Lorca, M. Et Al. 2022. Design of benzimidazoles, benzoxazoles, benzothiazoles and thiazolopyridines as leukotriene A4 hydrolase inhibitors through 3D-QSAR, docking and molecular dynamics. JOURNAL OF THE SERBIAN CHEMICAL SOCIETY , vol.88, no.00 , 25-39.

Lorca, M., Faúndez, M., Pessoa-Mahana, D., Recabarren-Gajardo, G., Diethelm-Varela, B., Millán, D., ... Celik, İ.(2022). Design of benzimidazoles, benzoxazoles, benzothiazoles and thiazolopyridines as leukotriene A4 hydrolase inhibitors through 3D-QSAR, docking and molecular dynamics. JOURNAL OF THE SERBIAN CHEMICAL SOCIETY , vol.88, no.00, 25-39.

Lorca, Marcos Et Al. "Design of benzimidazoles, benzoxazoles, benzothiazoles and thiazolopyridines as leukotriene A4 hydrolase inhibitors through 3D-QSAR, docking and molecular dynamics," JOURNAL OF THE SERBIAN CHEMICAL SOCIETY , vol.88, no.00, 25-39, 2022

Lorca, Marcos Et Al. "Design of benzimidazoles, benzoxazoles, benzothiazoles and thiazolopyridines as leukotriene A4 hydrolase inhibitors through 3D-QSAR, docking and molecular dynamics." JOURNAL OF THE SERBIAN CHEMICAL SOCIETY , vol.88, no.00, pp.25-39, 2022

Lorca, M. Et Al. (2022) . "Design of benzimidazoles, benzoxazoles, benzothiazoles and thiazolopyridines as leukotriene A4 hydrolase inhibitors through 3D-QSAR, docking and molecular dynamics." JOURNAL OF THE SERBIAN CHEMICAL SOCIETY , vol.88, no.00, pp.25-39.

@article{article, author={Marcos Lorca Et Al. }, title={Design of benzimidazoles, benzoxazoles, benzothiazoles and thiazolopyridines as leukotriene A4 hydrolase inhibitors through 3D-QSAR, docking and molecular dynamics}, journal={JOURNAL OF THE SERBIAN CHEMICAL SOCIETY}, year=2022, pages={25-39} }