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S2139349

72836-33-0

Synonym(s):
5-((4-Chlorobenzyl)sulfanyl)-1,3,4-thiadiazol-2-amine, Virulence Regulator RegA Inhibitor, NSC-523933;Regacin - CAS 72836-33-0 - Calbiochem

CAS NO.:72836-33-0

Empirical Formula: C9H8ClN3S2

Molecular Weight: 257.76

MDL number: MFCD00114062

Pack Size Price Stock Quantity
25mg RMB2239.02 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 168-169 °C(Solv: ethyl acetate (141-78-6))
Boiling point: 443.8±47.0 °C(Predicted)
Density  1.50±0.1 g/cm3(Predicted)
storage temp.  2-8°C
solubility  DMSO: 100mg/mL
pka 2.41±0.10(Predicted)
form  powder
color  pale yellow
InChI 1S/C9H8ClN3S2/c10-7-3-1-6(2-4-7)5-14-9-13-12-8(11)15-9/h1-4H,5H2,(H2,11,12)
InChIKey SPABJFQNGHSGMG-UHFFFAOYSA-N

Description and Uses

An orally bioavailable, non-toxic, thio-thiadiazolamine compound that specifically inhibits the DNA-binding capacity of virulence regulator, RegA (IC50 = 1.7 µM in E. coli strain MC4100 (kfc-lacZ, pACYC184-regA), by interacting with amino acid residues within a conserved region of the DNA-binding domain, but without affecting RegA dimerization. Interacts with the double helix-turn-helix (HTH) domain that results in a loss of binding affinity of RegA for its DNA targets. This interaction appears to involve W188 and R223 residues that are conserved in several RegA homologs including ToxT, AggR, RegR, and Rns. Shown to be highly effective in reducing Citrobacter rodentium colonization when administered perorally to mice (~50 mg/kg) either 15 minutes before or 12 hours after bacterial inoculation. Reduces the ability of Rns and RegR to activate the transcription of their target promoters, but does not affect the activity of AggR and ToxT.
Please note that the molecular weight for this compound is batch-specific due to variable water content.

Safety

Hazard Codes  Xi
WGK Germany  WGK 3
Hazard Note  Irritant
HS Code  2934999090
Storage Class 11 - Combustible Solids

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