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139290-65-6

中文名稱 139290-65-6
英文名稱 (R)-(+)-ALPHA-(2,3-DIMETHOXYPHENYL)-1-[2-(4-FLUORO-PHENYL)ETHYL]-4-PIPERIDINE METHANOL
CAS 139290-65-6
分子式 C22H28FNO3
分子量 373.46
MOL 文件 139290-65-6.mol
更新日期 2025/04/13 09:49:27
139290-65-6 結(jié)構(gòu)式 139290-65-6 結(jié)構(gòu)式

基本信息

中文別名
氟利色林
諾和靈 M100907
VOLINANSERIN MDL 100907 (R構(gòu)型)
Volinanserin MDL 100907 (R構(gòu)型)
英文別名
M 100907
MDL100907
R-MDL 100907
VOLINANSERIN
MDL 100907 NEW
MDL100907-L-tartrate
MDL100907 tartrate salt
MDL 100907 (MDL-100907
MDL-100907(Volinanserin)
Volinanserin (MDL100907)

物理化學(xué)性質(zhì)

熔點(diǎn)89-91°C
沸點(diǎn)499.4±45.0 °C(Predicted)
密度1.150±0.06 g/cm3(Predicted)
儲(chǔ)存條件-20°C冷凍
儲(chǔ)存條件2-8°C
溶解度二甲基亞砜:≥20mg/mL
酸度系數(shù)(pKa)13.93±0.20(Predicted)
形態(tài)粉末
顏色灰白色至淺棕色

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS09
警示詞警告
危險(xiǎn)性描述H400
防范說明P273
危險(xiǎn)品標(biāo)志N
危險(xiǎn)類別碼50
安全說明61
危險(xiǎn)品運(yùn)輸編號(hào)UN 3077 9 / PGIII
WGK Germany3
139290-65-6價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2025/02/08HY-14940139290-65-6
Volinanserin
139290-65-65mg1100元
2025/02/08HY-14940139290-65-6
Volinanserin
139290-65-610mM * 1mLin DMSO1210元
2025/02/08HY-14940139290-65-6
Volinanserin
139290-65-610mg1760元

常見問題列表

生物活性
Volinanserin (Volinanserin Hydrochloride Salt, MDL100907, M 100907, MDL-100,907)是一種高度選擇性的、有效的 5-HT2 receptor 的拮抗劑,其Ki值為0.36 nM。Volananserin 具有治療精神紊亂的藥物活性。
靶點(diǎn)
TargetValue
5-HT2 receptor
(Cell-free assay)
0.36 nM(Ki)
體外研究

Volinanserin (MDL 100907) is a potent antagonist at the 5-HT 2 receptor, with a K i of 0.36 nM, and shows 300-fold selectivity for 5-HT 2 receptor over 5-HT 1c receptor, alpha-1 and DA D 2 receptors. Volinanserin has antipsychotic activity.

體內(nèi)研究

Volinanserin (MDL 100907; 0.008-2.0 mg/kg, i.p.) significantly decreases d-amphetamine-stimulated locomotor activity in mice, with an ED 50 of 0.3 mg/kg, but shows no obvious reduction in the base-line locomotor activity in mice. Volinanserin produces atalepsy with an ED 50 of 10-50 mg/kg in rats. Volinanserin does not reduces apomorphine-induced stereotypies or produces catalepsy in rats. Volinanserin (M100907) combined with MK-801 significantly decreases reinforcers at 1 μg/kg, but dose-dependently (10, 100 μg/kg) antagonizes the disruptive effect of MK-801 in rats via i.p. administration. Volinanserin (6.25 μg/kg) enhances the antidepressant-like action of desipramine in rats performing under a DRL 72-s schedule, and elevates the antidepressant-like effect of tranylcypromine.

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