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Biological Activity 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
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 50 uM Kubo, M., et al. 1994. Studies on Anti-cataract Drugs from Natural Sources. I. Effects of a Methanolic Extract and the Alkaloidal Components from Corydalis Tuber on in vit Aldose Reductase Activity. Biol Pharm Bull, 17(3): 458-459.
List of Activity Plants.
Click on column headings to sort table by that column.
Plant Name Common Name Chemical Count Total Parts Per Million
Myrciaria cauliflora Jaboticaba 1 1, 770
Myrciaria dubia Camu-camu (Eng.,Peru,Scn.,Sp.); Rumberry (Eng.); Camo Camo (Peru); Araza de Agua (Sp.); Camu-camu Negro (Peru); Guapuro Blanco (Bol.) 5 0
Myrica cerifera Bayberry; Wax Myrtle; Southern Bayberry; Candle-Berry 4 2, 624
Myristica fragrans Mace; Nutmeg; Muskatnussbaum (Ger.); nogal moscado (Sp.); nuez moscada (Sp.) 10 1, 931, 915
Myroxylon balsamum Peru Balsam; Tolu Balsam 5 8, 000
Myrrhis odorata Garden Myrrh; Myrrh; Sweet Chervil; Sweet Cicely; Cicely 6 223, 000
Myrtus communis Myrtle; Myrte (Ger.); Arrayan (Sp.); Mirto (Sp.) 9 3, 988
Nandina domestica Heavenly Bamboo; Sacred Bamboo; Southern Heaven Bamboo; Nanten (Jap.) 3 400
Narcissus tazetta Daffodil 1 190
Nasturtium officinale Berro; Watercress 2 28, 120
Nelumbo nucifera Water Lotus 9 15
Neonotonia wightii not available 1 4.989999771118164
Nepeta cataria Catnip 4 7, 240
Nepeta racemosa Catmint 5 432
Nerium oleander Oleander 4 0
Nicotiana glauca Tree Tobacco 1 42, 000
Nicotiana tabacum Tobacco 11 20, 025
Nigella sativa Black Cumin; Roman Coriander; Fennel-Flower; Nutmeg-Flower; Black Caraway 3 16, 885
Ocimum basilicum Basil; Sweet Basil; Cuban Basil 19 606, 120
Ocimum canum Hoary Basil 4 270