isodiospyrin CAS 20175-84-2
Introduction:Basic information about isodiospyrin CAS 20175-84-2, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
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 |
| EINECS: | |
| Product Categories: | |
| 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 |
Safety Information
| 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:3.0.co;2-t">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 |
