니조페논

Methanone, (2-chlorophenyl)(2-(2-((diethylamino)methyl)-1H-imidazol-1-yl)-5-nitrophenyl)-, (2E)-2-butenedioate (1:1)

HCID 5282422CAS 54533-86-7

기본 정보

표준 SMILES
CCN(CC)Cc1nccn1-c1ccc([N+](=O)[O-])cc1C(=O)c1ccccc1Cl.O=C(O)/C=C/C(=O)O
InChIKey
JDQAUUIBFFFOOV-WLHGVMLRSA-N
분자식
C25H25ClN4O7
평균 분자량
528.9 g/mol
단동위원소 질량
528.14117682

개요

Nizofenone fumarate is a member of benzophenones.

이름 및 식별자

우선 이름
Methanone, (2-chlorophenyl)(2-(2-((diethylamino)methyl)-1H-imidazol-1-yl)-5-nitrophenyl)-, (2E)-2-butenedioate (1:1)
IUPAC
(E)-but-2-enedioic acid;(2-chlorophenyl)-[2-[2-(diethylaminomethyl)imidazol-1-yl]-5-nitrophenyl]methanone
현지명
니조페논
영어명
Nizofenone
분자식
C25H25ClN4O7
분자량
528.9416

이름 및 동의어

nizofenone fumarate54533-86-7EkonalDTXSID50486371I1Z517Z3YNSC-3158561-(2-(2-Chlorobenzoyl)-4-nitrophenyl)-2-(diethylaminomethyl)imidazole fumarateDTXCID601471513METHANONE, (2-CHLOROPHENYL)(2-(2-((DIETHYLAMINO)METHYL)-1H-IMIDAZOL-1-YL)-5-NITROPHENYL)-, (2E)-2-BUTENEDIOATE (1:1)RefChem:166179MidafenoneNizofenone fumarate [JAN]
이름 더 보기
니조페논(2-chlorophenyl)(2-{2-[(diethylamino)methyl]-1H-imidazol-1-yl}-5-nitrophenyl)methanone, maleate salt(2-Chlorophenyl)[2-[2-[(diethylamino)methyl]-1H-imidazol-1-yl]-5-nitrophenyl]methanone (E)-2-butenedioate
Y-9179Nizofenone (fumarate)(E)-but-2-enedioic acid;(2-chlorophenyl)-[2-[2-(diethylaminomethyl)imidazol-1-yl]-5-nitrophenyl]methanoneNizofenone fumarate (JAN)93929-95-4(2-chlorophenyl)(2-(2-((diethylamino)methyl)-1H-imidazol-1-yl)-5-nitrophenyl)methanone fumarateCAS-54533-86-7NSC315856

데이터베이스 식별자

CAS
54533-86-7、93929-95-4
PubChem CID
5282422
DTXSID
DTXSID5048637
ChEBI
CHEBI:31914
UNII
1I1Z517Z3Y

물성

구조 계산 물성

극성 표면적
159 Ų
수소 결합 공여자 수
2
수소 결합 수용자 수
9
회전 가능 결합 수
9
무거운 원자 수
37

물리화학적 성질

녹는점
157 · 157-158℃
저장 조건
2 · 2-8°C

안전 및 규제

안전 데이터

독성
LD50 in male, female mice, male, female rats (mg/kg): 495, 504, 1711, 1580 orally; 62, 70, 63, 65 i.v.; 270, 278, 1830, 1629 s.c. (Horizoe)

화학 및 산업

약리 정보

MeSH Pharmacological Classification · 2건

Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade.

Drugs intended to prevent damage to the brain or spinal cord from ischemia, stroke, convulsions, or trauma. Some must be administered before the event, but others may be effective for some time after. They act by a variety of mechanisms, but often directly or indirectly minimize the damage produced by endogenous excitatory amino acids.

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