Flucloxacillin

Flucloxacillin 구조식 이미지
카스 번호:
5250-39-5
상품명:
Flucloxacillin
동의어(영문):
Flopen;Flucil;Culpen;FK 900;Flupen;Penplus;Floxapen;Abboflox;BRL 2039;Staphylex
CBNumber:
CB8690991
분자식:
C19H17ClFN3O5S
포뮬러 무게:
453.87
MOL 파일:
5250-39-5.mol

Flucloxacillin 속성

끓는 점
677.3±55.0 °C(Predicted)
밀도
1.59±0.1 g/cm3(Predicted)
용해도
soluble in Methanol, Water
산도 계수 (pKa)
pKa 2.7 (Uncertain)
물리적 상태
고체
물리적 상태
단단한 모양
색상
하얀색
CAS 데이터베이스
5250-39-5(CAS DataBase Reference)

안전

Flucloxacillin C화학적 특성, 용도, 생산

개요

Chemically this is 3(2-chloro-6-fluorophenyl)-5-methyl-4-isoxazolyl penicillin; this differs from dicloxacillin only by the substitution of a fluorine for a chlorine atom (Sutherland et al., 1970). It comes as oral capsules of 250 and 500 mg, as a suspension of 25 and 50 mg/ml, and in an injectable formulation of 500 mg and 1 g.

용도

Antibacterial.

정의

ChEBI: A penicillin compound having a 6beta-[3-(2-chloro-6-fluorophenyl)-5-methyl-1,2-oxazole-4-carboxamido] side-chain.

Antimicrobial activity

There is complete cross-resistance with other penicillinase-stable penicillins.

일반 설명

Flucloxacillin was synthesized by Beecham Research Laboratories in 1962 as a penicillinase-stable and orally active semisynthetic penicillin. It shows almost the same activity as dicloxacillin, and it has slightly higher serum and tissue concentrations than dicloxacillin. This drug has been used to treat pyoderma, sepsis, and postoperative infections as well as ear and nose, respiratory tract, and other infections caused by Staphylococcus and Streptococcus, including benzylpenicillin-resistant strains.

Pharmacokinetics

Oral absorption: c. 80%
Cmax 250 mg (oral): 11 mg/L after 0.5–1 h
Plasma half-life: 2 h
Plasma protein binding: 95%
Absorption and distribution
It is well absorbed after oral administration and penetrates rapidly into extravascular exudates. Its high protein binding limits its diffusion, notably into the normal CSF.
Metabolism and excretion
Flucloxacillin is partly metabolized in the liver and about 10% of the plasma concentration is made up of metabolites. It is more slowly eliminated than cloxacillin. Some appears in the bile but about 50–80% of an oral dose is recovered from the urine, about 20% as metabolites.

Clinical Use

Uses are those of group 3 penicillins.

부작용

In patients treated by intravenous infusion, about 5% developed phlebitis by the first and 15% by the second day, after which the proportion rose dramatically. Side effects are otherwise those common to penicillins.

Flucloxacillin 준비 용품 및 원자재

원자재

준비 용품


Flucloxacillin 공급 업체

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Henan Tianfu Chemical Co.,Ltd.
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CONIER CHEM AND PHARMA LIMITED
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career henan chemical co
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SIMAGCHEM CORP
+86-13806087780
sale@simagchem.com China 17367 58
Career Henan Chemica Co
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laboratory@coreychem.com China 30255 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671
sales@tnjchem.com China 34572 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167
1026@dideu.com China 9126 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250
1026@dideu.com China 27945 58
AFINE CHEMICALS LIMITED
0571-85134551 18958018566;
info@afinechem.com China 15377 58

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