Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:6.2.1.1 (
ACS
)
78,556
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
A new class of benzothiazole-appended quinoline derivatives (
6
-
8
) was synthesized via one-pot TPGS micellar-mediated acid-catalyzed nucleophilic addition, followed by aerobic oxidative cyclization of 3-formylquinoline-2-one (
2
), 3-formylquinoline-2-thione (
3
), and 2-azidoquinoline-3-carbaldehyde (
4
) individually with 2-amino thiophenol (
5
). The structures of the prepared compounds were confirmed using suitable spectroscopic methods complemented with single-crystal X-ray diffraction analysis. Time-dependent density functional theory-based optimization of molecular structures, bond lengths, bond angles, HOMO-LUMO energy gaps, and molecular electrostatic potential maps was theoretically computed at the B3LYP/6-311++g(d) level. The molecular docking studies recommended that
6
-
8
bound to the active site cavity of CD81 effectively with the binding energies of -6.9, -6.3, and -6.5 kcal mol
-1
, respectively. Further, MD simulation studies of compound
6
suggested that the binding resulted in the stabilization of the
CD81 molecule
. Thus, all theoretical predictions associated with the experimental verifications motivated to discover novel approaches for cancer therapy.
ACS
Omega 2020 Jul 28
PMID:Green Synthesis, Experimental and Theoretical Studies to Discover Novel Binders of Exosomal Tetraspanin CD81 Protein. 3274 70