Results 161 to 170 of about 14,086 (252)

Synthesis, in vitro, and in silico studies of 7-fluorochromone based thiosemicarbazones as α-glucosidase inhibitors. [PDF]

Sci Rep
Noreen F, Ullah S, Mali SN, Khan A, Hussain J, Alshammari A, Albekairi NA, Jawarkar RD, Yadav S, Al-Harrasi A, Shafiq Z.   +10 more
europepmc   +1 more source

Synthesis, in vitro biological evaluation and in silico studies of novel pyrrolidine derived thiosemicarbazones as dihydrofolate reductase inhibitors. [PDF]

RSC Adv
Aftab H, Ullah S, Khan A, Al-Rashida M, Islam T, Alshammari A, Albekairi NA, Taslimi P, Al-Harrasi A, Shafiq Z, Alghamdi S.   +10 more
europepmc   +1 more source

Rational design of phenyl 2,4,5-trichlorobenzenesulfonate based thiosemicarbazones as α-glucosidase and α-amylase inhibitors: integrating enzymatic evaluation and molecular modeling. [PDF]

RSC Adv
Noreen F, Zaki MEA, Sadeghian N, Tokali FS, Taslimi P, Alharthy RD, Şenol H, Zhao X, Çakır F, Gomha SM, Shafiq Z.   +10 more
europepmc   +1 more source

Design, Synthesis, In Vitro, and In Silico Studies of 5-(Diethylamino)-2-Formylphenyl Naphthalene-2-Sulfonate Based Thiosemicarbazones as Potent Anti-Alzheimer Agents. [PDF]

Arch Pharm (Weinheim)
Farooq U, Islam M, Batool Z, Mali SN, Jawarkar RD, Gurav SS, Alharthy RD, Şenol H, Sadeghian N, Taslimi P, Shafiq Z, Schenone S.   +11 more
europepmc   +1 more source

Novel Copper(II) Coordination Compounds Containing Pyridine Derivatives of N⁴-Methoxyphenyl-Thiosemicarbazones with Selective Anticancer Activity. [PDF]

Molecules
Rusnac R, Garbuz O, Kravtsov V, Melnic E, Istrati D, Tsapkov V, Poirier D, Gulea A.   +7 more
europepmc   +1 more source

Aminopeptidase N: a multifunctional and promising target in medicinal chemistry. [PDF]

RSC Adv
Farsa O, Uher T.
europepmc   +1 more source

Cannabidiol-Based Thiosemicarbazones: A Preliminary Study Evaluating Their Anti-Tyrosinase Properties. [PDF]

Molecules
Peretz E, Ashkenazi N, Musa S.
europepmc   +1 more source

Design, Synthesis, Structural Insights, Tyrosinase Inhibition, and Sun Protection Factor of New Thiosemicarbazone Derivatives. [PDF]

Molecules
Masuri S, Era B, Pintus F, Floris S, Meloni F, Pettinau F, Podda E, Cabiddu MG, Fais A, Pivetta T.   +9 more
europepmc   +1 more source

Design, synthesis, QSAR modelling and molecular dynamic simulations of N-tosyl-indole hybrid thiosemicarbazones as competitive tyrosinase inhibitors. [PDF]

Sci Rep
Batool Z, Ullah S, Khan A, Mali SN, Gurav SS, Jawarkar RD, Alshammari A, Albekairi NA, Al-Harrasi A, Shafiq Z.   +9 more
europepmc   +1 more source

Antifungal activity of thiosemicarbazones, bis(thiosemicarbazones), and their metal complexes

Journal of Inorganic Biochemistry, 2021
Fungi are ubiquitous in nature, and typically cause little or no environmental or pathogenic damage to their plant, animal, and human hosts. However, a small but growing number of pathogenic fungi are spreading world-wide at an alarming rate threatening global ecosystem health and proliferation.
Kritika, Bajaj, Robert M, Buchanan, Craig A, Grapperhaus   +2 more
openaire   +3 more sources