Structure Information
Structure

Compound Identification

SMILES

F[B-](F)(F)F.C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@H]3C[C@H](N(C3)C(=O)OCC3=CC=C(C=C3)[N+]([O-])=O)C(=O)N3CC[S+](C)CC3)=C(N2C1=O)C(=O)OC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=ZQQKMMWOKLNCDO-MPYNIZJXSA-N

Formula

C34H38BF4N5O11S2

Mass

843.63

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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 - Phenol ester - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Nitrobenzene - Phenoxy compound - Pyrroline carboxylic acid or derivatives - Pyrroline carboxylic acid - Pyrrolidine-2-carboxamide - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine carboxylic acid - Nitroaromatic compound - Azepine - Benzenoid - Vinylogous thioester - 1,4-thiazinane - Monocyclic benzene moiety - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carbamic acid ester - Tertiary carboxylic acid amide - Pyrroline - Azetidine - Carboxamide group - Carboxylic acid ester - C-nitro compound - Organic nitro compound - Thioenolether - Secondary alcohol - Sulfenyl compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Alcohol - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic salt - Organic cation - 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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