Compound Identification
SMILES
CCCCCCC[C@H](O)C[C@@H]1CC[C@H]2C(C(=O)O[C@@H](C)CCCCCCC[C@@H]3C[C@@H]4CC[C@@H]5C[C@H](C)NC(N3)=[N+]45)=C(C)NC(N)=[N+]12
InChIKey
InChIKey=FDKCICQLNCXLJC-HCGOOJCFSA-P
Formula
C37H66N6O3
Mass
642.973
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Diazines
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Subclass
Pyrimidines and pyrimidine derivatives
- Level 5 Hydropyrimidines
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Subclass
Pyrimidines and pyrimidine derivatives
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Class
Diazines
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazines
Subclass
Pyrimidines and pyrimidine derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Hydropyrimidines
Alternative Parents
Vinylogous amides Pyrrolidines Enoate esters Secondary alcohols Guanidines Monocarboxylic acids and derivatives Carboximidamides Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Amines Organic cations
Molecular Framework
Aliphatic heteropolycyclic compounds
Substituents
Hydropyrimidine - 1,4,5,6-tetrahydropyrimidine - Pyrrolidine - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Vinylogous amide - Carboxylic acid ester - Guanidine - Secondary alcohol - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Carboximidamide - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Amine - Hydrocarbon derivative - Organooxygen compound - Alcohol - Carbonyl group - Organic cation - Aliphatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as hydropyrimidines. These are compounds containing a hydrogenated pyrimidine ring (i.e. containing less than the maximum number of double bonds.).
External Descriptors
Not available