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| | (22R,23R,25R)-5β,6β-Epoxy-4β,16β,20,22,23-pentahydroxy-1-oxoergost-2-en-26-oic acid γ-lactone Basic information |
| Product Name: | (22R,23R,25R)-5β,6β-Epoxy-4β,16β,20,22,23-pentahydroxy-1-oxoergost-2-en-26-oic acid γ-lactone | | Synonyms: | (22R,23R,25R)-5β,6β-Epoxy-4β,16β,20,22,23-pentahydroxy-1-oxoergost-2-en-26-oic acid γ-lactone;Ixocarpalactone A;Ergost-2-en-26-oic acid, 5,6-epoxy-4,16,20,22,23-pentahydroxy-1-oxo-, γ-lactone, (4β,5β,6β,16β,22R,23R,25R)- | | CAS: | 71801-45-1 | | MF: | C28H40O8 | | MW: | 504.62 | | EINECS: | | | Product Categories: | | | Mol File: | 71801-45-1.mol |  |
| | (22R,23R,25R)-5β,6β-Epoxy-4β,16β,20,22,23-pentahydroxy-1-oxoergost-2-en-26-oic acid γ-lactone Chemical Properties |
| Melting point | 290-292 °C | | Boiling point | 741.4±60.0 °C(Predicted) | | density | 1.36±0.1 g/cm3(Predicted) | | pka | 13.47±0.70(Predicted) |
| | (22R,23R,25R)-5β,6β-Epoxy-4β,16β,20,22,23-pentahydroxy-1-oxoergost-2-en-26-oic acid γ-lactone Usage And Synthesis |
| Definition | ChEBI: Ixocarpalactone A is a withanolide. | | Anticancer Research | This terpenoid compound is isolated from the edible plant Physalis philadelphica.The leaf and stem extract induces quinine reductase, a phase II enzyme, needed formetabolism of chemical carcinogens. The anticancer activity of ixocarpalactone isexerted through G2/M phase arrest in cell cycle, downregulation of E2F-1, DP-1,upregulation of hyper-phosphorylated retinoblastoma, and induction of apoptosis inSW480 human colon cancer cells (Balunas and Kinghorn 2005; Choi et al. 2006). |
| | (22R,23R,25R)-5β,6β-Epoxy-4β,16β,20,22,23-pentahydroxy-1-oxoergost-2-en-26-oic acid γ-lactone Preparation Products And Raw materials |
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