Dehydroabietylamine

• 常用名: Dehydroabietylamine
• 英文名: Dehydroabietylamine
• CAS号: 1078140-96-1
• 分子量: 285.5
• 密度: N/A
• 沸点: N/A
• 分子式: C₂₀H₃₁N
• 熔点: N/A
• 闪点: N/A

Dehydroabietylamine名称

• 英文名: Dehydroabietylamine

Dehydroabietylamine物理化学性质

• 分子式: C₂₀H₃₁N
• 分子量: 285.5
• InChIKey: JVVXZOOGOGPDRZ-SLFFLAALSA-N
• SMILES: CC(C)C1=CC2=C(C=C1)[C@]3(CCC[C@@]([C@@H]3CC2)(C)CN)C

Dehydroabietylamine靶点实验

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实验名称：Selectivity index, ratio of EC50 for mouse NIH/3T3 cells to EC50 for human MCF7 cells 来源：ChEMBL 靶标：N/A External Id：CHEMBL4273842

实验名称：Cytotoxicity against mouse NIH/3T3 cells after 96 hrs by sulforhodamine-B assay 来源：ChEMBL 靶标：NIH3T3 External Id：CHEMBL4273841

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：Cytotoxicity against human HT-29 cells after 96 hrs by sulforhodamine-B assay 来源：ChEMBL 靶标：HT-29 External Id：CHEMBL4273838

实验名称：Cytotoxicity against human A2780 cells after 96 hrs by sulforhodamine-B assay 来源：ChEMBL 靶标：A2780 External Id：CHEMBL4273837

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：Cytotoxicity against human SW1736 cells after 96 hrs by sulforhodamine-B assay 来源：ChEMBL 靶标：SW-1736 External Id：CHEMBL4273840

实验名称：Cytotoxicity against human MCF7 cells after 96 hrs by sulforhodamine-B assay 来源：ChEMBL 靶标：MCF7 External Id：CHEMBL4273839

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

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