VRX-0466617
CAS No. 926906-64-1
VRX-0466617( VRX 0466617 | VRX0466617 )
Catalog No. M16639 CAS No. 926906-64-1
A potent and selective Chk2 inhibitor with Ki/IC50 of 11 nM/120 nM; shows no inhibitory effect on Chk1 (>100 uM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 963 | Get Quote |
|
| 50MG | 1962 | Get Quote |
|
| 100MG | 2520 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameVRX-0466617
-
NoteResearch use only, not for human use.
-
Brief DescriptionA potent and selective Chk2 inhibitor with Ki/IC50 of 11 nM/120 nM; shows no inhibitory effect on Chk1 (>100 uM).
-
DescriptionA potent and selective Chk2 inhibitor with Ki/IC50 of 11 nM/120 nM; shows no inhibitory effect on Chk1 (>100 uM); inhibits the phosphorylation of Chk2 Ser(19) and Ser(33-35), but not of Chk2 Thr(68), prevents the IR-induced Chk2-dependent degradation of Hdmx and attenuates IR-induced apoptosis.
-
In Vitro——
-
In Vivo——
-
SynonymsVRX 0466617 | VRX0466617
-
PathwayAngiogenesis
-
TargetChk
-
RecptorChk
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number926906-64-1
-
Formula Weight462.366
-
Molecular FormulaC19H20BrN5O2S
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESN/C(C1=C(NC2=CC=C(NC3=CC=C(Br)C=C3)C=C2)SNC1=O)=N\C(C)CO
-
Chemical Name5-[4-(4-Bromoanilino)anilino]-N'-(1-hydroxypropan-2-yl)-3-oxo-1,2-thiazole-4-carboximidamide
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Carlessi L, et al. Mol Cancer Ther. 2007 Mar; 6(3):935-44.
2. Carlessi L, et al. Biochim Biophys Acta. 2010 Oct;1803(10):1213-23.
molnova catalog
related products
-
BAY-1816032
BAY-1816032 (BAY1816032) is a highly potent, selective, orally active BUB1 mitotic checkpoint serine/threonine kinase with IC50 of 7 nM.
-
MK 8776
MK 8776 (SCH 900776) is a potent and functionally selective CHK1 inhibitor (IC50=3 nM) with minimal intrinsic antagonistic properties.
-
Baricitinib
Baricitinib (LY3009104, INCB028050) is a selective JAK1 and JAK2 inhibitor with IC50 of 5.9 nM and 5.7 nM in cell-free assays.
Cart
sales@molnova.com