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HCID 3083708생성일: 2026년 11월 2일

폴리믹신 B 황산염

폴리믹신B황산염 · 폴리믹신B황산염(POLYMYXINBSULFATE) · POLYMYXIN B · POLYMYXIN B SULPHATE · POLYMIXIN B SULFATE · POLYMIXIN B SULPHATE · AEROSPORIN · polymyxin B sulfate usp

https://huagongshe.com/ko/chemical/3083708

폴리믹신 B 황산염 분자 구조식

식별자 및 물리적 특성

CAS No.1405-20-5
분자식C56H100N16O17S
평균 분자량1,301.56 g/mol
SMILESCC(C)CC1NC(=O)C(Cc2ccccc2)NC(=O)C(CCN)NC(=O)C(NC(=O)C(CCN)NC(=O)C(CCO)NC(=O)C(CCN)NC=O)CCNC(=O)C(CCO)NC(=O)C(CCN)NC(=O)C(CCN)NC1=O.O=S(=O)(O)O
PubChem CID3083708
현지명폴리믹신 B 황산염

화학 및 물리적 성질

녹는점217-220°C (dec.)
저장 조건2-8°C
용해도H2O: 50 mg/mL
pKa(산도 계수)pKa 8.9 (Uncertain)
물리적 상태가루
색상무색 또는 약간 노란색
pHpH (10g/L, 25℃) : 4.5~7.0
생물학적 소스Pseudomonas aeruginosa
용해도50mg/ml/n에서 물에 용해됨
Merck14,7573
안정성흡습성
InChIKeyHFMDLUQUEXNBOP-UHFFFAOYSA-N
LogP(분배 계수)-6.361 (est)
EPAPolymixin B sulfate (1405-20-5)

화학적 성질

White Solid

안전 및 규제

수질 위해 등급(WGK)3
RTECS 번호TR1150000
운송 번호(UN)3249
독성dog,LDLo,intracrebral,320ug/kg (0.32mg/kg),BEHAVIORAL: COMA,British Journal of Pharmacology and Chemotherapy. Vol. 23, Pg. 552, 1964.
관세 코드2941 90 00
위험 문구(R)22
위험 표시Xn
안전 문구(S)22-24/25
포장분류III
위험 등급6.1(b)Acute Tox. 4 Oral
기존화학 물질KE-05-1072
F 고인화성물질3-8-10
저장 분류11 - Combustible Solids

용도

개요

The polymyxins are cationic peptides originally isolated from B. polymyxa. They bind and kill Gram-negative bacteria. The B series of polymyxins consist of a cyclic heptapeptide and a tripeptide side chain acylated at the amino terminus by a fatty acid. Polymyxin B (sulfate) is a mixture of at least four closely related components, polymyxin B1 to B4, with polymyxin B1 and B2 being the two major components. Polymyxin B (sulfate) has rapid in vitro bactericidal activity against major multidrug-resistant Gram-negative bacteria, such as P. aeruginosa, A. baumannii, and K. pneumoniae.

용도

Polymyxin B sulfate is used as topical antibiotic agent, often used in combination with neomycin; products include ointments, creams, eye, and ear drops.

일반 설명

Polymyxin (Aerosporin) was discovered in 1947 almost simultaneouslyin three separate laboratories in the UnitedStates and Great Britain. As often happens whensimilar discoveries are made in widely separated laboratories,differences in nomenclature, referring to both theantibiotic-producing organism and the antibiotic itself, appearedin references to the polymyxins. Because the organismsfirst designated as Bacillus polymyxa and B.aerosporus Greer were found to be identical species, thename B. polymyxa is used to refer to all of the strains thatproduce the closely related polypeptides called polymyxins.Other organisms (e.g., see “Colistin” later) also producepolymyxins. Identified so far are polymyxins A, B1,B2, C, D1, D2, M, colistin A (polymyxin E1), colistin B(polymyxin E2), circulins A and B, and polypeptin. Theknown structures of this group and their properties havebeen reviewed by Vogler and Studer. Of these,polymyxin B as the sulfate usually is used in medicine because,when used systemically, it causes less kidney damagethan the others. Polymyxin B sulfate is a nearly odorless, white to buff powder. It is freely soluble in water and slightly soluble in alcohol.