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2-(1H-苯并[d]咪唑-2-基)喹啉

更新时间:2025-08-31 18:08:14

2-(1H-苯并[d]咪唑-2-基)喹啉结构式
2-(1H-苯并[d]咪唑-2-基)喹啉结构式
品牌特惠专场
常用名 2-(1H-苯并[d]咪唑-2-基)喹啉 英文名 2-(1H-Benzimidazol-2-yl)quinoline
CAS号 14044-48-5 分子量 245.27900
密度 N/A 沸点 N/A
分子式 C16H11N3 熔点 N/A
MSDS N/A 闪点 N/A

 2-(1H-苯并[d]咪唑-2-基)喹啉名称

中文名 2-(1H-苯并[d]咪唑-2-基)喹啉
英文名 2-(1H-Benzimidazol-2-yl)quinoline
英文别名 更多

 2-(1H-苯并[d]咪唑-2-基)喹啉物理化学性质

分子式 C16H11N3
分子量 245.27900
精确质量 245.09500
PSA 41.57000
LogP 3.77810
InChIKey XSJAMRUTJCSRNB-UHFFFAOYSA-N
SMILES c1ccc2nc(-c3nc4ccccc4[nH]3)ccc2c1

 2-(1H-苯并[d]咪唑-2-基)喹啉上下游产品

2-(1H-苯并[d]咪唑-2-基)喹啉上游产品  6

2-(1H-苯并[d]咪唑-2-基)喹啉下游产品  0

 2-(1H-苯并[d]咪唑-2-基)喹啉靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
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:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_SinglePoint_HTS_Activity
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:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
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 2-(1H-苯并[d]咪唑-2-基)喹啉英文别名

2-(benzimidazol-2-yl)quinoline
2-(1H-Benzo[d]imidazol-2-yl)quinoline
2-(1H-Benzoimidazol-2-yl)-quinoline
2-(2-quinolinyl)benzimidazole
2-benzo[d]imidazol-2-yl-quinoline
2-(2-quinolyl)benzimidazole
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