18607-76-6Relevant articles and documents
Pregnane glycosides from Gymnema inodorum and their α-glucosidase inhibitory activity
Trang, Do Thi,Yen, Duong Thi Hai,Cuong, Nguyen The,Anh, Luu The,Hoai, Nguyen Thi,Tai, Bui Huu,Doan, Vu Van,Yen, Pham Hai,Quang, Tran Hong,Nhiem, Nguyen Xuan,Minh, Chau Van,Kiem, Phan Van
, p. 2157 - 2163 (2019/11/03)
Two new pregnane glycosides, gyminosides A and B (1 and 2) and three known, tinctoroside B (3), tinctoroside C (4), and gymnepregoside F (5) were isolated from the leaves of Gymnema inodorum (Lour.) Decne. Their structures were elucidated by physical and chemical methods and comparing with those reported in the literature. All these compounds were evaluated for α-glucosidase assay. Compound 5 exhibited the most anti α-glucosidase activity with inhibitory percentage of 63.7 ± 3.9% at the concentration of 200 μM. Compounds 1–4 showed moderate anti α-glucosidase activity with inhibitory percentage ranging from 40.0 to 52.1%.
The anti-glycative potentials of pregnane glycosides from Gymnema sylvestre
Hung, Nguyen Van,Kiem, Phan Van,Kim, Seung Hyun,Kim, Sun Yeou,Lee, Jae Hyuk,Manh, Hoang Duc,Minh, Chau Van,Nhiem, Nguyen Xuan,Park, SeonJu,Tai, Bui Huu,Trang, Do Thi,Yen, Duong Thi Hai,Yen, Pham Hai
, p. 19 - 24 (2020/05/18)
Gymnema sylvestre is known for its potent antidiabetic activity. Phytochemical investigations of this plant led to the isolation of three new pregnane glycosides, gymnepregosides R-T (1-3) and four known analogues, 12β-acetyloxy-3β,8β,14β,17β-tetrahydroxypregn-5-en-20-one 3-O-β-D-glucopyranosyl-(1→4)-6-deoxy-3-O-methyl-β-D-allopyranosyl-(1→4)-β-D-oleandropyranosyl-(1→4)-β-D-cymaropyranosyl-(1→4)-β-D-cymaropyranoside (4), 12-O-(E)-cinnamoylgymnepregoside F (5), gymnepregoside F (6), and stephanoside I (7). Their structures were identified based on spectroscopic evidence and compared with those reported in the literature. All compounds were evaluated for antiglycative inhibitory activity. Compounds 1, 3, 5, and 6 showed the inhibitory effect on BSA-MGO formation ranging from 6.0 to 8.8 % at the concentrations of 400 μM. Compounds 1 and 2 showed significant breaking properties on MGO-AGE-protein crosslink with percent modification ranging from 54.6 to 58.4 %. Notably, a novel AGEs inhibitor (1) may inhibit the formation and accumulation of MGO-AGEs and protect cells from MGO-AGEs cross-linking damage.
A PREGNANE ESTER AND ITS GLYCOSIDE FROM ORTHENTHERA VIMINEA
Kaur, Kanwal J.,Khare, Maheshwari P.,Khare, Anakshi
, p. 3007 - 3010 (2007/10/02)
A new pregnane ester named ornogenin and its diglycoside designated as ornine were isolated from the dried twigs of Orthenthera viminea.On the basis of chemical and spectroscopic evidence, their structures were established as 12,20-di-O-cinnamoyl-sarcosti