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| | (R)-8,9-Dihydro-3,6,7-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4-one Basic information |
| Product Name: | (R)-8,9-Dihydro-3,6,7-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4-one | | Synonyms: | (R)-8,9-Dihydro-3,6,7-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4-one;Deoxyherqueinone;4H-Phenaleno[1,2-b]furan-4-one, 8,9-dihydro-3,6,7-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-, (9R)- | | CAS: | 20887-73-4 | | MF: | C20H20O6 | | MW: | 356.37 | | EINECS: | | | Product Categories: | | | Mol File: | 20887-73-4.mol | ![(R)-8,9-Dihydro-3,6,7-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4-one Structure](CAS/20180808/GIF/20887-73-4.gif) |
| | (R)-8,9-Dihydro-3,6,7-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4-one Chemical Properties |
| | (R)-8,9-Dihydro-3,6,7-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4-one Usage And Synthesis |
| Uses | Erabulenol A is the inhibitor for cholesteryl ester transfer protein that can be isolated from Penicillum sp.[1]. | | Definition | ChEBI: Deoxyherqueinone is an organic heterotetracyclic compound that is 8,9-dihydro-4H-phenaleno[1,2-b]furan substituted by methyl groups at positions 1,8,8 and 9R, hydroxy groups at positions 3,4 and 7, methoxy group at position 5 and oxo group at position 6. It is isolated from the soil fungus, Penicillium herquei. It has a role as a fungal metabolite and an antibacterial agent. It is an organic heterotetracyclic compound, a member of phenols, an enone and a polyketide. It is a conjugate acid of a deoxyherqueinone(1-). | | References | [1] Tabata N, et al., Erabulenols, inhibitors of cholesteryl ester transfer protein produced by Penicillium sp. FO-5637. II. Structure elucidation of erabulenols A and B. J Antibiot (Tokyo). 1998 Jul;51(7):624-8. DOI:10.7164/antibiotics.51.624 |
| | (R)-8,9-Dihydro-3,6,7-trihydroxy-5-methoxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4-one Preparation Products And Raw materials |
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