Compound Identification
SMILES
CC[C@H]1[C@H](CC2=N\C(=C\C3=C(CCC(O)=O)C(C)=C(C[C@@H]4NC(=O)[C@H](CC)[C@H]4C)N3)C(CCC(O)=O)=C2C)NC(=O)[C@@H]1C
InChIKey
InChIKey=TYOWQSLRVAUSMI-NPKPUNNESA-N
Formula
C33H46N4O6
Mass
594.753
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Tetrapyrroles and derivatives
- Subclass Bilirubins
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Class
Tetrapyrroles and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Tetrapyrroles and derivatives
Subclass
Bilirubins
Intermediate Tree Nodes
Not available
Direct Parent
Bilirubins
Alternative Parents
Dipyrrins Pyrrolidine-2-ones Dicarboxylic acids and derivatives Heteroaromatic compounds Secondary carboxylic acid amides Lactams Ketimines Propargyl-type 1,3-dipolar organic compounds Carboxylic acids Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Bilirubin skeleton - Dipyrrin - Dicarboxylic acid or derivatives - Pyrrolidone - 2-pyrrolidone - Substituted pyrrole - Pyrrole - Pyrrolidine - Heteroaromatic compound - Secondary carboxylic acid amide - Carboxamide group - Ketimine - Lactam - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Azacycle - Carboxylic acid derivative - Carboxylic acid - Imine - Organic oxide - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as bilirubins. These are organic compounds containing a dicarboxylic acyclic tetrapyrrole derivative.
External Descriptors
Not available