Compound library development guided by protein structure similarity clustering and natural product structure
about
Pharmacophore Models and Pharmacophore-Based Virtual Screening: Concepts and Applications Exemplified on Hydroxysteroid DehydrogenasesCharting biologically relevant chemical space: a structural classification of natural products (SCONP)Impairment of prostate cancer cell growth by a selective and reversible lysine-specific demethylase 1 inhibitor.Finding Inspiration in the Protein Data Bank to Chemically Antagonize Readers of the Histone Code.1,4-Dihydropyridine derivatives with T-type calcium channel blocking activity attenuate inflammatory and neuropathic pain.Natural products as an inspiration in the diversity-oriented synthesis of bioactive compound libraries.Principles, implementation, and application of biology-oriented synthesis (BIOS).Small molecule macroarray construction via palladium-mediated carbon-carbon bond-forming reactions: highly efficient synthesis and screening of stilbene arrays.Design, synthesis, and bioactivities screening of a diaryl ketone-inspired pesticide molecular library as derived from natural products.Recent trends and observations in the design of high-quality screening collections.Towards the systematic exploration of chemical space.Biology-oriented synthesis.Discovery of protein phosphatase inhibitor classes by biology-oriented synthesisBiology-oriented synthesis of a natural-product inspired oxepane collection yields a small-molecule activator of the Wnt-pathway.Mechanisms of disease: Selective inhibition of 11beta-hydroxysteroid dehydrogenase type 1 as a novel treatment for the metabolic syndrome.Similar interactions of natural products with biosynthetic enzymes and therapeutic targets could explain why nature produces such a large proportion of existing drugs.Chemogenomics in drug discovery: computational methods based on the comparison of binding sites.Predicting natural product value, an exploration of anti-TB drug space.Discovery of inhibitors of the Wnt and Hedgehog signaling pathways through the catalytic enantioselective synthesis of an iridoid-inspired compound collection.Development of highly potent inhibitors of the Ras-targeting human acyl protein thioesterases based on substrate similarity design.Mouse 11β-hydroxysteroid dehydrogenase type 2 for human application: homology modeling, structural analysis and ligand-receptor interaction.Synthesis of the B-seco limonoid core scaffold.Synthesis of natural-product-like molecules with over eighty distinct scaffoldsDiscovery of a new class of inhibitors of Mycobacterium tuberculosis protein tyrosine phosphatase B by biology-oriented synthesis.BIOS: Similarity-based design of natural product derived compound collections.Putting small molecules in the lead.Synthesis of the B-seco limonoid scaffoldA Scaffold-Tree-Merging Strategy for Prospective Bioactivity Annotation of γ-PyronesStereocomplementary synthesis of a natural product-derived compound collection on a solid phase
P2860
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P2860
Compound library development guided by protein structure similarity clustering and natural product structure
description
2004 nî lūn-bûn
@nan
2004 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Compound library development g ...... and natural product structure
@ast
Compound library development g ...... and natural product structure
@en
type
label
Compound library development g ...... and natural product structure
@ast
Compound library development g ...... and natural product structure
@en
prefLabel
Compound library development g ...... and natural product structure
@ast
Compound library development g ...... and natural product structure
@en
P2093
P2860
P356
P1476
Compound library development g ...... and natural product structure
@en
P2093
Alex Odermatt
Duraiswamy A Jeyaraj
Eleni Gourzoulidou
Kerstin Reinecke
Lars-Oliver Wittenberg
Marcus A Koch
Sudipta Basu
P2860
P304
16721-16726
P356
10.1073/PNAS.0404719101
P407
P577
2004-11-17T00:00:00Z