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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag auf Lager Startseite Anwendungen Enzyme Hydrolasen PSB-6426 - Moligand™ , Inhibitor of ectonucleoside triphosphate diphosphohydrolase 2, CAS No.P612993, Inhibitor of ectonucleoside triphosphate diphosphohydrolase 2 PSB-6426 - Moligand™ , Inhibitor of ectonucleoside triphosphate diphosphohydrolase 2, CAS No.P612993, Inhibitor of ectonucleoside triphosphate diphosphohydrolase 2
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.
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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 Spezifikationen & Reinheit
Moligand™
Mechanismus der Wirkung
Inhibitor of ectonucleoside triphosphate diphosphohydrolase 2
Namen und Kennungen Kanonisches Lächeln CCOP(=O)(Cc1ccc(cc1)NC(=O)CNC(=O)[C@H]1O[C@H]([C@@H]([C@@H]1O)O)n1ccc(=O)[nH]c1=O)OCC IUPAC Name (2S,3S,4R,5R)-N-[2-[4-(diethoxyphosphorylmethyl)anilino]-2-oxoethyl]-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolane-2-carboxamide InChIKey AEVBPXDFDKBGLT-YOUFYPILSA-N INCHI 1S/C22H29N4O10P/c1-3-34-37(33,35-4-2)12-13-5-7-14(8-6-13)24-16(28)11-23-20(31)19-17(29)18(30)21(36-19)26-10-9-15(27)25-22(26)32/h5-10,17-19,21,29-30H,3-4,11-12H2,1-2H3,(H,23,31)(H,24,28)(H,25,27,32)/t17-,18+,19-,21+/m0/s1 Isomere SMILES CCOP(=O)(CC1=CC=C(C=C1)NC(=O)CNC(=O)[C@@H]2[C@H]([C@H]([C@@H](O2)N3C=CC(=O)NC3=O)O)O)OCC PubChem CID 24949079
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 Klasse Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent N-acyl-alpha amino acids and derivatives Alternative Parents Alpha amino acid amides Glycosylamines Anilides N-arylamides Dialkyl alkylphosphonates Pyrimidones Hydropyrimidines Phosphonic acid esters Oxolanes Heteroaromatic compounds Vinylogous amides Secondary alcohols Lactams Secondary carboxylic acid amides 1,2-diols Ureas Oxacyclic compounds Azacyclic compounds Organophosphorus compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteromonocyclic compounds Substituents N-acyl-alpha amino acid or derivatives - Alpha-amino acid amide - Glycosyl compound - N-glycosyl compound - Anilide - N-arylamide - Dialkyl alkylphosphonate - Pyrimidone - Phosphonic acid diester - Monocyclic benzene moiety - Hydropyrimidine - Phosphonic acid ester - Pyrimidine - Benzenoid - Heteroaromatic compound - Oxolane - Vinylogous amide - Organophosphonic acid derivative - Urea - Secondary carboxylic acid amide - Secondary alcohol - 1,2-diol - Carboxamide group - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Organic nitrogen compound - Alcohol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organophosphorus compound - Aromatic heteromonocyclic compound Beschreibung This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. 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-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Lösungsrechner 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 Bewertungen 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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