The DOI matches its Crossref record; 65 of the 65 references it cites were found in a registry or an index.
Natural withanolides: an overview
Abstract
Withanolides are a group of naturally occurring C28 steroids built on an ergostane skeleton functionalized at carbons 1, 22 and 26, commonly known as the withanolide skeleton. Over the period of August 1996 to March 2010, 360 new naturally occurring withanolides were isolated and identified. This review provides a comprehensive summary of the structural classification and distribution of these new compounds. The diverse biological and pharmacological activities of natural withanolides are also discussed based on their structural features. A total of 211 references are cited in this review.
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Cites
Cyclooxygenases: Structural, cellular, and molecular biology
Smith, W. L., DeWitt, D. L., & Garavito, R. M. (2000) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.69.1.145 · Cited by 2,925
Benson, A. M., Hunkeler, M. J., & Talalay, P. (1980) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.77.9.5216 · Cited by 746
THE CHOLINERGIC HYPOTHESIS—TEN YEARS ON
Perry, E. K. (1986) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a072100 · Cited by 562
Neuritic regeneration and synaptic reconstruction induced by withanolide A
Kuboyama, T., Tohda, C., & Komatsu, K. (2005) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706122 · Cited by 339
Withaferin A targets heat shock protein 90 in pancreatic cancer cells
Yu, Y., Hamza, A., Zhang, T., Gu, M., Zou, P., Newman, B., Li, Y., Gunatilaka, A. A. L., Zhan, C.-G., & Sun, D. (2010) · Biochemical Pharmacology · doi:10.1016/j.bcp.2009.09.017 · Cited by 316
Kaileh, M., Vanden Berghe, W., Heyerick, A., Horion, J., Piette, J., Libert, C., De Keukeleire, D., Essawi, T., & Haegeman, G. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m606728200 · Cited by 301
Breast cancer and NSAID use: a meta-analysis
Khuder, S. A., & Mutgi, A. B. (2001) · British Journal of Cancer · doi:10.1054/bjoc.2000.1709 · Cited by 273
Malik, F., Kumar, A., Bhushan, S., Khan, S., Bhatia, A., Suri, K. A., Qazi, G. N., & Singh, J. (2007) · Apoptosis · doi:10.1007/s10495-007-0129-x · Cited by 254
Withanolides and related ergostane-type steroids
Glotter, E. (1991) · Natural Product Reports · doi:10.1039/np9910800415 · Cited by 241
Matsuda, H., Murakami, T., Kishi, A., & Yoshikawa, M. (2001) · Bioorganic & Medicinal Chemistry · doi:10.1016/s0968-0896(01)00024-4 · Cited by 219
Cited by
Medicinal Plants, Human Health and Biodiversity: A Broad Review
Sen, T., & Samanta, S. K. (2014) · Advances in Biochemical Engineering/Biotechnology · doi:10.1007/10_2014_273 · Cited by 330
Anticancer steroids: linking natural and semi-synthetic compounds
Salvador, J. A. R., Carvalho, J. F. S., Neves, M. A. C., Silvestre, S. M., Leitão, A. J., Silva, M. M. C., & Sá e Melo, M. L. (2013) · Nat. Prod. Rep. · doi:10.1039/c2np20082a · Cited by 276
Natural Withanolides in the Treatment of Chronic Diseases
White, P. T., Subramanian, C., Motiwala, H. F., & Cohen, M. S. (2016) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-319-41334-1_14 · Cited by 139
Metadata
- Authors
- Chen, L.-X., He, H., & Qiu, F.
- Venue
- Natural Product Reports
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2011
- Volume
- 28
- Issue
- 4
- Pages
- 705
- ISSN
- 0265-0568 (ISSN-L)
- 1460-4752
- OpenAlex
- W2106281303
- Cited by
- 358
- References
- 65
- FWCI
- 41.48
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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