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Propanedioic acid,2-(acetylamino)-2-[(5-nitro-1H-indol-3-yl)methyl]-, 1,3-diethyl ester

更新时间:2025-09-19 18:37:54

Propanedioic acid,2-(acetylamino)-2-[(5-nitro-1H-indol-3-yl)methyl]-, 1,3-diethyl ester结构式
Propanedioic acid,2-(acetylamino)-2-[(5-nitro-1H-indol-3-yl)methyl]-, 1,3-diethyl ester结构式
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常用名 Propanedioic acid,2-(acetylamino)-2-[(5-nitro-1H-indol-3-yl)methyl]-, 1,3-diethyl ester 英文名 Propanedioic acid,2-(acetylamino)-2-[(5-nitro-1H-indol-3-yl)methyl]-, 1,3-diethyl ester
CAS号 6958-33-4 分子量 391.37500
密度 1.342g/cm3 沸点 615.8ºC at 760mmHg
分子式 C18H21N3O7 熔点 N/A
MSDS N/A 闪点 326.2ºC

 名称

英文名 diethyl 2-acetamido-2-[(5-nitro-1H-indol-3-yl)methyl]propanedioate
英文别名 更多

 物理化学性质

密度 1.342g/cm3
沸点 615.8ºC at 760mmHg
分子式 C18H21N3O7
分子量 391.37500
闪点 326.2ºC
精确质量 391.13800
PSA 143.31000
LogP 2.53380
InChIKey IINRGTWFETXCNC-UHFFFAOYSA-N
SMILES CCOC(=O)C(Cc1c[nH]c2ccc([N+](=O)[O-])cc12)(NC(C)=O)C(=O)OCC
折射率 1.655

 合成线路

~%

Propanedioic acid,2-(acetylamino)-2-[(5-nitro-1H-indol-3-yl)methyl]-, 1,3-diethyl ester结构式

Propanedioic ac...

6958-33-4

文献:Cavallini; Ravenna Farmaco, Edizione Scientifica, 1958 , vol. 13, p. 105,109

 靶点实验

查看更多实验

实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
实验名称:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
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 英文别名

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