2-[5-methoxy-2-methyl-1-(4-methylbenzoyl)indol-3-yl]acetic acid

更新时间：2025-10-23 03:50:31

2-[5-methoxy-2-methyl-1-(4-methylbenzoyl)indol-3-yl]acetic acid结构式	常用名	2-[5-methoxy-2-methyl-1-(4-methylbenzoyl)indol-3-yl]acetic acid	英文名	2-[5-methoxy-2-methyl-1-(4-methylbenzoyl)indol-3-yl]acetic acid
	CAS号	16401-76-6	分子量	337.36900
	密度	N/A	沸点	N/A
	分子式	C₂₀H₁₉NO₄	熔点	N/A
	MSDS	N/A	闪点	N/A

英文名	2-[5-methoxy-2-methyl-1-(4-methylbenzoyl)indol-3-yl]acetic acid
英文别名	更多

分子式	C₂₀H₁₉NO₄
分子量	337.36900
精确质量	337.13100
PSA	68.53000
LogP	3.58230
InChIKey	ASIGZZOVSCNZDW-UHFFFAOYSA-N
SMILES	COc1ccc2c(c1)c(CC(=O)O)c(C)n2C(=O)c1ccc(C)cc1

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1412449-37-6

~82%

2-[5-methoxy-2-...

16401-76-6

文献：Liedtke, Andy J.; Marnett, Lawrence J.; Kim, Kwangho; Stec, Donald F.; Sulikowski, Gary A. Tetrahedron, 2012 , vol. 68, # 48 p. 10049 - 10058,10 Title/Abstract Full Text Show Details Liedtke, Andy J.; Kim, Kwangho; Stec, Donald F.; Sulikowski, Gary A.; Marnett, Lawrence J. Tetrahedron, 2012 , vol. 68, # 48 p. 10049 - 10058

4-甲氧基苯肼盐酸盐

19501-58-7

对甲基苯甲酰氯

874-60-2

乙酰丙酸

123-76-2

~23%

2-[5-methoxy-2-...

16401-76-6

文献：Rosenbaum, Claudia; Roehrs, Sonja; Mueller, Oliver; Waldmann, Herbert Journal of Medicinal Chemistry, 2005 , vol. 48, # 4 p. 1179 - 1187

5-甲氧基-2-甲基-3-吲哚乙酸

2882-15-7

2-[5-methoxy-2-...

16401-76-6

5-甲氧基-2-甲基-3-吲哚乙酸甲酯

7588-36-5

2-[5-methoxy-2-...

16401-76-6

实验名称：Effect of compound (10 uM) on doxorubicin-induced cytotoxicity towards T98G cell line...
来源：ChEMBL
靶标：T98G
External Id：CHEMBL835714

实验名称：Inhibition Assay from US Patent US9346803: "Indomethacin analogs for the treatment of...
来源：BindingDB
靶标：N/A
External Id：BindingDB_8047_1

实验名称：Inhibition of human recombinant AKR1C2-mediated NADP+-dependent oxidation of S-(+)-1,...
来源：ChEMBL
靶标：Aldo-keto reductase family 1 member C2
External Id：CHEMBL2329816

实验名称：Inhibition of human recombinant AKR1C3-mediated NADP+-dependent oxidation of S-(+)-1,...
来源：ChEMBL
靶标：Aldo-keto reductase family 1 member C3
External Id：CHEMBL2329815

实验名称：Selectivity ratio of IC50 for human recombinant AKR1C2 to IC50 for human recombinant ...
来源：ChEMBL
靶标：N/A
External Id：CHEMBL2329814

实验名称：Selectivity ratio of IC50 for human recombinant AKR1C1 to IC50 for human recombinant ...
来源：ChEMBL
靶标：N/A
External Id：CHEMBL2329813

实验名称：Inhibition of human recombinant AKR1C1-mediated NADP+-dependent oxidation of S-(+)-1,...
来源：ChEMBL
靶标：Aldo-keto reductase family 1 member C1
External Id：CHEMBL2329812

实验名称：Inhibition of human recombinant AKR1C4-mediated NADP+-dependent oxidation of S-(+)-1,...
来源：ChEMBL
靶标：Aldo-keto reductase family 1 member C4
External Id：CHEMBL2329811

实验名称：Selectivity ratio of IC50 for human recombinant AKR1C4 to IC50 for human recombinant ...
来源：ChEMBL
靶标：N/A
External Id：CHEMBL2329810

共9条，当前第1页，共1页

2-(5-methoxy-2-methyl-1-(4-methylbenzoyl)-1H-indol-3-yl)acetic acid

1-(p-Methylbenzoyl)-2-methyl-5-methoxy-3-indolessigsaeure

1-(p-Methylbenzoyl)-2-methyl-5-methoxy-3-carboxymethyl-indol

1H-Indole-3-acetic acid,5-methoxy-2-methyl-1-(4-methylbenzoyl)

[5-methoxy-2-methyl-1-(4-methyl-benzoyl)-indol-3-yl]-acetic acid

2-[5-methoxy-2-methyl-1-(4-methylbenzoyl)indol-3-yl]acetic acid

名称

物理化学性质

合成线路

靶点实验

英文别名

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