Compound Identification
SMILES
CC(C)CCN1C(C[NH+]2CCC[C@@H](CO)C2)=CN=C1S(=O)(=O)C(C)C
InChIKey
InChIKey=YOAWRNXUACGVPY-MRXNPFEDSA-O
Formula
C18H34N3O3S
Mass
372.55
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Azoles
-
Subclass
Imidazoles
-
Level 5
Substituted imidazoles
-
Level 6
Trisubstituted imidazoles
- Level 7 1,2,5-trisubstituted imidazoles
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Level 6
Trisubstituted imidazoles
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Level 5
Substituted imidazoles
-
Subclass
Imidazoles
-
Class
Azoles
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Azoles
Subclass
Imidazoles
Intermediate Tree Nodes
Substituted imidazoles - Trisubstituted imidazoles
Direct Parent
1,2,5-trisubstituted imidazoles
Alternative Parents
Aralkylamines Piperidines N-substituted imidazoles Sulfones Quaternary ammonium salts Heteroaromatic compounds 1,3-aminoalcohols Trialkylamines Azacyclic compounds Primary alcohols Organic oxides Hydrocarbon derivatives Organic cations
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
1,2,5-trisubstituted-imidazole - Aralkylamine - N-substituted imidazole - Piperidine - 1,3-aminoalcohol - Quaternary ammonium salt - Sulfone - Sulfonyl - Heteroaromatic compound - Tertiary aliphatic amine - Azacycle - Amine - Alcohol - Hydrocarbon derivative - Primary alcohol - Organic oxide - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Organic cation - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as 1,2,5-trisubstituted imidazoles. These are imidazoles in which the imidazole ring is substituted at positions 1, 2, and 5.
External Descriptors
Not available