Compound Identification
SMILES
CCSC([C@@H]1C[C@@H](CN1)SC1=C(N2[C@@H]([C@@H]([C@@H](C)O)C2=O)[C@H]1C)C(O)=O)C(=O)N(N)CC
InChIKey
InChIKey=ATTAVIYNHMJHPS-KDBYIVBFSA-N
Formula
C20H32N4O5S2
Mass
472.62
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
Beta amino acids and derivatives Alpha amino acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Tertiary carboxylic acid amides Pyrrolidines Thioenol ethers Amino acids Tertiary amines Azetidines Carboxylic acid hydrazides Secondary alcohols Carboxylic acids Azacyclic compounds Dialkylamines Dialkylthioethers Monocarboxylic acids and derivatives Sulfenyl compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Thienamycin - Beta amino acid or derivatives - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Carboxylic acid hydrazide - Carboxamide group - Azetidine - Amino acid or derivatives - Secondary alcohol - Tertiary amine - Amino acid - Thioenolether - Dialkylthioether - Monocarboxylic acid or derivatives - Sulfenyl compound - Carboxylic acid derivative - Secondary amine - Carboxylic acid - Secondary aliphatic amine - Azacycle - Thioether - Organic oxide - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Organosulfur compound - Alcohol - Amine - Organic nitrogen compound - Hydrocarbon derivative - 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