Compound Identification
SMILES
CC(C)OC(=O)OC(C)OC(=O)C1=C(SC2CNC(=O)C2)[C@H](C)C2C([C@@H](C)OC(=O)CN)C(=O)N12
InChIKey
InChIKey=LZGNIMBRUJUWAX-BJSXLXPESA-N
Formula
C22H31N3O9S
Mass
513.56
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Lactams
-
Subclass
Beta lactams
-
Level 5
Carbapenems
- Level 6 Thienamycins
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Level 5
Carbapenems
-
Subclass
Beta lactams
-
Class
Lactams
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Lactams
Subclass
Beta lactams
Intermediate Tree Nodes
Carbapenems
Direct Parent
Thienamycins
Alternative Parents
Alpha amino acid esters Pyrroline carboxylic acids Azepines Vinylogous thioesters Carbonic acid diesters Pyrrolidine-2-ones Dicarboxylic acids and derivatives Tertiary carboxylic acid amides Enoate esters Thioenol ethers Azetidines Secondary carboxylic acid amides Azacyclic compounds Acetals Sulfenyl compounds Organopnictogen compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives Monoalkylamines
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Thienamycin - Alpha-amino acid ester - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Carbonic acid diester - Dicarboxylic acid or derivatives - Vinylogous thioester - Pyrrolidone - 2-pyrrolidone - Pyrrolidine - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Tertiary carboxylic acid amide - Pyrroline - Amino acid or derivatives - Azetidine - Carboxamide group - Carboxylic acid ester - Carbonic acid derivative - Thioenolether - Secondary carboxylic acid amide - Acetal - Sulfenyl compound - Azacycle - Carboxylic acid derivative - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organosulfur compound - Primary amine - Primary aliphatic amine - Amine - Organonitrogen 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