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1338247-35-0

中文名稱 BMS-5
英文名稱 N-(5-(1-(2,6-dichlorophenyl)-3-(difluoroMethyl)-1H-pyrazol-5-yl)thiazol-2-yl)isobutyraMide
CAS 1338247-35-0
分子式 C17H14Cl2F2N4OS
分子量 431.29
MOL 文件 1338247-35-0.mol
更新日期 2024/10/28 15:27:44
1338247-35-0 結(jié)構(gòu)式 1338247-35-0 結(jié)構(gòu)式

基本信息

中文別名
化合物BMS5
BMS-5游離態(tài)
英文別名
LIMKI-3
CS-2190
BMS 5
BMS5
BMS-5 ≥95%
BMS-5, LIMKI-3
LIMKI-3
BMS5
BMS 5
LIMKI3
LIMKI 3
N-(5-(1-(2,6-dichlorophenyl)-3-(difluoroMethyl)-1H-pyrazol-5-yl)thiazol-2-yl)isobutyraMide
N-[5-[1-(2,6-Dichlorophenyl)-3-(difluoromethyl)-1H-pyrazol-5-yl]-2-thiazolyl]-2-methylpropanamide
Propanamide, N-[5-[1-(2,6-dichlorophenyl)-3-(difluoromethyl)-1H-pyrazol-5-yl]-2-thiazolyl]-2-methyl-
N-{5-[1-(2,6-Dichlorophenyl)-3-(difluoromethyl)-1H-pyrazol-5-yl]- 1,3-thiazol-2-yl}-2-methylpropanamide

物理化學性質(zhì)

密度1.54±0.1 g/cm3(Predicted)
儲存條件Sealed in dry,Store in freezer, under -20°C
溶解度DMSO:PBS (pH 7.2) (1:5):0.2(Max Conc. mg/mL);0.46(Max Conc. mM)
Ethanol:3.0(Max Conc. mg/mL);6.96(Max Conc. mM)
酸度系數(shù)(pKa)9.51±0.50(Predicted)
形態(tài)白色粉末
顏色White to off-white

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險性描述H302-H312-H332
防范說明P280
BMS-5價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/11/08S0185BMS-5
BMS-5
1338247-35-05mg857.46元
2024/11/08S0185BMS-5
BMS-5
1338247-35-025mg1775.47元
2024/11/08S0185BMS-51338247-35-0100mg6855.74元

常見問題列表

生物活性
BMS-5 (LIMKi 3) 是一種有效的 LIM kinases (LIMK) 的抑制劑,對LIMK1和LIMK2的IC50值分別為7 nM和8 nM。
靶點
TargetValue
LIMK1
(Cell-free assay)
7 nM
LIMK2
(Cell-free assay)
8 nM
體外研究

BMS-5 (LIMKi 3) inhibits cofilin-Ser3 phosphorylation in a dose-dependent manner in Nf2 ΔEx2 mouse Schwann cells (MSCs) with an IC 50 of ~2 μM. BMS-5 (LIMKi 3) reduces Nf2 ΔEx2 MSC viability in a dose-dependent manner with an IC 50 of 3.9 μM, but does not significantly reduce the viability of control Nf2 flox2/flox2 MSCs at equivalent BMS-5 concentrations. At 10 μM BMS-5, Nf2 ΔEx2 MSC viability is 40% compared to 83% for controls.

體內(nèi)研究

BMS-5 (LIMKi 3) (20 or 200 μM/side) is bilaterally infused into the hippocampus of rats immediately after contextual fear conditioning training. Rats are tested for memory consolidation 48 h after fear conditioning. Post hoc analysis shows that the group treated with 200 μM BMS-5 express lower freezing levels compared to the 20 μM and vehicle groups (P<0.01).

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