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N-[(3-fluorophenyl)-(2-methyl-1H-indol-3-yl)methyl]pyridin-2-amine

更新时间:2026-03-01 23:41:09

N-[(3-fluorophenyl)-(2-methyl-1H-indol-3-yl)methyl]pyridin-2-amine结构式
N-[(3-fluorophenyl)-(2-methyl-1H-indol-3-yl)methyl]pyridin-2-amine结构式
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常用名 N-[(3-fluorophenyl)-(2-methyl-1H-indol-3-yl)methyl]pyridin-2-amine 英文名 N-[(3-fluorophenyl)-(2-methyl-1H-indol-3-yl)methyl]pyridin-2-amine
CAS号 618404-94-7 分子量 331.4
密度 N/A 沸点 N/A
分子式 C21H18FN3 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 N-[(3-fluorophenyl)-(2-methyl-1H-indol-3-yl)methyl]pyridin-2-amine

 物理化学性质

分子式 C21H18FN3
分子量 331.4
InChIKey FLKMWFWTSZVEMZ-UHFFFAOYSA-N
SMILES CC1=C(C2=CC=CC=C2N1)C(C3=CC(=CC=C3)F)NC4=CC=CC=N4

 靶点实验

查看更多实验

实验名称:Permeability of the compound at pH 7.4 by PAMPA
来源:ChEMBL
靶标:N/A
External Id:CHEMBL2073150
实验名称:Inhibition of LG190178-induced VDR-LBD interaction to Alexa Fluor 647-labeled SRC2-3 ...
来源:ChEMBL
靶标:Vitamin D3 receptor
External Id:CHEMBL2073151
实验名称:Aqueous solubility of the compound in phosphate buffered saline at pH 7.4
来源:ChEMBL
靶标:N/A
External Id:CHEMBL2073149
实验名称:Cytotoxicity against human HEK293T cells assessed as cell viability at 20.8 uM by Cel...
来源:ChEMBL
靶标:HEK-293T
External Id:CHEMBL2073155
实验名称:Inhibitors of CDC25B-CDK2/CyclinA interaction
来源:Center for Chemical Genomics, University of Michigan
External Id:MScreen:TargetID_600
实验名称:Inhibition of VDR-LBD expressed in human HEK293T cells co-expressing GAL4-DBD assesse...
来源:ChEMBL
靶标:Vitamin D3 receptor
External Id:CHEMBL2073152
实验名称:Inhibition of VDR-LBD expressed in human HEK293T cells co-expressing GAL4-DBD assesse...
来源:ChEMBL
靶标:Vitamin D3 receptor
External Id:CHEMBL2073153
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