- Signaling Pathways
- Metabolic Enzyme/Protease
- Aldehyde Dehydrogenase (ALDH)
Aldehyde Dehydrogenase (ALDH)
Aldehyde Dehydrogenases (ALDHs) are a superfamily of NADP+-dependent enzymes that metabolize endogenous and exogenous aldehydes to corresponding carboxylic acids. This superfamily of proteins is comprised of 19 isozymes, with constitutive activity of at least one isozyme observed in a majority of mammalian tissues. The ALDHs play important roles, among other things, in cellular detoxification, the protection against ultraviolet radiation-induced damage, and amino acid metabolism.
The ALDH1A subfamily plays a pivotal role in embryogenesis and development by mediating retinoic acid signaling. ALDH2, as a key enzyme that oxidizes acetaldehyde, is crucial for alcohol metabolism. ALDH1A1 and ALDH3A1 are lens and corneal crystallins, which are essential elements of the cellular defense mechanism against ultraviolet radiation-induced damage in ocular tissues. Many ALDH isozymes are important in oxidizing reactive aldehydes derived from lipid peroxidation and thereby help maintain cellular homeostasis. Increased expression and activity of ALDH isozymes have been reported in various human cancers and are associated with cancer relapse. As a direct consequence of their significant physiological and toxicological roles, inhibitors of the ALDH enzymes have been developed to treat human diseases.
Aldehyde Dehydrogenase (ALDH) Isoform Specific Products
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Aldehyde Dehydrogenase (ALDH) Inhibitors
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Aldehyde Dehydrogenase (ALDH) Related Products (113)
Related Products (113)
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Antibodies (9)
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Aldehyde Dehydrogenase (ALDH) Isoform Comparison
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(6S)-CP-470711
0 Images(6S)-CP-470711 (Compound 8) is an inhibitor for sorbitol dehydrogenase, that inhibits human and rat SDH with IC50 of 19 nM and 27 nM. (6S)-CP-470711 ameliorates the Streptozotocin (HY-13753)-induced diabetes in rats models. -
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ALDH1A2-IN-1
0 ImagesALDH1A2-IN-1 is an active site-directed reversible ALDH1A2 inhibitor (IC50=0.91 μM; Kd=0.26 μM) with several hydrophobic interactions. -
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Sorbitol dehydrogenase-IN-1
0 ImagesSorbitol dehydrogenase-IN-1 is a potent and orally active sorbitol dehydrogenase inhibitor with IC50 s of 4, 5 nM for rat and human, respectively. Sorbitol Dehydrogenase (SDH) is an enzyme that belongs to the zinc-containing alcohol dehydrogenase (ADH) family. ADH and ALDH are enzymes that work together to metabolize alcohol. -
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Nitrefazole
0 ImagesSynonyms: EMD-15700Nitrefazole (EMD-15700) is an aldehyde dehydrogenase (ALDH) inhibitor. Nitrefazole specifically inhibits human liver ALDH I and human erythrocyte ALDH isozymes, but does not alter the activity of human liver ALDH II or human placental ALDH. Nitrefazole effectively promotes exosome secretion in prostate cancer cells by increasing the levels of Alix, nSMase2, Rab27a and p-ERK. Nitrefazole can be used in studies related to prostate cancer. -
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Daidzin (Standard)
0 ImagesSynonyms: Daidzoside (Standard); NPI-031D (Standard); Daidzein 7-O-glucoside (Standard)Daidzin (Standard) is the analytical standard of Daidzin. This product is intended for research and analytical applications. Daidzin is an isoflavone with antioxidant, anticancer, and antiatherosclerotic activities. Daidzin is a potent and selective inhibitor of mitochondrial ALDH-2. Daidzin reduces ethanol consumption. -
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NCT-505
0 ImagesNCT-505 is a potent and selective aldehyde dehydrogenase (ALDH1A1) inhibitor, with an IC50 of 7 nM, and weakly inhibits hALDH1A2, hALDH1A3, hALDH2, hALDH3A1 (IC50s, >57, 22.8, 20.1, >57 μM). -
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Citral (Standard)
0 ImagesCitral (Standard) is the analytical standard of Citral. This product is intended for research and analytical applications. Citral is an orally active monoterpene compound in lemon grass essential oil and a natural ALDH1A inhibitor, which can induce apoptosis and cycle arrest in breast cancer cell lines, and has analgesic, anti-injurious and anti-inflammatory effects. -
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Aldh2 Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS00570 -
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ABD-3001
0 ImagesCat. No.: HY-124766CAS No.: 350229-29-7ABD-3001 is an inhibitor of ALDH1. ABD-3001 can be studied in research on refractory/relapsed acute myeloid leukemia and high-risk myelodysplastic syndrome. -
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IGUANA-1 free base
0 ImagesSynonyms: STL5-T-0057 -
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- RV01
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CM026
0 ImagesCM026 is a selective aldehyde dehydrogenase 1A1 inhibitor with submicromolar inhibitory activity against aldehyde dehydrogenase 1A1. Its inhibitory mechanism is related to binding to the aldehyde binding pocket and utilizing a unique glycine residue. It can be used as a chemical tool to study the role of this enzyme in disease. -
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7-Hydroxy-4-phenylcoumarin
0 ImagesCat. No.: HY-W207195CAS No.: 2555-30-8Synonyms: 4-Phenylumbelliferone7-Hydroxy-4-phenylcoumarin is a dual ALDH-2 and MAO inhibitor, with IC50 values of 1.5 and 0.5 µM, respectively. -
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Dodecanal
0 ImagesDodecanal is an aliphatic aldehyde and serves as the major volatile metabolite in the leaves, stems and roots of Polygonum minus. Dodecanal acts as a substrate for oxidation reactions and is converted into dodecanoic acid by endogenous ALDH enzymes. Dodecanal is an intermediate in the biological oxidation pathway of n-dodecane and the biotransformation pathway of ω-aminododecane. -
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FSI-TN42
0 ImagesSynonyms: N42FSI-TN42 (N42) is a selective, orally active and irreversible ALDH1A1 inhibitor with an IC50 of 23 nM. FSI-TN42 shows 800-fold more potent against ALDH1A1 than ALDH1A2 (IC50obesity. -
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ALDH2 Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS00568 -
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CM121
0 ImagesCM121 is an active site-directed reversible ALDH1A2 inhibitor (IC50=0.54 μM;Kd=1.1 μM) with a variety of hydrophobic interactions. -
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- Taraxerone
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ALDH3A1-IN-4
0 ImagesALDH3A1-IN-4 is a selective ALDH3A1 inhibitor with an IC50 of 0.2 μM. ALDH3A1-IN-4 binds to the aldehyde-binding pocket of ALDH3A1 via hydrophobic interactions and van der Waals forces. ALDH3A1-IN-4 acts as a chemosensitizer that sensitizes ALDH3A1-expressing cancer cells to the antiproliferative effect of mafosfamide, but does not produce a sensitizing effect on non-cancer cells that do not express ALDH3A1. ALDH3A1-IN-4 is applicable to research related to lung adenocarcinoma and glioblastoma. -
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Coprine
0 ImagesCat. No.: HY-122373CAS No.: 58919-61-2Coprine is an orally active disulfiram (HY-B0240)-like component and an inhibitor of aldehyde dehydrogenase. Coprine is isolated from Coprinus atranentarius. Coprine inhibits low Km aldehyde dehydrogenase in rat liver and increases blood acetaldehyde levels during in vivo ethanol metabolism. Coprine does not inhibit semi-purified low Km aldehyde dehydrogenase from rat liver in vitro. Coprine can be used in studies related to alcoholism. -
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