葛杜宁

• 常用名: 葛杜宁
• 英文名: Gedunin
• CAS号: 2753-30-2
• 分子量: 482.56500
• 密度: 1.28g/cm3
• 沸点: 594.3ºC at 760mmHg
• 分子式: C₂₈H₃₄O₇
• 熔点: N/A
• 闪点: 313.2ºC

葛杜宁用途

格杜宁是一种具有抗癌、抗病毒、抗炎和杀虫活性的柠檬苦素。Gedunin作为一种有效的Hsp90抑制剂,诱导Hsp90依赖性客户蛋白的降解。2019冠状病毒疾病可能阻碍SARS COV-2病毒进入人类宿主细胞,可用于COVID-19研究[3 ]。

葛杜宁名称

• 中文名: 葛杜宁
• 英文名: gedunin

葛杜宁生物活性

• 描述: 格杜宁是一种具有抗癌、抗病毒、抗炎和杀虫活性的柠檬苦素。Gedunin作为一种有效的Hsp90抑制剂,诱导Hsp90依赖性客户蛋白的降解。2019冠状病毒疾病可能阻碍SARS COV-2病毒进入人类宿主细胞,可用于COVID-19研究[3 ]。
• 相关类别:
  研究领域 >> 癌症
  信号通路 >> 代谢酶/蛋白酶 >> HSP
  研究领域 >> 感染
  研究领域 >> 炎症/免疫
  信号通路 >> 细胞周期/DNA损伤 >> HSP
• 靶点实验:

  HSP90

• 体外研究: Gedunin(0.5-30μM)以剂量依赖性方式抑制CaCo-2结肠癌细胞增殖,IC50值为16.83μM[1]。
• 参考文献:

  [1]. Shaikh J Uddin, et al. Gedunin, a limonoid from Xylocarpus granatum, inhibits the growth of CaCo-2 colon cancer cell line in vitro. Phytother Res. 2007 Aug;21(8):757-61.

  [2]. Gary E L Brandt, et al. Gedunin, a novel hsp90 inhibitor: semisynthesis of derivatives and preliminary structure-activity relationships. J Med Chem. 2008 Oct 23;51(20):6495-502

  [3]. Seshu Vardhan, et al. Virtual screening by targeting proteolytic sites of furin and TMPRSS2 to propose potential compounds obstructing the entry of SARS-CoV-2 virus into human host cells. J Tradit Complement Med. 2021 Apr 12.

葛杜宁物理化学性质

• 密度: 1.28g/cm3
• 沸点: 594.3ºC at 760mmHg
• 分子式: C₂₈H₃₄O₇
• 分子量: 482.56500
• 闪点: 313.2ºC
• 精确质量: 482.23000
• PSA: 95.34000
• LogP: 4.56070
• InChIKey: YJXDGWUNRYLINJ-POZBICLPSA-N
• SMILES: CC(=O)OC1CC2C(C)(C)C(=O)C=CC2(C)C2CCC3(C)C(c4ccoc4)OC(=O)C4OC43C12C
• 外观性状: 白色至米白色固体
• 蒸汽压: 4.31E-14mmHg at 25°C
• 折射率: 1.581
• 储存条件: 20°C，惰性气体，干燥

葛杜宁靶点实验

查看更多实验

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：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：Tocris HTS for Inhibitors of Aerobactin Synthetase lucA 来源：23265 External Id：IucA Pilot Assay Tocris Library

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：MITF Measured in Cell-Based System Using Plate Reader - 2084-01_Activator_SinglePoint... 来源：Broad Institute 靶标：N/A External Id：2084-01_Activator_SinglePoint_HTS_Activity

实验名称：Counterscreen for inhibitors of the fructose-bisphosphate aldolase (FBA) of M. tuberc... 来源：The Scripps Research Institute Molecular Screening Center 靶标：N/A External Id：GDH-TPI_INH_ABS_1536_1X%INH CSRUN

实验名称：Antiviral activity determined as inhibition of SARS-CoV-2 induced cytotoxicity of Cac... 来源：ChEMBL 靶标：Severe acute respiratory syndrome coronavirus 2 External Id：CHEMBL4303805

实验名称：qHTS for Inhibitors of TGF-b: Cytotox Counterscreen 来源：NCGC 靶标：N/A External Id：SMAD3201

实验名称：uHTS identification of cystic fibrosis induced NFkb Inhibitors in a fluoresence assay 来源：Burnham Center for Chemical Genomics 靶标：cystic fibrosis transmembrane conductance regulator [Homo sapiens] External Id：SBCCG-A764-CF-PAF-Primary-Assay

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葛杜宁英文别名

• Gedunin,(1S,3aS,4aR,4bS,5R,6aR,10aR,10bR,12aS)-5-(Acetyloxy)-1-(3-furanyl)-1,5,6,6a,7,10a,10b,11,12,12a,decahydro-4b,7,7,10a,12a,-pentamethyloxireno[c]phenanthro[1,2-d]pyran-3,8(3aH,4bH)-dione
• Gedunine