1824609-67-7
Chemical Structure
Acloproxalap
Synonym(s): ADX-629
- CAS No.: 1824609-67-7
- Formula:C12H14N2O
- Molecular Weight:202.25
IUPAC Name: 4,4,4-trifluoro-1-(3-(trifluoromethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-en-8-yl)butan-1-one
InChIKey: NOFRQDXKZDAYGB-UHFFFAOYSA-N
SMILES: OC(C)(C)C1=NC2=C(C=C1N)C=CC=C2
Biological Activity: Acloproxalap (ADX-629) is an orally active reactive aldehyde species (RASP) inhibitor. Acloproxalap binds covalently to free aldehydes, sequesters reactive aldehyde species, malondialdehyde, acetaldehyde and preformed malondialdehyde-acetaldehyde adducts, and reduces elevated RASP levels. Acloproxalap decreases the formation of aldehyde adducts, reduces liver and serum triglyceride levels, hepatic fat accumulation, circulating anti-malondialdehyde-acetaldehyde adduct antibody levels, and inhibits the release of IL-6 and MCP-1. Acloproxalap improves cell viability of liver slices exposed to ethanol. Acloproxalap blocks ethanol-induced damage in animal models of alcoholic liver disease. Acloproxalap is applicable to research related to alcoholic liver disease, alcoholic fatty liver disease, non-alcoholic steatohepatitis, chronic cough, rheumatoid arthritis, ulcerative colitis and mild atopic asthma[1][2][3][4][5].
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Acloproxalap | 99.92% | Acloproxalap (ADX-629) is an orally active reactive aldehyde species (RASP) inhibitor. Acloproxalap binds covalently to free aldehydes, sequesters reactive aldehyde species, malondialdehyde, acetaldehyde and preformed malondialdehyde-acetaldehyde adducts, and reduces elevated RASP levels. Acloproxalap decreases the formation of aldehyde adducts, reduces liver and serum triglyceride levels, hepatic fat accumulation, circulating anti-malondialdehyde-acetaldehyde adduct antibody levels, and inhibits the release of IL-6 and MCP-1. Acloproxalap improves cell viability of liver slices exposed to ethanol. Acloproxalap blocks ethanol-induced damage in animal models of alcoholic liver disease. Acloproxalap is applicable to research related to alcoholic liver disease, alcoholic fatty liver disease, non-alcoholic steatohepatitis, chronic cough, rheumatoid arthritis, ulcerative colitis and mild atopic asthma. | ||||||||||||||||||||
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- [1]. Duryee MJ, Aripova N, Hunter CD, Ruskamp RJ, et al. A novel reactive aldehyde species inhibitor prevents the deleterious effects of ethanol in an animal model of alcoholic liver disease. Int Immunopharmacol. 2022 Dec;113(Pt A):109400. [Content Brief]
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[2]. Duncan Works, et al. In vitro comparison of Ethanol Metabolism in Precision Cut Liver
Slices from C57Bl/6, Balb/c, DBA/2J and 129S1/SvlmJ Mice and with the Aldeyra product ADX-629. - [3]. Guilleminault L, et al. Drugs Targeting Cough Receptors: New Therapeutic Options in Refractory or Unexplained Chronic Cough. Drugs. 2024 Jul;84(7):763-777. [Content Brief]
- [4]. Duncan R Works, et al. REACTIVE ALDEHYDE SPECIES (RASP) INHIBITORS SEQUESTER MAA-ADDUCTS AND REDUCE PRO-INFLAMMATORY CYTOKINES
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[5]. Couroux P, et al.
ADX-629, A Reactive Aldehyde Species (RASP) Inhibitor, Reduced Eosinophilia In Asthmatic Subjects After Bronchial Allergen Challenge (BAC) Journal of Allergy and Clinical Immunology, 151AB70
Keywords