Morin

CAS No. 480-16-0

Morin( Aluminum Ionophore I | LDN-0058388 | LY 002079 | NSC 19801 )

Catalog No. M14600 CAS No. 480-16-0

Morin is a chemical compound. It is a yellow color substance that can be isolated from Maclura pomifera (Osage orange), Maclura tinctoria (old fustic) and from leaves of Psidium guajava (common guava).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 41 In Stock
5MG 37 In Stock
10MG 52 In Stock
25MG 100 In Stock
50MG 144 In Stock
100MG 217 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Morin
  • Note
    Research use only, not for human use.
  • Brief Description
    Morin is a chemical compound. It is a yellow color substance that can be isolated from Maclura pomifera (Osage orange), Maclura tinctoria (old fustic) and from leaves of Psidium guajava (common guava).
  • Description
    Morin is a chemical compound. It is a yellow color substance that can be isolated from Maclura pomifera (Osage orange), Maclura tinctoria (old fustic) and from leaves of Psidium guajava (common guava). In a preclinical in vitro study, morin was found to be a weak inhibitor of fatty acid synthase with an IC50 of 2.33 μM.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Aluminum Ionophore I | LDN-0058388 | LY 002079 | NSC 19801
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    Other Indications
  • Indication
    ——

Chemical Information

  • CAS Number
    480-16-0
  • Formula Weight
    302.23
  • Molecular Formula
    C15H10O7
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 10 mM
  • SMILES
    InChI=1S/C15H10O7/c16-6-1-2-8(9(18)3-6)15-14(21)13(20)12-10(19)4-7(17)5-11(12)22-15/h1-5,16-19,21H
  • Chemical Name
    2',3,4',5,7-Pentahydroxyflavone

Shipping & Storage Information

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

Reference

1. Tian, WX. Current Medicinal Chemistry, 2006, 13 (8): 967–977.
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