224 related articles for article (PubMed ID: 7945258)
1. Phosphinic peptide analogues as potent inhibitors of Corynebacterium rathayii bacterial collagenase.
Yiotakis A; Lecoq A; Nicolaou A; Labadie J; Dive V
Biochem J; 1994 Oct; 303 ( Pt 1)(Pt 1):323-7. PubMed ID: 7945258
[TBL] [Abstract][Full Text] [Related]
2. Cyclic peptides with a phosphinic bond as potent inhibitors of a zinc bacterial collagenase.
Yiotakis A; Lecoq A; Vassiliou S; Raynal I; Cuniasse P; Dive V
J Med Chem; 1994 Aug; 37(17):2713-20. PubMed ID: 8064799
[TBL] [Abstract][Full Text] [Related]
3. Development of highly potent and selective phosphinic peptide inhibitors of zinc endopeptidase 24-15 using combinatorial chemistry.
Jirácek J; Yiotakis A; Vincent B; Lecoq A; Nicolaou A; Checler F; Dive V
J Biol Chem; 1995 Sep; 270(37):21701-6. PubMed ID: 7665587
[TBL] [Abstract][Full Text] [Related]
4. Phosphinic peptides, the first potent inhibitors of astacin, behave as extremely slow-binding inhibitors.
Yiallouros I; Vassiliou S; Yiotakis A; Zwilling R; Stöcker W; Dive V
Biochem J; 1998 Apr; 331 ( Pt 2)(Pt 2):375-9. PubMed ID: 9531473
[TBL] [Abstract][Full Text] [Related]
5. Hydroxyethylene isostere inhibitors of human immunodeficiency virus-1 protease: structure-activity analysis using enzyme kinetics, X-ray crystallography, and infected T-cell assays.
Dreyer GB; Lambert DM; Meek TD; Carr TJ; Tomaszek TA; Fernandez AV; Bartus H; Cacciavillani E; Hassell AM; Minnich M
Biochemistry; 1992 Jul; 31(29):6646-59. PubMed ID: 1637805
[TBL] [Abstract][Full Text] [Related]
6. Design, synthesis, and metal binding of novel Pseudo- oligopeptides containing two phosphinic acid groups.
Ye Y; Liu M; Kao JL; Marshall GR
Biopolymers; 2008 Jan; 89(1):72-85. PubMed ID: 17910046
[TBL] [Abstract][Full Text] [Related]
7. Development of the first potent and selective inhibitor of the zinc endopeptidase neurolysin using a systematic approach based on combinatorial chemistry of phosphinic peptides.
Jirácek J; Yiotakis A; Vincent B; Checler F; Dive V
J Biol Chem; 1996 Aug; 271(32):19606-11. PubMed ID: 8702656
[TBL] [Abstract][Full Text] [Related]
8. Synthesis of pseudo-peptide analogues of the C-terminal tetrapeptide of gastrin and evaluation of their biological activity on acid secretion.
Rodriguez M; Bali JP; Magous R; Castro B; Martinez J
Int J Pept Protein Res; 1986 Mar; 27(3):293-9. PubMed ID: 3011690
[TBL] [Abstract][Full Text] [Related]
9. Peptide inhibitors of E. collagenolyticum bacterial collagenase--effect of N-methylation. Consequences on biological activity and conformational properties.
Dive V; Yiotakis A; Roumestand C; Gilquin B; Labadie J; Toma F
Int J Pept Protein Res; 1992 Jun; 39(6):506-15. PubMed ID: 1399271
[TBL] [Abstract][Full Text] [Related]
10. Design, structure-activity, and molecular modeling studies of potent renin inhibitory peptides having N-terminal Nin-For-Trp (Ftr): angiotensinogen congeners modified by P1-P1' Phe-Phe, Sta, Leu psi[CH(OH)CH2]Val or leu psi[CH2NH]Val substitutions.
Sawyer TK; Pals DT; Mao B; Staples DJ; de Vaux AE; Maggiora LL; Affholter JA; Kati W; Duchamp D; Hester JB
J Med Chem; 1988 Jan; 31(1):18-30. PubMed ID: 3275777
[TBL] [Abstract][Full Text] [Related]
11. Effect of a novel selective and potent phosphinic peptide inhibitor of endopeptidase 3.4.24.16 on neurotensin-induced analgesia and neuronal inactivation.
Vincent B; Jiracek J; Noble F; Loog M; Roques B; Dive V; Vincent JP; Checler F
Br J Pharmacol; 1997 Jun; 121(4):705-10. PubMed ID: 9208137
[TBL] [Abstract][Full Text] [Related]
12. Potent and selective inhibition of zinc aminopeptidase A (EC 3.4.11.7, APA) by glutamyl aminophosphinic peptides: importance of glutamyl aminophosphinic residue in the P1 position.
Georgiadis D; Vazeux G; Llorens-Cortes C; Yiotakis A; Dive V
Biochemistry; 2000 Feb; 39(5):1152-5. PubMed ID: 10653662
[TBL] [Abstract][Full Text] [Related]
13. Crystallographic analysis of transition-state mimics bound to penicillopepsin: phosphorus-containing peptide analogues.
Fraser ME; Strynadka NC; Bartlett PA; Hanson JE; James MN
Biochemistry; 1992 Jun; 31(22):5201-14. PubMed ID: 1606144
[TBL] [Abstract][Full Text] [Related]
14. Aldehyde and ketone substrate analogues inhibit the collagenase of Clostridium histolyticum.
Grobelny D; Galardy RE
Biochemistry; 1985 Oct; 24(22):6145-52. PubMed ID: 3002433
[TBL] [Abstract][Full Text] [Related]
15. Peptide-derived transition state analogue inhibitors of thrombin; synthesis, activity and selectivity.
Jetten M; Peters CA; Visser A; Grootenhuis PD; van Nispen JW; Ottenheijm HC
Bioorg Med Chem; 1995 Aug; 3(8):1099-114. PubMed ID: 7582983
[TBL] [Abstract][Full Text] [Related]
16. Inhibition of Clostridium histolyticum collagenases by phosphonamide peptide inhibitors.
Dive V; Yiotakis A; Nicolaou A; Toma F
Eur J Biochem; 1990 Aug; 191(3):685-93. PubMed ID: 2167850
[TBL] [Abstract][Full Text] [Related]
17. Phosphonate analogues of carboxypeptidase A substrates are potent transition-state analogue inhibitors.
Hanson JE; Kaplan AP; Bartlett PA
Biochemistry; 1989 Jul; 28(15):6294-305. PubMed ID: 2790000
[TBL] [Abstract][Full Text] [Related]
18. Phosphorus amino acid analogues as inhibitors of leucine aminopeptidase.
Giannousis PP; Bartlett PA
J Med Chem; 1987 Sep; 30(9):1603-9. PubMed ID: 3625708
[TBL] [Abstract][Full Text] [Related]
19. RXP 407, a phosphinic peptide, is a potent inhibitor of angiotensin I converting enzyme able to differentiate between its two active sites.
Dive V; Cotton J; Yiotakis A; Michaud A; Vassiliou S; Jiracek J; Vazeux G; Chauvet MT; Cuniasse P; Corvol P
Proc Natl Acad Sci U S A; 1999 Apr; 96(8):4330-5. PubMed ID: 10200262
[TBL] [Abstract][Full Text] [Related]
20. The human erythrocyte anion-transport protein. Partial amino acid sequence, conformation and a possible molecular mechanism for anion exchange.
Brock CJ; Tanner MJ; Kempf C
Biochem J; 1983 Sep; 213(3):577-86. PubMed ID: 6615451
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]