Compound Identification
SMILES
CN(C)CCSC1=C(N2C(C1)C(C(O)C(F)(F)F)C2=O)C(O)=O
InChIKey
InChIKey=VESHJIFRSAIEGP-UHFFFAOYSA-N
Formula
C13H17F3N2O4S
Mass
354.34
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 acids and derivatives Pyrroline carboxylic acids Azepines Vinylogous thioesters Tertiary carboxylic acid amides Trialkylamines Thioenol ethers Secondary alcohols Amino acids Azetidines Fluorohydrins Sulfenyl compounds Azacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Organofluorides Carbonyl compounds Alkyl fluorides Hydrocarbon derivatives
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Thienamycin - Alpha-amino acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - Vinylogous thioester - Pyrroline - Tertiary carboxylic acid amide - Azetidine - Tertiary aliphatic amine - Thioenolether - Halohydrin - Tertiary amine - Secondary alcohol - Amino acid - Amino acid or derivatives - Carboxamide group - Fluorohydrin - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Carboxylic acid - Sulfenyl compound - Azacycle - Alcohol - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Organic nitrogen compound - Alkyl halide - Alkyl fluoride - 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