scispace - formally typeset
D

Devadasan Velmurugan

Researcher at University of Madras

Publications -  550
Citations -  3409

Devadasan Velmurugan is an academic researcher from University of Madras. The author has contributed to research in topics: Ring (chemistry) & Dihedral angle. The author has an hindex of 24, co-authored 544 publications receiving 2893 citations. Previous affiliations of Devadasan Velmurugan include SRM University & Bharathiar University.

Papers
More filters
Journal ArticleDOI

Bis(S-benzyl­isothio­uronium) tetra­chloridozincate(II)

TL;DR: The asymmetric unit of the title compound, (C8H11N2S)2[ZnCl4], contains two S-benzylisothio-uronium cations which differ in the C-C-S-C torsion angle [165.3
Posted ContentDOI

In silico and in vitro screening of FDA-approved drugs for potential repurposing against tuberculosis

TL;DR: The results suggest that lymecycline and cefpodoxime have potential to be repurposed for the treatment of tuberculosis.
Journal ArticleDOI

3-(4-Bromo­phen­yl)quinazolin-4(3H)-one

TL;DR: In the title compound, C14H9BrN2O, the quinazoline unit is essentially planar, with a mean deviation of 0.058 (2) Å from the least-squares plane defined by the ten constituent ring atoms.
Journal ArticleDOI

Methyl 11-hy­droxy-9-[1-(4-meth­oxy­phen­yl)-4-oxo-3-phen­oxy­azetidin-2-yl]-18-oxo-10-oxa-2-aza­penta­cyclo­[9.7.0.01,8.02,6.012,17]octa­deca-12(17),13,15-triene-8-carboxyl­ate

TL;DR: In the title compound, C34H32N2O8, one of the pyrrolidine rings in the p Pyrrolizidine ring system adopts a twist conformation, whereas the other ring adopts an envelope conformation (C atom as flap).
Journal ArticleDOI

4'-Amino-2,2''-dioxo-2,2'',3,3''-tetra-hydro-1H-indole-3-spiro-1'-cyclo-pent-3'-ene-2'-spiro-3''-1H-indole-3',5',5'-tricarbonitrile dihydrate.

TL;DR: In the title compound, C22H12N6O2·2H2O, the cyclopentene ring adopts an envelope conformation, with the spiro C atom bonded to the dicyano-substituted C atom deviating by 0.437 (2) Å from the plane of the remaining four atoms in the ring.