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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

95 related articles for article (PubMed ID: 1724664)

  • 1. Synthesis of a potent agonist of substance P by modifying the methionyl and glutaminyl residues of the C-terminal hexapeptide of substance P. Structure-activity relationships.
    Karagiannis K; Manolopoulou A; Stavropoulos G; Poulos C; Jordan CC; Hagan RM
    Int J Pept Protein Res; 1991 Oct; 38(4):350-6. PubMed ID: 1724664
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Synthesis and biological activity of analogues of the C-terminal hexapeptide of substance P with modifications at glutaminyl and methioninyl residues. Structure-activity studies.
    Antoniou M; Poulos C; Tsegenidis T
    Int J Pept Protein Res; 1992 Nov; 40(5):395-400. PubMed ID: 1282903
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis of potent antagonists of substance P by modifying the methionyl and glutaminyl residues of its C-terminal hexapeptide and without using D-amino acids.
    Manolopoulou A; Karagiannis K; Stavropoulos G; Poulos C; Jordan CC; Hagan RM
    Int J Pept Protein Res; 1993 Apr; 41(4):411-4. PubMed ID: 7684361
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analogues of the C-terminal fragments of neurokinins with modifications at their C-terminal methionyl residue. Structure-activity studies.
    Antoniou M; Poulos C
    Int J Pept Protein Res; 1994 Apr; 43(4):344-50. PubMed ID: 7519179
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthesis of a potent antagonist of substance P by replacing the CH2SCH3 and the alpha-carboxamide groups of the methionine at [Orn6]-SP6-11 by benzyl ester groups.
    Karagiannis K; Stavropoulos G; Poulos C; Jordan CC; Hagan RM
    Int J Pept Protein Res; 1993 Dec; 42(6):565-9. PubMed ID: 7508424
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis of potent agonists of substance P by replacement of Met11 with Glu(OBzl) and N-terminal glutamine with Glp of the C-terminal hexapeptide and heptapeptide of substance P.
    Stavropoulos G; Karagiannis K; Anagnostides S; Ministrouski I; Selinger Z; Chorev M
    Int J Pept Protein Res; 1995 Jun; 45(6):508-13. PubMed ID: 7558580
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis and biological activity of substance P C-terminal hexapeptide and heptapeptide analogues.
    Stavropoulos G; Karagiannis K; Cordopatis P; Halle D; Gilon C; Bar-Akiva G; Selinger Z; Chorev M
    Int J Pept Protein Res; 1991 Mar; 37(3):180-4. PubMed ID: 1714423
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Structure-activity studies on the C-terminal hexapeptide of substance P with modifications at the glutaminyl and methioninyl residues.
    Poulos C; Stavropoulos G; Brown JR; Jordan CC
    J Med Chem; 1987 Aug; 30(8):1512-5. PubMed ID: 2441056
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pseudopeptide analogues of substance P and leucine enkephalinamide containing the psi (CH2O) modification: synthesis and biological activity.
    Roubini E; Laufer R; Gilon C; Selinger Z; Roques BP; Chorev M
    J Med Chem; 1991 Aug; 34(8):2430-8. PubMed ID: 1714957
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synthesis and biological activity of NK1 substance P selective agonists by modifying the methionyl residue.
    Poulos C; Antoniou M; Patacchini R; Maggi CA; Pegoraro S; Rovero P
    Neuropeptides; 1994 Jul; 27(1):27-9. PubMed ID: 7526260
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis, biological activity, and conformational analysis of [pGlu6,N-MePhe8,Aib9] substance P (6-11): a selective agonist for the NK-3 receptor.
    Tallon M; Ron D; Halle D; Amodeo P; Saviano G; Temussi PA; Selinger Z; Naider F; Chorev M
    Biopolymers; 1993 Jun; 33(6):915-26. PubMed ID: 7686410
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neurokinin receptors in the guinea pig ileum.
    Nguyen-Le XK; Nguyen QT; Gobeil F; Jukic D; Chrétien L; Regoli D
    Pharmacology; 1996 Jan; 52(1):35-45. PubMed ID: 8966201
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis and biological activity of NK-1 selective, N-backbone cyclic analogs of the C-terminal hexapeptide of substance P.
    Byk G; Halle D; Zeltser I; Bitan G; Selinger Z; Gilon C
    J Med Chem; 1996 Aug; 39(16):3174-8. PubMed ID: 8759639
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A potent and selective agonist for NK-2 tachykinin receptor.
    Rovero P; Pestellini V; Patacchini R; Giuliani S; Santicioli P; Maggi CA; Meli A; Giachetti A
    Peptides; 1989; 10(3):593-5. PubMed ID: 2550911
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A synthetic glycopeptide of substance P analogue (SP6-11) with enhanced NK-1 receptor specificity.
    Haro I; Busquets MA; Torres JL; Valencia G; Garcia-Anton JM; Reig F
    J Pharm Sci; 1990 Jan; 79(1):74-6. PubMed ID: 1690289
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Tachykinin receptors in the guinea-pig isolated bronchi.
    Maggi CA; Patacchini R; Quartara L; Rovero P; Santicioli P
    Eur J Pharmacol; 1991 May; 197(2-3):167-74. PubMed ID: 1717290
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [pGlu6,Pro9]SP6-11, a selective agonist for the substance P P-receptor subtype.
    Laufer R; Gilon C; Chorev M; Selinger Z
    J Med Chem; 1986 Jul; 29(7):1284-8. PubMed ID: 2433445
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pharmacological receptors for substance P and neurokinins.
    Regoli D; Drapeau G; Dion S; D'Orléans-Juste P
    Life Sci; 1987 Jan; 40(2):109-17. PubMed ID: 2432376
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Synthesis and biological activity of substance P C-terminal hexapeptide analogues: structure-activity studies.
    Poulos C; Brown JR; Jordan CC
    J Med Chem; 1986 Jul; 29(7):1281-4. PubMed ID: 2433444
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis and biological activity of NK1 tachykinin antagonists not containing D-residues.
    Poulos C; Antoniou M; Patacchini R; Maggi CA; Rovero P
    Neuropeptides; 1994 Jan; 26(1):55-7. PubMed ID: 7512697
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.