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(2R-trans)-Oxazolam

HCID 62779
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Basic information

CAS
102916-82-5
Standard SMILES
C[C@@H]1CN2CC(=O)Nc3ccc(Cl)cc3[C@]2(c2ccccc2)O1
InChIKey
VCCZBYPHZRWKFY-KPZWWZAWSA-N
Molecular formula
C18H17ClN2O2
Average molar mass
328.8 g/mol
Monoisotopic mass
328.0978555

Overview

Oxazolam is a drug which is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. It is a prodrug for desmethyldiazepam.

Names & identifiers

Preferred name
(2R-trans)-Oxazolam
IUPAC
(2R,11bS)-10-chloro-2-methyl-11b-phenyl-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one
English name
trans-Oxazolam
Molecular formula
C18H17ClN2O2
Molecular weight
328.79

Names & synonyms

(2R-trans)-OxazolamDTXSID10860314102916-82-5RefChem:1049911DTXCID503401trans-Oxazolam27167-30-2(2R,11bS)-10-chloro-2-methyl-11b-phenyl-2,3,7,11b-tetrahydro[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6(5H)-oneSCHEMBL159582DTXSID50509533AKOS025311522NS00027565
Show more names
trans-10-chloro-2,3,7,11b-tetrahydro-2-methyl-11b-phenyl-oxazolo[3,2-d][1,4]benzodiazepin-6(5h)-one(2S,11bR)-10-chloro-2-methyl-11b-phenyl-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-oneOxazolo[3,2-d][1,4]benzodiazepin-6(5H)-one, 10-chloro-2,3,7,11b-tetrahydro-2-methyl-11b-phenyl-, trans- (9CI)
Q2759512

Database identifiers

CAS
102916-82-5、27167-30-2
PubChem CID
62779
DTXSID
DTXSID10860314

Properties

Computed structural properties

XLogP
3
Topological polar surface area
41.6 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
3
Rotatable bonds
1
Heavy atoms
23
Formal charge
0
Complexity
468

Experimental & physicochemical properties

DrugsPharmaceuticals -> Synthetic Cannabinoids or Psychoactive Compounds
Human DrugsPharmaceuticals

Physicochemical properties

Melting point
186 · 186-188°
Boiling point
495.8 · 495.8±45.0 °C(Predicted)
Density
1.37 · 1.37
pka
12.85 · 12.85±0.60(Predicted)

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Toxicology

Treatment · 1 item

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 item

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.

Carcinogen ClassificationNo indication of carcinogenicity to humans (not listed by IARC).

Chemistry & industry

Uses & manufacturing

Use ClassificationPharmaceuticals

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Compound notes

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