
SKLB 1028
CAS No. 1350544-93-2
SKLB 1028( —— )
Catalog No. M34711 CAS No. 1350544-93-2
SKLB 1028 (Ruserontinib) is a new type of oral multikinase inhibitor of EGFR, FLT3, and Abl. SKLB 1028 shows excellent activity in FLT3-driven AML models and considerable potency in CML models containing Abl mutants.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 78 | Get Quote |
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5MG | 116 | Get Quote |
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10MG | 187 | Get Quote |
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25MG | 365 | Get Quote |
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50MG | 542 | Get Quote |
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100MG | 759 | Get Quote |
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500MG | 1557 | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameSKLB 1028
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NoteResearch use only, not for human use.
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Brief DescriptionSKLB 1028 (Ruserontinib) is a new type of oral multikinase inhibitor of EGFR, FLT3, and Abl. SKLB 1028 shows excellent activity in FLT3-driven AML models and considerable potency in CML models containing Abl mutants.
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DescriptionRuserontinib (SKLB1028) is an orally active multikinase inhibitor of EGFR, FLT3 and Abl, with an IC50 value of 55 nM for human FLT3, and has antitumor activity.
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In Vitro——
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In VivoAnimal Model:MV4-11 and K562 xenograft NOD-SCID modelsDosage:5, 10, 20 mg/kg,70 mg/kg Administration:orally once daily, 18 days Result:Prevented tumor growth at a dose of 5 mg/kg, and caused rapid and complete tumor regression in both groups of mice at a dose of 10 or 20 mg/kg.Significantly inhibited the proliferation and induced apoptosis of MV4-11 and K562 cells at a dose of 70 mg/kg.
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Synonyms——
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PathwayAngiogenesis
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TargetEGFR
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RecptorEGFR | FLT | Bcr-Abl
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Research Area——
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Indication——
Chemical Information
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CAS Number1350544-93-2
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Formula Weight443.55
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Molecular FormulaC24H29N9
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (563.63 mM; Ultrasonic )
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SMILESC(C)(C)N1C=2C(N=C1NC=3C=CC=NC3)=CN=C(NC4=CC=C(C=C4)N5CCN(C)CC5)N2
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Z-X Cao, et al. SKLB1028, a novel oral multikinase inhibitor of EGFR, FLT3 and Abl, displays exceptional activity in models of FLT3-driven AML and considerable potency in models of CML harboring Abl mutants. Leukemia. 2012 Aug;26(8):1892-5.?
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