엔비오마이신

엔비오마이신
엔비오마이신 구조식 이미지
카스 번호:
33103-22-9
한글명:
엔비오마이신
동의어(한글):
엔비오마이신
상품명:
Enviomycin
동의어(영문):
Turn-n;enviomucin;Aids008855;Enviomycin;Aids-008855;Tuberactinomycin N;Tuberactin (*sulfate*);Tuberactinomycin N (8CI, 9CI);1,4,7,10,13-Pentaazacyclohexadecane, cyclic peptide deriv.;1-(L-Threo-3,6-diamino-4-hydroxy-hexanoic acid)-6-[T-2-(2-amino-1,4,5,6-tetrahydro-4-pyriminyl)glycine]viomycin
CBNumber:
CB41074158
분자식:
C25H43N13O10
포뮬러 무게:
685.69
MOL 파일:
33103-22-9.mol

엔비오마이신 속성

밀도
1.80±0.1 g/cm3(Predicted)
산도 계수 (pKa)
9.87±0.70(Predicted)

안전

엔비오마이신 C화학적 특성, 용도, 생산

개요

Enviomycin was found in the culture broth of Streptomyces griseoverticillatus var. tuberacticus by Toyo Jozo Co. in 1966 as a mixture of tuberactinomycins N and O. It is a water-soluble, basic peptide closely related to viomycin and showing selective activity against Mycobacterium species about twice as strong as that of viomycin. Enviomycin, in combination with other antituberculotic drugs, is used to treat tuberculosis caused by streptomycinresistant Mycobacterium.

Originator

Tuberactin,Toyo Jozo,Japan,1975

Manufacturing Process

Two liters of an aqueous medium consisting of glucose 3%, starch 2%, soybean meal 3% and sodium chloride 1.5% were equally divided and introduced into twenty 500-ml Erlenmeyer flasks, adjusted to pH 6, sterilized at 120°C for 30 minutes, inoculated with Streptomyces griseoverticillatus var. tuberacticus N6-130 and then rotatively shake-cultured (radius 2.5 cm, 330 rpm) at 30°C for 7 days, obtaining 1.5 liter of cultured broth containing 2,360 mcg/ml of tuberactinomycin-N.
Filtered broth was passed at 2.5 ml/min through a resin column (2.5 cm diameter, 28 cm length) packed with 150 ml of ion exchange resin Amberlite IRC-50 sodium type (Rohm and Haas Co., USA.). The column was washed with water, eluted with 0.5N HCl at a flow rate 1.3 ml/min. The eluates were fractionated each 10 ml and tuberactinomycin-N activity was found at fractions No. 45-63 observed by ultraviolet absorption method and bioassay.
The thus yielded active fraction, about 200 ml, was neutralized with sodium hydroxide, concentrated to about 15 ml in vacuo, separating the precipitated inorganic salts therefrom. After decolorization with active carbon, 150 ml of methanol was added, the mixture was allowed to stand overnight at 5°C and the precipitate was collected by filtration. The precipitate was washed withmethanol and dried in vacuo to yield crude tuberactinomycin-N hydrochloride (yield, 3.07 g; purity, 7 1.5%; recovery, 62%).

Therapeutic Function

Antitubercular

엔비오마이신 준비 용품 및 원자재

원자재

준비 용품


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