Triazole oxytocin antagonists: Identification of an aryloxyazetidine replacement for a biaryl substituent
- PMID: 19963374
- DOI: 10.1016/j.bmcl.2009.11.097
Triazole oxytocin antagonists: Identification of an aryloxyazetidine replacement for a biaryl substituent
Abstract
A series of aryloxyazetidines, aryloxypyrrolidines and aryloxypiperidines were designed based on structural overlap with previously reported arylpyrazine Oxytocin antagonists. Similarly high levels of Oxytocin antagonism were achievable in these new series. Several aryloxyazetidines also showed high levels of selectivity, with one compound, 25, displaying promising in vivo pharmacokinetics and significantly improved aqueous solubility over related compounds containing a biaryl substituent.
Copyright 2009 Elsevier Ltd. All rights reserved.
Similar articles
-
Triazole oxytocin antagonists: identification of aryl ether replacements for a biaryl substituent.Bioorg Med Chem Lett. 2008 Oct 1;18(19):5242-4. doi: 10.1016/j.bmcl.2008.08.066. Epub 2008 Aug 22. Bioorg Med Chem Lett. 2008. PMID: 18778939
-
Identification of amide bioisosteres of triazole oxytocin antagonists.Bioorg Med Chem Lett. 2010 Apr 1;20(7):2224-8. doi: 10.1016/j.bmcl.2010.02.018. Epub 2010 Feb 8. Bioorg Med Chem Lett. 2010. PMID: 20189387
-
Aryloxypyrazines as highly selective antagonists of Oxytocin.Bioorg Med Chem Lett. 2009 May 15;19(10):2634-6. doi: 10.1016/j.bmcl.2009.03.160. Epub 2009 Apr 5. Bioorg Med Chem Lett. 2009. PMID: 19376698
-
Peptide and non-peptide agonists and antagonists for the vasopressin and oxytocin V1a, V1b, V2 and OT receptors: research tools and potential therapeutic agents.Prog Brain Res. 2008;170:473-512. doi: 10.1016/S0079-6123(08)00437-8. Prog Brain Res. 2008. PMID: 18655903 Review.
-
Vasopressin and oxytocin in normal reproduction and in the pathophysiology of preterm labour and primary dysmenorrhoea. Development of receptor antagonists for therapeutic use in these conditions.Rocz Akad Med Bialymst. 2004;49:18-21. Rocz Akad Med Bialymst. 2004. PMID: 15631309 Review.
Cited by
-
Divergent, Strain-Release Reactions of Azabicyclo[1.1.0]butyl Carbinols: Semipinacol or Spiroepoxy Azetidine Formation.Angew Chem Int Ed Engl. 2021 Mar 22;60(13):7360-7365. doi: 10.1002/anie.202100583. Epub 2021 Feb 26. Angew Chem Int Ed Engl. 2021. PMID: 33555105 Free PMC article.
-
Synthesis of azetidines by aza Paternò-Büchi reactions.Chem Sci. 2020 Jun 12;11(29):7553-7561. doi: 10.1039/d0sc01017k. eCollection 2020 Aug 7. Chem Sci. 2020. PMID: 32832061 Free PMC article. Review.
-
Recent Progress in the Discovery and Development of 2-Nitroimidazooxazines and 6-Nitroimidazooxazoles to Treat Tuberculosis and Neglected Tropical Diseases.Molecules. 2020 Sep 10;25(18):4137. doi: 10.3390/molecules25184137. Molecules. 2020. PMID: 32927749 Free PMC article. Review.
-
Synthesis of azetidines via visible-light-mediated intermolecular [2+2] photocycloadditions.Nat Chem. 2020 Oct;12(10):898-905. doi: 10.1038/s41557-020-0541-1. Epub 2020 Sep 23. Nat Chem. 2020. PMID: 32968230
-
7-Substituted 2-Nitro-5,6-dihydroimidazo[2,1-b][1,3]oxazines: Novel Antitubercular Agents Lead to a New Preclinical Candidate for Visceral Leishmaniasis.J Med Chem. 2017 May 25;60(10):4212-4233. doi: 10.1021/acs.jmedchem.7b00034. Epub 2017 May 11. J Med Chem. 2017. PMID: 28459575 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Chemical Information