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Pinazepam

HCID 40391
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
52463-83-9
표준 SMILES
C#CCN1C(=O)CN=C(c2ccccc2)c2cc(Cl)ccc21
InChIKey
MFZOSKPPVCIFMT-UHFFFAOYSA-N
분자식
C18H13ClN2O
평균 분자량
308.8 g/mol
단동위원소 질량
308.0716407

개요

Pinazepam is a benzodiazepine.

이름 및 식별자

우선 이름
Pinazepam
IUPAC
7-chloro-5-phenyl-1-prop-2-ynyl-3H-1,4-benzodiazepin-2-one
영어명
pinazepam
분자식
C18H13ClN2O
분자량
308.76

이름 및 동의어

PinazepamDomar52463-83-9Pinazepamum7-Chloro-1,3-dihydro-5-phenyl-1-(2-propynyl)-2H-1,4-benzodiazepin-2-one7-Chloro-1-propargyl-5-phenyl-2H-1,4-benzodiazepin-2-one5286RBZ882DTXSID30234757-chloro-5-phenyl-1-(prop-2-yn-1-yl)-2,3-dihydro-1H-1,4-benzodiazepin-2-onepropazepamRefChem:929293DTXCID203475
이름 더 보기
Zami-905pinazepam USP/EP/BP7-chloro-5-phenyl-1-prop-2-ynyl-3H-1,4-benzodiazepin-2-one2H-1,4-Benzodiazepin-2-one, 7-chloro-1,3-dihydro-5-phenyl-1-(2-propyn-1-yl)-
N05BA147-chloro-5-phenyl-1-propargyl-1,4-benzodiazepin-2-one257-934-9Pinazepam [INN]ZAMI 905DunaZ-9052H-1,4-Benzodiazepin-2-one, 7-chloro-1,3-dihydro-5-phenyl-1-(2-propynyl)-

데이터베이스 식별자

CAS
52463-83-9
PubChem CID
40391
DTXSID
DTXSID3023475
ChEMBL
CHEMBL1213352
ChEBI
CHEBI:135315

물성

구조 계산 물성

XLogP
3.1
극성 표면적
32.7 Ų
수소 결합 공여자 수
0
수소 결합 수용자 수
2
회전 가능 결합 수
2
무거운 원자 수
22
형식 전하
0
복잡도
500

실험 및 물리화학적 성질

Drugs · 3건

DEA NFLIS-Drug Category -> Benzodiazepines

DEA Schedule IV Controlled Substance -> Depressants

Pharmaceuticals -> Synthetic Cannabinoids or Psychoactive Compounds

LogP2.87
Melting Point141 °C
Physical DescriptionSolid

물리화학적 성질

녹는점
140 · 140-142°
끓는 점
523.6 · 523.6±50.0 °C(Predicted)
밀도
1.2151 · 1.2151 (rough estimate)
굴절률
1.58 · 1.5800 (estimate)
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태
고체
산도 계수 (pKa)
2.34 · pKa 2.34 (Uncertain)
색상
미색부터 페일 베이지까지
안정성
감광성

안전 및 규제

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

유해성 정보

Regulatory InformationDEA schedule IV controlled substance

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.

Toxicity Summary · 1건

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).

화학 및 산업

약리 정보

ATC Code · 2건

N - Nervous system

QN - Nervous system

MeSH Pharmacological Classification · 1건

Agents that alleviate ANXIETY, tension, and ANXIETY DISORDERS, promote sedation, and have a calming effect without affecting clarity of consciousness or neurologic conditions. ADRENERGIC BETA-ANTAGONISTS are commonly used in the symptomatic treatment of anxiety but are not included here.

Cellular LocationsMembrane

응용 분야

용도Pinazepam is a is a benzodiazepine. Pinazepam possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. Pinazepam is less toxic than Diazepam. This is a contolled substance (depressant). Anxiolytic.

상·하류 제품 정보

상류 원료

Phthalimido Acetyl Chloride하이드라진, 모노수화물프로파길브로마이드2- 아미노 -5- 클로로 벤조Nordazepam

관련 반응

2건
반응 기록 만들기
HRID 1446802 반응식
HRID 1446802생성물로uspto-grants-1982_02
HRID 1446803 반응식
HRID 1446803생성물로uspto-grants-1982_02

화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
UNII
5286RBZ882
EC Number
257-934-9
Nikkaji
J9.933C

안전 데이터

ridadr
3249
독성
LD50 in mice, rats (mg/kg): 1355, 5819 orally; 266, 622 i.p. (Scrollini, 1975); Also reported as LD50 in mice (mg/kg): 670 orally (Podesva, Vagi)
포장분류
III
위험 등급
6.1(b)
DEA Controlled Substances
CSCN: 2883CSA SCH: Schedule IVNARC: No