[O-][Mo]([O-])=O.NC1=NC(=O)C2=C(N[C@@H]3O[C@H](COP([O-])([O-])=O)C([S-])=C([S-])[C@@H]3N2)N1

InChIKey=ZFTJTAWYOXYIKT-BKZHXLINSA-J

C10H10MoN5O9PS2

535.26

Organic compounds

Organoheterocyclic compounds

Pteridines and derivatives

Pterins and derivatives

Not available

Molybdopterins

Pyranopterins and derivatives Secondary alkylarylamines Pyrimidones Aminopyrimidines and derivatives Pyrans Primary aromatic amines Alkyl phosphates Vinylogous amides Heteroaromatic compounds Oxacyclic compounds Azacyclic compounds Organic transition metal salts Organosulfur compounds Hydrocarbon derivatives Organic oxides Organooxygen compounds Organopnictogen compounds Organic anions

Aromatic heteropolycyclic compounds

Molybdopterin - Pyranopterin - Aminopyrimidine - Pyrimidone - Secondary aliphatic/aromatic amine - Organic phosphoric acid derivative - Phosphoric acid ester - Primary aromatic amine - Pyran - Pyrimidine - Alkyl phosphate - Heteroaromatic compound - Vinylogous amide - Oxacycle - Azacycle - Organic metal salt - Organic transition metal salt - Secondary amine - Amine - Hydrocarbon derivative - Primary amine - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic anion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as molybdopterins. These are cofactors or analogs thereof, with a structure based on a furan ring fused to a pterin. In addition, the pyran ring features two thiolates, which serve as ligands in molybdo- and tungstoenzymes. In some cases, the alkyl phosphate group is replaced by an alkyl diphosphate nucleotide.

Not available