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trans-オキサゾラム

(2R-trans)-Oxazolam

HCID 62779
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基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
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基本情報

CAS
102916-82-5
標準SMILES
C[C@@H]1CN2CC(=O)Nc3ccc(Cl)cc3[C@]2(c2ccccc2)O1
InChIKey
VCCZBYPHZRWKFY-KPZWWZAWSA-N
分子式
C18H17ClN2O2
平均分子量
328.8 g/mol
単同位体質量
328.0978555

概要

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.

名称と識別子

優先名称
(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
現地名
trans-オキサゾラム
英語名
trans-Oxazolam
分子式
C18H17ClN2O2
分子量
328.79

名称と別名

(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
名称をさらに表示
trans-オキサゾラムrel-(2R*,11bS*)-10-クロロ-2,3,7,11b-テトラヒドロ-2-メチル-11b-フェニルオキサゾロ[3,2-d][1,4]ベンゾジアゼピン-6(5H)-オン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

データベース識別子

CAS
102916-82-5、27167-30-2

物性

構造計算による物性

XLogP
3
極性表面積
41.6 Ų
水素結合供与体数
1
水素結合受容体数
3
回転可能結合数
1
重原子数
23
形式電荷
0
複雑度
468

実験および物理化学的性質

DrugsPharmaceuticals -> Synthetic Cannabinoids or Psychoactive Compounds
Human DrugsPharmaceuticals

物理化学的性質

融点
186 · 186-188°
沸点
495.8 · 495.8±45.0 °C(Predicted)
比重(密度)
1.37 · 1.37
酸解離定数(Pka)
12.85 · 12.85±0.60(Predicted)

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

毒性情報

Treatment · 1 件

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 件

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).

化学と産業

用途と製造

Use ClassificationPharmaceuticals

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化合物ノート

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このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
PubChem CID
62779
DTXSID
DTXSID10860314
Nikkaji
J567.325I