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Dalbavancin Bacterial chemical

Cat.No.S4848

Dalbavancin is a lipoglycopeptide antibiotic that has bactericidal activity against Gram-positive bacteria including various staphylococci.
Dalbavancin Bacterial chemical Chemical Structure

Chemical Structure

Molecular Weight: 1816.69

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 1816.69 Formula

C88H100Cl2N10O28

Storage (From the date of receipt)
CAS No. 171500-79-1 -- Storage of Stock Solutions

Synonyms BI 397, MDL 63397 Smiles CNC1C(=O)NC2CC3=CC=C(OC4=C(OC5OC(C(O)C(O)C5NC(=O)CCCCCCCCC(C)C)C(O)=O)C6=CC(=C4)C(NC(=O)C(NC2=O)C7=CC(=CC(=C7Cl)O)OC8=CC=C1C=C8O)C(=O)NC9C(=O)NC(C(O)C%10=CC(=C(O6)C=C%10)Cl)C(=O)NC(C(=O)NCCCN(C)C)C%11

Solubility

In vitro
Batch:

DMSO : 100 mg/mL (55.04 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 100 mg/mL

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
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Mechanism of Action

In vitro
Dalbavancin's mechanism of action involves the formation of a complex with the C-terminal d-alanyl-d-alanine of growing peptidoglycan chains, thereby inhibiting bacterial cell wall biosynthesis. In addition, this compound appears to have the unique ability to dimerise and anchor its lipophilic side chain in the bacterial membranes. It possesses more potent in vitro bactericidal activity than vancomycin or teicoplanin against many resistant Gram-positive organisms[1].
In vivo
Dalbavancin has a half-life of 170-210 h in human. It exhibits linear, dose-dependent pharmacokinetics in healthy adults, following the administration of single intravenous doses of this compound 140-1120 mg. Total protein binding of this chemical is concentration independent, reversible and estimated to be 93%. Animal studies regarding tissue distribution have demonstrated tissue concentrations reaching maximal levels within 24 h, with the highest concentrations in the liver and kidneys[1].
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT05046860 Recruiting
Osteoarticular Infection
Centre Hospitalier Universitaire de Nice
March 7 2022 Not Applicable
NCT04959799 Completed
Diabetes|Infection
Aziende Chimiche Riunite Angelini Francesco S.p.A|Iqvia Pty Ltd
January 2 2022 --
NCT04485676 Completed
Skin Diseases Bacterial|Skin Diseases Infectious
Angelini Farmacéutica|Effice Servicios Para la Investigacion S.L.
July 15 2020 --
NCT06089044 Completed
Prosthesis-related Infections
Tourcoing Hospital
January 1 2020 --
NCT03696901 Terminated
Bacterial Infections
Correvio International Sarl|AMS Advanced Medical Services GmbH|PrimeVigilance|Advanz Pharma
November 21 2018 --

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