Title : Long-chain fatty acids inhibit human members of the aldo-keto reductase 1C subfamily.

Pub. Date : 2017 Nov 1

PMID : 28992312






1 Functional Relationships(s)
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1 The most potent inhibitors for AKR1C1, AKR1C2 and AKR1C4 were docosahexaenoic acid (Ki 0.77 microM), palmitoleic acid (Ki 0.41 microM) and linoleic acid (Ki 0.33 microM), respectively. palmitoleic acid aldo-keto reductase family 1 member C2 Homo sapiens