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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items ATPA - Moligand™, ≥98% , Agonist of GluK1, CAS No.140158-50-5, Agonist of GluK1
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
GTPL4140|HMS3260K20|Tox21_500139|CCG-204234|LP00139|NCGC00015027-02|NCGC00015027-03|NCGC00015027-04|NCGC00015027-05|NCGC00093629-01|NCGC00093629-02|NCGC00260824-01|EU-0100139|2-azaniumyl-3-(5-tert-butyl-3-oxo-2,3-dihydro-1,2-oxazol-4-yl)propanoate
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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
GTPL4140 | HMS3260K20 | Tox21_500139 | CCG-204234 | LP00139 | NCGC00015027-02 | NCGC00015027-03 | NCGC00015027-04 | NCGC00015027-05 | NCGC00093629-01 | NCGC00093629-02 | NCGC00260824-01 | EU-0100139 | 2-azaniumyl-3-(5-tert-butyl-3-oxo-2, 3-dihydro-1, 2-oxazol-4-yl)propanoate
Especificaciones y pureza
Moligand™, ≥98%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Mecanismo de acción
Agonist of GluK1
Nombres e identificadores Sonrisas canónicas CC(C)(C)C1=C(C(=O)NO1)CC(C(=O)O)N IUPAC Name 2-amino-3-(5-tert-butyl-3-oxo-1,2-oxazol-4-yl)propanoic acid InChIKey PIXJURSCCVBKRF-UHFFFAOYSA-N INCHI 1S/C10H16N2O4/c1-10(2,3)7-5(8(13)12-16-7)4-6(11)9(14)15/h6H,4,11H2,1-3H3,(H,12,13)(H,14,15) Isómeros SMILES CC(C)(C)C1=C(C(=O)NO1)CC(C(=O)O)N PubChem CID 2253 Peso molecular 228.24
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 Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Alpha amino acids Alternative Parents Aralkylamines Heteroaromatic compounds Isoxazoles Amino acids Carboxylic acid salts Lactams Azacyclic compounds Carboxylic acids Oxacyclic compounds Monocarboxylic acids and derivatives Monoalkylamines Organic zwitterions Hydrocarbon derivatives Organopnictogen compounds Carbonyl compounds Organic oxides Organic salts Molecular Framework Aromatic heteromonocyclic compounds Substituents Alpha-amino acid - Aralkylamine - Azole - Isoxazole - Heteroaromatic compound - Carboxylic acid salt - Amino acid - Lactam - Carboxylic acid - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Oxacycle - Azacycle - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organopnictogen compound - Organic zwitterion - Organic salt - Organic oxygen compound - Carbonyl group - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). External Descriptors Not available 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Sensibilidad Moisture sensitive Peso molecular 228.240 g/mol XLogP3 -1.900 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 4 Exact Mass 228.111 Da Monoisotopic Mass 228.111 Da Topological Polar Surface Area 102.000 Ų Heavy Atom Count 16 Formal Charge 0 Complexity 354.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 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 Reseñas 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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