β-Glucuronidase-IN-1

CAS No. 484006-66-8

β-Glucuronidase-IN-1( —— )

Catalog No. M33191 CAS No. 484006-66-8

β-Glucuronidase-IN-1 is an E. coli β-glucuronidase (β-glucuronidase) inhibitor with a potent, selective, non-competitive, and orally active IC50 and Ki value of 283 nM and 164 nM, respectively, against E. coli β-glucuronidase.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 93 In Stock
5MG 85 In Stock
10MG 132 In Stock
25MG 221 In Stock
50MG 323 In Stock
100MG 480 In Stock
200MG Get Quote In Stock
500MG 1014 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    β-Glucuronidase-IN-1
  • Note
    Research use only, not for human use.
  • Brief Description
    β-Glucuronidase-IN-1 is an E. coli β-glucuronidase (β-glucuronidase) inhibitor with a potent, selective, non-competitive, and orally active IC50 and Ki value of 283 nM and 164 nM, respectively, against E. coli β-glucuronidase.
  • Description
    β-Glucuronidase-IN-1 is a potent, selective, uncompetitive, and orally active E. coli bacterial β-glucuronidase inhibitor, exhibitingan IC50 and a Ki of 283 nM and 164 nM, respectively.
  • In Vitro
    β-Glucuronidase-IN-1 (Inhibitor 1) (0.01-100 μM) inhibits E. coli?β-glucuronidase activity as a dose-dependent manner and exhibits an IC50 and a Ki value with 283 nM and 164 nM, respectively.β-Glucuronidase-IN-1 (100 μM; 24-72 hours) maintains potent efficacy in living bacterial cells (EC50=17.7 nM), it does not affect bacterial cell growth under aerobic or anaerobic conditions or killing mammalian epithelial cells. Cell Viability AssayCell Line:CMT93, CaCO-2, HCT116 cells Concentration:100 μM Incubation Time:24hours, 48 hours and 72 hours Result:Did not impact mammalian cell survival and any reduction in cell viability were attributed to the presence of DMSO.
  • In Vivo
    β-Glucuronidase-IN-1 (oral gavage; 10 μg; twice per day; 11 days) protects the mouse GI epithelium from CPT-11–induced damage and protects the glandular structure of CPT-11-treated intestinal tissues.Animal Model:Healthy 6- to 8-week-old Balb/cJ mice Dosage:10 μg Administration:Oral gavage; twice per day; 11 daysResult:Alleviated CPT-11-induced toxicity in mice.
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Antibacterial
  • Recptor
    Antibacterial
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    484006-66-8
  • Formula Weight
    425.54
  • Molecular Formula
    C23H27N3O3S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (235.00 mM; Ultrasonic (<60°C)
  • SMILES
    CCOc1ccc(NC(=S)N(CCO)Cc2cc3cc(C)cc(C)c3[nH]c2=O)cc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Wallace BD, et al. Alleviating cancer drug toxicity by inhibiting a bacterial enzyme.Science.?2010 Nov 5;330(6005):831-5.?
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