Name | Mulberrofuran G |
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Synonyms |
(3aR,8aS,13bR,13cS)-8a-(2,4-Dihydroxyphenyl)-6-(6-hydroxy-1-benzofuran-2-yl)-2-methyl-1,8a,13b,13c-tetrahydro-3aH-benzo[3,4]isochromeno[1,8-bc]chromene-4,11-diol
albanol A Mulberrofuran G 3aH-Benzo[c][1]benzopyrano[4,3,2-ij][2]benzopyran-4,11-diol, 8a-(2,4-dihydroxyphenyl)-1,8a,13b,13c-tetrahydro-6-(6-hydroxy-2-benzofuranyl)-2-methyl-, (3aR,8aS,13bR,13cS)- |
Description | Mulberrofuran G protects ischemic injury-induced cell death via inhibition of NOX4-mediated ROS generation and ER stress[1]. Mulberrofuran G shows moderate inhibiting activity of hepatitis B virus (HBV) DNA replication with the |
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Related Catalog | |
References |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 695.1±55.0 °C at 760 mmHg |
Molecular Formula | C34H26O8 |
Molecular Weight | 562.57 |
Flash Point | 374.2±31.5 °C |
Exact Mass | 562.162781 |
PSA | 132.75000 |
LogP | 6.75 |
Vapour Pressure | 0.0±2.3 mmHg at 25°C |
Index of Refraction | 1.745 |
Storage condition | 2-8℃ |
Hazard Codes | Xi |
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~% 87085-00-5 |
Literature: Fukai, Toshio; Hano, Yoshio; Hirakura, Kazuhiro; Nomura, Taro; Uzawa, Jun; Fukushima, Kazutaka Heterocycles, 1984 , vol. 22, # 3 p. 473 - 477 |
Precursor 1 | |
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DownStream 0 |