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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
NEOASTILBIN 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.
NEPETIN ED50=1 uM Duke, 1992 *
NEPETRIN ED50=1-10 uM Duke, 1992 *
NEROLIDOL not available Duke, 1992 *
NEVADENSIN 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.
ORAPOSIDE IC50=0.15 uM Andary, C. Caffeic Acid Glycoside Esters and Pharmacology. Polyphenolic Phenom, 1993: 237-245.
OROXYLIN-A IC50=52 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.
OXYAYANIN-A IC27=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.
P-COUMARIC-ACID 4 ug/ml (weak activity) Ichikawa, K., et al. 1991. Isolation and Structure Determination of Aldose Reductase Inhibitors from Traditional Thai Medicine, and Syntheses of Their Derivatives. Sankyo Kenkyusho Nempo, 43: 99-110.
PECTOLINARIGENIN 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.
PECTOLINARIN IC42=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.
PENTABROMOPROPEN-2-YL-DIBROMO-ACETATE 4 ug/ml Sugano, M., Sato, A., Nagaki, H., Yoshioka, S., Shiraki, T., Horikoshi, H. 1990. Aldose Reductase Inhibitors from the Red Alga, Asparagopsis taxiformis. Tetrahedron Lett, 31(48): 7015-7016.
PENTABROMOPROPEN-2-YL-TRIBROMO-ACETATE 4 ug/ml Sugano, M., Sato, A., Nagaki, H., Yoshioka, S., Shiraki, T., Horikoshi, H. 1990. Aldose Reductase Inhibitors from the Red Alga, Asparagopsis taxiformis. Tetrahedron Lett, 31(48): 7015-7016.
PERILLOSIDE-A 0.1 mM/l rat Fujita, T., Ohira, K., Miyatake, K., Nakano, Y., Nakayama, M. 1995. Inhibitory Effect of Perillosides A and C, Related Monoterpene Glucosides on Aldose Reductase and Their Structure-Activity Relationships. Chem Pharm Bull, 43(6): 920-926.
PERILLOSIDE-A 0.1 mM/l hmn (weak activity) Fujita, T., Ohira, K., Miyatake, K., Nakano, Y., Nakayama, M. 1995. Inhibitory Effect of Perillosides A and C, Related Monoterpene Glucosides on Aldose Reductase and Their Structure-Activity Relationships. Chem Pharm Bull, 43(6): 920-926.
PERILLOSIDE-B 0.1 mM/l rat Fujita, T., Ohira, K., Miyatake, K., Nakano, Y., Nakayama, M. 1995. Inhibitory Effect of Perillosides A and C, Related Monoterpene Glucosides on Aldose Reductase and Their Structure-Activity Relationships. Chem Pharm Bull, 43(6): 920-926.
PERILLOSIDE-C 0.1 mM/l rat Fujita, T., Ohira, K., Miyatake, K., Nakano, Y., Nakayama, M. 1995. Inhibitory Effect of Perillosides A and C, Related Monoterpene Glucosides on Aldose Reductase and Their Structure-Activity Relationships. Chem Pharm Bull, 43(6): 920-926.
PERILLOSIDE-C 0.1 mM/l hmn (weak activity) Fujita, T., Ohira, K., Miyatake, K., Nakano, Y., Nakayama, M. 1995. Inhibitory Effect of Perillosides A and C, Related Monoterpene Glucosides on Aldose Reductase and Their Structure-Activity Relationships. Chem Pharm Bull, 43(6): 920-926.
PERILLOSIDE-D 0.1 mM/l rat Fujita, T., Ohira, K., Miyatake, K., Nakano, Y., Nakayama, M. 1995. Inhibitory Effect of Perillosides A and C, Related Monoterpene Glucosides on Aldose Reductase and Their Structure-Activity Relationships. Chem Pharm Bull, 43(6): 920-926.
PROTOPINE IC50=38.5 uM rat Al-Khalil, S. 1996. Inhibition of Lens Alkaloids Reductase by Protopine Alkaloids. Saudi Pharm J, 4(1): 45-47.
List of Activity Plants.
Click on column headings to sort table by that column.
Plant Name Common Name Chemical Count Total Parts Per Million
Cucumis melo Cantaloupe; Melon; Muskmelon; Netted Melon; Persian Melon; Nutmeg Melon 4 26, 220
Cucumis sativus Cucumber 2 0
Cucurbita pepo Pumpkin 5 6, 844
Cucurbita spp Summer Squash 1 2, 340
Cuminum cyminum Cumin 11 174, 336
Cunila origanoides Mountain Dittany; Frost Flower; Frost Mint; Maryland Dittany; American Dittany; Stone Mint; Dittany 4 63, 112
Curcuma longa Turmeric; Indian Saffron 10 29, 266
Cuscuta reflexa Amarbel 2 0
Cyamopsis tetragonoloba Guar; Cluster-Bean; Siam-Bean 9 9, 870
Cyclanthera pedata Achocha 1 2, 800
Cydonia oblonga Quince 3 960
Cymbopogon citratus West Indian Lemongrass; Lemongrass 6 7, 200
Cymbopogon flexuosus East Indian Lemongrass 1 0
Cymbopogon nardus Ceylon Citronella; Citronella 4 912
Cymbopogon parkeri Skhabar 2 70
Cymbopogon winterianus Java Citronella; Mahapengiri 2 294
Cynara cardunculus Artichoke 12 828
Cyperus rotundus Nutsedge 1 90
Cyphomandra betacea Tamarillo; Tree Tomato 1 4, 120
Cyrtosperma chamissonis Swamp Taro 1 762