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226226-39-7

中文名稱 226226-39-7
英文名稱 N-[2-[[(3R)-1-[(4-chlorophenyl)methyl]-3-pyrrolidinyl]amino]-2-oxoethyl]-3-(trifluoromethyl)benzamidehydrochloride
CAS 226226-39-7
分子式 C21H21ClF3N3O2
分子量 439.86
MOL 文件 226226-39-7.mol
226226-39-7 結(jié)構(gòu)式 226226-39-7 結(jié)構(gòu)式

基本信息

中文別名
CCR2 ANTAGONIST 4
英文別名
Teijin compound 1
CCR2 antagonist 4
Teijin compound 1 hydrochloride
N-[2-[[(3R)-1-[(4-chlorophenyl)methyl]pyrrolidin-3-yl]amino]-2-oxo-ethyl]-3-(trifluoromethyl)benzamide
Benzamide, N-[2-[[(3R)-1-[(4-chlorophenyl)methyl]-3-pyrrolidinyl]amino]-2-oxoethyl]-3-(trifluoromethyl)-
N-[2-[[(3R)-1-[(4-chlorophenyl)methyl]-3-pyrrolidinyl]amino]-2-oxoethyl]-3-(trifluoromethyl)benzamidehydrochloride

物理化學(xué)性質(zhì)

沸點(diǎn)597.9±50.0 °C(Predicted)
密度1.37±0.1 g/cm3(Predicted)
儲存條件Desiccate at +4°C
溶解度二甲基亞砜:≥20mg/mL
酸度系數(shù)(pKa)12.94±0.46(Predicted)
形態(tài)粉末
顏色白色至棕褐色

安全數(shù)據(jù)

WGK Germany3
226226-39-7價(jià)格(試劑級)
報(bào)價(jià)日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價(jià)格
2025/02/08HY-108323CCR2 antagonist 4226226-39-71 mg600元
2025/02/08HY-108323226226-39-7
CCR2 antagonist 4
226226-39-75mg1500元
2025/02/08HY-108323226226-39-7
CCR2 antagonist 4
226226-39-710mM * 1mLin DMSO1650元

常見問題列表

生物活性
CCR2 antagonist 4 (Teijin compound 1) 是一種高效、特異的 CCR2 拮抗劑,對 CCR2b 的 IC50 值為 180 nM。CCR2 antagonist 4 對 MCP-1 誘導(dǎo)的趨化作用有較強(qiáng)的抑制作用,其 IC50 為 24 nM。
靶點(diǎn)

CCR2b

180 nM (IC 50 )

體外研究

Ile263 and Thr292 in CCR2 contribute significantly to binding of Teijin compound 1 in CCR2. Residue Glu291 in TM7, a highly conserved residue in many CC chemokine receptors, contributes substantially to binding of the protonated CCR2 antagonist 4, and CCL2. His121 on TM3 and Ile263 on TM6 also strongly interact with CCR2 antagonist 4.
In ApoE-deficient mice, Vp-TSL targets specifically aortic plaque endothelial VCAM-1 and CCR2 antagonist 4 reduces the mouse monocyte/macrophage cell line (RAW 264.7) adhesion/ infiltration into the aorta.

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