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215804-67-4

CAS 215804-67-4
分子式 C28H30N4O
分子量 438.564
MOL 文件 215804-67-4.mol
更新日期 2023/03/20 15:41:27
215804-67-4 結(jié)構(gòu)式 215804-67-4 結(jié)構(gòu)式

物理化學(xué)性質(zhì)

儲(chǔ)存條件2-8°C
溶解度DMSO:可溶,2mg/mL,澄清(加熱)
形態(tài)粉末
顏色白色至米色

安全數(shù)據(jù)

WGK Germany3
化合物 SB-277011 HYDROCHLORIDE價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2024/11/08HY-10847BSB-277011 hydrochloride215804-67-45mg1000元
2024/11/08HY-10847BSB-277011 hydrochloride215804-67-410mM * 1mLin DMSO1050元
2024/11/08HY-10847BSB-277011 hydrochloride215804-67-410mg1600元

常見(jiàn)問(wèn)題列表

生物活性
SB-277011 hydrochloride (SB-277011A hydrochloride) 是一種強(qiáng)效、選擇性、口服生物利用度和腦透多巴胺 D3 受體(D3R) 拮抗劑,其 Ki 值在嚙齒動(dòng)物和人D3R 分別為 10.7 nM 和 11.2 nM。SB-277011 hydrochloride 對(duì) D3 受體比其他多巴胺受體表現(xiàn)出 80-100 倍的選擇性,,對(duì) D3,D2,5-HT1B?和 5-HT1D 受體的?pKi 值分別為 8.0,6.0,<5.2 和 5.9。
靶點(diǎn)

D 3 Receptor

10.7-11.2 nM (Ki)

D 2 Receptor

5-HT 1D Receptor

5-HT 1B Receptor

體內(nèi)研究

SB-277011 hydrochloride has an excellent pharmacokinetic profile, exhibits oral bioavailability 43%, half-life:2.0 h, plasma clearance 19 mL/min/kg) and to be highly brain-penetrant (brain:blood ratio of 3.6:1), with a clean P450 profile in the rat.SB-277011 hydrochloride (SB 277011; 3 mg/kg, p.o.) completely reverses the effects of quinelorane in the nucleus accumbens, but does not reverse the effects of quinelorane in the striatum at 93 mg/kg in rats.SB-277011 (intraperitoneal injection; 12.5-25 mg/kg) significantly and dose-dependently reduces intravenous cocaine self-administration under both low fixed-ratio and progressive-ratio reinforcement conditions in rats. When it increases to 50 mg/kg, SB-277011 can significantly inhibit basal and cocaine-enhanced locomotion in rats.

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