SR-4370

CAS No. 1816294-67-3

SR-4370( SR-4370 | SR 4370 | SR4370 )

Catalog No. M17385 CAS No. 1816294-67-3

SR- 4370 is an HDAC inhibitor. SR- 4370 exhibited IC50 values of 0.5 μM, 0.1 μM and 0.06 μM towards HDAC1, HDAC2 and HDAC3.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 61 In Stock
5MG 102 In Stock
10MG 177 In Stock
25MG 332 In Stock
50MG 500 In Stock
100MG 705 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SR-4370
  • Note
    Research use only, not for human use.
  • Brief Description
    SR- 4370 is an HDAC inhibitor. SR- 4370 exhibited IC50 values of 0.5 μM, 0.1 μM and 0.06 μM towards HDAC1, HDAC2 and HDAC3.
  • Description
    SR- 4370 is an HDAC inhibitor. SR- 4370 exhibited IC50 values of 0.5 μM, 0.1 μM and 0.06 μM towards HDAC1, HDAC2 and HDAC3, resp. SR- 4370 is reported in WO 2015153516.
  • In Vitro
    SR-4370 is an inhibitor of HDAC, with IC50s of 0.13 μM, 0.58 μM, 0.006 μM, 2.3 μM, and 3.4 μM for HDAC1, HDAC2, HDAC3, HDAC8, and HDAC6, respectively. SR-4370 is cytotoxic to the breast cancer cells (MDA-MB-231), with an IC50 of 12.6 μM.
  • In Vivo
    ——
  • Synonyms
    SR-4370 | SR 4370 | SR4370
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    GPR
  • Recptor
    HDAC1| HDAC2| HDAC3
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1816294-67-3
  • Formula Weight
    304.34
  • Molecular Formula
    C17H18F2N2O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 150 mg/mL; 492.89 mM
  • SMILES
    Fc1c(cccc1F)c2ccc(cc2)C(=O)NNCCCC
  • Chemical Name
    N'-butyl-2',3'-difluoro-[1,1'-biphenyl]-4-carbohydrazide

Shipping & Storage Information

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

Reference

1. D Liao, etal. HDAC Inhibitor Compounds and Methods of Treatment
molnova catalog
related products
  • CID1231538

    CID1231538 is a potent?GPR35?antagonist.

  • AMG-009

    AMG-009 is a selective and potent dual antagonist of CRTH2 and DP, with an IC50 value of 3 nM for CRTH2 and 12 nM for DP receptors.

  • PSN 375963

    PSN 375963 hydrochloride is a synthetic agonist of the endogenous ligand for GPR119.