Mezlocillin
- CAS No.
- 51481-65-3
- Chemical Name:
- Mezlocillin
- Synonyms
- Melocin;Bay-f 1353;Multocillin;MEZLOCILLIN;Meslocillin;Meloxacam acid;Mezlocillin acid;Melocillin sodium;Meloxicillin acid;antibioticbay-f1353
- CBNumber:
- CB9268151
- Molecular Formula:
- C21H25N5O8S2
- Molecular Weight:
- 539.58
- MOL File:
- 51481-65-3.mol
- MSDS File:
- SDS
- Modify Date:
- 2024/4/22 13:56:47
Density | 1.63±0.1 g/cm3(Predicted) |
---|---|
storage temp. | 2-8°C |
pka | pKa 2.7 (Uncertain) |
CAS DataBase Reference | 51481-65-3(CAS DataBase Reference) |
Mezlocillin Chemical Properties,Uses,Production
Description
Mezlocilin is an acylaminopenicillin, which has been shown to cause both immediate and delayed hypersensitivity in a nurse.
Uses
Like azlocillin, mezlocillin is used for infections of the urinary tract, gynecological infections, intraabdominal infections, skin infections, and respiratory tract infections. Synonyms of this drug are baypen, mezlin, and optocillin.
Definition
ChEBI: A penicillin in which the substituent at position 6 of the penam ring is a (2R)-2-[3-(methanesulfonyl)-2-oxoimidazolidine-1-carboxamido]-2-phenylacetamido group.
Antimicrobial activity
A semisynthetic acylureidopenicillin supplied as the sodium
salt for parenteral administration.
Ampicillin-susceptible strains of H. influenzae and Neisseria
spp. are very susceptible, but β-lactamase-producing organisms
are usually resistant. It is less active than azlocillin and
piperacillin against Ps. aeruginosa and has variable activity
against B. fragilis, independent of β-lactamase production. It
exhibits typical β-lactam synergy with aminoglycosides against
Ps. aeruginosa and enterobacteria.
It attains peak concentrations of 250 mg/L after a 2 g intravenous
infusion, with a plasma half-life of 55 min. Protein
binding is 20–30%. It distributes into multiple tissues and
human body fluids at therapeutically useful concentrations.
Up to 60% of the dose is recoverable unchanged from the
urine, with up to 2.5% excreted in the bile.
Toxicity and side effects are similar to those associated
with carboxypenicillins. Its clinical use is for serious infections
with susceptible organisms, including lower respiratory tract,
intra-abdominal, urinary tract and gynecological infections.
Commercial availability is quite limited.
General Description
Mezlocillin was synthesized by Bayer in 1974. The NH2 residue of ampicillin was acylated. Mezlocillin is a member of the so-called ureidopenicillins and shows two- to eightfold greater activity against Citrobacter, Enterobacter, Klebsiella, Escherichia coli, and Haemophilus influenzae than ampicillin, carbenicillin, or sulbenicillin. Its activity against gram-positive bacteria is almost the same as that of carbenicillin. Mezlocillin is used by intravenous administration for therapy of sepsis, meningitis, and respiratory tract, urinary tract, and abdominal infections.
Mezlocillin Preparation Products And Raw materials
Raw materials
Preparation Products
Supplier | Tel | Country | ProdList | Advantage | Inquiry |
---|---|---|---|---|---|
CHEMSWORTH | +91-261-2397244 | New Delhi, India | 6707 | 30 | Inquiry |
Hebei Mojin Biotechnology Co., Ltd | +8613288715578 | China | 12458 | 58 | Inquiry |
Ouhuang Engineering Materials (Hubei) Co., Ltd | +86-86177 | China | 2901 | 58 | Inquiry |
Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | China | 21669 | 55 | Inquiry |
Hebei Guanlang Biotechnology Co., Ltd. | +86-19930503282 | China | 8826 | 58 | Inquiry |
Xiamen AmoyChem Co., Ltd | +86-592-6051114 +8618959220845 | China | 6387 | 58 | Inquiry |
CONIER CHEM AND PHARMA LIMITED | +8618523575427 | China | 49391 | 58 | Inquiry |
career henan chemical co | +86-0371-86658258 +8613203830695 | China | 29826 | 58 | Inquiry |
SIMAGCHEM CORP | +86-13806087780 | China | 17367 | 58 | Inquiry |
Hefei TNJ Chemical Industry Co.,Ltd. | 0551-65418671 | China | 34571 | 58 | Inquiry |
Related articles
- Mezlocillin, Azlocillin: Antimicrobial Activity, Susceptibility, Administration and Dosage, Clinical Uses etc.
- Mezlocillin and Azlocillin are described together because they are often referred to as ‘‘newer antipseudomonal penicillins.’’....
- Mar 15,2022
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