Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Esther Alonso Becerra"'
Autor:
Iraida Spengler Salabarria, Zaida Trimiño Ayllón, Esther Alonso Becerra, Carlos Iglesias Pérez, Aristides Rosado Pérez
Publikováno v:
Revista CENIC Ciencias Químicas, Vol 32, Iss 2, Pp 061-064 (2001)
Muchas especies de plantas de la familia Amaryllidaceae son usadas en la medicina popular contra diferentes enfermedades, principalmente como citotóxicas, entre ellas se destaca el uso de varias especies de Zephyrantes en diferentes regiones del mun
Externí odkaz:
https://doaj.org/article/004b8f58b8954eb389f4dcbe6b7820b7
Autor:
Cercis Morera-Boado, Luis A. Montero-Cabrera, R. H. González-Jonte, Esther Alonso-Becerra, José Manuel García-de-la-Vega
Publikováno v:
Journal of Molecular Graphics and Modelling. 27:600-610
The interaction of three different brassinosteroids with water was studied by the Multiple Minima Hypersurface (MMH) procedure to model molecular interactions explicitly. The resulting thermodynamic data give useful information on properties of molec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d9f7c89305ad0331935f7dab094f37
https://doi.org/10.1016/j.jmgm.2008.09.013
https://doi.org/10.1016/j.jmgm.2008.09.013
Autor:
Yamilet Bernardo, Carlos Pérez, Ernesto Suárez, Esther Alonso-Becerra, Mitcheell Maestre, Reynier Suardíaz
Publikováno v:
The Journal of Physical Chemistry A. 112:8333-8336
The determination of the stereochemistry of brasinosteroid analogs with 22,23-epoxide groups can be easily achieved by means of 13C NMR spectroscopy. Here, we provide a rationalization of the 13C chemical shift pattern found in 22R,23R- and 22S,23S-e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2bb3e98099110d9881840df7a911b68
https://doi.org/10.1021/jp804570g
https://doi.org/10.1021/jp804570g
Publikováno v:
Journal of Molecular Structure: THEOCHEM. 819:109-120
Calculations on the molecular structure of three natural brassinosteroids using several semiempirical Hamiltonians: MNDO, AM1, PM3, PDDG/MNDO, PDDG/PM3 have been done to test their accuracy for predicting structural features of these molecules when c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edffe47e16ca47c918997480750d5cc9
https://doi.org/10.1016/j.theochem.2007.05.034
https://doi.org/10.1016/j.theochem.2007.05.034
Autor:
Carlos S. Perez-Martinez, Francisco Guerra-Martínez, Francisco Coll-Manchado, Yamilé Bernardo-Otero, Esther Alonso-Becerra, Guillermo Martínez-Massanet
Publikováno v:
Journal of Chemical Research. 2007:268-271
plant growth regulators, brassinosteroids, epoxide, steroids, stigmasterolBrassinosteroids (BS) are recognised as a new class of steroidal plant hormones that control many physiological and developmental processes. Extensive studies have been directe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58f6c1648abb8cb411bf6e7cd053fbb8
https://doi.org/10.3184/030823407x210884
https://doi.org/10.3184/030823407x210884
Autor:
Roberto Santana, Rachel Crespo, José Alberto Ruiz-García, Eladio Pardillo-Fontdevila, Yovani Marrero Ponce, Yoanna María Alvarez-Ginarte, Luis A. Montero-Cabrera, Esther Alonso-Becerra
Publikováno v:
QSAR & Combinatorial Science. 24:218-226
Predictive Quantitative Structure-Activity Relationship (QSAR) models of anabolic and androgenic activities for the 17b-hydroxy-5a-androstane steroid family were obtained by means of multi-linear regression using quantum and physicochemical molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed6e783dd76264bf8b61e2579508e1da
https://doi.org/10.1002/qsar.200430889
https://doi.org/10.1002/qsar.200430889
Autor:
R. H. González-Jonte, Cercis Morera-Boado, Luis A. Montero-Cabrera, Esther Alonso-Becerra, Nelaine Mora-Diez, José M. García de la Vega
Publikováno v:
Journal of molecular graphicsmodelling. 28(7)
The interaction of the most active natural brassinosteroid, brassinolide, with the twenty natural amino acids is studied applying the multiple minima hypersurface method to model the molecular interactions explicitly. The resulting thermodynamic data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b20cb112ea43285261a713102f96bb22
https://pubmed.ncbi.nlm.nih.gov/20106686
https://pubmed.ncbi.nlm.nih.gov/20106686
Autor:
Manuel Alonso-Tarajano, Juan Alexander Padrón-García, Yasser Ruiz, Colin Berry, Tim J. Winterburn, John Kay, Esther Alonso-Becerra
Publikováno v:
Proteins. 75(4)
The IA3 polypeptide inhibitor from Saccharomyces cerevisiae interacts potently and selectively with its target, the S. cerevisiae vacuolar aspartic proteinase (ScPr). Upon encountering the enzyme, residues 2–32 of the intrinsically unstructured IA3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0087960d8c8b9a8b22698d03a47e99a
https://pubmed.ncbi.nlm.nih.gov/19003993
https://pubmed.ncbi.nlm.nih.gov/19003993
Autor:
Reynier Suardíaz, Mitcheell Maestre, Ernesto Suárez, Yamilet Bernardo, Esther Alonso-Becerra, Carlos Pérez
Publikováno v:
Journal of Physical Chemistry A; Aug2008, Vol. 112 Issue 36, p8333-8336, 4p