LDC000067

CAS No. 1073485-20-7

LDC000067 ( LDC000067; LDC-000067; LDC 000067 )

Catalog No. M17138 CAS No. 1073485-20-7

LDC000067 is a highly specific and selective CDK9 inhibitor with an IC50 value of 44±10 nM.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 34 In Stock
5MG 43 In Stock
10MG 78 In Stock
25MG 156 In Stock
50MG 230 In Stock
100MG 341 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    LDC000067
  • Note
    Research use only, not for human use.
  • Brief Description
    LDC000067 is a highly specific and selective CDK9 inhibitor with an IC50 value of 44±10 nM.
  • Description
    LDC000067 is a potent and selective CDK9 inhibitor. LDC000067 inhibited in vitro transcription in an ATP-competitive and dose-dependent manner. Gene expression profiling of cells treated with LDC000067 demonstrated a selective reduction of short-lived mRNAs, including important regulators of proliferation and apoptosis. Analysis of de novoRNA synthesis suggested a wide ranging positive role of CDK9. At the molecular and cellular level, LDC000067 reproduced effects characteristic of CDK9 inhibition such as enhanced pausing of RNA polymerase II on genes and, most importantly, induction of apoptosis in cancer cells.
  • Synonyms
    LDC000067; LDC-000067; LDC 000067
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    CDK1; CDK2; CDK4; CDK6; CDK9
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1073485-20-7
  • Formula Weight
    370.43
  • Molecular Formula
    C18H18N4O3S
  • Purity
    98%
  • Solubility
    DMSO : ≥ 47 mg/mL 126.88 mM
  • SMILES
    COc1ccccc1c1cc(ncn1)Nc1cccc(c1)CS(=O)(=O)N
  • Chemical Name
    6-(6-(1-Methyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-ylthio)quinoline

Shipping & Storage Information

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

Reference

1. Albert TK, et al. Br J Pharmacol. 2014, 171(1), 55-68.
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