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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items D-quinurenina - Moligand™, ≥98% , Agonist of HCA 3 receptor, CAS No.13441-51-5, Agonist of HCA 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
KYNURENINE, (R)- | MFCD00133224 | CHEBI:86262 | D-2-Amino-4-[2-aminophenyl]-4-oxobutanoic acid | D-Kynurenine, free base | F19570 | NCGC00017339-01 | K-8980 | Kynurenine, D- | Benzenebutanoic acid, alpha,2-diamino-gamma-oxo-, (R)- | DTXSID50360767 | (R)-2
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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 Room temperature Ships Normal 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
KYNURENINE, (R)- | MFCD00133224 | CHEBI:86262 | D-2-Amino-4-[2-aminophenyl]-4-oxobutanoic acid | D-Kynurenine, free base | F19570 | NCGC00017339-01 | K-8980 | Kynurenine, D- | Benzenebutanoic acid, alpha, 2-diamino-gamma-oxo-, (R)- | DTXSID50360767 | (R)-2
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
La D-quinurenina puede utilizarse junto con la L-quinurenina para evaluar la especificidad y la cinética de las enzimas metabolizadoras de la cinurenina. La D-quinurenina se utiliza para estudiar la selectividad y la actividad del receptor acoplado a prot
Condiciones de almacenamiento de almacenamiento
Room temperature
Mecanismo de acción
Agonist of HCA 3 receptor
Nombres e identificadores Pubchem Sid 488191727 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488191727 Sonrisas canónicas C1=CC=C(C(=C1)C(=O)CC(C(=O)O)N)N IUPAC Name (2R)-2-amino-4-(2-aminophenyl)-4-oxobutanoic acid InChIKey YGPSJZOEDVAXAB-MRVPVSSYSA-N INCHI 1S/C10H12N2O3/c11-7-4-2-1-3-6(7)9(13)5-8(12)10(14)15/h1-4,8H,5,11-12H2,(H,14,15)/t8-/m1/s1 Isómeros SMILES C1=CC=C(C(=C1)C(=O)C[C@H](C(=O)O)N)N Peso molecular 208.21 Reaxy-Rn 2697333 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2697333&ln=
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 oxygen compounds Clase Organooxygen compounds Subclass Carbonyl compounds Intermediate Tree Nodes Ketones - Aryl ketones - Phenylketones Direct Parent Alkyl-phenylketones Alternative Parents Butyrophenones D-alpha-amino acids Gamma-keto acids and derivatives Benzoyl derivatives Aryl alkyl ketones Aniline and substituted anilines Beta-amino ketones Vinylogous amides Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Alkyl-phenylketone - Butyrophenone - Alpha-amino acid - Alpha-amino acid or derivatives - D-alpha-amino acid - Benzoyl - Gamma-keto acid - Aniline or substituted anilines - Aryl alkyl ketone - Monocyclic benzene moiety - Beta-aminoketone - Keto acid - Benzenoid - Vinylogous amide - Amino acid - Amino acid or derivatives - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Primary aliphatic amine - Amine - Hydrocarbon derivative - Organopnictogen compound - Organic oxide - Organic nitrogen compound - Organonitrogen compound - Primary amine - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. External Descriptors D-alpha-amino acid - kynurenine 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 Peso molecular 208.210 g/mol XLogP3 -2.200 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 4 Exact Mass 208.085 Da Monoisotopic Mass 208.085 Da Topological Polar Surface Area 106.000 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 255.000 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
Citations of This Product Referencias 1. Mengna Wang, Yuhong Liu, Yanshi Li, Tao Lu, Min Wang, Zhaobo Cheng, Lin Chen, Tongling Wen, Min Pan, Guohua Hu. (2024) Tumor Microenvironment-Responsive Nanoparticles Enhance IDO1 Blockade Immunotherapy by Remodeling Metabolic Immunosuppression. Advanced Science, [PMID:39661740 ] [10.1002/advs.202405845 ] 2. Jingqi Dong, Jialin Hu, Liqiang Liu, Aihua Qu, Hua Kuang, Chuanlai Xu. (2025) Colloidal gold immunochromatographic strips for the detection of kynurenine in clinical samples. Journal of Materials Chemistry B, [PMID:40297963 ] [10.1039/D5TB00188A ] 3. Chi Yan, Xingyu Chen, Wenqing Gao, Chunlan Tang, Liwen Du, Chengyi Xie, Feng Xu, Keqi Tang, Jiancheng Yu. (2025) Chiral Derivatization Enables High-Resolution Ion Mobility Spectrometry of 30 Amino Acid Enantiomers. ANALYTICAL CHEMISTRY, [PMID:41451537 ] [10.1021/acs.analchem.5c06382 ]
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