Arbekacin

Base Information Edit

Chemical Name:Arbekacin
CAS No.:51025-85-5
Molecular Formula:C22H44N6O10
Molecular Weight:552.626
Hs Code.:
UNII:G7V6SLI20L
DSSTox Substance ID:DTXSID8048319
Nikkaji Number:J33.173B
Wikipedia:Arbekacin
Wikidata:Q4784668
NCI Thesaurus Code:C76145
Metabolomics Workbench ID:43677
ChEMBL ID:CHEMBL426926
Mol file:51025-85-5.mol

Synonyms:1-N-((S)-4-amino-2-hydroxybutyryl)dibekacin;4-amino-2-hydroxybutylyldibekacin;arbekacin;arbekacin sulfate;habekacin;ME1100

Suppliers and Price of Arbekacin

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
ARBEKACIN 95.00%
1G
$ 5054.70

American Custom Chemicals Corporation
ARBEKACIN 95.00%
100MG
$ 1091.48

AHH
Arbekacin 98%
1g
$ 760.00

Total 58 raw suppliers

Chemical Property of Arbekacin Edit

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Refractive Index:1.634
Boiling Point:904 °C at 760 mmHg
PKA:13.07±0.70(Predicted)
Flash Point:500.5 °C
Density:1.47 g/cm³
XLogP3:-6.8
Hydrogen Bond Donor Count:11
Hydrogen Bond Acceptor Count:15
Rotatable Bond Count:10
Exact Mass:552.31189162
Heavy Atom Count:38
Complexity:757

Purity/Quality:

99% ^*data from raw suppliers

ARBEKACIN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(C(OC1CN)OC2C(CC(C(C2O)OC3C(C(C(C(O3)CO)O)N)O)NC(=O)C(CCN)O)N)N
Isomeric SMILES:C1C[C@H]([C@H](O[C@@H]1CN)O[C@@H]2[C@H](C[C@H]([C@@H]([C@H]2O)O[C@@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)N)O)NC(=O)[C@H](CCN)O)N)N
Recent ClinicalTrials:Phase II Study of NPC-14 (Arbekacin Sulfate) to Explore Safety, Tolerability, and Efficacy in Duchenne Muscular Dystrophy
Recent NIPH Clinical Trials:The efficacy of AN69 membrane for elimination of aminoglycoside.
Description Arbekacin is a semi-synthetic derivative of dibekacin useful in the treatment of bacterial infections. This aminoglycoside is active against a broad spectrum of bacteria, including some of the gentamycin-, kanamycin-, and tobramycin-resistant pathogens. Compared to amikacin and dibekacin, ototoxicity is reportedly milder.
Therapeutic Function Antibiotic

Technology Process of Arbekacin

There total 1 articles about Arbekacin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: