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Results 1 - 10 of 26 > >>
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EC Number Inhibitors Commentary Structure
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.13513-demethyl-13,14-dihydro-all-trans-retinyl trifluoroacetate competitive with respect to dipalmitoylphosphocholine, uncompetitive with respect to all-trans-retinol; reversible inhibitor Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.135all-trans-retinyl-alpha-bromoacetate irreversible inhibition Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.135all-trans-retinyl-alpha-bromoacetate - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.135all-trans-retinylbromoacetate - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.135Apo-cellular-retinol-binding protein - Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.135apo-CRBP-I i.e. apo-[cellular retinol-binding protein I], no inhibition by apo-CRBP-III Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.135fenretinide used clinically to presumably lower blood retinol-binding protein levels and thus decrease circulating retinol, targets the functional coupling of STRA6 and LRAT to increase cellular vitamin A uptake in peripheral tissues Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.135more inactivated by trivalent arsenicals Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.135more 1% dimethylsulfoxide does not inhibit LRAT activity Go to the Ligand Summary Page
Display the word mapDisplay the reaction diagram Show all sequences 2.3.1.135more 1-acyl-lysophosphatidylcholine does not inhibit LRAT up to 0.020 mM; product inhibition by retinyl ester can be ruled out Go to the Ligand Summary Page
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