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