Compound Identification
SMILES
Cl.CC1=NC=C(CO)C(CO)=C1O.CCC(C)(C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(=O)O3)[C@@H]12
InChIKey
InChIKey=YBNJGZUGWHMZQE-LYJWAQJISA-N
Formula
C33H50ClNO8
Mass
624.21
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Pyridines and derivatives
- Subclass Pyridoxines
-
Class
Pyridines and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Pyridines and derivatives
Subclass
Pyridoxines
Intermediate Tree Nodes
Not available
Direct Parent
Pyridoxines
Alternative Parents
Delta valerolactones Methylpyridines Hydroxypyridines Fatty acid esters Oxanes Dicarboxylic acids and derivatives Heteroaromatic compounds Secondary alcohols Carboxylic acid esters Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Hydrochlorides Organic oxides Organonitrogen compounds Carbonyl compounds Primary alcohols Aromatic alcohols
Molecular Framework
Not available
Substituents
Pyridoxine - Delta valerolactone - Fatty acid ester - Delta_valerolactone - Hydroxypyridine - Methylpyridine - Fatty acyl - Dicarboxylic acid or derivatives - Oxane - Heteroaromatic compound - Carboxylic acid ester - Secondary alcohol - Lactone - Oxacycle - Azacycle - Carboxylic acid derivative - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Primary alcohol - Carbonyl group - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - Aromatic alcohol - Hydrochloride - Organic oxide - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as pyridoxines. These are pyridoxal derivatives in which the carbaldehyde group at position 2 of the pyridoxal moiety is replaced by a hydroxymethyl group.
External Descriptors
Not available