Cart
sales@molnova.com
SD-70
CAS No. 332173-89-4
SD-70( SD70 )
Catalog No. M14117 CAS No. 332173-89-4
A small molecule tumor translocation inhibitor that inhibits the prostate cancer cell transcriptional program.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameSD-70
-
NoteResearch use only, not for human use.
-
Brief DescriptionA small molecule tumor translocation inhibitor that inhibits the prostate cancer cell transcriptional program.
-
DescriptionA small molecule tumor translocation inhibitor that inhibits the prostate cancer cell transcriptional program, in part by inhibition of the demethylase KDM4C (IC50=30 uM); represses AR transcriptional program, increases H3K9me2 levels in 293T cells; inhibits tumor growth in CWR22Rv1 prostate cancer xenograft mice model.
-
In Vitro——
-
In Vivo——
-
SynonymsSD70
-
PathwayChromatin/Epigenetic
-
TargetHistone Demethylase
-
RecptorHistone Demethylase
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number332173-89-4
-
Formula Weight310.353
-
Molecular FormulaC18H18N2O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILES——
-
Chemical NameN-(furan-2-yl(8-hydroxyquinolin-7-yl)methyl)isobutyramide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Jin C, et al. Proc Natl Acad Sci U S A. 2014 Jun 24;111(25):9235-40.
molnova catalog
related products
-
SGC-iMLLT
SGC-iMLLT is a potent and selective MLLT1/3-histone interactions inhibitor(IC50 = 0.26 μM),and is a first-in-class chemical probe displaying cellular target engagement of MLLT1(Kd = 0.129?μM) and MLLT3(Kd = 0.077?μM).
-
ORY-1001 dihydrochlo...
ORY-1001 dihydrochloride (RG-6016, Ladademstat) is a highly potent, selective inhibitor of lysine-specific demethylase KDM1A (LSD1) with IC50 of 18 nM.
-
MS049 2HCl
MS049 is a potent and selective inhibitor of PRMT4 (IC50 = 34 nM) and PRMT6 (IC50 = 43 nM).
