Compound Identification
SMILES
Cl.C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(SC3CN(CC4=CC=C(F)C=C4)C3)=C(N2C1=O)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O
InChIKey
InChIKey=WUNZQUSABUBNFL-NUVDOEAFSA-N
Formula
C27H29ClFN3O6S
Mass
578.05
Taxonomic Classification
Taxonomy Tree
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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 Benzyloxycarbonyls Nitrobenzenes Benzylamines Nitroaromatic compounds Phenylmethylamines Pyrroline carboxylic acids Aralkylamines Azepines Fluorobenzenes Aryl fluorides Vinylogous thioesters Tertiary carboxylic acid amides Enoate esters Secondary alcohols Thioenol ethers Azetidines Trialkylamines Propargyl-type 1,3-dipolar organic compounds Sulfenyl compounds Organic oxoazanium compounds Monocarboxylic acids and derivatives Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Hydrochlorides Organic oxides Organic zwitterions Organofluorides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Thienamycin - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Nitrobenzene - Nitroaromatic compound - Pyrroline carboxylic acid or derivatives - Pyrroline carboxylic acid - Benzylamine - Phenylmethylamine - Aralkylamine - Fluorobenzene - Halobenzene - Azepine - Monocyclic benzene moiety - Benzenoid - Aryl fluoride - Vinylogous thioester - Aryl halide - Alpha,beta-unsaturated carboxylic ester - Pyrroline - Tertiary carboxylic acid amide - Enoate ester - Organic nitro compound - Tertiary amine - Secondary alcohol - C-nitro compound - Amino acid or derivatives - Carboxamide group - Thioenolether - Tertiary aliphatic amine - Azetidine - Carboxylic acid ester - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Sulfenyl compound - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic zwitterion - Organic oxygen compound - Carbonyl group - Amine - Organic nitrogen compound - Organic salt - Hydrochloride - Organic oxide - Organosulfur compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organohalogen compound - Alcohol - Organofluoride - 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