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(2S,5R)-4-[6-(3-amino-1H-indazol-6-yl)-2-(methylamino)-4-pyrimidinyl]-N-cyclohexyl-5-methyl-2-morpholinecarboxamide

更新时间:2025-09-03 13:25:47

(2S,5R)-4-[6-(3-amino-1H-indazol-6-yl)-2-(methylamino)-4-pyrimidinyl]-N-cyclohexyl-5-methyl-2-morpholinecarboxamide结构式
(2S,5R)-4-[6-(3-amino-1H-indazol-6-yl)-2-(methylamino)-4-pyrimidinyl]-N-cyclohexyl-5-methyl-2-morpholinecarboxamide结构式
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常用名 (2S,5R)-4-[6-(3-amino-1H-indazol-6-yl)-2-(methylamino)-4-pyrimidinyl]-N-cyclohexyl-5-methyl-2-morpholinecarboxamide 英文名 (2S,5R)-4-[6-(3-amino-1H-indazol-6-yl)-2-(methylamino)-4-pyrimidinyl]-N-cyclohexyl-5-methyl-2-morpholinecarboxamide
CAS号 1227917-83-0 分子量 464.6
密度 N/A 沸点 N/A
分子式 C24H32N8O2 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 (2S,5R)-4-[6-(3-amino-1H-indazol-6-yl)-2-(methylamino)-4-pyrimidinyl]-N-cyclohexyl-5-methyl-2-morpholinecarboxamide

 物理化学性质

分子式 C24H32N8O2
分子量 464.6
InChIKey ANERBUIPYRATIP-VLIAUNLRSA-N
SMILES CNc1nc(-c2ccc3c(N)n[nH]c3c2)cc(N2CC(C(=O)NC3CCCCC3)OCC2C)n1

 靶点实验

查看更多实验

实验名称:GSK PKIS2: Screen against O. lienalis microfilariae, single point, at 3.1uM to assess...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL3988182
实验名称:Inhibition of PDK1-mediated RSK phosphorylation at Ser221 residue in human PC3 cells ...
来源:ChEMBL
靶标:3-phosphoinositide-dependent protein kinase 1
External Id:CHEMBL1768784
实验名称:Antiproliferative activity against human OCI-AML2 cells
来源:ChEMBL
靶标:OCI-AML2
External Id:CHEMBL1768787
实验名称:Antiproliferative activity against human K562 cells
来源:ChEMBL
靶标:K562
External Id:CHEMBL1768786
实验名称:Antiproliferative activity against human HEL 92.1.7 cells
来源:ChEMBL
靶标:HEL
External Id:CHEMBL1768789
实验名称:Antiproliferative activity against human OCI-AML3 cells
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL1768788
实验名称:Antiproliferative activity against human F-36P cells
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL1768790
实验名称:Inhibition of aurora A
来源:ChEMBL
靶标:Aurora kinase A
External Id:CHEMBL1768779
实验名称:Inhibition of PDK1
来源:ChEMBL
靶标:3-phosphoinositide-dependent protein kinase 1
External Id:CHEMBL1768778
实验名称:Inhibition of ALK5
来源:ChEMBL
靶标:TGF-beta receptor type-1
External Id:CHEMBL1768781
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