
SOS1-IN-15
CAS No. 2793404-47-2
SOS1-IN-15( —— )
Catalog No. M36502 CAS No. 2793404-47-2
SOS1-IN-15 is an orally active and potent SOS1 inhibitor with potential antitumor activity.SOS1-IN-15 is used in the study of colon cancer.
Purity : >98% (HPLC)






Size | Price / USD | Stock | Quantity |
2MG | 201 | Get Quote |
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5MG | 312 | Get Quote |
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10MG | 511 | Get Quote |
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25MG | 908 | Get Quote |
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50MG | 1609 | 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 NameSOS1-IN-15
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NoteResearch use only, not for human use.
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Brief DescriptionSOS1-IN-15 is an orally active and potent SOS1 inhibitor with potential antitumor activity.SOS1-IN-15 is used in the study of colon cancer.
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DescriptionSOS1-IN-15 (Compound 37) is an orally active SOS1 inhibitor with an IC50 of 5 nM. SOS1-IN-15 is a promising agent candidate for the research of KRAS-driven cancer.
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In VitroSOS1-IN-15 (Compound 37) (0.1 nM-0.1 mM; 72 h) displays prominent inhibitory activities in Mia-paca-2 cancer cells (IC50 = 178 ± 42 nM).SOS1-IN-15 has a limited inhibition of CYP and hERG.Cell Proliferation Assay Cell Line:Mia-paca-2 pancreas cancer cells Concentration:0.1 nM-0.1 mM Incubation Time:72 h Result:Inhibited the proliferation with an IC50 of 178 ± 42 nM.
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In VivoSOS1-IN-15 (Compound 37) (50 mg/kg; p.o.; daily for 22 days) inhibits tumor volume in mice.Animal Model:BALB/c nude mice bearing Mia-paca-2 pancreas tumorsDosage:50 mg/kg Administration:Oral administration, daily for 22 daysResult:Showed 49% tumor inhibition. No animal mortality and significant difference in the mice’s body weight were observed during the study period.Animal Model:Male CD-1 Mice Dosage:20 mg/kg Administration:Oral administration (Pharmacokinetic Analysis).a Compounds (20 mg/kg) were P.O. dosed in a mixture of 63% water + 30% PEG +5 % DMSO + 2% Tween 80 in male ICR mice (n = 3). Abbreviations: T1/2, elimination half-life; Tmax, plasma peak time after administration; Cmax, maximum plasma concentration; AUC, area under concentration-time curve. MRT, mean residence time; Kel, elimination rate constant.
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Synonyms——
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PathwayMAPK/ERK Signaling
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TargetRaf
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RecptorRaf
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Research Area——
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Indication——
Chemical Information
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CAS Number2793404-47-2
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Formula Weight536.548
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Molecular FormulaC28H27F3N6O2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 5 mg/mL (9.32 mM; Ultrasonic (<60°C)
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SMILESC(=O)(C1(C#N)CC1)N2C[C@]3(N(CC2)C=4C(OC3)=CC=5C(C4)=C(N[C@H](C)C6=C(F)C(C(F)F)=CC=C6)N=C(C)N5)[H]
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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. Zhang S, et al. Design and Structural Optimization of Orally Bioavailable SOS1 Inhibitors for the Treatment of KRAS-Driven Carcinoma. J Med Chem. 2022 Nov 17.?
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