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Cloxazolam

HCID 2816
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
24166-13-0
표준 SMILES
O=C1CN2CCOC2(c2ccccc2Cl)c2cc(Cl)ccc2N1
InChIKey
ZIXNZOBDFKSQTC-UHFFFAOYSA-N
분자식
C17H14Cl2N2O2
평균 분자량
349.2 g/mol
단동위원소 질량
348.0432331

개요

Cloxazolam is a hemiaminal ether and an oxazolobenzodiazepine.

이름 및 식별자

우선 이름
Cloxazolam
IUPAC
10-chloro-11b-(2-chlorophenyl)-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-one
영어명
CLOXAZOLAM
분자식
C17H14Cl2N2O2
분자량
349.21

이름 및 동의어

cloxazolamCloxazolazepamSepazonEnadelOlcadil24166-13-0CloxazolamumTolestanBetavelCloxamCS 370DTXSID0022854
이름 더 보기
cs370Lubalixmt14-411Sepazone
MT 14-411GYL649Z0HY10-chloro-11b-(2-chlorophenyl)-2,3,5,7-tetrahydro-[1,3]oxazolo[3,2-d][1,4]benzodiazepin-6-oneDTXCID902854CHEBI:3142610-Chloro-11b-(o-chlorophenyl)-2,3,7,11b-tetrahydro-oxazolo(3,2-d) (1,4)benzodiazepin-6(5H)-one10-Chloro-2,3,5,6,7,11b-hexahydro-11b-(o-chlorophenyl)benzo(6,7)-1,4-diazepino-(5,4-b)-oxazol-6-one10-chloro-11b-(2-chlorophenyl)-2,3,5,7-tetrahydro-(1,3)oxazolo(3,2-d)(1,4)benzodiazepin-6-one

데이터베이스 식별자

CAS
24166-13-0
PubChem CID
2816
DTXSID
DTXSID0022854
ChEMBL
CHEMBL2107254
ChEBI
CHEBI:31426
UNII
GYL649Z0HY
EC Number
815-874-6
Nikkaji
J3.158E

물성

구조 계산 물성

XLogP
3.2
극성 표면적
41.6 Ų
수소 결합 공여자 수
1
수소 결합 수용자 수
3
회전 가능 결합 수
1
무거운 원자 수
23
형식 전하
0
복잡도
478

실험 및 물리화학적 성질

Drugs · 3건

DEA NFLIS-Drug Category -> Benzodiazepines

DEA Schedule IV Controlled Substance -> Depressants

Pharmaceuticals -> Synthetic Cannabinoids or Psychoactive Compounds

Melting Point202-204

물리화학적 성질

녹는점
202 · 202-204° (dec)
끓는 점
172 °C · 172°C (rough estimate)
밀도
1.4125 · 1.4125 (rough estimate)
굴절률
1.61 · 1.6100 (estimate)
산도 계수 (pKa)
12.7 · 12.70±0.40(Predicted)

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

GHS 분류

GHS Classification · 4건

Warning

H302+H312+H332 (50%): Harmful if swallowed, in contact with skin or if inhaled [Warning Acute toxicity, oral; acute toxicity, dermal; acute toxicity, inhalation]

P203, P261, P264, P270, P271, P280, P301+P317, P302+P352, P304+P340, P317, P318, P319, P321, P330, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

유해성 정보

Regulatory InformationDEA schedule IV controlled substance
Hazard Classes and CategoriesAcute Tox. 4 (50%)

독성 정보

Treatment · 1건

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.

화학 및 산업

약리 정보

ATC Code · 3건

N05BA22

N - Nervous system

QN - Nervous system

Pharmacodynamics · 1건

Studies have shown a superiority of 4mg/day of cloxazepam to 12mg/day of bromazepam in terms of anxiety, depressed mood, and sleep; an insignificant difference in terms of sedative effect; and less muscle relaxant effects. [3] Cloxazolam, administered as a single oral dose of 3mg, when compared to a single 5 mg dose of diazepam in one study, showed similar subjective measures; however, there cloxazolam caused more fatigue, and less mood improvement. Cloxazolam also induced a significant increase in heart rate in the control group of this study. [3]

Mechanism of ActionCloxazolam is a long acting benzodiazepine. It acts as a prodrug, with pharmacologically active metabolites, which bind to to the GABAa receptor, which other benzodiazepines bind to, to illicit a physiological response.
Biological Half-Life65 hours
Metabolism/Metabolites · 2건

Cloxazolam is metabolised by the liver into the active metabolite chlordesmethyldiazepam (delorazepam). [5]

Cloxazolam is metabolised by the liver into the active metabolite chlordesmethyldiazepam (delorazepam). [5] Route of Elimination: Renal elimination. Half Life: 65 hours

Absorption, Distribution and ExcretionRenal elimination.

용도 및 제조

UsesUsed primarily as an anti-anxiety agent. Typically used short term, and may be given as a single dose of up to 100mcg/kg to reduce anxiety and tension experienced prior to surgery.

응용 분야

용도CLOXAZOLAM is a benzodiazepine derivative with anxiolytic, hypnotic and antihypertensive properties used as an anti-anxiety drug. It is metabolized into the active metabolite Delorezepam (D230675). Controlled Subs tance.

관련 반응

6건
반응 기록 만들기
HRID 305735 반응식
HRID 305735반응물로Training data from https://doi.org/10.1039/C8SC04228D (8/10)
HRID 328481 반응식
HRID 328481반응물로uspto-grants-1977_04
HRID 328493 반응식
HRID 328493반응물로uspto-grants-1977_04
HRID 597627 반응식
HRID 597627반응물로uspto-grants-1977_03
HRID 1658604 반응식
HRID 1658604반응물로uspto-grants-1976_06
HRID 1973528 반응식
HRID 1973528반응물로uspto-grants-1976_12

화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
Toxicity SummaryCloxazolam is a long acting benzodiazepine. It acts as a prodrug, with pharmacologically active metabolites, which bind to to the GABAa receptor, which other benzodiazepines bind to, to illicit a physiological response.
Signs and Symptoms · 1건

Drowsiness and ataxia are dose related. Central nervous system toxicity may result in respiratory depression and loss of consciousness. As such, pre-existing central nervous system depression and severe hepatic impairment are two particular contraindications for use.

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

안전 데이터

ridadr
3249
독성
LD50 in mice (g/kg): 3.3 orally; >2.0 i.p. (Kamioka)
포장분류
III
위험 등급
6.1(b)

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