Orellanine

CAS No. 37338-80-0

Orellanine ( 2-(1,3-dihydroxy-4-oxopyridin-2-yl)-1,3-dihydroxypyridin-4-one )

Catalog No. M28005 CAS No. 37338-80-0

Orellanine is a nephrotoxic compound extracted from the mushroom Cortinarius orellanus.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 872 Get Quote
10MG 1179 Get Quote
25MG 1737 Get Quote
50MG 2358 Get Quote
100MG 3177 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Orellanine
  • Note
    Research use only, not for human use.
  • Brief Description
    Orellanine is a nephrotoxic compound extracted from the mushroom Cortinarius orellanus.
  • Description
    Orellanine is a nephrotoxic compound extracted from the mushroom Cortinarius orellanus. Orellanine strongly inhibits the synthesis of macromolecules (Proteins, RNA and DNA) in Madin-Darby canine kidney cells and in rat liver mitochondria.
  • Synonyms
    2-(1,3-dihydroxy-4-oxopyridin-2-yl)-1,3-dihydroxypyridin-4-one
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    bradykinin B1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    37338-80-0
  • Formula Weight
    252.2
  • Molecular Formula
    C10H8N2O6
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Oc1cc[n+]([O-])c(c1O)-c1c(O)c(O)cc[n+]1[O-]
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Leeb-Lundberg LM, et al. International union of pharmacology. XLV. Classification of the kinin receptor family: from molecular mechanisms to pathophysiological consequences. Pharmacol Rev. 2005 Mar;57(1):27-77.
molnova catalog
related products
  • 2:PN:US20040072744 S...

    2: PN: US20040072744 SEQID: 2 claimed protein is a synthetic peptide, used for the research of Down’s syndrome and schizophrenia.

  • Thalidomide-O-amido-...

    Thalidomide-O-amido-PEG-C2-NH2 hydrochloride, a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker, can be used in the synthesis of PROTACs.

  • Ganoderiol F

    Ganoderiol F has anti-inflammatory, cytotoxic and anti-HIV activity, it inhibits activity of topoisomerases in vitro, and it inhibits human immunodeficiency virus-1 protease with IC(50) values of 20-40 microM.