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.
147 related articles for article (PubMed ID: 833810)
1. Synthesis and some pharmacological properties of [4-threonine, 7-glycine]oxytocin, [1-(L-2-hydroxy-3-mercaptopropanoic acid), 4-threonine, 7-glycine]oxytocin (hydroxy[Thr4, Gly7]oxytocin), and [7-Glycine]oxytocin, peptides with high oxytocic-antidiuretic selectivity. Lowbridge J; Manning M; Haldar J; Sawyer WH J Med Chem; 1977 Jan; 20(1):120-3. PubMed ID: 833810 [TBL] [Abstract][Full Text] [Related]
2. Synthesis and some pharmacological properties of [1-(L-2-hydroxy-3-mercaptopropanoic acid), 4-threonine]oxytocin (hydroxy [4-thr]oxytocin), a peptide with strikingly high oxytocic potency and of [1-(L-2-hydroxy-3-mercaptopropanoic acid)]oxytocin (hydroxy-oxytocin). Manning M; Lowbridge J; Sawyer WH; Haldar J J Med Chem; 1976 Mar; 19(3):376-80. PubMed ID: 943546 [TBL] [Abstract][Full Text] [Related]
3. Synthesis and some pharmacological properties of [4-threonine,7-sarcosine]oxytocin, a peptide with high oxytocic potency, and of [4-threonine,7-N-methylalanine]oxytocin. Grzonka Z; Lammek B; Gazis D; Schwartz IL J Med Chem; 1983 Dec; 26(12):1786-7. PubMed ID: 6685771 [TBL] [Abstract][Full Text] [Related]
4. An exploration of the effects of L- and D-tetrahydroisoquinoline-3-carboxylic acid substitutions at positions 2, 3 and 7 in cyclic and linear antagonists of vasopressin and oxytocin and at position 3 in arginine vasopressin. Manning M; Cheng LL; Stoev S; Bankowski K; Przybyiski J; Klis WA; Sawyer WH; Wo NC; Chan WY J Pept Sci; 1995; 1(1):66-79. PubMed ID: 9222985 [TBL] [Abstract][Full Text] [Related]
5. Design of oxytocin antagonists, which are more selective than atosiban. Manning M; Stoev S; Cheng LL; Wo NC; Chan WY J Pept Sci; 2001 Sep; 7(9):449-65. PubMed ID: 11587184 [TBL] [Abstract][Full Text] [Related]
6. [1-(L-2-hydroxy-3-mercaptopropanoic acid)] analogues of arginine-vasopressin, [8-D-arginine]vasopressin, and [4-valine,8-D-arginine]vasopressin. Lowbridge J; Manning M; Haldar J; Sawyer W J Med Chem; 1977 Sep; 20(9):1173-6. PubMed ID: 926117 [TBL] [Abstract][Full Text] [Related]
7. Combined high oxytocic with negligible antidiuretic and pressor activities in multisubstituted oxytocins. Stahl GL; Walter R J Med Chem; 1977 Apr; 20(4):492-5. PubMed ID: 850233 [TBL] [Abstract][Full Text] [Related]
8. Solid-phase synthesis of 16 potent (selective and nonselective) in vivo antagonists of oxytocin. Manning M; Kruszynski M; Bankowski K; Olma A; Lammek B; Cheng LL; Klis WA; Seto J; Haldar J; Sawyer WH J Med Chem; 1989 Feb; 32(2):382-91. PubMed ID: 2913298 [TBL] [Abstract][Full Text] [Related]
9. Design of neurohypophyseal peptides that exhibit selective agonistic and antagonistic properties. Manning M; Lowbridge J; Haldar J; Sawyer WH Fed Proc; 1977 May; 36(6):1848-52. PubMed ID: 323064 [TBL] [Abstract][Full Text] [Related]
10. An investigation of position 3 in arginine vasopressin with aliphatic, aromatic, conformationally-restricted, polar and charged amino acids. Stoev S; Cheng LL; Olma A; Klis WA; Manning M; Sawyer WH; Wo NC; Chan WY J Pept Sci; 1999 Mar; 5(3):141-53. PubMed ID: 10323558 [TBL] [Abstract][Full Text] [Related]
11. Potent antagonists of the antidiuretic responses to arginine-vasopressin based on modifications of [1-(beta-mercapto-beta,beta-cyclopentamethylenepropionic acid),2-D- phenylalanine,4-valine]arginine-vasopressin at position 4. Manning M; Olma A; Klis WA; Seto J; Sawyer WH J Med Chem; 1983 Nov; 26(11):1607-13. PubMed ID: 6631916 [TBL] [Abstract][Full Text] [Related]
12. Effects of a D-Cys6/L-Cys6 interchange in nonselective and selective vasopressin and oxytocin antagonists. Manning M; Cheng LL; Klis WA; Balaspiri L; Olma A; Sawyer WH; Wo NC; Chan WY J Med Chem; 1995 May; 38(10):1762-9. PubMed ID: 7752199 [TBL] [Abstract][Full Text] [Related]
13. Synthetic antagonists of in vivo responses by the rat uterus to oxytocin. Lowbridge J; Manning M; Seto J; Haldar J; Sawyer WH J Med Chem; 1979 May; 22(5):565-9. PubMed ID: 458806 [TBL] [Abstract][Full Text] [Related]
14. [1-Deaminopenicillamine,4-threonine]oxytocin, a potent inhibitor of oxytocin. Manning M; Lowbridge J; Seto J; Haldar J; Sawyer WH J Med Chem; 1978 Feb; 21(2):179-82. PubMed ID: 621712 [TBL] [Abstract][Full Text] [Related]
15. Synthesis and some pharmacological properties of oxytocin analogues having L-thiazolidine-4-carboxylic acid in position 7. Rosamond JD; Ferger MF J Med Chem; 1976 Jul; 19(7):873-6. PubMed ID: 940106 [TBL] [Abstract][Full Text] [Related]
16. Synthesis, pharmacological, conformational, and dynamic studies of the potent hormone antagonists [1-penicillamine, 4-threonine]-oxytocin and [1-penicillamine, 2-phenylalanine, 4-threonine]-oxytocin. Conformational and dynamic considerations in the design of antagonists. Hruby VJ; Mosberg HI; Hadley ME; Chan WY; Powell AM Int J Pept Protein Res; 1980 Nov; 16(5):372-81. PubMed ID: 7216613 [TBL] [Abstract][Full Text] [Related]
17. Some pharmacological actions of four synthetic analogues of oxytocin. BERDE B; DOEPFNER W; KONZETT H Br J Pharmacol Chemother; 1957 Jun; 12(2):209-14. PubMed ID: 13446374 [TBL] [Abstract][Full Text] [Related]
18. Synthesis and some pharmacological properties of two new antagonists of oxytocin. Rekowski P; Melin P; Lammek B Pol J Pharmacol Pharm; 1987; 39(3):303-7. PubMed ID: 3438212 [TBL] [Abstract][Full Text] [Related]
19. Oxytocin receptors from LLC-PK1 cells: expression in Xenopus oocytes. Cantau B; Barjon JN; Chicot D; Baskevitch PP; Jard S Am J Physiol; 1990 Apr; 258(4 Pt 2):F963-72. PubMed ID: 2158746 [TBL] [Abstract][Full Text] [Related]
20. Design of peptide oxytocin antagonists with strikingly higher affinities and selectivities for the human oxytocin receptor than atosiban. Manning M; Cheng LL; Stoev S; Wo NC; Chan WY; Szeto HH; Durroux T; Mouillac B; Barberis C J Pept Sci; 2005 Oct; 11(10):593-608. PubMed ID: 15880385 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]