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Haloxazolam

HCID 178805767
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Grundinformationen

CAS
88195-92-0
Standard-SMILES
O=C1CN2CCOC2(c2ccccc2F)c2cc(Br)ccc2N1
InChIKey
XDKCGKQHVBOOHC-UHFFFAOYSA-N
Summenformel
C17H14BrFN2O2
Durchschnittliche Molmasse
377,2 g/mol

Überblick

Haloxazolam is an organic molecular entity.

Namen und Bezeichner

Bevorzugter Name
Haloxazolam
IUPAC
10-bromo-11b-(2-fluorophenyl)-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one
Englischer Name
haloxazolam
Summenformel
C17H14BrFN2O2
Molmasse
377.21

Namen und Synonyme

haloxazolamSomelin59128-97-1HaloxazolamumCS-430M448L2V8XP10-Bromo-11b-(2-fluorophenyl)-2,3,7,11b-tetrahydrooxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-oneDTXSID6086674010-Bromo-11b-(2-fluorophenyl)-2,3,7,11b-tetrahydrooxazolo[3,2-d](1,4)benzodiazepin-6(5H)-oneRefChem:783374DTXCID90814996(11bRS)-10-Bromo-11b-(2-fluorophenyl)-2,3,7,11b-tetrahydro(1,3)oxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-one
Weitere Namen anzeigen
13-bromo-2-(2-fluorophenyl)-3-oxa-6,9-diazatricyclo(8.4.0.02,?)tetradeca-1(10),11,13-trien-8-one13-bromo-2-(2-fluorophenyl)-3-oxa-6,9-diazatricyclo(8.4.0.02,6)tetradeca-1(10),11,13-trien-8-one10-Bromo-11b-(o-fluorophenyl)-2,3,7,11b-tetrahydrooxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-oneHaloxazolam [INN:JAN]Haloxazolam (1.0mg/ml in Acetonitrile)10-Bromo-11b-(o-fluorophenyl)-2,3,7,11b-tetrahydrooxazolo[3,2-d][1,4]benzodiazepin-6(5H)-oneOxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-one, 2,3,7,11b-tetrahydro-10-bromo-11b-(2-fluorophenyl)-Oxazolo[3,2-d](1,4)benzodiazepin-6(5H)-one, 2,3,7,11b-tetrahydro-10-bromo-11b-(2-fluorophenyl)-

Datenbank-Bezeichner

CAS

Eigenschaften

Berechnete Struktureigenschaften

XLogP
2,8
Polarare Oberfläche (TPSA)
41,6 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
4
Frei drehbare Bindungen
1
Schwere Atome
23
Formalladung
0
Komplexität
480

Experimentelle und physikochemische Eigenschaften

Drugs · 3 Einträge

DEA NFLIS-Drug Category -> Benzodiazepines

DEA Schedule IV Controlled Substance -> Depressants

Pharmaceuticals -> Nervous system -> Anxiolytics

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Gefahrenhinweise

Regulatory InformationDEA schedule IV controlled substance

Toxikologische Informationen

Treatment · 1 Eintrag

General supportive measures should be employed, along with intravenous fluids, and an adequate airway maintained. Hypotension may be combated by the use of norepinephrine or metaraminol. Dialysis is of limited value. Flumazenil (Anexate) is a competitive benzodiazepine receptor antagonist that can be used as an antidote for benzodiazepine overdose. In particular, flumazenil is very effective at reversing the CNS depression associated with benzodiazepines but is less effective at reversing respiratory depression. Its use, however, is controversial as it has numerous contraindications. It is contraindicated in patients who are on long-term benzodiazepines, those who have ingested a substance that lowers the seizure threshold, or in patients who have tachycardia or a history of seizures. As a general rule, medical observation and supportive care are the mainstay of treatment of benzodiazepine overdose. Although benzodiazepines are absorbed by activated charcoal, gastric decontamination with activated charcoal is not beneficial in pure benzodiazepine overdose as the risk of adverse effects often outweigh any potential benefit from the procedure. It is recommended only if benzodiazepines have been taken in combination with other drugs that may benefit from decontamination. Gastric lavage (stomach pumping) or whole bowel irrigation are also not recommended.

Toxicity Summary · 1 Eintrag

Benzodiazepines bind nonspecifically to benzodiazepine receptors BNZ1, which mediates sleep, and BNZ2, which affects 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 the inhibitory neurotransmitter GABA to the site opens the chloride channel, resulting in a hyperpolarized cell membrane that prevents further excitation of the cell.

Chemie und Industrie

Verwendung und Herstellung

UsesHaloxazolam is indicated for the treatment insomnia.

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Auf dieser SeiteGrundinformationenÜberblickNamen und BezeichnerEigenschaftenSicherheit und RegulatorischesChemie und IndustrieZugehörige ReaktionenNotizen zur Verbindung
88195-92-0
ChEMBL
CHEMBL2104461
ChEBI
CHEBI:31666
UNII
M448L2V8XP
Nikkaji
J3.200J
Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).