Compound Identification
SMILES
C[C@@H](O)C1C2[C@@H](C)C(S[C@H]3C[C@H](N(C3)C(=O)OCC3=CC=C(C=C3)[N+]([O-])=O)C3=NC(CO)=C(C)S3)=C(N2C1=O)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O
InChIKey
InChIKey=LCMQKWWYKNANLT-XUSHFLBOSA-N
Formula
C34H35N5O11S2
Mass
753.8
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
-
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 acids and derivatives Benzyloxycarbonyls Nitrobenzenes 2,4,5-trisubstituted thiazoles Pyrroline carboxylic acids Pyrrolidine carboxylic acids Nitroaromatic compounds Azepines Vinylogous thioesters Tertiary carboxylic acid amides Carbamate esters Enoate esters Heteroaromatic compounds Thioenol ethers Secondary alcohols Azetidines Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Azacyclic compounds Sulfenyl compounds Organic oxoazanium compounds Organic oxides Primary alcohols Hydrocarbon derivatives Aromatic alcohols Carbonyl compounds Organic salts Organic zwitterions Organonitrogen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Thienamycin - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Nitrobenzene - 2,4,5-trisubstituted 1,3-thiazole - Nitroaromatic compound - Pyrrolidine carboxylic acid or derivatives - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Pyrrolidine carboxylic acid - Azepine - Vinylogous thioester - Monocyclic benzene moiety - Benzenoid - Pyrrolidine - Heteroaromatic compound - Azole - Pyrroline - Tertiary carboxylic acid amide - Thiazole - Carbamic acid ester - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Azetidine - Organic nitro compound - Carboxamide group - Carboxylic acid ester - C-nitro compound - Secondary alcohol - Thioenolether - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Allyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Sulfenyl compound - Organic oxoazanium - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Alcohol - Organic zwitterion - Organic nitrogen compound - Organic salt - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Primary alcohol - Aromatic alcohol - 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