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· · COA & SDS available for every product · Same-day shipping on in-stock items Spaglumic Acid - Moligand™, ≥98% , Agonist of mGlu 3 receptor, CAS No.3106-85-2, Agonist of mGlu 3 receptor
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98% Synonyms
AB00053333_02 | Acetyl-alpha-L-aspartylglutamic acid | SPBio_001502 | N-Acetyl-a-L-aspartyl-L-glutamic acid | Acido isospaglumico [Spanish] | Spectrum5_001840 | BDBM17658 | N-acetylaspartylglutamate (NAAG) | Acide isospaglumique [French] | NCGC00024569-02
Shipped In
Ice chest + Ice pads
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Why this grade Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
AB00053333_02 | Acetyl-alpha-L-aspartylglutamic acid | SPBio_001502 | N-Acetyl-a-L-aspartyl-L-glutamic acid | Acido isospaglumico [Spanish] | Spectrum5_001840 | BDBM17658 | N-acetylaspartylglutamate (NAAG) | Acide isospaglumique [French] | NCGC00024569-02
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
The most abundant peptide neurotransmitter in the mammalian CNS. A weak activator of NMDA receptors, and a highly selective agonist for mGlu3receptors. Neuroprotective under non-hydrolysing conditionsin vivo.
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Mechanism of action
Agonist of mGlu 3 receptor
Names and Identifiers Canonical Smiles CC(=O)NC(CC(=O)O)C(=O)NC(CCC(=O)O)C(=O)O IUPAC Name (2S)-2-[[(2S)-2-acetamido-3-carboxypropanoyl]amino]pentanedioic acid InChIKey OPVPGKGADVGKTG-BQBZGAKWSA-N INCHI 1S/C11H16N2O8/c1-5(14)12-7(4-9(17)18)10(19)13-6(11(20)21)2-3-8(15)16/h6-7H,2-4H2,1H3,(H,12,14)(H,13,19)(H,15,16)(H,17,18)(H,20,21)/t6-,7-/m0/s1 Isomeric SMILES CC(=O)N[C@@H](CC(=O)O)C(=O)N[C@@H](CCC(=O)O)C(=O)O PubChem CID 188803 Molecular Weight 304.25
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Class Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Peptides Direct Parent Dipeptides Alternative Parents Glutamic acid and derivatives Aspartic acid and derivatives N-acyl-L-alpha-amino acids Alpha amino acid amides Tricarboxylic acids and derivatives N-acyl amines Acetamides Secondary carboxylic acid amides Carboxylic acids Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents Alpha-dipeptide - Glutamic acid or derivatives - Aspartic acid or derivatives - N-acyl-l-alpha-amino acid - N-acyl-alpha-amino acid - N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - N-substituted-alpha-amino acid - Alpha-amino acid or derivatives - Tricarboxylic acid or derivatives - Fatty amide - N-acyl-amine - Fatty acyl - Acetamide - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Aliphatic acyclic compound Description This compound belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. External Descriptors dipeptide Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:water, Max Conc. mg/mL: 30.43, Max Conc. mM: 100 Molecular Weight 304.250 g/mol XLogP3 -2.100 Hydrogen Bond Donor Count 5 Hydrogen Bond Acceptor Count 8 Rotatable Bond Count 9 Exact Mass 304.091 Da Monoisotopic Mass 304.091 Da Topological Polar Surface Area 170.000 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 448.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 2 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
Citations of This Product References 1. Fen Xiong, Kaiyuan Jiang, Yali Wu, Cong Lou, Chengjie Ding, Wenli Zhang, Xi Zhang, Chen Li, Hong Zheng, Hongchang Gao. (2023) Intermittent fasting alleviates type 1 diabetes-induced cognitive dysfunction by improving the frontal cortical metabolic disorder. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, [PMID:37127173 ] [10.1016/j.bbadis.2023.166725 ] 2. Yang Wenjuan, Tang Sidi, Xu Rubing, Zhang Lu, Zhou Zihao, Yang Yong, Li Yanyan, Xiang Haibo. (2024) LC-MS based metabolomics identification of natural metabolites against Fusarium oxysporum. Frontiers in Plant Science, [PMID:39290733 ] [10.3389/fpls.2024.1435963 ]
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