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N-[2-(2-chlorophenyl)ethyl]-3-(8-oxo-6-sulfanylidene-5H-[1,3]dioxolo[4,5-g]quinazolin-7-yl)propanamide

更新时间:2026-03-27 14:07:06

N-[2-(2-chlorophenyl)ethyl]-3-(8-oxo-6-sulfanylidene-5H-[1,3]dioxolo[4,5-g]quinazolin-7-yl)propanamide结构式
N-[2-(2-chlorophenyl)ethyl]-3-(8-oxo-6-sulfanylidene-5H-[1,3]dioxolo[4,5-g]quinazolin-7-yl)propanamide结构式
委托求购
常用名 N-[2-(2-chlorophenyl)ethyl]-3-(8-oxo-6-sulfanylidene-5H-[1,3]dioxolo[4,5-g]quinazolin-7-yl)propanamide 英文名 N-[2-(2-chlorophenyl)ethyl]-3-(8-oxo-6-sulfanylidene-5H-[1,3]dioxolo[4,5-g]quinazolin-7-yl)propanamide
CAS号 688055-16-5 分子量 431.9
密度 N/A 沸点 N/A
分子式 C20H18ClN3O4S 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 N-[2-(2-chlorophenyl)ethyl]-3-(8-oxo-6-sulfanylidene-5H-[1,3]dioxolo[4,5-g]quinazolin-7-yl)propanamide

 物理化学性质

分子式 C20H18ClN3O4S
分子量 431.9
InChIKey MSVWQKLXHWOPPZ-UHFFFAOYSA-N
SMILES C1OC2=C(O1)C=C3C(=C2)C(=O)N(C(=S)N3)CCC(=O)NCCC4=CC=CC=C4Cl

 靶点实验

查看更多实验

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:Counterscreen for agonists of the human trace amine associated receptor 1 (hTAAR1): F...
来源:The Scripps Research Institute Molecular Screening Center
靶标:trace amine-associated receptor 1 [Homo sapiens]
External Id:TAAR1_ANT_FLUO8_1536_3XIC50 DCSRUN for TAAR1 AG
实验名称:Fluorescence-based cell-based high throughput dose response assay to identify agonist...
来源:The Scripps Research Institute Molecular Screening Center
靶标:trace amine-associated receptor 1 [Homo sapiens]
External Id:TAAR1_AG_FLUO8_1536_3XEC50 DRUN
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:Counterscreen for agonists of the human trace amine associated receptor 1 (TAAR1): Fl...
来源:The Scripps Research Institute Molecular Screening Center
靶标:guanine nucleotide-binding protein subunit alpha-15 [Homo sapiens]
External Id:CHO-GA16_ANT_FLUO8_1536_3XIC50 DCSRUN for TAAR1 AG
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
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