199 Results for "

ALDH

" in MedChemExpress (MCE) Product Catalog:
Products (199)

199 Results for "ALDH" in MCE Product Catalog:

Cat. No.: HY-W207195
CAS No.: 2555-30-8
Synonyms: 4-Phenylumbelliferone
7-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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Cat. No.: HY-D3183
CAS No.: 1623011-10-8
AldRed 659-A is a red-shifted fluorescent substrate for aldehyde dehydrogenase (ALDH). AldRed 659-A exhibits only minimal fluorescent uptake shift in comparison with DEAB (ALDH inhibitor)-treated control .
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Cat. No.: HY-W016645R
CAS No.: 120-21-8
Research Areas:  

Cancer

4-Diethylaminobenzaldehyde is a reversible aldehyde dehydrogenases (ALDHs) inhibitor, with a Ki of 4 nM for ALDH1. 4-Diethylaminobenzaldehyde displays potent anti-androgenic effect (IC50= 1.71μM) .
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Cat. No.: HY-D3182
CAS No.: 2252329-12-5
AldeRed 588-A is a fluorescent labeling reagent and a substrate for aldehyde dehydrogenase (ALDH). AldeRed 588-A is metabolized by functionally active ALDH enzymes, thereby specifically labeling viable ALDH bright cell populations with red-shifted fluorescence. AldeRed 588-A supports one-step isolation and sorting of ALDH-expressing cells (including normal stem cells and cancer stem cells), and can be used in combination with green fluorophores for multicolor experimental applications. AldeRed 588-A is widely applicable to research related to various cancers such as bladder cancer, breast cancer, and head and neck cancer .
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Cat. No.: HY-N0018R
CAS No.: 552-66-9
Synonyms: 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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Cat. No.: HY-157567
CAS No.: 2445840-25-3
Purity:  98.05%
Synonyms: N42
Research Areas:  

Metabolic Disease

FSI-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 (IC50
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Cat. No.: HY-177639A
CAS No.: 2728713-54-8
Synonyms: NN-6020 sodium
Research Areas:  

Metabolic Disease

Lefelsiran sodium is a siRNA targeted to ALDH2. It is used for the study of alcohol use disorder.
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Cat. No.: HY-D3185
CAS No.: 2243148-62-9
AlDeSense AM is a cell-permeable ALDH1A1-selective fluorescent reporter. AlDeSense AM is oxidized by ALDH1A1, which eliminates photoinduced electron transfer quenching and enhances the fluorescent signal. AlDeSense AM can be used to detect cells with cancer stem cell properties, as well as to monitor the plasticity of cancer stem cells in cell culture systems and animal models. AlDeSense AM is applicable to the study of cancers associated with cancer stem cells, including chronic myeloid leukemia, melanoma, and breast cancer .
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Cat. No.: HY-135214
CAS No.: 851053-64-0
Research Areas:  

Cancer

GA11 is an ALDH inhibitor that shows activity against glioblastoma both in vitro and in vivo .
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Cat. No.: HY-121817
CAS No.: 95-05-6
Purity:  96.35%
Sulfiram is a very weak aldehyde dehydrogenase (ALDH) inhibitor, with an IC50 value of 413 μM against Saccharomyces cerevisiae ALDH. As a photochemical precursor, Sulfiram undergoes photoconversion to form Disulfiram (HY-B0240), a potent ALDH inhibitor. Sulfiram inhibits the dimerization of the extracellular domain fragment (amino acid residues 230-624) of amyloid precursor protein (APP), alters the monomer-dimer equilibrium, induces conformational changes in the fragment, and enhances the production of sAPPα via α-cleavage of APP. Sulfiram can be used in research related to scabies and Alzheimer's disease .
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Cat. No.: HY-177639
CAS No.: 2765645-87-0
Synonyms: NN-6020
Research Areas:  

Metabolic Disease

Lefelsiran (NN-6020) is a siRNA targeted to ALDH2. It is used for the study of alcohol use disorder.
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Cat. No.: HY-18768A
CAS No.: 2080306-22-3
Research Areas:  

Cancer

NCT-501 hydrochloride is a potent and selective theophylline-based inhibitor of aldehyde dehydrogenase 1A1 (ALDH1A1), inhibits hALDH1A1 with IC50 of 40 nM, typically shows better selectivity over other ALDH isozymes and other dehydrogenases (hALDH1B1, hALDH3A1, and hALDH2, IC50 >57 μM) .
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Cat. No.: HY-B1877
CAS No.: 1836-75-5
Research Areas:  

Cancer

Nitrofen is a selective contact herbicide. Nitrofen is a retinal dehydrogenase (belongs to the ALDH family) and protoporphyrinogen oxidase inhibitor .
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Cat. No.: HY-112278
CAS No.: 2231098-99-8
Purity:  99.95%
Research Areas:  

Cancer

NCT-506 is an orally bioavailable aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitors with an IC50 of 7 nM .
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Cat. No.: HY-129314
CAS No.: 361156-54-9
Research Areas:  

Cancer

CM-39 is a non-covalent and reversible inhibitor for aldehyde dehydrogenase 1A (ALDH1A) with an IC50 of 0.9 μM .
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Cat. No.: HY-168985
CAS No.: 1804941-96-5
Mirivadelgat is an activator of aldehyde dehydrogenase 2 (ALDH2). Mirivadelgat is used for research on interstitial lung disease-associated pulmonary hypertension and cancer .
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Cat. No.: HY-122577
CAS No.: 2094547-67-6
Purity:  99.56%
Research Areas:  

Cancer

EN40 is a potent, selective aldehyde dehydrogenase 3A1 (ALDH3A1) inhibitor as a covalent ligand, exhibits an IC50 value of 2 uM
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Cat. No.: HY-124766
CAS No.: 350229-29-7
Research Areas:  

Cancer

ABD-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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Cat. No.: HY-139005
CAS No.: 247069-93-8
Synonyms: BAAA-DA
Target:  

Fluorescent Dye

Research Areas:  

Others

BODIPY aminoacetaldehyde diethyl acetal is a stable precursor to BODIPY-aminoacetaldehyde and can be converted into BODIPY-aminoacetaldehyde under acidic conditions. BODIPY-aminoacetaldehyde is a fluorescent substrate for aldehyde dehydrogenase (ALDH) .
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Cat. No.: HY-139032
CAS No.: 2204230-40-8
Research Areas:  

Others

CM121 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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