CDDO-3P-Im

CAS No. 1883650-95-0

CDDO-3P-Im( —— )

Catalog No. M26556 CAS No. 1883650-95-0

CDDO-3P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can reduce the size and severity of the lung tumors in the mouse lung cancer model.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 178 Get Quote
10MG 295 Get Quote
25MG 502 Get Quote
50MG 709 Get Quote
100MG 1008 Get Quote
500MG 2007 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    CDDO-3P-Im
  • Note
    Research use only, not for human use.
  • Brief Description
    CDDO-3P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can reduce the size and severity of the lung tumors in the mouse lung cancer model.
  • Description
    CDDO-3P-Im, an analog of CDDO-Imidazolide, has a chemopreventive effect. It can reduce the size and severity of the lung tumors in the mouse lung cancer model.(In Vitro):CDDO-3P-Im (30 nM) induces differentiation of U937 cells. In RAW264.7 cells, CDDO-3P-Im suppresses NO production (IC50 = 4.3 nM).(In Vivo):CDDO-3P-Im reduces the size and the severity of the lung tumors in mouse lung cancer models. In A/J mice, CDDO-3P-Im (50-200 mg/kg; diet) decreases the number, size, and severity of tumors. CDDO-3P-Im significantly elevates heme oxygenase-1 and quinone reductase mRNA and protein levels in various mouse tissues.
  • In Vitro
    CDDO-3P-Im (30-100 nM; 4 days) induces differentiation of U937 cells at 30 nM.CDDO-3P-Im suppresses NO production in RAW264.7 cells with an IC50 of 4.3 nM.Apoptosis Analysis Cell Line:U937 cells Concentration:30 nM, 100 nM Incubation Time:4 days Result:Induced differentiation of U937 cells at 30 nM.
  • In Vivo
    CDDO-3P-Im is more stable than CDDO-Im in pharmacokinetic studies.CDDO-3P-Im significantly elevates heme oxygenase-1 (HO-1) and quinone reductase (NQO1) mRNA and protein levels in various mouse tissues in vivo.CDDO-3P-Im (50-200 mg/kg; diet; for 16 weeks) decreases the number, the size and the severity of tumors in A/J mice. Animal Model:Seven week-old female A/J mice Dosage:50 mg/kg, 200 mg/kg Administration: Diet; for 16 weeks Result:Decreased the number, the size and the severity of tumors.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1883650-95-0
  • Formula Weight
    618.822
  • Molecular Formula
    C39H46N4O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 250 mg/mL (404.00 mM)
  • SMILES
    [H][C@@]12CC(C)(C)CC[C@@]1(CC[C@]1(C)[C@]2([H])C(=O)C=C2[C@@]3(C)C=C(C#N)C(=O)C(C)(C)[C@]3([H])CC[C@@]12C)C(=O)n1cnc(c1)-c1cccnc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Tabraiz S, et al. Temperature and immigration effects on quorum sensing in the biofilms of anaerobic membrane bioreactors. J Environ Manage. 2021 Sep 1;293:112947.
molnova catalog
related products
  • Pomalidomide-C2-acid

    Pomalidomide-C2-acid is a PROTAC building block.

  • Sinapaldehyde

    Sinapaldehyde has effects against 65 strains of Candida,Sinapaldehyde inhibits prostaglandin synthetase in a dose-dependent way, it dose-dependently inhibits ethyl phenylpropiolate-induced edema of the rat ear, and can inhibit electrically induced contractions of the guinea pig ileum in a dose-dependent way.

  • Catechin 7-O-beta-D-...

    Catechin 7-O-beta-D-glucopyranoside has intestinal anti-inflammatory activity.