Structure Information
Structure

Compound Identification

SMILES

[I-].C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@H]3C[C@@H](C[N+]4(CC(N)=O)CCCC4)N(C3)C(=O)OCC3=CC=C(C=C3)[N+]([O-])=O)=C(N2C1=O)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=SMOFKEUQGSRJBQ-XDFOCJBESA-N

Formula

C36H43IN6O11S

Mass

894.74

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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

Aromatic heteropolycyclic compounds

Substituents

Thienamycin - Alpha-amino acid amide - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Nitrobenzene - Nitroaromatic compound - Pyrrolidine carboxylic acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Pyrrolidine carboxylic acid - Azepine - Monocyclic benzene moiety - Vinylogous thioester - N-alkylpyrrolidine - Benzenoid - Tetraalkylammonium salt - Pyrrolidine - Pyrroline - Quaternary ammonium salt - Tertiary carboxylic acid amide - Carbamic acid ester - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Thioenolether - Organic nitro compound - Carboxamide group - Carboxylic acid ester - C-nitro compound - Primary carboxylic acid amide - Secondary alcohol - Azetidine - Azacycle - Carboxylic acid derivative - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Sulfenyl compound - Amine - Organic oxygen compound - Organic nitrogen compound - Organic salt - Carbonyl group - Organic iodide salt - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic zwitterion - Alcohol - Aromatic 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

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