UNC3866 TFA(1872382-47-2 free base)
CAS No. 1872382-48-3
UNC3866 TFA(1872382-47-2 free base)( —— )
Catalog No. M23852 CAS No. 1872382-48-3
UNC3866 TFA is a potent antagonist of the CBX7-H3 interaction as determined by AlphaScreen.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 105 | In Stock |
|
| 2MG | 29 | In Stock |
|
| 5MG | 46 | In Stock |
|
| 10MG | 81 | In Stock |
|
| 25MG | 160 | In Stock |
|
| 50MG | 233 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameUNC3866 TFA(1872382-47-2 free base)
-
NoteResearch use only, not for human use.
-
Brief DescriptionUNC3866 TFA is a potent antagonist of the CBX7-H3 interaction as determined by AlphaScreen.
-
DescriptionUNC3866 TFA is a potent antagonist of the CBX7-H3 interaction as determined by AlphaScreen.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayChromatin/Epigenetic
-
TargetHistone Demethylase
-
RecptorCBX7-H3
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number1872382-48-3
-
Formula Weight909.04
-
Molecular FormulaC45H67F3N6O10
-
Purity>98% (HPLC)
-
SolubilityDMSO:10 mM
-
SMILESCCN(CC)CCCC[C@@H](C(=O)N[C@@H](CO)C(=O)OC)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)C2=CC=C(C=C2)C(C)(C)C.C(=O)(C(F)(F)F)O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Stuckey JI, et al. A cellular chemical probe targeting the chromodomains of Polycomb repressive complex 1. Nat Chem Biol. 2016 Mar;12(3):180-7.
molnova catalog
related products
-
CCI 007
CCI 007 is a selective inhibitor of MLL-r, CALM-AF10 and SET-NUP214 leukemia with IC50 of 3.5 uM against MLL-r leukemia cell line PER-485
-
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).
-
LSD1-IN-27
LSD1-IN-27 is a potent LSD1 inhibitor with an IC50 value of 13 nM.LSD1-IN-27 inhibited the stemness and migration of gastric cancer cells.
Cart
sales@molnova.com