1.0 2016-10-03 18:13:06 UTC 2020-05-21 16:28:22 UTC BMDB0011117 BMDB11117 Se-Adenosylselenohomocysteine Se-adenosylselenohomocysteine belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives. Se-adenosylselenohomocysteine is possibly soluble (in water) and a very strong basic compound (based on its pKa). Se-adenosylselenohomocysteine participates in a number of enzymatic reactions, within cattle. In particular, Se-adenosylselenohomocysteine can be converted into selenohomocysteine and adenosine through its interaction with the enzyme adenosylhomocysteinase. In addition, Se-adenosylselenohomocysteine can be biosynthesized from se-adenosylselenomethionine; which is mediated by the enzyme methyltransferase-like protein 6. In cattle, se-adenosylselenohomocysteine is involved in the metabolic pathway called the selenoamino acid metabolism pathway. C14H20N6O5Se 431.31 432.066039608 2-amino-4-({[(2S,3S,4R,5S)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl}selanyl)butanoic acid se-adenosylselenohomocysteine NC(CC[Se]C[C@H]1O[C@@H]([C@H](O)[C@@H]1O)N1C=NC2=C(N)N=CN=C12)C(O)=O InChI=1S/C14H20N6O5Se/c15-6(14(23)24)1-2-26-3-7-9(21)10(22)13(25-7)20-5-19-8-11(16)17-4-18-12(8)20/h4-7,9-10,13,21-22H,1-3,15H2,(H,23,24)(H2,16,17,18)/t6?,7-,9-,10-,13+/m1/s1 UVSMMLABJBJNGH-WWJIDFMMSA-N belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives. Organic compounds Nucleosides, nucleotides, and analogues 5'-deoxyribonucleosides 5'-deoxyribonucleosides 1,2-diols 6-aminopurines Alpha amino acids Amino acids Aminopyrimidines and derivatives Azacyclic compounds Carbonyl compounds Carboxylic acids Glycosylamines Heteroaromatic compounds Hydrocarbon derivatives Imidolactams Monoalkylamines Monocarboxylic acids and derivatives N-substituted imidazoles Organic oxides Organopnictogen compounds Oxacyclic compounds Pentoses Secondary alcohols Selenoethers Tetrahydrofurans 1,2-diol 5'-deoxyribonucleoside 6-aminopurine Alcohol Alpha-amino acid Alpha-amino acid or derivatives Amine Amino acid Amino acid or derivatives Aminopyrimidine Aromatic heteropolycyclic compound Azacycle Azole Carbonyl group Carboxylic acid Carboxylic acid derivative Glycosyl compound Heteroaromatic compound Hydrocarbon derivative Imidazole Imidazopyrimidine Imidolactam Monocarboxylic acid or derivatives Monosaccharide N-glycosyl compound N-substituted imidazole Organic nitrogen compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Organoselenium compound Oxacycle Pentose monosaccharide Primary aliphatic amine Primary amine Purine Pyrimidine Secondary alcohol Selenoether Tetrahydrofuran Aromatic heteropolycyclic compounds Solid logp -2.54 ALOGPS logs -1.71 ALOGPS logp -5.3 ChemAxon pka_strongest_acidic 1.31 ChemAxon pka_strongest_basic 9.5 ChemAxon iupac 2-amino-4-({[(2S,3S,4R,5S)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl}selanyl)butanoic acid ChemAxon average_mass 431.31 ChemAxon mono_mass 432.066039608 ChemAxon smiles NC(CC[Se]C[C@H]1O[C@@H]([C@H](O)[C@@H]1O)N1C=NC2=C(N)N=CN=C12)C(O)=O ChemAxon formula C14H20N6O5Se ChemAxon inchi InChI=1S/C14H20N6O5Se/c15-6(14(23)24)1-2-26-3-7-9(21)10(22)13(25-7)20-5-19-8-11(16)17-4-18-12(8)20/h4-7,9-10,13,21-22H,1-3,15H2,(H,23,24)(H2,16,17,18)/t6?,7-,9-,10-,13+/m1/s1 ChemAxon inchikey UVSMMLABJBJNGH-WWJIDFMMSA-N ChemAxon polar_surface_area 182.63 ChemAxon refractivity 98.04 ChemAxon polarizability 36.91 ChemAxon rotatable_bond_count 7 ChemAxon acceptor_count 10 ChemAxon donor_count 5 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon number_of_rings 3 ChemAxon bioavailability 1 ChemAxon rule_of_five Yes ChemAxon ghose_filter Yes ChemAxon veber_rule Yes ChemAxon mddr_like_rule Yes ChemAxon Selenoamino Acid Metabolism SMP0087161 Specdb::MsMs 307981 Specdb::MsMs 307982 Specdb::MsMs 307983 Specdb::MsMs 352048 Specdb::MsMs 352049 Specdb::MsMs 352050 Specdb::MsMs 3056066 Specdb::MsMs 3056067 Specdb::MsMs 3056068 Specdb::MsMs 3110456 Specdb::MsMs 3110457 Specdb::MsMs 3110458 Specdb::CMs 18894 Specdb::CMs 39550 Specdb::CMs 151713 Specdb::NmrOneD 11262 Specdb::NmrOneD 11263 Specdb::NmrOneD 11264 Specdb::NmrOneD 11265 Specdb::NmrOneD 11266 Specdb::NmrOneD 11267 Specdb::NmrOneD 11268 Specdb::NmrOneD 11269 Specdb::NmrOneD 11270 Specdb::NmrOneD 11271 Specdb::NmrOneD 11272 Specdb::NmrOneD 11273 Specdb::NmrOneD 11274 Specdb::NmrOneD 11275 Specdb::NmrOneD 11276 Specdb::NmrOneD 11277 Specdb::NmrOneD 11278 Specdb::NmrOneD 11279 Specdb::NmrOneD 11280 Specdb::NmrOneD 11281 16682731 FDB027899 BMDBP01293 Adenosylhomocysteinase Q3MHL4 AHCY Enzyme BMDBP02842 tRNA N(3)-methylcytidine methyltransferase METTL2 Q0P5B2 METTL2 Enzyme