Conformationally locked thiosugars alpha-mannosidase inhibitors: Synthesis, and docking studies as potent biochemical


Autoria(s): Slvapriya, K; Hariharaputran, S; Suhas, VL; Chandra, N; Chandrasekaran, Srinivasan
Data(s)

01/09/2007

Resumo

series of thiosugar derivatives (thiolevomannosans) derived from mannose were synthesized and their inhibitory activity was tested against alpha-mannosidase (jack bean). These inhibitors were found to be more potent than the well-known inhibitors like kifunensine and deoxymannojirimycin based on docking and biochemical studies. The sulfone derivative 10 was shown to be the best inhibitor of alpha-mannosidase with the K-i value of 350 nM. (c) 2007 Elsevier Ltd. All rights reserved.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/26220/1/cf.pdf

Slvapriya, K and Hariharaputran, S and Suhas, VL and Chandra, N and Chandrasekaran, Srinivasan (2007) Conformationally locked thiosugars alpha-mannosidase inhibitors: Synthesis, and docking studies as potent biochemical. In: Bioorganic & Medicinal Chemistry, 15 (17). pp. 5659-5665.

Publicador

Elsevier Science

Relação

http://dx.doi.org/10.1016/j.bmc.2007.06.011

http://eprints.iisc.ernet.in/26220/

Palavras-Chave #Supercomputer Education & Research Centre #Organic Chemistry
Tipo

Journal Article

PeerReviewed