Name | 3',4',7-trihydroxyisoflavone |
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Synonyms |
7,3',4'-THIF
3-(3,4-Dihydroxyphenyl)-7-hydroxy-4H-chromen-4-one 3',4',7-Trihydroxyisoflavone 3`,4`,7-Trihydroxyisoflavone 4H-1-Benzopyran-4-one, 3-(3,4-dihydroxyphenyl)-7-hydroxy- 3l5r MFCD00143002 3-(3,4-Dihydroxy-phenyl)-7-hydroxy-chromen-4-on 3',4',7-trihydroxy isoflavone 3'-Hydroxydaidzein 3-(3,4-dihydroxyphenyl)-7-hydroxychromen-4-one 3-(3,4-dihydroxy-phenyl)-7-hydroxy-chromen-4-one 7,3',4'-Trihydroxyisoflavone 7-Hydroxy-3-(3,4-dihydroxyphenyl)-4H-chromen-4-one 4H-1-Benzopyran-4-one,3-(3,4-dihydroxyphenyl)-7-hydroxy |
Description | 7,3',4'-Trihydroxyisoflavone, a major metabolite of Daidzein, is an ATP-competitive inhibitor of Cot (Tpl2/MAP3K8) and MKK4. 7,3',4'-Trihydroxyisoflavone has anticancer, anti-angiogenic, chemoprotective, and free radical scavenging activities[1][2]. |
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Related Catalog | |
In Vitro | 7,3',4'-Trihydroxyisoflavone triggers cell cycle arrest at the G1 phase and displays an anti-proliferative effect against EGF receptor-positive skin cancer[1]. 7,3',4'-Trihydroxyisoflavone also significantly inhibits UVB-induced COX-2 expression by suppressing the NF-B transcription activity in mouse skin epidermal JB6 P+ cells[1]. |
In Vivo | In a mouse skin tumorigenesis model, 7,3',4'-Trihydroxyisoflavone strongly suppresses the incidence, multiplicity, and volume of UVB-induced mouse skin tumors. Consistent with the tumor data, 7,3',4'-Trihydroxyisoflavone clearly attenuates UVB-induced COX-2 expression in hairless mouse skin[2]. |
References |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 572.8±50.0 °C at 760 mmHg |
Melting Point | 280-282°C |
Molecular Formula | C15H10O5 |
Molecular Weight | 270.24 |
Flash Point | 224.0±23.6 °C |
Exact Mass | 270.052826 |
PSA | 90.90000 |
LogP | 2.58 |
Vapour Pressure | 0.0±1.6 mmHg at 25°C |
Index of Refraction | 1.732 |
Storage condition | -20°C Freezer |
Stability | Store in Freezer |
Risk Phrases | R36/37/38 |
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Safety Phrases | S22-S24/25 |
WGK Germany | 3 |
Precursor 8 | |
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DownStream 1 | |