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Murepavadin (POL7080)
  • 品牌:Chemstan
  • 产地:中国
  • 货号:LC-01
  • cas:944252-63-5
  • 发布日期: 2019-11-25
  • 更新日期: 2025-09-23
产品详请
产地 中国
品牌 Chemstan
货号 LC-01
用途 中间体
包装规格 20mg
纯度 98%%
CAS编号 944252-63-5
是否进口

联合知名大学科研院所及企业开发药食两用植物标准品和天然植物有效单体,主打中药对照品/标准品/天然植物有效单体,小分子化合物库,药物杂质。所有产品仅用作科学研究,我们不为任何个人用途提供产品和服务。


Fields of Application : 
Murepavadin is a novel class of highly specific outer membrane protein targeting antibiotic to treat resistant Pseudomonas infections.

CAS Number:944252-63-5
Purity:

>98%

Molecular Weight:1553.83
Molecular Formula:C73H112N22O16

Quality Control: HPLC、NMR、 LC/MS(Please contact us to get the QC report)

Synonyms:POL7080,Murepavadin,POL-7080,POL 7080
Chemical Name:
Storage:2 years -20°C Powder, 2 weeks4°C in DMSO,6 months-80°C in DMSO

Note: Products for research use only, not for human use

Description:
Murepavadin is a pathogen specific antimicrobial peptidomimetic with a novel, non-lytic mechanism of action, and is the first in class of outer membrane protein targeting antibiotics which are being developed. Murepavadin displays a potent in vitro activity including carbapenemase-producing and colistin-resistant P. aeruginosa. Murepavadin is active in pre-clinical animal models including infections with XDR isolates. The Pharmacokinetics is well characterized including subjects with impaired renal function and patients with VABP. Intravenous murepavadin is currently under clinical development for the treatment of HABP/VABP due to P. aeruginosa infection.Murepavadin, a pathogen-specific antibiotic, is being developed for hospital-acquired pneumonia (HAP) and ventilator-associated pneumonia (VAP) caused by Pseudomonas aeruginosa.Murepavadin fits well with the new trend in antibiotic use known as ‘antibiotic stewardship’ which, among other things, aims to reduce the excessive use of broad-spectrum products which generates resistance.Murepavadin has obtained QIDP (Qualified Infectious Disease Product) status and eligibility for priority review, with statutory exclusivity for an additional five years upon FDA approval.

References: 
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