M. K. Parai

发表

In vivo activity of thiophene-containing trisubstituted methanes against acute and persistent infection of non-tubercular Mycobacterium fortuitum in a murine infection model.

B. S. Srivastava, R. Shrivastava, G. Panda, 2012, The Journal of antimicrobial chemotherapy.

Effect of substituents on diarylmethanes for antitubercular activity.

Shagufta, A. Gaikwad, S. Das, 2007, European journal of medicinal chemistry.

Thiophene containing triarylmethanes as antitubercular agents.

G. Panda, V. Chaturvedi, S. Sinha, 2008, Bioorganic & medicinal chemistry letters.

A convenient synthesis of chiral amino acid derived 3,4-dihydro-2H-benzo[b][1,4]thiazines and antibiotic levofloxacin

G. Panda, M. K. Parai, 2009 .

An efficient synthesis of 6H,7H-chromeno[4,3-b]chromenes and 6,7-dihydrothio chromeno[3,2-c]chromenes as 9-substituted xanthene like analogs ☆

G. Panda, S. K. Manna, M. K. Parai, 2011 .

An unexpected reaction of phosphorous tribromide on chromanone, thiochromanone, 3,4-dihydro-2H-benzo[b]thiepin-5-one, 3,4-dihydro-2H-benzo[b]oxepin-5-one and tetralone derived allylic alcohols: a case study ☆

Shagufta, G. Panda, M. Kassack, 2008 .

Design, Synthesis and Antitubercular Activity of Compounds Containing Aryl and Heteroaryl Groups with Alkylaminoethyl Chains.

G. Panda, V. Chaturvedi, S. Sinha, 2009 .

Additional synthesis on thiophene-containing trisubstituted methanes (TRSMs) as inhibitors of M. tuberculosis and 3D-QSAR studies

P. Mishra, G. Panda, V. Chaturvedi, 2016, SAR and QSAR in environmental research.

A new strategy for the synthesis of aryl- and heteroaryl-substituted exocyclic olefins from allyl alcohols using PBr3

Shagufta, G. Panda, M. K. Parai, 2005 .

Application of Nazarov cyclization to access [6-5-6] and [6-5-5]tricyclic core embedded new heterocycles: an easy entry to structures related to taiwaniaquinoids.

G. Panda, Ritesh Singh, M. K. Parai, 2009, Organic & biomolecular chemistry.

Development of a Novel Lead that Targets M. tuberculosis Polyketide Synthase 13

Lisa K. Woolhiser, S. Norval, J. Sacchettini, 2017, Cell.

SAR and Lead Optimization of an HIV-1 Vif-APOBEC3G Axis Inhibitor.

T. Rana, M. Stevenson, N. Sharova, 2012, ACS medicinal chemistry letters.

Optimization of TAM16, a Benzofuran That Inhibits the Thioesterase Activity of Pks13; Evaluation toward a Preclinical Candidate for a Novel Antituberculosis Clinical Target

Robert H Bates, L. Stojanovski, K. Read, 2021, Journal of medicinal chemistry.

Design, synthesis, and biological and structural evaluations of novel HIV-1 protease inhibitors to combat drug resistance.

B. Tidor, C. Schiffer, T. Rana, 2012, Journal of medicinal chemistry.

Mycobacterium tuberculosis Malate Synthase Structures with Fragments Reveal a Portal for Substrate/Product Exchange*

J. Sacchettini, I. Krieger, Hsiao-Ling Huang, 2016, The Journal of Biological Chemistry.

Thiophene containing trisubstituted methanes [TRSMs] as identified lead against Mycobacterium tuberculosis.

P. Mishra, G. Panda, Priyanka Trivedi, 2015, European journal of medicinal chemistry.