These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
126 related articles for article (PubMed ID: 30579793)
1. The role of N-terminal heterocycles in hydrogen bonding to α-chymotrypsin. Schumann NC; Bruning J; Marshall AC; Abell AD Bioorg Med Chem Lett; 2019 Feb; 29(3):396-399. PubMed ID: 30579793 [TBL] [Abstract][Full Text] [Related]
2. Synthesis and structure-activity relationships of peptidyl alpha-keto heterocycles as novel inhibitors of prolyl endopeptidase. Tsutsumi S; Okonogi T; Shibahara S; Ohuchi S; Hatsushiba E; Patchett AA; Christensen BG J Med Chem; 1994 Oct; 37(21):3492-502. PubMed ID: 7932578 [TBL] [Abstract][Full Text] [Related]
3. Ring-deactivated hydroxyalkylpyrrole-based inhibitors of alpha-chymotrypsin: synthesis and mechanism of action. Martyn DC; Vernall AJ; Clark BM; Abell AD Org Biomol Chem; 2003 Jun; 1(12):2103-10. PubMed ID: 12945901 [TBL] [Abstract][Full Text] [Related]
4. Design of serine protease inhibitors with conformation restricted by amino acid side-chain-side-chain CH/pie interaction. Shimohigashi Y; Nose T; Yamauchi Y; Maeda I Biopolymers; 1999; 51(1):9-17. PubMed ID: 10380349 [TBL] [Abstract][Full Text] [Related]
5. Ring-deactivated hydroxymethylpyrroles as inhibitors of alpha-chymotrypsin. Abell AD; Nabbs BK Bioorg Med Chem; 2001 Mar; 9(3):621-8. PubMed ID: 11310596 [TBL] [Abstract][Full Text] [Related]
6. X-ray crystal structure of a dipeptide-chymotrypsin complex in an inhibitory interaction. Kashima A; Inoue Y; Sugio S; Maeda I; Nose T; Shimohigashi Y Eur J Biochem; 1998 Jul; 255(1):12-23. PubMed ID: 9692896 [TBL] [Abstract][Full Text] [Related]
7. Peptidyl human heart chymase inhibitors. 1. Synthesis and inhibitory activity of difluoromethylene ketone derivatives bearing P' binding subsites. Eda M; Ashimori A; Akahoshi F; Yoshimura T; Inoue Y; Fukaya C; Nakajima M; Fukuyama H; Imada T; Takai S; Shiota N; Miyazaki M; Nakamura N Bioorg Med Chem Lett; 1998 Apr; 8(8):913-8. PubMed ID: 9871511 [TBL] [Abstract][Full Text] [Related]
8. Quantifying tetrahedral adduct formation and stabilization in the cysteine and the serine proteases. Cleary JA; Doherty W; Evans P; Malthouse JP Biochim Biophys Acta; 2015 Oct; 1854(10 Pt A):1382-91. PubMed ID: 26169698 [TBL] [Abstract][Full Text] [Related]
9. Crystal structure of gamma-chymotrypsin in complex with 7-hydroxycoumarin. Ghani U; Ng KK; Atta-ur-Rahman ; Choudhary MI; Ullah N; James MN J Mol Biol; 2001 Nov; 314(3):519-25. PubMed ID: 11846564 [TBL] [Abstract][Full Text] [Related]
10. 1H-pyrrolo[2,3-b]pyridine: A new scaffold for human neutrophil elastase (HNE) inhibitors. Crocetti L; Giovannoni MP; Schepetkin IA; Quinn MT; Khlebnikov AI; Cantini N; Guerrini G; Iacovone A; Teodori E; Vergelli C Bioorg Med Chem; 2018 Nov; 26(21):5583-5595. PubMed ID: 30385225 [TBL] [Abstract][Full Text] [Related]
11. Leucine-phenylalanine dipeptide-based N-mesyloxysuccinimides: synthesis of all four stereoisomers and their assay against serine proteases. Abell AD; Oldham MD Bioorg Med Chem Lett; 1999 Feb; 9(3):497-500. PubMed ID: 10091709 [TBL] [Abstract][Full Text] [Related]
12. Noncovalent inhibition of the serine proteases, alpha-chymotrypsin and trypsin by trifluoro(organo)borates. Smoum R; Rubinstein A; Srebnik M Org Biomol Chem; 2005 Mar; 3(5):941-4. PubMed ID: 15731882 [TBL] [Abstract][Full Text] [Related]
13. A mechanistic study on the inhibition of α-chymotrypsin by a macrocyclic peptidomimetic aldehyde. Zhang X; Bruning JB; George JH; Abell AD Org Biomol Chem; 2016 Aug; 14(29):6970-8. PubMed ID: 27349772 [TBL] [Abstract][Full Text] [Related]
14. Three-dimensional structure of chymotrypsin inactivated with (2S)-N-acetyl-L-alanyl-L-phenylalanyl alpha-chloroethane: implications for the mechanism of inactivation of serine proteases by chloroketones. Kreutter K; Steinmetz AC; Liang TC; Prorok M; Abeles RH; Ringe D Biochemistry; 1994 Nov; 33(46):13792-800. PubMed ID: 7947790 [TBL] [Abstract][Full Text] [Related]
15. Exploration of nitrogen heterocycle scaffolds for the development of potent human neutrophil elastase inhibitors. Cantini N; Khlebnikov AI; Crocetti L; Schepetkin IA; Floresta G; Guerrini G; Vergelli C; Bartolucci G; Quinn MT; Giovannoni MP Bioorg Med Chem; 2021 Jan; 29():115836. PubMed ID: 33218895 [TBL] [Abstract][Full Text] [Related]
16. Novel diphenyl esters of peptidyl alpha-aminoalkylphosphonates as inhibitors of chymotrypsin and subtilisin. Pietrusewicz E; Sieńczyk M; Oleksyszyn J J Enzyme Inhib Med Chem; 2009 Dec; 24(6):1229-36. PubMed ID: 19912056 [TBL] [Abstract][Full Text] [Related]
17. N-heterocyclic dipeptide aldehyde calpain inhibitors. Jones SA; Jones MA; McNabb SB; Aitken SG; Coxon JM; Abell AD Protein Pept Lett; 2009; 16(12):1466-72. PubMed ID: 20001909 [TBL] [Abstract][Full Text] [Related]