Hydroxysteroid dehydrogenase like 1 (HSDL1) is an enzyme encoded by the HSDL1 gene, and it prominently showcases oxidoreductase activity. It's primarily localized within the intermediate filament cytoskeleton and the mitochondrion. As an oxidoreductase, this enzyme is fundamental in catalyzing oxidation-reduction reactions, which involve the transfer of electrons between different molecules. Such reactions are pivotal for various metabolic pathways, ensuring that cells can efficiently process nutrients, detoxify poisons, and manage energy resources. Given its fundamental role, any modulation of HSDL1's function can have significant effects on cellular metabolism and overall physiological balance.
The class of compounds that inhibit HSDL1 can be broadly categorized based on their mode of action and the pathways they influence. These inhibitors often target the oxidoreductase functionality of the enzyme. Some of them work by directly binding to the enzyme's active site, thus stopping the substrate from interacting with the enzyme and subsequently hindering the catalytic process. Others might exert their inhibitory effect by altering the enzyme's redox state, making it either too reduced or too oxidized to function efficiently. In addition, some inhibitors might modulate the enzyme's function by influencing associated pathways or molecules, thereby creating an environment where HSDL1's activity is indirectly affected. Another subset of inhibitors might work by modifying key amino acid residues in the enzyme, rendering it inactive.
SEE ALSO...
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
Originally an aldehyde dehydrogenase inhibitor, disulfiram may influence the oxidoreductase function of HSDL1 by altering its redox state. | ||||||
Cyanamide | 420-04-2 | sc-239592 sc-239592A | 5 g 25 g | $21.00 $77.00 | ||
As an inhibitor of aldehyde dehydrogenases, cyanamide might indirectly influence the oxidoreductase activity of HSDL1. | ||||||
Fomepizole | 7554-65-6 | sc-252838 | 1 g | $74.00 | 1 | |
This compound is an inhibitor of alcohol dehydrogenase and might show cross-reactivity with other oxidoreductases. | ||||||
Raloxifene | 84449-90-1 | sc-476458 | 1 g | $802.00 | 3 | |
Though primarily an estrogen receptor modulator, it can influence the oxidoreductase activity in some enzymes indirectly. | ||||||
IBMX | 28822-58-4 | sc-201188 sc-201188B sc-201188A | 200 mg 500 mg 1 g | $159.00 $315.00 $598.00 | 34 | |
Being a non-selective inhibitor of phosphodiesterases, it can alter cellular cAMP levels, possibly influencing HSDL1 indirectly. | ||||||
α-Iodoacetamide | 144-48-9 | sc-203320 | 25 g | $250.00 | 1 | |
A general cysteine protease inhibitor which can modify enzyme active sites containing cysteine and might impact HSDL1 activity indirectly. | ||||||
Phenethyl-hydrazine | 51-71-8 | sc-331686 | 500 mg | $388.00 | ||
Known as a monoamine oxidase inhibitor, its broad activity might theoretically influence the oxidoreductase activity of HSDL1. |