Walker B - Search Results

1

Peptidyl inverse esters of p-methoxybenzoic acid: a novel class of potent inactivator of the serine proteases.

Lynas J, Walker B. Lynas J, et al. Among authors: walker b. Biochem J. 1997 Aug 1;325 ( Pt 3)(Pt 3):609-16. doi: 10.1042/bj3250609. Biochem J. 1997. PMID: 9271079 Free PMC article.

2

Evaluation of dipeptide alpha-keto-beta-aldehydes as new inhibitors of cathepsin S.

Walker B, Lynas JF, Meighan MA, Brömme D. Walker B, et al. Biochem Biophys Res Commun. 2000 Aug 28;275(2):401-5. doi: 10.1006/bbrc.2000.3311. Biochem Biophys Res Commun. 2000. PMID: 10964677

3

Strategies for the inhibition of serine proteases.

Walker B, Lynas JF. Walker B, et al. Cell Mol Life Sci. 2001 Apr;58(4):596-624. doi: 10.1007/PL00000884. Cell Mol Life Sci. 2001. PMID: 11361094 Free PMC article. Review.

4

Peptides containing acylated C-terminal gem diamines: novel irreversible inactivators of the cysteine and serine proteinases.

Gilmore BF, Lynas JF, Harriott P, Healy A, Walker B. Gilmore BF, et al. Among authors: walker b. Chem Biol Drug Des. 2006 May;67(5):364-9. doi: 10.1111/j.1747-0285.2006.00390.x. Chem Biol Drug Des. 2006. PMID: 16784461

5

Irreversible inhibition of the bacterial cysteine protease-transpeptidase sortase (SrtA) by substrate-derived affinity labels.

Scott CJ, McDowell A, Martin SL, Lynas JF, Vandenbroeck K, Walker B. Scott CJ, et al. Among authors: walker b. Biochem J. 2002 Sep 15;366(Pt 3):953-8. doi: 10.1042/BJ20020602. Biochem J. 2002. PMID: 12069686 Free PMC article.

6

Dipeptide proline diphenyl phosphonates are potent, irreversible inhibitors of seprase (FAPalpha).

Gilmore BF, Lynas JF, Scott CJ, McGoohan C, Martin L, Walker B. Gilmore BF, et al. Among authors: walker b. Biochem Biophys Res Commun. 2006 Jul 28;346(2):436-46. doi: 10.1016/j.bbrc.2006.05.175. Biochem Biophys Res Commun. 2006. PMID: 16769036

7

Peptide glyoxals: a novel class of inhibitor for serine and cysteine proteinases.

Walker B, McCarthy N, Healy A, Ye T, McKervey MA. Walker B, et al. Biochem J. 1993 Jul 15;293 ( Pt 2)(Pt 2):321-3. doi: 10.1042/bj2930321. Biochem J. 1993. PMID: 8343111 Free PMC article.

8

Inhibitors of the chymotrypsin-like activity of proteasome based on di- and tri-peptidyl alpha-keto aldehydes (glyoxals).

Lynas JF, Harriott P, Healy A, McKervey MA, Walker B. Lynas JF, et al. Among authors: walker b. Bioorg Med Chem Lett. 1998 Feb 17;8(4):373-8. doi: 10.1016/s0960-894x(98)00030-4. Bioorg Med Chem Lett. 1998. PMID: 9871688

9

Solid-phase synthesis and biological screening of N-alpha-mercaptoamide template-based matrix metalloprotease inhibitors.

Lynas JF, Martin SL, Walker B, Baxter AD, Bird J, Bhogal R, Montana JG, Owen DA. Lynas JF, et al. Among authors: walker b. Comb Chem High Throughput Screen. 2000 Feb;3(1):37-41. doi: 10.2174/1386207003327738. Comb Chem High Throughput Screen. 2000. PMID: 10702612

10

Potent new leucine aminopeptidase inhibitor of novel structure synthesised by a modified Wadsworth-Emmons (Horner) Wittig procedure.

Walker B, Darkins PA, McKervey MA, Moncrieff HM, Lynas JF. Walker B, et al. Bioorg Med Chem Lett. 2000 Jul 3;10(13):1481-2. doi: 10.1016/s0960-894x(00)00261-4. Bioorg Med Chem Lett. 2000. PMID: 10888337

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