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Search Results for " aldh "

20

Compounds

Cat No. Product Name Synonyms Targets
T4778 3-Hydroxybenzaldehyde Others , Dehydrogenase
3-Hydroxybenzaldehyde is a compound useful in organic synthesis.
TJS1382 Taraxerone Dehydrogenase
Taraxerone has allelopathic and antifungal effects.Taraxerone prevents catalase, superoxide dismutase, and reduces glutathione concentrations from the decrease induced by ethanol administration with the concentration dep...
T12196 NCT-505 Dehydrogenase
NCT-505 is a potent and selective inhibitor of aldehyde dehydrogenase (ALDH1A1, IC50 = 7 nM) and a weak inhibitor of hALDH1A2, hALDH1A3, hALDH2, hALDH3A1 with IC50 values of >57 μM, 22.8 μM, 20.1 μM, >57 μM respectively...
T6903 NCT-501 NCT501 Dehydrogenase
NCT-501 is a potent and selective inhibitor of Aldehyde Dehydrogenase 1A1 (ALDH1A1) with IC50 of 40 nM.
T2662 Alda-1 Alda 1 Apoptosis , Dehydrogenase
Alda-1 is an ALDH2 agonist, a cell-permeable activator of both the wild-type ALDH2*1 and the Asian E487K mutant ALDH2*2 forms of mitochondrial aldehyde dehydrogenase 2 (mtALDH2).
T4S0878 Prunetin Prunusetin ERK , Dehydrogenase , NF-κB
1. Prunetin (Prunusetin) significantly reduces serum levels of inflammatory cytokines and mortality in mice challenged with lipopolysaccharide. 2. Prunetin mediates anti-obesity/adipogenesis effects by suppressing obesit...
T10140 4-Diethylaminobenzaldehyde Dehydrogenase
4-Diethylaminobenzaldehyde is a reversible aldehyde dehydrogenase (ALDH) inhibitor (Ki: 4 nM for ALDH1). It displays a potent anti-androgenic effect (IC50: 1.71μM).
T23533 WIN 18446 Dehydrogenase
inhibitor of aldehyde dehydrogenase 1a2 (ALDH1a2)
T7835 CM10 CM 10 Dehydrogenase
CM10 is an aldehyde dehydrogenase 1A family(ALDH1A) inhibitor.
T10148 4-Hydroxynonenal 4-HNE Dehydrogenase , Endogenous Metabolite
4-Hydroxynonenal (4-HNE) (4-HNE) is an oxidative/nitrosative stress biomarker. It is a substrate and an inhibitor of acetaldehyde dehydrogenase 2 (ALDH2).
T0054 Disulfiram Tetraethylthiuram disulfide,NSC 190940,TETD Dehydrogenase , Interleukin , Pyroptosis
Disulfiram (TETD) is an inhibitor of the acetaldehyde dehydrogenase ALDH, inhibiting hALDH1 and hALDH2 (IC50=0.15/1.45 μM) with specificity. Disulfiram is acutely sensitized to alcohol and also inhibits GSDMD pore format...
T1389 Dyclonine hydrochloride Dyclocaine hydrochloride,Dyclonine HCl Sodium Channel , Antibacterial , Antifungal
Dyclonine hydrochloride (Dyclonine HCl) , an over the counter throat lozenge, is found in Sucretswith local anesthetic effect .
T15022 CVT-10216 Dehydrogenase
CVT-10216 is a Potent and selective, reversible inhibitor of aldehyde dehydrogenase 2 (ALDH2) (IC50: 29 nM). CVT-10216 also has inhibitory effect of ALDH-1 (IC50: 1.3 μM). CVT-10216 can reduce excessive alcohol drinking...
T39675 ALDH1A2-IN-1 ALDH1A2-IN-1
ALDH1A2-IN-1 is a reversible inhibitor of the active site of ALDH1A2, showing a significant affinity for the enzyme with an IC50 value of 0.91 μM and a Kd value of 0.26 μM. This compound interacts hydrophobically with th...
T60240 ALDH1A3-IN-2 Dehydrogenase
ALDH1A3-IN-2 is a potent ALDH1A3 inhibitor with an IC50 of 0.30 μM.ALDH1A3-IN-2 has potential for cancer disease research.
T67832 ALDH2 modulator 1 Dehydrogenase
ALDH2 modulator 1 is a potent and orally active modulator of acetaldehyde dehydrogenase-2 (ALDH2), which reduces blood alcohol levels in mice.
T63341 ALDH1A1-IN-2 Dehydrogenase
ALDH1A1-IN-2 is a potent aldehyde dehydrogenase 1a1 (aldh1a1) inhibitor with anticancer activity.ALDH1A1-IN-2 may be used in the study of breast cancer, inflammation or obesity.
T60372 ALDH3A1-IN-1
ALDH3A1-IN-1 (Compound 18) is a potent ALDH3A1 inhibitor with an IC 50 of 1.61 μM. ALDH3A1-IN-1 is more potent than DEAB against patient-derived primary prostate tumor epithelial cells, as single agents or in combination...
T64347 ALDH1A3-IN-3 Dehydrogenase
ALDH1A3-IN-3 (compound 16), a powerful ALDH1A3 inhibitor with an IC50 of 0.26 μM, serves as an effective ALDH3A1 substrate. It is utilized in prostate cancer research.
T60275 ALDH3A1-IN-2
ALDH3A1-IN-2 (Compound 19), a potent inhibitor of aldehyde dehydrogenases (ALDHs), demonstrates high efficacy against ALDH3A1 with an IC50 of 1.29 μM. Given the overexpression of ALDHs in multiple tumor types, including ...
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