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4,6-bis(benzylsulfanyl)pyrimidin-2-amine

更新时间:2026-07-15 19:08:22

4,6-bis(benzylsulfanyl)pyrimidin-2-amine结构式
4,6-bis(benzylsulfanyl)pyrimidin-2-amine结构式
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常用名 4,6-bis(benzylsulfanyl)pyrimidin-2-amine 英文名 4,6-bis(benzylsulfanyl)pyrimidin-2-amine
CAS号 6307-33-1 分子量 339.47800
密度 1.3g/cm3 沸点 570.4ºC at 760 mmHg
分子式 C18H17N3S2 熔点 N/A
MSDS N/A 闪点 298.8ºC

 4,6-bis(benzylsulfanyl)pyrimidin-2-amine名称

英文名 4,6-bis(benzylsulfanyl)pyrimidin-2-amine
英文别名 更多

 4,6-bis(benzylsulfanyl)pyrimidin-2-amine物理化学性质

密度 1.3g/cm3
沸点 570.4ºC at 760 mmHg
分子式 C18H17N3S2
分子量 339.47800
闪点 298.8ºC
精确质量 339.08600
PSA 102.40000
LogP 5.22460
InChIKey VUNFZODSSSDAPR-UHFFFAOYSA-N
SMILES Nc1nc(SCc2ccccc2)cc(SCc2ccccc2)n1
折射率 1.704

 4,6-bis(benzylsulfanyl)pyrimidin-2-amine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:Confirm compound inhibition to esBAF complex through repress target gene Fgf4 in qPCR...
来源:Broad Institute
靶标:N/A
External Id:2141-03_Inhibitor_SinglePoint_CherryPick_Activity
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
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 4,6-bis(benzylsulfanyl)pyrimidin-2-amine英文别名

4,6-bis-benzylsulfanyl-pyrimidin-2-ylamine
HMS3085A13
2-Amino-4,6-di-(benzylmercapto)-pyrimidin
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