The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.
Chalcones as potent tyrosinase inhibitors: the importance of a 2,4-substituted resorcinol moiety
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Citations
Cites
Tyrosinase: a comprehensive review of its mechanism
Sánchez-Ferrer, Á., Neptuno Rodríguez-López, J., García-Cánovas, F., & García-Carmona, F. (1995) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/0167-4838(94)00204-t · Cited by 1,239
Chemical and Instrumental Approaches to Treat Hyperpigmentation
Briganti, S., Camera, E., & Picardo, M. (2003) · Pigment Cell Research · doi:10.1034/j.1600-0749.2003.00029.x · Cited by 837
Mushroom Tyrosinase: Recent Prospects
Seo, S.-Y., Sharma, V. K., & Sharma, N. (2003) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf020826f · Cited by 809
Vaya, J., Belinky, P. A., & Aviram, M. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00089-0 · Cited by 549
Self-citationA Quantum Chemical Explanation of the Antioxidant Activity of Flavonoids
van Acker, S. A. B. E., de Groot, M. J., van den Berg, D.-J., Tromp, M. N. J. L., Donné-Op den Kelder, G., van der Vijgh, W. J. F., & Bast, A. (1996) · Chemical Research in Toxicology · doi:10.1021/tx9600964 · Cited by 408
Oxyresveratrol and Hydroxystilbene Compounds
Kim, Y. M., Yun, J., Lee, C.-K., Lee, H., Min, K. R., & Kim, Y. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200678200 · Cited by 323
Glabrene and isoliquiritigenin as tyrosinase inhibitors from licorice roots
Nerya, O., Vaya, J., Musa, R., Izrael, S., Ben-Arie, R., & Tamir, S. (2003) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf020935u · Cited by 297
Self-citationChalcones as potent tyrosinase inhibitors: the effect of hydroxyl positions and numbers
Nerya, O., Musa, R., Khatib, S., Tamir, S., & Vaya, J. (2004) · Phytochemistry · doi:10.1016/j.phytochem.2004.04.016 · Cited by 285
Self-citationInhibition of the catecholase activity of biomimetic dinuclear copper complexes by kojic acid
Battaini, G., Monzani, E., Casella, L., Santagostini, L., & Pagliarin, R. (2000) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s007750050370 · Cited by 180
Inhibition of LDL oxidation by flavonoids in relation to their structure and calculated enthalpy
Vaya, J., Mahmood, S., Goldblum, A., Aviram, M., Volkova, N., Shaalan, A., Musa, R., & Tamir, S. (2002) · Phytochemistry · doi:10.1016/s0031-9422(02)00445-4 · Cited by 152
Self-citation
Cited by
Hypopigmenting agents: an updated review on biological, chemical and clinical aspects
Solano, F., Briganti, S., Picardo, M., & Ghanem, G. (2006) · Pigment Cell Research · doi:10.1111/j.1600-0749.2006.00334.x · Cited by 696
Natural and Synthetic Tyrosinase Inhibitors as Antibrowning Agents: An Update
Loizzo, M. R., Tundis, R., & Menichini, F. (2012) · Comprehensive Reviews in Food Science and Food Safety · doi:10.1111/j.1541-4337.2012.00191.x · Cited by 317
Ji, S., Li, Z., Song, W., Wang, Y., Liang, W., Li, K., Tang, S., Wang, Q., Qiao, X., Zhou, D., et al. (2016) · Journal of Natural Products · doi:10.1021/acs.jnatprod.5b00877 · Cited by 242
Metadata
- Authors
- Khatib, S., Nerya, O., Musa, R., Shmuel, M., Tamir, S., & Vaya, J.
- Venue
- Bioorganic & Medicinal Chemistry
- Publisher
- Elsevier BV
- Published
- 2005-01
- Volume
- 13
- Issue
- 2
- Pages
- 433-441
- ISSN
- 0968-0896 (ISSN-L)
- OpenAlex
- W2058844545
- Cited by
- 340
- References
- 14
- FWCI
- 4.39
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Chalcones as potent tyrosinase inhibitors: the importance of a 2,4-substituted resorcinol moiety. https://app.cochat.ai/papers/10.1016/j.bmc.2004.10.010
- The paper
- Khatib, S., Nerya, O., Musa, R., Shmuel, M., Tamir, S., & Vaya, J. (2005). Chalcones as potent tyrosinase inhibitors: the importance of a 2,4-substituted resorcinol moiety. Bioorganic & Medicinal Chemistry. https://doi.org/10.1016/j.bmc.2004.10.010
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.
