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

• 常用名: N-[(3-bromophenyl)(2-methyl-1H-indol-3-yl)methyl]pyridin-2-amine
• 英文名: N-[(3-bromophenyl)(2-methyl-1H-indol-3-yl)methyl]pyridin-2-amine
• CAS号: 618404-88-9
• 分子量: 392.3
• 密度: N/A
• 沸点: N/A
• 分子式: C₂₁H₁₈BrN₃
• 熔点: N/A
• 闪点: N/A

名称

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

物理化学性质

• 分子式: C₂₁H₁₈BrN₃
• 分子量: 392.3
• InChIKey: VGXNPIDAUCMBNF-UHFFFAOYSA-N
• SMILES: CC1=C(C2=CC=CC=C2N1)C(C3=CC(=CC=C3)Br)NC4=CC=CC=N4

靶点实验

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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：Screen for inhibitors of RMI FANCM (MM2) intereaction 来源：11908 靶标：N/A External Id：RMI-FANCM-MM2

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：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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