Comparative Metabolomic Analysis and Antinociceptive Effect of Methanolic Extracts from Salvia cinnabarina , Salvia lavanduloides and Salvia longispicata.

Autor: Ortiz-Mendoza, Nancy^1,2 (AUTHOR) nancy_om@ciencias.unam.mx, Monribot-Villanueva, Juan L.³ (AUTHOR) juan.monribot@inecol.mx, Guerrero-Analco, José A.³ (AUTHOR) joseantonio.guerrero@inecol.mx, Martínez-Gordillo, Martha J.⁴ (AUTHOR) mjmg@ciencias.unam.mx, Basurto-Peña, Francisco A.⁵ (AUTHOR) abasurto@ib.unam.mx, Aguirre-Hernandez, Eva¹ (AUTHOR) joseantonio.guerrero@inecol.mx, Soto-Hernández, Marcos⁶ (AUTHOR) msoto@colpos.mx

Publikováno v: Molecules. Nov2024, Vol. 29 Issue 22, p5465. 18p.

Antimicrobial Peptides From Different Sources: Isolation, Purification, and Characterization to Potential Applications.

Autor: Ahmed SAH; College of Pharmaceutical Sciences, Hangzhou Institute of Innovative Medicine & Institute of Drug Metabolism and Pharmaceutical Analysis, Zhejiang University, Hangzhou, China., Saif B; Key Laboratory of Applied Surface and Colloid Chemistry, School of Chemistry and Chemical Engineering, Ministry of Education, Shaanxi Normal University, Xi'an, China.; Chemistry Department, Faculty of Science, Ibb University, Ibb, Yemen., Qian L; College of Pharmaceutical Sciences, Hangzhou Institute of Innovative Medicine & Institute of Drug Metabolism and Pharmaceutical Analysis, Zhejiang University, Hangzhou, China.

Publikováno v: Journal of separation science [J Sep Sci] 2024 Dec; Vol. 47 (23), pp. e70043.

The discovery of new potent non-peptide Angiotensin II AT1 receptor blockers:A concise synthesis, molecular docking studies and biological evaluation of N-substituted 5-butylimidazole derivatives

Autor: G. Agelis, A. Resvani, S. Durdagi, K. Spyridaki , T.Tumová,J. Slaninová, P. Giannopoulos, D. Vlahakos, G. Liapakis,T.Mavromoustakos

A convenient and facile synthesis, in silico docking studies and in vitro biological evaluation of N-substituted 5-butylimidazole derivatives as potent Angiotensin II (ANG II) receptor type 1 (AT1) blockers (ARBs) has been reported in the current stu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2127::d845412b1ba15e1660e466fa06ba3f77
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2956946

Influence of 1-aminocyclohexane-1-carboxylic acid in position 2 or 3 of AVP and its analogues on their pharmacological properties

Autor: B, Jastrzebska, I, Derdowska, W, Kowalczyk, A, Machova, J, Slaninová, B, Lammek

Publikováno v: The journal of peptide research : official journal of the American Peptide Society. 62(2)

In this study we describe the synthesis and some pharmacological properties of seven new analogues of arginine vasopressin (AVP) substituted in position 2 or 3 with 1-aminocyclohexane-1-carboxylic acid (Acc). All peptides were tested for the pressor,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::62e89a04c2a6f645bd97599533cb080b
https://pubmed.ncbi.nlm.nih.gov/12823619

Magnesium and biological activity of oxytocin analogues modified on aromatic ring of amino acid in position 2

Autor: J, Slaninová, L, Maletínská, J, Vondrásek, Z, Procházka

Publikováno v: Journal of peptide science : an official publication of the European Peptide Society. 7(8)

For the purpose of evaluating substitution effects in the ortho, meta or para positions of the aromatic ring of tyrosine or phenylalanine in position 2 of oxytocin on uterotonic activity in vitro in the presence and absence of magnesium ions, six new

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::60b687ab4a61e66b8f90a68b6cca6719
https://pubmed.ncbi.nlm.nih.gov/11548057