Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Adicionar filtros








Intervalo de ano
1.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 500-504, 2021.
Artigo em Inglês | WPRIM | ID: wpr-888778

RESUMO

Two new lignan glucosides, tinsinlignans A and B (1 and 2), two new oxyneolignans, tinsinlignans C and D (3 and 4), along with one known analogue (5), were isolated from the stems of Tinospora sinensis. The structures of the new compounds were elucidated based on analysis of spectroscopic data, and the absolute configuration of 1 was determined through electronic circular dichroism (ECD) calculation based on the time-dependent density functional theory (TD-DFT). Compounds 1-4 were evaluated for their inhibitory effects on nitric oxide (NO) production induced by lipopolysaccharide (LPS) in murine RAW264.7 macrophage cells and compounds 1 and 2 exhibited moderate inhibitory activities with IC


Assuntos
Animais , Camundongos , Glucosídeos/farmacologia , Lignanas/farmacologia , Lipopolissacarídeos , Estrutura Molecular , Óxido Nítrico , Compostos Fitoquímicos/farmacologia , Tinospora/química
2.
Chinese Journal of Natural Medicines (English Ed.) ; (6): 303-307, 2019.
Artigo em Inglês | WPRIM | ID: wpr-776882

RESUMO

Four new octadecanoid derivatives (1-4) including a pair of enantiomers (1/2), along with 12 known analogues (5-16), were isolatedfrom the seeds of Ipomoea nil. Their structures were determined by detailed spectroscopic analyses and comparison with reported data of structurally related compounds, with the absolute configurations of 1 and 2 being assigned by an in situ dimolybdenum ECD method. Our bioassays revealed that these isolates did not show ABTS radical scavenging activity while 10 and 13 displayed better α-glucosidase inhibitory activity than the positive control acarbose (IC 167.7 ± 1.55 μmol·L), with IC of 92.73 ± 3.12 and 11.39 ± 2.18μmol·L, respectively.


Assuntos
Ácidos Graxos , Química , Metabolismo , Inibidores de Glicosídeo Hidrolases , Química , Metabolismo , Concentração Inibidora 50 , Ipomoea nil , Química , Estrutura Molecular , Extratos Vegetais , Química , Metabolismo , Sementes , Química
3.
China Biotechnology ; (12)2006.
Artigo em Chinês | WPRIM | ID: wpr-685265

RESUMO

The hom gene encoding for homoserine dehydrogenase was amplified from the genomic DNA of Corynebacterium glutamicum ATCC 13032.After the kanamycin-resistant gene(Km)cassette from plasmid pET28a was inserted into the center of hom,the hom::Km cassette was then electroporated into the competent cell of C.glutamicum ATCC 13032.And kanamycin-resistant clones were obtained.PCR was performed to confirm whether the Km gene was integrated into the hom gene of these clones and the recombinant strains of hom-disrupted were screened out.Fermentation results showed that the lysine yield of the hom-disrupted strain C.g-hom::Km-8 reached 4.7 g/L,which was 6.7 times that of C.glutamicum ATCC 13032.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA