CX-6258 HCl
CAS No. 1353859-00-3
CX-6258 HCl( CX-6258 Hydrochloride | CX 6258 Hydrochloride )
Catalog No. M17253 CAS No. 1353859-00-3
CX-6258 HCl is an effective, orally efficacious Pim1/2/3 kinase inhibitor (IC50: 5/25/16 nM).
CX-6258 HCl is an effective, orally efficacious Pim1/2/3 kinase inhibitor (IC50: 5/25/16 nM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
2MG | 46 | In Stock |
|
5MG | 72 | In Stock |
|
10MG | 132 | In Stock |
|
25MG | 240 | In Stock |
|
50MG | 402 | In Stock |
|
100MG | 579 | In Stock |
|
500MG | 1197 | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product NameCX-6258 HCl
-
NoteResearch use only, not for human use.
-
Brief DescriptionCX-6258 HCl is an effective, orally efficacious Pim1/2/3 kinase inhibitor (IC50: 5/25/16 nM).
-
DescriptionCX-6258 HCl is a potent, selective, and orally efficacious pan-Pim kinases inhibitor.
-
In VitroWestern Blot Analysis Cell Line:MV-4-11 human AML cells.Concentration:0.1 μM, 1 μM, 10 μM.Incubation Time:2 hours.Result:Caused dose dependent inhibition of the phosphorylation of two pro-survival proteins, Bad and 4E-BP1, at the Pim kinase specific sites S112 and S65 and T37/46, respectively.
-
In VivoAnimal Model:Nude mice, MV-4-11 xenograft modelsDosage:50 mg/kg, 100 mg/kg.Administration:Oral administration; once daily; over a period of 21 days.Result:Exhibitd dose dependent efficacy, with a 50 mg/kg dose producing 45% tumor growth inhibition (TGI) and a 100 mg/kg dose producing 75% TGI.
-
SynonymsCX-6258 Hydrochloride | CX 6258 Hydrochloride
-
PathwayOthers
-
TargetOther Targets
-
RecptorPim1| Pim2| Pim3
-
Research AreaCancer
-
Indication——
Chemical Information
-
CAS Number1353859-00-3
-
Formula Weight498.4
-
Molecular FormulaC26H24ClN3O3·HCl
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 10 mg/mL (20.06 mM)
-
SMILESCN1CCCN(CC1)C(=O)c1cccc(c1)c1ccc(o1)/C=C/1\c2c(ccc(c2)Cl)NC1=O.Cl
-
Chemical Name(3E)-5-Chloro-3-[[5-[3-[(hexahydro-4-methyl-1H-1,4-diazepin-1-yl)carbonyl]phenyl]-2-furanyl]methylene]-1,3-dihydro-2H-indol-2-one hydrochloride
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Haddach M, et al. ACS Medicinal Chemistry Letters, 3 (2) , 135-139
molnova catalog
related products
-
Nitecapone
Nitecapone is a reversible inhibitor of S-COMT (IC50 values of 300 nM in rat liver).
-
Guaiacylglycerol 8-O...
The herbs of Juniperus formosana.
-
Sulfachloropyridazin...
A sulfonamide antimicrobial used for urinary tract infections and in veterinary medicine.