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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Xanthurenic acid - 10mM in DMSO , CAS No.59-00-7
Disponível para encomenda
GRADE & PURITY 10mM in DMSO
Synonyms
BDBM50113313 | Xanthurenate; 8-Hydroxykynurenic acid; 4,8-Dihydroxyquinaldic acid | 4-oxoxanthurenic acid | IDI1_000262 | NSC401570 | NSC-401570 | KBioSS_000733 | NCGC00094846-05 | 4,8-Dihydroxy-2-quinolinecarboxylic acid | 4,8-Dihydroxy-quinoline-2-carbo
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs 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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
BDBM50113313 | Xanthurenate; 8-Hydroxykynurenic acid; 4,8-Dihydroxyquinaldic acid | 4-oxoxanthurenic acid | IDI1_000262 | NSC401570 | NSC-401570 | KBioSS_000733 | NCGC00094846-05 | 4,8-Dihydroxy-2-quinolinecarboxylic acid | 4,8-Dihydroxy-quinoline-2-carbo
Especificações e pureza
10mM in DMSO
Mecanismos bioquímicos e fisiológicos
Shown to selectively activate group II mGlu receptors in transfected HEK293 cells at nanomolar concentrations. Attenuates cAMP formation in mouse cortical slices expressing mGlu2and mGlu3receptors.
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores Sorrisos canónicos
C1=CC2=C(C(=C1)O)NC(=CC2=O)C(=O)O
IUPAC Name
8-hydroxy-4-oxo-1H-quinoline-2-carboxylic acid
InChIKey
FBZONXHGGPHHIY-UHFFFAOYSA-N
INCHI
1S/C10H7NO4/c12-7-3-1-2-5-8(13)4-6(10(14)15)11-9(5)7/h1-4,12H,(H,11,13)(H,14,15)
SMILES isoméricas
C1=CC2=C(C(=C1)O)NC(=CC2=O)C(=O)O
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 Organoheterocyclic compounds Classe Quinolines and derivatives Subclass Quinoline carboxylic acids Intermediate Tree Nodes Not available Direct Parent Quinoline carboxylic acids Alternative Parents 8-hydroxyquinolines Hydroxyquinolines Hydroquinolones Hydroquinolines Pyridinecarboxylic acids 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Vinylogous amides Heteroaromatic compounds Azacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Organooxygen compounds Organopnictogen compounds Organic oxides Hydrocarbon derivatives Organonitrogen compounds Molecular Framework Aromatic heteropolycyclic compounds Substituents Quinoline-2-carboxylic acid - Dihydroquinolone - Hydroxyquinoline - 8-hydroxyquinoline - Dihydroquinoline - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Pyridine - Benzenoid - Heteroaromatic compound - Vinylogous amide - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Azacycle - Organonitrogen compound - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Aromatic heteropolycyclic compound Descrição This compound belongs to the class of organic compounds known as quinoline carboxylic acids. These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions. External Descriptors quinolinemonocarboxylic acid - dihydroxyquinoline 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 Ponto de fusão (°C) 297-298°C Peso molecular 205.170 g/mol XLogP3 0.900 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 1 Exact Mass 205.038 Da Monoisotopic Mass 205.038 Da Topological Polar Surface Area 86.600 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 336.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 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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