Cart
sales@molnova.com
Home - Products - Others - Other Targets - Peonidin-3-O-[6-O-(E)-Caffeoyl-2-O-{6-O-Caffeoyl-β-D-glucoside}-β-D-glucoside]-5-O-β-D-glucoside

Peonidin-3-O-[6-O-(E)-Caffeoyl-2-O-{6-O-Caffeoyl-β-D-glucoside}-β-D-glucoside]-5-O-β-D-glucoside

CAS No. 145919-39-7

Peonidin-3-O-[6-O-(E)-Caffeoyl-2-O-{6-O-Caffeoyl-β-D-glucoside}-β-D-glucoside]-5-O-β-D-glucoside( ——— )

Catalog No. M39763 CAS No. 145919-39-7

Peonidin-3-O-[6-O-(E)-Caffeoyl-2-O-{6-O-Caffeoyl-β-D-glucoside}-β-D-glucoside]-5-O-β-D-glucoside

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG Get Quote Get Quote
50MG Get Quote Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote
Get Quotation Bulk Inquiry Add to Cart

Biological Information

  • Product Name
    Peonidin-3-O-[6-O-(E)-Caffeoyl-2-O-{6-O-Caffeoyl-β-D-glucoside}-β-D-glucoside]-5-O-β-D-glucoside
  • Note
    Research use only, not for human use.
  • Brief Description
    Peonidin-3-O-[6-O-(E)-Caffeoyl-2-O-{6-O-Caffeoyl-β-D-glucoside}-β-D-glucoside]-5-O-β-D-glucoside
  • Description
    Peonidin-3-O-[6-O-(E)-Caffeoyl-2-O-{6-O-Caffeoyl-β-D-glucoside}-β-D-glucoside]-5-O-β-D-glucoside
  • In Vitro
    ———
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ———
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    145919-39-7
  • Formula Weight
    ———
  • Molecular Formula
    ———
  • Purity
    >98% (HPLC)
  • Solubility
    ———
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog
related products

  • BGB 15025

    HPK1-IN-32 is a potent and selective HPK1 inhibitor with an IC50 of 65 nM. HPK1-IN-32 can be used for the research of HPK1 related disorders or diseases.

  • AC1NS4RE

    SU5614 is a potent and selective FLT3 inhibitor. SU5614 has inhibitory activity for FLT3 and selectively induces growth arrest, apoptosis, and cell cycle arrest in Ba/F3 and AML cell lines expressing a constitutively activated FLT3.

  • Clindamycin

    Clindamycin inhibits protein synthesis by acting on the 50S ribosomal.

Sign In Join Free