UNC1999
CAS No. 1431612-23-5
UNC1999 ( UNC1999; UNC 1999; UNC-1999 )
Catalog No. M11830 CAS No. 1431612-23-5
UNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 with IC50 of 2 nM and 45 nM in cell-free assays, respectively.
Purity : >98%(HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 40 | In Stock |
|
5MG | 59 | In Stock |
|
10MG | 88 | In Stock |
|
25MG | 168 | In Stock |
|
50MG | 272 | In Stock |
|
100MG | 489 | In Stock |
|
500MG | 1071 | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameUNC1999
-
NoteResearch use only, not for human use.
-
Brief DescriptionUNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 with IC50 of 2 nM and 45 nM in cell-free assays, respectively.
-
DescriptionUNC1999 is a potent, orally bioavailable and selective inhibitor of EZH2 and EZH1 with IC50 of 2 nM and 45 nM in cell-free assays, respectively, showing >1000-fold selectivity over a broad range of epigenetic and non-epigenetic targets.
-
SynonymsUNC1999; UNC 1999; UNC-1999
-
PathwayChromatin/Epigenetic
-
TargetHMTase
-
RecptorEZH1; EZH2
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number1431612-23-5
-
Formula Weight569.74
-
Molecular FormulaC33H43N7O2
-
Purity>98%(HPLC)
-
SolubilityEthanol: 100 mg/mL (175.51 mM); DMSO: 100 mg/mL (175.51 mM)
-
SMILESO=C(NCC1=C(CCC)C=C(C)NC1=O)C2=C3C(N(C(C)C)N=C3)=CC(C4=CC=C(N5CCN(C(C)C)CC5)N=C4)=C2
-
Chemical Name1-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
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Konze KD, et al. ACS Chem. Biol. 2013, 8 (6), 1324–1334.
molnova catalog
related products
-
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.
-
PFI-2
A first-in-class, potent and selective inhibitor of SETD7 methyltransferase with Ki app/IC50 of 0.33/2 nM.
-
MMSET-IN-1
MMSET-IN-1 is a potent, selective epigenetic oncogene MMSET (aka NSD2 or WHSC1) inhibitor with Ki/IC50 of 1.6/3.3 uM.