NC1NC(=O)C2=C(N1)N[C@@H]1O[C@H](COP(O)(O)=O)C(S)=C(S)[C@@H]1N2

InChIKey=WOVOXSWXFIURJE-VJTMLDAESA-N

C10H16N5O6PS2

397.36

Organic compounds

Organoheterocyclic compounds

Pteridines and derivatives

Pterins and derivatives

Not available

Molybdopterins

Pyranopterins and derivatives Alpha amino acid amides Monoalkyl phosphates Pyrans Hydropyrimidines Vinylogous amides Secondary carboxylic acid amides Lactams Orthocarboxylic acid derivatives Ortho amides Alkylthiols Thioenols Azacyclic compounds Dialkylamines Oxacyclic compounds Enamines Hydrocarbon derivatives Primary amines Carbonyl compounds Organic oxides

Aliphatic heteropolycyclic compounds

Molybdopterin - Pyranopterin - Alpha-amino acid amide - Alpha-amino acid or derivatives - Monoalkyl phosphate - Organic phosphoric acid derivative - Phosphoric acid ester - Pyran - Alkyl phosphate - Hydropyrimidine - 1,2,3,4-tetrahydropyrimidine - Vinylogous amide - Orthocarboxylic acid derivative - Secondary carboxylic acid amide - Lactam - Ortho amide - Amino acid or derivatives - Carboxamide group - Alkylthiol - Carboxylic acid derivative - Secondary aliphatic amine - Enamine - Oxacycle - Azacycle - Thioenol - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Amine - Organic oxide - Carbonyl group - Primary amine - Organosulfur compound - Organonitrogen compound - Organooxygen compound - Aliphatic 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