DescriptionCurator's Comment: description was created based on several sources, including
http://reference.medscape.com/drug/neo-fradin-myciguent-neomycin-po-342515
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
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL2363135 Sources: https://www.ncbi.nlm.nih.gov/pubmed/18060665 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Preventing | CVP TRIPLE ANTIBIOTIC Approved UseUses: first aid to help prevent infection in minor: cuts, scrapes, burns Launch Date1995 |
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Palliative | NEO-FRADIN Approved UseHepatic 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 Date2001 |
PubMed
Title | Date | PubMed |
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Synthesis and anti-HIV activity of guanidinoglycosides. | 2000 Dec 29 |
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A simple classification method for residual antibiotics using E. coli cells transformed by the calcium chloride method and drug resistance plasmid DNA. | 2001 |
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Targeted site-specific cleavage of HIV-1 viral Rev responsive element by copper aminoglycosides. | 2001 Feb |
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Split-thickness skin graft donor site dressing: preliminary results of a controlled, clinical comparative study of MEBO and Sofra-Tulle. | 2001 Jan |
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Agenesis of the skull bones. | 2001 Jul |
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Simultaneous side effects of both clozapine and valproate. | 2001 May |
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Aminoglycoside binding to human and bacterial A-Site rRNA decoding region constructs. | 2001 Oct |
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A hole in the drum. An overview of tympanic membrane perforations. | 2002 Aug |
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Stereospecificity of aminoglycoside-ribosomal interactions. | 2002 Aug 20 |
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Electron paramagnetic resonance dynamic signatures of TAR RNA-small molecule complexes provide insight into RNA structure and recognition. | 2002 Dec 17 |
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Small molecule modulators of HIV Rev/Rev response element interaction identified by random screening. | 2002 Jun |
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Inhibition of Klenow DNA polymerase and poly(A)-specific ribonuclease by aminoglycosides. | 2002 Nov |
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Reexamination of neomycin B degradation: efficient preparation of its CD and D rings as protected glycosyl donors. | 2002 Oct 3 |
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Are topical antibiotics necessary in the management of otitis externa? | 2003 Aug |
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Comparison of compliance between topical aural medications. | 2003 Aug |
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The Tat antagonist neomycin B hexa-arginine conjugate inhibits gp-120-induced death of human neuroblastoma cells. | 2003 Mar |
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Structure-activity relationship of neomycin, paromomycin, and neamine-arginine conjugates, targeting HIV-1 gp120-CXCR4 binding step. | 2003 Nov |
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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 |
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Aminoglycoside antibiotics reduce glucose reabsorption in kidney through down-regulation of SGLT1. | 2003 Sep 5 |
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Integrated, long term, sustainable, cost effective biosolids management at a large Canadian wastewater treatment facility. | 2004 |
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An approach to enhance specificity against RNA targets using heteroconjugates of aminoglycosides and chloramphenicol (or linezolid). | 2004 Feb 25 |
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New agents active against Mycobacterium avium complex selected by molecular topology: a virtual screening method. | 2004 Jan |
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Optimizing the quadruple-potential waveform for the pulsed amperometric detection of neomycin. | 2004 Jun 11 |
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Randomized, double-blind trial comparing topical nitroglycerine with xylocaine and Proctosedyl in idiopathic chronic anal fissure. | 2004 May-Jun |
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Lipoprotein lipase in hemodialysis patients: indications that low molecular weight heparin depletes functional stores, despite low plasma levels of the enzyme. | 2004 Nov 3 |
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Delayed neurotrophic treatment preserves nerve survival and electrophysiological responsiveness in neomycin-deafened guinea pigs. | 2004 Oct 1 |
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A peptide nucleic acid-neamine conjugate that targets and cleaves HIV-1 TAR RNA inhibits viral replication. | 2004 Sep 23 |
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Neamine inhibits xenografic human tumor growth and angiogenesis in athymic mice. | 2005 Dec 15 |
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Prescription pattern for treatment of hemorrhoids under the universal coverage policy of Thailand. | 2005 Jul |
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The RNA-bound conformation of neamine as determined by transferred NOE experiments. | 2005 Jul |
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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 |
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Contact allergy to neomycin sulfate: results of a multifactorial analysis. | 2005 Oct |
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Analysis of neomycin sulfate and framycetin sulfate by high-performance liquid chromatography using evaporative light scattering detection. | 2005 Sep 16 |
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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 |
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Rapid analysis of native neomycin components on a portable capillary electrophoresis system with potential gradient detection. | 2006 Aug |
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Synthesis and antibacterial activity of novel neamine derivatives. | 2006 Dec 15 |
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Mixed-type noncompetitive inhibition of anthrax lethal factor protease by aminoglycosides. | 2006 Jul |
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Biosolids from two-stage bioleaching could produce compost for unrestricted use. | 2006 Jun |
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Removal of p-xylene with Pseudomonas sp. NBM21 in biofilter. | 2006 Oct |
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Selectively guanidinylated derivatives of neamine. Syntheses and inhibition of anthrax lethal factor protease. | 2006 Oct 1 |
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Determination of neomycin sulfate and impurities using high-performance anion-exchange chromatography with integrated pulsed amperometric detection. | 2007 Jan 4 |
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27405449
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
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on
Edited
Fri Dec 15 16:39:57 GMT 2023
by
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on
Fri Dec 15 16:39:57 GMT 2023
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Record UNII |
I16QD7X297
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Record Status |
Validated (UNII)
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Classification Tree | Code System | Code | ||
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CFR |
21 CFR 524.154
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WHO-VATC |
QD06AX04
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NDF-RT |
N0000007853
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WHO-VATC |
QS03AA01
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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
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WHO-ATC |
D06AX04
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EPA PESTICIDE CODE |
6303
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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
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WHO-ATC |
S01AA03
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LIVERTOX |
NBK547874
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WHO-ATC |
A01AB08
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CFR |
21 CFR 524.1484J
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CFR |
21 CFR 524.155
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CFR |
21 CFR 524.1484H
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WHO-ATC |
S02AA07
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CFR |
21 CFR 524.960
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WHO-VATC |
QJ01GB05
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CFR |
21 CFR 520.1484
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WHO-VATC |
QS02AA07
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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
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CFR |
21 CFR 520.82B
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WHO-ATC |
B05CA09
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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
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D009355
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4247
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NEOMYCIN
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Neomycin
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SUB03406MIG
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215-766-3
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C683
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I16QD7X297
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m7809
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DTXSID9041073
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232
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3242
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CHEMBL184618
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7299
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7507
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709
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DB00994
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I16QD7X297
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