Antimicrobial drugs bearing guanidine moieties: A review
SH Kim, D Semenya, D Castagnolo - European Journal of Medicinal …, 2021 - Elsevier
Compounds incorporating guanidine moieties constitute a versatile class of biologically
interesting molecules with a wide array of applications. As such, guanidines have been …
interesting molecules with a wide array of applications. As such, guanidines have been …
Heterocyclic compounds as a magic bullet for diabetes mellitus: a review
Diabetes mellitus (DM) is a major metabolic disorder due to hyperglycemia, which is
increasing all over the world. From the last two decades, the use of synthetic agents has …
increasing all over the world. From the last two decades, the use of synthetic agents has …
Aminopyrimidines: Recent synthetic procedures and anticancer activities
E Venturini Filho, EMC Pinheiro, S Pinheiro, SJ Greco - Tetrahedron, 2021 - Elsevier
The pyrimidine scaffold represents one of the privileged structures in chemistry, and there
has been an increase in number of studies utilizing this scaffold and its derivatives. The …
has been an increase in number of studies utilizing this scaffold and its derivatives. The …
Novel 2-amino-4-aryl-6-pyridopyrimidines and N-alkyl derivatives: Synthesis, characterization and investigation of anticancer, antibacterial activities and DNA/BSA …
A series of new 2-amino-4-aryl-6-pyridopyrimidines, and their N-alkyl bromide derivatives
were designed and synthesized by employing methyl substituted azachalcones. These …
were designed and synthesized by employing methyl substituted azachalcones. These …
Synthesis of novel spirooxindolo-pyrrolidines, pyrrolizidines, and pyrrolothiazoles via a regioselective three-component [3+ 2] cycloaddition and their preliminary …
G Wu, L Ouyang, J Liu, S Zeng, W Huang, B Han… - Molecular …, 2013 - Springer
A series of spirooxindolo-pyrrolidines, pyrrolizidines, and pyrrolothiazoles hybrid
compounds were prepared in good yields by regioselective, three-component, 1, 3-dipolar …
compounds were prepared in good yields by regioselective, three-component, 1, 3-dipolar …
Synthesis, in vitro biological activities and in silico study of dihydropyrimidines derivatives
A Barakat, MS Islam, AM Al-Majid, HA Ghabbour… - Bioorganic & Medicinal …, 2015 - Elsevier
We describe here the synthesis of dihydropyrimidines derivatives 3a–p, and evaluation of
their α-glucosidase enzyme inhibition activities. Compounds 3b (IC 50= 62.4±1.5 μM), 3c (IC …
their α-glucosidase enzyme inhibition activities. Compounds 3b (IC 50= 62.4±1.5 μM), 3c (IC …
Synthesis and evaluation of small libraries of triazolylmethoxy chalcones, flavanones and 2-aminopyrimidines as inhibitors of mycobacterial FAS-II and PknG
A synthetic strategy to access small libraries of triazolylmethoxy chalcones 4 {1–20},
triazolylmethoxy flavanones 5 {1–10} and triazolylmethoxy aminopyrimidines 6 {1–17} from …
triazolylmethoxy flavanones 5 {1–10} and triazolylmethoxy aminopyrimidines 6 {1–17} from …
Novel synthesis of dihydropyrimidines for α-glucosidase inhibition to treat type 2 diabetes: In vitro biological evaluation and in silico docking
A convenient and efficient new method has been established for the synthesis of
dihydropyrimidines by inexpensive and non-toxic N-acetyl glycine (NAG) catalysed reaction …
dihydropyrimidines by inexpensive and non-toxic N-acetyl glycine (NAG) catalysed reaction …
Nonclassical antifolates, part 5. Benzodiazepine analogs as a new class of DHFR inhibitors: Synthesis, antitumor testing and molecular modeling study
A new series of tetrahydro-quinazoline and tetrahydro-1H-dibenzo [b, e][1, 4] diazepine
analogs were synthesized and tested for their DHFR inhibition and in vitro antitumor activity …
analogs were synthesized and tested for their DHFR inhibition and in vitro antitumor activity …
In Silico Molecular Docking and In Vitro Antidiabetic Studies of Dihydropyrimido[4,5‐a]acridin‐2‐amines
An in vitro antidiabetic activity on α‐amylase and α–glucosidase activity of novel 10‐chloro‐
4‐(2‐chlorophenyl)‐12‐phenyl‐5, 6‐dihydropyrimido [4, 5‐a] acridin‐2‐amines (3a–3f) …
4‐(2‐chlorophenyl)‐12‐phenyl‐5, 6‐dihydropyrimido [4, 5‐a] acridin‐2‐amines (3a–3f) …