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Structure of Alda-1
CAS No.: 349438-38-6
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
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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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 |
GHS Pictogram: |
![]() ![]() |
Signal Word: | Danger |
Hazard Statements: | H301-H400 |
Precautionary Statements: | P273-P301+P310 |
Class: | 6.1 |
UN#: | 2811 |
Packing Group: | Ⅲ |
In Vitro:
Cell Line
|
Concentration | Treated Time | Description | References |
recombinant ALDH2 | 20 μM | 1 hour | Alda-1 prevented nitroglycerin-induced ALDH2 inactivation | PMC3547591 |
H9c2 cells | 20 μM | 12 hours | Alda-1 treatment significantly increased ALDH2 activation in H9c2 cells and promoted mitochondrial respiration. | PMC7809100 |
cardiomyocytes | 20 μM | 12 hours | Alda-1 treatment significantly increased ALDH2 activation in cardiomyocytes and promoted mitochondrial respiration. | PMC7809100 |
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. | PMC9792909 |
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. | PMC6506700 |
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. | PMC6506700 |
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. | PMC10731778 |
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. | PMC8724276 |
Human renal proximal tubular epithelial cells (HK-2) | 20μM | 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. | PMC9860042 |
H4IIEC3 rat hepatoma cells | 100 μM acetaldehyde or 10 μM 4-HNE | 3 days | To define the link between aldehydes and hepatotoxicity, results showed that acetaldehyde or 4-HNE treatment caused transcription factor inactivation, ER stress, and apoptosis. | PMC7949737 |
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. | PMC7218264 |
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. | PMC7218264 |
Cardiac fibroblasts | 20 µM | 96 hours | Alda-1 treatment reduced fibroblast proliferation under aldehydic load stress | PMC4155470 |
ALDH2*1 | 0.03–0.06 μM | To study the activation effect of Alda-1 on ALDH2*1 dehydrogenase activity | PMC2857674 | |
ALDH2*2 | 0.3–0.5 μM | To study the activation effect of Alda-1 on ALDH2*2 dehydrogenase activity | PMC2857674 | |
HepG2 cells | 40 μM | Alda-1 prevented HNE-induced HepG2 cell death by activating ALDH2 to degrade HNE | PMC9500440 | |
Huh-7 cells | 40 μM | Alda-1 prevented HNE-induced Huh-7 cell death by activating ALDH2 to degrade HNE | PMC9500440 |
In Vivo:
Species
|
Animal Model
|
Administration | Dosage | Frequency | Description | References |
C57BL/6J mice | Alcoholic liver disease model | Intraperitoneal injection | 5 mg/kg body weight | 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. | PMC7949737 |
Mouse | 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. | PMC6310045 |
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. | PMC4234033 |
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 | PMC3547591 |
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. | PMC9629059 |
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 | PMC4155470 |
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. | PMC6880805 |
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 | PMC9500440 |
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. | PMC9860042 |
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. | PMC5434792 |
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. | PMC10731778 |
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 |
Tags: Alda-1 | Alda1 | Alda 1 | Aldehyde Dehydrogenase | Apoptosis | ALDH2 Agonist | aldehyde dehydrogenase 2 | acetaldehyde | 349438-38-6
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P263 | Avoid contact during pregnancy/while nursing. |
P264 | Wash hands thoroughly after handling. |
P265 | Wash skin thouroughly after handling. |
P270 | Do not eat, drink or smoke when using this product. |
P271 | Use only outdoors or in a well-ventilated area. |
P272 | Contaminated work clothing should not be allowed out of the workplace. |
P273 | Avoid release to the environment. |
P280 | Wear protective gloves/protective clothing/eye protection/face protection. |
P281 | Use personal protective equipment as required. |
P282 | Wear cold insulating gloves/face shield/eye protection. |
P283 | Wear fire/flame resistant/retardant clothing. |
P284 | Wear respiratory protection. |
P285 | In case of inadequate ventilation wear respiratory protection. |
P231 + P232 | Handle under inert gas. Protect from moisture. |
P235 + P410 | Keep cool. Protect from sunlight. |
Response | |
Code | Phrase |
P301 | IF SWALLOWED: |
P304 | IF INHALED: |
P305 | IF IN EYES: |
P306 | IF ON CLOTHING: |
P307 | IF exposed: |
P308 | IF exposed or concerned: |
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P310 | Immediately call a POISON CENTER or doctor/physician. |
P311 | Call a POISON CENTER or doctor/physician. |
P312 | Call a POISON CENTER or doctor/physician if you feel unwell. |
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P322 | |
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P337 | If eye irritation persists: |
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P340 | Remove victim to fresh air and keep at rest in a position comfortable for breathing. |
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P378 | |
P380 | Evacuate area. |
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P391 | Collect spillage. Hazardous to the aquatic environment |
P301 + P310 | IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. |
P301 + P312 | IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell. |
P301 + P330 + P331 | IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. |
P302 + P334 | IF ON SKIN: Immerse in cool water/wrap in wet bandages. |
P302 + P350 | IF ON SKIN: Gently wash with plenty of soap and water. |
P303 + P361 + P353 | IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower. |
P304 + P312 | IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell. |
P304 + P340 | IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. |
P304 + P341 | IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. |
P305 + P351 + P338 | IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. |
P306 + P360 | IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes. |
P307 + P311 | IF exposed: call a POISON CENTER or doctor/physician. |
P308 + P313 | IF exposed or concerned: Get medical advice/attention. |
P309 + P311 | IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician. |
P332 + P313 | IF SKIN irritation occurs: Get medical advice/attention. |
P333 + P313 | IF SKIN irritation or rash occurs: Get medical advice/attention. |
P335 + P334 | Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages. |
P337 + P313 | IF eye irritation persists: Get medical advice/attention. |
P342 + P311 | IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician. |
P370 + P376 | In case of fire: Stop leak if safe to Do so. |
P370 + P378 | In case of fire: |
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Storage | |
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H231 | May react explosively even in the absence of air at elevated pressure and/or temperature |
H240 | Heating may cause an explosion |
H241 | Heating may cause a fire or explosion |
H242 | Heating may cause a fire |
H250 | Catches fire spontaneously if exposed to air |
H251 | Self-heating; may catch fire |
H252 | Self-heating in large quantities; may catch fire |
H260 | In contact with water releases flammable gases which may ignite spontaneously |
H261 | In contact with water releases flammable gas |
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H271 | May cause fire or explosion; strong oxidizer |
H272 | May intensify fire; oxidizer |
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H281 | Contains refrigerated gas; may cause cryogenic burns or injury |
H290 | May be corrosive to metals |
Health hazards | |
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H302 | Harmful if swallowed |
H303 | May be harmful if swallowed |
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H305 | May be harmful if swallowed and enters airways |
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H311 | Toxic in contact with skin |
H312 | Harmful in contact with skin |
H313 | May be harmful in contact with skin |
H314 | Causes severe skin burns and eye damage |
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H316 | Causes mild skin irritation |
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H318 | Causes serious eye damage |
H319 | Causes serious eye irritation |
H320 | Causes eye irritation |
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H335 | May cause respiratory irritation |
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H340 | May cause genetic defects |
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H350 | May cause cancer |
H351 | Suspected of causing cancer |
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H361d | Suspected of damaging the unborn child |
H362 | May cause harm to breast-fed children |
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H372 | Causes damage to organs through prolonged or repeated exposure |
H373 | May cause damage to organs through prolonged or repeated exposure |
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H411 | Toxic to aquatic life with long-lasting effects |
H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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