Literature for peptidase C03.005: hepatitis A virus-type picornain 3C
(References are filtered for relevance to Inhibitor. To remove the filter click here. See explanation.)
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Sureshan,M., Brintha,S. and Jothi,A.
Identification of Mulberrofuran as a potent inhibitor of hepatitis A virus 3C(pro) and RdRP enzymes through structure-based virtual screening, dynamics simulation, and DFT studies
Mol Divers28, 1609-1628. PubMed Europe PubMed DOI I -
Al-Salahi,R., Anouar,E.H., Marzouk,M. and Abuelizz,H.A.
Anti-HAV evaluation and molecular docking of newly synthesized 3-benzyl(phenethyl)benzo[g]quinazolines
Bioorg Med Chem Lett29, 1614-1619. PubMed Europe PubMed DOI I -
Banerjee,K., Bhat,R., Rao,V.U.B., Nain,A., Rallapalli,K.L., Gangopadhyay,S., Singh,R.P., Banerjee,M. and Jayaram,B.
Toward development of generic inhibitors against the 3C proteases of picornaviruses
FEBS J286, 765-787. PubMed Europe PubMed DOI I -
Kassem,A.F., Batran,R.Z., Abbas,E.M.H., Elseginy,S.A., Shaheen,M.N.F. and Elmahdy,E.M.
New 4-phenylcoumarin derivatives as potent 3C protease inhibitors: design, synthesis, anti-HAV effect and molecular modeling
Eur J Med Chem168, 447-460. PubMed Europe PubMed DOI I -
Blaum,B.S., Wunsche,W., Benie,A.J., Kusov,Y., Peters,H., Gauss-Muller,V., Peters,T. and Sczakiel,G.
Functional binding of hexanucleotides to 3C protease of hepatitis A virus
Nucleic Acids Res40, 3042-3055. PubMed Europe PubMed DOI I -
Huitema,C., Zhang,J., Yin,J., James,M.N., Vederas,J.C. and Eltis,L.D.
Heteroaromatic ester inhibitors of hepatitis A virus 3C proteinase: evaluation of mode of action
Bioorg Med Chem16, 5761-5777. PubMed Europe PubMed DOI T I -
Sperry,J. and Brimble,M.A.
An efficient enantioselective synthesis of the 3C protease inhibitor (-)-thysanone
Synlett2008, 1910-1912. DOI I -
[YEAR:7-7-2006]Yin,J., Cherney,M.M., Bergmann,E.M., Zhang,J., Huitema,C., Pettersson,H., Eltis,L.D., Vederas,J.C. and James,M.N.
An episulfide cation (thiiranium ring) trapped in the active site of HAV 3C proteinase inactivated by peptide-based ketone inhibitors
J Mol Biol361, 673-686. PubMed Europe PubMed DOI S I -
[YEAR:14-10-2005]Yin,J., Bergmann,E.M., Cherney,M.M., Lall,M.S., Jain,R.P., Vederas,J.C. and James,M.N.
Dual modes of modification of hepatitis A virus 3C protease by a serine-derived beta-lactone: selective crystallization and formation of a functional catalytic triad in the active site
J Mol Biol354, 854-871. PubMed Europe PubMed DOI S I -
Lall,M.S., Jain,R.P. and Vederas,J.C.
Inhibitors of 3C cysteine proteinases from Picornaviridae
Curr Top Med Chem4, 1239-1253. PubMed Europe PubMed DOI I -
[YEAR:8-3-2002]Lall,M.S., Ramtohul,Y.K., James,M.N. and Vederas,J.C.
Serine and threonine beta-lactones: a new class of hepatitis a virus 3C cysteine proteinase inhibitors
J Org Chem67, 1536-1547. PubMed Europe PubMed DOI I -
[YEAR:17-5-2002]Ramtohul,Y.K., James,M.N. and Vederas,J.C.
Synthesis and evaluation of keto-glutamine analogues as inhibitors of hepatitis A virus 3C proteinase
J Org Chem67, 3169-3178. PubMed Europe PubMed DOI I -
[YEAR:5-12-1999]Bergmann,E.M., Cherney,M.M., Mckendrick,J., Frormann,S., Luo,C., Malcolm,B.A., Vederas,J.C. and James,M.N.
Crystal structure of an inhibitor complex of the 3C proteinase from hepatitis A virus (HAV) and implications for the polyprotein processing in HAV
Virology265, 153-163. PubMed Europe PubMed DOI S I -
Huang,Y., Malcolm,B.A. and Vederas,J.C.
Synthesis and testing of azaglutamine derivatives as inhibitors of hepatitis A virus (HAV) 3C proteinase
Bioorg Med Chem7, 607-619. PubMed Europe PubMed DOI I -
Morris,T.S., Frormann,S., Shechosky,S., Lowe,C., Lall,M.S., Gauss-Muller,V., Purcell,R.H., Emerson,S.U., Vederas,J.C. and Malcolm,B.A.
In vitro and ex vivo inhibition of hepatitis A virus 3C proteinase by a peptidyl monofluoromethyl ketone
Bioorg Med Chem5, 797-807. PubMed Europe PubMed DOI I -
Malcolm,B.A., Lowe,C., Shechosky,S., McKay,R.T., Yang,C.C., Shah,V.J., Simon,R.J., Vederas,J.C. and Santi,D.V.
Peptide aldehyde inhibitors of hepatitis A virus 3C proteinase
Biochemistry34, 8172-8179. PubMed Europe PubMed DOI I
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