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177943-33-8

中文名稱 (S)-3-aMino-1-hydroxy-3,4-dihydroquinolin-2(1H)-one hydrochloride
CAS 177943-33-8
分子式 C9H11ClN2O2
分子量 214.649
MOL 文件 177943-33-8.mol
177943-33-8 結(jié)構(gòu)式 177943-33-8 結(jié)構(gòu)式

基本信息

英文別名
177943-33-8
PF04859989 hydrochloride
PF-4859989 hydrochloride
PF-04859989 hydrochloride
PF-04859989 hydrochloride >=98% (HPLC)
(3S)-3-Amino-1-hydroxy-3,4-dihydroquinolin-2(1H)-one
L-3-Amino-3,4-dihydro-1-hydroxycarbstyril hydrochloride
(S)-3-aMino-1-hydroxy-3,4-dihydroquinolin-2(1H)-one hydrochloride
2(1H)-Quinolinone, 3-amino-3,4-dihydro-1-hydroxy-, monohydrochloride, (S)- (9CI)
PF 04859989 hydrochloride - L-3-Amino-3,4-dihydro-1-hydroxycarbstyril hydrochloride

物理化學(xué)性質(zhì)

儲存條件room temp
溶解度在水中的溶解度為20mg/mL,澄清
形態(tài)粉末
顏色白色至米色

常見問題列表

生物活性
PF-04859989 hydrochloride 是一種可透過血腦屏障的,不可逆的犬尿氨酸轉(zhuǎn)氨酶 KAT II 抑制劑,對 hKATⅡ 和 rKATⅡ 的 IC50 分別為 23 和 263 nM。PF-04859989 hydrochloride 對 KATⅡ 的選擇性高于人 KATⅠ、KATⅢ 和 KATⅣ (IC50 分別為22、11和 >50 μM)。
體內(nèi)研究

In vivo pharmacokinetic and efficacy studies in rat show that PF-04859989 is a brain-penetrant, irreversible inhibitor and is capable of reducing brain kynurenic acid by 50% at a dose of 10 mg/kg (sc).
Rats receiving PF-04859989 (5 mg/kg; i.p.) exhibited a significantly lower number of spontaneously active DA neurons pertrack.

Animal Model: Male Sprague-Dawley rats
Dosage: 5 mg/kg
Administration: I.p.
Result: Exhibited a significantly lower number of spontaneously active dopamine (DA) neurons pertrack compared to controls.
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