Ceftizoxime

Ceftizoxime 구조식 이미지
카스 번호:
68401-81-0
상품명:
Ceftizoxime
동의어(영문):
Cefimx;Ceftizox;EPOCELIN;FR-13749;Ceftisomin;CEFTIZOXIME;Ceftizoxime >CEFTIZOXIME ACID;Ceftizoxime (350 mg);Ceftizoxime, ≥ 98.0%
CBNumber:
CB1717299
분자식:
C13H13N5O5S2
포뮬러 무게:
383.4
MOL 파일:
68401-81-0.mol

Ceftizoxime 속성

녹는점
227° (dec)
밀도
1.89±0.1 g/cm3(Predicted)
저장 조건
under inert gas (nitrogen or Argon) at 2–8 °C
용해도
Aqueous Base (Slightly), DMSO (Slightly, Heated), Methanol (Slightly, Heated, Sonicated)
물리적 상태
고체
물리적 상태
단단한 모양
산도 계수 (pKa)
pKa 2.1 (Uncertain)
색상
흰색에서 연한 노란색
Merck
14,1951
안정성
흡습성
InChIKey
NNULBSISHYWZJU-LLKWHZGFSA-N
SMILES
N12[C@@]([H])([C@H](NC(/C(/C3=CSC(N)=N3)=N\OC)=O)C1=O)SCC=C2C(O)=O
CAS 데이터베이스
68401-81-0(CAS DataBase Reference)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
RTECS 번호 XI0367375
HS 번호 2941906000
독성 LD50 intravenous in rat: 8gm/kg
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
예방조치문구:
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
P332+P313 피부 자극이 생기면 의학적인 조치· 조언을 구하시오.
P337+P313 눈에 대한 자극이 지속되면 의학적인 조치· 조언를 구하시오.
NFPA 704
0
2 0

Ceftizoxime C화학적 특성, 용도, 생산

개요

In ceftizoxime, the whole C-3 side chain has been omitted to prevent deactivation by hydrolysis. It rather resembles cefotaxime in its properties; however, not being subject to metabolism, its pharmacokinetic properties are much less complex.

용도

Ceftizoxime is used for bacterial infections of the lower respiratory tract, infections of the urinary tract, infections of the bones, joints, skin, soft tissues, and abdominal infections. Synonyms of this drug are ceftix and eposerin.

정의

ChEBI: A parenteral third-generation cephalosporin, bearing a 2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl]amino group at the 7beta-position.

Antimicrobial activity

A semisynthetic cephalosporin supplied as the sodium salt. The properties are very similar to those of cefotaxime, but it lacks the acetoxymethyl group at position C-4 and is therefore not subject to deacetylation. Activity against common pathogenic bacteria (Table 13.4) is very similar to that of cefotaxime.
A 500 mg intramuscular injection achieves a plasma concentration of around 14 mg/L. A concentration of 85–90 mg/L is produced 30 min at the end of a 30-min intravenous infusion. The plasma half-life is 1.3–1.9 h. Protein binding is 30%. It is well distributed. In children with meningitis receiving 200–250 mg/kg per day in four equally divided doses for 14–21 days, mean CSF concentrations 2 h after a dose were 6.4 mg/L on day 2 and 3.6 mg/L on day 14.
About 70–90% of the dose is recovered in the urine in the first 24 h, principally by glomerular filtration. Probenecid increases the plasma half-life by about 50%. In patients receiving 1 g intravenously over 30 min, the plasma elimination half-life rose to 35 h when the corrected creatinine clearance was <10 mL/ min. It is partly removed by peritoneal and hemodialysis.
Adverse reactions and clinical use are similar to those of cefotaxime.

Ceftizoxime 준비 용품 및 원자재

원자재

준비 용품


Ceftizoxime 공급 업체

글로벌( 214)공급 업체
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Shenzhen Excellent Biomedical Technology Co.,Ltd.
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Henan Tianfu Chemical Co.,Ltd.
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Shanghai Zheyan Biotech Co., Ltd.
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career henan chemical co
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CONIER CHEM AND PHARMA LIMITED
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sales@conier.com China 49391 58
SIMAGCHEM CORP
+86-13806087780
sale@simagchem.com China 17367 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167
1026@dideu.com China 9126 58
AFINE CHEMICALS LIMITED
0571-85134551 18958018566;
info@afinechem.com China 15377 58
Hebei Guanlang Biotechnology Co,.LTD
+86-19930503253; +8619930503252
daisy@crovellbio.com China 5957 58

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