Product Information
- 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
- 4',5,7-Trihydroxyflavone
- Pelargidenon 1449
- 4′,5,7-Trihydroxyflavone
- 5,7,4'-Trihydroxyflavone
- 5,7-Dihidroxi-2-(4-Hidroxifenil)-4-Benzopirona
- 5,7-Dihydroxy-2-(4-Hydroxyphenyl)-4-Benzopyrone
- 5,7-Dihydroxy-2-(4-Hydroxyphenyl)chromen-4-one
- 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-benzopyron
- 5,7-Dihydroxy-2-p-hydroxyphenyl-4-chromenone
- See more synonyms
- Apegenin
- Apigenine
- Apigenol
- Chamomile
- Flavone, 4',5,7-trihydroxy-
- Flavone, 4′,5,7-trihydroxy-
- Ly 080400
- Nsc 83244
- St 056301
- Uccf 031
- Versulin
Applications Induces the reversion of transformed phenotypes of v-H-ras-transformed NIH 3T3 cells at low concentration (12.5 uM) by inhibiting MAP kinase activity. Also inhibits the proliferation of malignant tumor cells by G2/M arrest and induces morphological differentiation. Apigenin has also been reported to enhance the gap juntion intracellular communication in liver cells.uv(max)ethanol: 269, 340 nm (e= 18,800, 20,900) moderately sol. in hot alcohol
References Chaumontet, C., et al.: Carcinogenesis, 15, 2325 (1994); Sato, F., et al.: Biochem. Biophys. Res. Commun., 204, 578 (1994); Kuo, M.L. et al.: Biochem. Biophys. Res. Commun., 212, 767 (1995);
Chemical properties
Technical inquiry about: TR-A726500 Apigenin
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