An official website of the United States government.

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

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
7-O-ACETYL-8-EPI-LOGANIC-ACID not available Kohda, H., Tanaka, S., Yamaoka, Y., Yahara, S., Nohara, T., Tanimoto, T., Tanaka, A. 1989. Studies on Lens-Aldose-Reductase Inhibitor in Medicinal Plants.II Active Constituents of Monochasma savatierii FRANCH, et MAXIM. Chem. Pharm. Bull. 37(11):3153-3154
8,9-DIHYDROXY-3-METHOXYCOUMESTAN 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.
8-METHOXY-CIRSILINEOL 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.
ACACETIN not available Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
ACACETIN-7-O-(6''-ALPHA-L-RHAMNOPYRANOSYL)-BETA-D-GLUCOPYRANOSIDE IC50=4.7 uM rat Yoshikawa, M., et al. 1999. Medicinal Flowers. I. Aldose Reductase Inhibitors and Three New Eudesmane-Type Sesquiterpenes, Kikkanols A, B, and C, From the Flowers of Chrysanthemum inducum L. Chem Pharm Bull, 47(3): 340-345.
ACARBOSE 0.4 g/kg diet rat Cohen-Melamed, E., Nyska, A., Pollack, A., Madar, Z. 1995. Aldose Reductase (EC 1.1.1.21) Activity and Reduced-Glutatione Content in Lenses of Diabetic Sand Rats (Psammomys obesus) Fed with Acarbose. Brit J Nutr, 74(5): 607-615.
ACETOSIDE IC50=0.4 ppm Kohda, H., Tanaka, S., Yamaoka, Y., Yahara, S., Nohara, T., Tanimoto, T., Tanaka, A. 1989. Studies on Lens-Aldose-Reductase Inhibitor in Medicinal Plants.II Active Constituents of Monochasma savatierii FRANCH, et MAXIM. Chem. Pharm. Bull. 37(11):3153-3154
ACETYL-TRISULFATE-QUERCETIN IC50=0.1 uM Duke, 1992 *
ACTEOSIDE IC50=0.39 uM Murata, M., Yamakoshi, Y., Homma, S., Arai, K., and Nakamura, Y. 1992. Macrocarpals, Antibacterial Compounds from Eucalyptus, Inhibit Aldose Reductase. Biosci. Biotech. Biochem., 56(12): 2062-2063, 1992.
AESCULETIN IC50=0.74 ug/ml cow Okada,Y,et al.1995.Search for Naturally Occurring Substances to Prevent the Complications of Diabetes.II.Inhibitory Effect of Coumarin and Flavonoid Derivatives on Bovine Lens Aldose Reductase and Rabbit Platelet Aggregation.Chem Pharm Bull43(8):1385-1387
AESCULIN 10 ug/ml cow Okada,Y,et al.1995.Search for Naturally Occurring Substances to Prevent the Complications of Diabetes.II.Inhibitory Effect of Coumarin and Flavonoid Derivatives on Bovine Lens Aldose Reductase and Rabbit Platelet Aggregation.Chem Pharm Bull43(8):1385-1387
ALLO-CYMENE 100 ug/ml (weak activity) Okamura, K., Iwakami, S., Matsunaga, T. 1992. Biological Activity of Monoterpenes from Trees. Toyama-Ken Yakuji Kenkyusho Nenpo, (20): 95-101.
ALLOCRYPTOPINE IC50=27.9 uM rat Al-Khalil, S. 1996. Inhibition of Lens Alkaloids Reductase by Protopine Alkaloids. Saudi Pharm J, 4(1): 45-47.
ALPHA-TERPINENE 100 ug/ml Okamura, K., Iwakami, S., Matsunaga, T. 1992. Biological Activity of Monoterpenes from Trees. Toyama-Ken Yakuji Kenkyusho Nenpo, (20): 95-101.
ALPHA-TERPINEOL 100 ug/ml Okamura, K., Iwakami, S., Matsunaga, T. 1992. Biological Activity of Monoterpenes from Trees. Toyama-Ken Yakuji Kenkyusho Nenpo, (20): 95-101.
AMENTOFLAVONE IC25=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.
APIIN not available Jeffery B. Harborne and H. Baxter, eds. 1983. Phytochemical Dictionary. A Handbook of Bioactive Compounds from Plants. Taylor & Frost, London. 791 pp.
ARENARIOSIDE IC50=2.38 uM Andary, C. Caffeic Acid Glycoside Esters and Pharmacology. Polyphenolic Phenom, 1993: 237-245.
ASCORBIC-ACID not available Challem, J., Berkson, Burt, and Smith, Melissa Dianne. 2000.
Syndrome X - The complete nutritional program to prevent and reservse insulin resistance. John Wiley & Sons, New York. 272 pp. $24.95
ASTILBIN 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.
List of Activity Plants.
Click on column headings to sort table by that column.
Plant Name Common Name Chemical Count Total Parts Per Million
Eucalyptus siderophloia not available 4 77.20000000298023
Eucalyptus sideroxylon not available 4 227
Eucalyptus sparsa not available 4 670
Eucalyptus stoatei not available 4 384
Eucalyptus tereticornis not available 4 208.10000000149012
Eucalyptus tetraptera not available 4 365
Eucalyptus viridis not available 4 11
Eucommia ulmoides Tu Chung; Du Zhong; Gutta-Percha Tree 2 0
Eugenia brasiliensis Brazil Cherry; Grumichama 1 2, 580
Eugenia floribunda Black rumberry; Camu-camu arbol; Camu-camu negro 1 5, 355
Eugenia uniflora Pitanga; Surinam Cherry 1 4, 230
Eupatorium perfoliatum Boneset 7 0
Eupatorium triplinerve Triplinerved eupatorium 1 150
Euphorbia hirta Queensland Asthma Herb 8 443
Euphorbia lathyris Caper Spurge; Mole Plant 3 0
Euphorbia pulcherrima Poinsettia 3 0
Euphorbia tirucalli Aveloz 1 0
Euphrasia officinalis Eyebright 10 17, 567
Fagopyrum esculentum Buckwheat 11 495, 858
Fallopia japonica Japanese Knotweed; Giant Knotweed; Mexican Bamboo; Hu-Zhang 5 50, 800