Structure Information
Structure

Compound Identification

SMILES

[K+].OC\C=C1/O[C@@H]2CC(=O)N2[C@H]1C([O-])=O.C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@H]3CN[C@@H](C3)C(=O)N(C)C)=C(N2C1=O)C(O)=O

InChIKey

InChIKey=TYWXJWDDZSTOAL-XYYFGJEJSA-M

Formula

C25H33KN4O10S

Mass

620.72

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Lactams

Subclass

Beta lactams

Intermediate Tree Nodes

Carbapenems

Direct Parent

Thienamycins

Alternative Parents

Molecular Framework

Not available

Substituents

Thienamycin - Proline or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Clavam - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Para-oxazepine - Azepine - Vinylogous thioester - Oxazolidine - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Amino acid or derivatives - Amino acid - Azetidine - Carboxamide group - Carboxylic acid salt - Secondary alcohol - Tertiary amine - Thioenolether - Organic alkali metal salt - Azacycle - Secondary amine - Oxacycle - Sulfenyl compound - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Secondary aliphatic amine - Alcohol - Hydrocarbon derivative - Organonitrogen compound - Organic oxide - Organooxygen compound - Organic oxygen compound - Carbonyl group - Organic potassium salt - Organic salt - Organic zwitterion - Organosulfur compound - Amine - Primary alcohol - Organic nitrogen compound - Aliphatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as thienamycins. These are beta-lactam antibiotics that differ from penicillins in having the thiazolidine sulfur atom replaced by carbon, the sulfur then becoming the first atom in the side chain.

External Descriptors

Not available

Previous Back Next