
STX-0119
CAS No. 851095-32-4
STX-0119( —— )
Catalog No. M35353 CAS No. 851095-32-4
STX-0119 is a selective, orally active STAT3 dimerization inhibitor that suppresses STAT3 transcription with an IC50 of 74 μM.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
5MG | 55 | Get Quote |
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10MG | 88 | Get Quote |
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25MG | 172 | Get Quote |
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50MG | 273 | Get Quote |
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100MG | 403 | Get Quote |
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500MG | Get Quote | Get Quote |
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1G | Get Quote | Get Quote |
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Biological Information
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Product NameSTX-0119
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NoteResearch use only, not for human use.
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Brief DescriptionSTX-0119 is a selective, orally active STAT3 dimerization inhibitor that suppresses STAT3 transcription with an IC50 of 74 μM.
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DescriptionSTX-0119 is a selective, orally active STAT3 dimerization inhibitor. STX-0119 inhibits STAT3 transcription with an IC50 of 74 μM.
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In VitroSTX-0119 (10-50 μM; 24 h) inhibits STAT3 dimerization through a direct interaction with the STAT3 protein and not via the modulation of upstream regulators such as JAK in HEK293 and MDA-MB-468 cells.STX-0119 (10-50 μM; 24 h) reduces the expression of STAT3 target proteins.Western Blot Analysis Cell Line:MDA-MB-468 cells Concentration:10, 20 and 50 μM Incubation Time:24 h Result:Reduced the expression of STAT3 target proteins, namely, c-myc, cyclin D1, and survivin, in a concentration-dependent manner. Did not suppress the expression of those STAT3-regulated oncoproteins.
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In VivoSTX-0119 (160 mg/kg; oral gavage; daily for 4 days) inhibits SCC-3 tumor growth in mice.The plasma concentration of STX-0119 (160 mg/kg; oral gavage) is maintained at >100 μg/mL (>260 μM), even at 8 h after administration.Animal Model:Male BALB/cA-ν/ν nude mice, SCC-3 lymphoma xenograft model Dosage:160 mg/kg Administration:Oral gavage, daily for 4 days Result:Suppressed the growth of SCC-3 cells significantly on the fourth day.
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Synonyms——
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PathwayJAK/STAT Signaling
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TargetSTAT
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RecptorSTAT
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Research Area——
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Indication——
Chemical Information
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CAS Number851095-32-4
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Formula Weight382.37
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Molecular FormulaC22H14N4O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 13.33 mg/mL (34.86 mM; Ultrasonic (<60°C)
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SMILESC(NC=1OC(=NN1)C2=CC=CO2)(=O)C=3C4=C(N=C(C3)C5=CC=CC=C5)C=CC=C4
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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. Matsuno K, et al. Identification of a New Series of STAT3 Inhibitors by Virtual Screening. ACS Med Chem Lett. 2010 Jul 13;1(8):371-5.?
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