기본 정보
- CAS
359-83-1- 표준 SMILES
CC(C)=CCN1CCC2(C)c3cc(O)ccc3CC1C2C- InChIKey
VOKSWYLNZZRQPF-UHFFFAOYSA-N- 분자식
- C19H27NO
- 평균 분자량
- 285.4 g/mol
- 단동위원소 질량
- 285.20926449
개요
Talwin is a benzazocine.
이름 및 식별자
- 우선 이름
- Talwin
- IUPAC
- 1,13-dimethyl-10-(3-methylbut-2-enyl)-10-azatricyclo[7.3.1.02,7]trideca-2(7),3,5-trien-4-ol
- 영어명
- 1,2,3,4,5,6-hexahydro-6,11-dimethyl-3-(3-methylbut-2-enyl)-2,6-methano-3-benzazocin-8-ol
- 분자식
- C19H27NO
- 분자량
- 285.42
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
359-83-1、39188-58-4、55643-30-6、7488-49-5- PubChem CID
- 4736
- DTXSID
DTXSID30859346- ChEMBL
CHEMBL100116- ChEBI
CHEBI:182080- EC Number
- 259-735-2、811-426-9
- Nikkaji
- J267.040B
물성
구조 계산 물성
- XLogP
- 3.3
- 극성 표면적
- 23.5 Ų
- 수소 결합 공여자 수
- 1
- 수소 결합 수용자 수
- 2
- 회전 가능 결합 수
- 2
- 무거운 원자 수
- 21
- 형식 전하
- 0
- 복잡도
- 414
실험 및 물리화학적 성질
안전 및 규제
GHS 분류
GHS Classification
Warning
H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]
P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)
The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.
유해성 정보
독성 정보
Treatment
Adequate measures to maintain ventilation and general circulatory support should be employed. Assisted or controlled ventilation, intravenous fluids, vasopressors, and other supportive measures should be employed as indicated. Consideration should be given to gastric lavage and gastric aspiration. For respiratory depression due to overdosage or unusual sensitivity to pentazocine, parenteral naloxone is a specific and effective antagonist. Initial doses of 0.4 to 2.0 mg of naloxone are recommended, repeated at 2-3 minute intervals, if needed, up to a total of 10 mg. Anti
화학 및 산업
약리 정보
Pharmacodynamics
Pentazocine is a potent analgesic which when administered orally in a 50 mg dose appears equivalent in analgesic effect to 60 mg (1 grain) of codeine. Onset of significant analgesia usually occurs between 15 and 30 minutes after oral administration, and duration of action is usually three hours or longer. Onset and duration of action and the degree of pain relief are related both to dose and the severity of pretreatment pain. Pentazocine weakly antagonizes the analgesic effects of morphine and meperidine; in addition, it produces incomplete reversal of cardiovascular, respiratory, and behavioral depression induced by morphine and meperidine. Pentazocine has about 1/50 the antagonistic activity of nalorphine. It also has sedative activity.
Metabolism/Metabolites
Hepatic
Hepatic Half Life: 2 to 3 hours
MeSH Pharmacological Classification
Compounds with activity like OPIATE ALKALOIDS, acting at OPIOID RECEPTORS. Properties include induction of ANALGESIA or NARCOSIS.
Agents that are administered in association with anesthetics to increase effectiveness, improve delivery, or decrease required dosage.
Agents inhibiting the effect of narcotics on the central nervous system.
Agents that induce NARCOSIS. Narcotics include agents that cause somnolence or induced sleep (STUPOR); natural or synthetic derivatives of OPIUM or MORPHINE or any substance that has such effects. They are potent inducers of ANALGESIA and OPIOID-RELATED DISORDERS.
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