Compound Identification
SMILES
CCCOC(=O)CCC1C2=CC3=NC(C(CCC(=O)OCCC)C3(C)C)=C(C)C3=NC(C(CC(=O)OCCC)C3(C)CCC(=O)OCCC)C3(C)N=C(C(CCC(=O)OCCC)C3(C)CC(=O)OCCC)C(C)=C(N2)C1(C)CC(=O)OCCC
InChIKey
InChIKey=BLLUNPSEYAIXAX-UHFFFAOYSA-N
Formula
C66H102N4O14
Mass
1175.556
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Tetrapyrroles and derivatives
-
Subclass
Corrinoids
- Level 5 Precorrins
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Subclass
Corrinoids
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Class
Tetrapyrroles and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Tetrapyrroles and derivatives
Subclass
Corrinoids
Intermediate Tree Nodes
Not available
Direct Parent
Precorrins
Alternative Parents
Fatty acid esters Pyrrolines Pyrrolidines Ketimines Carboxylic acid esters Propargyl-type 1,3-dipolar organic compounds Enamines Dialkylamines Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Precorrin - Fatty acid ester - Fatty acyl - Pyrrolidine - Pyrroline - Carboxylic acid ester - Ketimine - Carboxylic acid derivative - Secondary aliphatic amine - Enamine - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic oxide - Imine - Organic oxygen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Amine - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as precorrins. These are intermediates formed by methylation at one or more of the four rings prior to the formation of the macrocyclic corrin ring.
External Descriptors
Not available