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Antimo Gioiello

Showing results (51-60 of 88) with videos related to

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Medchemcomm|November 2, 2019
Dissecting the allosteric FXR modulation: a chemical biology approach using guggulsterone as a chemical toolDaniela Passeri, Andrea Carotti, Jose M Ramos Pittol, et al.
Free Radical Biology & Medicine|April 23, 2019
LC-MS/MS assay for the simultaneous determination of tocopherols, polyunsaturated fatty acids and their metabolites in human plasma and serumDanilo Giusepponi, Roberta Galarini, Carolina Barola, et al.
Chemmedchem|October 2, 2015
Concepts and Molecular Aspects in the Polypharmacology of PARP-1 InhibitorsDaniela Passeri, Emidio Camaioni, Paride Liscio, et al.
Journal of Chromatography. A|July 26, 2020
Integrating experimental and computational techniques to study chromatographic enantioresolutions of chiral tetrahydroindazole derivativesFederica Ianni, Bruno Cerra, Shiva Tali Shandiz, et al.
Journal of Medicinal Chemistry|August 20, 2004
Bile acid derivatives as ligands of the farnesoid X receptor. Synthesis, evaluation, and structure-activity relationship of a series of body and side chain modified analogues of chenodeoxycholic acidRoberto Pellicciari, Gabriele Costantino, Emidio Camaioni, et al.
Journal of Chemical Information and Modeling|August 14, 2008
Molecular field analysis and 3D-quantitative structure-activity relationship study (MFA 3D-QSAR) unveil novel features of bile acid recognition at TGR5Antonio Macchiarulo, Antimo Gioiello, Charles Thomas, et al.
Chemmedchem|October 21, 2020
The Stone Guest: How Does pH Affect Binding Properties of PD-1/PD-L1 Inhibitors?Alessandra Riccio, Alice Coletti, Daniela Dolciami, et al.
ACS Chemical Biology|August 30, 2016
Bile Acid Recognition by NAPE-PLDEleonora Margheritis, Beatrice Castellani, Paola Magotti, et al.
Journal of Medicinal Chemistry|July 11, 2006
Back door modulation of the farnesoid X receptor: design, synthesis, and biological evaluation of a series of side chain modified chenodeoxycholic acid derivativesRoberto Pellicciari, Antimo Gioiello, Gabriele Costantino, et al.
Journal of Medicinal Chemistry|February 28, 2024
Discovery and Structure-Activity Relationships of Novel <i>ss</i>DAF-12 Receptor ModulatorsGiada Ceccarelli, Laura Goracci, Andrea Carotti, et al.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
Medchemcomm|November 2, 2019
Dissecting the allosteric FXR modulation: a chemical biology approach using guggulsterone as a chemical toolDaniela Passeri, Andrea Carotti, Jose M Ramos Pittol, et al.
Free Radical Biology & Medicine|April 23, 2019
LC-MS/MS assay for the simultaneous determination of tocopherols, polyunsaturated fatty acids and their metabolites in human plasma and serumDanilo Giusepponi, Roberta Galarini, Carolina Barola, et al.
Chemmedchem|October 2, 2015
Concepts and Molecular Aspects in the Polypharmacology of PARP-1 InhibitorsDaniela Passeri, Emidio Camaioni, Paride Liscio, et al.
Journal of Chromatography. A|July 26, 2020
Integrating experimental and computational techniques to study chromatographic enantioresolutions of chiral tetrahydroindazole derivativesFederica Ianni, Bruno Cerra, Shiva Tali Shandiz, et al.
Journal of Medicinal Chemistry|August 20, 2004
Bile acid derivatives as ligands of the farnesoid X receptor. Synthesis, evaluation, and structure-activity relationship of a series of body and side chain modified analogues of chenodeoxycholic acidRoberto Pellicciari, Gabriele Costantino, Emidio Camaioni, et al.
Journal of Chemical Information and Modeling|August 14, 2008
Molecular field analysis and 3D-quantitative structure-activity relationship study (MFA 3D-QSAR) unveil novel features of bile acid recognition at TGR5Antonio Macchiarulo, Antimo Gioiello, Charles Thomas, et al.
Chemmedchem|October 21, 2020
The Stone Guest: How Does pH Affect Binding Properties of PD-1/PD-L1 Inhibitors?Alessandra Riccio, Alice Coletti, Daniela Dolciami, et al.
ACS Chemical Biology|August 30, 2016
Bile Acid Recognition by NAPE-PLDEleonora Margheritis, Beatrice Castellani, Paola Magotti, et al.
Journal of Medicinal Chemistry|July 11, 2006
Back door modulation of the farnesoid X receptor: design, synthesis, and biological evaluation of a series of side chain modified chenodeoxycholic acid derivativesRoberto Pellicciari, Antimo Gioiello, Gabriele Costantino, et al.
Journal of Medicinal Chemistry|February 28, 2024
Discovery and Structure-Activity Relationships of Novel <i>ss</i>DAF-12 Receptor ModulatorsGiada Ceccarelli, Laura Goracci, Andrea Carotti, et al.
Pageof 9