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887401-92-5

中文名稱 INCB-3284
英文名稱 INCB 3284
CAS 887401-92-5
分子式 C26H31F3N4O4
分子量 520.54
MOL 文件 887401-92-5.mol
更新日期 2024/11/15 18:20:29
887401-92-5 結(jié)構(gòu)式 887401-92-5 結(jié)構(gòu)式

基本信息

英文別名
INCB-003284
N-({1-[4-Hydroxy-4-(6-methoxy-pyridin-3-yl)-cyclohexyl]-pyrrolidin-3-ylcarbamoyl}-methyl)-3-trifluoromethyl-benzamide
Benzamide, N-[2-[[(3R)-1-[trans-4-hydroxy-4-(6-methoxy-3-pyridinyl)cyclohexyl]-3-pyrrolidinyl]amino]-2-oxoethyl]-3-(trifluoromethyl)-

物理化學(xué)性質(zhì)

沸點703.7±60.0 °C(Predicted)
密度1.35±0.1 g/cm3(Predicted)
儲存條件-20°C儲存
溶解度可溶于DMSO(少許)、甲醇(少許)
酸度系數(shù)(pKa)12.94±0.46(Predicted)
形態(tài)固體
顏色黃色至深黃色

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-H315-H319-H335

常見問題列表

生物活性
INCB 3284 是一種有效的,選擇性的人 CCR2 拮抗劑,能夠抑制單核細(xì)胞趨化蛋白 1 與 hCCR2 結(jié)合,IC50 值為 3.7 nM。INCB 3284 可用于急性肝功能衰竭的研究。
靶點

MCP-1-hCCR2

3.7 nM (IC 50 )

體外研究

INCB 3284 is a pentent, selective and orally bioavailable human CCR2 antagonist, inhibiting monocyte chemoattractant protein-1 binding to hCCR2, with an IC 50 of 3.7 nM. INCB 3284 also causes an IC 50 of 4.7 nM in antagonism of chemotaxis activity, an IC 50 of 84 μM in inhibition of the hERG potassium current. However, INCB 3284 has no effec on CCR1, CCR3, CCR5, CXCR3, and CXCR5, or additional GPCRs at a concentration of 1 μM. Moreover, INCB 3284 potently inhibits CCR2-mediated signaling events such as intracellular calcium mobilization and ERK phosphorylation with IC 50 values of 6 and 2.6 nM, respectively.

體內(nèi)研究

INCB 3284 (1 mg/kg/day, ip) reduces liver damage, and decreases microglia activation in AOM-treated mice via inhibition on CCR2. INCB 3284 also significantly reduces the pERK1/2 to tERK1/2 ratio, as well as G-protein signaling pathway activity and proinflammatory cytokine production in cortex lysates from mice administed with azoxymethane.

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