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Farmacología y terapéutica(7)
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3D-QSAR, synthesis, and antimicrobial activity of 1-alkylpyridinium compounds as potential agents to improve food safety
ArticleAbstract: Cetylpyridinium chloride (CPC), an alkylpyridinium compound has been recently approved by the US FooPalabras claves:3D-QSAR, Alkylpyridinium analogues, Cetylpyridinium chloride, CoMFA analysis, MIC activityAutores:Breen P.J., Castillo R., Cesar M. Compadre, Compadre R.L., Rodriguez-Morales S.Fuentes:scopusErratum: Corrigendum to ‘Synthesis of (2R,8′S,3′E)-δ-tocodienol, a tocoflexol family member designed to have a superior pharmacokinetic profile compared to δ-tocotrienol’ (Tetrahedron (2016) 72(27–28) (4001–4006))
OtherAbstract: The authors regret that the following statement was omitted from the Acknowledgements section of thePalabras claves:Autores:Boerma M., Cesar M. Compadre, Crooks P.A., Gujarathi S., Hauer-Jensen M., Liu X., Shao L., Zhang X., Zheng G., Zhou D.Fuentes:scopusMolecular modeling analysis of the inhibition of mitochondrial cytochrome bc1 complex activity by tocol derivatives
Conference ObjectAbstract: The biological functions of vitamin E related compounds have been of interest in biomedical researchPalabras claves:3D-QSAR, CoMFA, Mitochondrial Cytochrome bc1 Complex, Tocopherols, TocopherylquinonesAutores:Cesar M. Compadre, Hauer-Jensen M., Kumar K.S., Singh A.Fuentes:scopusMolecular dynamics guided design of tocoflexol: A new radioprotectant tocotrienol with enhanced bioavailability
ArticleAbstract: Preclinical Research There is a pressing need to develop safe and effective radioprotector/radiomitiPalabras claves:Bioavailability, countermeasures, molecular dynamics, radiation protection, tocoflexol, tocotrienolAutores:Boerma M., Breen P.J., Cesar M. Compadre, Ghosh S., Hauer-Jensen M., Kiaei M., Singh A., Thakkar S., Varughese K.I., Zheng G.Fuentes:scopusIsolation of 6-O-(p-coumaroyl)-catalpol from Tabebuia rosea
ArticleAbstract:Palabras claves:Autores:Cesar M. Compadre, Enriquez R.G., Jauregui J.F., Nathan P.J.Fuentes:scopusSeparation of electronic and hydrophobic effects for the papain hydrolysis of substituted N-benzoylglycine esters
ArticleAbstract: The role of hydrophobic and electronic effects on the kinetic constants kcat and Km for the papain hPalabras claves:Enzymic hydrolysis, Glycinate ester, N-Benzoylglycine ester, Papain, QSAR, SARAutores:Cesar M. Compadre, Hansch C., Klein T.E., Nelson Smith R., Petridou-Fischer J., Selassie C., Steinmetz W., Yang C., Yang G.Fuentes:scopusSesquiterpene lactones from Gynoxys verrucosa and their anti-MRSA activity
ArticleAbstract: Ethnopharmacological relevance: Because of its virulence and antibiotic resistance, Staphylococcus aPalabras claves:Dehydroleucodine, Gynoxys verrucosa, Leucodine, MRSA, STAPHYLOCOCCUS AUREUS, STAPHYLOCOCCUS EPIDERMIDISAutores:B. Berry, Berry B., Breen P.J., C. Compadre, C. Quave, Cesar M. Compadre, K. Varughese, M. Smeltzer, O. Malagon Aviles, Omar Malagòn, P. Breen, P. Ordóñez Vivanco, Paola E. Ordóñez, Quave C.L., Reynolds W.F., Smeltzer M., Varughese K.I., W. ReynoldsFuentes:googlerraaescopusSolution conformation of a pentapeptide by nmr and molecular modeling studies
ArticleAbstract: High resolution NMR studies and molecular modeling calculations were performed on a linear pentapeptPalabras claves:2D NMR, cis-trans isomerization, Hydrogen bond, molecular modeling, β-TurnAutores:Cesar M. Compadre, Ramaprasad S.Fuentes:scopusSynthesis, crystallography, and anti-leukemic activity of the amino adducts of dehydroleucodine
ArticleAbstract: Dehydroleucodine is a bioactive sesquiterpene lactone. Herein, four dehydroleucodine amino derivativPalabras claves:Amino adducts, Anti-leukemic activity, Dehydroleucodine, Sesquiterpene lactoneAutores:Burns D.C., Cesar M. Compadre, Enriquez R.G., Guzman M.L., Jones D.E., Mery D.E., Nemu S., Omar Malagòn, Paola E. Ordóñez, Reynolds W.F., Sharma K.K.Fuentes:googlescopusThe Intensely Sweet Sesquiterpene Hernandulcin: Isolation, Synthesis, Characterization, and Preliminary Safety Evaluation
ArticleAbstract: Details are provided of the isolation of an intensely sweet compound, hernandulcin, from Lippia dulcPalabras claves:Autores:Cesar M. Compadre, Hussain R., Kinghorn A.D., Lopez de Compadre R., Pezzuto J.M.Fuentes:scopus