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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 ... |