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Dr. Duke's Phytochemical and Ethnobotanical Databases
U.S. Department of Agriculture
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Aldose-Reductase-Inhibitor

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List of activity chemicals.
Click on column headings to sort table by that column. *Unless otherwise noted all references are to (Duke, 1992)
Chemical Name Dosage Reference
SIDEROXYLONAL-A IC50=1.25 uM Satoh, H., Etoh, H., Watanobe, N., Kawagishi, H., Arai, K., Ina, K. Structures of Sideroxylonals from Eucalyptus sideroxylon. Chem Lett, 1992(10): 1917-1920.
SIDEROXYLONAL-B IC50=2.47 uM Satoh, H., Etoh, H., Watanobe, N., Kawagishi, H., Arai, K., Ina, K. Structures of Sideroxylonals from Eucalyptus sideroxylon. Chem Lett, 1992(10): 1917-1920.
SKULLCAPFLAVONE-II 500 uM rat Shin, K. H., Chae, Y. J., Chung, M. S., Lee, H. J. 1994. Effect of Flavonoids from Scutellariae radix on Cataract Formation and Polyol Accumulation in Rat Lens. Korean J Pharmacog, 25(1): 41-46.
SOPHORICOSIDE IC18=10uM Shimizu, M., Ito, T., Terashima, S., Hayashi, T., Arisawa, M., Morita, N., Kurokawa, S., Ito, K., and Hashimoto, Y. 1984. Inhibition of Lens Aldose Reductase by Flavonoids. Phytochemistry, 23: 1885-1888.
SORBARIN IC70=10uM; IC14=1uM Shimizu, M., Ito, T., Terashima, S., Hayashi, T., Arisawa, M., Morita, N., Kurokawa, S., Ito, K., and Hashimoto, Y. 1984. Inhibition of Lens Aldose Reductase by Flavonoids. Phytochemistry, 23: 1885-1888.
SPIRAEOSIDE IC9=1 uM *
SPIRAEOSIDE IC51=10 uM Shimizu, M., Ito, T., Terashima, S., Hayashi, T., Arisawa, M., Morita, N., Kurokawa, S., Ito, K., and Hashimoto, Y. 1984. Inhibition of Lens Aldose Reductase by Flavonoids. Phytochemistry, 23: 1885-1888.
SUDACHIIN-A 10 uM Okuda, I., Muwa, B., Inagakat, K., Horie, T., Nakayama, M. 1982. Inhibition of Aldose Reductases from Rat and Bovine Lenses by Flavonoids. Biochem Pharmacol, 31(23): 3807-3822.
SUDACHITIN 10 uM Okuda, I., Muwa, B., Inagakat, K., Horie, T., Nakayama, M. 1982. Inhibition of Aldose Reductases from Rat and Bovine Lenses by Flavonoids. Biochem Pharmacol, 31(23): 3807-3822.
SUDACHITIN-7-O-BETA-D-GLUCOSIDE 10 uM Okuda, I., Muwa, B., Inagakat, K., Horie, T., Nakayama, M. 1982. Inhibition of Aldose Reductases from Rat and Bovine Lenses by Flavonoids. Biochem Pharmacol, 31(23): 3807-3822.
SUGIOL Tezuka, Y., Kasimu, R., Basnet, P., Namba, T., Kadota, S. 1997. Aldose Reductase Inhibitory Constituents of the Root of Salvia miltiorhiza Bunge. Chem Pharm Bull, 45(8): 1306-1311.
TANNIC-ACID IC50=1.8 ug/ml Sawada, H., Hamatake, M., Hara, A., Nakagawa, M., Nakayama, T. 1989. Inhibition of Human Placenta Aldose Reductase by Tannic Acid. Chem Pharm Bull, 37(6): 1662-1664.
TANSHINONE-I IC50=4.8 uM rat *
TANSHINONE-II-A IC50=1.14 uM rat *
TAXIFOLIN 60 uM pig Haraguchi, H., Ohmi, I., Masuda, H., Tamura, Y., Mizutani, K., Tanaka, O., Chou, W. H. 1996. Inhibition of Aldose Reductase by Dihydroflavonols in Engelhardtia chrysolepis and Effects on Other Enzymes. Experientia, 52(6): 564-567.
THERMORUBIN IC50=0.006 uM cow Nakayama, M., et al. 1996. Thermorubin from Cultured Thermoactinomyces UAT-8 as Aldose Reductase Inhibitor and Pharmaceutical Compositions Containing Thermorubin for Diabetic Complications. Patent, Japan Kokai Tokkyo Koho-08 59,462. 5pp.
THIAZOCIN-A IC50=0.455 uM Ozasa, T., Yoneda, T., Hirasawa, M., Suzuki, K., Tanaka, K., Kadota, S., Iwanami, M. 1991. Thiazocins, New Aldose Reductase Inhibitors from Actinosynnema sp. I. Fermentation, Isolation and Characterization. J Antibiot, 44(7): 768-773.
THIAZOCIN-B IC50=0.220 uM Ozasa, T., Yoneda, T., Hirasawa, M., Suzuki, K., Tanaka, K., Kadota, S., Iwanami, M. 1991. Thiazocins, New Aldose Reductase Inhibitors from Actinosynnema sp. I. Fermentation, Isolation and Characterization. J Antibiot, 44(7): 768-773.
THYMONIN 10 uM Okuda, I., Muwa, B., Inagakat, K., Horie, T., Nakayama, M. 1982. Inhibition of Aldose Reductases from Rat and Bovine Lenses by Flavonoids. Biochem Pharmacol, 31(23): 3807-3822.
THYMUSIN 10 uM Okuda, I., Muwa, B., Inagakat, K., Horie, T., Nakayama, M. 1982. Inhibition of Aldose Reductases from Rat and Bovine Lenses by Flavonoids. Biochem Pharmacol, 31(23): 3807-3822.
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List of Activity Plants.
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Plant Name Common Name Chemical Count Total Parts Per Million
Echinacea spp Coneflower; Echinacea 11 6, 050
Echinospartium horridum 1 0
Elaeagnus angustifolia Russian Olive; Silver Berry 7 1, 000
Elaeagnus commutata Silver Berry 1 725
Elaeagnus pungens Thorny Silver Berry 1 0
Elaeagnus umbellatus Russian Olive 1 57
Elaeis guineensis African Oil Palm 1 163
Eleocharis dulcis Water chestnut 1 317
Elettaria cardamomum Cardamom 9 1, 013, 601
Eleutherococcus senticosus Eleuthero Ginseng; Siberian Ginseng; Spiny Ginseng; Wu jia; Ci wu jia (Pinyin) 9 42, 418.499994277954
Elsholtzia blanda Bantaluki; Bantulsi 2 8.800000011920929
Elsholtzia cristata Furan Chemotype 2 38.100000001490116
Elsholtzia eriostachya 'Dwarf' Bush Mint 1 0.10000000149011612
Elsholtzia pilosa Hairy Mint Shrub 4 137
Elsholtzia polystachya Bush Mint 6 133.60000005364418
Ephedra gerardiana Pakistani Ephedra 1 0
Ephedra sinica Ma Huang; Chinese Ephedra 8 1, 754
Equisetum arvense Field Horsetail; Horsetail 14 16, 416
Equisetum hyemale Horsetail; Scouring Rush 1 0
Erinacea anthyllis 1 0