Dalbavancin
[CAS# 171500-79-1]

Identification

• Classification: API >> Antibiotics >> Peptide drug
• Name: Dalbavancin
• Synonyms: MDL 63397
• Molecular Formula: C₈₈H₁₀₀Cl₂N₁₀O₂₈
• Molecular Weight: 1816.69
• CAS Registry Number: 171500-79-1
• EC Number: 857-318-5
• SMILES: CC(C)CCCCCCCCC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1OC2=C3C=C4C=C2OC5=C(C=C(C=C5)[C@H]([C@H]6C(=O)N[C@@H](C7=C(C(=CC(=C7)O)O[C@@H]8[C@H]([C@H]([C@@H]([C@H](O8)CO)O)O)O)C9=C(C=CC(=C9)[C@H](C(=O)N6)NC(=O)[C@@H]4NC(=O)[C@@H]1C2=C(C(=CC(=C2)OC2=C(C=CC(=C2)[C@H](C(=O)N[C@H](CC2=CC=C(O3)C=C2)C(=O)N1)NC)O)O)Cl)O)C(=O)NCCCN(C)C)O)Cl)C(=O)O)O)O

Properties

• Solubility: Insoluble (2.0E^-5 g/L) (25 ºC), Calc.^*
• Density: 1.59±0.1 g/cm³ (20 ºC 760 Torr), Calc.^*
• Index of Refraction: 1.729, Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS08;GHS09 Warning
• Hazard Statements: H361-H373-H400-H410
• Precautionary Statements: P203-P260-P273-P280-P318-P319-P391-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Reproductive toxicity	Repr.	2	H361
Specific target organ toxicity - repeated exposure	STOT RE	2	H373
Chronic hazardous to the aquatic environment	Aquatic Chronic	1	H410
Acute hazardous to the aquatic environment	Aquatic Acute	1	H400

Discovory and Applicatios

Dalbavancin is a second-generation lipoglycopeptide antibiotic developed to combat Gram-positive bacterial infections, particularly those caused by multidrug-resistant pathogens. Its discovery is linked to modifications of earlier glycopeptides such as vancomycin, aiming to enhance antimicrobial activity and pharmacokinetic properties. Dalbavancin is a semisynthetic derivative of the natural product A40926, which was originally isolated from Nonomuraea species. Researchers focused on structural modifications to improve stability, enhance potency against resistant bacteria, and extend the drug’s half-life, ultimately leading to its clinical approval. The United States Food and Drug Administration approved dalbavancin in 2014 for the treatment of acute bacterial skin and skin structure infections, providing a valuable alternative to conventional glycopeptides.

Dalbavancin functions by inhibiting bacterial cell wall synthesis, a mechanism similar to other glycopeptides. It binds to the terminal D-Ala-D-Ala residues of peptidoglycan precursors, blocking transpeptidation and transglycosylation processes essential for cell wall formation. The result is bacterial cell lysis and death. Dalbavancin exhibits a prolonged elimination half-life of approximately 14 days, allowing for an extended dosing interval. Unlike traditional glycopeptides requiring daily administration, dalbavancin is typically administered as a single intravenous infusion or two doses one week apart, improving patient compliance and reducing hospital stays. This feature makes it particularly useful for outpatient therapy and long-term infection management.

The synthesis of dalbavancin involves a semisynthetic approach based on the core A40926 structure, which is modified through selective acylation reactions. Key steps include protection and deprotection of functional groups, as well as site-specific chemical modifications to enhance its pharmacokinetic profile. The ability to optimize chemical modifications has led to improvements in drug solubility, stability, and overall therapeutic efficacy. Advances in process chemistry have made large-scale production feasible, ensuring a stable supply for clinical applications.

Dalbavancin is primarily used for the treatment of acute bacterial skin and skin structure infections, particularly those caused by methicillin-resistant Staphylococcus aureus and other drug-resistant Gram-positive bacteria. Additionally, clinical trials have explored its efficacy in osteomyelitis, catheter-related bloodstream infections, and prosthetic joint infections, conditions that often require prolonged antibiotic therapy. The long-acting profile of dalbavancin makes it an attractive option for treating persistent bacterial infections, reducing the burden of frequent dosing and hospitalization. Research is ongoing to assess its potential in combination therapies and expand its indications beyond skin infections.

The widespread use of dalbavancin is limited by its high cost, which can restrict accessibility despite its clinical advantages. However, its effectiveness against multidrug-resistant bacteria and its ability to streamline antibiotic therapy continue to drive interest in its application. With increasing antibiotic resistance posing a global challenge, dalbavancin remains a crucial component of modern antimicrobial strategies. Future studies will likely explore its role in combination regimens and broader therapeutic applications, reinforcing its importance in infectious disease management.