Synthesis and Structure–activity relationships of 1-arylmethyl-3-(1-methyl-2-amino)ethyl-5-aryl-6-methyluracils as antagonists of the human GnRH Receptor
- 26 July 2003
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 13 (19) , 3317-3322
- https://doi.org/10.1016/s0960-894x(03)00619-x
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Identification of 1-Arylmethyl-3- (2-aminoethyl)-5-aryluracil as Novel Gonadotropin-Releasing Hormone Receptor AntagonistsJournal of Medicinal Chemistry, 2003
- Design and Structure−Activity Relationships of 2-Alkyl-3-aminomethyl-6-(3-methoxyphenyl)-7-methyl-8-(2-fluorobenzyl)imidazolo[1,2-a]pyrimid-5-ones as Potent GnRH Receptor AntagonistsJournal of Medicinal Chemistry, 2003
- A novel synthesis of 7-aryl-8-fluoro-pyrrolo[1,2-a]pyrimid-4-ones as potent, stable GnRH receptor antagonistsBioorganic & Medicinal Chemistry Letters, 2002
- Synthesis and initial structure–Activity relationships of a novel series of imidazolo[1,2-a]pyrimid-5-ones as potent GnRH receptor antagonistsBioorganic & Medicinal Chemistry Letters, 2002
- Design, synthesis and structure–Activity relationships of novel imidazolo[1,2-a]pyrimid-5-ones as potent GnRH receptor antagonistsBioorganic & Medicinal Chemistry Letters, 2002
- A Novel Synthesis of 2-Arylpyrrolo[1,2-a]pyrimid-7-ones and Their Structure–Activity Relationships as Potent GnRH Receptor AntagonistsBioorganic & Medicinal Chemistry Letters, 2001
- Initial Structure–Activity Relationship Studies of a Novel Series of Pyrrolo[1,2-a]pyrimid-7-ones as GnRH Receptor AntagonistsBioorganic & Medicinal Chemistry Letters, 2001