Amikacin EP Impurity E is a pharmaceutical impurity reference standard used in the quality control and manufacturing of the aminoglycoside antibiotic amikacin. It serves as a reference compound for identifying and quantifying related impurities during drug development and production.
콘텐츠 범위: 이 페이지의 정보는 화학물질 식별 및 산업 공급·연구개발·제조 맥락을 대상으로 합니다. 치료 효능 주장, 의료 조언 또는 의약품 사용 지침에 해당하지 않습니다.
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CAS 50866-72-3
1,6'-Di-HABA Kanamycin A
amikacin impurity reference standard
Ephedrine hemihydrate
active pharmaceutical ingredient
Mizoribine
immunosuppressive drug
Diatrizoic acid dihydrate
X-ray contrast medium
PROCAINE HYDROCHLORIDE
local anesthetic active pharmaceutical ingredient
Amikacin EP Impurity G
Amikacin impurity reference standard
Amikacin hydrate
active pharmaceutical ingredient
Amikacin
antibiotic active pharmaceutical ingredient
(2S)-4-amino-N-[[(2R,3S,4S,5R,6R)-6-[(1R,2R,3S,4R,6S)-4,6-diamino-3-[(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl]-2-hydroxybutanamide
PABPVMHDINVPAE-PVLUVTDWSA-N
C1[C@H]([C@@H]([C@H]([C@@H]([C@H]1N)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CNC(=O)[C@H](CCN)O)O)O)O)O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)N)O)N