CC(C)(C)OC(=O)N[C@@H](CC1=CC=CC=C1)[C@@H](O)CC(=O)NCCCCCC(=O)NC1=NC(=O)N(C=C1)[C@H]1CS[C@@H](CO)O1

InChIKey=RCWDJPGPAFDRKH-ABMRFVCESA-N

C30H43N5O8S

633.76

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

3'-thia pyrimidine nucleosides

Not available

3'-thia pyrimidine nucleosides

Gamma amino acids and derivatives Amphetamines and derivatives N-arylamides Pyrimidones Hydropyrimidines Imidolactams N-acyl amines Carbamate esters Heteroaromatic compounds Oxathiolanes Monothioacetals Secondary carboxylic acid amides Secondary alcohols Organic carbonic acids and derivatives Azacyclic compounds Oxacyclic compounds Carbonyl compounds Primary alcohols Hydrocarbon derivatives Organopnictogen compounds Organic oxides

Aromatic heteromonocyclic compounds

3'-thia pyrimidine nucleoside - Gamma amino acid or derivatives - Amphetamine or derivatives - N-arylamide - Pyrimidone - Monocyclic benzene moiety - Fatty amide - Hydropyrimidine - N-acyl-amine - Pyrimidine - Benzenoid - Imidolactam - Fatty acyl - Heteroaromatic compound - Carbamic acid ester - Oxathiolane - Monothioacetal - Secondary carboxylic acid amide - Secondary alcohol - Carboxamide group - Carbonic acid derivative - Oxacycle - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Organic oxide - Alcohol - Organic oxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Primary alcohol - Organic nitrogen compound - Carbonyl group - Organopnictogen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as 3'-thia pyrimidine nucleosides. These are nucleoside analogues with a structure that consists of a pyrimidine base, which is N-substituted at the 1-position with a 3'-thia derivative (1,3-oxazolidine) of the ribose moiety that is characteristic of nucleosides.

Not available