Structure Information
Structure

Compound Identification

SMILES

CC[Si](CC)(CC)O[C@H](C)[C@@H]1[C@H]2[C@@H](C)C(S[C@H]3CN(C(=O)C3)[Si](CC)(CC)CC)=C(N2C1=O)C(=O)OCOC(=O)C(C)(C)C

InChIKey

InChIKey=VTXCKTWZPTTYLI-DWTKAHDNSA-N

Formula

C32H56N2O7SSi2

Mass

669.04

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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

Aliphatic heteropolycyclic compounds

Substituents

Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Acylal - Dicarboxylic acid or derivatives - Pyrrolidone - 2-pyrrolidone - Vinylogous thioester - Pyrroline - Tertiary carboxylic acid amide - Trialkylheterosilane - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Silyl ether - Carboxylic acid ester - Thioenolether - Carboxamide group - Azetidine - Acetal - N-silyl compound - Carboxylic acid derivative - Organoheterosilane - Azacycle - Organic metalloid salt - Sulfenyl compound - Organonitrogen compound - Organic metalloid moeity - Organic oxide - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Organosilicon 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

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