MOMIPP

CAS No. 1363421-46-8

MOMIPP( —— )

Catalog No. M27997 CAS No. 1363421-46-8

MOMIPP is a PIKfyve inhibitor and a macropinocytosis inducer. MOMIPP readily penetrates the blood-brain barrier and is moderately effective in suppressing progression of intracerebral glioblastoma xenografts.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 245 In Stock
5MG 155 In Stock
10MG 250 In Stock
25MG 455 In Stock
50MG 616 In Stock
100MG 923 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    MOMIPP
  • Note
    Research use only, not for human use.
  • Brief Description
    MOMIPP is a PIKfyve inhibitor and a macropinocytosis inducer. MOMIPP readily penetrates the blood-brain barrier and is moderately effective in suppressing progression of intracerebral glioblastoma xenografts.
  • Description
    MOMIPP is a PIKfyve inhibitor and a macropinocytosis inducer. MOMIPP readily penetrates the blood-brain barrier and is moderately effective in suppressing progression of intracerebral glioblastoma xenografts.(In Vitro):MOMIPP can induce intense macropinocytosis, leading to methuosis in cultured glioblastoma cells at low micromolar concentrations. MOMIPP(3 μM) induces cell vacuolization in U373 and Hs683 cell lines. The cytotoxic IPP compound, MOMIPP, causes early disruptions of glucose uptake and glycolytic metabolism. Coincident with these metabolic changes, MOMIPP selectively activates the JNK1/2 stress kinase pathway, resulting in phosphorylation of c-Jun, Bcl-2 and Bcl-xL.(In Vivo):MOMIPP (80 mg/kg; i.p.; once daily; for 15 consecutive days) shows result that MOMIPP is moderately effective in suppressing progression of intracerebral glioblastoma xenografts.
  • In Vitro
    Western Blot Analysis Cell Line:U251 cells Concentration:10?μM Incubation Time:4?h or 24?h Result:Activated the JNK stress kinase pathway.
  • In Vivo
    Animal Model:Athymic CrTac:NCR-Foxn1 mice (female, 7-8?weeks)Dosage:80?mg/kg.Administration:i.p.;once daily; for 15 consecutive days Result:Suppressed progression of intracerebral glioblastoma xenografts.
  • Synonyms
    ——
  • Pathway
    PI3K/Akt/mTOR signaling
  • Target
    PI3K
  • Recptor
    SOS1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1363421-46-8
  • Formula Weight
    292.338
  • Molecular Formula
    C18H16N2O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 31.25 mg/mL (106.90 mM)
  • SMILES
    COc1ccc2[nH]c(C)c(\C=C\C(=O)c3ccncc3)c2c1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Matthew Arnold Marx, et al. Sos1 inhibitors. WO2021127429 A1.
molnova catalog
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