508213-33-0Relevant academic research and scientific papers
Design of inhibitors of scytalone dehydratase: Probing interactions with an asparagine carboxamide
Basarab, Gregory S.,Jordan, Douglas B.,Gehret, Troy C.,Schwartz, Rand S.
, p. 4143 - 4154 (2007/10/03)
Among the active-site residues of scytalone dehydratase, the side-chain carboxamide of asparagine 131 has the greatest potential for strong electrostatic interactions. Structure-based inhibitor design aimed at enhancing interactions with this residue led to the synthesis of a series of highly potent inhibitors that have a five- or six-membered ring containing a carbonyl functionality for hydrogen bonding. To achieve a good orientation for hydrogen bonding, the inhibitors incorporate a phenyl substituent that displaces a phenylalanine residue away from the five- or six-membered rings. Without the phenyl substituent, inhibitor binding potency is diminished by three orders of magnitude. Larger Ki values of a site-directed mutant (Asn131Ala) of scytalone dehydratase in comparison to those of wild-type enzyme validate the design concept. The most potent inhibitor (Ki=15 pM) contains a tetrahydrothiophenone that can form a single hydrogen bond with the asparagine carboxamide. Inhibitors with a butyrolactam that can form two hydrogen bonds with the asparagine carboxamide demonstrate excellent in vivo fungicidal activity.
Design of scytalone dehydratase inhibitors as rice blast fungicides: Derivatives of norephedrine
Basarab, Gregory S.,Jordan, Douglas B.,Gehret, Troy C.,Schwartz, Rand S.,Wawrzak, Zdzislaw
, p. 1613 - 1618 (2007/10/03)
Five X-ray crystal structures of scytalone dehydratase complexed with different inhibitors have delineated conformationally flexible regions of the binding pocket. This information was used for the design and synthesis of a norephedrine-derived cyanoacetamide class of inhibitors leading to potent fungicides.
