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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 349438-38-6 Chemical Structure| 349438-38-6

Structure of Alda-1
CAS No.: 349438-38-6

Chemical Structure| 349438-38-6

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Alda-1 is a potent and selective ALDH2 agonist that activates wild-type ALDH2 and restores near wild-type activity to ALDH2*2.

4.5 *For Research Use Only !

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Product Details of Alda-1

CAS No. :349438-38-6
Formula : C15H11Cl2NO3
M.W : 324.16
SMILES Code : O=C(NCC1=CC=C(OCO2)C2=C1)C3=C(Cl)C=CC=C3Cl
MDL No. :MFCD02055160
InChI Key :NMKJFZCBCIUYHI-UHFFFAOYSA-N
Pubchem ID :831629

Safety of Alda-1

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H400
Precautionary Statements:P273-P301+P310
Class:6.1
UN#:2811
Packing Group:

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Recombinant ALDH2 20 µM 1 hour Alda-1 prevented nitroglycerin-induced ALDH2 inactivation Sci Transl Med. 2011 Nov 2;3(107):107ra111.
H9c2 cells 20 µM 12 hours Alda-1 treatment significantly increased ALDH2 activation in H9c2 cells and promoted mitochondrial respiration. Bioact Mater. 2021 Jan 8;6(7):2058-2069.
Cardiomyocytes 20 µM 12 hours Alda-1 treatment significantly increased ALDH2 activation in cardiomyocytes and promoted mitochondrial respiration. Bioact Mater. 2021 Jan 8;6(7):2058-2069.
T84 human colon cells 20 µM 12 hours Alda-1 restored the levels of ALDH2 protein and activity, and significantly blocked ethanol-induced increase in cell permeability and reduction in TJ/AJ protein levels. Redox Biol. 2023 Feb;59:102577.
A549 cells 0 nM, 100 nM, 350 nM, 1 µM 2 days Alda-1 treatment significantly reduced the side population of A549 cells, indicating that Alda-1 inhibits the stem cell-like properties of lung cancer cells. Neoplasia. 2019 Jun;21(6):602-614.
H1299 cells 0 nM, 100 nM, 1 µM 2 days Alda-1 treatment significantly reduced the CD44+/CD24− population of H1299 cells, indicating that Alda-1 inhibits the stem cell-like properties of lung cancer cells. Neoplasia. 2019 Jun;21(6):602-614.
H9C2 cells 20 µM 2 hours To evaluate the protective effect of Alda-1 on LPS-induced apoptosis and inflammation in H9C2 cells, the results showed that Alda-1 pretreatment significantly reduced LPS-induced mitochondrial membrane permeability, ROS levels, and apoptosis rate, and decreased the expression of inflammatory factors. Mol Med. 2023 Dec 20;29(1):171.
H9C2 myoblasts 20 µM 24 hours To evaluate the protective effect of Alda-1 on Aβ-induced lipid peroxidation, results showed that Alda-1 significantly alleviated Aβ-induced lipid peroxidation. Acta Pharmacol Sin. 2022 Jan;43(1):39-49.
Human renal proximal tubular epithelial cells (HK-2) 20 µM 24 hours To evaluate the effect of Alda-1 on MA-induced mitochondrial dysfunction and apoptosis in HK-2 cells. Results showed that Alda-1 treatment significantly improved mitochondrial function and reduced apoptosis. Cell Death Dis. 2023 Jan 20;14(1):45.
3T3 cells 20 µM 48 hours Evaluate the activation effect of Alda-1 on ALDH2 variants. The results showed that Alda-1 increased the activity of the ALDH2*2 variant by approximately 14-fold, but had limited activation effects on other variants. EBioMedicine. 2020 May;55:102753.
Human-derived fibroblasts 20 µM 48 hours Evaluate the activation effect of Alda-1 on ALDH2 variants. The results showed that Alda-1 had poor activation effects on ALDH2*3 and ALDH2*6 variants, and did not significantly improve their activity. EBioMedicine. 2020 May;55:102753.
Cardiac fibroblasts 20 µM 96 hours Alda-1 treatment reduced fibroblast proliferation under aldehydic load stress Cardiovasc Res. 2014 Sep 1;103(4):498-508.
ALDH2*1 0.03–0.06 µM To study the activation effect of Alda-1 on ALDH2*1 dehydrogenase activity Nat Struct Mol Biol. 2010 Feb;17(2):159-64.
ALDH2*2 0.3–0.5 µM To study the activation effect of Alda-1 on ALDH2*2 dehydrogenase activity Nat Struct Mol Biol. 2010 Feb;17(2):159-64.
HepG2 cells 40 µM Alda-1 prevented HNE-induced HepG2 cell death by activating ALDH2 to degrade HNE Cell Mol Gastroenterol Hepatol. 2022;14(4):925-944.
Huh-7 cells 40 µM Alda-1 prevented HNE-induced Huh-7 cell death by activating ALDH2 to degrade HNE Cell Mol Gastroenterol Hepatol. 2022;14(4):925-944.

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
C57BL/6 mice LPS-induced myocardial injury model Intraperitoneal injection 10 mg/kg Single injection, lasting 12 hours To evaluate the protective effect of Alda-1 on LPS-induced cardiac dysfunction, inflammation, and apoptosis, the results showed that Alda-1 pretreatment significantly improved cardiac function, reduced the expression of cardiac injury markers CKMB and LDH, and decreased the levels of inflammatory cytokines and apoptosis rate. Mol Med. 2023 Dec 20;29(1):171.
C57BL/6 mice Intestinal ischemia-reperfusion injury model Intraperitoneal injection 10 mg/kg Single dose, 1 hour before ischemia Alda-1 pretreatment significantly alleviated intestinal ischemia-reperfusion injury, accompanied by up-regulated ALDH2 activity and reduced accumulation of 4-HNE and MDA. Clin Sci (Lond). 2017 Jun 1;131(11):1123-1136
Rats Myocardial infarction-induced heart failure model Subcutaneous injection 10 mg/kg/day Continuous for 6 weeks Alda-1 treatment improved cardiac function, reduced left ventricular dilation, and decreased myocardial hypertrophy and cardiac fibrosis Cardiovasc Res. 2014 Sep 1;103(4):498-508.
Wistar rats Myocardial infarction model Continuous infusion via Alzet pump 16 mg/kg/day 16 hours Alda-1 prevented nitroglycerin-induced increase in myocardial infarction injury Sci Transl Med. 2011 Nov 2;3(107):107ra111.
Mice and rats ALDH2*1/*2 knock-in mice and Wistar rats Subcutaneous injection 2 mg/kg 15 minutes before, and again at 30 and 150 minutes after Alda-1 reduced the response to nociceptive stimulus in ALDH2*1/*2 mice and reversed the carrageenan-induced pain behavior, restoring thresholds to baseline values for both wild type and ALDH2*1/*2 mice. Sci Transl Med. 2014 Aug 27;6(251):251ra118
Mice Choline-deficient, amino acid-defined (CDAA) mouse model Intraperitoneal injection 20 mg/kg 3 times a week for 8 weeks Alda-1 reduced liver inflammation and fibrosis by degrading HNE Cell Mol Gastroenterol Hepatol. 2022;14(4):925-944.
C57BL/6 mice Cisplatin or maleic acid-induced acute kidney injury model Intraperitoneal injection 20 mg/kg Once daily for 3 days To evaluate the protective effect of Alda-1 on cisplatin or maleic acid-induced acute kidney injury. Results showed that Alda-1 pretreatment significantly improved renal function and reduced tubular injury and apoptosis. Cell Death Dis. 2023 Jan 20;14(1):45.
C57BL/6 mice Bile duct ligation model Subcutaneous injection 20 mg/kg Once daily for 14 days Alda-1 accelerates aldehyde degradation by activating ALDH2, reducing BDL-induced liver necrosis, inflammation, and fibrosis, indicating that aldehydes play an important role in the pathogenesis of cholestatic liver injury and fibrosis. Free Radic Biol Med. 2019 Dec;145:136-145
Mice GSNO-R−/− mice Perfusion 20 μmol/L 10 minutes prior to the onset of ischemia and for 10 minutes at the start of reperfusion Alda-1 significantly reduced infarct size in female GSNO-R?/? hearts, suggesting that excess mitochondrial formaldehyde may exacerbate I/R injury in female hearts with the disruption of GSNO-R. Circ Res. 2018 Nov 9;123(11):1232-1243
C57BL/6J mice Alcoholic liver disease model Intraperitoneal injection 5 mg/kg Every other day for 10 days To test the therapeutic potential of Alda-1 for alcoholic liver disease, results showed that Alda-1 treatment alleviated liver damage, reduced hepatic steatosis, and apoptosis. J Hepatol. 2015 Jun;62(6):1375-81.
C57BL/6J mice GFP-LC3 transgenic mice Intraperitoneal injection 50 mg/kg Single dose Alda-1 pretreatment reduced ethanol-induced mitochondrial depolarization and GFP-LC3 puncta formation. Autophagy. 2022 Nov;18(11):2671-2685

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.08mL

0.62mL

0.31mL

15.42mL

3.08mL

1.54mL

30.85mL

6.17mL

3.08mL

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