• ChemBase ID: 169214
• Molecular Formular: C19H37N5O7
• Molecular Mass: 447.52638
• Monoisotopic Mass: 447.26929855
• SMILES: [C@H]1(O[C@H]2[C@@H](C([C@@H](CC2N)N)O[C@@H]2[C@@H](C([C@](CO2)(O)C)NC)O)O)OC(CCC1N)C(N*)*
• Canonical SMILES: *NC(C1CCC([C@H](O1)O[C@@H]1C(N)C[C@H](C([C@H]1O)O[C@H]1OC[C@](C([C@H]1O)NC)(C)O)N)N)*
• InChI: InChI=

NAMES AND DATABASE IDS

Names

• Synonyms: Alcomicin; Bristagen; Cidomycin; Duragentam; Garamycin; Garasol; Genoptic; Gentacidin; Gentacin; Gentaglyde; Gentalyn; Gentamicin C Complex Citrate; Gentibioptal; Genticin; Gentocin; Gentogram; Gent-Ophtal; Getalline; GM; Gentamicin Deuterated (C Complex) Pentaacetate Salt(Contains d0)

Database IDs

• PubChem SID: 162263346
• PubChem CID: 71316867

PROPERTIES

Physical Property

• Solubility: DMSO; Water
• Apperance: White Solid
• Melting Point: 117-122°C

Safety Information

• Storage Condition: Hygroscopic, -20°C Freezer, Under Inert Atmosphere

DETAILS

Toronto Research Chemicals - G360602

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 complex

REFERENCES

• Holt, H.A., et al.: J. Antimicrob. Chemother., 34, 747 (1994)
• Wilschanski, M., et al.: Am. J. Respir. Crit. Care Med., 161, 860 (1994)