Other grades of this product :
| cucurbitacins Basic information | | Uses |
| 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 | | EINECS: | | Product Categories: | chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract | | Mol File: | 60137-06-6.mol |
| cucurbitacins Chemical Properties |
| density | 1.22±0.1 g/cm3 (20 ºC 760 Torr) |
| 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. |
| cucurbitacins Preparation Products And Raw materials |
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