Compound Identification
SMILES
CC(O)[C@@H]1[C@H]2[C@@H](C)C(S[C@@]3(CNC(=O)C3)C(=O)N3CCN(CC(=O)OCC4=CC=C(C=C4)[N+]([O-])=O)CC3)=C(N2C1=O)C(O)=O
InChIKey
InChIKey=APUUSVHMBMNCHG-YZDNTSIVSA-N
Formula
C28H33N5O10S
Mass
631.66
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Lactams
-
Subclass
Beta lactams
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Level 5
Carbapenems
- Level 6 Thienamycins
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Level 5
Carbapenems
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Subclass
Beta lactams
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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 Beta amino acids and derivatives Benzyloxycarbonyls Nitrobenzenes Pyrroline carboxylic acids Pyrrolidinecarboxamides Nitroaromatic compounds Azepines N-alkylpiperazines Vinylogous thioesters Dicarboxylic acids and derivatives Pyrrolidine-2-ones Tertiary carboxylic acid amides Trialkylamines Thioenol ethers Azetidines Carboxylic acid esters Secondary carboxylic acid amides Amino acids Secondary alcohols Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Carboxylic acids Azacyclic compounds Organic oxoazanium compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Thienamycin - Alpha-amino acid ester - Beta amino acid or derivatives - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Nitrobenzene - Pyrroline carboxylic acid - Nitroaromatic compound - Pyrrolidine-3-carboxamide - Pyrrolidine carboxylic acid or derivatives - Pyrroline carboxylic acid or derivatives - Azepine - N-alkylpiperazine - Piperazine - Benzenoid - Monocyclic benzene moiety - Pyrrolidone - 2-pyrrolidone - Dicarboxylic acid or derivatives - Vinylogous thioester - 1,4-diazinane - Tertiary carboxylic acid amide - Pyrrolidine - Pyrroline - Amino acid or derivatives - Azetidine - Amino acid - Carboxamide group - Carboxylic acid ester - Organic nitro compound - C-nitro compound - Tertiary aliphatic amine - Thioenolether - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Azacycle - Sulfenyl compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Carboxylic acid - Organic 1,3-dipolar compound - Organic oxoazanium - Amine - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Alcohol - Carbonyl group - Organic salt - Organic oxide - Organic zwitterion - Hydrocarbon derivative - 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