Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Alberto A. Ghini"'
Publikováno v:
Eclética Química, Vol 36, Iss 2, Pp 128-141 (2018)
Humic substances (HS) were isolated from the sediments of Lobos Pond (Argentina) using mild conditions to preserve their native structure. The HS (humic and fulvic acids) were characterized by means of elemental analysis and FTIR spectroscopy. Also a
Externí odkaz:
https://doaj.org/article/d131deefe2e140d18503206615162efd
Publikováno v:
ARKIVOC, Vol 2005, Iss 12, Pp 154-162 (2005)
Externí odkaz:
https://doaj.org/article/948d484b6a074d86bd850d47c009e797
Publikováno v:
ARKIVOC, Vol 2003, Iss 10, Pp 468-476 (2003)
Externí odkaz:
https://doaj.org/article/117489a375454d1d877c2f58c5382355
Publikováno v:
Eclética Química, Vol 36, Iss 2, Pp 128-141 (2018)
Eclética Química v.36 n.2 2011
Eclética Química
Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP)
instacron:UNESP
SEDICI (UNLP)
Universidad Nacional de La Plata
instacron:UNLP
Eclética Química v.36 n.2 2011
Eclética Química
Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP)
instacron:UNESP
SEDICI (UNLP)
Universidad Nacional de La Plata
instacron:UNLP
Humic substances (HS) were isolated from the sediments of Lobos Pond (Argentina) using mild conditions to preserve their native structure. The HS (humic and fulvic acids) were characterized by means of elemental analysis and FTIR spectroscopy. Also a
Autor:
Maria Sol Kruse, Mariana Rey, Adriana S. Veleiro, Gerardo Burton, Alberto A. Ghini, Héctor Coirini
Publikováno v:
Neuroscience. 290:138-146
Neuroactive steroids (NAS), like allopregnanolone (A) and pregnanolone (P), bind to specifics sites on the GABAA receptor complex and modulate receptor function. They are capable to inhibit or stimulate the binding of GABAA receptor specific ligands,
Synthesis and activity evaluation of a series of cholanamides as modulators of the liver X receptors
Autor:
Mario David Martinez, Lautaro D. Alvarez, Adriana S. Veleiro, Adali Pecci, M. Virginia Dansey, Gerardo Burton, Alberto A. Ghini
Publikováno v:
Bioorganicmedicinal chemistry. 26(5)
The Liver X receptors (LXRs) are members of the nuclear receptor family, that play fundamental roles in cholesterol transport, lipid metabolism and modulation of inflammatory responses. In recent years, the synthetic steroid N,N-dimethyl-3β-hydroxyc
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Neurosteroids like 3α-OH-5α-pregnan-20-one (allopregnanolone) and 3α-OH-5β-pregnan-20-one (pregnanolone) modulate the γ-aminobutyric acid-A (GABAA) receptor function and produce several effects that can be considered for therapeutical pruposes l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ae1ee807930f0028c0cb51275c022cf
https://www.omicsonline.org/open-access/synthetic-epoxypregnan-steroids-effects-on-anxiety-behavior-in-rats-2157-7536-1000167.php?aid=68053
https://www.omicsonline.org/open-access/synthetic-epoxypregnan-steroids-effects-on-anxiety-behavior-in-rats-2157-7536-1000167.php?aid=68053
Publikováno v:
Eclética Química, Vol 36, Iss 2, Pp 128-141 (2011)
Humic substances (HS) were isolated from the sediments of Lobos Pond (Argentina) using mild conditions to preserve their native structure. The HS (humic and fulvic acids) were characterized by means of elemental analysis and FTIR spectroscopy. Also a
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Lipase-catalyzed transesterification of the 20 hydroxyl group in a series of pregnanes afforded novel 20-ethyl succinates that are not possible to prepare following the traditional synthetic methods. The reaction is stereoselective. The enzyme reacts
Publikováno v:
Tetrahedron. 62:4762-4768
A procedure is described for the preparation of 6-thiapregnanes in five steps from pregnenolone via a 5-oxo-7-iodo-secopregnane intermediate. The 6-thiasteroid obtained was converted into 6-thia-allopregnanolone and its sulfoxide and sulfone derivati