The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
Recent developments and biological activities of thiazolidinone derivatives: A review
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Cites
Synthesis and anticancer activity of some novel 2-substituted benzimidazole derivatives
Refaat, H. M. (2010) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2010.03.022 · Cited by 279
Novel 4-thiazolidinone derivatives as potential antifungal and antibacterial drugs
Omar, K., Geronikaki, A., Zoumpoulakis, P., Camoutsis, C., Soković, M., Ćirić, A., & Glamočlija, J. (2010) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2009.10.041 · Cited by 271
Synthesis and anticancer activity evaluation of 4-thiazolidinones containing benzothiazole moiety
Havrylyuk, D., Мосула, Л. М., Zimenkovsky, B. S., Vasylenko, O., Gzella, A. K., & Lesyk, R. (2010) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2010.08.008 · Cited by 249
Kamel, M. M., Ali, H. I., Anwar, M. M., Mohamed, N. A., & Soliman, A. M. (2010) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2009.10.044 · Cited by 180
2-Imino-thiazolidin-4-one Derivatives as Potent, Orally Active S1P1Receptor Agonists
Bolli, M. H., Abele, S., Binkert, C., Bravo, R., Buchmann, S., Bur, D., Gatfield, J., Hess, P., Kohl, C., Mangold, C., et al. (2010) · Journal of Medicinal Chemistry · doi:10.1021/jm100181s · Cited by 179
Zhou, H., Wu, S., Zhai, S., Liu, A., Sun, Y., Li, R., Zhang, Y., Ekins, S., Swaan, P. W., Fang, B., et al. (2008) · Journal of Medicinal Chemistry · doi:10.1021/jm7012024 · Cited by 179
Geronikaki, A. A., Lagunin, A. A., Hadjipavlou-Litina, D. I., Eleftheriou, P. T., Filimonov, D. A., Poroikov, V. V., Alam, I., & Saxena, A. K. (2008) · Journal of Medicinal Chemistry · doi:10.1021/jm701496h · Cited by 176
Babaoglu, K., Page, M. A., Jones, V. C., McNeil, M. R., Dong, C., Naismith, J. H., & Lee, R. E. (2003) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/s0960-894x(03)00673-5 · Cited by 175
Ottanà, R., Carotti, S., Maccari, R., Landini, I., Chiricosta, G., Caciagli, B., Vigorita, M. G., & Mini, E. (2005) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2005.05.093 · Cited by 154
Amin, K. M., KAMEL, M. M., Anwar, M. M., Khedr, M. A., & Syam, Y. M. (2010) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2009.12.078 · Cited by 147
Cited by
Ilardi, E. A., Vitaku, E., & Njardarson, J. T. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm401375q · Cited by 1,604
Nepali, K., Sharma, S., Sharma, M., Bedi, P. M. S., & Dhar, K. L. (2014) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2014.03.018 · Cited by 435
Thiazole-containing compounds as therapeutic targets for cancer therapy
Sharma, P. C., Bansal, K. K., Sharma, A., Sharma, D., & Deep, A. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.112016 · Cited by 382
Thiazolidinediones as antidiabetic agents: A critical review
Nanjan, M. J., Mohammed, M., Prashantha Kumar, B. R., & Chandrasekar, M. J. N. (2018) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2018.02.009 · Cited by 316
Effects of Antidiabetic Drugs on Gut Microbiota Composition
Montandon, S., & Jornayvaz, F. (2017) · Genes · doi:10.3390/genes8100250 · Cited by 135
Metadata
- Authors
- Jain, A. K., Vaidya, A., Ravichandran, V., Kashaw, S. K., & Agrawal, R. K.
- Venue
- Bioorganic & Medicinal Chemistry
- Publisher
- Elsevier BV
- Published
- 2012-06
- Volume
- 20
- Issue
- 11
- Pages
- 3378-3395
- ISSN
- 0968-0896 (ISSN-L)
- OpenAlex
- W2126508060
- Cited by
- 461
- References
- 32
- FWCI
- 10.79
- Type
- journal article
- Language
- en
- Open access
- green
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- Jain, A. K., Vaidya, A., Ravichandran, V., Kashaw, S. K., & Agrawal, R. K. (2012). Recent developments and biological activities of thiazolidinone derivatives: A review. Bioorganic & Medicinal Chemistry. https://doi.org/10.1016/j.bmc.2012.03.069
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
