蛇床素

• 常用名: 蛇床素
• 英文名: Cnidicin
• CAS号: 14348-21-1
• 分子量: 354.396
• 密度: 1.2±0.1 g/cm3
• 沸点: 519.0±50.0 °C at 760 mmHg
• 分子式: C₂₁H₂₂O₅
• 熔点: N/A
• 闪点: 267.7±30.1 °C

蛇床素用途

Cnidicin 是一种来自 Angelica koreana 根的香豆素,可抑制肥大细胞脱颗粒和 RAW 264.7 细胞产生一氧化氮 (NO).

蛇床素名称

• 中文名: 蛇床素
• 英文名: cnidicin

蛇床素生物活性

• 描述: Cnidicin 是一种来自 Angelica koreana 根的香豆素,可抑制肥大细胞脱颗粒和 RAW 264.7 细胞产生一氧化氮 (NO).
• 相关类别:
  研究领域 >> 其他
  信号通路 >> 其他 >> 其他
• 体外研究: Cnidicin对从培养的RBL-2H3细胞中以剂量依赖性方式(IC50=25μM)释放β-己糖胺酶和从活化的RAW264.7细胞(IC50=7.5μM)产生一氧化氮显示出显着的抑制作用[1]。
• 参考文献:

  [1]. Ryu SY, et al. Cnidicin, a coumarin, from the root of Angelica koreana, inhibits the degranulation of mast cell and the NO generation in RAW 264.7 cells. Planta Med. 2001 Mar;67(2):172-4.

蛇床素物理化学性质

• 密度: 1.2±0.1 g/cm3
• 沸点: 519.0±50.0 °C at 760 mmHg
• 分子式: C₂₁H₂₂O₅
• 分子量: 354.396
• 闪点: 267.7±30.1 °C
• 精确质量: 354.146729
• PSA: 61.81000
• LogP: 6.07
• InChIKey: HJMDOAWWVCOEDW-UHFFFAOYSA-N
• SMILES: CC(C)=CCOc1c2ccoc2c(OCC=C(C)C)c2oc(=O)ccc12
• 蒸汽压: 0.0±1.4 mmHg at 25°C
• 折射率: 1.580
• 储存条件: 2-8℃

蛇床素靶点实验

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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

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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：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：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

实验名称：Absorbance-based primary biochemical high throughput screening assay to identify acti... 来源：The Scripps Research Institute Molecular Screening Center 靶标：caspase-3 preproprotein [Homo sapiens] External Id：PROCASPASE3_ACT_EPIABS_1536_1X%ACT PRUN

实验名称：uHTS identification of small molecule modulators of NR3A 来源：Burnham Center for Chemical Genomics 靶标：N/A External Id：SBCCG-A1015-NR3A-Primary-Assay

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蛇床素英文别名

• 4,9-Bis[(3-methyl-2-buten-1-yl)oxy]-7H-furo[3,2-g]chromen-7-one