Synthesis of New Chiral (R)BINOL Derivatives under Microwave Irradiation andEvaluation of their Antibacterial and Glucosidase Inhibitory Activity.
Chemistry select, Google scholar, 2019, accepted, 00
Rational design, molecular docking and synthesis of novel homopiperazinelinked imidazo[1,2a]pyrimidine derivatives as potent cytotoxic andantimicrobial agents.
Bioorganic & Medicinal Chemistry Letters, Scopus, 2019, 0, 00
Synthesis, Characterization and Antibacterial Activity of Some NovelC7Substituted2morpholinoN(pyridin2ylmethyl)quinazolin4amine Derivatives.
Der Pharma Chemica, , Others, 2018, 10, 40-48
Design, Synthesis and Biological Evaluation of 2(((5aryl1,2,4oxadiazol3yl)methyl)thio)benzo[d]oxazolesNew Antiinflammatory and Antioxidant Agents.
Chemistry select, Scopus, 2018, 3, 1-7
Focused library design and synthesis of 2mercapto benzothiazolelinked 1,2,4oxadiazoles as COX25LOX inhibitors.
Journal of Molecular Structure , Scopus, 2018, 1159, 193-204
Synthesis and biological potentials of some new 1,3,4oxadiazoleanalogues.
Medicinal chemistry research , Scopus, 2018, 27, 864-883
Stabilityindicating method ofentacaponerelated substances usingUPLC in finished dosage form.
CURRENT SCIENCE, Scopus, 2018, 114, 644
Synthesis, Biological Evaluation and Docking Studies of 1,3,4OxadiazoleFused Benzothiazole Derivatives for Anticancer Drugs.
Letters in Drug Design & Discovery, Scopus, 2018, 15, 199-1307
An approach towards the oxidation of 2amino4Hchromenes to 2imino2Hchromenes.
Tetrahedron Letters , Scopus, 2018, 59, 4616-4619
Molecular hybrid design, synthesis and biological evaluation of Nphenyl sulfonamide linked Nacyl hydrazone derivatives functioning as COX2 inhibitors new antiinflammatory, antioxidant and antibacterial agents.
NEW JOURNAL OF CHEMISTRY, Scopus, 2017, 41, 13516-13532
New AntiInflammatory Hybrid NAcyl HydrazoneLinked Isoxazole Derivatives as COX2 InhibitorsRational Design, Synthesis and Biological Evaluation .
Chemistry selective, Scopus, 2017, 2, 8091-8100
A diversity oriented synthesis of natural product inspired molecular libraries.
Organic & Biomolecular Chemistry, Scopus, 2017, 15, 9108-9120
Synthesis, molecular docking and in vitroantiproliferative activity of novel pyrano[3,2c]carbazole derivatives.
New J. Chem.,, Scopus, 2016, 40, 8305--8315
DESIGNING NOVEL MEK1 INHIBITORS AS ANTICANCER AGENTS.
IJLP, Google scholar, 2016, 6, 22-33
Ionic liquidwater mixture promoted organictransformations.
RSC Adv., , 5, , Scopus, 2015, 5, 51035-51054
Design, synthesis, and biological evaluation of quinazolinederivatives as aglucosidase inhibitors.
Medicinal chemistry research , Scopus, 2015, 24, 2227-2237
Boronic acidcontaining CXCR12 antagonists optimization ofmetabolic stability, in vivo evaluation, and a proposed receptorbinding model.
BMCL, Web of science, 2015, 25, 2280-2284
Design, synthesis and screening studies of potent thiazol2amine derivatives as fibroblast growth factor receptor 1 inhibitors. .
Current Topics in Medicinal Chemistry, Web of science, 2014, 14, 2031-2041
Pyrrolidine and piperidine based chiral spiro andfused scaffolds via buildcouplepair approach. .
RSC Adv, Scopus, 2014, 14, 10619-10626
A reagent based DOS strategy via Evans chiral auxiliaryhighly stereoselective Michael reaction towardsoptically active quinolizidinones, piperidinones andpyrrolidinones3.
RSC Adv., Scopus, 2013, 3, 2404-2411
Diversity Oriented Synthesis of Macrocyclic Diaryl Ethers by DtzBenzannulation.
Asian J. Org. Chem, Web of science, 2013, 2, 862-868
Synthesis of Privileged Scaffolds by Using DiversityOriented Synthesis.
Chem. Asian J. 2013, 00, 0 0, Web of science, 2013, 0, 00
Fibroblast Growth Factor Receptor Inhibitors.
Current Pharmaceutical Design, Web of science, 2013, 19, 687-701
Development of glucosidase inhibitors by roomtemperature CC cross couplings of quinazolinones.
Org. Biomol. Chem, Scopus, 2013, 11, 4778-4791
ReagentBased DOS Developing a Diastereoselective Methodology toAccess Spirocyclic and Fused Heterocyclic Ring Systems**.
Chem. Asian J., Web of science, 2012, 7, 2351-2360
Molecular modeling of Bt Cry1Ac (DIDII)ASAL (Allium sativum lectin)fusionprotein and its interaction with aminopeptidase N (APN) receptor ofManduca sexta.
Journal of Molecular Graphics and Modelling , Scopus, 2012, 33, 61-67
Discovery and Preclinical Evaluation of a Novel Class of Cytotoxic Propynoic Acid Carbamoyl Methyl Amides (PACMAs).
J. Med. Chem., Scopus, 2011, 54, 2902-2914
Virtual screening studies on HIV1 reverse transcriptase inhibitorsto design potent leads.
European Journal of Medicinal Chemistry, Scopus, 2011, 46, 851-859
A wideranging review on Nasicon type materials.
J Mater Sci, Scopus, 2011, 46, 2821-2837
A threedimensional pharmacophoremodelling of ITK inhibitors and virtualscreening for novel inhibitors.
SAR and QSAR in Environmental Research, Scopus, 2011, 22, 171-190
Ligandbased and structurebased approaches in identifyingideal pharmacophore against cJun Nterminal kinase3.
J Mol Model, Scopus, 2011, 17, 151-163
Insilico studies on anthrax lethal factor inhibitors Pharmacophore modeling andvirtual screening approaches towards designing of novel inhibitors for a killer.
Journal of Molecular Graphics and Modelling , Scopus, 2010, 29 , 256-265
Three Dimensional Molecular Field Analysis of Thiomorpholine Analogs of TACE Inhibitors Using Receptor Based Alignment.
Letters in Drug Design & Discovery, Web of science, 2010, 7 , 269-274
Combined pharmacophore and structureguided studies to identify diverseHSP90 inhibitors.
Journal of Molecular Graphics and Modelling, Scopus, 2010, 28, 472-477
Modeling of human caspase5 protein and docking studies of caspase5 inhibitors against modeled caspase5.
Journal of Global Pharma Technology , Google scholar, 2010, 2, 1-5
Discovery of potential ZAP70 kinase inhibitors Pharmacophore design,database screening and docking studies.
European Journal of Medicinal Chemistry, Scopus, 2009, 44, 4793-4800
Knowledge basedidentification of MAOB selective inhibitors using pharmacophore and structure based virtual screening models.
European Journal of Medicinal Chemistry, Scopus, 2009, 44, 3584-3590
Discovery of Novel SmallMolecule Inhibitors of Human Epidermal Growth Factor Receptor2Combined Ligand and TargetBased Approach.
J. Med. Chem. , Scopus, 2008, 51, 3367-3377
Discovery of 3acetyl4hydroxy2pyranone derivatives and theirdifluoridoborate complexes as a novel class of HIV1 integrase Inhibitors.
Bioorganic & Medicinal Chemistry, Scopus, 2008, 16, 8988-8998
QSAR analysis of 1,3diaryl4,5,6,7tetrahydro2Hisoindolederivatives as selective COX2 inhibitors.
European Journal of Medicinal Chemistry , Scopus, 2008, 43, 1559-1569
Powder Xray diffraction, infrared and conductivity studiesof AgSbMP3O12 (M Al, Ga, Fe and Cr).
Materials Research Bulletin , Scopus, 2008, 43, 1509-1518
Pharmacophore modeling and virtual screening studies to designsome potential histone deacetylase inhibitors as new leads.
Journal of Molecular Graphics and Modelling , Scopus, 2008, 26, 935-946
HIV1 Integrase Inhibitors2005^2006 Update.
Medicinal Research Reviews, Scopus, 2008, 28, 118-154
Preparation, characterization and conductivity studiesof a Nasicon system Ag32xTaxAl2x (PO4)3.(a) 204, No. .
phys. stat. sol. , Web of science, 2007, 10, 3454-3462
Preparation, characterization, conductivity and thermalexpansion studies of Ca0.5SbMP3O12 (M Al, Fe, Cr).
J Mater Sci, Web of science, 2007, 42, 3613-3620
Pharmacophore mapping of diverse classesof farnesyltransferase inhibitors. .
Bioorganic & Medicinal Chemistry Letters, Scopus, 2007, 17, 1594-1600
Preparation, characterization, and impedance studies of Li Sb M ( P O 4 ) 3 ( M Al , Fe,and Cr) .
JOURNAL OF APPLIED PHYSICS, Web of science, 2006, 100, 083707
Ligand Coordinate Analysis of SC558 from the Active Site to the Surface of COX2 AMolecular Dynamics Study. .
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Synthesis, molecular docking, antiproliferative, and antimicrobialactivity of novel pyrano[3,2c]carbazole derivatives.
Med Chem Res, Scopus, 2006, 25, 2093-2103
A REVIEW ON ANTIHCV AGENTS TARGETING ACTIVE SITE AND ALLOSTERIC SITES OF NONSTRUCTURALPROTEIN 5B [NS5B].
International Journal of Pharmacy and Pharmaceutical Sciences, Google scholar, 2006, 8, 1-18
Preparation, characterization and impedance study of AgTaMP3O12(MAl, Ga, In, Cr, Fe and Y).
Solid State Ionics, Web of science, 2005, 176, 2701-2710
Virtual Screening of 4Anilinoquinazoline Analogues as EGFR Kinase InhibitorsImportance of Hydrogen Bonds in the Evaluation of Poses and Scoring Functions.
J. Chem. Inf. Model, Web of science, 2005, 45, 725-738
Design of EGFR Kinase Inhibitors A LigandBased Approachand Its Confirmation with StructureBased Studies.
Bioorganic & Medicinal Chemistry , Scopus, 2003, 11, 4643-4653
Analogue Based Design of MMP13 (Collagenase3) Inhibitors. .
Bioorganic & Medicinal Chemistry Letters, Scopus, 2002, 12, 2689-2693
Title of the project | NHeterocyclic CarbeneStabilized Silaallenes, Silacumulenes, Phosphaallenes and Phosphacumulenes. |
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Funded by | DST |
Duration | 36 months |
Sanctioned date | 26 October, 2017 |
Title of the project | Traditional and New Approaches Towards the Discovery of Dengue Protease Inhibitors Potent and Druglike Antiviral Agents against Dengue Fever |
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Funded by | SERB_DST |
Duration | 36 months |
Sanctioned date | 04 June, 2016 |
Title of the book | ComputerAided Techniques in Design of HIV1 Integrase Inhibitors |
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Book / Chapter | Chapters |
Name of the publisher | Wiley Series |
Subject area | Medicinal Chemistry |
Edition | 10 |
Page numbers | 389-413 |
ISBN | 9780470184745 |
Published year | 2011 |
Title | Pesticidal Compositions And Processes Related Thereto |
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Application number | US 9,615,576 B2 |
Category | US |
Submitted date | 17 February, 2017 |
Title | Pesticidal Compositions And Processes Related Thereto |
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Application number | US 20140206537A1 |
Category | US |
Submitted date | 25 March, 2014 |
Title | Pesticidal Compositions And Processes Related Thereto |
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Application number | US 9,615,576 B2 |
Category | US |
Submitted date | 21 June, 2012 |
Seminar name | Future India innovations in pharmaceutical Sciences |
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Organized by | Nalanda college of pharmacy, Nalgonda |
More info... |
Seminar name | Materials in Healthcare |
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Organized by | GITAM, Hyederabd |
More info... |
Seminar name | Big Data Applications in Drug Repurposing (BDADR 17) |
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Organized by | GITAM |
More info... |
Seminar name | CRSI National symposium in chemistry |
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Organized by | hyderabad |
More info... |
Seminar name | Innovations and developments in Emerging research in chemical sciences |
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Organized by | Tara Govt. College ,Sangareddy |
More info... |
Seminar name | Modern Trends in Drug Discovery and Development (MTDDD 16 |
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Organized by | GITAM |
More info... |
Seminar name | Advanced Techniques in Chemical Research |
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Organized by | SKSD mahila college, Tanuku |
More info... |
Seminar name | Old and Recent Trends in Chemical Science |
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Organized by | Tara Govt. College ,Sangareddy |
More info... |
Seminar name | international conference on molecular spectroscopy |
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Organized by | MGU, KOTTAYAM, KERALA |
More info... |
Seminar name | international conference on drug design |
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Organized by | jnu |
More info... |
Seminar name | centre for chemical sciences and technology |
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Organized by | jntuh |
More info... |
Seminar name | Recent Advances in computational Drug Design |
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Organized by | Schrodinger |
More info... |
Seminar name | Biotechnology in Pharma and Food Industries |
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Organized by | GITAM |
More info... |
Seminar name | World congress on biotechnology |
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Organized by | OMICS |
More info... |
Title of the thesis | DEVELOPMENT AND VALIDATION OF NOVEL STABILITY INDICATING METHODS FOR SELECTED DRUGS OF CANCER AND PARKINSON DISEASES USING RPHPLC AND UPLC TECHNIQUES |
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Name of the student | Naresh Konduru |
Name of the college / university | GITAM |
Major subject area | Analytical Chemistry |
Year of admission | 2018 |
Type of admission | Part time |
Thesis specification | PhD |
Title of the thesis | Rational Design, Synthesis of hetero cyclic compouds of anti cancer agents |
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Name of the student | Madhu Sudhana Reddy Gangireddy |
Name of the college / university | GITAM |
Major subject area | Medicinal Chemistry |
Year of admission | 2015 |
Type of admission | Part time |
Thesis specification | PhD |
Title of the thesis | Novel Design, Synthesis of hetero cyclic compouds of anti cancer agents |
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Name of the student | Manohar Mantipally |
Name of the college / university | GITAM |
Major subject area | Medicinal Chemistry |
Year of admission | 2015 |
Type of admission | Part time |
Thesis specification | PhD |
Title of the thesis | Design, Synthesis of hetero cyclic compouds of anti viral agents |
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Name of the student | Venkatnarayana chowdary Maddipati |
Name of the college / university | GITAM |
Major subject area | Medicinal Chemistry |
Year of admission | 2015 |
Type of admission | Part time |
Thesis specification | PhD |
Title of the thesis | Design, Synthesis of hetero cyclic compouds of anti cancer agents |
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Name of the student | Gopal Muddasani |
Name of the college / university | GITAM |
Major subject area | Medicinal Chemistry |
Year of admission | 2015 |
Type of admission | Part time |
Thesis specification | PhD |
Title of the thesis | Novel Design, Synthesis of hetero cyclic compouds of anti cancer agents |
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Name of the student | Kalisavali |
Name of the college / university | GITAM |
Major subject area | Medicinal Chemistry |
Year of admission | 2015 |
Type of admission | Part time |
Thesis specification | PhD |
Title of the thesis | Design, Synthesis of hetero cyclic compouds of anti viral agents |
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Name of the student | Sidvilas |
Name of the college / university | GITAM |
Major subject area | Medicinal Chemistry |
Year of admission | 2015 |
Type of admission | Part time |
Thesis specification | PhD |
Title of the thesis | Design, Synthesis of hetero cyclic compouds of anti cancer agents |
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Name of the student | Anil Kumar |
Name of the college / university | GITAM |
Major subject area | Medicinal Chemistry |
Year of admission | 2015 |
Type of admission | Part time |
Thesis specification | PhD |
Title of the thesis | Design, synthesis and insilco studies of BenzothiazoleBenzooxazole based hetrero cyclic agents as a COX2 inhibitors |
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Name of the student | Satyanarayan.Y |
Name of the college / university | GITAM |
Major subject area | Medicinal Chemistry |
Year of admission | 2014 |
Type of admission | Part time |
Thesis specification | PhD |
Title of the thesis | Identification, synthesis and biological evaluation of new Quinazoline and BINOL based Antidiabetic and Antibacterial agents |
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Name of the student | Ashok Reddy.A |
Name of the college / university | GITAM |
Major subject area | Medicinal Chemistry |
Year of admission | 2014 |
Type of admission | Part time |
Thesis specification | PhD |
Organization name | Indian Science Congress Association |
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Membership category | Life |
Membership type | Member |
Name of the award | Best Researcher |
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Awarded by | GITAM |
Awarded year | 2017 |
Name of the award | Best Employee |
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Awarded by | GVKBIO |
Awarded year | 2012 |
Board name | Wiley |
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Journal name | Chemistry Select |
Board name | Elsevier |
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Journal name | Journal Molecular Structure |