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1260181-14-3

1260181-14-3 Structure

1260181-14-3 Structure
IdentificationBack Directory
[Name]

TCS 21311
[CAS]

1260181-14-3
[Synonyms]

TCS 21311
NIBR-3049
TCS21311; TCS-21311
JAK3/GSK-3β/PKCα Inhibitor - CAS 1260181-14-3 - Calbiochem
3-{5-[4-(2-hydroxy-2-methylpropionyl)piperazin-1-yl]-2-trifluoromethylphenyl}-4-(1H-indol-3-yl)pyrrole-2,5-dione
3-[5-[4-(2-Hydroxy-2-Methyl-1-oxopropyl)-1-piperazinyl]-2-(trifluoroMethyl)phenyl]-4-(1H-indol-3-yl)-1H-pyrrole-2,5-dione
1H-Pyrrole-2,5-dione, 3-[5-[4-(2-hydroxy-2-methyl-1-oxopropyl)-1-piperazinyl]-2-(trifluoromethyl)phenyl]-4-(1H-indol-3-yl)-
[Molecular Formula]

C27H25F3N4O4
[MOL File]

1260181-14-3.mol
[Molecular Weight]

526.51
Chemical PropertiesBack Directory
[Boiling point ]

793.0±60.0 °C(Predicted)
[density ]

1.436±0.06 g/cm3(Predicted)
[storage temp. ]

+2C to +8C
[solubility ]

<52.65mg/ml in DMSO
[form ]

Yellow solid
[pka]

7.91±0.60(Predicted)
Hazard InformationBack Directory
[Uses]

A potent JAK3 inhibitor; selective for JAK3 over JAK1, JAK2 and TYK2. It also inhibits GSK-3β, PKCα and PKCθ.
[Biological Activity]

tcs 21311 is a potent and selective jak3 inhibitor with the ic50 values of 8 nm. tcs 21311 shows high selectivity for jak3 over jak1, jak2 and tyk2. the ic50 values are 1017, 2550 and 8055 nm respectively. tcs 21311 exihibits inhibitory effect on gsk-3β, pkcα and pkcθ with the ic50 values of 3, 13 and 68 nm, respectively [1].janus kinases (jak) belong to a small family of cytoplasmic protein tyrosine kinases including jak1, jak2, tyk2, and jak3, which play important roles in initiating the cytokine-triggered signaling events by activators of transcription (stat) proteins via tyrosine phosphorylation [2]. due to its association with relevant cytokine signaling pathways, jak3 serves as an important target for therapeutic intervention in the treatment of inflammatory diseases, autoimmune disorders and organ transplant rejection [2].
[storage]

Desiccate at RT
[References]

[1] thoma g, nuninger f, falchetto r, et al. identification of a potent janus kinase 3 inhibitor with high selectivity within the janus kinase family[j]. journal of medicinal chemistry, 2010, 54(1): 284-288.
[2] clark m p, george k m, bookland r g, et al. development of new pyrrolopyrimidine-based inhibitors of janus kinase 3 (jak3)[j]. bioorganic & medicinal chemistry letters, 2007, 17(5): 1250-1253.
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