에브로티딘

에브로티딘
에브로티딘 구조식 이미지
카스 번호:
100981-43-9
한글명:
에브로티딘
동의어(한글):
에브로티딘
상품명:
Ebrotidine
동의어(영문):
FI3542;Ulsanic;FI-3542;FI 3542;Ebrotidine;FI 3542; ULSANIC; FI-3542; FI3542;Ebrotidine,FI 3542,Histamine Receptor,inhibit,Inhibitor,FI-3542;(E)-N-[[[2-[[[2-[(Aminoiminomethyl)amino]-4-thiazolyl]methyl]thio]ethyl]amino]methylene]-4-bromobenzenesulfonamide;N-(4-bromophenyl)sulfonyl-N'-[2-[[2-(diaminomethylideneamino)-1,3-thiazol-4-yl]methylsulfanyl]ethyl]methanimidamide;Benzenesulfonamide, N-[[[2-[[[2-[(aminoiminomethyl)amino]-4-thiazolyl]methyl]thio]ethyl]amino]methylene]-4-bromo-, [N(E)]-
CBNumber:
CB71074199
분자식:
C14H17BrN6O2S3
포뮬러 무게:
477.42
MOL 파일:
100981-43-9.mol

에브로티딘 속성

녹는점
142.5-146℃
끓는 점
633.0±65.0 °C(Predicted)
밀도
1.73±0.1 g/cm3(Predicted)
저장 조건
Amber Vial, -20°C Freezer, Under inert atmosphere
용해도
DMSO(약간 용해됨), 메탄올(약간 용해됨)
산도 계수 (pKa)
5.25±0.40(Predicted)
물리적 상태
고체
물리적 상태
단단한 모양
색상
흰색에서 황백색까지
안정성
감광성

안전

에브로티딘 C화학적 특성, 용도, 생산

개요

Ebrocit was launched in Spain as a gastroprotective agent. It was prepared from 4-bromobenzenesulfonamide in two steps. Ebrocit's activity arises from its ability to antagonize histamine H2-receptors (the first of a new generation) showing 1.5-2.5 times higher affinity than Ranitidine and 2-fold greater affinity than cimetidine which correlates to an antisecretory potency of 1 times and 4-10 times respectively. Cytoand gastroprotection arises from increased gastric mucus production, enhanced physiochemical properties (decreased permeability of H+), and an increase in mucin glycosylation and sulfation. It acts on gastric mucosal EGF and PDGF receptor expression. Nitric oxide was also found to be involved. Ebrocit caused enhanced mucosal blood flow with anti H.pylori activity. It has diminished P450 binding which eliminates the possibility of mutagenic nitrosoamine formation.

용도

Ebrotidine is a H2 receptor antagonist that has shown gastroprotective properties against gastric mucosal damange.

에브로티딘 준비 용품 및 원자재

원자재

준비 용품


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