GW 841819X
CAS No. 146135-18-4
GW 841819X ( GW841819X )
Catalog No. M11985 CAS No. 146135-18-4
GW 841819X is an analogue of (+)-JQ1 and a novel inhibitor of BET bromodomain.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 873 | Get Quote |
|
50MG | 1782 | Get Quote |
|
100MG | 2250 | Get Quote |
|
200MG | Get Quote | Get Quote |
|
500MG | Get Quote | Get Quote |
|
1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameGW 841819X
-
NoteResearch use only, not for human use.
-
Brief DescriptionGW 841819X is an analogue of (+)-JQ1 and a novel inhibitor of BET bromodomain.
-
DescriptionGW 841819X is an analogue of (+)-JQ1 and a novel inhibitor of BET bromodomain that displays activity in vivo against NUT-midline carcinoma, multiple myeloma, mixed-lineage leukemia, and acute myeloid leukemia.
-
SynonymsGW841819X
-
PathwayChromatin/Epigenetic
-
TargetBromodomain
-
RecptorBromodomain
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number146135-18-4
-
Formula Weight487.94
-
Molecular FormulaC26H22ClN5O3
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESO=C(OCC1=CC=CC=C1)N[C@H]2C3=NN=C(C)N3C4=CC=C(OC)C=C4C(C5=CC=C(Cl)C=C5)=N2
-
Chemical Name(R)-benzyl (6-(4-chlorophenyl)-8-methoxy-1-methyl-4H-benzo[f][1,2,4]triazolo[4,3-a][1,4]diazepin-4-yl)carbamate
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Chung CW, et al. J Med Chem. 2011 Jun 9;54(11):3827-38.
2. Baud MG, et al. Science. 2014 Oct 31;346(6209):638-41.
2. Baud MG, et al. Science. 2014 Oct 31;346(6209):638-41.
molnova catalog
related products
-
MS-417
MS-417 (GTPL-7512) is a highly specific BET bromodomain inhibitor that binds to BRD4-BD1 and BRD4 BD2 with Kd of 36.1 uM and 25.4 uM respectively.
-
AU1
AU1 (GSK 1379725A) is the first selective small molecule inhibitor of BPTF bromodomain (bromodomain PHD finger transcription factor) with Kd of 2.8 uM in a cell-based reporter assay.
-
PFI-3
PFI-3 is a potent and cell active BRG/PB1 bromodomains inhibitor with Kd of 54-97 nM.