Catalog |
name |
Description |
price |
R-R-2969 |
BAY-293 CAS No.2244904-70-7 |
BAY-293/CAS No.2244904-70-7, 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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R-R-2970 |
GGTI298 Trifluoroacetate CAS No.1217457-86-7 |
GGTI298 Trifluoroacetate/CAS No.1217457-86-7 is a CAAZ peptidomimetic geranylgeranyltransferase I (GGTase I) inhibitor, which can inhibit Rap1A with IC50 of 3 μM; little effect on Ha-Ras with IC50 of >20 μM. |
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R-R-2971 |
MBQ-167 CAS No.2097938-73-1 |
MBQ-167/CAS No.2097938-73-1 is a dual Rac/Cdc42 inhibitor, with IC50s of 103 nM for Rac 1/2/3 and 78 nM for Cdc42 in MDA-MB-231 cells, respectively. |
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R-R-2972 |
MRTX0902 CAS No.2654743-22-1 |
MRTX0902/CAS No.2654743-22-1 is an orally active and potent SOS1 inhibitor with an IC50 of 46 nM (WO2021127429A1; Example 12-10). |
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R-R-2973 |
Opnurasib CAS No.2653994-08-0 |
Opnurasib (JDQ-443) (NVP-JDQ443)/CAS No.2653994-08-0 is an orally active, potent, selective, and covalent KRAS G12C inhibitor (extracted from patent WO2021120890A1). Opnurasib shows antitumor activity. |
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R-R-2974 |
LC-2 CAS No.2502156-03-6 |
LC-2/CAS No.2502156-03-6 is a potent and first-in-class von Hippel-Lindau-based PROTAC capable of degrading endogenous KRAS G12C, with DC50s between 0.25 and 0.76 μM. LC-2 covalently binds KRAS G12C with a MRTX849 warhead and recruits the E3 ligase VHL, inducing rapid and sustained KRAS G12C degradation leading to suppression of MAPK signaling in both homozygous and heterozygous KRAS G12C cell lines. |
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R-C-1275 |
JNJ 31020028 CAS No. 1094873-14-9 |
JNJ-31020028 is a selective brain penetrant antagonist of neuropeptide Y2 receptor with high affinity(pIC50=8.07,human;pIC50=8.22 rat);>100-fold selective versus human Y1/Y4/Y5 receptors. |
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R-R-2975 |
RMC-6291 CAS No.2641998-63-0 |
RMC-6291/CAS No.2641998-63-0 is an orally active and covalent inhibitor of KRASG12C(ON). RMC-6291 forms a tri-complex within tumor cells between KRASG12C(ON) and cyclophilin A (CypA). Thus, RMC-6291 prevents KRASG12C(ON) from signaling via steric blockade of RAS effector binding. RMC-6291 inhibits ERK signaling and induced apoptosis in KRASG12C-mutant H358 cells. RMC-6291 also inhibits the proliferation of KRASG12C mutant cells with a median IC50 of 0.11 nM. |
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R-R-2976 |
CASIN CAS No.425399-05-9 |
CASIN/CAS No.425399-05-9 is a selective GTPase Cdc42 inhibitor with an IC50 of 2 uM. CASIN can be used for the research of cancer. |
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R-R-2977 |
Salirasib CAS No.162520-00-5 |
Salirasib/CAS No.162520-00-5 is a Ras inhibitor that inhibits specifically both oncogenically activated Ras and growth factor receptor-mediated Ras activation, resulting in the inhibition of Ras-dependent tumor growth. |
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