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| | mulberrofuran G Basic information |
| Product Name: | mulberrofuran G | | Synonyms: | mulberrofuran G;albanol A;Mulberrofuran G（(+)-Albanol A,Albanol A）;3aH-Benzo[3,4][2]benzopyrano[1,8-bc][1]benzopyran-4,11-diol, 8a-(2,4-dihydroxyphenyl)-1,8a,13b,13c-tetrahydro-6-(6-hydroxy-2-benzofuranyl)-2-methyl-, (3aS,8aS,13bS,13cR)-;Mulberrofuran G, 10 mM in DMSO | | CAS: | 87085-00-5 | | MF: | C34H26O8 | | MW: | 562.57 | | EINECS: | | | Product Categories: | | | Mol File: | 87085-00-5.mol |  |
| | mulberrofuran G Chemical Properties |
| Boiling point | 695.1±55.0 °C(Predicted) | | density | 1.484±0.06 g/cm3(Predicted) | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | form | Powder | | pka | 8.87±0.60(Predicted) | | color | White to off-white | | LogP | 6.346 (est) |
| | mulberrofuran G Usage And Synthesis |
| Uses | 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 IC50 of 3.99 μM[2]. | | target | HBV | | IC 50 | NOX4 | | References | [1] Hong S, Kwon J, Kim DW, Lee HJ, Lee D, Mar W. Mulberrofuran G Protects Ischemic Injury-induced Cell Death via Inhibition of NOX4-mediated ROS Generation and ER Stress.Phytother Res. 2017;31(2):321-329. DOI:10.1002/ptr.5754
[2] Geng CA, Ma YB, Zhang XM, et al. Mulberrofuran G and isomulberrofuran G from Morus alba L.: anti-hepatitis B virus activity and mass spectrometric fragmentation.J Agric Food Chem. 2012;60(33):8197-8202. DOI:10.1021/jf302639b |
| | mulberrofuran G Preparation Products And Raw materials |
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