Compound Identification
SMILES
CCOC(=O)C1=C(N2[C@@H](CC1)[C@H](NC(=O)OC(C)(C)C)C2=O)C(O)=O
InChIKey
InChIKey=FQFVXIYIVUKVPS-UWVGGRQHSA-N
Formula
C16H22N2O7
Mass
354.359
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Lactams
-
Subclass
Beta lactams
- Level 5 Carbacephems
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Subclass
Beta lactams
-
Class
Lactams
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Lactams
Subclass
Beta lactams
Intermediate Tree Nodes
Not available
Direct Parent
Carbacephems
Alternative Parents
Alpha amino acids and derivatives Tetrahydropyridines Dicarboxylic acids and derivatives Vinylogous amides Tertiary carboxylic acid amides Enoate esters Carbamate esters Tertiary amines Azetidines Amino acids Carboxylic acids Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Carbacephem - Alpha-amino acid or derivatives - Tetrahydropyridine - Dicarboxylic acid or derivatives - Tertiary carboxylic acid amide - Carbamic acid ester - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Vinylogous amide - Azetidine - Carboxylic acid ester - Tertiary amine - Amino acid or derivatives - Carboxamide group - Amino acid - Carboxylic acid - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as carbacephems. These are a new class of beta-lactam antibiotics similar in structure to the cephalosporins. They differ from cephalosporins, however, in the substitution of a sulfur atom in the dihydrothiazine ring with a methylene group to form a tetrahydropyridine ring.
External Descriptors
Not available