Acetylsalicylic acid
CAS No. 50-78-2
Acetylsalicylic acid( Acetylsalicylic Acid )
Catalog No. M14736 CAS No. 50-78-2
Aspirin (Acetylsalicylic acid) is a potent and selective inhibitor of cyclooxygenase (COX) with a broad range of pharmacological activities including anti-inflammation and pain relief.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
200MG | 28 | In Stock |
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500MG | 41 | In Stock |
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1G | 48 | In Stock |
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Biological Information
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Product NameAcetylsalicylic acid
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NoteResearch use only, not for human use.
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Brief DescriptionAspirin (Acetylsalicylic acid) is a potent and selective inhibitor of cyclooxygenase (COX) with a broad range of pharmacological activities including anti-inflammation and pain relief.
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DescriptionAspirin (Acetylsalicylic acid) is a potent and selective inhibitor of cyclooxygenase (COX) with a broad range of pharmacological activities including anti-inflammation and pain relief. Multiple studies have accumulated sufficient evidence to establish the association between the use of aspirin and a reduced risk of Ys including prostate Y, breast Y, colorectal Y, endometrial Y, and ovarian Y. Aspirin suppresses ovarian Y cells harboring COX-1 by acting as histone deacetylase inhibitors to up-regulate cell cycle arrest protein p21. Aspirin also inhibits the expression of COX-2 in human umbilical vein endothelial cells and neonatal rat ventricular cardiomyocytes resulting in reduced PG production and the down-regulation of ERK and NF-KB respectively.(In Vitro):Aspirin inhibits COX-1 and COX-2 in human articular chondrocytes, with IC50 values of 3.57 μM and 29.3 μM, respectively.Aspirin acetylates serine-530 of COX-1, thereby blocking thromboxane A synthesis in platelets and reducing platelet aggregation.Aspirin inhibits COX-2 protein expression through interference with binding of CCAAT/enhancer binding protein beta (C/EBPbeta) to its cognate site on COX-2 promoter/enhancer.Aspirin inhibits NF-κB-dependent transcription from the lgκ enhancer and the human immunodeficiency virus (HIV) long terminal repeat (LTR) in transfected T cells.Aspirin induces apoptosis by the activation of caspases, the activation of p38 MAP kinase, release of mitochondrial cytochrome c, and activation of the ceramide pathway.(In Vivo):Aspirin (5-150 mg/kg, PO, once) shows significant antipyretic activity in adult yeast-fevered male rats.
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In Vitro——
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In VivoAnimal Model:Male albino Charles River rats (200-250 g, 8 animals/group, fever was induced by 20 ml/kg of a 20 % aqueous suspension of brewer’s yeast which was injected SC in the back below the nape of the neck)Dosage:5, 25, 50, 100 and 150 mg/kg Administration:PO, once Result:Produced a statistically significant decrease of 0.23 ℃ at 15 min post-drug at the dose of 150 mg/kg. Antipyretic effect gradually increased in magnitude until a peak effect of 1.96 ℃ was reached at 120 min post-drug. The ED50 of aspirin was found to be 10.3 mg/kg with confidence limits of 1.8-23.0 mg/kg. The antipyretic response to aspirin is dependent on the dose of the compound administered.
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SynonymsAcetylsalicylic Acid
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PathwayChromatin/Epigenetic
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TargetCOX
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RecptorCOX-1| COX-2
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Research AreaInflammation/Immunology
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Indication——
Chemical Information
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CAS Number50-78-2
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Formula Weight180.16
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Molecular FormulaC9H8O4
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Purity>98% (HPLC)
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SolubilityEthanol: 36 mg/mL (199.82 mM); DMSO: 36 mg/mL (199.82 mM)
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SMILESO=C(O)C1=CC=CC=C1OC(C)=O
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Chemical NameBenzoic acid, 2-(acetyloxy)-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Kopp E, et al. Science, 1994, 265(5174), 956-959.
molnova catalog
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