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1.
Chem Pharm Bull (Tokyo) ; 69(3): 291-297, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-33642479

RESUMEN

Alkaline hydrolysis of crude resin glycoside fraction of the seeds of Ipomoea muricata (L.) Jacq. (Convolvulaceae) yielded a new glycosidic acid, muricatic acid D; three known glycosidic acids, namely, muricatic acids A, B, and C; and three known organic acids, namely, isobutyric, 2S-methylbutyric, and 2S-methyl-3S-hydroxybutyric acid. Two new genuine resin glycosides with macrolactone structures (jalapins), muricatins X and XI, were also isolated from the fraction. Their structures were determined using spectroscopic data and chemical evidence.


Asunto(s)
Glicósidos/química , Ipomoea/química , Extractos Vegetales/química , Resinas de Plantas/química , Semillas/química , Butiratos/química , Cromatografía Liquida , Convolvulaceae/química , Hidrólisis , Espectroscopía de Resonancia Magnética , Estructura Molecular , Solventes/química
2.
Chem Pharm Bull (Tokyo) ; 64(9): 1408-10, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27581646

RESUMEN

A new resin glycoside, named muricatin IX (1), was isolated from the seeds of Ipomoea muricata (L.) JACQ. (Convolvulaceae). The structure of 1 was determined on the basis of spectroscopic data as well as chemical evidence. Compound 1 is the first representative of resin glycosides in which an organic acid connects the sugar moiety and the aglycone moiety to form macrocyclic ester ring.


Asunto(s)
Glicósidos/aislamiento & purificación , Ipomoea/química , Resinas de Plantas/aislamiento & purificación , Semillas/química , Glicósidos/química , Conformación Molecular , Resinas de Plantas/química
3.
Nat Prod Res ; : 1-10, 2022 Sep 23.
Artículo en Inglés | MEDLINE | ID: mdl-36148550

RESUMEN

Two new resin glycosides, muricatins XII (1) and XIII (2), were isolated from the crude resin glycoside fraction of the seeds of Ipomoea muricata (L.) Jacq. (Convolvulaceae), along with three known ones, muricatins V (3), VI (4), and IX (5). Compounds 1 and 2 contained new glycosidic acids, muricatic acids E (1a) and F (2a), respectively. The structures of these compounds were determined using data obtained from spectroscopy measurements and chemical evidence. The results suggested that 1 and 2 have macrolactone structures (jalapins). Furthermore, the cytotoxic activity of the crude resin glycoside fraction and 3-5 against HL-60 human promyelocytic leukaemia cells was evaluated. All tested samples demonstrated cytotoxic activities.

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