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Scopus Author ID: 23090957600

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Works (34)

Rational design, molecular docking and synthesis of novel homopiperazine linked imidazo[1,2-a]pyrimidine derivatives as potent cytotoxic and antimicrobial agents

Bioorganic and Medicinal Chemistry Letters
2019 | Journal article
DOI: 10.1016/j.bmcl.2019.06.031
EID:

2-s2.0-85067566195
Contributors: Mantipally, M.; Gangireddy, M.R.; Gundla, R.; Badavath, V.N.; Mandha, S.R.; Maddipati, V.C.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Synthesis of New Chiral (R)-BINOL Derivatives under Microwave Irradiation and Evaluation of Their Antibacterial and α-Glucosidase Inhibitory Activity

ChemistrySelect
2019 | Journal article
DOI: 10.1002/slct.201803937
EID:

2-s2.0-85066291911
Contributors: Ankireddy, A.R.; Paidikondala, K.; Gundla, R.; Balaraju, T.; Pagadala, R.; Banothu, V.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

An approach towards the oxidation of 2-amino-4H-chromenes to 2-imino-2H-chromenes

Tetrahedron Letters
2018 | Journal article
DOI: 10.1016/j.tetlet.2018.11.046
EID:

2-s2.0-85056831901
Contributors: Mantipally, M.; Gundla, R.; Gangireddy, M.R.; Vijayan, V.; Devadasan, V.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Design, Synthesis and Biological Evaluation of 2 (((5-aryl-1,2,4-oxadiazol-3-yl)methyl)thio)benzo[d]oxazoles: New Antiinflammatory and Antioxidant Agents

ChemistrySelect
2018 | Journal article
DOI: 10.1002/slct.201801558
EID:

2-s2.0-85054584795
Contributors: Yatam, S.; Jadav, S.S.; Gundla, R.; Gundla, K.P.; Reddy, G.M.; Ahsan, M.J.; Chimakurthy, J.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Focused library design and synthesis of 2-mercapto benzothiazole linked 1,2,4-oxadiazoles as COX-2/5-LOX inhibitors

Journal of Molecular Structure
2018 | Journal article
DOI: 10.1016/j.molstruc.2018.01.060
EID:

2-s2.0-85041455344
Contributors: Yatam, S.; Gundla, R.; Jadav, S.S.; Pedavenkatagari, N.R.; Chimakurthy, J.; Rani B, N.; Kedam, T.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Stability-indicating method of entacapone-related substances using UPLC in finished dosage form

Current Science
2018 | Journal article
DOI: 10.18520/cs/v114/i03/644-649
EID:

2-s2.0-85041528530
Contributors: Konduru, N.; Gundla, R.; Katari, N.K.; Madhuri, G.V.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Synthesis and biological potentials of some new 1,3,4-oxadiazole analogues

Medicinal Chemistry Research
2018 | Journal article
DOI: 10.1007/s00044-017-2109-1
EID:

2-s2.0-85034222776
Contributors: Jawed Ahsan, M.; Meena, R.; Dubey, S.; Khan, V.; Manda, S.; Singh Jadav, S.; Sharma, P.; Geesi, M.H.; Hassan, M.Z.; Afroz Bakht, M. et al.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Synthesis, biological evaluation and docking studies of 1,3,4-oxadiazole fused benzothiazole derivatives for anticancer drugs

Letters in Drug Design and Discovery
2018 | Journal article
DOI: 10.2174/1570180815666180219165119
EID:

2-s2.0-85054882903
Contributors: Subramanyam, M.; Sreenivasulu, R.; Gundla, R.; Rao, M.V.B.; Rao, K.P.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

A diversity oriented synthesis of natural product inspired molecular libraries

Organic and Biomolecular Chemistry
2017 | Journal article
DOI: 10.1039/c7ob02230a
EID:

2-s2.0-85033406207
Contributors: Chauhan, J.; Luthra, T.; Gundla, R.; Ferraro, A.; Holzgrabe, U.; Sen, S.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Molecular hybrid design, synthesis and biological evaluation of N-phenyl sulfonamide linked N-acyl hydrazone derivatives functioning as COX-2 inhibitors: New anti-inflammatory, anti-oxidant and anti-bacterial agents

New Journal of Chemistry
2017 | Journal article
DOI: 10.1039/c7nj03332j
EID:

2-s2.0-85034624415
Contributors: Gorantla, V.; Gundla, R.; Jadav, S.S.; Anugu, S.R.; Chimakurthy, J.; Nidasanametla, S.K.; Korupolu, R.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

New Anti-Inflammatory Hybrid N-Acyl Hydrazone-Linked Isoxazole Derivatives as COX-2 Inhibitors:Rational Design, Synthesis and Biological Evaluation

ChemistrySelect
2017 | Journal article
DOI: 10.1002/slct.201701421
EID:

2-s2.0-85038096454
Contributors: Gorantla, V.; Gundla, R.; Jadav, S.S.; Anugu, S.R.; Chimakurthy, J.; Rao ns, K.; Korupolu, R.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

A review on anti-HCV agents targeting active site and allosteric sites of nonstructural protein 5B [NS5B]

International Journal of Pharmacy and Pharmaceutical Sciences
2016 | Journal article
DOI: 10.22159/ijpps.2016v8i11.13965
EID:

2-s2.0-84994888091
Contributors: Polamreddy, P.; Vishwakarma, V.; Gundla, R.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Boronic acid-containing CXCR1/2 antagonists: Optimization of metabolic stability, in vivo evaluation, and a proposed receptor binding model

Bioorganic and Medicinal Chemistry Letters
2015 | Journal article
DOI: 10.1016/j.bmcl.2015.04.041
EID:

2-s2.0-84937762524
Contributors: Maeda, D.Y.; Peck, A.M.; Schuler, A.D.; Quinn, M.T.; Kirpotina, L.N.; Wicomb, W.N.; Auten, R.L.; Gundla, R.; Zebala, J.A.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Design, synthesis, and biological evaluation of quinazoline derivatives as α-glucosidase inhibitors

Medicinal Chemistry Research
2015 | Journal article
DOI: 10.1007/s00044-014-1293-5
EID:

2-s2.0-84939993456
Contributors: Gurram, V.; Garlapati, R.; Thulluri, C.; Madala, N.; Kasani, K.S.; Machiraju, P.K.; Doddapalla, R.; Addepally, U.; Gundla, R.; Patro, B. et al.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Erratum: Synthesis of privileged scaffolds by using diversity-oriented synthesis (Chemistry - An Asian Journal (2013) 8 DOI: 10.1002/asia.201201203)

Chemistry - An Asian Journal
2014 | Journal article
DOI: 10.1002/asia.201402552
EID:

2-s2.0-84903218403
Contributors: Surakanti, R.; Sanivarapu, S.; Thulluri, C.; Iyer, P.S.; Tangirala, R.S.; Gundla, R.; Addepally, U.; Murthy, Y.L.N.; Velide, L.; Sen, S.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Pyrrolidine and piperidine based chiral spiro and fused scaffolds via build/couple/pair approach

RSC Advances
2014 | Journal article
DOI: 10.1039/c3ra47714b
EID:

2-s2.0-84894473831
Contributors: Mamidala, R.; Babu Damerla, V.S.; Gundla, R.; Chary, M.T.; Murthy, Y.L.N.; Sen, S.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

A reagent based DOS strategy via Evans chiral auxiliary: Highly stereoselective Michael reaction towards optically active quinolizidinones, piperidinones and pyrrolidinones

RSC Advances
2013 | Journal article
DOI: 10.1039/c2ra22115b
EID:

2-s2.0-84872698221
Contributors: Sen, S.; Kamma, S.R.; Gundla, R.; Adepally, U.; Kuncha, S.; Thirnathi, S.; Prasad, U.V.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Development of α-glucosidase inhibitors by room temperature C-C cross couplings of quinazolinones

Organic and Biomolecular Chemistry
2013 | Journal article
DOI: 10.1039/c3ob40636a
EID:

2-s2.0-84880096750
Contributors: Garlapati, R.; Pottabathini, N.; Gurram, V.; Kasani, K.S.; Gundla, R.; Thulluri, C.; MacHiraju, P.K.; Chaudhary, A.B.; Addepally, U.; Dayam, R. et al.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Diversity Oriented Synthesis of Macrocyclic Diaryl Ethers by Dötz Benzannulation

Asian Journal of Organic Chemistry
2013 | Journal article
DOI: 10.1002/ajoc.201300125
EID:

2-s2.0-84899835385
Contributors: Sen, S.; Mamidala, R.; Gundla, R.; Charya, M.T.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Fibroblast growth factor receptor inhibitors

Current Pharmaceutical Design
2013 | Journal article
EID:

2-s2.0-84876698366
Contributors: Suneel Kumar, B.V.S.; Narasu, L.; Gundla, R.; Dayam, R.; Sarma, J.A.R.P.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Synthesis of privileged scaffolds by using diversity-oriented synthesis

Chemistry - An Asian Journal
2013 | Journal article
DOI: 10.1002/asia.201201203
EID:

2-s2.0-84878318244
Contributors: Surakanti, R.; Sanivarapu, S.; Thulluri, C.; Iyer, P.S.; Tangirala, R.S.; Gundla, R.; Addepally, U.; Murthy, Y.L.N.; Velide, L.; Sen, S.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Molecular modeling of Bt Cry1Ac (DI-DII)-ASAL (Allium sativum lectin)-fusion protein and its interaction with aminopeptidase N (APN) receptor of Manduca sexta

Journal of Molecular Graphics and Modelling
2012 | Journal article
DOI: 10.1016/j.jmgm.2011.11.001
EID:

2-s2.0-84855215423
Contributors: Tajne, S.; Sanam, R.; Gundla, R.; Gandhi, N.S.; Mancera, R.L.; Boddupally, D.; Vudem, D.R.; Khareedu, V.R.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Reagent-based DOS: Developing a diastereoselective methodology to access spirocyclic- and fused heterocyclic ring systems

Chemistry - An Asian Journal
2012 | Journal article
DOI: 10.1002/asia.201200385
EID:

2-s2.0-84866371648
Contributors: Damerla, V.S.B.; Tulluri, C.; Gundla, R.; Naviri, L.; Adepally, U.; Iyer, P.S.; Murthy, Y.L.N.; Prabhakar, N.; Sen, S.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Computer-Aided Techniques in Design of HIV-1 Integrase Inhibitors

HIV-1 Integrase: Mechanism and Inhibitor Design
2011 | Book chapter
Part of DOI: 10.1002/9781118015377.ch26
EID:

2-s2.0-84873093524
Contributors: Serrao, E.; Gundla, R.; Deng, J.; Odde, S.; Neamati, N.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Discovery and preclinical evaluation of a novel class of cytotoxic propynoic acid carbamoyl methyl amides (PACMAs)

Journal of Medicinal Chemistry
2011 | Journal article
DOI: 10.1021/jm101655d
EID:

2-s2.0-79955409571
Contributors: Yamada, R.; Cao, X.; Butkevich, A.N.; Millard, M.; Odde, S.; Mordwinkin, N.; Gundla, R.; Zandi, E.; Louie, S.G.; Petasis, N.A. et al.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Ligand-based and structure-based approaches in identifying ideal pharmacophore against c-Jun N-terminal kinase-3

Journal of Molecular Modeling
2011 | Journal article
DOI: 10.1007/s00894-010-0701-0
EID:

2-s2.0-78651438310
Contributors: Kumar, B.V.S.S.; Kotla, R.; Buddiga, R.; Roy, J.; Singh, S.S.; Gundla, R.; Ravikumar, M.; Sarma, J.A.R.P.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Virtual screening studies on HIV-1 reverse transcriptase inhibitors to design potent leads

European Journal of Medicinal Chemistry
2011 | Journal article
DOI: 10.1016/j.ejmech.2010.12.022
EID:

2-s2.0-79951682045
Contributors: Vadivelan, S.; Deeksha, T.N.; Arun, S.; MacHiraju, P.K.; Gundla, R.; Sinha, B.N.; Jagarlapudi, S.A.R.P.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Combined pharmacophore and structure-guided studies to identify diverse HSP90 inhibitors

Journal of Molecular Graphics and Modelling
2010 | Journal article
DOI: 10.1016/j.jmgm.2009.11.002
EID:

2-s2.0-75049084371
Contributors: Sanam, R.; Tajne, S.; Gundla, R.; Vadivelan, S.; Machiraju, P.K.; Dayam, R.; Narasu, L.; Jagarlapudi, S.; Neamati, N.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Insilico studies on anthrax lethal factor inhibitors: Pharmacophore modeling and virtual screening approaches towards designing of novel inhibitors for a killer

Journal of Molecular Graphics and Modelling
2010 | Journal article
DOI: 10.1016/j.jmgm.2010.07.002
EID:

2-s2.0-77956270965
Contributors: Roy, J.; Kumar, U.C.; Machiraju, P.K.; Muttineni, R.K.; Suneel Kumar, S.B.V.S.; Gundla, R.; Dayam, R.; Sarma, J.A.R.P.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Three dimensional molecular field analysis of thiomorpholine analogs of TACE inhibitors using receptor based alignment

Letters in Drug Design and Discovery
2010 | Journal article
DOI: 10.2174/157018010790945779
EID:

2-s2.0-77949696765
Contributors: Bahia, M.S.; Bagga, N.; Gundla, R.; Silakari, O.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Corrigendum to "Discovery of 3-acetyl-4-hydroxy-2-pyranone derivatives and their difluoridoborate complexes as a novel class of HIV-1 integrase inhibitors" [Bioorg. Med. Chem. 16 (2008) 8988-8998] (DOI:10.1016/j.bmc.2008.08.067)

Bioorganic and Medicinal Chemistry
2009 | Journal article
DOI: 10.1016/j.bmc.2008.08.082
EID:

2-s2.0-58549117849
Contributors: Ramkumar, K.; Tambov, K.V.; Gundla, R.; Manaev, A.V.; Yarovenko, V.; Traven, V.F.; Neamati, N.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Discovery of 3-acetyl-4-hydroxy-2-pyranone derivatives and their difluoridoborate complexes as a novel class of HIV-1 integrase Inhibitors

Bioorganic and Medicinal Chemistry
2008 | Journal article
DOI: 10.1016/j.bmc.2008.08.067
EID:

2-s2.0-52949115265
Contributors: Ramkumar, K.; Tambov, K.V.; Gundla, R.; Manaev, A.V.; Yarovenko, V.; Traven, V.F.; Neamati, N.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

Discovery of novel small-molecule inhibitors of human epidermal growth factor receptor-2: Combined ligand and target-based approach

Journal of Medicinal Chemistry
2008 | Journal article
DOI: 10.1021/jm7013875
EID:

2-s2.0-45749146280
Contributors: Gundla, R.; Kazemi, R.; Sanam, R.; Muttineni, R.; Sarma, J.A.R.P.; Dayam, R.; Neamati, N.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier

HIV-1 integrase inhibitors: 2005-2006 Update

Medicinal Research Reviews
2008 | Journal article
DOI: 10.1002/med.20116
EID:

2-s2.0-37249086122
Contributors: Dayam, R.; Gundla, R.; Al-Mawsawi, L.Q.; Neamati, N.
Source: Self-asserted source
Rambabu Gundla via Scopus - Elsevier
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