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Cat. No. Product Name Information
PC-62495

ARS-1630

ARS-1630 is the R-conformational atropisomer of ARS-1620, 1,000-fold less potent than ARS-1620 (1.2 ± 0.6 M-1s-1) and thus acts as a unique inactive control compound..
PC-62494

ARS-1620

KRAS G12C inhibitor

ARS-1620 is a potent, specific and covalent KRAS G12C inhibitor with an observed rate of 1,100±200 M-1S-1, shows >10-fold improved potency over the initial ARS-853.
PC-62490

NSC 658497

SOS1 inhibitor

NSC 658497 is a small molecule inhibitor of Ras GEF, SOS1, binds to SOS1 with Kd of 7 uM but no H-Ras, competitively suppresses SOS1-Ras interaction, and dose-dependently inhibits SOS1 GEF activity.
PC-62207

SCH 54292

Ras-GEF inhibitor

SCH 54292 is a potent Ras-GEF interaction inhibitor with IC50 of 0.7 uM.
PC-61154

Deltasonamide 2

Deltasonamide 2 (Deltasonamide-2) is a novel small molecule inhibitor of PDE6δ/KRas interaction with Kd of 385 pM.
PC-61153

Deltasonamide 1

PDE6δ/KRas inhibitor

Deltasonamide 1 is a novel small molecule inhibitor of PDE6δ/KRas interaction with Kd of 203 pM.
PC-61152

Deltazinone 1

Deltazinone 1 (Deltazinone1) is a novel highly selective PDEδ inhibitor that inhibits PDEδ/Ras interaction with Kd of 8±4 nM.
PC-60886

UC-857993

SOS1-Ras inhibitor

UC-857993 is a small molecule inhibitor of guanine nucleotide exchange factor (GEF) catalytic activity that binds to SOS1 (Kd=14.7 uM) and disrupts GEF-Ras interaction.
PC-60885

UC-773587

SOS1-Ras inhibitor

UC-773587 is a small molecule inhibitor of guanine nucleotide exchange factor (GEF) catalytic activity that binds to SOS1 (Kd=3.4 uM) and disrupts GEF-Ras interaction.
PC-70154

ML-162

ML-162 (ML162) is a small-molecule probe that selectively kills cells induced to express mutant RAS, inhibits BJeLR (expressing HRAS G12V) cell lines with IC50 of 25 nM.
PC-45721

ML-098

Ras activator

ML-098 (CID-7345532) is a small molecule pan activator families of Ras-related GTPases (EC50=77-588 nM for Rab7, Rab-2A, Cdc42, Rac1).
PC-45673

ARS-853

KRAS G12C inhibitor

ARS-853 (ARS853) is a mutant-specific, covalent inhibitor of KRAS G12C with IC50 of 2.5 uM.

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