TBBD

CAS No. 476-66-4

TBBD ( Ellagic acid )

Catalog No. M14590 CAS No. 476-66-4

TBBD is a specific inhibitor of coactivator-associated arginine methyltransferase 1 (CARM1; PRMT4) that selectively inhibits methylation at arginine 17 of histone H3 (H3R17).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
500MG 41 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    TBBD
  • Note
    Research use only, not for human use.
  • Brief Description
    TBBD is a specific inhibitor of coactivator-associated arginine methyltransferase 1 (CARM1; PRMT4) that selectively inhibits methylation at arginine 17 of histone H3 (H3R17).
  • Description
    TBBD is a specific inhibitor of coactivator-associated arginine methyltransferase 1 (CARM1; PRMT4) that selectively inhibits methylation at arginine 17 of histone H3 (H3R17); shows no significant effect on the HMTase activity of G9a, as well as on the HAT activity of p300/CBP-associated factor.
  • Synonyms
    Ellagic acid
  • Pathway
    Chromatin/Epigenetic
  • Target
    HMTase
  • Recptor
    Carbonicanhydrase;CK2;PKA;PKC;Smoothened;Syk
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    476-66-4
  • Formula Weight
    302.19
  • Molecular Formula
    C14H6O8
  • Purity
    >98% (HPLC)
  • Solubility
    Ethanol: 0.2 mg/mL (0.65 mM) ( < 1 mg/ml refers to the product slightly soluble or insoluble )
  • SMILES
    O=C1C2=CC(O)=C(O)C(O3)=C2C4=C(C3=O)C=C(O)C(O)=C4O1
  • Chemical Name
    2,3,7,8-tetrahydroxychromeno[5,4,3-cde]chromene-5,10-dione

Shipping & Storage Information

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

Reference

1. Selvi BR, et al. J Biol Chem. 2010 Mar 5;285(10):7143-52.
2. Hatanaka Y, et al. Cell Rep. 2017 Sep 19;20(12):2756-2765.
molnova catalog
related products
  • XY1

    XY1 is the inactive control compound of SGC-707.

  • CMP-5 hydrochloride

    CMP-5 (PRMT5-IN-5)is a first-in-class, small-molecule PRMT5-specific inhibitor that blocks EBV-driven B-lymphocyte transformation and survival.

  • A-196

    A potent, selective and substrate-competitive inhibitor of protein lysine methyltransferases (PKMTs) SUV420H1 and SUV420H2 with IC50 of 25 nM and 144 nM, respectively.