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9H-Purine,9-(2-chloroethyl)-6-[(phenylmethyl)thio]

更新时间:2025-08-25 18:11:14

9H-Purine,9-(2-chloroethyl)-6-[(phenylmethyl)thio]结构式
9H-Purine,9-(2-chloroethyl)-6-[(phenylmethyl)thio]结构式
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常用名 9H-Purine,9-(2-chloroethyl)-6-[(phenylmethyl)thio] 英文名 9H-Purine,9-(2-chloroethyl)-6-[(phenylmethyl)thio]
CAS号 299-13-8 分子量 304.79800
密度 1.37g/cm3 沸点 498.8ºC at 760mmHg
分子式 C14H13ClN4S 熔点 N/A
MSDS N/A 闪点 255.5ºC

 名称

英文名 6-benzylsulfanyl-9-(2-chloroethyl)purine
英文别名 更多

 物理化学性质

密度 1.37g/cm3
沸点 498.8ºC at 760mmHg
分子式 C14H13ClN4S
分子量 304.79800
闪点 255.5ºC
精确质量 304.05500
PSA 68.90000
LogP 3.35740
InChIKey HCWAMVQMVMQQNI-UHFFFAOYSA-N
SMILES ClCCn1cnc2c(SCc3ccccc3)ncnc21
蒸汽压 4.39E-10mmHg at 25°C
折射率 1.694

 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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 英文别名

hms3080h18
bc 76
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