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ChemicalBook--->CAS DataBase List--->172998-24-2

172998-24-2

172998-24-2 Structure

172998-24-2 Structure
IdentificationBack Directory
[Name]

BUFORIN II
[CAS]

172998-24-2
[Synonyms]

BUFORIN II
L-Threonyl-L-arginyl-L-seryl-L-seryl-L-arginyl-L-alanylglycyl-L-leucyl-L-glutaminyl-L-phenylalanyl-L-prolyl-L-valylglycyl-L-arginyl-L-valyl-L-histidyl-L-arginyl-L-leucyl-L-leucyl-L-arginyl-L-lysine
[Molecular Formula]

C106H184N40O26
[MDL Number]

MFCD01311893
[MOL File]

172998-24-2.mol
[Molecular Weight]

2434.85
Chemical PropertiesBack Directory
[density ]

1.47±0.1 g/cm3(Predicted)
[storage temp. ]

−20°C
[form ]

Solid
[color ]

White to off-white
Hazard InformationBack Directory
[Uses]

Buforin II, derived from buforin I, a protein isolated from the stomach of the Asian toad Bufo bufo gargarizans, is a potent antimicrobial peptide. Buforin II has antimicrobial activity against a broad spectrum of Gram-positive and Gram-negative bacteria[1].
[in vivo]

Buforin II (intravenously a single dose, 1 mg/kg) has potent antibacterial activity that effectively reduces lethality and leads to a significant reduction in plasma endotoxin and cytokine concentrations in male Wistar rat model of sepsis[1].

Animal Model:Male Wistar rats weighing 200 to 300 g with A. baumannii?ATCC 19606[1]
Dosage:1 mg/kg
Administration:Intravenously a single dose
Result:Reduced mortality by 40% in the treatment group and by 20% in the rifampicin (10 mg/kg) combination group.
Reduced TNF, IL-6 and endotoxin plasma levels by 33%, 25% and 32%, respectively.
Animal Model:Male Wistar rats weighing 200 to 300 g with the multiresistant strain[1]
Dosage:1 mg/kg
Administration:Intravenously a single dose
Result:Reduced mortality by 46.6% in the treatment group and by 20% in the rifampicin (10 mg/kg) combination group.
Reduced TNF, IL-6 and endotoxin plasma levels by 46%, 20% and 28%, respectively.
[References]

[1] Oscar Cirioni, et al. Therapeutic efficacy of buforin II and rifampin in a rat model of Acinetobacter baumannii sepsis. Crit Care Med. 2009 Apr;37(4):1403-7. DOI:10.1097/CCM.0b013e31819c3e22
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