TY - JOUR
T1 - Nematocidal Alkaloids from the Roots of Stemona mairei (H.Lév.)K.Krause and identification of their pharmacophoric moiety
AU - Shi, Bao-Bao
AU - Kongkiatpaiboon, Sumet
AU - Chen, Gao
AU - Schinnerl, Johann
AU - Cai, Xiang-hai
N1 - Publisher Copyright:
© 2022
PY - 2023/1
Y1 - 2023/1
N2 - Fifteen undescribed Stemona alkaloids, named as stemarines A–O (1–15), along with 25 known alkaloids (16–40), were isolated and identified from the roots of Stemona mairei (H.Lév.)K.Krause (Stemonaceae). Their structures were elucidated through the analysis of the NMR spectra, mass data, and computational chemistry. All the hitherto undescribed compounds possess a pyrrolo[1,2-α]azepine core structure but differ in important structural features, which reflects their nematocidal activities. Alkaloids 3–6 featured a carboxylic side chain and exhibited significant nematocidal activity against the nematode Caenorhabditis elegans. Transections of fresh roots combined with application of the Dragendorff’ reagent on the tissue indicated accumulation of alkaloids mainly in the epidermis and the pith. These results suggest the key pharmacophore of these alkaloids lies in the aliphatic side chain of these compounds and its spatial distribution in the roots indicate protective effects against underground herbivores.
AB - Fifteen undescribed Stemona alkaloids, named as stemarines A–O (1–15), along with 25 known alkaloids (16–40), were isolated and identified from the roots of Stemona mairei (H.Lév.)K.Krause (Stemonaceae). Their structures were elucidated through the analysis of the NMR spectra, mass data, and computational chemistry. All the hitherto undescribed compounds possess a pyrrolo[1,2-α]azepine core structure but differ in important structural features, which reflects their nematocidal activities. Alkaloids 3–6 featured a carboxylic side chain and exhibited significant nematocidal activity against the nematode Caenorhabditis elegans. Transections of fresh roots combined with application of the Dragendorff’ reagent on the tissue indicated accumulation of alkaloids mainly in the epidermis and the pith. These results suggest the key pharmacophore of these alkaloids lies in the aliphatic side chain of these compounds and its spatial distribution in the roots indicate protective effects against underground herbivores.
UR - http://www.scopus.com/inward/record.url?scp=85141541199&partnerID=8YFLogxK
U2 - 10.1016/j.bioorg.2022.106239
DO - 10.1016/j.bioorg.2022.106239
M3 - Article
SN - 0045-2068
VL - 130
JO - Bioorganic Chemistry
JF - Bioorganic Chemistry
M1 - 106239
ER -