| Identification | Back Directory | [Name]
5,5a-Dihydro-1,5a,9,13-tetrahydroxy-3,7-dimethyl-4H,10H,12H,16H-dibenzo[de,d'e']furo[2,3-g:5,4-i']bis[2]benzopyran-4,10,16-trione | [CAS]
76706-63-3 | [Synonyms]
Bacillosporin C
5,5a-Dihydro-1,5a,9,13-tetrahydroxy-3,7-dimethyl-4H,10H,12H,16H-dibenzo[de,d'e']furo[2,3-g:5,4-i']bis[2]benzopyran-4,10,16-trione | [Molecular Formula]
C26H18O10 | [MOL File]
76706-63-3.mol | [Molecular Weight]
490.415 |
| Chemical Properties | Back Directory | [Melting point ]
>280 °C | [Boiling point ]
1002.6±65.0 °C(Predicted) | [density ]
1.84±0.1 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
DMF: soluble; DMSO: soluble; Ethanol: soluble; Methanol: soluble | [form ]
A solid | [pka]
7.15±0.40(Predicted) |
| Hazard Information | Back Directory | [Description]
Bacillosporin C is an oxaphenalenone dimer originally isolated from T. bacillosporus. Bacillosporin C, an anhydride, is formed from the lactone bacillosporin D in the mangrove endophytic fungus SBE-14. Similar oxaphenalenone dimers have antibiotic activity and inhibit acetylcholinesterase. | [Uses]
Bacillosporin C is an oxaphenalenone dimer originally isolated from T. bacillosporus. Bacillosporin C, an anhydride, is formed from the lactone bacillosporin D in the mangrove endophytic fungus SBE-14. Similar oxaphenalenone dimers have antibiotic activity and inhibit acetylcholinesterase. | [storage]
Store at -20°C | [References]
[1] Yamazaki, et al. Isolation and structures of oxaphenalenone dimers from Talaromyces bacillosporus. Chem. Pharm. Bull. 28(12), 3649-3655 (1980). |
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