The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Synthesis of derivatives of methyl rosmarinate and their inhibitory activities against matrix metalloproteinase-1 (MMP-1)
Abstract
A series of MMP-1 inhibitors have been identified based upon a methyl rosmarinate scaffold using structure-based drug design methods. The best compound in the series showed an IC50 value of 0.4 μM. A docking study was conducted for compound (S)-10n in order to investigate its binding interactions with MMP-1. The structure-activity relationships (SAR) were also briefly discussed. Useful SAR was established which provides important guidelines for the design of future generations of potent inhibitors against MMP-1.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“It exhibits inhibitory activities against tyrosinase, α-glucosidase, and matrix metalloproteinase-1 (MMP-1) [61,62,63,64].”
In the citing paper
“Methyl rosmarinate stands out for its antioxidative properties and antifungal activities.”
Citations
Cites
Matrix metalloproteinases as modulators of inflammation and innate immunity
Parks, W. C., Wilson, C. L., & López-Boado, Y. S. (2004) · Nature Reviews Immunology · doi:10.1038/nri1418 · Cited by 1,929
Research works printed but not linked: 32
- Huxley-Jones, 2008, Drug Discov. Today, 13, 685, 10.1016/j.drudis.2008.05.005 · DOI
- Hidalgo, 2001, J. Natl. Cancer Inst., 93, 178, 10.1093/jnci/93.3.178 · DOI
- Roach, 2008, Expert Opin. Drug Discov., 3, 475, 10.1517/17460441.3.5.475 · DOI
- Dahlberg, 2000, Arthritis Rheum., 43, 673, 10.1002/1529-0131(200003)43:3<673::AID-ANR25>3.0.CO;2-8 · DOI
- Ikeda, 2003, Clin. Cardiol., 26, 55, 10.1002/clc.4960260203 · DOI
- Pilcher, 1999, Ann. N.Y. Acad. Sci., 878, 12, 10.1111/j.1749-6632.1999.tb07671.x · DOI
- Rowan, 2008, Expert Opin. Ther. Targets, 12, 1, 10.1517/14728222.12.1.1 · DOI
- Fingleton, 2007, Curr. Pharm. Des., 13, 333, 10.2174/138161207779313551 · DOI
- Lefèvre, 2009, Nat. Med., 15, 1414, 10.1038/nm.2050 · DOI
- Rush, 2004, Curr. Top. Med. Chem., 4, 1311, 10.2174/1568026043387999 · DOI
- Verma, 2007, Bioorg. Med. Chem., 15, 2223, 10.1016/j.bmc.2007.01.011 · DOI
- Gross, 1962, Proc. Natl. Acad. Sci. U. S. A., 48, 1014, 10.1073/pnas.48.6.1014 · DOI
- Sternlicht, 2001, Annu. Rev. Cell. Dev. Biol., 17, 463, 10.1146/annurev.cellbio.17.1.463 · DOI · Paper page
- Egeblad, 2002, Nat. Rev. Cancer, 2, 161, 10.1038/nrc745 · DOI · Paper page
- Stamenkovic, 2003, J. Pathol., 200, 448, 10.1002/path.1400 · DOI
- Galis, 2002, Circ. Res., 90, 251, 10.1161/res.90.3.251 · DOI
- Elkington, 2011, J. Clin. Invest., 121, 1827, 10.1172/JCI45666 · DOI
- Lovejoy, 1994, Science, 263, 375, 10.1126/science.8278810 · DOI
- Borkakoti, 1994, Nat. (London) Struct. Biol., 1, 106, 10.1038/nsb0294-106 · DOI
- Lovejoy, 1999, Nat. Struct. Mol. Biol., 6, 217, 10.1038/6657 · DOI
- Whittaker, 1999, Chem. Rev., 99, 2735, 10.1021/cr9804543 · DOI
- .Rao, 2005, Curr. Pharm. Des., 11, 295, 10.2174/1381612053382115 · DOI
- Skiles, 2004, Curr. Med. Chem., 11, 2911, 10.2174/0929867043364018 · DOI
- Rosenbaum, 2005, Clin. Cancer Res., 11, 4437, 10.1158/1078-0432.CCR-04-2252 · DOI
- Bissett, 2005, J. Clin. Oncol., 23, 842, 10.1200/JCO.2005.03.170 · DOI
- Hemmings, 2001, Rheumatology, 40, 537, 10.1093/rheumatology/40.5.537 · DOI
- Paul Beckett, 1996, Expert Opin. Ther. Pat., 6, 1305, 10.1517/13543776.6.12.1305 · DOI
- Queffélec, 2008, Eur. J. Med. Chem., 43, 2268, 10.1016/j.ejmech.2007.12.013 · DOI
- Wong, 1992, Synthesis, 8, 793, 10.1055/s-1992-26228 · DOI
- Kunz, 1984, Angew. Chem. Int. Ed., 23, 71, 10.1002/anie.198400711 · DOI
- Minamikawa, 1978, Tetrahedron Lett., 34, 3085, 10.1016/S0040-4039(01)94947-0 · DOI
- Donini, 2000, J. Med. Chem., 43, 4180, 10.1021/jm000040d · DOI
Cited by
Xiao, Z., Yang, S., Chen, J., Li, C., Zhou, C., Hong, P., Sun, S., & Qian, Z.-J. (2020) · Journal of Functional Foods · doi:10.1016/j.jff.2020.104198 · Cited by 54
Hadi, N., Drioiche, A., Bouchra, E. M., Baammi, S., Abdelaziz Shahat, A., Tagnaout, I., Radi, M., Remok, F., Bouzoubaa, A., & Zair, T. (2024) · Pharmaceuticals · doi:10.3390/ph17070862 · Cited by 30
Metadata
- Authors
- Yuan, H., Lu, W., Wang, L., Shan, L., Li, H., Huang, J., Sun, Q., & Zhang, W.
- Venue
- European Journal of Medicinal Chemistry
- Publisher
- Elsevier BV
- Published
- 2013-04
- Volume
- 62
- Pages
- 148-157
- ISSN
- 0223-5234
- Cited by
- 35
- References
- 1
- Language
- en
- Funders
- NCET Foundation
- NSFC (30725045)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
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.