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171500-79-1

171500-79-1 structure
171500-79-1 structure
  • Name: Dalbavancin
  • Chemical Name: dalbavancin
  • CAS Number: 171500-79-1
  • Molecular Formula: C88H100Cl2N10O28
  • Molecular Weight: 1816.692
  • Catalog: API Antibiotics Peptide
  • Create Date: 2018-08-27 19:33:51
  • Modify Date: 2024-01-02 14:17:58
  • Dalbavancin is a lipoglycopeptide antibiotic agent that is active against gram-positive pathogens.

Name dalbavancin
Synonyms Dalvance
Zeven
Dalbavancin
(1S,2R,19R,22R,33S,36R,39R,51S)-5,31-Dichloro-51-{[3-(dimethylamino)propyl]carbamoyl}-2,25,30,43,48-pentahydroxy-46-(α-D-mannopyranosyloxy)-22-(methylamino)-21,34,37,53,55,58-hexaoxo-7,13,27-triox a-20,35,38,52,54,57-hexaazaundecacyclo[37.14.2.2.2.2.2.1.1.1.0.0]hexahexaconta-3,5,8(64),9,11,14,16,23,25,28(59),29,31,40(56),41,43,45,47,49 ,60,62,65-henicosaen-64-yl 2-deoxy-2-[(10-me
Description Dalbavancin is a lipoglycopeptide antibiotic agent that is active against gram-positive pathogens.
Related Catalog
Target

MIC90: 0.06 μg/mL (Staphylococcus aureus) and 0.25 μg/mL (Bacillus anthracis)[1][2]

In Vitro Dalbavancin is a parenterally administered semisynthetic lipoglycopeptide developed to combat infections caused by resistant gram-positive pathogens. Dalbavancin exhibits potent in vitro bactericidal activity against gram-positive pathogens including S. aureus (MRSA), VISA, and non-VanA strains of VRE. Dalbavancin is developed for the treatment of complicated skin and skin structure infections (cSSSIs), predominantly those caused by MRSA and β-hemolytic streptococci, organisms against which it has shown greater potency than existing glycopeptide therapeutic agents[1][2].
In Vivo Dalbavancin (15-240 mg/kg; intraperitoneal injection; every 36 h or 72 h; for 14 days; female BALB/c mice) treatment has a survival rate of 80% to 100% of mice with all dose regimens[1]. Animal Model: Female BALB/c mice (6-8 weeks) challenged with Ames strain of B. anthracis[1] Dosage: 15 mg/kg, 30 mg/kg, 60 mg/kg, 120 mg/kg, 240 mg/kg Administration: Intraperitoneal injection; every 36 h or 72 h; for 14 days Result: The efficacy was 80 to 100%, as determined by the rate of survival at 42 days, when treatment was initiated 24 h postchallenge with regimens of 15 to 120 mg/kg every 36 h or 30 to 240 mg/kg every 72 h.
References

[1]. Heine HS, et al. Activity of dalbavancin against Bacillus anthracis in vitro and in a mouse inhalation anthrax model. Antimicrob Agents Chemother. 2010 Mar;54(3):991-6.

[2]. Bennett JW, et al. Dalbavancin in the treatment of complicated skin and soft-tissue infections: a review. Ther Clin Risk Manag. 2008 Feb;4(1):31-40.

Density 1.6±0.1 g/cm3
Molecular Formula C88H100Cl2N10O28
Molecular Weight 1816.692
Exact Mass 1814.608521
PSA 572.51000
LogP 2.94
Index of Refraction 1.729
Storage condition -20℃