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· · COA & SDS available for every product · Same-day shipping on in-stock items AB-NECA - Moligand™ , Agonist of A 2B receptor, CAS No.A607329, Agonist of A 2B 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. Synonyms
aminobenzyl-5'-N-ethylcarboxamidoadenosine
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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 Synonyms
aminobenzyl-5'-N-ethylcarboxamidoadenosine
Specifications & Purity
Moligand™
Mechanism of action
Agonist of A 2B receptor
Names and Identifiers Canonical Smiles CCNC(=O)C(=O)Nc1nc(Nc2ccccc2)c2c(n1)n(cn2)[C@@H]1O[C@@H]([C@H]([C@H]1O)O)CO IUPAC Name N'-[6-anilino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]purin-2-yl]-N-ethyloxamide InChIKey ZLZSAUQLHYWSOL-HLFSEMCJSA-N INCHI 1S/C20H23N7O6/c1-2-21-17(31)18(32)26-20-24-15(23-10-6-4-3-5-7-10)12-16(25-20)27(9-22-12)19-14(30)13(29)11(8-28)33-19/h3-7,9,11,13-14,19,28-30H,2,8H2,1H3,(H,21,31)(H2,23,24,25,26,32)/t11-,13-,14-,19-/m1/s1 Isomeric SMILES CCNC(=O)C(=O)NC1=NC(=C2C(=N1)N(C=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)NC4=CC=CC=C4 PubChem CID 57340157
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 Nucleosides, nucleotides, and analogues Class Purine nucleosides Subclass Not available Intermediate Tree Nodes Not available Direct Parent Purine nucleosides Alternative Parents Alpha amino acid amides Glycosylamines 6-aminopurines Pentoses Aniline and substituted anilines N-arylamides Aminopyrimidines and derivatives Imidolactams N-substituted imidazoles Oxolanes Heteroaromatic compounds Secondary carboxylic acid amides 1,2-diols Secondary alcohols Azacyclic compounds Secondary amines Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Primary alcohols Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents Purine nucleoside - Alpha-amino acid amide - Glycosyl compound - N-glycosyl compound - 6-aminopurine - Alpha-amino acid or derivatives - Pentose monosaccharide - Imidazopyrimidine - Purine - Aniline or substituted anilines - N-arylamide - Aminopyrimidine - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Imidolactam - Benzenoid - Pyrimidine - Azole - Heteroaromatic compound - Oxolane - Imidazole - Secondary carboxylic acid amide - Secondary alcohol - Amino acid or derivatives - 1,2-diol - Carboxamide group - Oxacycle - Organoheterocyclic compound - Carboxylic acid derivative - Secondary amine - Azacycle - Organic oxide - Carbonyl group - Amine - Primary alcohol - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organic nitrogen compound - Alcohol - Organonitrogen compound - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety. 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.
3D Structure Associated Targets(Human) Certificates（CoA,COO,BSE/TSE and Analysis Chart) Solution Calculators Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Reviews 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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