1.0 2016-09-30 22:31:39 UTC 2020-04-22 15:03:51 UTC BMDB0000497 BMDB00497 5,6-Dihydrouridine 1-beta-D-Ribofuranosylhydrouracil 3,4-Dihydrouridine D 1-b-D-Ribofuranosylhydrouracil 1-Β-D-ribofuranosylhydrouracil Dihydro-1-b-D-ribofuranosyl-2,4(1H,3H)-pyrimidinedione Dihydro-1-beta-delta-ribofuranosyl-2,4(1H,3H)-pyrimidinedione Dihydrouridine 5,6-Dihydrouridine C9H14N2O6 246.2173 246.08518619 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3-diazinane-2,4-dione dihydrouridine 5627-05-4 OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1CCC(=O)NC1=O InChI=1S/C9H14N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h4,6-8,12,14-15H,1-3H2,(H,10,13,16)/t4-,6-,7-,8-/m1/s1 ZPTBLXKRQACLCR-XVFCMESISA-N belongs to the class of organic compounds known as glycosylamines. Glycosylamines 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). Organic compounds Organic oxygen compounds Organooxygen compounds Carbohydrates and carbohydrate conjugates Glycosylamines Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Hydropyrimidines Organic carbonic acids and derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds Oxacyclic compounds Pentoses Primary alcohols Propargyl-type 1,3-dipolar organic compounds Pyrimidones Secondary alcohols Tetrahydrofurans 1,2,5,6-tetrahydropyrimidine Alcohol Aliphatic heteromonocyclic compound Azacycle Carbonic acid derivative Carbonyl group Hydrocarbon derivative Hydropyrimidine Monosaccharide N-glycosyl compound Organic 1,3-dipolar compound Organic nitrogen compound Organic oxide Organoheterocyclic compound Organonitrogen compound Organopnictogen compound Oxacycle Pentose monosaccharide Primary alcohol Propargyl-type 1,3-dipolar organic compound Pyrimidine Pyrimidone Secondary alcohol Tetrahydrofuran Aliphatic heteromonocyclic compounds uridines Solid logp -2.10 ALOGPS logs -0.03 ALOGPS logp -2.8 ChemAxon pka_strongest_acidic 11.59 ChemAxon pka_strongest_basic -3 ChemAxon iupac 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,3-diazinane-2,4-dione ChemAxon average_mass 246.2173 ChemAxon mono_mass 246.08518619 ChemAxon smiles OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1CCC(=O)NC1=O ChemAxon formula C9H14N2O6 ChemAxon inchi InChI=1S/C9H14N2O6/c12-3-4-6(14)7(15)8(17-4)11-2-1-5(13)10-9(11)16/h4,6-8,12,14-15H,1-3H2,(H,10,13,16)/t4-,6-,7-,8-/m1/s1 ChemAxon inchikey ZPTBLXKRQACLCR-XVFCMESISA-N ChemAxon polar_surface_area 119.33 ChemAxon refractivity 52.34 ChemAxon polarizability 22.98 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 6 ChemAxon donor_count 4 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon number_of_rings 2 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Specdb::CMs 9997 Specdb::CMs 37571 Specdb::CMs 136540 Specdb::CMs 144274 Specdb::CMs 1064112 Specdb::CMs 1064114 Specdb::CMs 1064116 Specdb::CMs 1064118 Specdb::CMs 1064120 Specdb::CMs 1064121 Specdb::CMs 1064123 Specdb::CMs 1064125 Specdb::CMs 1064127 Specdb::CMs 1064129 Specdb::CMs 1064131 Specdb::CMs 1064133 Specdb::CMs 1064134 Specdb::CMs 1064136 Specdb::CMs 1064138 Specdb::CMs 1064140 Specdb::CMs 1064141 Specdb::CMs 1064143 Specdb::CMs 1064145 Specdb::CMs 1064147 Specdb::CMs 1064149 Specdb::NmrOneD 6922 Specdb::NmrOneD 6923 Specdb::NmrOneD 6924 Specdb::NmrOneD 6925 Specdb::NmrOneD 6926 Specdb::NmrOneD 6927 Specdb::NmrOneD 6928 Specdb::NmrOneD 6929 Specdb::NmrOneD 6930 Specdb::NmrOneD 6931 Specdb::NmrOneD 6932 Specdb::NmrOneD 6933 Specdb::NmrOneD 6934 Specdb::NmrOneD 6935 Specdb::NmrOneD 6936 Specdb::NmrOneD 6937 Specdb::NmrOneD 6938 Specdb::NmrOneD 6939 Specdb::NmrOneD 6940 Specdb::NmrOneD 6941 Specdb::MsMs 79047 Specdb::MsMs 79048 Specdb::MsMs 79049 Specdb::MsMs 139545 Specdb::MsMs 139546 Specdb::MsMs 139547 Specdb::MsMs 2357787 Specdb::MsMs 2357788 Specdb::MsMs 2357789 Specdb::MsMs 2604311 Specdb::MsMs 2604312 Specdb::MsMs 2604313 FDB022076 85115 94312 23774 Dihydrouridine 5483 Cerutti, Peter; Kondo, Yoshikazu; Landis, W. R.; Witkop, Bernhard. Photoreduction of uridine and reduction of dihydrouridine with sodium borohydride. Journal of the American Chemical Society (1968), 90(3), 771-5.