InChI
InChI=1S/C22H43N5O12.H2O4S/c1-22(35)6-36-20(15(33)18(22)26-2)39-17-8(27-19(34)9(28)4-23)3-7(25)16(14(17)32)38-21-13(31)12(30)11(29)10(5-24)37-21;1-5(2,3)4/h7-18,20-21,26,28-33,35H,3-6,23-25H2,1-2H3,(H,27,34);(H2,1,2,3,4)/t7-,8+,9-,10+,11+,12-,13+,14-,15+,16+,17-,18+,20+,21+,22-;/m0./s1
InChI key
DDXRHRXGIWOVDQ-MGAUJLSLSA-N
SMILES string
C[C@@]1(CO[C@@H]([C@@H]([C@H]1NC)O)O[C@H]2[C@@H](C[C@@H]([C@H]([C@@H]2O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CN)O)O)O)N)NC(=O)[C@H](CN)O)O.OS(=O)(=O)O
assay
≥68%
form
powder
color
white to off-white
antibiotic activity spectrum
Gram-negative bacteria, Gram-positive bacteria
mode of action
protein synthesis | inhibits
storage temp.
2-8°C
Quality Level
General description
Isepamicin Sulfate is a semisynthetic aminoglycoside antibiotic derived from gentamicin with a spectrum of activity against Gram-positive bacteria, Gram-negative bacteria, and fungi.
Biochem/physiol Actions
Sepamicin Sulfate inhibits bacterial protein synthesis by binding to the bacterial 30S ribosomal subunit, leading to the misreading of genetic information and inhibition of protein synthesis, and ultimately, bacterial cell death.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
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