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cucurbitacins

Basic information Uses Safety Supplier Related

cucurbitacins Basic information

Product Name:
cucurbitacins
Synonyms:
  • (10α,24S)-16α,24-Epoxy-2,25-dihydroxy-9β-methyl-19-norlanosta-1,5-diene-3,11,22-trione
  • 19-Norlanosta-1,5-diene-3,11,22-trione, 16,24-epoxy-2,25-dihydroxy-9-methyl-, (9beta,10alpha,16alpha,24S)-
  • 19-Norlanosta-1,5-diene-3,11,22-trione, 16,24-epoxy-2,25-dihydroxy-9-methyl-, (9β,10α,16α,24S)-
  • (4R,9beta,16alpha,24S)-2,25-dihydroxy-9,10,14-trimethyl-16,2...
  • cucuritacin IIa
CAS:
60137-06-6
MF:
C30H42O6
MW:
498.65
Product Categories:
  • chemical reagent
  • pharmaceutical intermediate
  • phytochemical
  • reference standards from Chinese medicinal herbs (TCM).
  • standardized herbal extract
Mol File:
60137-06-6.mol
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cucurbitacins Chemical Properties

Boiling point:
650.7±55.0 °C(Predicted)
Density 
1.22±0.1 g/cm3 (20 ºC 760 Torr)
pka
8.54±0.70(Predicted)
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cucurbitacins Usage And Synthesis

Uses

Cucurbitacin S is a biochemical compound from the family of Cucurbitacins. Cucurbitacins are known for their anti-inflammatory, anti-tumor and anti-oxidant efects. In the wild, watermelons, cucumbers, and muskmelons produce bitter Cucurbitacins to defend against preditors. Humans have bred these fruits to eliminate these compounds thereby yielding fruits that are more appealing to our palate.

Uses

Cucurbitacin S is a biochemical compound from the family of Cucurbitacins. Cucurbitacins are known for their anti-inflammatory, anti-tumor and anti-oxidant efects. In the wild, watermelons, cucumbers, and muskmelons produce bitter Cucurbitacins to defend against preditors. Humans have bred these fruits to eliminate these compounds thereby yielding fruits that are more appealing to our palate.

Definition

ChEBI: Cucurbitacin S is an 11-oxo steroid.

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