KANAMYCIN SULFATE

Kanamycin sulfate is an aminoglycoside antibiotic that inhibits bacterial protein synthesis by binding the 30S ribosomal subunit. It is used for severe gramnegative and some mycobacterial infections. Benefits include potent bactericidal activity. Side effects include nephrotoxicity, irreversible ototoxicity, neuromuscular blockade, and need for serum level monitoring. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 5acd369f2d0e Category: Tag:

Product Description


Mechanism of Action

KANAMYCIN SULFATE exhibits a structured and multilayered biochemical activity profile involving modulation of enzymatic cascades, receptorbinding dynamics, intracellular signalling architecture, and metabolicflux regulation. Its molecular characteristics indicate potential interactions with catalytic pockets, allosteric surfaces, and regulatory protein domains. Through these interactions, the compound influences phosphorylation patterns, mitochondrial bioenergetics, oxidativestress networks, membrane potential stabilization, and transcriptional pathway responsiveness.

In cellular systems, mechanistic effects may include modulation of calcium flux, ROS equilibrium, structuralprotein turnover, and adaptive stressresponse activation. The compound may act as a pathway booster, suppressor, or modulator depending on dosing, cellular environment, and metabolic state.

Benefits and Advantages

This compound is widely used in biochemical, pharmacological and mechanistic research settings, including:

  • Receptorligand interaction studies and affinitymapping assays
  • Enzyme kinetics and catalyticpathway modelling
  • Mitochondrialfunction, ROSregulation and redoxbalance experiments
  • Transcriptomic, proteomic and metabolomic profiling
  • Cellstress signalling, apoptosis/autophagy pathway mapping and cytoskeletaldynamics studies
  • Pharmacodynamic simulation and SAR (structureactivity relationship) analysis

Side Effects and Risks

Risks may include unintended oxidative imbalance, mitochondrial overload, receptor crosstalk effects, disruption of ionchannel homeostasis, and dosedependent cytotoxicity. At elevated concentrations, the compound may trigger apoptosis, autophagy, or compensatory metabolic rewiring. Longterm exposure can influence transcriptional stability, signalling thresholds, and cellular resilience.

Use only in controlled laboratory environments following strict biosafety and handling protocols. Not intended for human or veterinary use.

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

Datasheet


Molecular Formula

C18H38N4O15S

Molecular Weight

582.6 g/mol

CAS Number

25389-94-0

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

Kanamycin A sulfate; Kanamycin A sulphate; J80EX28SMQ; DTXSID1047524; EINECS 223-347-1

IUPAC/Chemical Name

(2R,3S,4S,5R,6R)-2-(aminomethyl)-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]oxyoxane-3,4,5-triol;sulfuric acid

InChl Key

OOYGSFOGFJDDHP-KMCOLRRFSA-N

InChl Code

InChI=1S/C18H36N4O11.H2O4S/c19-2-6-10(25)12(27)13(28)18(30-6)33-16-5(21)1-4(20)15(14(16)29)32-17-11(26)8(22)9(24)7(3-23)31-17;1-5(2,3)4/h4-18,23-29H,1-3,19-22H2;(H2,1,2,3,4)/t4-,5+,6-,7-,8+,9-,10-,11-,12+,13-,14-,15+,16-,17-,18-;/m1./s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/441374;

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