hydrocotarnine

CAS No. 550-10-7

hydrocotarnine( —— )

Catalog No. M28624 CAS No. 550-10-7

hydrocotarnine?is an inhibitor of Cbl.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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Biological Information

  • Product Name
    hydrocotarnine
  • Note
    Research use only, not for human use.
  • Brief Description
    hydrocotarnine?is an inhibitor of Cbl.
  • Description
    hydrocotarnine?is an inhibitor of Cbl.(In Vivo):In vivo, inhibition of Cbl with an analgesic drug, hydrocotarnine, increases inflammasome-mediated IL-18 secretion in the colon, and protects mice from dextran sulphate sodium-induced colitis. Together, our novel findings provide new insights into the role of the SFK-Cbl axis in suppressing NLRP3 inflammasome activation and identify a novel clinical utility of hydrocortanine for disease treatment.
  • In Vitro
    Hydrocotarnine is an analgesic agent (CRIN-2), with the patent ID of WO2011160016A2.Hydrocotarnine (10 μM; 1 h) elevates the secretion of IL-1β and IL-18, and (0.1-10 μM; 1 h) increases the global level of tyrosine-phosphorylated proteins in THP-1 cells. Hydrocotarnine (50 μM; 0-100 min) increases the glycolytic capacity and glycolytic reserve capacity in THP-1-derived macrophages.Hydrocotarnine (50 μM; 16 h) inhibits Cbl and increases the total GLUT1 protein in THP-1-derived macrophages.Hydrocotarnine is known to enhance the analgesic effect of opioids, and alleviates cancer pain. Western Blot Analysis Cell Line:THP-1 cells Concentration:0.1, 1, 10 μM Incubation Time:1 hour Result:Induced p-Pyk2 loss and increased the level of tyrosine-phosphorylated proteins in a dose-dependent manner.
  • In Vivo
    Hydrocotarnine (10 mg/kg/d; i.p.; 9 d) shows inhibitory effect on Cbl and results in increasing IL-18 levels, indicating that NLRP3 inflammasome activation is enhanced in mice.Hydrocotarnine (10 mg/kg/d; i.p.; 9 d) protects mice from DSS-induced colitis, with low scores of pathological evaluation of inflammation, epithelial defects, and crypt atrophy. Animal Model:DSS-induced colitis model in C57BL/6 mice (6-9 weeks old) Dosage:10 mg/kg Administration:Intraperitoneal injection; once daily; 9 days while 2.5% DSS treatment began on day 1 and ended on day 7 Result:Significantly attenuated the weight loss of DSS-induced colitis mice compared to PBS-treated control mice, indicating that decreasing negative regulation of the NLRP3 inflammasome activation could attenuate colitis in an animal model.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    550-10-7
  • Formula Weight
    221.25
  • Molecular Formula
    C12H15NO3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : ≥ 100 mg/mL (451.98 mM)
  • SMILES
    CN(CC1)Cc2c1cc1OCOc1c2OC
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Pedro Molina, et al. Iminophosphorane-mediated imidazole ring formation: A new and general entry to aplysinopsin-type alkaloids of marine origin. Tetrahedron Lett. 1994;50(7): 2241-2254
molnova catalog
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