| Identification | Back Directory | [Name]
Kazinol A | [CAS]
99624-28-9 | [Synonyms]
Kazinol A
4-[(2S)-7-hydroxy-3,4-dihydro-2H-chromen-2-yl]-3,6-bis(3-methylbut-2-enyl)benzene-1,2-diol
4-[(2S)-7-hydroxy-3,4-dihydro-2H-chromen-2-yl]-3,6-bis(3-methylbut-2-en-1-yl)benzene-1,2-diol
4-[(2S)-3,4-Dihydro-7-hydroxy-2H-1-benzopyran-2-yl]-3,6-bis(3-methyl-2-buten-1-yl)-1,2-benzenediol
1,2-Benzenediol, 4-[(2S)-3,4-dihydro-7-hydroxy-2H-1-benzopyran-2-yl]-3,6-bis(3-methyl-2-buten-1-yl)- | [Molecular Formula]
C25H30O4 | [MDL Number]
MFCD31693119 | [MOL File]
99624-28-9.mol | [Molecular Weight]
394.5 |
| Chemical Properties | Back Directory | [Melting point ]
129-130 °C | [Boiling point ]
583.5±50.0 °C(Predicted) | [density ]
1.166±0.06 g/cm3(Predicted) | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [form ]
Powder | [pka]
9.91±0.40(Predicted) | [color ]
Colorless to light yellow |
| Hazard Information | Back Directory | [Description]
Kazinol A shows strong inhibition of arachidonic acid (AA)-induced platelet aggregation.
Kazinol A possesses potent antioxidant activity against 2,2-diphenyl-l-picrylhydrazyl and 2,2′-azino-bis-ethylbenzthiazoline-6-sulfonic acid (ABTS) radicals. | [Uses]
Kazinol A induces cytotoxic effects in human bladder cancer cells, including the cisplatin-resistant T24R2[1]. | [Definition]
ChEBI: Kazinol A is a hydroxyflavonoid. | [References]
[1] Park S, et al. Cytotoxic effects of kazinol A derived from Broussonetia papyrifera on human bladder cancer cells, T24 and T24R2.?Phytomedicine. 2016;23(12):1462-1468. DOI:10.1016/j.phymed.2016.08.005 |
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cjbscvictory
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13348960310 |
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https://www.weikeqi-biotech.com/ |
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