ML133 HCl

CAS No. 1222781-70-5

ML133 HCl( —— )

Catalog No. M17888 CAS No. 1222781-70-5

ML133 HCl is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 39 Get Quote
10MG 55 Get Quote
25MG 97 Get Quote
50MG 156 Get Quote
100MG 259 Get Quote
200MG 336 Get Quote
500MG 566 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    ML133 HCl
  • Note
    Research use only, not for human use.
  • Brief Description
    ML133 HCl is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.
  • Description
    ML133 HCl is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 and weak activity for Kir4.1 and Kir7.1.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    CDK
  • Recptor
    Kir2.1
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    1222781-70-5
  • Formula Weight
    313.82
  • Molecular Formula
    C19H19NO·HCl
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 125 mg/mL; 398.32 mM
  • SMILES
    Cl.COC1=CC=C(CNCC2=CC=CC3=C2C=CC=C3)C=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Wang HR, et al. ACS Chem Biol, 2011, 6(8), 845-856.
molnova catalog
related products
  • PNU-112455A

    PNU-112455A is an ATP-competitive CDK2/5 inhibitor with Ki of 2 uM and 2 uM for cdk2·GST-cyclin E and cdk5·GST-p25 respectively.

  • CDK7 and 9 inhibitor...

    A potent, selective transcriptional CDK inhibitor with Ki of 2.3 and 0.38 nM for CDK7 and CDK9, respectively; displays >30-fold selectivity over CDK1/2/4, inhibits VEGFR2 with IC50 of 180 nM in a panel of non-CDK kinases.

  • BS-181 hydrochloride

    BS-181 is a potent, selective CDK7 inhibitor with IC50 of 21 nM.