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Biological Activity Aldose-Reductase-Inhibitor

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 Duke, 1992 *
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 not available 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 Duke, 1992 *
TANSHINONE-II-A IC50=1.14 uM rat Duke, 1992 *
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.
List of Activity Plants.
Click on column headings to sort table by that column.
Plant Name Common Name Chemical Count Total Parts Per Million
Pouteria caimito Abiu; Caimito 1 3, 780
Pouteria campechiana Canistel 1 1, 475
Pouteria viridis Green Sapote; Sapote Verde 1 2, 720
Prosopis juliflora Mesquite 1 0
Prunella vulgaris Self-Heal; Heal-All 12 492, 000
Prunus aequinoctialis not available 1 0
Prunus africana Bitter Almond; Red Stinkwood 1 220
Prunus armeniaca Apricot 13 36, 145
Prunus avium Cereza; Sweet Cherry 1 0
Prunus cerasus Sour Cherry 16 873
Prunus domestica Plum 6 699
Prunus dulcis Almond 8 63
Prunus laurocerasus Cherry Laurel 6 15, 000
Prunus mahaleb not available 1 0
Prunus maximowiczii not available 1 0
Prunus nipponica not available 1 0
Prunus persica Peach 11 1, 127
Prunus salicifolia Capulin; Wild Cherry 1 2, 830
Prunus serotina Black Cherry; Wild Cherry 6 31, 124
Prunus spinosa Blackthorn; Sloe 6 0