isodiospyrin
isodiospyrin Basic information
- Product Name:
- isodiospyrin
- Synonyms:
-
- isodiospyrin
- [1,2’-Binaphtalene]-5,5’,8,8’-tet
- 1,2’-Binaphthalene-5,5’,8,8’-tet
- [1,2'-BINAPHTHALENE]-5,5',8,8'
- Isoquinone
- (-)-1',4-Dihydroxy-2,3'-dimethyl-(1,2'-binaphthalene)-5,5',8,8'-tetrone
- Isodiospirin
- [1,2'-Binaphthalene]-5,5',8,8'-tetrone,1',4-dihydroxy-2,3'-dimethyl-, (1R)-
- CAS:
- 20175-84-2
- MF:
- C22H14O6
- MW:
- 374.34
- Mol File:
- 20175-84-2.mol
isodiospyrin Chemical Properties
- Melting point:
- 233 °C
- Boiling point:
- 712.0±60.0 °C(Predicted)
- Density
- 1.495±0.06 g/cm3(Predicted)
- pka
- 5.66±0.20(Predicted)
- form
- Solid
- color
- Orange to red
isodiospyrin Usage And Synthesis
Uses
Isodiospyrin, a natural dimeric naphthoquinone, is a human DNA topoisomerase I (Topoisomerase) inhibitor. Isodiospyrin can prevent both DNA relaxation and kinase activities of human topoisomerase I. Isodiospyrin shows anticancer, antibacterial and antifungal activities[1][2][3].
Definition
ChEBI: Isodiospyrin is a member of biphenyls.
IC 50
Topoisomerase I
References
[1] Chun-Yuan Ting, et al. Isodiospyrin as a novel human DNA topoisomerase I inhibitor. Biochem Pharmacol. 2003 Nov 15;66(10):1981-91. DOI:10.1016/j.bcp.2003.07.003
[2] B A Adeniyi, et al. Antibacterial activity of diospyrin, isodiospyrin and bisisodiospyrin from the root of Diospyros piscatoria (Gurke) (Ebenaceae). Phytother Res. 2000 Mar;14(2):112-7. DOI:10.1002/(sici)1099-1573(200003)14:2<112::aid-ptr488>3.0.co;2-t
[3] Xiaoning Wang, et al. Antifungal metabolites from the roots of Diospyros virginiana by overpressure layer chromatography. Chem Biodivers. 2011 Dec;8(12):2331-40. DOI:10.1002/cbdv.201000310
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