6 Results for "

son of sevenless 1

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "son of sevenless 1" in MCE Product Catalog:

12
12 Cited Publications
Cat. No.: HY-125817
CAS No.: 2230836-55-0
Purity:  99.95%
Target:  

SOS1 Ras p38 MAPK

Research Areas:  

Cancer

BI-3406 (compound I-6) is an orally active, highly potent and selective inhibitor of the interaction between KRAS and Son of Sevenless 1 (SOS1) with an IC50 of 6 nM. BI-3406 potently reduces the formation of GTP-loaded KRAS, and inhibits MAPK pathway signaling. BI-3406 has anticancer activity .
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2
2 Cited Publications
Cat. No.: HY-114398
CAS No.: 2244904-70-7
Purity:  98.97%
Target:  

SOS1 Ras

Research Areas:  

Cancer

BAY-293, a valuable chemical probe, blocks RAS activation via disruption of the KRAS-SOS1 interaction with an IC50 of 21 nM. BAY-293 is a potent inhibitor of Son of Sevenless 1 (SOS1). SOS1 is the guanine nucleotide exchange factor (GEF) and activator of RAS .
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Cat. No.: HY-176170
Target:  

SOS1

Research Areas:  

Cancer

SOS1-IN-19 (Compound 10i) is a potent inhibitor of SOS1 (Son of Sevenless 1) with an IC50 value of 165.2 nM. SOS1-IN-19 blocks KRAS activation by preventing GDP/GTP exchange in KRAS signaling pathway. SOS1-IN-19 is promising for research of KRAS-driven cancers (e.g., NSCLC and colorectal cancer) .
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Cat. No.: HY-161655
CAS No.: 3043923-70-9
Research Areas:  

Cancer

SOS1 Ligand intermediate-5 is the ligand for son of sevenless 1 (SOS1). SOS1 Ligand intermediate-5 is utilized for synthesis of PROTAC SOS1 degrader-10 (HY-161654) .
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Cat. No.: HY-172221
Target:  

SOS1 Ras ERK

Research Areas:  

Cancer

SOS1-IN-18 (Compound 8) is the inhibitor for Son of Sevenless 1 protein (SOS1) with a KD of 2.6 nM, and inhibits SOS1-KRAS G12C interaction with an IC50 of 3.4 nM. SOS1-IN-18 inhibits the phosphorylation of ERK in H358 with an IC50 of 31 nM, inhibits the proliferation of H358 with an IC50 of 5 nM .
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Cat. No.: HY-175326
CAS No.: 2767633-04-3
Target:  

SOS1

Research Areas:  

Cancer

SOS1-IN-21 is an orally active inhibitor of son of Sevenless 1 (SOS1) with an IC50 of 15 nM. SOS1 is a guanine nucleotide exchange factor (GEF) that activates KRAS by facilitating the exchange of GDP for GTP. SOS1-IN-21 exhibits potent antiproliferative activity, with IC50 values of 16 nM in NCI-H358 and 17 nM in Mia Paca-2 cell proliferation assays. SOS1-IN-21 exhibits significant antitumor activity in the Mia Paca-2 xenograft model. SOS1-IN-21 can be used for the study of KRAS mutant tumors, such as pancreatic cancer .
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