Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/54568
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dc.contributor.authorRohane, Sachin H-
dc.contributor.authorChauhan, Ashlesha J-
dc.date.accessioned2020-06-22T09:59:10Z-
dc.date.available2020-06-22T09:59:10Z-
dc.date.issued2020-05-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/54568-
dc.description700-709en_US
dc.description.abstractMolecular docking of 1 to 51 compounds has been performed in Small-Molecule Drug Discovery Suite of Schrödinger. Fifty one compounds have been targeted on 2NSD and 2X22 involved in tuberculosis activity. Aryloxy moiety on refluxing with chloroethyl acetate in the presence of potassium carbonate and acetone has yielded ethyl aryloxy acetate (A), which have been reacted with hydrazine hydrate to produce aryloxyacetyl hydrazine (B), which on treatment with aromatic aldehydes or ketones yield hydrazones (C). The novel series of compounds have been elucidated on the basis of spectral studies and screened for antimycobacterial activity. The compounds are significantly sensitive at concentration 50 and 100 μg/mL. Compound 11 shows sensitivity at 25 μg/mL. The antibacterial activity is strongly connected with the position of the substituent on aromatic aldehyde or ketones in relation to the hydrazide skeleton.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.59B(05) [May 2020]en_US
dc.subjectHydrazoneen_US
dc.subjectMolecular dockingen_US
dc.subjectAntimycobacterial activityen_US
dc.titleAntimycobacterial potential of novel hydrazone derivativesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.59B(05) [May 2020]

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