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· · COA & SDS available for every product · Same-day shipping on in-stock items 8-Azaadenosine - ≥98%(HPLC) , CAS No.10299-44-2
Synonyms
(2R,3R,4S,5R)-2-{7-amino-3H-[1,2,3]triazolo[4,5-d]pyrimidin-3-yl}-5-(hydroxymethyl)oxolane-3,4-diol | 3-?-D-Ribofuranosyl-3H-1,2,3-triazolo[4,5-d]pyrimidin-7-amine | 8-Azaadenosine | 8-Aza-adenosine | Q27105620 | HY-115686 | 3-beta-D-Ribofuranosyl-3H-1,2,
Storage
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
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Why this grade ≥98%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C,Argon charged Ships Ice chest + Ice pads 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
(2R, 3R, 4S, 5R)-2-{7-amino-3H-[1, 2, 3]triazolo[4, 5-d]pyrimidin-3-yl}-5-(hydroxymethyl)oxolane-3, 4-diol | 3-?-D-Ribofuranosyl-3H-1, 2, 3-triazolo[4, 5-d]pyrimidin-7-amine | 8-Azaadenosine | 8-Aza-adenosine | Q27105620 | HY-115686 | 3-beta-D-Ribofuranosyl-3H-1, 2,
Specifications & Purity
≥98%(HPLC)
Biochemical and Physiological Mechanisms
ADAR1 (adenosine deaminases acting on double-stranded RNA) inhibitor. Reduces A-to-I editing activity in a leukemia cell line, restoreslet-7and inhibits leukemia stem cells self-renewalin vitro.
Storage
Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles C1=NC(=C2C(=N1)N(N=N2)C3C(C(C(O3)CO)O)O)N IUPAC Name (2R,3R,4S,5R)-2-(7-aminotriazolo[4,5-d]pyrimidin-3-yl)-5-(hydroxymethyl)oxolane-3,4-diol InChIKey OAUKGFJQZRGECT-UUOKFMHZSA-N INCHI 1S/C9H12N6O4/c10-7-4-8(12-2-11-7)15(14-13-4)9-6(18)5(17)3(1-16)19-9/h2-3,5-6,9,16-18H,1H2,(H2,10,11,12)/t3-,5-,6-,9-/m1/s1 Isomeric SMILES C1=NC(=C2C(=N1)N(N=N2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)N Molecular Weight 268.23 Reaxy-Rn 1226020 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1226020&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 Class Organooxygen compounds Subclass Carbohydrates and carbohydrate conjugates Intermediate Tree Nodes Glycosyl compounds Direct Parent Glycosylamines Alternative Parents Pentoses Triazolopyrimidines Aminopyrimidines and derivatives Imidolactams Triazoles Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents N-glycosyl compound - Pentose monosaccharide - Triazolopyrimidine - Aminopyrimidine - Monosaccharide - Pyrimidine - Imidolactam - Azole - Heteroaromatic compound - 1,2,3-triazole - Triazole - Tetrahydrofuran - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Primary amine - Primary alcohol - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organic nitrogen compound - Amine - Alcohol - Aromatic heteropolycyclic compound Description This compound belongs to the class of organic compounds known as glycosylamines. These are compounds consisting of an amine with a beta-N-glycosidic bond to a carbohydrate, thus forming a cyclic hemiaminal ether bond (alpha-amino ether). External Descriptors N-glycosyl compound 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) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 26.82, Max Conc. mM: 100 Sensitivity Moisture sensitive Molecular Weight 268.230 g/mol XLogP3 -2.200 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 9 Rotatable Bond Count 2 Exact Mass 268.092 Da Monoisotopic Mass 268.092 Da Topological Polar Surface Area 152.000 Ų Heavy Atom Count 19 Formal Charge 0 Complexity 336.000 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
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