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Lancovutide

Basic information Safety Supplier Related

Lancovutide Basic information

Product Name:
Lancovutide
Synonyms:
  • 2-l-lysine-6-(3-aminoalanine)-10-l-phenylalanine-12-l-phenylalanine-ancoveni
  • antibioticpa48009
  • cyclic6-19)-imine
  • leucopeptin
  • DURAMYCIN
  • duramycin from streptoverticillium*cinnamoneus
  • lancovutide
  • duramycin from streptoverticillium*ci·Namoneus
CAS:
1391-36-2
MF:
C89H125N23O25S3
MW:
2013.28
Product Categories:
  • A - KAntibiotics
  • Antibacterial
  • Antibiotics A to
  • Antibiotics A-FAntibiotics
  • Chemical Structure Class
  • Interferes with Protein SynthesisAntibiotics
  • Mechanism of Action
  • Spectrum of Activity
  • Tetracyclines
Mol File:
1391-36-2.mol
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Lancovutide Chemical Properties

Melting point:
271-273 ºC
Density 
1.0238 (rough estimate)
refractive index 
1.6680 (estimate)
storage temp. 
2-8°C
solubility 
0.1 M HCl: soluble10mg/mL
form 
powder
pka
3.15±0.11(Predicted)
color 
Off-White to Pale Yellow
Sequence
Cys-Lys-Gln-Cys-Cys-Ala-Phe-Gly-Pro-Phe-{Abu}-Phe-Val-Cys-Asp-Gly-Asn-{Abu}-Lys-NH2 (Disulfide bridge: Cys1-Abu18, Cys4-Cys14, Cys5-Abu11)
Stability:
Hygroscopic
InChIKey
BPIFGBWRBGTMHX-OHSSMEBINA-N
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Safety Information

WGK Germany 
3
RTECS 
BV7100000
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Lancovutide Usage And Synthesis

Uses

Duramycin is a chloride secretion enhancer in airway epithelium.

Synthesis

Duramycin is a natural product produced by certain bacteria that binds to phosphatidylethanolamine (PE). We report here the genes that are involved in duramycin biosynthesis, and we produced duramycin by expressing those genes in Escherichia coli. We show that duramycin analogs can also be produced.

in vivo

Evaluation of [68Ga]NODAGA-Duramycin as a positron emission tomography (PET) tracer of cell death for whole-body detection of chemotherapy-induced organ toxicity. Organ uptake is analyzed in untreated and doxorubicin, busulfan, and cisplatin-treated mice 2 h after intravenous injection of [68Ga]NODAGA-Duramycin. [68Ga]NODAGA-Duramycin PET/CT is successfully applied to non-invasively detect chemotherapy-induced organ toxicity with high sensitivity in mice[3].

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