Download MendeleySynthesis of glutamic acid analogs as potent inhibitors of leukotriene A4 hydrolase.
Kirkland, T.A., Adler, M., Bauman, J.G., Chen, M., Haeggstrom, J.Z., King, B., Kochanny, M.J., Liang, A.M., Mendoza, L., Phillips, G.B., Thunnissen, M., Trinh, L., Whitlow, M., Ye, B., Ye, H., Parkinson, J., Guilford, W.J.(2008) Bioorg Med Chem 16: 4963-4983
- PubMed: 18394906
- DOI: https://doi.org/10.1016/j.bmc.2008.03.042
- Primary Citation of Related Structures:
3CHO, 3CHP, 3CHQ, 3CHR, 3CHS - PubMed Abstract:
Leukotriene B(4) (LTB(4)) is a potent pro-inflammatory mediator that has been implicated in the pathogenesis of multiple diseases, including psoriasis, inflammatory bowel disease, multiple sclerosis and asthma. As a method to decrease the level of LTB(4) and possibly identify novel treatments, inhibitors of the LTB(4) biosynthetic enzyme, leukotriene A(4) hydrolase (LTA(4)-h), have been explored. Here we describe the discovery of a potent inhibitor of LTA(4)-h, arylamide of glutamic acid 4f, starting from the corresponding glycinamide 2. Analogs of 4f are then described, focusing on compounds that are both active and stable in whole blood. This effort culminated in the identification of amino alcohol 12a and amino ester 6b which meet these criteria.
Organizational Affiliation:
Department of Medicinal Chemistry, Berlex Biosciences, 2600 Hilltop Drive, Richmond, CA 94804, United States. [email protected]
