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162760-96-5

中文名稱 WAY-100635;WAY 100635; WAY100635
英文名稱 CYCLOHEXANECARBOXAMIDE, N-[2-[4-(2-METHOXYPHENYL)-1-PIPERAZINYL]ETHYL]-N-2-PYRIDINYL-, HYDROCHLORIDE (1:3)
CAS 162760-96-5
分子式 C25H34N4O2
分子量 422.56
MOL 文件 162760-96-5.mol
更新日期 2024/12/03 15:40:35
162760-96-5 結(jié)構(gòu)式 162760-96-5 結(jié)構(gòu)式

基本信息

中文別名
化合物 T21561
N-(2-(4-(2-甲氧基苯基)哌嗪-1-基)乙基)-N-(吡啶-2-基)環(huán)己甲酰胺
英文別名
WAY 100635
WAY100635
WAY100635 TRIHYDROCHLORIDE
WAY-100635
WAY 100635
WAY100635
Cyclohexanecarboxamide,N-[2-[4-(2-methoxyphenyl)-1-piperazinyl]ethyl]-N-2-pyridinyl-
N-{2-[4-(2-Methoxyphenyl)piperazin-1-yl]ethyl}-N-(pyridin-2-yl)cyclohexanecarboxaMide
CYCLOHEXANECARBOXAMIDE, N-[2-[4-(2-METHOXYPHENYL)-1-PIPERAZINYL]ETHYL]-N-2-PYRIDINYL-, HYDROCHLORIDE (1:3)
CYCLOHEXANECARBOXYLIC ACID (2-[4-(2-METHOXY-PHENYL)-PIPERAZIN-1-YL]-ETHYL)-PYRIDIN-2-YL-AMIDE TRIHYDROCHLORIDE

物理化學(xué)性質(zhì)

熔點(diǎn)>145oC (dec.)
沸點(diǎn)594.8±50.0 °C(Predicted)
密度1.154±0.06 g/cm3(Predicted)
儲(chǔ)存條件Sealed in dry,Room Temperature
溶解度少許溶于甲醇和水
酸度系數(shù)(pKa)6.84±0.10(Predicted)
形態(tài)固體
顏色灰白色至淡黃色
穩(wěn)定性吸濕性

常見(jiàn)問(wèn)題列表

生物活性
WAY-100635 是一種有效且具有選擇性的 5-hydroxytryptamine 1A (5-HT1A) 受體拮抗劑,其 IC50 值為 0.91 nM,Ki 值為 0.39 nM。WAY-100635 對(duì)于 5-HT1A 和 α1-腎上腺素的 pIC50 值分別為 8.9 和 6.6。WAY-100635 也是一種有效的多巴胺 D4 受體激動(dòng)劑。
靶點(diǎn)

5-HT 1A Receptor

8.87 (pIC 50 )

5-HT 1A Receptor

9.71 (pA2)

體外研究

The functional properties and binding affinities of WAY-100635 are evaluated in HEK 293 cells stably expressing dopamine D 2L or D 4.4 receptors.
WAY-100635 displays 940, 370, and 16 nM binding affinities at D 2L , D 3 , and D 4.2 receptors, respectively. Saturation analyses demonstrat that the K d of [ 3 H] WAY-100635 at D 4.2 receptors is 2.4 nM. WAY-100635 is potent agonist in HEK-D 4.4 cells with EC 50 of 9.7 nM. WAY-100635 possesses high affinity for D 4.4 receptor (3.3 nM) .

體內(nèi)研究

WAY-100635 (1 mg/kg; subcutaneous injection; male Sprague-Dawley rats) treatment abolishes the reduction of the severity of abstinence signs induced by Rhodiola rosea administration in nicotine-dependent rat.

Animal Model: Male Sprague-Dawley rats (220-240 g)
Dosage: 1 mg/kg
Administration: Subcutaneous injection (Pharmacokinetic study)
Result: Reduced total abstinence score, increased immobility time and the burying behavior was increased.
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