기본 정보
- CAS
156-51-4- 표준 SMILES
NNCCc1ccccc1.O=S(=O)(O)O- InChIKey
RXBKMJIPNDOHFR-UHFFFAOYSA-N- 분자식
- C8H14N2O4S
- 평균 분자량
- 234.28 g/mol
- 단동위원소 질량
- 234.06742811
이름 및 식별자
- 우선 이름
- Phenelzine Sulfate
- IUPAC
- 2-phenylethylhydrazine;sulfuric acid
- 현지명
- 페넬진황산염
- 영어명
- Phenelzine Sulfate
- 분자식
- C8H14N2O4S
- 분자량
- 234.27
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
156-51-4- PubChem CID
- 61100
- DTXSID
DTXSID3021144- ChEMBL
CHEMBL1200895- ChEBI
CHEBI:8061- UNII
- 2681D7P965
- EC Number
- 205-856-0
물성
구조 계산 물성
- 극성 표면적
- 121 Ų
- 수소 결합 공여자 수
- 4
- 수소 결합 수용자 수
- 6
- 회전 가능 결합 수
- 3
- 무거운 원자 수
- 15
- 형식 전하
- 0
- 복잡도
- 159
물리화학적 성질
- 녹는점
- 166.5 · 166.5-167.5 °C
- 저장 조건
- 2 · 2-8°C
- 용해도
- 물에 자유롭게 용해됩니다. 에탄올(96%)과 에테르에는 거의 녹지 않습니다.
- 물리적 상태
- 고체
- 색상
- White to off-white
- 생물학적 소스
- synthetic
- 수용성
- 50 mg/mL, · water: 50mg/mL, clear to slightly hazy, colorless to faintly yellow
- Merck
- 13 · 13,7300
- 주요 응용
- 의약품(소분자)
- InChI
- InChI=1S/C8H12N2.H2O4S/c9-10-7-6-8-4-2-1-3-5-8;1-5(2,3)4/h1-5,10H,6-7,9H2;(H2,1,2,3,4)
- InChIKey
- RXBKMJIPNDOHFR-UHFFFAOYSA-N
- SMILES
- C1(CCNN)C=CC=CC=1.S(=O)(=O)(O)O
화학적 성질
A white powder or pearly platelets.
안전 및 규제
GHS 분류
GHS Classification
Danger
H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]
P264, P270, P301+P316, P321, P330, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 39 reports by companies from 1 notifications to the ECHA C&L Inventory.;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
유해성 정보
독성 정보
Carcinogen Classification
Phenelzine sulfate
Group 3: Not classifiable as to its carcinogenicity to humans
Volume 24: (1980) Some Pharmaceutical Drugs;Volume Sup 7: Overall Evaluations of Carcinogenicity: An Updating of IARC Monographs Volumes 1 to 42, 1987; 440 pages; ISBN 92-832-1411-0 (out of print)
1987
1987
Drug Induced Liver Injury
Drug Induced Liver Injury Rank (DILIrank 2.0)
Phenelzine sulfate
vLess-DILI-concern
3
Adverse reactions
DOI:10.1016/j.drudis.2016.02.015
안전 데이터
- wgk
- 3
- rtecs
- MV8750000
- ridadr
- UN 2811 6.1/PG 3
- 독성
- LD50 orally in mice: 156 mg/kg (Gylys)
- HS 번호
- 2928002500
- risk_code
- 22
- hazard_code
- Xn
- 포장분류
- III
- 위험 등급
- 6.1(b)
- Hazard Classifications
- Acute Tox. 3 Oral
- 스토리지 클래스
- 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
화학 및 산업
약리 정보
FDA Pharmacological Classification
PHENELZINE SULFATE
Monoamine Oxidase Inhibitors [MoA]; Monoamine Oxidase Inhibitor [EPC]
MeSH Pharmacological Classification
Mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. Several MONOAMINE OXIDASE INHIBITORS are useful as antidepressants apparently as a long-term consequence of their modulation of catecholamine levels. The tricyclic compounds useful as antidepressive agents (ANTIDEPRESSIVE AGENTS, TRICYCLIC) also appear to act through brain catecholamine systems. A third group (ANTIDEPRESSIVE AGENTS, SECOND-GENERATION) is a diverse group of drugs including some that act specifically on serotonergic systems.
A chemically heterogeneous group of drugs that have in common the ability to block oxidative deamination of naturally occurring monoamines. (From Gilman, et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed, p414)
응용 분야
용도Phenelzine Sulfate is a hydrazine derivative that is a non-selective and irreversible monoamine oxidase inhibitor (MAOI) and also inhibits GABA-transaminase (GABA-T), markedly increasing brain GABA levels. It is an antidep ressant and anxiolytic used in the treatment of major depressive disorder (MDD) as well as other neural disorders.
일반 설명Phenelzine sulfate, 2-(phenylethyl)hydrazine sulfate(Nardil), is an effective antidepressant agent. A mechanismbasedinactivator, it irreversibly inactivates the enzyme orits cofactor, presumably after oxidation to the diazine,which can then break up into molecular nitrogen, a hydrogen atom, and a phenethyl free radical. The latter would bethe active species in irreversible inhibition.
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