Project description:Graphical abstract Two new apotirucallane triterpenoids, namely chisiamols G (1) and H (2), featuring a 21,23-lactone, together with five known triterpenoids, were isolated from the twigs of Chisocheton paniculatus. The structures of the new compounds were elucidated on the basis of spectroscopic and chemical methods. Electronic Supplementary Material Supplementary material is available for this article at 10.1007/s13659-012-0065-5 and is accessible for authorized users.
| S-EPMC4131609 | biostudies-literature
Project description:Celastrus angulatus
| PRJNA509758 | ENA
Project description:RNA Sequencing of Celastrus orbiculatus
Project description:Mallotus paniculatus (Lam.) Müll. Arg. 1865 (Euphorbiaceae) is a shrub or small tree with medicinal properties that is distributed across Southeast Asia. In this study, we sequenced the complete chloroplast genome of M. paniculatus to study phylogenetic relationships within the family Euphorbiaceae Juss. The complete chloroplast genome of M. paniculatus was 164,455 bp in length, with an overall GC content of 35.3%. It was found to consist of a long single copy region of 89,021 bp, a small single copy region of 18,524 bp, and a pair of inverted repeats of 28,455 bp. Results indicated that the chloroplast genome contains a total of 131 genes, including 78 protein-coding genes, 37 tRNA genes, eight rRNA genes, and eight pseudogenes. The phylogenetic tree showed that M. paniculatus is closely related to Mallotus japonicus and Mallotus peltatus.
Project description:This research aimed to explore the eco-friendly green synthesis of copper nanoparticles (CuNPs) using Celastrus paniculatus leaves extract. Primarily, the biosynthesized CuNPs characterized by UV-vis spectroscopy showed an absorption peak at 269 nm. Further, The SEM and TEM studies revealed the spherical shape of particles with size ranged between 2-10 nm with an average particle diameter of 5 nm. FT-IR analysis confirmed the presence of functional groups -OH, C[bond, double bond]C and C-H triggers the synthesis of CuNPs. The negative zeta potential -22.2 mV indicated the stability of CuNPs was confirmed by DLS and the composition and purity by EDS studies. Further, the photocatalytic property of the CuNPs was divulged by their methylene blue dye degradation potential. The reaction kinetics followed pseudo-first-order with k-values (rate constant) 0.0172 min-1. In addition, this material was found to be a good antifungal agent against plant pathogenic fungi Fusarium oxysporum showed 76.29 ± 1.52 maximum mycelial inhibition.