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27223-35-4 molecular structure
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14-chloro-4,10-dimethyl-2-phenyl-3-oxa-7,10-diazatricyclo[9.4.0.02,7]pentadeca-1(11),4,12,14-tetraene-6,9-dione

ChemBase ID: 1365
Molecular Formular: C20H17ClN2O3
Molecular Mass: 368.81358
Monoisotopic Mass: 368.09277009
SMILES and InChIs

SMILES:
Clc1cc2C3(OC(=CC(=O)N3CC(=O)N(c2cc1)C)C)c1ccccc1
Canonical SMILES:
CC1=CC(=O)N2C(O1)(c1ccccc1)c1cc(Cl)ccc1N(C(=O)C2)C
InChI:
InChI=1S/C20H17ClN2O3/c1-13-10-18(24)23-12-19(25)22(2)17-9-8-15(21)11-16(17)20(23,26-13)14-6-4-3-5-7-14/h3-11H,12H2,1-2H3
InChIKey:
PWAJCNITSBZRBL-UHFFFAOYSA-N

Cite this record

CBID:1365 http://www.chembase.cn/molecule-1365.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
14-chloro-4,10-dimethyl-2-phenyl-3-oxa-7,10-diazatricyclo[9.4.0.02,7]pentadeca-1(11),4,12,14-tetraene-6,9-dione
14-chloro-4,10-dimethyl-2-phenyl-3-oxa-7,10-diazatricyclo[9.4.0.0^{2,7}]pentadeca-1(11),4,12,14-tetraene-6,9-dione
IUPAC Traditional name
ketazolam
Synonyms
Ketazolam
11-Chloro-8,12b-dihydro-2,8-dimethyl-12b-phenyl-4H-[1,3]oxazino[3,2-d][1,4]benzodiazepine-4,7(6H)-dione
(±)-Ketazolam
Anseren
Ansieten
Anxon
Contamex
Loftran
NSC 338158
U 28774
Unakalm
CAS Number
27223-35-4
PubChem SID
160964825
46507008
PubChem CID
33746
ATC CODE
N05BA10
Chemspider ID
31110
DrugBank ID
DB01587
KEGG ID
D04650
Unique Ingredient Identifier
92A214MD7Y
Wikipedia Title
Ketazolam

DATA SOURCES

DATA SOURCES

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Data Source Data ID Price
TRC
K165650 external link Add to cart Please log in.

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem ALOGPS 2.1
Acid pKa 14.1983595  H Acceptors
H Donor LogD (pH = 5.5) 3.0128675 
LogD (pH = 7.4) 3.0128675  Log P 3.0128677 
Molar Refractivity 99.781 cm3 Polarizability 37.913918 Å3
Polar Surface Area 49.85 Å2 Rotatable Bonds
Lipinski's Rule of Five true 
Log P 2.6  LOG S -3.64 
Solubility (Water) 8.39e-02 g/l 

PROPERTIES

PROPERTIES

Safety Information Pharmacology Properties Product Information Bioassay(PubChem)
MSDS Link
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Admin Routes
Oral expand Show data source
Excretion
Renal expand Show data source
Half Life
26-200 hours expand Show data source
Metabolism
Hepatic expand Show data source
Legal Status
Schedule IV(US) expand Show data source
Certificate of Analysis
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DETAILS

DETAILS

DrugBank DrugBank Wikipedia Wikipedia TRC TRC
DrugBank - DB01587 external link
Item Information
Drug Groups approved
Description Ketazolam is a drug which is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. Ketazolam is not approved for sale in the United States or Canada.
Indication Ketazolam could be used for the treatment of anxiety. In approved countries, it is indicated for the treatment of anxiety, tension, irritability and similar stress related symptoms.
Pharmacology Benzodiazepines enhance the effect of the neurotransmitter gamma-aminobutyric acid (GABA), which results in sedative, hypnotic, anxiolytic, anticonvulsant, muscle relaxant and amnesic action.
Benzodiazepines bind nonspecifically to benzodiazepine receptors which mediate sleep, affects muscle relaxation, anticonvulsant activity, motor coordination, and memory. As benzodiazepine receptors are thought to be coupled to gamma-aminobutyric acid-A (GABAA) receptors, this enhances the effects of GABA by increasing GABA affinity for the GABA receptor. Binding of GABA to the site opens the chloride channel, resulting in a hyperpolarized cell membrane that prevents further excitation of the cell.
Toxicity Symptoms of overdose include somnolence, confusion, coma, and diminished reflexes. Respiration, pulse and blood pressure should be monitored.
Biotransformation Ketazolam breaks down in the blood to diazepam which breaks down to demoxepam which breaks down to desmethyldiazepam.
Half Life 26-200 hours
Elimination Diazepam and its metabolites are excreted mainly in the urine, predominantly as their glucuronide conjugates.
External Links
Wikipedia
Toronto Research Chemicals - K165650 external link
A psychotropic benzodiazepine derivative with hypnotic and anxiolytic properties. Controlled Substance.

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
  • • Sethy, V.H. et al.: Naun.-Schmeid. Atch. Pharmacol., 301, 157 (1978)
  • • Moore, S. et al.: Curr. Therap. Res., 29, 704 (1978)
  • • Gutierrez, S.F. et al.: Cien. Pharmac., 5, 37 (1978)
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PATENTS

PATENTS

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INTERNET

INTERNET

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