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타일로신

Tylosin

HCID 6474983
노트반응

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기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
1401-69-0
표준 SMILES
CC[C@H]1OC(=O)C[C@@H](O)[C@H](C)[C@@H](O[C@@H]2O[C@H](C)[C@H](O[C@H]3C[C@@](C)(O)[C@@H](O)[C@H](C)O3)[C@H](N(C)C)[C@H]2O)[C@@H](CC=O)C[C@@H](C)C(=O)/C=C/C(C)=C/[C@@H]1COC1O[C@H](C)[C@@H](O)[C@@H](OC)[C@H]1OC
분자식
C46H77NO17
평균 분자량
916.1 g/mol

이름 및 식별자

우선 이름
Tylosin
현지명
타일로신
영어명
Tylosin
분자식
C46H77NO17
분자량
916.1

이름 및 동의어

타일로신틸로신TylosineTylosin ATylonVetilTYLOSINTYLAN50tylocineVetil(R)Tylan 100fradizine

데이터베이스 식별자

CAS
1401-69-0
PubChem CID
6474983

물성

물리화학적 성질

녹는점
135 · 135-137°C
끓는 점
796.05 °C · 796.05°C (rough estimate)
밀도
1.1424 · 1.1424 (rough estimate)
굴절률
1.528 · 1.5280 (estimate)
저장 조건
2 · Sealed in dry,2-8°C
용해도
30 mg/ml; · DMF: 30 mg/ml; DMSO: 25 mg/ml; Ethanol: 30 mg/ml
물리적 상태
결정성 고체
산도 계수 (pKa)
7.73 · pKa 7.73(H2O t = 25 I = 0.167) (Uncertain)
색상
White to light yellow
수용성
2 O: · H2O: 가용성 50mg/mL
Henry's Law Constant
1.7 · 1.7×1032 mol/(m3Pa) at 25℃, HSDB (2015)
안정성
4 · Solutions are stable at pH 4-9 (most stable at pH 7); Below pH 4 tylosin B (desmycosin) is formed as a result of acid hydrolysis; In neutral and alkaline pH – tylosin aldol (TAD) is formed together with polar degradation products of unknown identity; When tylosin solution is exposed to daylight, a photodegradation product - isotylosin A (isoTA) is formed.
주요 응용
제약소분자 약용
InChIKey
WBPYTXDJUQJLPQ-VMXQISHHSA-N
EPA
Tylosin (1401-69-0)
화학적 성질 · 1건

Off-White to Pale Yellow Solid. Tylosin is a macrolide antibiotic which is active against certain Gram-positive and Gram-negative bacteria and Gram-positive mycoplasmas. It consists predominantly of tylosin(factor A), but varying amounts of desmycosin (factor B), macrocin (factor C) and relomycin(factor D) may also be present, depending on the manufacturing source. Most of themicrobiological activity resides with tylosin factor A. Tylosin is a weak organic base with a high degree of lipid solubility, thus it is well distributed to the organs and tissues of animals (Burrows, 1980). Tylosin is used in pigs, cattle and poultryfor the treatment of conditions caused by sensitive organisms. It may be administered by oral orparenteral routes. Tylosin is not used in human medicine.

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

안전 데이터

wgk
WGK 2
독성
Tylosin base and its salts were shown to be of low acute oral toxicity with LD50 values in excess 5000 mg/kg bw in the rat and mouse and greater than 800 mg/kg bw in the dog.
HS 번호
2941906000
risk_code
42/43-50
hazard_code
Xn,N
safety_code
36-61-45-36/37-22
기존화학 물질
KE-35033
Hazard Classifications
Resp. Sens. 1Skin Sens. 1
스토리지 클래스
11 - Combustible Solids
유해 물질 데이터
1401-69-0(Hazardous Substances Data)

화학 및 산업

응용 분야 · 2건

개요Tylosin is a macrolide antibiotic produced by S. fradiae that has bacteriostatic activity against Gram-positive bacteria. It is a mixture of tylosin A, B, C, and D, with tylosin A contributing 80% of its bacteriostatic activity. Tylosin has MIC values of 9.6, 16.4, 0.1, 1, and 0.5 μg/ml for F. necrophorum, A. pyogenes, M. gallisepticum, S. aureus, and S. uberis, respectively.,, Formulations containing tylosin have been used for the prevention of liver abscesses in cattle. Tylosin is an environmental contaminant because it is not fully metabolized by treated livestock and enters the environment through manure-based fertilizers.

용도Tylosin is a 16-membered macrocyclic lactone isolated from Streptomyces fradiae in 1961. Tylosin has broad spectrum antibacterial activity and was developed as a veterinary pharmaceutical for treatment of bacterial infections in a range of domestic animals . Tylosin acts by binding to the 50S ribosomal subunit resulting in the inhibition of protein synthesis in bacteria.

상·하류 제품 정보

하류 제품

Tilmicosin phosphateCefepime hydrochloride

공급사100 곳

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Baoji Guokang Healthchem co.,ltd+8615604608665 15604608665 · [email protected]
Hebei Henghe Import and Export Trading Co. LTD+8618032935937 18032916000 · [email protected]
Hebei Yanxi Chemical Co., Ltd.

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추가 설명

정의ChEBI: A macrolide antibiotic that is tylonolide having mono- and diglycosyl moieties attached to two of its hydroxy groups. It is found naturally as a fermentation product of Streptomyces fradiae.