| Identification | Back Directory | [Name]
6,8-Dihydroxy-7-methoxy-3-methyl-1H-2-benzopyran-1-one | [CAS]
26246-41-3 | [Synonyms]
K 251-1
Reticulol
Nsc 294978
6,8-Dihydroxy-7-methoxy-3-methylisocoumarin
6,8-Dihydroxy-7-methoxy-3-methyl-1H-2-benzopyran-1-one
1H-2-Benzopyran-1-one, 6,8-dihydroxy-7-methoxy-3-methyl- | [Molecular Formula]
C11H10O5 | [MOL File]
26246-41-3.mol | [Molecular Weight]
222.19 |
| Chemical Properties | Back Directory | [Melting point ]
193-193.5℃ | [Boiling point ]
473.2±45.0 °C(Predicted) | [density ]
1.424±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
Soluble in DMSO | [form ]
A powder | [pka]
7.19±0.20(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Description]
Reticulol is an isocoumarin derivative produced by certain species of Streptomyces that inhibits cAMP phosphodiesterase (IC50 = 41 μM). It also inhibits DNA topoisomerase I when used at a concentration of 45 μM in B16F10 melanoma cells. Reticulol has antifungal activity against T. mentagrophyes with a MIC of 1.8 μM. It is cytotoxic against A427 human lung and B16F10 mouse melanoma cells at concentrations of 25 and 200 μM, respectively, and inhibits lung metastasis in mice. | [Uses]
Reticulol is an isocoumarin metabolite produced by selected species of Streptomyces. Reticulol was first described as a potent inhibitor of cyclic nucleotide phosphodiesterase but more recent research has demonstrated a topoisomerase I inactivation mechanism. Reticulol also causes dose dependent inhibition of lung metastasis in the B16F10 melanoma model. | [Uses]
Reticulol is an isocoumarin metabolite shown to inactivate topoisomerase I. | [storage]
Store at -20°C |
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