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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Inosine - Moligand™, 10mM in DMSO , CAS No.58-63-9
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. 10mM in DMSO Synonyms
inosine|58-63-9|Hypoxanthosine|Ribonosine|Atorel|Oxiamin|Hypoxanthine riboside|Trophicardyl|Selfer|Pantholic-L|Panholic-L|beta-Inosine|Hypoxanthine D-riboside|(-)-Inosine|Hypoxanthine ribonucleoside|9-beta-D-Ribofuranosylhypoxanthine|Hypoxanthine nucleosi
Shipped In
Dry ice packs + Cold packs
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Why this grade Moligand™, 10mM in DMSO Moligand™ 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 76 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
inosine | 58-63-9 | Hypoxanthosine | Ribonosine | Atorel | Oxiamin | Hypoxanthine riboside | Trophicardyl | Selfer | Pantholic-L | Panholic-L | beta-Inosine | Hypoxanthine D-riboside | (-)-Inosine | Hypoxanthine ribonucleoside | 9-beta-D-Ribofuranosylhypoxanthine | Hypoxanthine nucleosi
Especificações e pureza
Moligand™, 10mM in DMSO
Mecanismos bioquímicos e fisiológicos
Purine nucleoside and adenosine metabolite. Cell-permeable. Displays neuroprotective and immunomodulatory effects. Potent vasodilator and axon growth stimulator.
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
OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3C(=O)NC=Nc23
IUPAC Name
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one
InChIKey
UGQMRVRMYYASKQ-KQYNXXCUSA-N
INCHI
1S/C10H12N4O5/c15-1-4-6(16)7(17)10(19-4)14-3-13-5-8(14)11-2-12-9(5)18/h2-4,6-7,10,15-17H,1H2,(H,11,12,18)/t4-,6-,7-,10-/m1/s1
SMILES isoméricas
C1=NC2=C(C(=O)N1)N=CN2[C@H]3[C@@H]([C@@H]([C@H](O3)CO)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 Nucleosides, nucleotides, and analogues Classe Purine nucleosides Subclass Not available Intermediate Tree Nodes Not available Direct Parent Purine nucleosides Alternative Parents Glycosylamines 6-oxopurines Pentoses Hypoxanthines Pyrimidones N-substituted imidazoles Vinylogous amides Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds Primary alcohols Molecular Framework Aromatic heteropolycyclic compounds Substituents Purine nucleoside - Glycosyl compound - N-glycosyl compound - 6-oxopurine - Hypoxanthine - Pentose monosaccharide - Purinone - Imidazopyrimidine - Purine - Pyrimidone - Pyrimidine - Monosaccharide - N-substituted imidazole - Vinylogous amide - Tetrahydrofuran - Heteroaromatic compound - Azole - Imidazole - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Alcohol - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Aromatic heteropolycyclic compound Descrição 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 inosines 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 Rotação específica [α] -52 ° (C=1, H2O) Ponto de fusão (°C) 218°C Peso molecular 268.230 g/mol XLogP3 -1.300 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 2 Exact Mass 268.081 Da Monoisotopic Mass 268.081 Da Topological Polar Surface Area 129.000 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 405.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 4 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
FAQs e artigos Citations of This Product Calculadoras de soluções Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
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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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