TG4-155

CAS No. 1164462-05-8

TG4-155( —— )

Catalog No. M20218 CAS No. 1164462-05-8

TG4-155 is a brain penetrant EP2 antagonist (KB = 2.4 nM) that is over 1000-fold less effective at EP4 (KB = 11.4 μM) and a panel of other receptors and channels.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 40 In Stock
5MG 61 In Stock
10MG 98 In Stock
25MG 208 In Stock
50MG 361 In Stock
100MG 537 In Stock
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Biological Information

  • Product Name
    TG4-155
  • Note
    Research use only, not for human use.
  • Brief Description
    TG4-155 is a brain penetrant EP2 antagonist (KB = 2.4 nM) that is over 1000-fold less effective at EP4 (KB = 11.4 μM) and a panel of other receptors and channels.
  • Description
    TG4-155 is a brain penetrant EP2 antagonist (KB = 2.4 nM) that is over 1000-fold less effective at EP4 (KB = 11.4 μM) and a panel of other receptors and channels.
  • In Vitro
    TG4-155 inhibits the serotonin 5-HT2B receptor with IC50=2.6 μM and hERG (human Ether-à-go-go-Related Gene) with IC50=12 μM.PGE2 (0.1-10 μM) stimulation significantly enhances human prostate cancer cell line PC3 cell growth in a concentration-dependent manner with a maximal response being obtained at approximately 1 μM. This PGE2-induced cancer cell proliferation is significantly suppressed by TG4-155 (0.01-1μM ; 48 hours) in a concentration-dependent manner. Cell Viability Assay Cell Line:PC3 cells Concentration:48 hours Incubation Time:0.01, 0.1, and 1 μM Result:Significantly suppressed PGE2-induced cancer cell proliferation in a concentration-dependent manner.
  • In Vivo
    Administration of TG4-155 (5 mg/kg, i.p.; at 1 and 12 h) significantly reducesstatus epilepticus (SE)-induced neurodegeneration scores in C57BL/6 mice.TG4-155 (3 mg/kg; i.p.) displays a bioavailability of 61% (i.p. route compared with i.v.), a plasma half-life (t1/2) of 0.6 h, and a brain/plasma ratio of 0.3 in C57BL/6 mice. Animal Model:C57BL/6 mice (8-12 wk old)Dosage:5 mg/kg Administration:I.p.; at 1 and 12 h Result:Administration significantly reduced SE-induced neurodegeneration scores by 91% in hippocampal subregions CA1, by 80% in CA3, and by 63% in hilus.Animal Model:C57BL/6 miceDosage:3 mg/kg Administration:I.p.Result:Displayed a bioavailability of 61% (i.p. route compared with i.v.), t1/2 of 0.6 h, and a brain/plasma ratio of 0.3.
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Prostaglandin Receptor
  • Recptor
    EP2
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1164462-05-8
  • Formula Weight
    394.47
  • Molecular Formula
    C23H26N2O4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:125 mg/mL?(316.89 mM)
  • SMILES
    COc1cc(\C=C\C(=O)NCCn2c(C)cc3ccccc23)cc(OC)c1OC
  • Chemical Name
    (E)-N-[2-(2-methylindol-1-yl)ethyl]-3-(345-trimethoxyphenyl)prop-2-enamide

Shipping & Storage Information

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

Reference

1.Jiang J Ganesh T Du Y et al. Small molecule antagonist reveals seizure-induced mediation of neuronal injury by prostaglandin E2 receptor subtype EP2[J]. Proceedings of the National Academy of Sciences 2012 109(8):3149-3154.
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