Cart
sales@molnova.com
Home - Products - GPCR/G Protein - Antibacterial - Nilofabicin

Nilofabicin

CAS No. 934628-27-0

Nilofabicin( CG-400549 | CG 400549 | CG400549 | CG-0549 | CG 0549 | CG0549 | )

Catalog No. M27115 CAS No. 934628-27-0

Nilofabicin is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated acute.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 36 In Stock
5MG 31 In Stock
10MG 46 In Stock
25MG 74 In Stock
50MG 116 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock
Get Quotation Bulk Inquiry Add to Cart

Biological Information

  • Product Name
    Nilofabicin
  • Note
    Research use only, not for human use.
  • Brief Description
    Nilofabicin is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated acute.
  • Description
    Nilofabicin is a potent inhibitor of enoyl-(acyl-carrier-protein) reductase fall(FabI) and can be used in studies about the treatment of complicated acute. (In Vitro):Nilofabicin had an MIC90 of 0.5 μg/ml for Staphylococcus aureus strains and was more potent than either linezolid or vancomycin. Among 203 strains of Staphylococcus aureus, the MICs of Nilofabicin were 0.06 to 1.0 μg/ml, with MIC(50) and MIC(90) values of 0.25 μg/ml each. All strains were susceptible to linezolid and quinupristin-dalfopristin (MICs, 0.25 to 2.0 μg/ml).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    CG-400549 | CG 400549 | CG400549 | CG-0549 | CG 0549 | CG0549 |
  • Pathway
    GPCR/G Protein
  • Target
    Antibacterial
  • Recptor
    Prostacyclin receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    934628-27-0
  • Formula Weight
    340.44
  • Molecular Formula
    C19H20N2O2S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (293.74 mM)
  • SMILES
    Cc1c(N)cccc1Cn1ccc(OCCc2cccs2)cc1=O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Bexis S, et, al. Vascular actions of the prostacyclin receptor antagonist BAY 73-1449 in the portal hypertensive rat. Eur J Pharmacol. 2008 Aug 20;590(1-3):322-6.
Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog
related products

  • Sortase-IN-6e

    A small molecule inhibitor of Staphylococcus aureus sortase with IC50 of 9.3 uM.

  • LpxH-IN-AZ1

    LpxH-IN-AZ1 is a potent inhibitor of the UDP-2,3-diacylglucosamine pyrophosphate hydrolase, LpxH, and sulfonylpiperazine compounds.

  • (+)-pinoresinol-β-D-...

    Pinoresinol 4-O-β-D-glucopyranoside ((+)-Pinoresinol 4-O-β-D-glucopyranoside) is the major active furofuran type?lignans?in Fructus Forsythiae.

Sign In Join Free