Molecular dynamics analysis of novel statin analogs shows that binding induces superior stabilization of HMG‐CoA reductase. As shown by the solvent‐accessible surface area profile, ligand‐induced rigidity offers a new, effective strategy for drug design. Cardiovascular diseases remain a leading cause of global mortality.
Yoshua B. Mtulo +4 more
wiley +1 more source
Terpenes as Naturally Occurring Stereochemical Templates: Conformationally Driven Discovery of Reactivity. [PDF]
Arto O +6 more
europepmc +1 more source
Absolute stereochemistry of fungal metabolites: icterinoidins A1 and B1, and atrovirins B1 and B2
Melvyn Gill, Peter M. Morgan
openalex +2 more sources
Stereochemical Studies of Monoterpene Compounds. VI. The Stereochemistry of 2-Hydroxypinocamphone and Its Reduction Products [PDF]
Takayuki Suga +3 more
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Diverse reactivity of maleimides in polymer science and beyond
This mini‐review provides a thorough overview of maleimide chemistry, highlighting its diverse reactivity in polymer and materials science applications. Abstract Maleimides are remarkably versatile functional groups, capable of participating in homo‐ and copolymerizations, Diels–Alder and (photo)cycloadditions, Michael additions, and other reactions ...
Bruce E Kirkpatrick +2 more
wiley +1 more source
Ancient gene clusters govern the initiation of monoterpenoid indole alkaloid biosynthesis and C3 stereochemistry inversion. [PDF]
Hwang J +21 more
europepmc +1 more source
The Stereochemistry of N-tert-Butyl-4-(4-hydroxyphenyl)-4-phenyl-2-butylamines. [PDF]
Anne Helander +8 more
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Enhancing Lipidomics With High‐Resolution Ion Mobility‐Mass Spectrometry
ABSTRACT Lipids, indispensable yet structurally intricate biomolecules, serve as critical regulators of cellular function and disease progression. Conventional lipidomics, constrained by limited resolution for isomeric and low‐abundance species, has been transformed by ion mobility‐mass spectrometry (IM‐MS).
Gaoyuan Lu +3 more
wiley +1 more source
Biosynthesis of the 5-Isoxazolidinone-Containing Hexacyclic Structure of Parnafungin. [PDF]
Sun Z, Yost KM, Bills GF, Tang Y.
europepmc +1 more source

