Drug ID:Drug46
Drug Name:Neomycin
CID:8378
DrugBank ID:DB00994
Modality:Small Molecule
Groups:approved
US Approved:YES
Other Approved:YES
Identifier: NCT02765256, , NCT00355602
Molecular Formula:C23H46N6O13
Molecular Weight:614.6 g/mol
Isomeric SMILES:C1[C@H]([C@@H]([C@H]([C@@H]([C@H]1N)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CN)O)O)N)O[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O[C@@H]4[C@@H]([C@H]([C@@H]([C@@H](O4)CN)O)O)N)O)O)N
Synonyms:Framycetin; neomycin; NEOMYCIN B; 119-04-0; Fradiomycin; Mycifradin; Soframycin; NEOMYCIN SULFATE; Enterfram; Framygen
Phase 0: 5
Phase 1: 4
Phase 2: 8
Phase 3: 5
Phase 4: 8
Description:A component of neomycin that is produced by Streptomyces fradiae. On hydrolysis it yields neamine and neobiosamine B. (From Merck Index, 11th ed). Neomycin is a bactericidal aminoglycoside antibiotic that binds to the 30S ribosome of susceptible organisms. Binding interferes with mRNA binding and acceptor tRNA sites and results in the production of non-functional or toxic peptides.

Molecular Structure

2D Molecular Structure

Knowledge Graph

dtIDCIDCompound NameGene IDGene NameSpeciesPubMed IDsAction
dt423 8378 Framycetin 1161 ERCC8 Homo sapiens (human) Inhibitor
dt424 8378 Framycetin 2434 FRA10D Homo sapiens (human) Inhibitor
dt425 8378 Framycetin 3791 KDR Homo sapiens (human) 17441906 None
dt426 8378 Framycetin 1815 DRD4 Homo sapiens (human) Inhibitor
dt427 8378 Framycetin 45025515 lef Bacillus anthracis 16386899 None
dt428 8378 Framycetin 45025515 lef Bacillus anthracis 16870442 None
dt429 8378 Framycetin 24247 Casr Rattus norvegicus (Norway rat) 7816802 Full agonist
dt430 8378 Framycetin None -- None 11983334 None
dt431 8378 Framycetin 846 CASR Homo sapiens (human) 17537980 None
dt432 8378 Framycetin 595 CCND1 Homo sapiens (human) Agonist

  • No data available

Phase Distribution
Phase Description
  • Phase 0: Exploratory trials to assess drug behavior in humans
  • Phase 1: Safety trials to determine safe dosage range
  • Phase 2: Efficacy trials to evaluate therapeutic effects
  • Phase 3: Large-scale trials to confirm efficacy and safety
  • Phase 4: Post-marketing surveillance for long-term safety and efficacy

Trial IDTitlePhaseStatusSponsorIndicationsInterventions
NCT02765256 Fundamental Modification of the Gut Microbiota in the Treatment of Refractory Crohn's Disease PHASE2 COMPLETED University of Pennsylvania Crohn's Disease DRUG: Fluconazole|DRUG: Vancomycin|DRUG: Neomycin… Details
NCT03042091 Neomycin and Metronidazole Hydrochloride With or Without Polyethylene Glycol in Reducing Infection in Patients Undergoing Elective Colorectal Surgery EARLY_PHASE1 UNKNOWN Thomas Jefferson University Colorectal Neoplasms; Diverticulitis; Inflammator… DRUG: Polyethylene Glycol; DRUG: Neomycin; DRUG: … Details
NCT00355602 Antibiotics for the Treatment of Ulcerative Colitis None COMPLETED University of Dundee Colitis, Ulcerative DRUG: Cefuroxime|DRUG: Ciprofloxacin|DRUG: Clarit… Details

Disease IDDisease NameDefinitionCategoryRelated DrugsMechanism
No data available

Strategy IDTherapeutic StrategySynonymsRelated DrugsMechanism
S03 Anti-TNF agents Tumor necrosis factor infliximab; adalimumab; golimumab; certolizumab pegol TNF is produced by various immune and non-immune cells in t… Details
S04 T-cell homing and retention T-cell trafficking vedolizumab; anti-MAdCAM1 antibodies ; etrolizumab Inhibition of the interaction between α4β7 integrins on T c… Details
S07 Blockade of cytokine Cytokine signalling apremilast; roflumilast; filgotinib; tofacitinib; ABT494; ABT-874; ustekinumab; isankizumab; LY-2525623; AMG139; MEDI2079; guselkumab Various T-cell subsets, their differentiation pathways and … Details
S11 Improveming Intestinal Microecology the intestinal microbiota antibiotics; probiotics; prebiotics; postbiotics; synbiotics; fecal microbiota transplantation (FMT) The imbalance between beneficial bacteria and harmful patho… Details

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