Cerdulatinib (PRT062070)
Catalog No.: GC11209Purity:>99.50%Synonyms: PRT062070, PRT2070
Le cerdulatinib (PRT062070) (PRT062070) est un inhibiteur sélectif de Tyk2 avec une IC50 de 0,5 nM. Le cerdulatinib (PRT062070) (PRT062070) est également un double inhibiteur de JAK et SYK avec des IC50 de 12, 6, 8 et 32 pour JAK1, 2, 3 et SYK, respectivement.
Les produits sont exclusivement destinés à la recherche. Ils ne doivent pas être utilisés chez l’être humain. Nous ne vendons pas aux patients.
Cas No.: 1198300-79-6
10mM (in 1mL DMSO)In Stock
$45.00
1
1mgIn Stock
$25.00
1
5mgIn Stock
$45.00
1
10mgIn Stock
$61.00
1
25mgIn Stock
$103.00
1
50mgIn Stock
$151.00
1
100mgIn Stock
$231.00
1
200mgIn Stock
$323.00
1
| Pack Size | Price | Availability | Quantity | Action |
|---|---|---|---|---|
| 10mM (in 1mL DMSO) | $45.00 | In Stock | 1 | |
| 1mg | $25.00 | In Stock | 1 | |
| 5mg | $45.00 | In Stock | 1 | |
| 10mg | $61.00 | In Stock | 1 | |
| 25mg | $103.00 | In Stock | 1 | |
| 50mg | $151.00 | In Stock | 1 | |
| 100mg | $231.00 | In Stock | 1 | |
| 200mg | $323.00 | In Stock | 1 |
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Citations
1 publicationsPublications de chercheurs utilisant ce produitDescription
Cerdulatinib (PRT062070) is a potent and selective inhibitor of Syk and JAK.[1]
The JAK/STAT cascade, which has been implicated in hematopoiesis and cytokine signaling, is present in humans and flies. Worms. The SYK/ZAP70 kinases play an important role in human T and B cell signaling.[3]
Cerdulatinib can induce apoptosis via down-regulation of MCL1 protein and PARP cleavage. Through the inhibition of RB phosphorylation and down-regulation of cyclin E,the Cerdulatinib can also block G1/S transition and cause cell cycle arrest. Further analyses of the cell signaling activities showed that STAT3 phosphorylation was sensitive to inhibition by cerdulatinib in ABC cell lines while phosphorylation of SYK, PLCg2, AKT and ERK is reported to be sensitive to inhibition by cerdulatinib in GCB cell lines.[2]
Cerdulatinib is effective in rodent models of B-cell lymphoma and autoimmune disease and has exhibited anti-tumor activity in genetically diverse B-cell lymphoma cell lines and is more effective than Syk- or Jak- selective inhibitors alone.[1]
References:
[1] Manish Patel , Pau Hamlin, MD, etal. , A Phase I Open-Label, Multi-Dose Escalation Study of the Dual Syk/Jak Inhibitor PRT062070 (Cerdulatinib) in Patients with Relapsed/Refractory B Cell Malignancies. Blood: 124 (21) ; December 6, 2014.
[2] Y. Lynn Wang, MD PhD, Jiao Ma, PhD, etal., SYK and STAT3 Are Active in Diffuse Large B-Cell Lymphoma: Activity of Cerdulatinib, a Dual SYK/JAK Inhibitor. Blood: 124 (21) ; December 6, 2014.
[3]Morrison DK, Murakami MS, Cleghon V. Protein kinases and phosphatases in the Drosophila genome. J Cell Biol. 2000 Jul 24;150(2):F57-62.
Protocole (Protocol)
| Cell experiment [1]: | |
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Cell lines |
DLBCL (diffuse large B-cell lymphoma) cells: germinal center B-cell (GCB) subtype, activated B-cell (ABC) subtype. |
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Preparation method |
Limited solubility. General tips for obtaining a higher concentration: Please warm the tube at 37 ℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months. |
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Reaction Conditions |
6 h |
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Applications |
Cerdulatinib induces apoptosis in both GCB and ABC cell lines by caspase 3 and PARP cleavage. Cerdulatinib also triggers apoptosis and cell cycle arrest in BCR-stimulated DLBCL cells. Cerdulatinib blocks JAK/STAT and BCR signaling in both ABC and GCB cell lines as well. |
| Animal experiment [2]: | |
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Animal models |
Female Lewis rats collagen-induced arthritis (CIA) model |
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Dosage form |
Oral gavage twice daily. |
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Applications |
3 mg/kg of Cerdulatinib suppresses the inflammation and reverses relative to pretreatment levels at 5 mg/kg. Cerdulatinib also dose-dependently leads to significant improvements in inflammatory infiltrate within the synovium and the integrity of the articular cartilage. Moreover, Cerdulatinib treatment affects anticollagen antibody formation and reduces 50% of circulating antibody titers at the 1.5, 3, and 5 mg/kg doses. |
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Other notes |
Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal. |
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References: 1. Ma J, Xing W, Coffey G et al. Cerdulatinib, a novel dual SYK/JAK kinase inhibitor, has broad anti-tumor activity in both ABC and GCB types of diffuse large B cell lymphoma. Oncotarget. 2015 Nov 5. 2. Coffey G, Betz A, DeGuzman F et al.The novel kinase inhibitor PRT062070 (Cerdulatinib)demonstrates efficacy in models of autoimmunity and B-cell cancer. J Pharmacol Exp Ther. 2014 Dec;351(3):538-48. |
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Documents produit (Product Documents)
Purity:>99.50%Appearance:A solid
Propriétés chimiques (Chemical Properties)
N° CAS
1198300-79-6
Synonymes
PRT062070, PRT2070
Nom chimique
4-(cyclopropylamino)-2-((4-(4-(ethylsulfonyl)piperazin-1-yl)phenyl)amino)pyrimidine-5-carboxamide
SMILES
NC(C1=CN=C(NC2=CC=C(N3CCN(S(=O)(CC)=O)CC3)C=C2)N=C1NC4CC4)=O
Formule moléculaire
C20H27N7O3S
Masse moléculaire
445.54
Solubilité
≥ 22.3mg/mL in DMSO
Conservation
Desiccate at -20°C
Conseils généraux
Choisissez un solvant adapté selon les données de solubilité du produit. Après préparation, répartissez la solution mère en aliquotes afin d’éviter les cycles répétés de congélation-décongélation.
Utilisez les solutions mères dans les 6 mois si elles sont conservées à -80°C, ou dans le mois si elles sont conservées à -20°C.
Pour améliorer la solubilité, réchauffez le tube à 37°C et soniquez-le pendant une durée appropriée.
Utilisez les solutions mères dans les 6 mois si elles sont conservées à -80°C, ou dans le mois si elles sont conservées à -20°C.
Pour améliorer la solubilité, réchauffez le tube à 37°C et soniquez-le pendant une durée appropriée.
Conditions d’expédition
Les échantillons d’évaluation sont expédiés avec des blocs réfrigérants. Les autres formats sont expédiés à température ambiante ou, sur demande, avec des blocs réfrigérants.
Calculateurs (Calculators)Molarité / Dilution / Masse moléculaire / Conversion d’unités / Formulation in vivo / Solubilité
g/mol
Reviews
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