XL-844
CAS No. 631864-00-1
XL-844( EXEL-9844 | EXEL9844 | XL844 )
Catalog No. M15387 CAS No. 631864-00-1
A potent, specific, orally available, ATP competitive inhibitor of Chk1 and Chk2 with Ki of 2.2 nM and 0.07 nM, respectively.
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 NameXL-844
-
NoteResearch use only, not for human use.
-
Brief DescriptionA potent, specific, orally available, ATP competitive inhibitor of Chk1 and Chk2 with Ki of 2.2 nM and 0.07 nM, respectively.
-
DescriptionA potent, specific, orally available, ATP competitive inhibitor of Chk1 and Chk2 with Ki of 2.2 nM and 0.07 nM, respectively; increases gemcitabine-induced H2AX phosphorylation, blocks Cdc25A phosphorylation, and induces premature mitotic entry; significantly enhances gemcitabine antitumor activity in a PANC-1 xenograft model.Blood Cancer Phase 1 Discontinued.
-
In Vitro——
-
In Vivo——
-
SynonymsEXEL-9844 | EXEL9844 | XL844
-
PathwayAngiogenesis
-
TargetChk
-
RecptorChk
-
Research AreaCancer
-
IndicationBlood cancer
Chemical Information
-
CAS Number631864-00-1
-
Formula Weight287.323
-
Molecular FormulaC14H17N5O2
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESC1=CC=C(C(=C1)NC(=O)NC2=NC=CN=C2)OCCCN
-
Chemical Name1-[2-(3-aminopropoxy)phenyl]-3-pyrazin-2-ylurea
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
PV-1115
A potent and highly selective Chk2 inhibitor with IC50 of 0.14 nM; displays greater than 100 uM for Chk1 in vitro.
-
SAR-020106
SAR-020106 is a potent, ATP-competitive, and selective CHK1 inhibitor with an IC50 of 13.3 nmol/L on the isolated human enzyme.SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an IC(50) of 13.3 nmol/L on the isolated human enzyme. This compound abrogates an etoposide-induced G(2) arrest with an IC(50) of 55 nmol/L in HT29 cells, and significantly enhances the cell killing of gemcitabine and SN38 by 3.0- to 29-fold in several colon tumor lines in vitro and in a p53-dependent fashion.
-
CCT241533
A potent and selective ATP-competitive inhibitor of CHK2 K5777:N5777with IC50 of 3 nM.
Cart
sales@molnova.com