The DOI matches its Crossref record; 118 of the 118 references it cites were found in a registry or an index.
Clerodane diterpenes: sources, structures, and biological activities
Open accessAbstract
The clerodane diterpenoids are a widespread class of secondary metabolites and have been found in several hundreds of plant species from various families and in organisms from other taxonomic groups.
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Cites
Salvinorin A: A potent naturally occurring nonnitrogenous κ opioid selective agonist
Roth, B. L., Baner, K., Westkaemper, R., Siebert, D., Rice, K. C., Steinberg, S., Ernsberger, P., & Rothman, R. B. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182234399 · Cited by 784
Comprehensive Medicinal Chemistry
(1991) · Quantitative Structure-Activity Relationships · doi:10.1002/qsar.19910100410 · Cited by 745
Waldhoer, M., Bartlett, S. E., & Whistler, J. L. (2004) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.73.011303.073940 · Cited by 740
Two rings in them all: The labdane-related diterpenoids
Peters, R. J. (2010) · Natural Product Reports · doi:10.1039/c0np00019a · Cited by 433
Salvia divinorum and salvinorin A: new pharmacologic findings
Siebert, D. J. (1994) · Journal of Ethnopharmacology · doi:10.1016/0378-8741(94)90116-3 · Cited by 279
Salvinorin, a new trans-neoclerodane diterpene from Salvia divinorum(Labiatae)
Ortega, A., Blount, J. F., & Manchand, P. S. (1982) · Journal of the Chemical Society, Perkin Transactions 1 · doi:10.1039/p19820002505 · Cited by 226
Groer, C. E., Tidgewell, K., Moyer, R. A., Harding, W. W., Rothman, R. B., Prisinzano, T. E., & Bohn, L. M. (2007) · Molecular Pharmacology · doi:10.1124/mol.106.028258 · Cited by 224
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Wang, Y., Tang, K., Inan, S., Siebert, D., Holzgrabe, U., Lee, D. Y. W., Huang, P., Li, J.-G., Cowan, A., & Liu-Chen, L.-Y. (2005) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.104.073668 · Cited by 191
Cited by
Phytoecdysteroid and Clerodane Content in Three Wild Ajuga Species in Israel
Taha-Salaime, L., Davidovich-Rikanati, R., Sadeh, A., Abu-Nassar, J., Marzouk-Kheredin, S., Yahyaa, Y., Ibdah, M., Ghanim, M., Lewinsohn, E., Inbar, M., et al. (2019) · ACS Omega · doi:10.1021/acsomega.8b03029 · Cited by 10
Metadata
- Authors
- Li, R., Morris-Natschke, S. L., & Lee, K.-H.
- Venue
- Natural Product Reports
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2016
- Volume
- 33
- Issue
- 10
- Pages
- 1166-1226
- ISSN
- 0265-0568 (ISSN-L)
- 1460-4752
- OpenAlex
- W2500606803
- Cited by
- 256
- References
- 118
- FWCI
- 8.58
- Type
- journal article
- Language
- en
- Open access
- green
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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.
