20,24-Dihydroxydammar-25-en-3-one
20,24-Dihydroxydammar-25-en-3-one Basic information
- Product Name:
- 20,24-Dihydroxydammar-25-en-3-one
- Synonyms:
-
- 20,24-Dihydroxydammar-25-en-3-one
- Dammar-25-en-3-one, 20,24-dihydroxy-, (24S)-
- CAS:
- 75069-59-9
- MF:
- C30H50O3
- MW:
- 458.72
- Mol File:
- 75069-59-9.mol
20,24-Dihydroxydammar-25-en-3-one Chemical Properties
- Boiling point:
- 556.3±35.0 °C(Predicted)
- Density
- 1.027±0.06 g/cm3(Predicted)
- pka
- 14.53±0.20(Predicted)
20,24-Dihydroxydammar-25-en-3-one Usage And Synthesis
Uses
20(S),24(S)-Dihydroxydammar-25-en-3-one (compound 19) is a kind of triterpene. 20(S),24(S)-Dihydroxydammar-25-en-3-one can be isolated from the floral spikes of Betula platyphylla var. 20(S),24(S)-Dihydroxydammar-25-en-3-one has cytotoxicity against Human Cancer Cell Lines[1].
Definition
ChEBI: 20S,24S-dihydroxydammer-25-en-3-one is a tetracyclic triterpenoid that is dammer-25-ene substituted by hydroxy groups at positions 20 and 24 and an oxo group at position 3 (the 24S-stereoisomer). It has been isolated from the stems of Aglaia abbreviata. It has a role as a plant metabolite. It is a tetracyclic triterpenoid, a cyclic terpene ketone and a diol. It derives from a hydride of a dammarane.
References
[1] Yoshiki Kashiwada, et al. Triterpenoids from the floral spikes of Betula platyphylla var. japonica and their reversing activity against multidrug-resistant cancer cells. J Nat Prod. 2007, 70, 4. DOI:10.1021/np060631s
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