ChemicalBook--->CAS DataBase List--->26246-41-3

26246-41-3

26246-41-3 Structure

26246-41-3 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312-H319
[Precautionary statements ]

P264-P270-P280-P301+P312-P302+P352-P305+P351+P338-P321-P330-P362+P364-P337+P313-P501
Hazard InformationBack 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.
[in vivo]

Reticulol (10 mg/kg, 50 mg/kg; iv; day 3 and day 5 after tumor implanted) inhibits tumor growth in mice bearing B16F10 melanoma, and shows lung metastasis-blocking effect[1].

Animal Model:Pathogen-free female C57BL/6J mice[1]
Dosage:10 mg/kg, 50 mg/kg
Administration:IV via the tail vein; day 3 and day 5 after tumor implanted
Result:Inhibited tumor growth.
[storage]

Store at -20°C
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