金石蚕苷

• 常用名: 金石蚕苷
• 英文名: Poliumoside
• CAS号: 94079-81-9
• 分子量: 770.728
• 密度: 1.6±0.1 g/cm3
• 沸点: 1023.2±65.0 °C at 760 mmHg
• 分子式: C₃₅H₄₆O₁₉
• 熔点: N/A
• 闪点: 316.2±27.8 °C

金石蚕苷用途

Poliumoside是天然产物，能显著地抑制糖基化终产物的形成。

金石蚕苷名称

• 中文名: 金石蚕苷
• 英文名: [6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

金石蚕苷生物活性

• 描述: Poliumoside是天然产物,能显著地抑制糖基化终产物的形成。
• 相关类别:
  信号通路 >> 其他 >> 其他
  研究领域 >> 代谢疾病
  天然产物 >> 苯丙酸类
• 参考文献:

  [1]. Yu SY, et al. Caffeoylated phenylpropanoid glycosides from Brandisia hancei inhibit advanced glycation end product formation and aldose reductase in vitro and vessel dilation in larval zebrafish in vivo. Planta Med. 2013 Dec;79(18):1705-9.

金石蚕苷物理化学性质

• 密度: 1.6±0.1 g/cm3
• 沸点: 1023.2±65.0 °C at 760 mmHg
• 分子式: C₃₅H₄₆O₁₉
• 分子量: 770.728
• 闪点: 316.2±27.8 °C
• 精确质量: 770.263306
• PSA: 304.21000
• LogP: 2.63
• InChIKey: YMWRMAOPKNYHMZ-YOQCIRBJSA-N
• SMILES: CC1OC(OCC2OC(OCCc3ccc(O)c(O)c3)C(O)C(OC3OC(C)C(O)C(O)C3O)C2OC(=O)C=Cc2ccc(O)c(O)c2)C(O)C(O)C1O
• 蒸汽压: 0.0±0.3 mmHg at 25°C
• 折射率: 1.685
• 储存条件: 室温

金石蚕苷安全信息

• 危害码 (欧洲): Xi

金石蚕苷靶点实验

查看更多实验

实验名称：Antimicrobial activity against Candida albicans ATCC 10231 after 48 hrs by microbroth... 来源：ChEMBL 靶标：Candida albicans External Id：CHEMBL4425002

实验名称：Antifungal activity against Candida parapsilosis ATCC 22019 after 24 hrs by micro bro... 来源：ChEMBL 靶标：Candida parapsilosis External Id：CHEMBL4425003

实验名称：Antifungal activity against Cryptococcus neoformans isolate T1444 after 48 hrs by mic... 来源：ChEMBL 靶标：Cryptococcus neoformans External Id：CHEMBL4425004

实验名称：Antifungal activity against Cryptococcus neoformans ATCC 24067 after 48 hrs by micro ... 来源：ChEMBL 靶标：Cryptococcus neoformans External Id：CHEMBL4425005

实验名称：Antiproliferative activity against PDGF-BB-induced rat VSMC proliferation at 50 uM af... 来源：ChEMBL 靶标：NON-PROTEIN TARGET External Id：CHEMBL1781466

实验名称：Small-molecule inhibitors of ST2 (IL1RL1) 来源：20881 靶标：interleukin-1 receptor-like 1 isoform [homo sapiens] External Id：ST2_IL33_Inhibitors_Primary_Screening_77700

实验名称：Inhibition of human recombinant PKCalpha 来源：ChEMBL 靶标：Protein kinase C alpha type External Id：CHEMBL997396

实验名称：Discovering small molecule activators of G protein-gated inwardly-rectifying potassiu... 来源：15621 靶标：G protein-activated inward rectifier potassium channel 2 External Id：VANDERBILT_HTS_GIRK2_MPD

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金石蚕苷英文别名

• 2-(1H-TETRAZOL-1-YL)ISONICOTINIC ACID
• poliumoside
• Y0162
• 2-(3,4-Dihydroxyphenyl)ethyl 6-deoxy-α-L-mannopyranosyl-(1->3)-[6-deoxy-α-L-mannopyranosyl-(1->6)]-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-β-D-glucopyranoside