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133 related items for PubMed ID: 1894448

  • 1. Solid phase synthesis of a fully active analogue of cholecystokinin using the acid-stable Boc-Phe (p-CH2) SO3H as a substitute for Boc-Tyr(SO3H) in CCK8.
    Gonzalez-Muniz R, Cornille F, Bergeron F, Ficheux D, Pothier J, Durieux C, Roques BP.
    Int J Pept Protein Res; 1991 Apr; 37(4):331-40. PubMed ID: 1894448
    [Abstract] [Full Text] [Related]

  • 2. Full agonists of CCK8 containing a nonhydrolyzable sulfated tyrosine residue.
    Marseigne I, Roy P, Dor A, Durieux C, Pélaprat D, Reibaud M, Blanchard JC, Roques BP.
    J Med Chem; 1989 Feb; 32(2):445-9. PubMed ID: 2464062
    [Abstract] [Full Text] [Related]

  • 3. Synthesis and binding affinities of cyclic and related linear analogues of CCK8 selective for central receptors.
    Charpentier B, Dor A, Roy P, England P, Pham H, Durieux C, Roques BP.
    J Med Chem; 1989 Jun; 32(6):1184-90. PubMed ID: 2724293
    [Abstract] [Full Text] [Related]

  • 4. Synthesis and biological evaluation of cholecystokinin analogs in which the Asp-Phe-NH2 moiety has been replaced by a 3-amino-7-phenylheptanoic acid or a 3-amino-6-(phenyloxy)hexanoic acid.
    Amblard M, Rodriguez M, Lignon MF, Galas MC, Bernad N, Artis-Noël AM, Hauad L, Laur J, Califano JC, Aumelas A.
    J Med Chem; 1993 Oct 01; 36(20):3021-8. PubMed ID: 7692048
    [Abstract] [Full Text] [Related]

  • 5. Synthesis of human CCK26-33 and CCK-33 related analogues on 2,4-DMBHA and TMBHA.
    Miranda MT, Liddle RA, Rivier JE.
    J Med Chem; 1993 Jun 11; 36(12):1681-8. PubMed ID: 7685390
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  • 8. Boc-Trp-Orn(Z)-Asp-NH2 and derivatives: a new family of CCK antagonists.
    Gonzalez-Muniz R, Bergeron F, Marseigne I, Durieux C, Roques BP.
    J Med Chem; 1990 Dec 11; 33(12):3199-204. PubMed ID: 1701834
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  • 10. Plant peptide hormone phytosulfokine (PSK-alpha): synthesis of new analogues and their biological evaluation.
    Bahyrycz A, Matsubayashi Y, Ogawa M, Sakagami Y, Konopińska D.
    J Pept Sci; 2004 Jul 11; 10(7):462-9. PubMed ID: 15298181
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  • 11. Facile solid-phase synthesis of sulfated tyrosine-containing peptides: total synthesis of human big gastrin-II and cholecystokinin (CCK)-39.
    Kitagawa K, Aida C, Fujiwara H, Yagami T, Futaki S, Kogire M, Ida J, Inoue K.
    J Org Chem; 2001 Jan 12; 66(1):1-10. PubMed ID: 11429884
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  • 12. Synthetic CCK8 analogs with antagonist activity on pancreatic receptors: in vivo study in the rat, compared to non-peptidic antagonists.
    Nagain C, Galas MC, Lignon MF, Rodriguez M, Martinez J, Rozé C.
    Pancreas; 1991 May 12; 6(3):275-81. PubMed ID: 1713671
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  • 13. Carboxylic acids and tetrazoles as isosteric replacements for sulfate in cholecystokinin analogues.
    Tilley JW, Danho W, Lovey K, Wagner R, Swistok J, Makofske R, Michalewsky J, Triscari J, Nelson D, Weatherford S.
    J Med Chem; 1991 Mar 12; 34(3):1125-36. PubMed ID: 2002454
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  • 14. Cyclic cholecystokinin analogues with high selectivity for central receptors.
    Charpentier B, Pelaprat D, Durieux C, Dor A, Reibaud M, Blanchard JC, Roques BP.
    Proc Natl Acad Sci U S A; 1988 Mar 12; 85(6):1968-72. PubMed ID: 3162318
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  • 15. Total synthesis, purification, and characterization of human [Phe(p-CH2SO 3Na)52, Nle32,53,56, Nal55]-CCK20-58, [Tyr52, Nle32,53,56, Nal55]-CCK-58, and [Phe(p-CH2SO3Na)52, Nle32,53,56, Nal55]-CCK-58.
    Miranda MT, Craig AG, Miller C, Liddle RA, Rivier JE.
    J Protein Chem; 1993 Oct 12; 12(5):533-44. PubMed ID: 7511387
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  • 16. Application of 2-chlorotrityl resin in solid phase synthesis of (Leu15)-gastrin I and unsulfated cholecystokinin octapeptide. Selective O-deprotection of tyrosine.
    Barlos K, Gatos D, Kapolos S, Poulos C, Schäfer W, Yao WQ.
    Int J Pept Protein Res; 1991 Dec 12; 38(6):555-61. PubMed ID: 1819590
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  • 17. Stabilized (111)in-labeled sCCK8 analogues for targeting CCK2-receptor positive tumors: synthesis and evaluation.
    Roosenburg S, Laverman P, Joosten L, Eek A, Oyen WJ, de Jong M, Rutjes FP, van Delft FL, Boerman OC.
    Bioconjug Chem; 2010 Apr 21; 21(4):663-70. PubMed ID: 20302291
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  • 19. Solid phase synthesis of peptides containing the non-hydrolysable analog of (O)phosphotyrosine, p(CH2PO3H2)Phe. Application to the synthesis of 344-357 sequences of the beta 2 adrenergic receptor.
    Garbay-Jaureguiberry C, Ficheux D, Roques BP.
    Int J Pept Protein Res; 1992 Jun 21; 39(6):523-7. PubMed ID: 1383166
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  • 20. A new series of photoactivatable and iodinatable linear vasopressin antagonists.
    Carnazzi E, Aumelas A, Barberis C, Guillon G, Seyer R.
    J Med Chem; 1994 Jun 10; 37(12):1841-9. PubMed ID: 8021923
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