Compound Identification
SMILES
[Co++].CC1C2=NC(C)(CC3=C(CCC(O)=O)C(C)(CC(O)=O)C(=N3)C(C)=C3[N-]C(C)(C4N=C1C(C)(CCC(O)=O)C4CC(O)=O)C(C)(CC(O)=O)C3CCC(O)=O)C(C)=C2CCC(O)=O
InChIKey
InChIKey=DPVDDBUQBNNVPO-UHFFFAOYSA-M
Formula
C45H59CoN4O14
Mass
938.914
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Tetrapyrroles and derivatives
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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
Sesterterpenoids Metallotetrapyrroles Pyrrolines Pyrrolidines Ketimines Carboxylic acids Carbene-type 1,3-dipolar compounds Azacyclic compounds Organic oxides Organic cobalt salts Hydrocarbon derivatives Carbonyl compounds Organic cations
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Precorrin - Sesterterpenoid - Metallotetrapyrrole skeleton - Pyrrolidine - Pyrroline - Ketimine - Organic transition metal salt - Carboxylic acid derivative - Carbene-type 1,3-dipolar compound - Carboxylic acid - Azacycle - Organic cobalt salt - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Imine - Organic salt - Organic cation - 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