N-Acetylneuraminic acid

Synonyms: Neu5Ac, NeuAc, Acido aceneuramico, Acide aceneuramique, Acidium aceneuramicum, Sialic acid

N-Acetylneuraminic acid (Neu5Ac, NeuAc, Acido aceneuramico, Acide aceneuramique, Acidium aceneuramicum, Sialic acid, NANA) is the predominant sialic acid found in mammalian cells. Sialic acids are negatively charged monosaccharides attached to the end of sugar chains, giving rise to a wide variety of glycoproteins and glycolipids in biological fluids and cell membranes.

N-Acetylneuraminic acid Chemical Structure

N-Acetylneuraminic acid Chemical Structure

CAS: 131-48-6

Selleck's N-Acetylneuraminic acid has been cited by 2 publications

Purity & Quality Control

Batch: Purity: 99.82%
99.82

N-Acetylneuraminic acid Related Products

Biological Activity

Description N-Acetylneuraminic acid (Neu5Ac, NeuAc, Acido aceneuramico, Acide aceneuramique, Acidium aceneuramicum, Sialic acid, NANA) is the predominant sialic acid found in mammalian cells. Sialic acids are negatively charged monosaccharides attached to the end of sugar chains, giving rise to a wide variety of glycoproteins and glycolipids in biological fluids and cell membranes.
In Vivo
In vivo N-Acetylneuraminic acid (Neu5Ac) could improve lipid metabolism and hyperlipidemia-associated coagulation. It prevents HFD-induced hypercholesterolemia and hypercoagulation through regulation of serum lipid levels, metabolic indices, and coagulation-related indices[2].
Animal Research Animal Models Sprague-Dawley rats
Dosages 20 mg/kg
Administration i.p.
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT03545568 Completed
N-Acetylneuraminic Acid Storage Disease
University of Lausanne|University of Modena and Reggio Emilia
May 1 2018 Not Applicable
NCT02346461 Completed
GNE Myopathy
National Human Genome Research Institute (NHGRI)|National Center for Advancing Translational Sciences (NCATS)|National Institutes of Health Clinical Center (CC)
February 5 2015 Phase 2
NCT01236898 Completed
Nonaka Myopathy|Hereditary Inclusion Body Myopathy
Tohoku University
November 2010 Phase 1

Chemical Information & Solubility

Molecular Weight 309.27 Formula

C11H19NO9

CAS No. 131-48-6 SDF Download N-Acetylneuraminic acid SDF
Smiles CC(=O)NC1C(CC(OC1C(C(CO)O)O)(C(=O)O)O)O
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 62 mg/mL ( (200.47 mM); Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : 62 mg/mL

Ethanol : Insoluble


Molecular Weight Calculator

In vivo
Batch:

Add solvents to the product individually and in order.


In vivo Formulation Calculator

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In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Tech Support

Answers to questions you may have can be found in the inhibitor handling instructions. Topics include how to prepare stock solutions, how to store inhibitors, and issues that need special attention for cell-based assays and animal experiments.

Handling Instructions

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