BIP-135

CAS No. 941575-71-9

BIP-135( —— )

Catalog No. M26630 CAS No. 941575-71-9

BIP-135 is a potent and selective ATP-competitive GSK-3 inhibitor. With IC50s of 16 nM and 21 nM for GSK-3α and GSK-3β, respectively. BIP 135 exhibits neuroprotective effect.

Purity : >98% (HPLC)

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Biological Information

  • Product Name
    BIP-135
  • Note
    Research use only, not for human use.
  • Brief Description
    BIP-135 is a potent and selective ATP-competitive GSK-3 inhibitor. With IC50s of 16 nM and 21 nM for GSK-3α and GSK-3β, respectively. BIP 135 exhibits neuroprotective effect.
  • Description
    BIP-135 is a potent and selective ATP-competitive GSK-3 inhibitor. With IC50s of 16 nM and 21 nM for GSK-3α and GSK-3β, respectively. BIP 135 exhibits neuroprotective effect.(In Vitro):BIP-135 (20 μM; 48 hours) is a superior neuroprotective agent in the model of oxidative stress. BIP-135 (20-30 μM; 72 hours) increases the survival motor neuron (SMN) protein levels at a dose of 25 μM in human SMA fibroblasts. And the typical bell-shaped dose-response curve is observed due to some toxicity at higher concentrations.(In Vivo):BIP-135 (75 mg/kg; i.p.; daily; from postnatal day 0 to 21) prolongs the median survival time of Δ7 SMA KO mouse model of spinal muscular atrophy. And it does not appear to be toxic and was well-tolerated by the animals (no decrease in body weight).
  • In Vitro
    BIP-135 (20-30 μM; 72 hours) increases the survival motor neuron (SMN) protein levels at a dose of 25 μM in human SMA fibroblasts. And the typical bell-shaped dose-response curve is observed due to some toxicity at higher concentrations.BIP-135 (20 μM; 48 hours) is a superior neuroprotective agent in the model of oxidative stress. Western Blot Analysis Cell Line:Human SMA fibroblasts Concentration:20 μM, 25 μM, 30 μM Incubation Time:72 hours Result:Led to a 7-fold increase in SMN levels at 25 μM.
  • In Vivo
    BIP-135 does not appear to be toxic and was well-tolerated by the animals (no decrease in body weight).BIP-135 (75 mg/kg; i.p.; daily; from postnatal day 0 to 21) prolongs the median survival time of Δ7 SMA KO mouse model of spinal muscular atrophy. Animal Model:Male and female SMN2+/+, SMN2Δ7+/+, Smn+/– mice Dosage:75 mg/kg Administration:Intraperitoneal injection; daily; from postnatal day 0 to 21Result:Caused a modest extension in the median survival of SMA KO animals by two days.
  • Synonyms
    ——
  • Pathway
    PI3K/Akt/mTOR signaling
  • Target
    GSK-3
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    941575-71-9
  • Formula Weight
    421.25
  • Molecular Formula
    C21H13BrN2O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 62.5 mg/mL (148.37 mM)
  • SMILES
    Cn1cc(C2=C(C(=O)NC2=O)c2coc3ccccc23)c2cc(Br)ccc12
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Au?ynait? A, et al. Identification of a 2'-O-Methyluridine Nucleoside Hydrolase Using the Metagenomic Libraries. Molecules. 2018;23(11):2904. Published 2018 Nov 7.
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