Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Maite Beltrán"'
Autor:
Jorge Washington Soxo-Andachi, Jeremy Alexander Toinga-Cayambe, Nayeli Maite Beltrán-Ureña, Alison Estefanía Rea-Reinoso
Publikováno v:
CIENCIAMATRIA. 8:1231-1239
En la presente investigación el objetivo general fue analizar el patriarcado como origen de la violencia. Se apoyó en la perspectiva cuantitativa, de tipo documental bibliográfica. Esto en vista de que a partir de la revisión documental y el estu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d06ea425c511f64a9401bf04cce8830
https://doi.org/10.35381/cm.v8i4.962
https://doi.org/10.35381/cm.v8i4.962
Autor:
Maite Beltrán, Yolanda Pérez, Vicente Marchán, Anna Grandas, Enrique Pedroso, Jordi Robles, Isaura Travesset
Publikováno v:
Tetrahedron. 58:6965-6978
Nucleopeptides with no restriction in the amino acid composition can be synthesized using stepwise solid-phase methodology. Best conditions for the protection of arginine and cysteine, as well as for the final deprotection treatment are established,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3f825a4b81bb47d44e0a06894faaefc
https://doi.org/10.1016/s0040-4020(02)00793-7
https://doi.org/10.1016/s0040-4020(02)00793-7
Publikováno v:
JBIC Journal of Biological Inorganic Chemistry. 4:701-707
A histidine-2'-deoxyguanosine hybrid, Phac-Hse(p5'dG)-His-OH (I), was synthesized, and its reaction with cisplatin was monitored by reversed-phase HPLC and 1HNMR. Two new compounds, II and III, were observed to be simultaneously formed, II in larger
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8bc0c49bfb726170cbeed331a153810
https://doi.org/10.1007/s007750050342
https://doi.org/10.1007/s007750050342
Autor:
Jordi Robles, Maite Beltrán, Vicente Marchán, Yolanda Pérez, Isaura Travesset, Enrique Pedroso, Anna Grandas
Publikováno v:
Tetrahedron. 55:13251-13264
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c4a564c461c18cbcd88d891eb48fb08
https://doi.org/10.1016/s0040-4020(99)00815-7
https://doi.org/10.1016/s0040-4020(99)00815-7
Publikováno v:
Tetrahedron Letters. 39:4115-4118
Protection of the imidazole ring of the histidine residue is not required for the elongation of an oligonucleotide chain at the side chain hydroxyl group of an amino acid residue by the phosphite triester approach. For the assembly of the peptide cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3f90f60fd5469b6c727e5e5c5a4812e
https://doi.org/10.1016/s0040-4039(98)00669-8
https://doi.org/10.1016/s0040-4039(98)00669-8
Publikováno v:
Bioconjugate Chemistry. 8:785-788
Nucleopeptides Ac-Tyr(p3' dACGT)-Ala-Phe-Gly-NH2, Ac-Thr(p3'dACGT)-Ala-Phe-Gly-OH, Ac-Ser(p3'dACGT)-Ala-Phe-Gly-OH, and Phac-Hse(p3'dACGT)-Ala-Phe-Gly-OH, in which the 3'-end of a tetradeoxyribonucleotide is linked by a phosphodiester bond to a hydro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfb673e6304054dd957311b2c4dd38e8
https://doi.org/10.1021/bc970051u
https://doi.org/10.1021/bc970051u
Publikováno v:
ResearcherID
Covalently linked peptide-oligonucleotide hybrids are good candidates for antisense or anti-gene therapeutics. The use of homoserine as the linking amino acid allows nucleopeptide analogues with a base-stable amino acid-nucleoside phosphate diester l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::966eb8518784da2447cd34ef8e1a4292
https://doi.org/10.1007/bf02443527
https://doi.org/10.1007/bf02443527
Autor:
Vicente Marchán, I. Travesset, Maite Beltrán, Jordi Robles, Enrique Pedroso, A. Grandas, G. Fábregas, Laurent Debéthune
Publikováno v:
Nucleosides and Nucleotides. 18:1493-1494
The preparation of nucleopeptides containing tryptophan and basic residues (lysine, arginine) is described. Different solid supports and the necessity of primary carboxamide protection have also been evaluated.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dd858a79884eefcbf9b74b40c28b57b
https://doi.org/10.1080/07328319908044765
https://doi.org/10.1080/07328319908044765
Publikováno v:
Nucleosides and Nucleotides. 16:1487-1488
Hydroxylated amino acids can be introduced in nucleopeptides using the acetyl group for their side chain protection. Base-stable nucleopeptide analogues are obtained if homoserine is used as the linking residue.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c281346f1654469557d181dc4dad3dfd
https://doi.org/10.1080/07328319708006212
https://doi.org/10.1080/07328319708006212