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1.
J Pept Res ; 65(2): 284-91, 2005 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-15705170

RESUMO

Degarelix is a potent very long-acting GnRH antagonist after subcutaneous administration. In this paper, we describe the synthesis of two analogs of degarelix incorporating racemic 3-(2-methoxy-5-pyridyl)-alanine (2-OMe-5Pal, 5) at position 3. The two diastereomers were separated by reverse-phase high-performance liquid chromatography (RP-HPLC) and the absolute stereochemistry at position 3 in the peptides was determined by enzymatic digestion with proteinase K. These analogs were tested in vitro for their ability to antagonize the GnRH receptor and in vivo for duration of action in a castrated male rat assay. Analog 7 with D2-OMe-5Pal was potent in vitro (IC50 = 5.22 nM); however, analog 8 with L2-OMe-5Pal at position 3 in degarelix lost potency as an antagonist of the human GnRH receptor (IC50 = 36.95 nM). Both the analogs were found to be short-acting in vivo.


Assuntos
Alanina/análogos & derivados , Alanina/síntese química , Hormônio Liberador de Gonadotropina/antagonistas & inibidores , Piridinas/síntese química , Alanina/farmacologia , Animais , Masculino , Oligopeptídeos/química , Piridinas/farmacologia , Ratos , Receptores LHRH/antagonistas & inibidores
2.
J Am Chem Soc ; 123(24): 5619-24, 2001 Jun 20.
Artigo em Inglês | MEDLINE | ID: mdl-11403591

RESUMO

A novel family of cystine-based spirobicyclic peptides (cystinospiranes) has been synthesized by a single-step procedure involving condensation of pentaerythritol-derived tetrachloride with either the simple L-cystine dimethyl ester or its C,C'-extended bispeptides leading to a variety of 19-membered spirobicyclic peptides or its N,N'-extended bispeptides affording the ring-expanded 25-membered cystinospiranes. The design is flexible with respect to the ring size that can be adjusted depending upon the length of the N,N'-extended cystine bispeptide, and the choice of an amino acid, as illustrated here with the preparation of a large number of cystinospiranes containing a wide variety of amino acids. X-ray crystal structure of the parent spirane (5a) revealed nanotube formation by vertical stacking of relatively flat spirobicyclic molecules through contiguous NH- - -O==C hydrogen bonding. The fused pair of parallel nanotubes is open-ended, hollow, and extends to infinity. Crystallographic parameters are the following: C(33)H(52)N(4)O(16)S(4), space group C2, a = 42.181(3) A, b = 5.1165(7) A, c = 11.8687(9) A, beta = 106.23(1) degrees.


Assuntos
Cistina/química , Peptídeos Cíclicos/síntese química , Compostos de Espiro/síntese química , Cristalização , Cristalografia por Raios X , Ligação de Hidrogênio , Estrutura Molecular , Peptídeos Cíclicos/química , Estrutura Secundária de Proteína , Compostos de Espiro/química
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