about
Microbial and Natural Metabolites That Inhibit Splicing: A Powerful Alternative for Cancer TreatmentDesign, synthesis and initial biological evaluation of a novel pladienolide analog scaffold.Twelve-membered macrolactones: privileged scaffolds for the development of new therapeutics.Enantioselective total synthesis of pladienolide B: a potent spliceosome inhibitorTherapeutic targeting of splicing in cancer.Stabilized cyclopropane analogs of the splicing inhibitor FD-895Structure of FD-895 revealed through total synthesisOptimization of antitumor modulators of pre-mRNA splicing.Total synthesis, proof of absolute configuration, and biosynthetic origin of stylopsal, the first isolated sex pheromone of strepsiptera.
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
name
A synthetic entry to pladienolide B and FD-895
@ast
A synthetic entry to pladienolide B and FD-895
@en
A synthetic entry to pladienolide B and FD-895.
@nl
type
label
A synthetic entry to pladienolide B and FD-895
@ast
A synthetic entry to pladienolide B and FD-895
@en
A synthetic entry to pladienolide B and FD-895.
@nl
prefLabel
A synthetic entry to pladienolide B and FD-895
@ast
A synthetic entry to pladienolide B and FD-895
@en
A synthetic entry to pladienolide B and FD-895.
@nl
P2093
P2860
P1476
A synthetic entry to pladienolide B and FD-895
@en
P2093
Alexander L Mandel
Brian D Jones
James J La Clair
Michael D Burkart
P2860
P304
P356
10.1016/J.BMCL.2007.06.094
P407
P577
2007-07-07T00:00:00Z