Identification | Back Directory | [Name]
Tectorigenin | [CAS]
548-77-6 | [Synonyms]
Tectrigenin Tectorigenine 4',5,7-Trihydroxy-6-methoxyisoflavone 5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-methoxychromone 5,7-Dihydroxy-3-(4-hydroxy-phenyl)-6-methoxy-chromen-4-one 5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one 5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one 6-Methoxy-5,7-dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 4H-1-Benzopyran-4-one, 5,7-dihydroxy-3-(4-hydroxyphenyl)-6-methoxy- Tectorigenin
5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one | [Molecular Formula]
C16H12O6 | [MDL Number]
MFCD00597094 | [MOL File]
548-77-6.mol | [Molecular Weight]
300.26 |
Chemical Properties | Back Directory | [Melting point ]
225-226° | [Boiling point ]
361.5°C (rough estimate) | [density ]
1.512 | [refractive index ]
1.4600 (estimate) | [storage temp. ]
2-8°C | [solubility ]
DMSO : 150 mg/mL (499.57 mM; Need ultrasonic and warming) | [form ]
powder to crystal | [pka]
6.49±0.20(Predicted) | [color ]
White to Orange to Green | [BRN ]
305601 | [CAS DataBase Reference]
548-77-6 |
Hazard Information | Back Directory | [Uses]
Tectorigenin is identified as an α-glucosidase inhibitors. Potent lactate dehydrogenase (LDH) inhibitor. | [Definition]
ChEBI: A methoxyisoflavone that is isoflavone substituted by a methoxy group at position 6 and hydroxy groups at positions 5, 7 and 4' respectively. | [Synthesis Reference(s)]
Synthetic Communications, 38, p. 525, 2008 DOI: 10.1080/00397910701796725 |
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