Basic information Safety Supplier Related

N-[2-CARBAMOYL-5-(4-CHLORO-PHENYL)-THIOPHEN-3-YL]-SUCCINAMIC ACID

Basic information Safety Supplier Related

N-[2-CARBAMOYL-5-(4-CHLORO-PHENYL)-THIOPHEN-3-YL]-SUCCINAMIC ACID Basic information

Product Name:
N-[2-CARBAMOYL-5-(4-CHLORO-PHENYL)-THIOPHEN-3-YL]-SUCCINAMIC ACID
Synonyms:
  • N-[2-CARBAMOYL-5-(4-CHLORO-PHENYL)-THIOPHEN-3-YL]-SUCCINAMIC ACID
  • Butanoic acid, 4-[[2-(aminocarbonyl)-5-(4-chlorophenyl)-3-thienyl]amino]-4-oxo-
CAS:
676995-91-8
MF:
C15H13ClN2O4S
MW:
352.79
Mol File:
Mol File
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N-[2-CARBAMOYL-5-(4-CHLORO-PHENYL)-THIOPHEN-3-YL]-SUCCINAMIC ACID Chemical Properties

Boiling point:
637.9±55.0 °C(Predicted)
Density 
1.497±0.06 g/cm3(Predicted)
pka
4.59±0.10(Predicted)
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N-[2-CARBAMOYL-5-(4-CHLORO-PHENYL)-THIOPHEN-3-YL]-SUCCINAMIC ACID Usage And Synthesis

Uses

FtsZ-IN-10 is a bacterial division inhibitor that interferes with the normal assembly of FtsZ. FtsZ-IN-10 specifically binds to Bacillus subtilis FtsZ monomers, thereby affecting their polymerization behavior. FtsZ-IN-10 may also activate nucleotide-free archaeal FtsZ to form ordered polymers. FtsZ-IN-10 can hinder the localization of FtsZ in the Z ring and inhibit bacterial cell division. Chlorinated analogs of FtsZ-IN-10 show the ability to inhibit the growth of antibiotic-resistant clinical isolates such as Staphylococcus aureus and Enterococci[1].

References

[1] Synthetic inhibitors of bacterial cell division targeting the GTP-binding site of FtsZ DOI:10.1021/cb400208z

N-[2-CARBAMOYL-5-(4-CHLORO-PHENYL)-THIOPHEN-3-YL]-SUCCINAMIC ACIDSupplier

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