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Haridas B. Rode

Observed names: H B Rode, H Rode, H. B. Rode, H. RODE, H.B. Rode, Haridas B Rode, Haridas Rode, Rode, H.B., Rode, Haridas B, Rode, Haridas B.
Observed institutions: Broad Institute, Jikei University School of Medicine, Brigham and Women's Hospital, Max Planck Society, University of Cape Town, University of Cologne, University of the Witwatersrand, Universität Greifswald, Dana-Farber Cancer Institute, Max Planck Institute of Molecular Physiology, Chemical Genomics Centre, Indian Institute of Chemical Technology, Council of Scientific and Industrial Research, Academy of Scientific and Innovative Research
ORCID: 0000-0003-3958-1802
Observed ORCID: 0000-0003-3958-1802
OpenAlex ID: A5022988094
Chemogenomic Profiling Provides Insights into the Limited Activity of Irreversible EGFR Inhibitors in Tumor Cells Expressing the T790M EGFR Resistance Mutation
2010 · Martin L. Sos, Haridas B. Rode, et al. · Cancer Research · 220
Structure-guided development of affinity probes for tyrosine kinases using chemical genetics
2007 · Jimmy A Blair, Daniel Rauh, et al. · Nature Chemical Biology · 203
Hybrid Compound Design To Overcome the Gatekeeper T338M Mutation in cSrc
2009 · Matthäus Getlik, Christian Grütter, et al. · Journal of Medicinal Chemistry · 146
A new screening assay for allosteric inhibitors of cSrc
2009 · Jeffrey R Simard, Sabine Klüter, et al. · Nature Chemical Biology · 129
Structural insights into how irreversible inhibitors can overcome drug resistance in EGFR
2008 · Anja Michalczyk, Sabine Klüter, et al. · Bioorganic & Medicinal Chemistry · 91
Synthesis and Biological Evaluation of 4-Anilinoquinolines as Potent Inhibitors of Epidermal Growth Factor Receptor
2010 · Vijaykumar G. Pawar, Martin L. Sos, et al. · Journal of Medicinal Chemistry · 61
Synthesis and biological evaluation of 2,4,5-trisubstituted thiazoles as antituberculosis agents effective against drug-resistant tuberculosis
2019 · Uttam B. Karale, Vagolu Siva Krishna, et al. · European Journal of Medicinal Chemistry · 46
Characterization of Irreversible Kinase Inhibitors by Directly Detecting Covalent Bond Formation: A Tool for Dissecting Kinase Drug Resistance
2010 · Sabine Klüter, Jeffrey R. Simard, et al. · ChemBioChem · 46
Novel 1,3,4-oxadiazoles As Antitubercular Agents With Limited Activity Against drug-resistant Tuberculosis
2019 · Vitthal B Makane, Vagolu Siva Krishna, et al. · Future Medicinal Chemistry · 43
Synthesis and evaluation of α-aminoacyl amides as antitubercular agents effective on drug resistant tuberculosis
2019 · Vitthal B. Makane, Vagolu Siva Krishna, et al. · European Journal of Medicinal Chemistry · 33
On water direct arylation of imidazo[1,2- a ]pyridines with aryl halides
2017 · Saradhi Kalari, Dattatraya A. Babar, et al. · Tetrahedron Letters · 31
Strategies towards the synthesis of anti-tuberculosis drugs
2019 · Haridas B. Rode, Dhanaji M. Lade, et al. · Organic & Biomolecular Chemistry · 29
Crosslinked enzyme aggregates (CLEA) of phytase with soymilk proteins
2018 · Harini Tirunagari, Shalini Basetty, et al. · Journal of Biotechnology · 28
A Chemical Genetic Approach for Covalent Inhibition of Analogue-Sensitive Aurora Kinase
2012 · André Koch, Haridas B. Rode, et al. · ACS Chemical Biology · 27
Difluorinative-hydroxylation and C-3 functionalization (halogenation/SCN/NO) of imidazopyridine using Selectfluor as fluorine source or oxidant respectively
2021 · Saradhi Kalari, Sridhar Balasubramanian, et al. · Tetrahedron Letters · 26
Selectfluor-Mediated Synthesis of β-Acyl Allyl Sulfones/β-Acyl Allyl Benzotriazoles from Ketones/Acetylenes, Aryl Sulfinates/Benzotriazole, and DMSO as a Dual-Carbon Synthon
2022 · Saradhi Kalari, Uttam B. Karale, et al. · The Journal of Organic Chemistry · 25
Analysis of Compound Synergy in High-Throughput Cellular Screens by Population-Based Lifetime Modeling
2010 · Martin Peifer, Jonathan Weiss, et al. · PLoS ONE · 24
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Identification of New Molecular Entities (NMEs) as Potential Leads against Tuberculosis from Open Source Compound Repository
2015 · Sudha Sravanti Kotapalli, Sri Satya Anila Nallam, et al. · PLoS ONE · 22
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Methylene-Tethered Arylsulfonation and Benzotriazolation of Aryl/Heteroaryl C–H Bonds with DMSO as a One-Carbon Surrogate
2021 · Saradhi Kalari, Akash U. Shinde, et al. · The Journal of Organic Chemistry · 21
Cobalt‐Catalyzed Direct Arylation of Imidazo[1,2‐a]pyridine with Aryl Iodides
2020 · Dattatraya A. Babar, Haridas B. Rode · European Journal of Organic Chemistry · 18
A sustainable approach for nickel nanoparticles synthesis: expeditious access to N-heterocycles under heterogeneous condition and photophysical studies
2023 · Thrilokraj R., Rajeev V. Hegde, et al. · New Journal of Chemistry · 17
Ligand-free Pd-catalysed decarboxylative arylation of imidazo[1,2-a]pyridine-3-carboxylic acids with aryl bromides
2016 · Uttam B. Karale, Saradhi Kalari, et al. · RSC Advances · 17
3‐Aryl‐substituted imidazo[1,2‐a]pyridines as antituberculosis agents
2021 · Uttam B. Karale, Akash U. Shinde, et al. · Archiv der Pharmazie · 15
Synthesis of novel 4,5‐dihydropyrrolo[1,2‐ a ]quinoxalines, pyrrolo[1,2‐ a ]quinoxalin]‐2‐ones and their antituberculosis and anticancer activity
2020 · Vitthal B. Makane, Eruva Vamshi Krishna, et al. · Archiv der Pharmazie · 15
Catalyst- and Additive-Free Approach to Constructing Benzo-oxazine, Benzo-oxazepine, and Benzo-oxazocine: O Atom Transfer and C═O, C–N, and C–O Bond Formation at Room Temperature
2021 · Arnab Ghosh, Rajeev V. Hegde, et al. · Organic Letters · 14
Works count: 93
Citation count: 1,516
H-index: 19
I10-index: 32
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