Compound Identification
SMILES
CC1(CN2C=NC3=C2N=C(Cl)N=C3N)CC1CO
InChIKey
InChIKey=BABZHNOIVBRFFY-UHFFFAOYSA-N
Formula
C11H14ClN5O
Mass
267.72
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Nucleosides, nucleotides, and analogues
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Class
Nucleoside and nucleotide analogues
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Subclass
Cyclopropyl nucleosides
- Level 5 Cyclopropyl purine nucleosides
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Subclass
Cyclopropyl nucleosides
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Class
Nucleoside and nucleotide analogues
-
Superclass
Nucleosides, nucleotides, and analogues
Kingdom
Organic compounds
Superclass
Nucleosides, nucleotides, and analogues
Class
Nucleoside and nucleotide analogues
Subclass
Cyclopropyl nucleosides
Intermediate Tree Nodes
Not available
Direct Parent
Cyclopropyl purine nucleosides
Alternative Parents
6-aminopurines Aminopyrimidines and derivatives 2-halopyrimidines N-substituted imidazoles Imidolactams Aryl chlorides Heteroaromatic compounds Azacyclic compounds Primary amines Primary alcohols Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Cyclopropyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - 2-halopyrimidine - Halopyrimidine - Aryl chloride - Aryl halide - Imidolactam - Pyrimidine - N-substituted imidazole - Heteroaromatic compound - Azole - Imidazole - Organoheterocyclic compound - Azacycle - Organochloride - Organohalogen compound - Primary amine - Amine - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as cyclopropyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclopropane that is substituted a the 1-position with a hydroxyl group and at the 2- position with either a purine base.
External Descriptors
Not available