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
1. Riesterer O, et al. Invest New Drugs. 2011 Jun;29(3):514-22.
2. Matthews DJ, et al. Cell Cycle. 2007 Jan 1;6(1):104-10.
molnova catalog
related products
-
Prexasertib dihydroc...
A potent, selective, ATP-competitive inhibitor of CHK1 with Ki of 0.9 nM.
-
PHI-101
PHI-101 is an orally available and selective checkpoint kinase 2 (Chk2) inhibitor for the study of refractory acute myelogenous leukemia (AML) and ovarian cancer.
-
PF-00477736
PF-00477736 (PF-477736) is a potent, selective, ATP-competitive inhibitor of Chk1 with Ki of 0.49 nM, also inhibits Chk2 (Ki=47 nM) and poorly inhibits CDK1 activity (Ki=9.9 uM).
Cart
sales@molnova.com