局部用于青光眼或高眼壓癥。
體外研究

Pretreatment with Unoprostone (0.01, 0.1, 1 μM; 1 h before H 2 O 2 treatment) protects against H 2 O 2 -induced cell death in a concentration-dependent manner and the effect is significant at 0.1 μM and 1 μM concentrations.
Pretreatment with Unoprostone at concentrations of 0.1 to 3 μM protects against light-induced cell death in a concentration-dependent manner; the effect is significant at the 1 and 3 μM concentrations. Unoprostone reduces the morphological change, and it significantly inhibits the low mitochondrial membrane potential and cell death induced by light irradiation.
Unoprostone has prostaglandin F receptors (FP) binding affinity with a K i of 3.86 μM.

Cell Viability Assay

Cell Line: H 2 O 2 -induced photoreceptor cell
Concentration: 0.01, 0.1, 1 μM
Incubation Time: 1 hour before H 2 O 2 treatment
Result: Protected against H 2 O 2 -induced cell death in a concentration-dependent manner.
體內(nèi)研究

Unoprostone (0.06%, 0.12%; topical instillation; 3 μl) reduces mouse intraocular pressure (IOP) in a dose-dependent manner.

Animal Model: Male mice (6 weeks old)
Dosage: 0.06%, 0.12%
Administration: Topical instillation; 3 μl
Result: Reduced mouse IOP in a dose-dependent manner.
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