1.0 2016-09-30 22:45:59 UTC 2020-05-21 16:27:06 UTC BMDB0001440 BMDB01440 dGTP 2'-Deoxyguanosine 5'-triphosphate Deoxyguanosine 5'-triphosphate Deoxyguanosine triphosphate 2'-Deoxyguanosine 5'-triphosphoric acid Deoxyguanosine 5'-triphosphoric acid Deoxyguanosine triphosphoric acid 2'-Deoxyguanosine triphosphate Deoxy-GTP Deoxyguanosine triphosphate, 3H-labeled C10H16N5O13P3 507.181 506.995745159 ({[({[(2R,3S,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)phosphonic acid dGTP 2564-35-4 NC1=NC2=C(N=CN2[C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)C(=O)N1 InChI=1S/C10H16N5O13P3/c11-10-13-8-7(9(17)14-10)12-3-15(8)6-1-4(16)5(26-6)2-25-30(21,22)28-31(23,24)27-29(18,19)20/h3-6,16H,1-2H2,(H,21,22)(H,23,24)(H2,18,19,20)(H3,11,13,14,17)/t4-,5+,6+/m0/s1 HAAZLUGHYHWQIW-KVQBGUIXSA-N belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside triphosphates. These are purine nucleotides with triphosphate group linked to the ribose moiety lacking a hydroxyl group at position 2. Organic compounds Nucleosides, nucleotides, and analogues Purine nucleotides Purine deoxyribonucleotides Purine 2'-deoxyribonucleoside triphosphates Azacyclic compounds Heteroaromatic compounds Hydrocarbon derivatives Hydroxypyrimidines Monoalkyl phosphates N-substituted imidazoles Organic oxides Organonitrogen compounds Organopnictogen compounds Oxacyclic compounds Purines and purine derivatives Secondary alcohols Tetrahydrofurans Alcohol Alkyl phosphate Aromatic heteropolycyclic compound Azacycle Azole Heteroaromatic compound Hydrocarbon derivative Hydroxypyrimidine Imidazole Imidazopyrimidine Monoalkyl phosphate N-substituted imidazole Organic nitrogen compound Organic oxide Organic oxygen compound Organic phosphoric acid derivative Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Oxacycle Phosphoric acid ester Purine Purine 2'-deoxyribonucleoside triphosphate Pyrimidine Secondary alcohol Tetrahydrofuran Aromatic heteropolycyclic compounds Deoxyribonucleotides deoxyguanosine phosphate guanyl deoxyribonucleotide purine 2'-deoxyribonucleoside 5'-triphosphate Solid logp -0.61 ALOGPS logs -1.96 ALOGPS logp -3.2 ChemAxon pka_strongest_acidic 1.03 ChemAxon pka_strongest_basic 0.33 ChemAxon iupac ({[({[(2R,3S,5R)-5-(2-amino-6-oxo-6,9-dihydro-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)phosphonic acid ChemAxon average_mass 507.181 ChemAxon mono_mass 506.995745159 ChemAxon smiles NC1=NC2=C(N=CN2[C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)O2)C(=O)N1 ChemAxon formula C10H16N5O13P3 ChemAxon inchi InChI=1S/C10H16N5O13P3/c11-10-13-8-7(9(17)14-10)12-3-15(8)6-1-4(16)5(26-6)2-25-30(21,22)28-31(23,24)27-29(18,19)20/h3-6,16H,1-2H2,(H,21,22)(H,23,24)(H2,18,19,20)(H3,11,13,14,17)/t4-,5+,6+/m0/s1 ChemAxon inchikey HAAZLUGHYHWQIW-KVQBGUIXSA-N ChemAxon polar_surface_area 274.58 ChemAxon refractivity 95.73 ChemAxon polarizability 39.09 ChemAxon rotatable_bond_count 8 ChemAxon acceptor_count 13 ChemAxon donor_count 7 ChemAxon physiological_charge -3 ChemAxon formal_charge 0 ChemAxon number_of_rings 3 ChemAxon bioavailability 0 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Purine Metabolism SMP0087239 Specdb::NmrTwoD 1073 Specdb::NmrTwoD 1649 Specdb::MsMs 26018 Specdb::MsMs 26019 Specdb::MsMs 26020 Specdb::MsMs 32576 Specdb::MsMs 32577 Specdb::MsMs 32578 Specdb::MsMs 2245240 Specdb::MsMs 2247002 Specdb::MsMs 2247303 Specdb::MsMs 2319788 Specdb::MsMs 2319789 Specdb::MsMs 2319790 Specdb::MsMs 2618450 Specdb::MsMs 2618451 Specdb::MsMs 2618452 Specdb::NmrOneD 1708 Specdb::NmrOneD 4956 Specdb::NmrOneD 4957 Specdb::CMs 26341 Specdb::CMs 38075 58613 FDB022623 65103 C00286 16497 DB02181 C00019346 34502 Deoxyguanosine triphosphate 6248 DGTP BMDBP00486 Nucleoside diphosphate kinase 7 Q5E9Y9 NME7 Enzyme