SML3924
INCB3344
≥98% (HPLC)
别名:
INCB-3344, INCB 3344, trans-N-(2-{1-[4-(Benzo[d][1,3]dioxol-5-yl)-4-hydroxycyclohexyl]-4-ethoxypyrrolidin-3-ylamino}-2-oxoethyl)-3-(trifluoromethyl)benzamide
登录 查看组织和合同定价。
选择规格
变更视图
关于此项目
经验公式（希尔记法）:
C29H34F3N3O6
化学文摘社编号:
分子量:
577.59
UNSPSC Code:
51111800
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
powder
Quality Segment
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
-10 to -25°C
Biochem/physiol Actions
Orally active, potent and selective CCR2 antagonist in vitro and in vivo.
INCB3344 is an orally active, potent and selective CCR2 antagonist (human/mouse/rat/cynomolgus IC50 = 5.1/9.5/7.3/16 nM by competitive binding assays, IC50 = 3.8/7.8/2.7/6.2 nM by chemotaxis assays) with >100-fold selectivity over other homologous chemokine receptors. INCB3344 shows in vivo efficacy in a murine EAE model (thioglycolate-induced peritonitis in mice; 30-100 mg/kg bid. p.o. against peritoneal macrophage influx) and a rat adjuvant arthritis model (100 mg/kg bid. p.o. against adjuvant-induced macrophages infiltration of the joint).
INCB3344 is an orally active, potent and selective CCR2 antagonist (human/mouse/rat/cynomolgus IC50 = 5.1/9.5/7.3/16 nM by competitive binding assays, IC50 = 3.8/7.8/2.7/6.2 nM by chemotaxis assays) with >100-fold selectivity over other homologous chemokine receptors. INCB3344 shows in vivo efficacy in a murine EAE model (thioglycolate-induced peritonitis in mice; 30-100 mg/kg bid. p.o. against peritoneal macrophage influx) and a rat adjuvant arthritis model (100 mg/kg bid. p.o. against adjuvant-induced macrophages infiltration of the joint).
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable