Details
Stereochemistry | RACEMIC |
Molecular Formula | C17H14BrFN2O2 |
Molecular Weight | 377.208 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
FC1=CC=CC=C1C23OCCN2CC(=O)NC4=CC=C(Br)C=C34
InChI
InChIKey=XDKCGKQHVBOOHC-UHFFFAOYSA-N
InChI=1S/C17H14BrFN2O2/c18-11-5-6-15-13(9-11)17(12-3-1-2-4-14(12)19)21(7-8-23-17)10-16(22)20-15/h1-6,9H,7-8,10H2,(H,20,22)
CNS Activity
Originator
Approval Year
PubMed
Title | Date | PubMed |
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[The behavior of 1,4-benzodiazepine drugs in the acidic media. I. Proton and carbon 13 nuclear magnetic resonance spectra of oxazolam, cloxazolam and haloxazolam in the acidic media]. | 1984 Jun |
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The behavior of 1,4-benzodiazepine drugs in acidic media. V. Kinetics of hydrolysis of flutazolam and haloxazolam in aqueous solution. | 1986 Jan |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C1012
Created by
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DEA NO. |
2771
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1357
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DTXSID60866740
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3563
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C83744
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Haloxazolam
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C018779
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m5908
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4295
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DB01476
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100000083946
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SUB08010MIG
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CHEMBL2104461
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59128-97-1
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M448L2V8XP
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ACTIVE MOIETY