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Chemical Structure| 1431612-23-5 Chemical Structure| 1431612-23-5

Structure of UNC1999
CAS No.: 1431612-23-5

Chemical Structure| 1431612-23-5

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UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 with IC50 of 2 nM and 45 nM, respectively.

4.5 *For Research Use Only! Not for Human Use. We Do Not Sell to Patients.

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Product Details of UNC1999

CAS No. :1431612-23-5
Formula : C33H43N7O2
M.W : 569.74
SMILES Code : O=C(C1=CC(C2=CC=C(N3CCN(C(C)C)CC3)N=C2)=CC4=C1C=NN4C(C)C)NCC5=C(CCC)C=C(C)NC5=O
English Name :1-Isopropyl-6-(6-(4-isopropylpiperazin-1-yl)pyridin-3-yl)-N-((6-methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl)-1H-indazole-4-carboxamide
MDL No. :MFCD26960958
InChI Key :DPJNKUOXBZSZAI-UHFFFAOYSA-N
Pubchem ID :72551585

Safety of UNC1999

Related Pathways of UNC1999

epigenetics

Isoform Comparison

Biological Activity

Target
  • Histone Methyltransferase

    EZH2, IC50:2 nM

    EZH1, IC50:45 nM

In Vitro:

Cell Line
Concentration Treated Time Description References
IdHPCs 1 μM 4 days Inhibit EZH1/2 activity, reduce H3K27me3 deposition Nat Commun. 2022 Nov 28;13(1):7159.
DLD-1 2.5 μM 24 hours To evaluate UNC1999-induced autophagy, results showed that UNC1999 increased the formation of autophagic vacuoles. Am J Cancer Res. 2016 Aug 1;6(8):1661-80
HCT116 5 μM 6 or 18 hours To investigate the effect of EZH2 inhibitors on LC3B gene expression, results showed that UNC1999 and GSK343 transiently increased the mRNA level of LC3B gene. Am J Cancer Res. 2016 Aug 1;6(8):1661-80

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.76mL

0.35mL

0.18mL

8.78mL

1.76mL

0.88mL

17.55mL

3.51mL

1.76mL

References

 

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