Compound Identification
SMILES
C[C@@H](O)[C@@H]1[C@H]2[C@@H](C)C(S[C@H]3C[C@H](N(C3)C(=O)OCC3=CC=C(C=C3)[N+]([O-])=O)C(=O)N3CCN(CC(N)=O)CC3)=C(N2C1=O)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O
InChIKey
InChIKey=IYFPZGFYHJQCNN-BNLXNNPZSA-N
Formula
C36H41N7O12S
Mass
795.82
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 acid amides Benzyloxycarbonyls N-piperazineacetamides Nitrobenzenes Pyrroline carboxylic acids Pyrrolidinecarboxamides Pyrrolidine carboxylic acids Nitroaromatic compounds Azepines N-alkylpiperazines Vinylogous thioesters Tertiary carboxylic acid amides Carbamate esters Enoate esters Primary carboxylic acid amides Secondary alcohols Thioenol ethers Trialkylamines Azetidines Propargyl-type 1,3-dipolar organic compounds Sulfenyl compounds Monocarboxylic acids and derivatives Azacyclic compounds Organic oxoazanium compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic salts Organic zwitterions
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Thienamycin - Alpha-amino acid amide - Alpha-amino acid or derivatives - N-piperazineacetamide - Benzyloxycarbonyl - Nitrobenzene - Nitroaromatic compound - Pyrrolidine carboxylic acid - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Pyrroline carboxylic acid - Pyrroline carboxylic acid or derivatives - Azepine - N-alkylpiperazine - 1,4-diazinane - Vinylogous thioester - Piperazine - Benzenoid - Monocyclic benzene moiety - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Pyrrolidine - Pyrroline - Tertiary carboxylic acid amide - Carbamic acid ester - Carboxylic acid ester - Organic nitro compound - C-nitro compound - Carboxamide group - Azetidine - Primary carboxylic acid amide - Secondary alcohol - Tertiary amine - Tertiary aliphatic amine - Thioenolether - Amino acid or derivatives - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Carboxylic acid derivative - Azacycle - Monocarboxylic acid or derivatives - Sulfenyl compound - Propargyl-type 1,3-dipolar organic compound - Amine - Organic salt - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organosulfur compound - Organic oxide - Alcohol - Organic nitrogen compound - Organic oxygen compound - Organic zwitterion - 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