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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock [¹⁴C]glutamine - Moligand™ , Sodium-coupled neutral amino acid transporter 3, CAS No.C614004, Sodium-coupled neutral amino acid transporter 3
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. Synonyms
BRN 1723797 | EINECS 200-292-1 | Glutamine (L-Glutamine) | Levoglutamida | NSC 27421 | Glutamic acid-5-amide | L-glutamine | L-Glutaminsaeure-5-amid | Nutrestore (TN) | UNII-0RH81L854J | 0RH81L854J | 4-04-00-03038 (Beilstein Handbook Reference) | DTXSID10
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Why this grade Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonymes
BRN 1723797 | EINECS 200-292-1 | Glutamine (L-Glutamine) | Levoglutamida | NSC 27421 | Glutamic acid-5-amide | L-glutamine | L-Glutaminsaeure-5-amid | Nutrestore (TN) | UNII-0RH81L854J | 0RH81L854J | 4-04-00-03038 (Beilstein Handbook Reference) | DTXSID10
Spécifications et pureté
Moligand™
Conditions de stockage de stockage
Room temperature
Mécanisme d'action
Sodium-coupled neutral amino acid transporter 3
Noms et identifiants Sourires canoniques NC(=O)CC[C@@H](C(=O)O)N IUPAC Name (2S)-2-amino-4-carbamoylbutanoic acid InChIKey ZDXPYRJPNDTMRX-VKHMYHEASA-N INCHI 1S/C5H10N2O3/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H2,7,8)(H,9,10)/t3-/m0/s1 Isomères SMILES C(CC(=O)N)[C@@H](C(=O)O)N PubChem CID 5961
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 Classe Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids Direct Parent L-alpha-amino acids Alternative Parents Fatty acids and conjugates Amino acids Monocarboxylic acids and derivatives Carboxylic acids Carboximidic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents L-alpha-amino acid - Fatty acid - Amino acid - Carboximidic acid - Carboximidic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Amine - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary aliphatic amine - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound Description This compound belongs to the class of organic compounds known as l-alpha-amino acids. These are alpha amino acids which have the L-configuration of the alpha-carbon atom. External Descriptors Common amino acids 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Poids moléculaire 146.140 g/mol XLogP3 -3.100 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 4 Exact Mass 146.069 Da Monoisotopic Mass 146.069 Da Topological Polar Surface Area 106.000 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 146.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 1 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
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Reconstitution Calculator Avis Need help choosing the grade? Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Moligand™ grade guide →
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