AMYKACIN

Amykacin (amikacin variant) is an aminoglycoside antibiotic that inhibits bacterial protein synthesis, effective against severe gramnegative infections. Benefits include activity against resistant strains. Side effects include nephrotoxicity, ototoxicity, and neuromuscular blockade, requiring drug-level monitoring and renal dose adjustment. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 687ac7d28778 Category: Tag:

Product Description


Mechanism of action

Amykacin (likely variant of amikacin or aminoglycoside derivative) exerts bactericidal effects by binding the 30S ribosomal subunit, inhibiting accurate tRNA positioning and causing mistranslation and halted protein synthesis.

Benefits and advantages

Useful in comparative aminoglycoside studies, ribosomal binding kinetics research and antimicrobial resistance profiling.

Side effects and risks

Nephrotoxicity, ototoxicity, neuromuscular blockade. Strict antimicrobial handling required.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C22H43N5O13

Molecular Weight

585.61 g/mol

CAS Number

37517-28-5

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

DTXSID60860546; 4-amino-n-{5-amino-2-[(3-amino-3-deoxyhexopyranosyl)oxy]-4-[(6-amino-6-deoxyhexopyranosyl)oxy]-3-hydroxycyclohexyl}-2-hydroxybutanamide; 4-Amino-N-(5-amino-2-((3-amino-3-deoxyhexopyranosyl)oxy)-4-((6-amino-6-deoxyhexopyranosyl)oxy)-3-hydroxycyclohexyl)-2-hydroxybutanamide; RefChem:1070310; DTXCID10209183

IUPAC/Chemical Name

4-amino-N-[5-amino-2-[4-amino-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-3-hydroxycyclohexyl]-2-hydroxybutanamide

InChl Key

LKCWBDHBTVXHDL-UHFFFAOYSA-N

InChl Code

InChI=1S/C22H43N5O13/c23-2-1-8(29)20(36)27-7-3-6(25)18(39-22-16(34)15(33)13(31)9(4-24)37-22)17(35)19(7)40-21-14(32)11(26)12(30)10(5-28)38-21/h6-19,21-22,28-35H,1-5,23-26H2,(H,27,36)

References

https://pubchem.ncbi.nlm.nih.gov/#query=37517-28-5;

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