S. Kabilan

2.6k total citations
124 papers, 2.2k citations indexed

About

S. Kabilan is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, S. Kabilan has authored 124 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Organic Chemistry, 31 papers in Molecular Biology and 23 papers in Inorganic Chemistry. Recurrent topics in S. Kabilan's work include Synthesis and biological activity (66 papers), Crystal structures of chemical compounds (22 papers) and Synthesis and Characterization of Heterocyclic Compounds (19 papers). S. Kabilan is often cited by papers focused on Synthesis and biological activity (66 papers), Crystal structures of chemical compounds (22 papers) and Synthesis and Characterization of Heterocyclic Compounds (19 papers). S. Kabilan collaborates with scholars based in India, South Korea and United States. S. Kabilan's co-authors include G. Aridoss, P. Parthiban, Shankar Balasubramanian, R. Ramachandran, Chennan Ramalingan, R. Elancheran, Yeon Tae Jeong, Jibon Kotoky, Venkatachalam Ramkumar and Meena Ramanathan and has published in prestigious journals such as Angewandte Chemie International Edition, SHILAP Revista de lepidopterología and The Journal of Organic Chemistry.

In The Last Decade

S. Kabilan

120 papers receiving 2.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
S. Kabilan India	28	1.6k	470	290	277	242	124	2.2k
Qing‐Shan Li China	27	1.3k 0.9×	401 0.9×	350 1.2×	335 1.2×	167 0.7×	103	2.1k
Amir Azam India	31	1.5k 1.0×	454 1.0×	442 1.5×	539 1.9×	238 1.0×	62	2.3k
Assem Barakat Saudi Arabia	33	3.1k 2.0×	777 1.7×	377 1.3×	648 2.3×	248 1.0×	313	4.1k
Sham M. Sondhi India	26	2.0k 1.3×	794 1.7×	143 0.5×	319 1.2×	143 0.6×	101	2.6k
Ali A. El‐Emam Saudi Arabia	31	2.8k 1.8×	490 1.0×	462 1.6×	291 1.1×	269 1.1×	262	3.7k
Abdullah Mohammed Al‐Majid Saudi Arabia	27	1.9k 1.2×	471 1.0×	165 0.6×	276 1.0×	114 0.5×	154	2.4k
Xiaoyan Ma China	28	1.1k 0.7×	551 1.2×	240 0.8×	391 1.4×	390 1.6×	99	2.3k
Koray Sayın Türkiye	29	886 0.6×	289 0.6×	154 0.5×	377 1.4×	697 2.9×	121	1.9k
Vivek K. Gupta India	30	2.3k 1.5×	484 1.0×	542 1.9×	564 2.0×	477 2.0×	321	3.4k
Braulio Insuasty Colombia	39	4.0k 2.5×	790 1.7×	177 0.6×	120 0.4×	367 1.5×	258	4.7k

Countries citing papers authored by S. Kabilan

Since Specialization

Citations

This map shows the geographic impact of S. Kabilan'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 S. Kabilan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Kabilan more than expected).

Fields of papers citing papers by S. Kabilan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. Kabilan. 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 S. Kabilan. The network helps show where S. Kabilan may publish in the future.

Co-authorship network of co-authors of S. Kabilan

This figure shows the co-authorship network connecting the top 25 collaborators of S. Kabilan. A scholar is included among the top collaborators of S. Kabilan 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 S. Kabilan. S. Kabilan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Elancheran, R., et al.. (2024). Single crystal XRD analysis, Molecular docking, DFT studies, Hirshfeld analysis, antioxidant and anticancer activities of three natural carboxylic acids identified in Carica papaya leaves. Journal of Molecular Structure. 1318. 139131–139131. 2 indexed citations

Elancheran, R., et al.. (2022). Screening of 1,3,4-Thiadiazole Derivatives by in silico Molecular Docking to Target Estrogen Receptor for Breast Cancer. Biointerface Research in Applied Chemistry. 13(2). 160–160. 7 indexed citations

Kabilan, S., et al.. (2019). Polyherbal Formulation as Potent Nutraceutical: Antioxidant and Antibacterial Activity. International Journal of Engineering and Advanced Technology. 9(1s4). 803–806. 2 indexed citations

Elancheran, R., et al.. (2018). In silico Molecular Modelling of Selected Natural Ligands and their Binding Features with Estrogen Receptor Alpha. Current Computer - Aided Drug Design. 15(1). 89–96. 28 indexed citations

Elancheran, R., et al.. (2018). Pleiotropic Effect of Mahanine and Girinimbine Analogs: Anticancer Mechanism and its Therapeutic Versatility. Anti-Cancer Agents in Medicinal Chemistry. 18(14). 1983–1990. 5 indexed citations

Saravanan, K., R. Elancheran, S. Divakar, et al.. (2017). Design, synthesis and biological evaluation of 2-(4-phenylthiazol-2-yl) isoindoline-1,3-dione derivatives as anti-prostate cancer agents. Bioorganic & Medicinal Chemistry Letters. 27(5). 1199–1204. 27 indexed citations

Harries, Mark, Aliki Taylor, Lars Holmberg, et al.. (2014). Incidence of bone metastases and survival after a diagnosis of bone metastases in breast cancer patients. Cancer Epidemiology. 38(4). 427–434. 62 indexed citations

Venkatraman, R., et al.. (2013). ENHANCEMENT OF MICROSTRUCTURE AND MECHANICAL PROPERTIES THROUGH EQUAL CHANNEL ANGULAR PRESSING OF ALUMINIUM PROCESSED BY POWDER METALLURGY ROUTE. International Journal of Innovative Research in Science Engineering and Technology. 2(9). 4964–4976. 1 indexed citations

Sakkiah, Sugunadevi, et al.. (2013). Pharmacophore Design, Virtual Screening, Molecular Docking and Optimization Approaches to Discover Potent Thrombin Inhibitors. Combinatorial Chemistry & High Throughput Screening. 16(9). 702–720. 3 indexed citations

10.

Shanmugam, Mani, et al.. (2012). Synthesis, spectral characterization and antimicrobial studies of novel s-triazine derivatives. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 105. 383–390. 21 indexed citations

11.

Ramachandran, R., et al.. (2011). Synthesis, spectral, crystal structure and in vitro antimicrobial evaluation of imidazole/benzotriazole substituted piperidin-4-one derivatives. European Journal of Medicinal Chemistry. 46(5). 1926–1934. 70 indexed citations

12.

Bhaskar, B., et al.. (2011). Synthesis, stereochemistry, antimicrobial evaluation and QSAR studies of 2,6-diaryltetrahydropyran-4-one thiosemicarbazones. European Journal of Medicinal Chemistry. 46(4). 1415–1424. 28 indexed citations

13.

Ramachandran, R., et al.. (2011). Synthesis, stereochemistry and in vitro antimicrobial evaluation of novel 2-[(2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-ylidene)hydrazono]-4-phenyl-2,3-dihydrothiazoles. Bioorganic & Medicinal Chemistry Letters. 21(21). 6301–6304. 7 indexed citations

14.

Dutkiewicz, Grzegorz, H.S. Yathirajan, R. Ramachandran, S. Kabilan, & Maciej Kubicki. (2010). Different hydrogen-bonding modes in two closely related oximes. Acta Crystallographica Section C Crystal Structure Communications. 66(6). o274–o278. 1 indexed citations

15.

Parthiban, P., S. Kabilan, Venkatachalam Ramkumar, & Yeon Tae Jeong. (2010). Stereocontrolled facile synthesis and antimicrobial activity of oximes and oxime ethers of diversely substituted bispidines. Bioorganic & Medicinal Chemistry Letters. 20(22). 6452–6458. 22 indexed citations

16.

Bhaskar, B., et al.. (2010). Synthesis, antimicrobial evaluation and QSAR studies of novel piperidin-4-yl-5-spiro-thiadiazoline derivatives. Bioorganic & Medicinal Chemistry Letters. 20(23). 6909–6914. 37 indexed citations

17.

Ramachandran, R., et al.. (2009). 2-(2,4-Diphenyl-3-azabicyclo[3.3.1]nonan-9-ylidenehydrazono)-1,3-thiazolidin-4-one. Acta Crystallographica Section E Structure Reports Online. 65(3). o584–o584. 2 indexed citations

18.

Aridoss, G., S. Amirthaganesan, Ashok Kumar Nanjundan, et al.. (2008). A facile synthesis, antibacterial, and antitubercular studies of some piperidin-4-one and tetrahydropyridine derivatives. Bioorganic & Medicinal Chemistry Letters. 18(24). 6542–6548. 78 indexed citations

19.

Aridoss, G., Shankar Balasubramanian, P. Parthiban, & S. Kabilan. (2007). Synthesis and NMR spectral studies of N-chloroacetyl-2,6-diarylpiperidin-4-ones. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 68(5). 1153–1163. 32 indexed citations

20.

Parthiban, P., Shankar Balasubramanian, G. Aridoss, & S. Kabilan. (2007). Synthesis and NMR spectral studies of some 2,6-diarylpiperidin-4-one O-benzyloximes. Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy. 70(1). 11–24. 24 indexed citations

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