| E7260 |
Tolrestat
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Tolrestat is a potent, orally active aldose reductase inhibitor with IC50 of 35 nM.
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| E7937 |
Fidarestat
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Fidarestat (SNK 860) is an inhibitor of aldose reductase, with IC50s of 26 nM, 33 μM, and 1.8 μM for aldose reductase, AKR1B10 and V301L AKR1B10, respectively; this compound has the potential to treat diabetic disease.
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| S1202 |
Dutasteride
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Dutasteride (GI198745, GG-745) is a dual 5-α reductase inhibitor that inhibits conversion of testosterone to dihydrotestosterone (DHT).
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Chemical and Pharmaceutical Bulletin, 2025, 857-867
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Neoplasia, 2024, 101045
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Neoplasia, 2024, 57:101045
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| S2404 |
Isoliquiritigenin
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Isoliquiritigenin, an anti-tumor flavonoid from the root of Glycyrrhiza glabra, inhibits aldose reductase with an IC50 of 320 nM.
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Proceedings of the National Academy of Sciences, October 16 2018, E9869-E9878
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The American Journal of Chinese Medicine, November 04 2023, 2221-2241
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J Nutr Biochem, 2024, 136:109808
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| S1197 |
Finasteride
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Finasteride (MK-906) is a potent, reversible inhibitor of the rat type 1 5 alpha-reductase with Ki of 10.2 nM, used in the treatment of benign prostatic hyperplasia (BPH) and male pattern baldness (MPB).
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PLoS One, June 2, 2016, e0156549
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Frontiers in Pharmacology, February 20, 2023, 1038039
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Biochem Pharmacol, 2025, 241:117171
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| S2035 |
Epalrestat
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Epalrestat is an aldose reductase inhibitor with IC50 of 72 nM.
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Cell Rep Med, 2023, 4(6):101056
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Free Radic Biol Med, 2021, 163:220-233
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J Agric Food Chem, 2020, 68(42):11747-11757
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| S9170 |
Engeletin
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Engeletin (Dihydrokaempferol 3-rhamnoside), a bioactive flavonoid, has multiple biological activities such as anti-diabetic and anti-inflammatory effects. engeletin againsts LPS-stimulated endometritis in mice via negative regulation of pro-inflammatory mediators via the TLR4-regulated NF-κB pathway.
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Journal of Inflammation Research, October 10, 2022, 5767-5783
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Journal of Inflammation Research, 2022, 5767-5783
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J Inflamm Res, 2022, 15:5767-5783
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| S5803 |
Alrestatin
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Alrestatin is an inhibitor of aldose reductase which is involved in the pathogenesis of complications of diabetes mellitus, including diabetic neuropathy.
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iScience, 2022, 25(4):104153
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| S5910 |
Alpha-Estradiol
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Alpha-Estradiol (α-Estradiol, 17 alpha-Estradiol, Alfatradiol, Epiestradiol, Epiestrol, Alora, 17 α-E2), a natural, non-feminizing stereoisomer, a hormonally almost inactive isomer of physiological 17 beta-estradiol (17 β-E2), is a weak inhibitor of estrogen.
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Biomater Res, 2024, 28:0010
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| S1074 |
Poliumoside
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Poliumoside exhibits significant inhibition of advanced glycation end product formation with IC50 values of 19.69 µM. In the rat lens aldose reductase assay. This compound exhibits greater inhibitory effects on rat lens aldose reductase(RLAR) with IC50 values of 8.47 µM.
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| S5446 |
2-Chloro-1-(4-fluorobenzyl)benzimidazole
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2-Chloro-1-(4-fluorobenzyl)benzimidazole is an aldose reductase (ALR2) inhibitor which is used for preparation of disubstituted benzimidazole derivative.
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| E5720 |
Isocurcumenol
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Isocurcumenol, an estrogen receptor alpha (ERα) inhibitor isolated from Curcuma zedoaria Rhizomes, possesses anti-tumor acticity, with IC50 values of 99.1μg/mL and 178.2 μg/mL in DLA and KB cells, respectively.
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