Conformationally locked thiosugars alpha-mannosidase inhibitors: Synthesis, and docking studies as potent biochemical
Data(s) |
01/09/2007
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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 |