The DOI matches its Crossref record; 233 of the 239 references it cites were found in a registry or an index.
Polyhydroxylated alkaloids—Natural occurrence and therapeutic applications
Abstract
Over one hundred polyhydroxylated alkaloids have been isolated from plants and micro-organisms. These alkaloids can be potent and highly selective glycosidase inhibitors and are arousing great interest as tools to study cellular recognition and as potential therapeutic agents. However, only three of the natural products so far have been widely studied for therapeutic potential due largely to the limited commercial availability of the other compounds.
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
“Swainsonine (mannose analogue) and castanospermine (glucose analogue) are iminosugar alkaloid glycosidases inhibitors, which also express anticancer properties and act on the protein-folding machinery [248].”
From GANAB and N-Glycans Substrates Are Relevant in Human Physiology, Polycystic Pathology and Multiple Sclerosis: A Review (2022) · cites this paper as [248]
Citations
Cites
Alkaloids: Chemical and Biological Perspectives
(1992) · Springer eBooks · doi:10.1007/978-1-4612-2908-7 · Cited by 1,305
Dose: A critical factor in cancer chemotherapy
Frei, E., & Canellos, G. P. (1980) · The American Journal of Medicine · doi:10.1016/0002-9343(80)90472-6 · Cited by 838
Hakomori, S. (1985) · PubMed · Cited by 805
Lysosomes and storage diseases
Hers, H. G., & HOOF, F. V. (1973) · Medical Entomology and Zoology · Cited by 744
Fan, J., Ishii, S., Asano, N., & Suzuki, Y. (1999) · Nature Medicine · doi:10.1038/4801 · Cited by 616
Legler, G. (1990) · Advances in carbohydrate chemistry and biochemistry · doi:10.1016/s0065-2318(08)60034-7 · Cited by 553
Sears, P. S., & Wong, C. (1999) · Angewandte Chemie International Edition · doi:10.1002/(sici)1521-3773(19990816)38:16 · Cited by 516
Amino-sugar glycosidase inhibitors: versatile tools for glycobiologists
WINCHESTER, B. G., & Fleet, G. W. J. (1992) · Glycobiology · doi:10.1093/glycob/2.3.199 · Cited by 497
Tulsiani, D. R. P., Harris, T. M., & Touster, O. (1982) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)34274-1 · Cited by 461
Analysis of dose intensity for adjuvant chemotherapy trials in stage II breast cancer.
Hryniuk, W. M., & Levine, M. N. (1986) · Journal of Clinical Oncology · doi:10.1200/jco.1986.4.8.1162 · Cited by 457
Research works printed but not linked: 9
- Bowen, 1993, A preliminary pharmacokinetics evaluation of the antimetastatic immunomodulator swainsonine, Anticancer Res., 13, 841
- Bowen, 1997, Interaction of swainsonine with lymphoid and highly perfused tissues, Anticancer Res., 17, 4345
- Cox, 1994, Therapeutic advances in Gaucher's disease, Trends Exp. Clin. Med., 4, 144
- Griffiths, R.C., 1998. Polyhydroxylated Alkaloids and their Ability to Inhibit Glycosidases. PhD thesis, University of Wales, UK.
- Hakomori, 1985, Aberrant glycosylation in cancer cell membranes as focused on glycolipids, Cancer Res., 45, 2405
- Jolly, 1981, Mannosidosis, J. Appl. Biochem., 3, 273
- Menzies, 1979, A neurological disease associated with Solanum dimidiatum, Southwest. Vet., 32, 45
- Pienaar, 1976, Maldronksiekte in cattle, Onderstepoort J. Vet. Res., 43, 67
- Richmond, 1996, Efficacy and safety of MDL 28,574A in HIV-positive patients with baseline CD4 values of 301-500, Proc. Int. Conf. AIDS, 11, 80
Cited by
Sorted by citations
Items 301–400 of 732
Izquierdo, I., Plaza, M. T., Tamayo, J. A., & Sánchez‐Cantalejo, F. (2007) · Tetrahedron Asymmetry · doi:10.1016/j.tetasy.2007.09.014 · Cited by 21
Total synthesis of (+)-swainsonine and (+)-8-epi-swainsonine
Trajković, M., Balanac, V., Ferjancic, Z. B., & Saičić, R. N. (2014) · RSC Advances · doi:10.1039/c4ra11978a · Cited by 21
Histochemistry of simple hairs from the foliar cavities of Azolla filiculoides
Pereira, A. L., & Carrapico, F. J. (2007) · Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology · doi:10.1080/11263500701627588 · Cited by 21
Preparative isolation of swainsonine from locoweed: extraction and purification procedures
Gardner, D. R., Lee, S. T., Molyneux, R. J., & Edgar, J. A. (2003) · Phytochemical Analysis · doi:10.1002/pca.713 · Cited by 21
Asymmetric synthesis of hydroxy-skipped bishomo-inositols as potential glycosidase inhibitors
Mahapatra, T., & Nanda, S. (2010) · Tetrahedron Asymmetry · doi:10.1016/j.tetasy.2010.07.033 · Cited by 21
Singh, D., & Kaur, G. (2011) · Journal of Basic Microbiology · doi:10.1002/jobm.201100255 · Cited by 21
Annona muricata (Graviola): Toxic or Therapeutic
Mohanty, S., Hollinshead, J., Jones, L., Jones, P. W., Thomas, D., Watson, A. A., Watson, D. G., Gray, A. I., Molyneux, R. J., & Nash, R. J. (2008) · Natural Product Communications · doi:10.1177/1934578x0800300107 · Cited by 21
Takahashi, M., Maehara, T., Sengoku, T., Fujita, N., Takabe, K., & Yoda, H. (2008) · Tetrahedron · doi:10.1016/j.tet.2008.03.029 · Cited by 21
Xie, Y., Yao, Y., Sun, H., Yan, T., Liu, J., & Kang, T. (2011) · Molecules · doi:10.3390/molecules16108745 · Cited by 20
Quan, N., Nie, L., Zhu, R., Shi, X., Ding, W., & Lü, X. (2013) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201300804 · Cited by 20
Stereoselective synthesis of (−)-8-epi-swainsonine starting with a chiral aziridine
Lee, B. K., Choi, H. G., Roh, E. J., Lee, W. K., & Sim, T. (2012) · Tetrahedron Letters · doi:10.1016/j.tetlet.2012.11.087 · Cited by 20
Total synthesis of 1-deoxy-7,8a-di-epi-castanospermine and formal synthesis of pumiliotoxin-251D
Sultane, P. R., Mohite, A. R., & Bhat, R. G. (2012) · Tetrahedron Letters · doi:10.1016/j.tetlet.2012.08.061 · Cited by 20
Kalamkar, N. B., Puranik, V. G., & Dhavale, D. D. (2011) · Tetrahedron · doi:10.1016/j.tet.2011.02.030 · Cited by 20
Li, Y., Kinami, K., Hirokami, Y., Kato, A., Su, J., Jia, Y., Fleet, G. W. J., & Yu, C. (2016) · Organic & Biomolecular Chemistry · doi:10.1039/c5ob02474a · Cited by 20
Kumar, R. S., Almansour, A. I., Arumugam, N., Mohammad, F., Alshahrani, W. S., Kotresha, D., Altaf, M., Azam, M., & Menéndez, J. C. (2018) · RSC Advances · doi:10.1039/c8ra07985d · Cited by 20
Zoidl, M., Müller, B., Torvisco, A., Tysoe, C., Benazza, M., Siriwardena, A. H., Withers, S. G., & Wrodnigg, T. M. (2014) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2014.03.069 · Cited by 20
Akbarzadeh, R., Amanpour, T., Khavasi, H. R., & Bazgir, A. (2013) · Tetrahedron · doi:10.1016/j.tet.2013.12.011 · Cited by 20
Crepidtumines A and B, Two Novel Indolizidine Alkaloids from Dendrobium crepidatum
Xu, X., Chen, X., Yang, R., Li, Z.-S., Zhou, H., Bai, Y., Yu, M., Li, B., & Ding, G. (2020) · Scientific Reports · doi:10.1038/s41598-020-66552-2 · Cited by 20
Cyclisations and Strategies for Stereoselective Synthesis of Piperidine Iminosugars
Dhara, D., Dhara, A., Bennett, J., & Murphy, P. V. (2021) · The Chemical Record · doi:10.1002/tcr.202100221 · Cited by 20
Synthesis and glycosidase inhibitory activity of pseudo-di-(or tri-)saccharides
McCort‐Tranchepain, I., SANIERE, M., & Merrer, Y. L. (2003) · Tetrahedron · doi:10.1016/s0040-4020(03)00257-6 · Cited by 20
Synthesis of polyhydroxylated 7-aminopyrrolizidines and 8-aminoindolizidines
Stecko, S., Jurczak, M., Staszewska‐Krajewska, O., Solecka, J., & Chmielewski, M. (2009) · Tetrahedron · doi:10.1016/j.tet.2009.06.043 · Cited by 20
Gopalakrishnan, M., Thanusu, J., & Kanagarajan, V. (2007) · Medicinal Chemistry Research · doi:10.1007/s00044-007-9051-6 · Cited by 20
De Masi, R., & Orlando, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23137373 · Cited by 20
“Swainsonine (mannose analogue) and castanospermine (glucose analogue) are iminosugar alkaloid glycosidases inhibitors, which also express anticancer properties and act on the protein-folding machinery [248].”
BackgroundGavale, K. S., Chavan, S. R., Khan, A., Joshi, R. S., & Dhavale, D. D. (2015) · Organic & Biomolecular Chemistry · doi:10.1039/c5ob00668f · Cited by 19
Selva, V., Larrañaga, O., Castelló, L. M., Nájera, C., Sansano, J. M., & de Cózar, A. (2017) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.7b00903 · Cited by 19
Zanardi, M. M., Sortino, M. A., & Sarotti, A. M. (2019) · Carbohydrate Research · doi:10.1016/j.carres.2019.01.011 · Cited by 19
Regiochemistry‐Directed Syntheses of Polyhydroxylated Alkaloids from Chiral Aziridines
Eum, H., Choi, J., Cho, C., & Ha, H. (2015) · Asian Journal of Organic Chemistry · doi:10.1002/ajoc.201500285 · Cited by 19
Safar, P. J., Žúžiová, J., Bobošı́ková, M., Marchalı́n, Š., Prónayová, N., Comesse, S., & Daı̈ch, A. (2009) · Tetrahedron Asymmetry · doi:10.1016/j.tetasy.2009.08.010 · Cited by 19
Stereodivergent Synthesis of Iminosugars from Stannylated Derivatives of (S)-Vinylglycinol
Lumbroso, A., Beaudet, I., TOUPET, L. J., Grognec, E. L., & Quintard, J. (2012) · Organic Letters · doi:10.1021/ol303213r · Cited by 19
Marjanovic, J., Divjaković, V., Matović, R., Ferjancic, Z. B., & Saičić, R. N. (2013) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201300716 · Cited by 19
Stöckigt, J. H. H., Chen, Z., & Ruppert, M. (2010) · Topics in current chemistry · doi:10.1007/128_2010_80 · Cited by 19
Construction of protected hydroxylated pyrrolidines using nitrogen-centered radical cyclizations
Zhai, H., Zlotorzynska, M., & Sammis, G. M. (2009) · Chemical Communications · doi:10.1039/b914757h · Cited by 19
Cordero, F. M., Bonanno, P., Khairnar, B. B., Cardona, F., Brandi, A., Macchi, B., Minutolo, A., Grelli, S., & Mastino, A. (2012) · ChemPlusChem · doi:10.1002/cplu.201100069 · Cited by 18
Synthesis and Glycosidase Inhibition of Broussonetine M and Its Analogues
Wu, Q., Kinami, K., Kato, A., Li, Y., Jia, Y., Fleet, G. W. J., & Yu, C. (2019) · Molecules · doi:10.3390/molecules24203712 · Cited by 18
3,4-Dihydroxypyrrolidine as Glycosidase Inhibitor
Suzuki, K., Nakahara, T., & Kanie, O. (2009) · Current Topics in Medicinal Chemistry · doi:10.2174/156802609787354315 · Cited by 18
Asymmetric syntheses of 6-deoxyfagomin, d-deoxyrhamnojirimycin, and d-rhamnono-1,5-lactam
Fu, R., Du, Y., Li, Z.-Y., Xu, W.-X., & Huang, P. (2009) · Tetrahedron · doi:10.1016/j.tet.2009.09.083 · Cited by 18
Detection of polyhydroxyalkaloids in Lonchocarpus extracts by GC‐MS of acetylated derivatives
Magalhães, A. F., Santos, C. C., Magalhães, E. G., & Diaz, M. A. N. (2002) · Phytochemical Analysis · doi:10.1002/pca.645 · Cited by 18
Korvorapun, K., Soorukram, D., Kuhakarn, C., Tuchinda, P., Reutrakul, V., & Pohmakotr, M. (2014) · Chemistry - An Asian Journal · doi:10.1002/asia.201403023 · Cited by 18
α-Glucosidase-inhibitory iminosugars from the leaves of Suregada glomerulata
Yan, R.-Y., Wang, H., Liu, C., Kang, J., & Chen, R.-Y. (2013) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2013.07.048 · Cited by 18
Gopalakrishnan, M., Thanusu, J., Kanagarajan, V., & Govindaraju, R. (2008) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.1080/14756360801906632 · Cited by 18
Ring-closing double reductive amination route to aza-heteroannulated sugars
Laventine, D. M., Davies, M., Evinson, E. L., Jenkins, P. R., Cullis, P. M., & Fawcett, J. (2004) · Tetrahedron Letters · doi:10.1016/j.tetlet.2004.11.032 · Cited by 18
Gkizis, P. L., Argyropoulos, N. G., & Coutouli‐Argyropoulou, E. (2013) · Tetrahedron · doi:10.1016/j.tet.2013.07.098 · Cited by 18
Kumar, N. S., Kuntz, D. A., Wen, X., Pinto, B. M., & Rose, D. R. (2007) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.21850 · Cited by 18
Curtis, K. L., Evinson, E. L., Handa, S., & Singh, K. (2007) · Organic & Biomolecular Chemistry · doi:10.1039/b711994a · Cited by 18
Csatayová, K., Davies, S. G., Fletcher, A. M., Ford, J. G., Klauber, D. J., Roberts, P. M., & Thomson, J. E. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo501952t · Cited by 17
Xerardo Garcia-mera, B., Rodríguez-Borges, J. E., Vale, M. L. C., & Alves, M. J. (2011) · Tetrahedron · doi:10.1016/j.tet.2011.06.097 · Cited by 17
Development of a practical biocatalytic process for ( S )- N -Boc-3-hydroxypiperidine synthesis
Chen, L.-F., Fan, H., Zhang, Y., Wu, K., Wang, H., Lin, J., & Wei, D. (2017) · Tetrahedron Letters · doi:10.1016/j.tetlet.2017.03.037 · Cited by 17
Flexible approach for the asymmetric synthesis of (−)-hyacinthacine A1 and its 7a-epimer
Si, C., Mao, Z., Ren, R., Du, Z., & Wei, B. (2014) · Tetrahedron · doi:10.1016/j.tet.2014.08.056 · Cited by 17
Tripathi, P., Tripathi, A. C., Chawla, V., & Saraf, S. K. (2014) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2014.05.080 · Cited by 17
Design and syntheses of some iminosugar derivatives as potential immunosuppressants
Zhang, G., Zheng, X., Zhang, L., & Ye, X. (2011) · MedChemComm · doi:10.1039/c1md00098e · Cited by 17
First Total Synthesis of (+)‐Adenophorine, a Naturally Occurring Inhibitor of Glycosidases
Pearson-Long, M. S. M., Evain, M., Mathé‐Allainmat, M., & Lebreton, J. (2007) · European Journal of Organic Chemistry · doi:10.1002/ejoc.200700459 · Cited by 17
Synthesis of the New 7S‐Aminolentiginosine and Derivatives
Cordero, F. M., Bonanno, P., Neudeck, S., Vurchio, C., & Brandi, A. (2009) · Advanced Synthesis & Catalysis · doi:10.1002/adsc.200800806 · Cited by 17
Lin, C., Pan, Y.-S., Patkar, L. N., Lin, H., Tzou, D. M., Subramanian, T., & Lin, C. (2004) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2004.03.064 · Cited by 17
A ring-closing metathesis route to 7-membered aza-heteroannulated sugars
Laventine, D. M., Jenkins, P. R., & Cullis, P. M. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.02.007 · Cited by 17
Izquierdo, I., Plaza, M. T., & Tamayo, J. A. (2006) · Journal of Carbohydrate Chemistry · doi:10.1080/07328300600735181 · Cited by 17
Total synthesis of pyrrolidine alkaloid, Radicamine-B via Stille coupling
Mallesham, P., Vijaykumar, B. V. D., Shin, D., & Chandrasekhar, S. (2011) · Tetrahedron Letters · doi:10.1016/j.tetlet.2011.09.034 · Cited by 16
A divergent asymmetric approach to aza-spiropyran derivative and (1S,8aR)-1-hydroxyindolizidine
Zheng, J., Chen, W., Huang, S., Ye, J., & Huang, P. (2007) · Beilstein Journal of Organic Chemistry · doi:10.1186/1860-5397-3-41 · Cited by 16
Li, Y., Shimada, Y., Adachi, I., Kato, A., Jia, Y., Fleet, G. W. J., Xiao, M., & Yu, C. (2015) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.5b00571 · Cited by 16
Massicot, F., Plantier‐Royon, R., Vasse, J., & Behr, J. (2018) · Carbohydrate Research · doi:10.1016/j.carres.2018.05.004 · Cited by 16
Ntsoelinyane, P.-M.-A. H., & Mashele, S. S. (2014) · Bangladesh Journal of Pharmacology · doi:10.3329/bjp.v9i1.16967 · Cited by 16
Isolation of the pyrrolizidine alkaloid 1-epialexine from Castanospermum australe
Jones, L., Hollinshead, J., Fleet, G. W. J., Thompson, A. L., Watkin, D. J., Gál, Z. A., Jenkinson, S. F., Kato, A., & Nash, R. J. (2010) · Phytochemistry Letters · doi:10.1016/j.phytol.2010.04.003 · Cited by 16
Tiecco, M., Testaferri, L., Bagnoli, L., & Scarponi, C. (2008) · Tetrahedron Asymmetry · doi:10.1016/j.tetasy.2008.10.006 · Cited by 16
Chen, G., Huang, H., Ye, J., Wang, A., Huang, H., Zhang, H., & Huang, P. (2012) · Chemistry - An Asian Journal · doi:10.1002/asia.201100809 · Cited by 16
Wu, H., Zeng, W., Chen, G., Guo, Y., Yao, C., Li, J., & Liang, Z. (2018) · Spectrochimica Acta Part A Molecular and Biomolecular Spectroscopy · doi:10.1016/j.saa.2018.08.013 · Cited by 16
Synthesis of (+)-7a-epi-7-deoxycasuarine via cross metathesis
Koch, D., Maechling, S., & Blechert, S. (2007) · Tetrahedron · doi:10.1016/j.tet.2007.05.007 · Cited by 16
Tricase, A. F., Cavalluzzi, M. M., Catalano, A. A., Bellis, M. D., Palma, A. D., Basile, G., Sinicropi, M. S., & Lentini, G. (2025) · Molecules · doi:10.3390/molecules30153213 · Cited by 15
Mancebo‐Aracil, J., Nájera, C., Castelló, L. M., Sansano, J. M., Larrañaga, O., de Cózar, A., & Cossío, F. P. (2015) · Tetrahedron · doi:10.1016/j.tet.2015.10.064 · Cited by 15
A route to selective functionalization of polyhydroxypyrrolidines
Sousa, C. A. D., Rizzo-Aguiar, F., Vale, M. L. C., Xerardo Garcia-mera, B., Caamaño, O., & Rodríguez-Borges, J. E. (2011) · Tetrahedron Letters · doi:10.1016/j.tetlet.2011.12.037 · Cited by 15
Glawar, A. F. G., Jenkinson, S. F., Newberry, S. J., Thompson, A. L., Nakagawa, S., Yoshihara, A., Akimitsu, K., Izumori, K., Butters, T. D., Kato, A., et al. (2013) · Organic & Biomolecular Chemistry · doi:10.1039/c3ob41334a · Cited by 15
Tamayo, J. A., Franco, F., & Sánchez‐Cantalejo, F. (2011) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201101126 · Cited by 15
Mironiuk‐Puchalska, E., Rowicki, T., Sas, W., & Koszytkowska‐Stawińska, M. (2013) · Tetrahedron · doi:10.1016/j.tet.2013.09.008 · Cited by 15
Kato, A., Nakagome, I., Hata, M., Nash, R. J., Fleet, G. W. J., Natori, Y., Yoshimura, Y., Adachi, I., & Hirono, S. (2020) · Molecules · doi:10.3390/molecules25122843 · Cited by 15
Novel one-pot synthesis of 1,2,4-triazolidin-3-thiones comprising piperidine moiety
Gopalakrishnan, M., Kanagarajan, V., & Thanusu, J. (2008) · Green Chemistry Letters and Reviews · doi:10.1080/17518250802644617 · Cited by 15
Pandey, G. D., Grahacharya, D., Shashidhara, K. S., Khan, M. I., & Puranik, V. G. (2009) · Organic & Biomolecular Chemistry · doi:10.1039/b907007a · Cited by 15
Aouadi, K., Abdoul‐Zabar, J., Msaddek, M., & Praly, J. (2014) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201402215 · Cited by 15
Synthesis of thioswainsonine as a potential glycosidase inhibitor
Kumar, N. S., & Pinto, B. M. (2006) · Carbohydrate Research · doi:10.1016/j.carres.2006.04.009 · Cited by 15
Lorin, S., Rajaraman, D., Selvam, S., Ramakrishnan, J., Kumaradhas, P., Nagaraj, K., & Kaliyaperumal, R. (2024) · Zeitschrift für Physikalische Chemie · doi:10.1515/zpch-2023-0397 · Cited by 15
Davies, S. G., Foster, E. M., Lee, J. A., Roberts, P. M., & Thomson, J. E. (2014) · The Journal of Organic Chemistry · doi:10.1021/jo5018298 · Cited by 14
Zhuang, J.-J., Ye, J., Zhang, H., & Huang, P. (2011) · Tetrahedron · doi:10.1016/j.tet.2011.12.063 · Cited by 14
Li, Q. R., Dong, G. R., Park, S. J., Hong, Y. R., Kim, I. S., & Jung, Y. H. (2013) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201300308 · Cited by 14
Unique Diastereoselectivity Trends in Aminyl Radical Cyclizations onto Silyl Enol Ethers
Zlotorzynska, M., Zhai, H., & Sammis, G. M. (2009) · The Journal of Organic Chemistry · doi:10.1021/jo902426z · Cited by 14
Nuti, F., Paolini, I., Cardona, F., Chelli, M., Lolli, F., Brandi, A., Goti, A., Rovero, P., & Papini, A. M. (2007) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2007.04.007 · Cited by 14
Beniazza, R., Desvergnes, V., Mehta, G., Blanchard, N., Robert, F., & Landais, Y. (2011) · The Journal of Organic Chemistry · doi:10.1021/jo101945h · Cited by 14
Eight Stereoisomers of Homonojirimycin from d -Mannose
Lenagh‐Snow, G. M. J., Jenkinson, S. F., Newberry, S. J., Kato, A., Nakagawa, S., Adachi, I., Wormald, M. R., Yoshihara, A., Morimoto, K., Akimitsu, K., et al. (2012) · Organic Letters · doi:10.1021/ol3005744 · Cited by 14
Zoidl, M., Santana, A. G., Torvisco, A., Tysoe, C., Siriwardena, A. H., Withers, S. G., & Wrodnigg, T. M. (2016) · Carbohydrate Research · doi:10.1016/j.carres.2016.04.006 · Cited by 14
Kawamura, M. Y., Talero, A., Santiago, J., Vilca, E. E. G., Rosset, I. G., & Burtoloso, A. C. B. (2016) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.6b01575 · Cited by 14
Miyawaki, S., Hirokami, Y., Kinami, K., Hoshino, M., Minehira, D., Miyamoto, D., Nash, R. J., Fleet, G. W. J., Adachi, I., Toyooka, N., et al. (2016) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2016.10.015 · Cited by 14
Bdira, F. B., Artola, M., Overkleeft, H. S., Ubbink, M., & Aerts, J. M. F. G. (2018) · Journal of Lipid Research · doi:10.1194/jlr.r086629 · Cited by 14
Synthesis of Glycosylated 1‐Deoxynojirimycins Starting from Natural and Synthetic Disaccharides
Liu, B., van Mechelen, J., van den Berg, R. J. B. H. N., van den Nieuwendijk, A. M. C. H., Aerts, J. M. F. G., van der Marel, G. A., Codée, J. D. C., & Overkleeft, H. S. (2018) · European Journal of Organic Chemistry · doi:10.1002/ejoc.201801461 · Cited by 14
Synthesis of 1,2-Dihydroxyindolizidines from 1-(2-Pyridyl)-2-propen-1-ol
Giomi, D., Alfini, R., Micoli, A., Calamai, E., Faggi, C., & Brandi, A. (2011) · The Journal of Organic Chemistry · doi:10.1021/jo201830b · Cited by 14
Koyama, R., Kano, Y., Kikushima, K., Mizutani, A., Soeda, Y., Miura, K., Hirano, T., Nishio, T., & Hakamata, W. (2020) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2020.115492 · Cited by 14
Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines C, O and P
Ribes, C., Falomir, E., Murga, J., Cardá, M., & Marco, J. A. (2009) · Tetrahedron · doi:10.1016/j.tet.2009.10.066 · Cited by 14
Gopalakrishnan, M., Thanusu, J., & Kanagarajan, V. (2008) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.1080/14756360802323902 · Cited by 14
Kato, A., Nakagome, I., Kise, M., Yoshimura, K., Tanaka, N., Nash, R. J., Fleet, G. W. J., Kobayashi, Y., Ikeda, H., Okada, T., et al. (2023) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.3c00637 · Cited by 13
Plant Secondary Metabolites and Their Impact on Human Health
Lal, N., Sahu, N., Shirale, A. O., Gurav, P., Rani, K., MEENA, B. P., Diwan, G., & Biswas, A. K. (2023) · Sustainable plant nutrition in a changing world · doi:10.1007/978-3-031-35147-1_15 · Cited by 14
Total synthesis of radicamine B and 5-epi-radicamine B
Jagadeesh, Y., & Rao, B. V. (2011) · Tetrahedron Letters · doi:10.1016/j.tetlet.2011.09.043 · Cited by 13
Avaliação de extratos vegetais no controle de mosca-branca, Bemisia tabaci biótipo B em abóbora
Lima, B. M. F. V., Moreira, J. O. T., & Aragão, C. A. (2013) · Ciência Agronômica/Revista ciência agronômica · doi:10.1590/s1806-66902013000300026 · Cited by 13
Naresh, A., Marumudi, K., Kunwar, A. C., & Rao, B. V. (2017) · Organic Letters · doi:10.1021/acs.orglett.7b00441 · Cited by 13
An α-glucoside of 1,4-dideoxy-1,4-imino-d-lyxitol with an eleven carbon side chain
Kato, A., Hollinshead, J., Yamashita, Y., Nakagawa, S., Koike, Y., Adachi, I., Yu, C., Fleet, G. W. J., & Nash, R. J. (2010) · Phytochemistry Letters · doi:10.1016/j.phytol.2010.08.006 · Cited by 13
Malik, M., & Jarosz, S. (2016) · Organic & Biomolecular Chemistry · doi:10.1039/c5ob02573g · Cited by 13
Metadata
- Authors
- Watson, A. A., Fleet, G. W. J., Asano, N., Molyneux, R. J., & Nash, R. J.
- Affiliations
- University of Oxford (GB)
- Hokuriku University (JP)
- Western Regional Research Center (US)
- Aberystwyth University (GB)
- Corresponding author
- Nash, Robert J.
- Venue
- Phytochemistry
- Publisher
- Elsevier BV
- Published
- 2001-02
- Volume
- 56
- Issue
- 3
- Pages
- 265-295
- ISSN
- 0031-9422 (ISSN-L)
- OpenAlex
- W2085285145
- Cited by
- 714
- References
- 239
- Citations by year
- 2026: 10 · 2025: 10 · 2024: 17 · 2023: 12 · 2022: 20 · 2021: 21 · 2020: 25 · 2019: 28 · 2018: 20 · 2017: 18 · 2016: 33 · 2015: 29 · 2014: 51 · 2013: 49 · 2012: 41
- FWCI
- 2.11
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Phytochemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Alkaloids: synthesis and pharmacology
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Phytochemistry and Biological Activities
- Physical Sciences › Chemistry › Organic Chemistry › Carbohydrate Chemistry and Synthesis
- Keywords
- polyhydroxylated alkaloids, natural products, glycosidase inhibitors, plant alkaloids, cellular recognition, therapeutic applications, natural product isolation
- MeSH terms
- Alkaloids, Animals, Enzyme Inhibitors, Glycoside Hydrolases, Toxicity Tests
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