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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque ATPA - Moligand™, ≥98% , Agonist of GluK1, CAS No.140158-50-5, Agonist of GluK1
Disponível para encomenda
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
Especificações e pureza
Moligand™, ≥98%
Condições de armazenamento de armazenamento
Store at -20°C
Enviado em
Ice chest + Ice pads
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Mecanismo de ação
Agonist of GluK1
Nomes e identificadores Sorrisos canónicos 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) SMILES isoméricas 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 Classe 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 Descrição 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.
Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Sensibilidade 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 Revisões 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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