Details
Stereochemistry | RACEMIC |
Molecular Formula | C16H22ClN3O |
Molecular Weight | 307.818 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(CCCNCCO)NC1=CC=NC2=C1C=CC(Cl)=C2
InChI
InChIKey=XFICNUNWUREFDP-UHFFFAOYSA-N
InChI=1S/C16H22ClN3O/c1-12(3-2-7-18-9-10-21)20-15-6-8-19-16-11-13(17)4-5-14(15)16/h4-6,8,11-12,18,21H,2-3,7,9-10H2,1H3,(H,19,20)
Molecular Formula | C16H22ClN3O |
Molecular Weight | 307.818 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/28031899
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28031899
Cletoquine is a metabolite of a disease-modifying anti-rheumatic and antimalarial drug hydroxychloroquine. It is produced by oxidative N-deethylation of hydroxychloroquine.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:07:14 GMT 2023
by
admin
on
Sat Dec 16 17:07:14 GMT 2023
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Record UNII |
83CVD213TU
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Record Status |
Validated (UNII)
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Record Version |
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2583
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C79524
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100000080195
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SUB06654MIG
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4298-15-1
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71826
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DTXSID70863361
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83CVD213TU
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CHEMBL580132
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admin on Sat Dec 16 17:07:14 GMT 2023 , Edited by admin on Sat Dec 16 17:07:14 GMT 2023
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Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
Related Record | Type | Details | ||
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PARENT -> METABOLITE ACTIVE |
Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |