Description
A cAMP phosphodiesterase inhibitor (IC50 = 41 µM); inhibits DNA topoisomerase I at a concentration of 45 µM in B16F10 melanoma cells; has antifungal activity against T. mentagrophyes with a MIC 1.8 µM; cytotoxic against A427 human lung and B16F10 mouse melanoma cells at concentrations of 25 and 200 µM, respectively; inhibits lung metastasis in mice
Formal name: 6,8-dihydroxy-7-methoxy-3-methyl-1H-2-benzopyran-1-one
Synonyms: 6,8-dihydroxy-7-methoxy-3-methyl Isocoumarin|NSC 294978
Molecular weight: 222.2
CAS: 26246-41-3
Purity: >95%
Formulation: A powder
Product Type|Biochemicals|Antifungals||Product Type|Biochemicals|Natural Products|Coumarins||Product Type|Biochemicals|Natural Products|Microbial Metabolites||Product Type|Biochemicals|Small Molecule Inhibitors|MMPs||Product Type|Biochemicals|Small Molecule Inhibitors|Phosphodiesterases||Product Type|Biochemicals|Small Molecule Inhibitors|Topoisomerases||Research Area|Cancer|Cell Death||Research Area|Cancer|Cell Migration & Metastasis||Research Area|Cancer|Cell Signaling|cAMP Signaling||Research Area|Cancer|DNA Damage and Repair|Topoisomerase||Research Area|Cell Biology|Cell Signaling|cAMP Signaling||Research Area|Epigenetics, Transcription, & Translation|RNA, DNA, & Protein Synthesis||Research Area|Immunology & Inflammation||Research Area|Infectious Disease|Fungal Diseases|Ringworm