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303149-14-6

中文名稱 1-PHENYL-3-[[3-(TRIFLUOROMETHYL)PHENYL]IMINO]-1H-INDOL-2-ONE
英文名稱 HT-2157
CAS 303149-14-6
分子式 C21H13F3N2O
分子量 366.34
MOL 文件 303149-14-6.mol
更新日期 2024/12/23 09:08:15
303149-14-6 結(jié)構(gòu)式 303149-14-6 結(jié)構(gòu)式

基本信息

中文別名
化合物HT-2157
英文別名
HT-2157
SNAP 37889
HT-2157(SNAP37889)
SNAP-37889 (HT-2157)
SNAP 37889, CID1471834
1-phenyl-3-[3-(trifluoromethyl)phenyl]iminoindol-2-one
1-PHENYL-3-[[3-(TRIFLUOROMETHYL)PHENYL]IMINO]-1H-INDOL-2-ONE
2H-Indol-2-one, 1,3-dihydro-1-phenyl-3-[[3-(trifluoromethyl)phenyl]imino]-
所屬類別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

熔點(diǎn)141-144 °C
沸點(diǎn)484.0±55.0 °C(Predicted)
密度1.29±0.1 g/cm3(Predicted)
儲(chǔ)存條件-20°C儲(chǔ)存
溶解度DMF:30.0(Max Conc. mg/mL);81.89(Max Conc. mM)
DMSO:44.0(Max Conc. mg/mL);120.11(Max Conc. mM)
Ethanol:7.0(Max Conc. mg/mL);19.11(Max Conc. mM)
酸度系數(shù)(pKa)-0.36±0.20(Predicted)
形態(tài)固體
顏色Yellow to orange
1-PHENYL-3-[[3-(TRIFLUOROMETHYL)PHENYL]IMINO]-1H-INDOL-2-ONE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
2024/11/08HY-1007171-PHENYL-3-[[3-(TRIFLUOROMETHYL)PHENYL]IMINO]-1H-INDOL-2-ONE
HT-2157
303149-14-61mg900元
2024/11/08HY-1007171-PHENYL-3-[[3-(TRIFLUOROMETHYL)PHENYL]IMINO]-1H-INDOL-2-ONE
HT-2157
303149-14-610mM * 1mLin DMSO2176元
2024/11/08HY-1007171-PHENYL-3-[[3-(TRIFLUOROMETHYL)PHENYL]IMINO]-1H-INDOL-2-ONE
HT-2157
303149-14-65mg2700元

常見(jiàn)問(wèn)題列表

生物活性
HT-2157(SNAP 37889) 是一種選擇性的高親和力甘丙肽-3 受體 (Gal3) 競(jìng)爭(zhēng)性拮抗劑。
靶點(diǎn)

Galanin-3 receptor

體外研究

HT-2157 (SNAP 37889) binds with high affinity to membranes from transiently transfected LMTK - cells expressing the human Gal 3 receptor (K i =17.44±0.01 nM; n>100) and is highly selective for Gal 3 over the Gal 1 and Gal 2 subtypes (K i >10,000 nM for each subtype; n=46 of each subtype). When tested for the antagonism of galanin-evoked inhibition of adenylyl cyclase, HT-2157 (0.1-10 μM) produces concentration-dependent rightward shifts of the concentration-effect curve to galanin.

體內(nèi)研究

The galanin-3 receptor antagonist, HT-2157 (SNAP 37889), reduces operant responding for ethanol in alcohol-preferring rats. The novel selective GALR3 antagonist, HT-2157, to reduce anxiety-like behaviour and voluntary ethanol consumption in the iP (alcohol-preferring) rat. Male iP rats treated with HT-2157 at a dose of 30 mg/kg (i.p.) do not show altered locomotor activity or changes in anxiety-like behaviour in the elevated plus maze or light-dark paradigms. Treatment with HT-2157 (30 mg/kg, i.p.) reduces operant responding for solutions containing ethanol, sucrose and saccharin. Collectively, results from the current study shows that HT-2157 (30 mg/kg, i.p.) is effective in reducing operant responding for ethanol, independent of a sedative effect.

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