겜핍로질

겜핍로질
겜핍로질 구조식 이미지
카스 번호:
25812-30-0
한글명:
겜핍로질
동의어(한글):
젬피브로질;겜핍로질;겜핍로질(GEMFIBROZIL)
상품명:
Gemfibrozil
동의어(영문):
lopid;2,2-Dimethyl-5-(2,5-Dimethylphenoxy)Valeric;CI-7;Jezil;Genlip;C1-719;Lipttr;ci-719;Lipozid;Decrelip
CBNumber:
CB9154247
분자식:
C15H22O3
포뮬러 무게:
250.33
MOL 파일:
25812-30-0.mol
MSDS 파일:
SDS

겜핍로질 속성

녹는점
61-63°C
끓는 점
158-159 C
밀도
1.1109 (rough estimate)
굴절률
1.5020 (estimate)
저장 조건
2-8°C
용해도
물에는 거의 녹지 않으며, 염화메틸렌에는 잘 녹고, 무수 에탄올과 메탄올에는 잘 녹습니다.
물리적 상태
가루
산도 계수 (pKa)
4.75±0.45(Predicted)
색상
흰색에서 황백색까지
수용성
>0.5g/L(온도는 명시되지 않음)
Merck
14,4388
BCS Class
2
CAS 데이터베이스
25812-30-0(CAS DataBase Reference)
IARC
3 (Vol. 66) 1996
EPA
Pentanoic acid, 5-(2,5-dimethylphenoxy)-2,2-dimethyl- (25812-30-0)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,Xi
위험 카페고리 넘버 22-63-62-46-36/38-21
안전지침서 36-53-36/37-26-25
WGK 독일 3
RTECS 번호 YV7120000
위험 등급 IRRITANT
HS 번호 2918992090
유해 물질 데이터 25812-30-0(Hazardous Substances Data)
독성 LD50 in mice, rats (mg/kg): 3162, 4786 orally (Kurtz)
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H302 삼키면 유해함 급성 독성 물질 - 경구 구분 4 경고 GHS hazard pictograms P264, P270, P301+P312, P330, P501
예방조치문구:
NFPA 704
0
2 0

겜핍로질 MSDS


Gemfibrozil

겜핍로질 C화학적 특성, 용도, 생산

개요

Gemfibrozil is a peroxisome proliferator-activated receptor α (PPARα) and PPARγ agonist (EC50s = 193.3 and 147.8 μM, respectively, in transactivation assays). In vivo, gemfibrozil (50 mg/kg, p.o.) reduces serum total cholesterol, triglyceride, and LDL levels in a rat model of high-cholesterol diet-induced hyperlipidemia. Gemfibrozil (100 mg/kg per day) reduces atherosclerotic plaque area, superoxide production, and expression of the genes encoding the NF-κB subunit p65 and chemokine (C-C) motif ligand 2 (CCL2) in ApoE-/- mice. Formulations containing gemfibrozil have been used in the treatment of high cholesterol.

화학적 성질

White Crystalline Powder

용도

Gemfibrozil has been used to to study its effects on cell cycle progression in yeast. It has been used to study the effects of fibrates on cell proliferation and gene expression in human cell lines.

World Health Organization (WHO)

Gemfibrozil, an antihyperlipidaemic derivative of clofibrate, was introduced in the early 1980's. It is registered in several countries for the treatment of hyperlipidaemia unresponsive to dietary measures. (See also the WHO comment for clofibrate).

일반 설명

Gemfibrozil, 5-(2,5-dimethylphenoxy)-2,2-dimethylpentanoic acid (Lopid), is a congener of clofibratethat was used first in the treatment of hyperlipoproteinemia inthe mid-1970s. Its mechanism of action and use are similar tothose of clofibrate. Gemfibrozil reduces plasma levels ofVLDL triglycerides and stimulates clearance of VLDL fromplasma. The drug has little effect on cholesterol plasma levelsbut does cause an increase of HDL.
Gemfibrozil is absorbed quickly from the gut and excretedunchanged in the urine. The drug has a plasma half-life of1.5 hours, but reduction of plasma VLDL concentration takesbetween 2 and 5 days to become evident. The peak effect of its hypolipidemic action may take up to 4 weeks to becomemanifest.

Mechanism of action

From the chemical point of view, gemfibrozil is somewhat related to clofibrate and has analogous pharmacological use. The primary action of gemibrozil as well as clofibrate consists of a significant reduction in the level of very low-density proteins in the plasma and an increase in high-density protein formation.

겜핍로질 준비 용품 및 원자재

원자재

준비 용품


겜핍로질 공급 업체

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