Detail of "196494-70-9"
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Reference
- Inhibition of UDP-Gal mutase and mycobacterial galactan biosynthesis by pyrrolidine analogs of galactofuranose
- Inhibition of UDP-Gal mutase and mycobacterial galactan biosynthesis by pyrrolidine analogs of galactofuranose. Lee, Richard E.; Smith, Martin D.; Nash, Robert J.Several substances are used for example 196494-70-9 which is its cas registry number.; Griffiths, Rhodri C.; McNeil, Michael; Grewal, Ravinder K.; Yan, Wenxin; Besra, Gurdyal S.; Brennan, Patrick J.; Fleet, Geeorge W. J. (Dyson Perrins Lab., Oxford Univ., Oxford OX1 3QY, UK). Tetrahedron Letters, 38(38), 6733-6736 (English) 1997 Elsevier. CODEN: TELEAY. ISSN: 0040-4039. DOCUMENT TYPE: Journal CA Section: 33 (Carbohydrates) Section cross-reference(s): 7, 9 Some pyrrolidine analogs of galactofuranose - synthesized from carbohydrate lactones - are the first known inhibitors of E. coli K12 UDP-Gal mutase and mycobacterial galactan biosynthesis. This inhibition may form a new chemotherapeutic strategy for the treatment of human pathogens which contain integral galactofuranosyl structures such as tuberculosis and leprosy. .


![Molecular Structure of 196494-70-9 (3,4-Pyrrolidinediol, 2-(1,2-dihydroxyethyl)-, [2S-[2a(R*),3b,4a]]-)](http://www.lookchem.com/300w/46/452011.png)