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Kanamycin
Kantrex, Klebcil (kanamycin) is a small molecule pharmaceutical. Kanamycin was first approved as Kantrex on 1982-01-01. It is used to treat acinetobacter infections, bacterial infections, escherichia coli infections, hepatic encephalopathy, and klebsiella infections amongst others in the USA.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
infectionsD007239
digestive system diseasesD004066
respiratory tract diseasesD012140
nervous system diseasesD009422
nutritional and metabolic diseasesD009750
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
No data
Labels
FDA
EMA
No data
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
acinetobacter infectionsEFO_1000792D000151
bacterial infectionsD001424A49
escherichia coli infectionsEFO_1001318D004927B96.20
hepatic encephalopathyD006501K72.91
klebsiella infectionsEFO_1001353D007710
mycobacterium infectionsD009164A31.9
proteus infectionsEFO_1001130D011512
respiratory tract infectionsD012141J06.9
serratia infectionsEFO_1001421D016868
staphylococcal infectionsD013203A49.01
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
A: Alimentary tract and metabolism drugs
A07: Antidiarrheals, intestinal antiinflammatory/antiinfective agents
A07A: Intestinal antiinfectives
A07AA: Antibiotics, intestinal
A07AA08: Kanamycin
J: Antiinfectives for systemic use
J01: Antibacterials for systemic use
J01G: Aminoglycoside antibacterials
J01GB: Other aminoglycosides in atc
J01GB04: Kanamycin
S: Sensory organ drugs
S01: Ophthalmologicals
S01A: Antiinfective ophthalmologics
S01AA: Antibiotics, ophthalmologic
S01AA24: Kanamycin
HCPCS
Code
Description
J1840
Injection, kanamycin sulfate, up to 500 mg
J1850
Injection, kanamycin sulfate, up to 75 mg
Clinical
Clinical Trials
16 clinical trials
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Indications Phases 4
No data
Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Kidney calculiD007669EFO_0004253N20.0212
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
LipomaD008067D17.9111
Atrial fibrillationD001281EFO_0000275I48.011
UreteroscopyD01866611
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Autonomic nervous system diseasesD001342EFO_0009532G90112
Orthostatic intoleranceD054971112
Healthy volunteers/patients22
Orthostatic hypotensionD007024I95.111
ObesityD009765EFO_0001073E66.911
VasodilationD01466411
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Postural orthostatic tachycardia syndromeD054972G90.A22
Anorexia nervosaD000856EFO_0004215F50.022
HypotensionD007022EFO_0005251I9511
Heart failureD006333EFO_0003144I5011
Cardiovascular diseasesD002318EFO_0000319I9811
Cardiac arrhythmiasD001145EFO_0004269I49.911
TachycardiaD013610HP_0001649R00.011
Primary dysautonomiasD05496911
Intraoperative awarenessD05892611
Long qt syndromeD008133HP_0001657I45.8111
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameKANAMYCIN
INNkanamycin
Description
Kanamycin A is a member of kanamycins. It has a role as a bacterial metabolite. It is a conjugate base of a kanamycin A(4+).
Classification
Small molecule
Drug classantibiotics (Streptomyces strain)
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O
Identifiers
PDB
CAS-ID59-01-8
RxCUI1727573
ChEMBL IDCHEMBL1384
ChEBI ID17630
PubChem CID6032
DrugBankDB01172
UNII IDRUC37XUP2P (ChemIDplus, GSRS)
Target
Agency Approved
No data
Alternate
No data
Variants
Clinical Variant
Identifier
Target mutation
Effect
Evaluation
Status
VCV000009631MT-RNR1drug response2021-06-151A
Financial
No data
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 109,821 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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251 adverse events reported
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