Cyclocalopin A
CAS: 486430-94-8
Ref. 3D-LUA43094
| 1mg | To inquire | ||
| 5mg | To inquire | ||
| 10mg | To inquire | ||
| 25mg | To inquire |
Product Information
- Spiro[3-cyclohexene-1,3′(2′H)-[7H]furo[2,3-c]pyran]-5,7′-dione, 3′a,4′,5′,7′a-tetrahydro-2′,6-dihydroxy-2′,4,4′-trimethyl-, (1S,2′R,3′aR,4′S,6S,7′aS)-rel-(-)-
- rel-(-)-(1S,2′R,3′aR,4′S,6S,7′aS)-3′a,4′,5′,7′a-Tetrahydro-2′,6-dihydroxy-2′,4,4′-trimethylspiro[3-cyclohexene-1,3′(2′H)-[7H]furo[2,3-c]pyran]-5,7′-dione
- Spiro[4-cyclohexene-1,3′(3′aH)-[2H]furo[2,3-c]pyran]-3,7′(7′aH)-dione, 4′,5′-dihydro-2,2′-dihydroxy-2′,4,4′-trimethyl-, (1R,2R,2′S,3′aS,4′R,7′aR)-rel-(-)-
Cyclocalopin A is a natural product that has been isolated from the fungus Boletus rubripes. Cyclocalopin A has been shown to have antifungal and anticancer properties, as well as having anti-inflammatory and anti-diabetic activities. Cyclocalopin A is a glyoxylate with a stereoselective bioactivity, showing activity towards fungal cells but not mammalian cells in vitro. The bioavailability of cyclocalopin A has been shown to be improved by epimerization, which converts the hydroxyl group into the hydroxy group. The structure of cyclocalopin A was first determined using spectroscopic methods and later confirmed by X-ray crystallography. This compound is currently being used as a model compound for other biologically active compounds due to its availability, stability, and low cost.
Chemical properties
Technical inquiry about: 3D-LUA43094 Cyclocalopin A
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