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1155877-97-6

中文名稱 D159687
英文名稱 1-(4-((3'-Chloro-6-Methoxy-[1,1'-biphenyl]-3-yl)Methyl)phenyl)urea
CAS 1155877-97-6
分子式 C21H19ClN2O2
分子量 366.84
MOL 文件 1155877-97-6.mol
更新日期 2024/11/08 11:24:23
1155877-97-6 結(jié)構(gòu)式 1155877-97-6 結(jié)構(gòu)式

基本信息

中文別名
化合物D 159687
1-(4-((3'-氯-6-甲氧基-[1,1'-聯(lián)苯]-3-基)甲基)苯基)脲
1-(4-((3'-氯-6-甲氧基-[1,1'-聯(lián)苯]-3-基)甲基)苯基)脲
英文別名
D159687
D159687
D-159687
D 159687
1-(4-((3'-chloro-6-methoxybiphenyl-3-yl)methyl)phenyl)urea
1-(4-((3'-Chloro-6-Methoxy-[1,1'-biphenyl]-3-yl)Methyl)phenyl)urea
Urea, N-[4-[(3'-chloro-6-methoxy[1,1'-biphenyl]-3-yl)methyl]phenyl]-

物理化學(xué)性質(zhì)

沸點(diǎn)502.0±50.0 °C(Predicted)
密度1.263±0.06 g/cm3(Predicted)
儲(chǔ)存條件Sealed in dry,Room Temperature
溶解度DMSO : 150 mg/mL (408.90 mM)
酸度系數(shù)(pKa)14.48±0.50(Predicted)
形態(tài)Solid
顏色White to off-white

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H315-H319-H335
防范說(shuō)明P261-P305+P351+P338
D159687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-15444D159687
D159687
1155877-97-65mg600元
2024/11/08HY-15444D159687
D159687
1155877-97-610mM * 1mLin DMSO660元
2024/11/08HY-15444D159687
D159687
1155877-97-610mg960元

常見(jiàn)問(wèn)題列表

生物活性
D159687 是一種選擇性 PDE4D 抑制劑。
靶點(diǎn)

PDE4D

體外研究

D159687 (1 μM, 0-24?hours) induces a transient increase in CREB phosphorylation which peaked at 6?hours after treatment.
D159687 (0.01-1 μM, 6 hours) causes optimal CREB phosphorylation at 1?μM.

Western Blot Analysis

Cell Line: HT-22 (mouse hippocampal cell line)
Concentration: 1 μM
Incubation Time: 0, 1, 3, 6, 12, 24?hours
Result: Induced a transient increase in CREB phosphorylation which peaked at 6?hours after treatment.

Western Blot Analysis

Cell Line: HT-22 (mouse hippocampal cell line)
Concentration: 0.01 μM, 0.1 μM, 1 μM
Incubation Time: 6 hours
Result: CREB phosphorylation was optimal at 1?μM.
體內(nèi)研究

D159687 (0.05-5 mg/kg; oral daily for a week) shows a potential recruitment or enhancement of synaptic function with increased task difficulty in female Cynomolgus macaques.

Animal Model: Female Cynomolgus macaques (4–6 year old)
Dosage: 0.05, 0.5, 5 mg/kg
Administration: Oral daily for a week
Result: A potential recruitment or enhancement of synaptic function with increased task difficulty.
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