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Ras Ras

Cat.No.  Name Information
M2562 ZCL278 ZCL278 is a selective Cdc42 GTPase inhibitor with Kd of 11.4 μM.
M6282 NSC 23766 NSC 23766 is an inhibitor of Rac GTPase targeting Rac activation by guanine nucleotide exchange factors (GEFs) with IC50 of ~50 μM in a cell-free assay; does not inhibit the closely related targets, Cdc42 or RhoA.
M9356 AMG-510 (Sotorasib) AMG-510 (Sotorasib) is a potent KRAS G12C covalent inhibitor.
M9428 MRTX849 (Adagrasib) MRTX849 (Adagrasib) is a potent, highly selective, oral available KRAS G12C inhibitor.
M45161 ARS-3248 ARS-3248 is a novel KRAS G12C inhibitor.
M45160 LY3499446 LY3499446 is a KRAS G12C covalent inhibitor for studies related to non-small cell lung cancer (NSCLC).
M45053 ACBI3 ACBI3 is a selective and potent pan-KRAS degrader.
M43844 MK-1084 MK-1084 is a KRAS G12C inhibitor that can be used in studies related to solid tumors.
M41938 CFL-120 CFL-120 is a potent KRasG12C inhibitor.
M41937 CFL-137 CFL-137 is a potent KRasG12C inhibitor.
M41936 Oligomycin D Oligomycin D (Rutamycin A) is an antibiotic.
M41935 KRAS inhibitor-22 KRAS inhibitor-22 is a potent inhibitor of K-Ras.
M41934 pan-KRAS-IN-3 pan-KRAS-IN-3 is a pan-KRAS inhibitor.
M41933 KRASG12C IN-2 KRASG12C IN-2 is an orally active KRASG12C inhibitor.
M41932 Rac1-IN-3 Rac1-IN-3 is a Rac1 inhibitor with an IC50 of 46.1 μM.
M41931 PAT-IN-2 PAT-IN-2 is a protein acyl transferases (PAT) inhibitor.
M41930 PAT-IN-1 PAT-IN-1 is a protein acyl transferases (PAT) inhibitor.
M41929 RMC-4998 RMC-4998 is a molecular glue compound with good antitumor activity.
M41928 SCH54292 SCH54292 is a potent Ras-GEF interaction inhibitor with IC50 of 0.7 μM.
M41927 KRAS G12C inhibitor 58 KRAS G12C inhibitor 58 is a KRAS G12C inhibitor, used in cancer research.
M41926 SOS1-IN-16 SOS1-IN-16 is a selective inhibitor of SOS1 with an IC50 of 7.2 nM.
M41925 PROTAC KRAS G12C degrader-3 PROTAC KRAS G12C degrader-3 is a potent KRAS G12C degrader for cancer research.
M41924 pan-KRAS-IN-4 pan-KRAS-IN-4 is a potent inhibitor of KRAS with IC50s of 0.37 nM (Kras G12C), 0.19 nM (Kras G12V), respectively.
M41923 TH-Z816 TH-Z816 is a reversible inhibitor againstKRAS(G12D)mutation with an IC50 value of 14 μM, which can be used in cancer research.




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