Catalogue number | C104671 |
Chemical name | Momordicoside F1 |
CAS Number | 81348-81-4 |
Synonyms | b-D-Glucopyranoside,1,3,4,8,10,11,12,13,14,15,16,17-dodecahydro-17-(5-methoxy-1,5-dimethyl-3-hexenyl)-4,4,13,14-tetramethyl-5,9-(epoxymethano)-2H-cyclopenta[a]phenanthren-3-yl,[3S-[3a,5a,8a,9a,10b,13a,14b,17a(1S*,3E)]]-; 5,9-(Epoxymethano)-2H-cyclopenta[a]phenanthrene, b-D-glucopyranoside deriv.; b-D-Glucopyranoside,(3S,5R,8S,9S,10S,13R,14S,17R)-1,3,4,8,10,11,12,13,14,15,16,17-dodecahydro-17-[(1R)-5-methoxy-1,5-dimethyl-3-hexenyl]-4,4,13,14-tetramethyl-5,9-(epoxymethano)-2H-cyclopenta[a]phenanthren-3-yl |
Molecular Weight | C37H60O8 |
Formula | 632.9 |
Purity | 98% |
Physical Description | Powder |
Solvent | Chloroform, Dichloromethane,DMSO |
Storage | Stored at 2-8°C, Protected from air and light, refrigerate or freeze |
Applications | Antidiabetic activities.
Momordicosides enhanced fatty acid oxidation and glucose disposal during glucose tolerance tests in both insulin-sensitive and insulin-resistant mice. These findings indicate that cucurbitane triterpenoids, the characteristic constituents of M. charantia, may provide leads as a class of therapeutics for diabetes and obesity. |
References | 1. Chemical and Pharmaceutical Bulletin, 2001, 49(1), 54-63. 2. Chemistry & Biology, 2008, 15(3), 263-273. 3. Journal of Medicinal Plants Research, 2009, 3(13), 1264-1269. |
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After Receiving
The packaging of the product may have turned upside down during transportation, resulting in the product adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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