Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Mahmud Tareq Hassan Khan"'
Autor:
Samaneh Zolghadri, Asieh Bahrami, Mahmud Tareq Hassan Khan, J. Munoz-Munoz, F. Garcia-Molina, F. Garcia-Canovas, Ali Akbar Saboury
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 279-309 (2019)
Tyrosinase is a multi-copper enzyme which is widely distributed in different organisms and plays an important role in the melanogenesis and enzymatic browning. Therefore, its inhibitors can be attractive in cosmetics and medicinal industries as depig
Externí odkaz:
https://doaj.org/article/d47c752989394920b8eb4a45d1b52433
Autor:
Giordana Feriotto, Federico Tagliati, Riccardo Giriolo, Fabio Casciano, Claudio Tabolacci, Simone Beninati, Mahmud Tareq Hassan Khan, Carlo Mischiati
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 4, p 1644 (2021)
Among the phenolic acids tested on the K562 cell line, a model of chronic myeloid leukemia (CML), caffeic acid (CA) was biologically active on sensitive and imatinib (IM)-resistant cells at micro-molar concentration, either in terms of reduction of c
Externí odkaz:
https://doaj.org/article/2d800605f2144989b860d987df8e8e38
Autor:
Mahmud Tareq Hassan Khan, Ali Akbar Saboury, Asieh Bahrami, Jose Munoz-Munoz, Francisco Garcia-Molina, Francisco García-Cánovas, Samaneh Zolghadri
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 34, Iss 1, Pp 279-309 (2019)
Journal of Enzyme Inhibition and Medicinal Chemistry
Journal of Enzyme Inhibition and Medicinal Chemistry
Tyrosinase is a multi-copper enzyme which is widely distributed in different organisms and plays an important role in the melanogenesis and enzymatic browning. Therefore, its inhibitors can be attractive in cosmetics and medicinal industries as depig
Autor:
Mahmud Tareq Hassan Khan, Claudio Tabolacci, Carlo Mischiati, Giordana Feriotto, Simone Beninati, Federico Tagliati, Fabio Casciano, Riccardo Giriolo
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 1644, p 1644 (2021)
Volume 22
Issue 4
International Journal of Molecular Sciences, Vol 22, Iss 1644, p 1644 (2021)
Volume 22
Issue 4
Among the phenolic acids tested on the K562 cell line, a model of chronic myeloid leukemia (CML), caffeic acid (CA) was biologically active on sensitive and imatinib (IM)-resistant cells at micro-molar concentration, either in terms of reduction of c
Publikováno v:
Journal of Molecular Graphics and Modelling. 54:54-61
Butyrylcholinesterase (BChE) exists mainly at neuromuscular junctions and plays an important role in the hydrolyzing mechanism of neurotransmitter acetylcholine. A variety of compounds have been produced in order to inhibit the function of BChE. We h
Publikováno v:
Current Bioactive Compounds. 10:31-36
Publikováno v:
Current Topics in Medicinal Chemistry. 14:1486-1493
Tyrosinase (EC 1.14.18.1), also known as polyphenols oxidase, is a glycosylated multi-copper monooxygenase enzyme widely distributed in many different organisms. The enzyme is responsible for the pigmentation of skin, eyes and hair in mammals and in
Autor:
Mahmud Tareq Hassan Khan, Yovani Marrero-Ponce, Antonio Rescigno, Huong Le-Thi-Thu, Juan A. Castillo-Garit, Concepción Abad, Gerardo M. Casañola-Martin, Francisco Torrens
Publikováno v:
Scopus-Elsevier
CIÊNCIAVITAE
CIÊNCIAVITAE
The tyrosinase enzyme (EC 1.14.18.1) is an oxidoreductase inside the general enzyme classification and is involved in the oxidation and reduction process in the epidermis. These chemical reactions that the enzyme catalyzes are of principal importance
Autor:
Mahmud Tareq Hassan Khan
Publikováno v:
Current Bioinformatics. 8:416-428
Autor:
Mahmud Tareq Hassan Khan, Kundapura Umesha, Veerakyathappa Bhanuprakash, R. Raghavendra, Chenna Govindaraju Darshan Raj, Balladka Kunhanna Sarojini, R. Yogisharadhya
Publikováno v:
Medicinal Chemistry Research. 23:168-180
In the present study, we report the synthesis, characterization of new series of thiazolo[3,2-a]pyrimidine-6-carboxylate derivatives 3a–f and 4a–f. The newly synthesized compounds were screened for in vitro antimicrobial and antiviral activities.