RNPA2000
CAS No. 329214-04-2
RNPA2000 ( RNPA 2000 )
Catalog No. M14084 CAS No. 329214-04-2
RNPA2000 is a small-molecule inhibitor of Staphylococcus aureus RnpA-mediated RNA turnover and tRNA processing (IC50=130 uM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
100MG | Get Quote | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameRNPA2000
-
NoteResearch use only, not for human use.
-
Brief DescriptionRNPA2000 is a small-molecule inhibitor of Staphylococcus aureus RnpA-mediated RNA turnover and tRNA processing (IC50=130 uM).
-
DescriptionRNPA2000 is a small-molecule inhibitor of Staphylococcus aureus RnpA-mediated RNA turnover and tRNA processing (IC50=130 uM); inhibits both RnpA-associated RNA degradation and tRNA maturation activities both in vitro and within S. aureus.
-
SynonymsRNPA 2000
-
PathwayGPCR/G Protein
-
TargetAntibacterial
-
RecptorAntibacterial
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number329214-04-2
-
Formula Weight361.42
-
Molecular FormulaC17H19N3O4S
-
Purity>98% (HPLC)
-
Solubility——
-
SMILES——
-
Chemical NameN-(2-(2-(4-isopropylphenoxy)acetyl)hydrazine-1-carbonothioyl)furan-2-carboxamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Eidem TM, et al. Antimicrob Agents Chemother. 2015 Apr;59(4):2016-28.
2. Lounsbury N, et al. Bioorg Med Chem Lett. 2018 Apr 1;28(6):1127-1131.
2. Lounsbury N, et al. Bioorg Med Chem Lett. 2018 Apr 1;28(6):1127-1131.
molnova catalog
related products
-
VB-82252
VB-82252 is a highly potent, orally active inhibitor of C. difficile toxins TcdA and TcdB, potently inhibits UDP glucose hydrolysis activity of TcdB (IC50=32 nM).
-
Ceftobiprole medocar...
Ceftobiprole medocaril is the parenteral prodrug of Ceftobiprole. Ceftobiprole is a broad-spectrum cephalosporin with activity against Methicillin-resistant staphylococcus aureus (MRSA).
-
GSK-729
A potent, small molecule inhibitor of Mycobacterium tuberculosis enoyl-coenzyme A (CoA) hydratase EchA6 with IC50 of 1.8 uM.