U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Description
Curator's Comment: description was created based on several sources, including http://reference.medscape.com/drug/neo-fradin-myciguent-neomycin-po-342515

Neomycin is an aminoglycoside antibiotic found in many topical medications such as creams, ointments, and eye drops. In vitro tests have demonstrated that neomycin is bactericidal and acts by inhibiting the synthesis of protein in susceptible bacterial cells. It is effective primarily against gram-negative bacilli but does have some activity against gram-positive organisms. Neomycin is active in vitro against Escherichia coli and the Klebsiella-Entero. Topical uses include treatment for superficial eye infections caused by susceptible bacteria (used in combination with other anti-infective), treatment of otitis externa caused by susceptible bacteria, treatment or prevention of bacterial infections in skin lesions, and use as a continuous short-term irrigant or rinse to prevent bacteriuria and gram negative rod bacteremia in bacteriuria patients with indwelling catheters. May be used orally to treat hepatic encephalopathy, as a perioperative prophylactic agent, and as an adjunct to fluid and electrolyte replacement in the treatment of diarrhea caused to enter pathogenic E. coli (EPEC). Neomycin sulfate has been shown to be effective adjunctive therapy in hepatic coma by reduction of the ammonia forming bacteria in the intestinal tract. The subsequent reduction in blood ammonia has resulted in neurologic improvement. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Neomycin Sulfate Oral Solution and other antibacterial drugs, susceptible bacteria should use Neomycin Sulfate Oral Solution only to treat or prevent infections that are proven or strongly suspected to be caused. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Neomycin binds to four nucleotides of 16S rRNA and a single amino acid of protein S12. This interferes with decoding site near nucleotide 1400 in 16S rRNA of 30S subunit. This region interacts with the wobble base in the anticodon of tRNA. This leads to interference with the initiation complex, misreading of mRNA so incorrect amino acids are inserted into the polypeptide leading to nonfunctional or toxic peptides and the breakup of polysomes into nonfunctional monosomes

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
CVP TRIPLE ANTIBIOTIC

Approved Use

Uses: first aid to help prevent infection in minor: cuts, scrapes, burns

Launch Date

1995
Palliative
NEO-FRADIN

Approved Use

Hepatic coma (portal-systemic encephalopathy): Neomycin sulfate has been shown to be effective adjunctive therapy in hepatic coma by reduction of the ammonia forming bacteria in the intestinal tract. The subsequent reduction in blood ammonia has resulted in neurologic improvement. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Neomycin Sulfate Oral Solution and other antibacterial drugs, Neomycin Sulfate Oral Solution should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Launch Date

2001
PubMed

PubMed

TitleDatePubMed
Synthesis and anti-HIV activity of guanidinoglycosides.
2000 Dec 29
A simple classification method for residual antibiotics using E. coli cells transformed by the calcium chloride method and drug resistance plasmid DNA.
2001
Targeted site-specific cleavage of HIV-1 viral Rev responsive element by copper aminoglycosides.
2001 Feb
Split-thickness skin graft donor site dressing: preliminary results of a controlled, clinical comparative study of MEBO and Sofra-Tulle.
2001 Jan
Agenesis of the skull bones.
2001 Jul
Simultaneous side effects of both clozapine and valproate.
2001 May
Aminoglycoside binding to human and bacterial A-Site rRNA decoding region constructs.
2001 Oct
A hole in the drum. An overview of tympanic membrane perforations.
2002 Aug
Stereospecificity of aminoglycoside-ribosomal interactions.
2002 Aug 20
Electron paramagnetic resonance dynamic signatures of TAR RNA-small molecule complexes provide insight into RNA structure and recognition.
2002 Dec 17
Small molecule modulators of HIV Rev/Rev response element interaction identified by random screening.
2002 Jun
Inhibition of Klenow DNA polymerase and poly(A)-specific ribonuclease by aminoglycosides.
2002 Nov
Reexamination of neomycin B degradation: efficient preparation of its CD and D rings as protected glycosyl donors.
2002 Oct 3
Are topical antibiotics necessary in the management of otitis externa?
2003 Aug
Comparison of compliance between topical aural medications.
2003 Aug
The Tat antagonist neomycin B hexa-arginine conjugate inhibits gp-120-induced death of human neuroblastoma cells.
2003 Mar
Structure-activity relationship of neomycin, paromomycin, and neamine-arginine conjugates, targeting HIV-1 gp120-CXCR4 binding step.
2003 Nov
Structural investigation of a high-affinity MnII binding site in the hammerhead ribozyme by EPR spectroscopy and DFT calculations. Effects of neomycin B on metal-ion binding.
2003 Oct 6
Aminoglycoside antibiotics reduce glucose reabsorption in kidney through down-regulation of SGLT1.
2003 Sep 5
Integrated, long term, sustainable, cost effective biosolids management at a large Canadian wastewater treatment facility.
2004
An approach to enhance specificity against RNA targets using heteroconjugates of aminoglycosides and chloramphenicol (or linezolid).
2004 Feb 25
New agents active against Mycobacterium avium complex selected by molecular topology: a virtual screening method.
2004 Jan
Optimizing the quadruple-potential waveform for the pulsed amperometric detection of neomycin.
2004 Jun 11
Randomized, double-blind trial comparing topical nitroglycerine with xylocaine and Proctosedyl in idiopathic chronic anal fissure.
2004 May-Jun
Lipoprotein lipase in hemodialysis patients: indications that low molecular weight heparin depletes functional stores, despite low plasma levels of the enzyme.
2004 Nov 3
Delayed neurotrophic treatment preserves nerve survival and electrophysiological responsiveness in neomycin-deafened guinea pigs.
2004 Oct 1
A peptide nucleic acid-neamine conjugate that targets and cleaves HIV-1 TAR RNA inhibits viral replication.
2004 Sep 23
Neamine inhibits xenografic human tumor growth and angiogenesis in athymic mice.
2005 Dec 15
Prescription pattern for treatment of hemorrhoids under the universal coverage policy of Thailand.
2005 Jul
The RNA-bound conformation of neamine as determined by transferred NOE experiments.
2005 Jul
A simple structural-based approach to prevent aminoglycoside inactivation by bacterial defense proteins. Conformational restriction provides effective protection against neomycin-B nucleotidylation by ANT4.
2005 Jun 15
Contact allergy to neomycin sulfate: results of a multifactorial analysis.
2005 Oct
Analysis of neomycin sulfate and framycetin sulfate by high-performance liquid chromatography using evaporative light scattering detection.
2005 Sep 16
Neamine derivatives having a nucleobase with a lysine or an arginine as a linker, their synthesis and evaluation as potential inhibitors for HIV TAR-Tat.
2006 Apr 15
Rapid analysis of native neomycin components on a portable capillary electrophoresis system with potential gradient detection.
2006 Aug
Synthesis and antibacterial activity of novel neamine derivatives.
2006 Dec 15
Mixed-type noncompetitive inhibition of anthrax lethal factor protease by aminoglycosides.
2006 Jul
Biosolids from two-stage bioleaching could produce compost for unrestricted use.
2006 Jun
Removal of p-xylene with Pseudomonas sp. NBM21 in biofilter.
2006 Oct
Selectively guanidinylated derivatives of neamine. Syntheses and inhibition of anthrax lethal factor protease.
2006 Oct 1
Determination of neomycin sulfate and impurities using high-performance anion-exchange chromatography with integrated pulsed amperometric detection.
2007 Jan 4
Patents

Sample Use Guides

Hepatic coma: 4-12 grams per day given in the following regimen: 1. Withdraw protein from diet. Avoid use of diuretic agents. 2. Give supportive therapy including blood products, as indicated. 3. Give NEO-FRADIN Oral Solution in doses of four to twelve grams of neomycin sulfate per day in divided doses. Treatment should be continued over a period of five to six days during which time protein should be returned incrementally to the diet.
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: TRMU, tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase, is expressed in both hair cells and HEI-OC-1 cells, and its expression is significantly decreased after 24 h neomycin treatment. Downregulated TRMU expression with siRNA and found that cell death and apoptosis were significantly increased after neomycin injury.
Unknown
Substance Class Mixture
Created
by admin
on Fri Dec 15 16:39:57 GMT 2023
Edited
by admin
on Fri Dec 15 16:39:57 GMT 2023
Record UNII
I16QD7X297
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEOMYCIN
HSDB   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
NEOMIN
Brand Name English
NEOMYCIN [HSDB]
Common Name English
PIMAVECORT
Brand Name English
NEOMYCIN [VANDF]
Common Name English
Neomycin [WHO-DD]
Common Name English
ANTIBIOTIC COMPLEX COMPOSED OF NEOMYCINS A, B AND C PRODUCED BY STREPTOMYCES FRADIAE
Common Name English
NEOMYCIN [MI]
Common Name English
NEOMAS
Brand Name English
neomycin [INN]
Common Name English
NEOLATE
Brand Name English
KAOMYCINE
Brand Name English
VONAMYCIN
Brand Name English
FRADIOMYCIN
Common Name English
Classification Tree Code System Code
CFR 21 CFR 524.154
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
WHO-VATC QD06AX04
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NDF-RT N0000007853
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WHO-VATC QS03AA01
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
CFR 21 CFR 520.1921
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WHO-VATC QB05CA09
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CFR 21 CFR 524.1484E
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NCI_THESAURUS C2363
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CFR 21 CFR 333.120
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CFR 21 CFR 524.1484
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CFR 21 CFR 524.1484K
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WHO-VATC QG51AG03
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
WHO-ATC D06AX04
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EPA PESTICIDE CODE 6303
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
WHO-ATC A07AA01
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WHO-VATC QA01AB08
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WHO-ATC A07AA51
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WHO-VATC QG51AG06
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WHO-VATC QJ51RG01
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WHO-VATC QA07AA51
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
WHO-ATC S01AA03
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LIVERTOX NBK547874
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WHO-ATC A01AB08
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
CFR 21 CFR 524.1484J
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
CFR 21 CFR 524.155
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
CFR 21 CFR 524.1484H
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
WHO-ATC S02AA07
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CFR 21 CFR 524.960
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WHO-VATC QJ01GB05
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
CFR 21 CFR 520.1484
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WHO-VATC QS02AA07
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
CFR 21 CFR 524.1484D
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WHO-ATC R02AB01
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WHO-VATC QS01AA03
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WHO-ATC J01GB05
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WHO-VATC QS02AA57
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CFR 21 CFR 524.1484F
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CFR 21 CFR 524.1484I
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WHO-ATC S03AA01
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WHO-VATC QA07AA01
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CFR 21 CFR 524.1484B
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CFR 21 CFR 556.430
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CFR 21 CFR 524.1600A
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CFR 21 CFR 558.455
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NDF-RT N0000175477
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
CFR 21 CFR 520.82B
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
WHO-ATC B05CA09
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
CFR 21 CFR 524.1484C
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CFR 21 CFR 524.981C
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CFR 21 CFR 524.1484G
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CFR 21 CFR 524.1600B
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WHO-VATC QR02AB01
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
Code System Code Type Description
MESH
D009355
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
DRUG CENTRAL
4247
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
WIKIPEDIA
NEOMYCIN
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
LACTMED
Neomycin
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
EVMPD
SUB03406MIG
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
ECHA (EC/EINECS)
215-766-3
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
NCI_THESAURUS
C683
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
DAILYMED
I16QD7X297
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
MERCK INDEX
m7809
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID9041073
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PRIMARY
INN
232
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PRIMARY
HSDB
3242
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PRIMARY
ChEMBL
CHEMBL184618
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
RXCUI
7299
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PRIMARY RxNorm
CHEBI
7507
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PRIMARY
IUPHAR
709
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
CAS
1404-04-2
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
DRUG BANK
DB00994
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
FDA UNII
I16QD7X297
Created by admin on Fri Dec 15 16:39:57 GMT 2023 , Edited by admin on Fri Dec 15 16:39:57 GMT 2023
PRIMARY
All of the following components must be present:
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY
Definition References