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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
REYNOUTRIN IC34=1 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.
RHAMNETIN IC23=1 uM Duke, 1992 *
RHAMNETIN IC57=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.
RHAMNOCITRIN 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
RHOIFOLIN IC32=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.
ROSMARINIC-ACID not available Duke, 1992 *
RUTIN 4 ug/ml 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.
RUTIN 100 uM Duke, 1992 *
SALBOSTATIN IC50=0.7 mM Vertesy, L., Fehlhaber, H., Schulz, a. 1994. The Trehalase Inhibitor Salbostatin, a Novel Metabolite from Streptomyces albus, ATCC21838. Angew Chem Int Ed Engl, 33(18): 1844-1846.
SALFREDIN-A-4 not available Matsumoto, K., et al. 1995. Salfredins, New Aldose Reductase Inhibitors Produced by Crucibulum sp. RF-3817. I. Fermentation, Isolation and Structures of Salfredins. J Antibiot, 48(6): 439-446.
SALFREDIN-C-2 not available Matsumoto, K., et al. 1995. Salfredins, New Aldose Reductase Inhibitors Produced by Crucibulum sp. RF-3817. I. Fermentation, Isolation and Structures of Salfredins. J Antibiot, 48(6): 439-446.
SALICYLIC-ACID 724.6 uM Toyomizu, M., Sugiyama, S., Jin, R. L., Nakatsu, T. 1993. Alpha-Glucosidase and Aldose Reductase Inhibitors: Constituents of Cashew, Anacardium occidentale, Nut Shell Liquids. Phytotherapy Research, 7(3): 252-254.
SALVIANOLIC-ACID-A 0.01 uM rat Du, G. H., Qiu, Y., Tian, Y. E., Zhang, J. T. 1995. Prevention of Galactose-Induced Cataractogenesis in Rats by Salvianolic Acid A. Yao Hsueh Hsueh Pao, 30(8): 561-566.
SAMBUNIGRIN 0.1 mM/l rat (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.
SANGGENONE-C 100 uM Yamaguchi, T., Sato, J., Mihashi, H., Nomura, T. 1991. Aldose Reductase Inhibitors Containing Benzopyrans for Treatment of Diseases Associated with Diabetes. Patent, Japan Kokai Tokkyo Koho-03 68,517. 9pp.
SAPPANCHALCONE 0.1 uM Morota, T., Takeda, H., Sasaki, H., Sato, S. 1990. Aldose Reductase Inhibitors Containing Phenol of Caesalpinia sappan. Patent, Japan Kokai Tokkyo Koho-02 264,718.
SCOPARONE 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
SCOPOLETIN IC50=6.2 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
SCUTELLAREIN IC56=10uM; IC10=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.
SIDERITOFLAVONE not available Duke, 1992 *
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