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メキサゾラム

Mexazolam

HCID 4177
ノート反応
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
31868-18-5
標準SMILES
CC1COC2(c3ccccc3Cl)c3cc(Cl)ccc3NC(=O)CN12
InChIKey
ANUCDXCTICZJRH-UHFFFAOYSA-N
分子式
C18H16Cl2N2O2
平均分子量
363.2 g/mol
単同位体質量
362.0588831

概要

Mexazolam is a hemiaminal ether and an oxazolobenzodiazepine.

名称と識別子

優先名称
Mexazolam
IUPAC
10-chloro-11b-(2-chlorophenyl)-3-methyl-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one
現地名
メキサゾラム
英語名
mexazolam
分子式
C18H16Cl2N2O2
分子量
363.24

名称と別名

mexazolamMelex31868-18-5CS-386MexazolamumDTXSID9057715DTXCID0031504S5969B6237CHEBI:3184210-Chloro-11b-(2-chlorophenyl)-2,3,7,11b-tetrahydro-3-methyloxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-one10-chloro-2,3,7,11b-tetrahydro-3-methyl-11b-(2-chlorophenyl)oxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-oneRefChem:818798
名称をさらに表示
メキサゾラム10-クロロ-11b-(o-クロロフェニル)-2,3,7,11b-テトラヒドロ-3-メチルオキサゾロ[3,2-d][1,4]ベンゾジアゼピン-6(5H)-オン10-クロロ-2,3,7,11b-テトラヒドロ-3-メチル-11b-(o-クロロフェニル)オキサゾロ[3,2-d][1,4]ベンゾジアゼピン-6(5H)-オン10-クロロ-11b-(2-クロロフェニル)-2,3,7,11b-テトラヒドロ-3-メチルオキサゾロ[3,2-d][1,4]ベンゾジアゼピン-6(5H)-オンメキサゾラム (JAN)13-クロロ-2-(2-クロロフェニル)-5-メチル-3-オキサ-6,9-ジアザトリシクロ[8.4.0.02,6]テトラデカ-1(14),10,12-トリエン-8-オンSedoxilmexazolam APImexazolam USP/EP/BPMexazolam (1 mg/mL in Acetonitrile)MexazolamQ: What is Mexazolam Q: What is the CAS Number of Mexazolam
13-chloro-2-(2-chlorophenyl)-5-methyl-3-oxa-6,9-diazatricyclo(8.4.0.0^(2,6))tetradeca-1(10),8,11,13-tetraen-8-ol13-chloro-2-(2-chlorophenyl)-5-methyl-3-oxa-6,9-diazatricyclo(8.4.0.02,6)tetradeca-1(10),8,11,13-tetraen-8-ol10-chloro-11b-(2-chlorophenyl)-3-methyl-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one10-Chloro-11b-(o-chlorophenyl)-2,3,7,11b-tetrahydro-3-methyloxazolo(3,2-d)(1,4)benzodiazepin-6(5H)-oneMexazolam [INN:JAN]Mexazolamum [INN-Latin]Mexazolam (1.0mg/ml in Acetonitrile)CS 386

物性

構造計算による物性

XLogP
3.7
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
24
形式電荷
0
複雑度
505

物理化学的性質

融点
172 · 172-175°
沸点
522.2 · 522.2±50.0 °C(Predicted)
比重(密度)
1.3817 · 1.3817 (rough estimate)
屈折率
1.61 · 1.6100 (estimate)
溶解性
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
外見
Solid
酸解離定数(Pka)
6.69 · 6.69(at 25℃)
色
White to Off-White

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).

安全データ

毒性
LD50 in male, female mice; male, female rats (mg/kg): 4687, 4571, 810, 4500 orally; >6000, >6000, >4000, >4000 i.p. or s.c. (Masuda)

化学と産業

薬理情報

ATC Code · 2 件

N - Nervous system

QN - Nervous system

Protein BindingMexazolam is >90% protein bound in plasma.
Mechanism of ActionMexazolam is a benzodiazepine that binds to benzodiazepine-type receptors, inhibiting gamma-aminobutyric acid.
Biological Half-LifeMexazolam follows a 2 compartment model with a first half life of 1.4h and a second half life of 76h.
Metabolism/MetabolitesMexazolam is rapidly metabolized to the active metabolites chloronordiazepam and chloroxazepam.
Absorption, Distribution and Excretion · 2 件

The active metabolite chloronordiazepam has a Tmax of 1-2h.

Mexazolam is mainly eliminated in the bile and feces, with <10% eliminated as metabolites in the urine. >50% of a dose of mexazolam is eliminated as the metabolite chloroxazepam.

用途と製造

Uses · 1 件

Mexazolam has been trialed for anxiety and was found to be effective in alleviating anxiety at one week follow-up, however, after three weeks of therapy mexazolam had lost its therapeutic anxiolytic properties becoming no more effective than placebo, presumably due to benzodiazepine tolerance.

応用分野

説明Mexazolam is a benzodiazepine anxiolytic closely related to flutazolam. It is reported to be particularly effective against psychosomatic essential hypertension, peptic ulcer, irritable colon and autonomic dystonia.

使用Mexazolam is a benzodiazepine derivative and have been investigated for its therapeutic value in treating anxiety. Mexazolam is known to be metabolized via the CYP3A4 pathway.

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化合物ノート

読み込み中…

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

データベース識別子

CAS
31868-18-5
PubChem CID
4177
DTXSID
DTXSID9057715
ChEMBL
CHEMBL1743261
ChEBI
CHEBI:31842
UNII
S5969B6237
Nikkaji
J3.491F

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