H. M. Vagdevi

573 total citations
33 papers, 483 citations indexed

About

H. M. Vagdevi is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, H. M. Vagdevi has authored 33 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Organic Chemistry, 4 papers in Molecular Biology and 3 papers in Toxicology. Recurrent topics in H. M. Vagdevi's work include Synthesis and biological activity (24 papers), Synthesis and Characterization of Heterocyclic Compounds (13 papers) and Synthesis and Biological Evaluation (11 papers). H. M. Vagdevi is often cited by papers focused on Synthesis and biological activity (24 papers), Synthesis and Characterization of Heterocyclic Compounds (13 papers) and Synthesis and Biological Evaluation (11 papers). H. M. Vagdevi collaborates with scholars based in India, Saudi Arabia and South Korea. H. M. Vagdevi's co-authors include V. P. Vaidya, Guru S. Gadaginamath, K.A. Vishnumurthy, Kodihalli C. Ravindra, H. Manjunatha, Basavaraj Padmashali, Sandeep Telkar, Bhadrapura Lakkappa Dhananjaya, Venkatrao H. Kulkarni and Momin Khan and has published in prestigious journals such as SHILAP Revista de lepidopterología, European Journal of Medicinal Chemistry and Journal of Molecular Structure.

In The Last Decade

H. M. Vagdevi

31 papers receiving 444 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
H. M. Vagdevi India 11 384 91 50 40 30 33 483
Neira Gamboa de Domı́nguez Venezuela 9 344 0.9× 141 1.5× 59 1.2× 54 1.4× 34 1.1× 13 492
Maurício Silva dos Santos Brazil 11 566 1.5× 89 1.0× 72 1.4× 40 1.0× 18 0.6× 29 705
S. Rajakumar India 7 269 0.7× 85 0.9× 55 1.1× 24 0.6× 40 1.3× 9 404
Sharad C. Karad India 10 583 1.5× 120 1.3× 65 1.3× 34 0.8× 28 0.9× 19 650
Gabriel Marc Romania 15 359 0.9× 175 1.9× 61 1.2× 51 1.3× 35 1.2× 49 556
Marcelo do Nascimento Gomes Brazil 9 342 0.9× 132 1.5× 72 1.4× 68 1.7× 21 0.7× 10 525
Jyotirmaya Sahoo India 10 303 0.8× 106 1.2× 40 0.8× 47 1.2× 17 0.6× 33 452
Nitin Kumar India 11 366 1.0× 128 1.4× 37 0.7× 26 0.7× 65 2.2× 19 492
Hülya Karaca Türkiye 11 565 1.5× 178 2.0× 78 1.6× 72 1.8× 33 1.1× 37 697
Viresh H. Shah India 14 607 1.6× 149 1.6× 31 0.6× 49 1.2× 51 1.7× 70 675

Countries citing papers authored by H. M. Vagdevi

Since Specialization
Citations

This map shows the geographic impact of H. M. Vagdevi's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by H. M. Vagdevi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H. M. Vagdevi more than expected).

Fields of papers citing papers by H. M. Vagdevi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H. M. Vagdevi. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by H. M. Vagdevi. The network helps show where H. M. Vagdevi may publish in the future.

Co-authorship network of co-authors of H. M. Vagdevi

This figure shows the co-authorship network connecting the top 25 collaborators of H. M. Vagdevi. A scholar is included among the top collaborators of H. M. Vagdevi based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with H. M. Vagdevi. H. M. Vagdevi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
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Vagdevi, H. M., et al.. (2023). Synthesis of Novel 3-methyl-1-(5-methyl-1,3-benzoxazol-2-yl)-1H-pyrazol-5-amine Derivatives and In-vitro Evaluation of their Antitumor and Antibacterial Activities. Journal of Pharmaceutical Research International. 35(13). 25–35. 1 indexed citations
4.
Vagdevi, H. M., et al.. (2022). Design, Synthesis, Computational Docking and Biological Evaluation of Novel 4-Chloro-1,3-Benzoxazole Derivatives as Anticancer Agents. Biosciences Biotechnology Research Asia. 19(4). 895–915. 2 indexed citations
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Vagdevi, H. M., et al.. (2020). An efficient synthesis of 2-(6-methoxy-2-napthyl)-1,3-benzoxazole derivatives using IBD/LTA: Reactivity, DFT, Anticancer and Larvicidal activities. Asian Journal of Research in Chemistry. 13(5). 312–318. 1 indexed citations
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Vagdevi, H. M., et al.. (2015). In vitro antioxidant and antitubercular activity of Leucas marrubioides Desf. root extracts. Journal of Applied Pharmaceutical Science. 137–142. 4 indexed citations
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Vagdevi, H. M., et al.. (2012). Synthesis, Characterization and evaluation of Antibacterial Activity of some 3-Substitutedphenylquinazoline -2,4-diones. Der pharma chemica. 4(4). 1754–1758. 4 indexed citations
10.
Vagdevi, H. M., et al.. (2012). Synthesis, characterization and antimicrobial activity of 7-methoxyquinoline-4- substituted 1, 2, 3-triazole derivatives. Der pharma chemica. 4(1). 272–281. 2 indexed citations
11.
Vagdevi, H. M., et al.. (2012). In vitro antimicrobial and molecular docking of dichloro substituted benzoxazole derivatives. Medicinal Chemistry Research. 21(12). 4193–4199. 9 indexed citations
12.
Vishnumurthy, K.A., et al.. (2011). Synthesis, in vitro antioxidant, anthelmintic and molecular docking studies of novel dichloro substituted benzoxazole-triazolo-thione derivatives. European Journal of Medicinal Chemistry. 46(7). 3078–3084. 67 indexed citations
13.
Vagdevi, H. M., et al.. (2010). Synthesis and Antibacterial Activity of Novel Organoselenium Compounds. International Journal of Chemistry. 2(2). 13 indexed citations
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Ravindra, Kodihalli C., H. M. Vagdevi, & V. P. Vaidya. (2008). Synthesis, characterization and pharmacological studies on some triazolothiadiazines and triazolothiadiazoles containing naphtho[2,b]furan. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 47(8). 1271–1276. 4 indexed citations
15.
Vagdevi, H. M., et al.. (2008). Evaluation of antimicrobial and analgesic activities of Aporosa lindleyana (euphorbiaceae) bark extract. International Journal of Green Pharmacy. 2(3). 155. 8 indexed citations
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Ravindra, Kodihalli C., H. M. Vagdevi, V. P. Vaidya, & Basavaraj Padmashali. (2007). Synthesis, Antimicrobial and Antiinflammatory Activities of 1,3,4‐Oxadiazoles Linked to Naphtho[2,1‐b]furan.. ChemInform. 38(8). 12 indexed citations
18.
Ravindra, Kodihalli C., H. M. Vagdevi, V. P. Vaidya, & Basavaraj Padmashali. (2006). Synthesis, antimicrobial and antiinflammatory activities of 1,3,4-oxadiazoles linked to naphtho[2,1- b ]furan. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 45(11). 2506–2511. 12 indexed citations
19.
Vaidya, V. P., et al.. (2004). Synthesis of naphtho[2,1-b]furo[3,2-e]-1,4-diazepin-2-ones and naphtho[2,1- b]furo[3,2-e]-1,3,4-triazepin-2-ones of pharmacological interest. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 43(7). 1537–1543. 3 indexed citations
20.
Mahadevan, K. M., V. P. Vaidya, & H. M. Vagdevi. (2003). Synthesis of novel naphtho(2, I-b )furopyrimidine deri vati yes. Indian Journal of Chemistry Section B-organic Chemistry Including Medicinal Chemistry. 42(8). 1931–1936. 4 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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