Kanamycin
An aminoglycoside antibiotic used to treat serious bacterial infections including tuberculosis, working by binding to bacterial ribosomes to inhibit protein synthesis. It has also been studied as an inhaled therapy for asthma-related bacterial infections.
分子量
484.5000 g/mol
LogP
-6.90
TPSA
283.00 Ų
Lipinski 五规则
不符合
治疗领域
作用机制
Binds irreversibly to the 30S ribosomal subunit, causing misreading of mRNA codons and inhibition of translocation. This leads to production of aberrant proteins and disruption of the bacterial cell membrane.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Binds irreversibly to the 30S ribosomal subunit, causing misreading of mRNA codons and inhibition of translocation. This leads to production of aberrant proteins and disruption of the bacterial cell membrane.
二维结构
Cite this structure
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SMILES
NC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H](N)C[C@@H]2N)[C@H](O)[C@@H](O)[C@@H]1O
InChI
InChI=1S/C18H36N4O11/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/h4-18,23-29H,1-3,19-22H2/t4-,5+,6-,7-,8+,9-,10-,11-,12+,13-,14-,15+,16-,17-,18-/m1/s1
Molecular Formula
C18H36N4O11
HBD / HBA
11 / 15
可旋转键数
6
重原子数
33
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
常见问题
An aminoglycoside antibiotic used to treat serious bacterial infections including tuberculosis, working by binding to bacterial ribosomes to inhibit protein synthesis. It has also been studied as an inhaled therapy for asthma-related bacterial infections.
Binds irreversibly to the 30S ribosomal subunit, causing misreading of mRNA codons and inhibition of translocation. This leads to production of aberrant proteins and disruption of the bacterial cell membrane.
Yes, Kanamycin is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1384. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 6032. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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