Informazioni sul prodotto
- Pateamine
- 4,12-Dioxa-20-thia-21-azabicyclo[16.2.1]heneicosa-1(21),6,8,18-tetraene-5,13-dione, 15-amino-3-[7-(dimethylamino)-2,5-dimethyl-1,3,5-heptatrienyl]-9,11,17-trimethyl-, [3S-[3R*(1E,3E,5E),6Z,8E,11R*,15S*,17R*]]-
- 4,12-Dioxa-20-thia-21-azabicyclo[16.2.1]heneicosa-1(21),6,8,18-tetraene-5,13-dione, 15-amino-3-[(1E,3E,5E)-7-(dimethylamino)-2,5-dimethyl-1,3,5-heptatrien-1-yl]-9,11,17-trimethyl-, (3S,6Z,8E,11S,15R,17S)-
- 4,12-Dioxa-20-thia-21-azabicyclo[16.2.1]heneicosa-1(21),6,8,18-tetraene-5,13-dione, 15-amino-3-[(1E,3E,5E)-7-(dimethylamino)-2,5-dimethyl-1,3,5-heptatrienyl]-9,11,17-trimethyl-, (3S,6Z,8E,11S,15R,17S)-
- (3S,6Z,8E,11S,15R,17S)-15-Amino-3-[(1E,3E,5E)-7-(dimethylamino)-2,5-dimethyl-1,3,5-heptatrien-1-yl]-9,11,17-trimethyl-4,12-dioxa-20-thia-21-azabicyclo[16.2.1]heneicosa-1(21),6,8,18-tetraene-5,13-dione
Pateamine A is a natural compound that was originally isolated from the marine sponge Mycale sp. It has been shown to have anticancer properties by inhibiting motilin-induced calcium mobilization in human urine and inhibiting cancer cell growth in Chinese hamster ovary cells. Pateamine A has also been found to be a potent inhibitor of kinases, including vildagliptin, which is used to treat type 2 diabetes. This compound induces apoptosis in tumor cells and can be used as an analog for studying the effects of kinase inhibitors on cancer development. Its potential as an anticancer agent makes it a promising candidate for future research into cancer treatments.
Proprietà chimiche
Richiesta tecnica su: 3D-XP183225 Pateamine A
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