Angelol H

• 常用名: Angelol H
• 英文名: Angelol H
• CAS号: 83247-73-8
• 分子量: 376.400
• 密度: 1.3±0.1 g/cm3
• 沸点: 579.1±50.0 °C at 760 mmHg
• 分子式: C₂₀H₂₄O₇
• 熔点: N/A
• 闪点: 203.1±23.6 °C

Angelol H用途

Angelol H 是从 Angelica pubescens MAXIM 中分离出来的天然化合物。

Angelol H名称

• 英文名: (1R,2R)-2,3-Dihydroxy-1-(7-methoxy-2-oxo-2H-chromen-6-yl)-3-methylbutyl (2E)-2-methyl-2-butenoate

Angelol H生物活性

• 描述: Angelol H 是从 Angelica pubescens MAXIM 中分离出来的天然化合物。
• 相关类别:
  研究领域 >> 其他
  信号通路 >> 其他 >> 其他
• 参考文献:

  [1]. BABA, K., et al. (1982). Studies on coumarins from the root of Angelica pubescens Maxim. V. Stereochemistry of angelols A-H. CHEMICAL & PHARMACEUTICAL BULLETIN, 30(6), 2036-2044.

Angelol H物理化学性质

• 密度: 1.3±0.1 g/cm3
• 沸点: 579.1±50.0 °C at 760 mmHg
• 分子式: C₂₀H₂₄O₇
• 分子量: 376.400
• 闪点: 203.1±23.6 °C
• 精确质量: 376.152191
• LogP: 2.25
• InChIKey: BAHUBXAYVOCLNA-OEQDPHDDSA-N
• SMILES: CC=C(C)C(=O)OC(c1cc2ccc(=O)oc2cc1OC)C(O)C(C)(C)O
• 蒸汽压: 0.0±1.7 mmHg at 25°C
• 折射率: 1.567

Angelol H靶点实验

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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：qHTS Assay for Inhibitors of the Phosphatase Activity of Eya2 来源：NCGC 靶标：eyes absent homolog 2 isoform a [Homo sapiens] External Id：EYA2477

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：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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Angelol H英文别名

• (1R,2R)-2,3-Dihydroxy-1-(7-methoxy-2-oxo-2H-chromen-6-yl)-3-methylbutyl (2E)-2-methyl-2-butenoate