WebSep 1, 2005 · Phoslactomycin B (PLM-B), a potent and selective inhibitor of serine threonine phosphatase is of interest for its antitumor, antifungal and antiviral activity. Described … WebAn efficient and highly convergent total synthesis of Leustroducsin B was achieved in 17 longest linear and 39 total steps by disconnecting the molecule into three fragments having similar levels of complexity.
Modular polyketide synthases and cis-double bond formation ...
Web(+)-Phoslactomycin B was synthesized by a highly enantio- and stereoselective approach involving asymmetric pentenylation, Suzuki−Miyaura coupling, ring-closing metathesis, … WebA Convergent Approach toward the C1−C11 Subunit of Phoslactomycins and Formal Synthesis of Phoslactomycin B. Organic Letters, 11(4), 935–938. doi:10.1021/ol8029142 . how fast can a tornado move
Prolactin: What It Is, Function & Symptoms - Cleveland Clinic
Phoslactomycin (PLM) is a natural product from the isolation of Streptomyces species. This is an inhibitor of the protein serine/threonine phosphatase which is the protein phosphate 2A (PP2A). The PP2A involves the growth factor of the cell such as to induce the formation of mitogen-activated protein interaction … See more The domains in the polyketide synthase type I: • ACP: acyl carrier protein (serves as chaperone) • AT: acyl transferase (transfers acyl group form CoA to ACP) See more The PKS of phoslactomycin has one loading domain, 7 modules and 6 proteins that encode PnA, PnB, PnC, PnD, PnE, and PnF. The biosynthesis starts the loading with the cyclohexyl- … See more 1. ^ Klaasen and Watkins II. (2015). Casarett & Doull's Essentials of Tocicology (Third ed.). McGraw Hill, Lange. p. 29. ISBN 978-0-07-184709-4. 2. ^ "Phoslactomycin B C25H40NO8P ChemSpider" See more Isolation from Streptomyces platensis, PLM is produces. Genes PnT1 and PnT2 regulate the post-synthesis of PLM to form PLM B by the phosphorylation and added the amine group . … See more WebFeb 1, 2009 · The preparation of the C1-C11 subunit of phoslactomycins, and a formal synthesis of phoslactomycin B, were achieved by a convergent strategy involving the chelation-controlled addition of an alkynyl Grignard reagent to an alpha-alkoxy ketone. WebVersatile synthon for the preparation of chiral compounds including κ-opioid receptor agonists, 1α,25-dihydroxyvitamin D3 analogue, and phoslactomycin B. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. highcourt partners