Arbekacin

Small moleculeexperimental

Arbekacin (INN) is a semisynthetic aminoglycoside antibiotic which was derived from kanamycin. It is primarily used for the treatment of infections caused by multi-resistant bacteria including methicillin-resistant Staphylococcus aureus (MRSA). Arbekacin was originally synthesized from dibekacin in 1973 by Hamao Umezawa and collaborators. It has been registered and marketed in Japan since 1990 under the trade name Habekacin. Arbekacin is no longer covered by patent and generic versions of the drug are also available under such trade names as Decontasin and Blubatosine. — Wikipedia

Clinical trial activity

5 trials · 7 clinical orgs · 0 marketing orgs

Phase 1
3
Phase 2
1
Phase 3
0
Phase 4
0

Earliest trial started Aug 3, 2012 (NCT01659515)

Timeline

2010s

  1. Jan 1, 2013

    Earliest Phase 1 Sponsor(trial)

  2. Jan 1, 2013

    Earliest Phase 2 Sponsor(trial)

Indications

Mechanism of action

Chemistry & pharmacology

Loading structure…

SMILES

NCC[C@H](O)C(=O)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CN)CC[C@H]2N)[C@H](O)[C@H]1O[C@H]1O[C@H](CO)[C@@H](O)[C@H](N)[C@H]1O
Mol. weight
552.63 g/mol
Lipinski Ro5
3 violation(s)
Rule of 3
No
Chirality
Single Stereoisomer
Inorganic
No
Polymer
No

Oral

No

Parenteral

No

Topical

No

Sources

Also known as

  • 1-n-((s)-4-amino-2-hydroxybutyryl)dibekacin
  • 4-amino-2-hydroxybutylyldibekacin
  • abk
  • abk
  • ahb-dkb
  • arbekacin
  • arbekacin
  • arbekacin
  • arbekacin
  • arbekacin
  • arbekacin
  • arbekacin
  • arbekacin
  • arbekacina
  • arbekacina
  • arbekacine
  • arbekacine
  • arbekacin sulfate
  • arbekacin sulfate
  • arbekacin sulfate
  • arbekacinum
  • arbekacinum
  • d-streptamine, o-3-amino-3-deoxy-alpha-d-glucopyranosyl-(1->6)-o-(2,6-diamino-2,3,4,6-tetradeoxy-alpha-d-erythro-hexopyranosyl-(1->4))-n1-((2s)-4-amino-2-hydroxy-1-oxobutyl)-2-deoxy-, sulfate
  • haba-dkb
  • habekacin
  • habekacin
  • habekacin
  • habekacin
  • haberacin
  • haberacin
  • o-3-amino-3-deoxy-alpha-d-glucopyranosyl-(1->4)-o-(2,6-diamino-2,3,4,6-tetradeoxy-alpha-d-erythro-hexopyranosyl-(1->6))-n'-((2s)-4-amino-2-hydroxybutyryl)-2-deoxy-l-streptamine

Clinical trials

NCT IDPhaseStart dateSponsor(s)
NCT02459158Phase 1Sep 1, 2015Meiji Seika Pharma Co., Ltd.
NCT01961830Phase 1Sep 1, 2013Meiji Seika Pharma Co., Ltd.
NCT01918384Phase 2Aug 1, 2013Hyogo Medical University, Japan Medical Association, Kobe University, Nobel Pharmaceuticals
NCT01907776Phase 1Jul 1, 2013Meiji Seika Pharma Co., Ltd.
NCT01659515N/AAug 3, 2012Meiji Seika Pharma Co., Ltd., Uniformed Services University of the Health Sciences, United States Army
Showing 5 of 5 trials
Page 1 / 1

Organizations

Research & Development (7)

OrganizationOrg typeTrialsAs lead sponsorPhasesEarliest year
Meiji Seika Pharma Co., Ltd.For profit4322012
Hyogo Medical UniversityAcademic/Hospital1012013
Japan Medical AssociationAcademic/Hospital1012013
Kobe UniversityAcademic/Hospital1112013
Nobel PharmaceuticalsFor profit1012013
Uniformed Services University of the Health SciencesGovernment1012012
United States ArmyGovernment1112012
7 organizations
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