Bavachinin

CAS No. 19879-30-2

Bavachinin ( 7-O-Methylbavachin; Bavachinin A )

Catalog No. M18196 CAS No. 19879-30-2

Bavachinin(7-O-Methylbavachin) is a natural compound isolated from the Chinese herb Fructus Psoraleae with potent anti-angiogenic activity.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 53 In Stock
10MG 76 In Stock
25MG 123 In Stock
50MG 176 In Stock
100MG 266 In Stock
500MG 651 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Bavachinin
  • Note
    Research use only, not for human use.
  • Brief Description
    Bavachinin(7-O-Methylbavachin) is a natural compound isolated from the Chinese herb Fructus Psoraleae with potent anti-angiogenic activity.
  • Description
    Bavachinin(7-O-Methylbavachin) is a natural compound isolated from the Chinese herb Fructus Psoraleae with potent anti-angiogenic activity.
  • Synonyms
    7-O-Methylbavachin; Bavachinin A
  • Pathway
    Metabolic Enzyme/Protease
  • Target
    Dehydrogenase
  • Recptor
    Others
  • Research Area
    Inflammation/Immunology
  • Indication
    ——

Chemical Information

  • CAS Number
    19879-30-2
  • Formula Weight
    338.4
  • Molecular Formula
    C21H22O4
  • Purity
    98%
  • Solubility
    DMSO : ≥ 250 mg/mL; 738.77 mM
  • SMILES
    [C@H]1(CC(=O)c2c(O1)cc(c(c2)CC=C(C)C)OC)c1ccc(cc1)O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Chen X, et al. FEBS Lett. 2013 Sep 17;587(18):2930-5.
molnova catalog
related products
  • DS-1001b

    DS-1001b is an ?inhibitor of ?mutant IDH-1 (Isocitrate Dehydrogenase-1).

  • AVN944

    AVN-944(VX-944) is a selective, noncompetitive inhibitor of the enzyme directed against human IMPDH with Ki of 6-10 nM for IMPDH1/IMPDH2.

  • Tiazofurin

    Tiazofurin is a synthetic nucleoside analogue with antineoplastic activity. Tiazofurin is anabolized intracellularly to tiazole-4-carboxamide adenine dinucleotide (TAD), a potent inhibitor of IMP dehydrogenase (IMPDH) .