Details
Stereochemistry | RACEMIC |
Molecular Formula | C13H14N2O.ClH |
Molecular Weight | 250.724 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.OC(CNC1=CC=CC=N1)C2=CC=CC=C2
InChI
InChIKey=HYYDHUILGLWOOP-UHFFFAOYSA-N
InChI=1S/C13H14N2O.ClH/c16-12(11-6-2-1-3-7-11)10-15-13-8-4-5-9-14-13;/h1-9,12,16H,10H2,(H,14,15);1H
Approval Year
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sources: https://www.ncbi.nlm.nih.gov/pubmed/13999595 |
Primary | Analexin Approved UseAnalgesic, Muscle relaxant Launch Date1959 |
Doses
Dose | Population | Adverse events |
---|---|---|
400 mg 2 times / day multiple, oral Dose: 400 mg, 2 times / day Route: oral Route: multiple Dose: 400 mg, 2 times / day Sources: |
unhealthy, 70 years n = 1 Health Status: unhealthy Age Group: 70 years Sex: M Population Size: 1 Sources: |
Disc. AE: Liver injury... AEs leading to discontinuation/dose reduction: Liver injury Sources: |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Liver injury | Disc. AE | 400 mg 2 times / day multiple, oral Dose: 400 mg, 2 times / day Route: oral Route: multiple Dose: 400 mg, 2 times / day Sources: |
unhealthy, 70 years n = 1 Health Status: unhealthy Age Group: 70 years Sex: M Population Size: 1 Sources: |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29696
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admin on Fri Dec 15 15:39:05 GMT 2023 , Edited by admin on Fri Dec 15 15:39:05 GMT 2023
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17777
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100000086987
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C84055
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206-308-3
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9469
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M574V6XQH7
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326-43-2
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CHEMBL1697767
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m8702
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SUB02134MIG
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ACTIVE MOIETY
SUBSTANCE RECORD