120 related articles for article (PubMed ID: 2156864)
1. Thiol-based inhibitors of mammalian collagenase. Substituted amide and peptide derivatives of the leucine analogue, 2-[(R,S)-mercaptomethyl]-4-methylpentanoic acid.
Darlak K; Miller RB; Stack MS; Spatola AF; Gray RD
J Biol Chem; 1990 Mar; 265(9):5199-205. PubMed ID: 2156864
[TBL] [Abstract][Full Text] [Related]
2. Phosphoramidate peptide inhibitors of human skin fibroblast collagenase.
Kortylewicz ZP; Galardy RE
J Med Chem; 1990 Jan; 33(1):263-73. PubMed ID: 2153207
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Inhibition of purified collagenase from alkali-burned rabbit corneas.
Burns FR; Stack MS; Gray RD; Paterson CA
Invest Ophthalmol Vis Sci; 1989 Jul; 30(7):1569-75. PubMed ID: 2545645
[TBL] [Abstract][Full Text] [Related]
5. Comparison of vertebrate collagenase and gelatinase using a new fluorogenic substrate peptide.
Stack MS; Gray RD
J Biol Chem; 1989 Mar; 264(8):4277-81. PubMed ID: 2538433
[TBL] [Abstract][Full Text] [Related]
6. Application of N-carboxyalkyl peptides to the inhibition and affinity purification of the porcine matrix metalloproteinases collagenase, gelatinase, and stromelysin.
Stack MS; Emberts CG; Gray RD
Arch Biochem Biophys; 1991 Jun; 287(2):240-9. PubMed ID: 1654808
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Characterization of the P2' and P3' specificities of thrombin using fluorescence-quenched substrates and mapping of the subsites by mutagenesis.
Le Bonniec BF; Myles T; Johnson T; Knight CG; Tapparelli C; Stone SR
Biochemistry; 1996 Jun; 35(22):7114-22. PubMed ID: 8679538
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Design and synthesis of novel imidazole-substituted dipeptide amides as potent and selective inhibitors of Candida albicans myristoylCoA:protein N-myristoyltransferase and identification of related tripeptide inhibitors with mechanism-based antifungal activity.
Devadas B; Freeman SK; Zupec ME; Lu HF; Nagarajan SR; Kishore NS; Lodge JK; Kuneman DW; McWherter CA; Vinjamoori DV; Getman DP; Gordon JI; Sikorski JA
J Med Chem; 1997 Aug; 40(16):2609-25. PubMed ID: 9258368
[TBL] [Abstract][Full Text] [Related]
11. Inhibition of collagenase from Clostridium histolyticum by phosphoric and phosphonic amides.
Galardy RE; Grobelny D
Biochemistry; 1983 Sep; 22(19):4556-61. PubMed ID: 6313042
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Vertebrate collagenase inhibitor. II. Tetrapeptidyl hydroxamic acids.
Odake S; Okayama T; Obata M; Morikawa T; Hattori S; Hori H; Nagai Y
Chem Pharm Bull (Tokyo); 1991 Jun; 39(6):1489-94. PubMed ID: 1657422
[TBL] [Abstract][Full Text] [Related]
14. New thiol inhibitors of Clostridium histolyticum collagenase. Importance of the P3' position.
Yiotakis A; Hatgiyannacou A; Dive V; Toma F
Eur J Biochem; 1988 Mar; 172(3):761-6. PubMed ID: 2832171
[TBL] [Abstract][Full Text] [Related]
15. Design, synthesis, and evaluation of matrix metalloprotease inhibitors bearing cyclopropane-derived peptidomimetics as P1' and P2' replacements.
Reichelt A; Gaul C; Frey RR; Kennedy A; Martin SF
J Org Chem; 2002 Jun; 67(12):4062-75. PubMed ID: 12054939
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Protein kinase inhibitor-(6-22)-amide peptide analogs with standard and nonstandard amino acid substitutions for phenylalanine 10. Inhibition of cAMP-dependent protein kinase.
Glass DB; Lundquist LJ; Katz BM; Walsh DA
J Biol Chem; 1989 Aug; 264(24):14579-84. PubMed ID: 2760075
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Inhibition of mammalian collagenases by thiol-containing peptides.
Gray RD; Miller RB; Spatola AF
J Cell Biochem; 1986; 32(1):71-7. PubMed ID: 3021790
[TBL] [Abstract][Full Text] [Related]
20. Primary structural determinants essential for potent inhibition of cAMP-dependent protein kinase by inhibitory peptides corresponding to the active portion of the heat-stable inhibitor protein.
Glass DB; Cheng HC; Mende-Mueller L; Reed J; Walsh DA
J Biol Chem; 1989 May; 264(15):8802-10. PubMed ID: 2722799
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
