1.0 2026-09-22 22:22:09 UTC 2026-09-22 22:22:09 UTC FDB118973 Vidarabine (2R,3S,4S,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol (2R,3S,4S,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol C10H13N5O4 267.2413 267.096753929 (2R,3S,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol armes NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O InChI=1S/C10H13N5O4/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(18)6(17)4(1-16)19-10/h2-4,6-7,10,16-18H,1H2,(H2,11,12,13)/t4-,6-,7+,10-/m1/s1 OIRDTQYFTABQOQ-UHTZMRCNSA-N belongs to the class of organic compounds known as purine nucleosides. Purine nucleosides are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety. Purine nucleosides Organic compounds Nucleosides, nucleotides, and analogues Purine nucleosides Aromatic heteropolycyclic compounds 6-aminopurines Aminopyrimidines and derivatives Azacyclic compounds Glycosylamines Heteroaromatic compounds Hydrocarbon derivatives Imidolactams N-substituted imidazoles Organopnictogen compounds Oxacyclic compounds Pentoses Primary alcohols Primary amines Secondary alcohols Tetrahydrofurans 6-aminopurine Alcohol Amine Aminopyrimidine Aromatic heteropolycyclic compound Azacycle Azole Glycosyl compound Heteroaromatic compound Hydrocarbon derivative Imidazole Imidazopyrimidine Imidolactam Monosaccharide N-glycosyl compound N-substituted imidazole Organic nitrogen compound Organic oxygen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Oxacycle Pentose monosaccharide Primary alcohol Primary amine Purine Purine nucleoside Pyrimidine Secondary alcohol Tetrahydrofuran beta-D-arabinoside purine nucleoside logp -1.21 ALOGPS logs -1.28 ALOGPS solubility 1.40e+01 g/l ALOGPS logp -2.1 ChemAxon pka_strongest_acidic 12.45 ChemAxon pka_strongest_basic 4.99 ChemAxon iupac (2R,3S,4S,5R)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol ChemAxon average_mass 267.2413 ChemAxon mono_mass 267.096753929 ChemAxon smiles NC1=NC=NC2=C1N=CN2[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O ChemAxon formula C10H13N5O4 ChemAxon inchi InChI=1S/C10H13N5O4/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(18)6(17)4(1-16)19-10/h2-4,6-7,10,16-18H,1H2,(H2,11,12,13)/t4-,6-,7+,10-/m1/s1 ChemAxon inchikey OIRDTQYFTABQOQ-UHTZMRCNSA-N ChemAxon polar_surface_area 139.54 ChemAxon refractivity 63.2 ChemAxon polarizability 24.49 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 8 ChemAxon donor_count 4 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 19946 Specdb::CMs 40281 Specdb::CMs 132720 Specdb::CMs 140454 Specdb::NmrOneD 100438 Specdb::NmrOneD 100439 Specdb::NmrOneD 100440 Specdb::NmrOneD 100441 Specdb::NmrOneD 100442 Specdb::NmrOneD 100443 Specdb::NmrOneD 100444 Specdb::NmrOneD 100445 Specdb::NmrOneD 100446 Specdb::NmrOneD 100447 Specdb::NmrOneD 100448 Specdb::NmrOneD 100449 Specdb::NmrOneD 100450 Specdb::NmrOneD 100451 Specdb::NmrOneD 100452 Specdb::NmrOneD 100453 Specdb::NmrOneD 100454 Specdb::NmrOneD 100455 Specdb::NmrOneD 100456 Specdb::NmrOneD 100457 Specdb::MsMs 80160 Specdb::MsMs 80161 Specdb::MsMs 80162 Specdb::MsMs 140946 Specdb::MsMs 140947 Specdb::MsMs 140948 Specdb::MsMs 374735 Specdb::MsMs 451397 Specdb::MsMs 2813672 Specdb::MsMs 2813673 Specdb::MsMs 2813674 Specdb::MsMs 2891730 Specdb::MsMs 2891731 Specdb::MsMs 2891732