| Identification | |
| Name: | Gentamycin sulfate |
| Synonyms: | Gentalline;Pred-G S.O.P.;Gentocin (Veterinary);Gentocin (*sulfate*);Garamycin (TN);Gentacin;Geramycin;Gentocin;Prestwick_240;Septopal;Gentamicin,sulfate (salt);Gentamicin C complex sulfate;Gentamicins;Topagen (Veterinary);Gentamycin sulphat;Gentamycin Solution;Gentamicin sulphate;Alcomicin;Garasol (Veterinary); |
| CAS: | 1405-41-0 |
| EINECS: | 215-778-9 |
| Molecular Formula: | C21H43N5O7.H2SO4 |
| Molecular Weight: | 575.67 |
| InChI: | InChI=1/C19H39N5O7.H2O4S/c1-19(27)7-28-18(13(26)16(19)24-2)31-15-11(23)5-10(22)14(12(15)25)30-17-9(21)4-3-8(6-20)29-17;1-5(2,3)4/h8-18,24-27H,3-7,20-23H2,1-2H3;(H2,1,2,3,4)/t8-,9+,10-,11+,12-,13+,14+,15-,16+,17+,18+,19-;/m0./s1 |
| Molecular Structure: |  |
| Properties | |
| Density: | == |
| Stability: | Stable under normal temperatures and pressures. |
| Solubility: | water: 50 mg/mL |
| Appearance: | White to buff-colored powder. Odorless. |
| Specification: |
?Gentamycin sulfate , its cas register number is 1405-41-0. It also can be called Garamycin ; and 2-[4,6-Diamino-3-[3-amino-6-(1-methylaminoethyl)oxan-2-yl]oxy-2-hydroxy-cyclohexoxy]-5-methyl-4-methylamino-oxane-3,5-diol sulphate . |
| Usage: | Inhibits protein synthesis by binding to L6 protein of 50S ribosomal subunit. Antibacterial. Antibiotic complex consists of three closely related components, gentamicins C1, C2, C1a, and also gentamicin A which differs from the other members of the |
| Safety Data | |
| Hazard Symbols |
Xn:Harmful
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