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
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