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Benzo[g]pteridine-2,4(3H,7H)-dione, 6,8,9, 10-tetrahydro-10-methyl-3-phenyl

更新时间:2025-09-19 07:27:18

Benzo[g]pteridine-2,4(3H,7H)-dione, 6,8,9, 10-tetrahydro-10-methyl-3-phenyl结构式
Benzo[g]pteridine-2,4(3H,7H)-dione, 6,8,9, 10-tetrahydro-10-methyl-3-phenyl结构式
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常用名 Benzo[g]pteridine-2,4(3H,7H)-dione, 6,8,9, 10-tetrahydro-10-methyl-3-phenyl 英文名 Benzo[g]pteridine-2,4(3H,7H)-dione, 6,8,9, 10-tetrahydro-10-methyl-3-phenyl
CAS号 61369-40-2 分子量 308.33500
密度 1.42g/cm3 沸点 460.4ºC at 760 mmHg
分子式 C17H16N4O2 熔点 N/A
MSDS N/A 闪点 232.3ºC

 名称

英文名 10-methyl-3-phenyl-6,7,8,9-tetrahydrobenzo[g]pteridine-2,4-dione
英文别名 更多

 物理化学性质

密度 1.42g/cm3
沸点 460.4ºC at 760 mmHg
分子式 C17H16N4O2
分子量 308.33500
闪点 232.3ºC
精确质量 308.12700
PSA 69.78000
LogP 1.35820
InChIKey SRGWNININRDPRD-UHFFFAOYSA-N
SMILES Cn1c2nc(=O)n(-c3ccccc3)c(=O)c-2nc2c1CCCC2
折射率 1.726

 合成线路

~79%

Benzo[g]pteridine-2,4(3H,7H)-dione, 6,8,9, 10-tetrahydro-10-methyl-3-phenyl结构式

Benzo[g]pteridi...

61369-40-2

文献:Fleury, Jean-Pierre Heterocycles, 1980 , vol. 14, # 10 p. 1581 - 1602

~%

Benzo[g]pteridine-2,4(3H,7H)-dione, 6,8,9, 10-tetrahydro-10-methyl-3-phenyl结构式

Benzo[g]pteridi...

61369-40-2

文献:Lacroix, Alain; Schabat, Dominique; Clerin, Daniel; Fleury, Jean-Pierre Bulletin de la Societe Chimique de France, 1987 , # 6 p. 1065 - 1072

~%

Benzo[g]pteridine-2,4(3H,7H)-dione, 6,8,9, 10-tetrahydro-10-methyl-3-phenyl结构式

Benzo[g]pteridi...

61369-40-2

文献:Lacroix, Alain; Schabat, Dominique; Clerin, Daniel; Fleury, Jean-Pierre Bulletin de la Societe Chimique de France, 1987 , # 6 p. 1065 - 1072

~%

Benzo[g]pteridine-2,4(3H,7H)-dione, 6,8,9, 10-tetrahydro-10-methyl-3-phenyl结构式

Benzo[g]pteridi...

61369-40-2

文献:Fleury, Jean-Pierre Heterocycles, 1980 , vol. 14, # 10 p. 1581 - 1602

 靶点实验

查看更多实验

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: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
实验名称:High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
来源:Southern Research Institute
靶标:HIV-1 Vif
External Id:HIV1-VIF_MS
实验名称:Primary and Confirmatory Screening for Flavivirus Genomic Capping Enzyme Inhibition
来源:Southern Research Specialized Biocontainment Screening Center
靶标:Chain A, Crystal Structure Of Dengue-2 Virus Methyltransferase Complexed With S-Adenosyl-L-Homocysteine
External Id:CEGtase_01
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
实验名称:Luciferase Reporter Cell Based HTS to identify inhibitors of N-linked Glycosylation M...
来源:Broad Institute
靶标:N/A
External Id:2146-01_Inhibitor_SinglePoint_HTS_Activity
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 英文别名

methyl-10-phenyl-3-tetrahydro-6,7,8,9-iso-alloxazine
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