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首页-小分子抑制剂&激动剂-Ras-Raf-MAPK-ERK Pathway-Ras

Request The Product List ofRas Ras

Cat. No. Product Name Information
PC-45476

K-Ras G12C-IN-1

KRAS G12C inhibitor

K-Ras G12C-IN-1 is a novel and irreversible inhibitor of mutant K-ras G12C.
PC-28768

RO7783903

KRAS G12C inhibitor

RO7783903 (RO3903) is a covalent KRAS G12C tricomplex inhibitor, over comes secondary KRAS mutations that drive clinical resistance to guanosine diphosphate (GDP)-bound (OFF) state inhibitors.
PC-27893

SCH51344

Ras/Rac inhibitor, MTH1 inhibitor

SCH51344 (SCH 51344) is a potent inhibitor of RAS transformation, specifically blocks membrane ruffling induced by activated forms of H-RAS, K-RAS, N-RAS and RAC, also potently inhibits MTH1 (NUDT1) with IC50 of 215 nM, 410 nM, and 675 nM for MTH1 substrates dGTP, 8-oxo-dGTP, and 2-OH-dATP.
PC-27417

Debecarasib

KRAS G12D inhibitor

Debecarasib is a potent and orally bioavailable inhibitor of GDP-bound KRAS G12D, shows highly selectivity for KRAS G12D against wild-type KRAS and other RAS mutations or amplifications.
PC-27366

AM-2383

pan-KRAS inhibitor

AM-2383 is a potent, selective pan-KRAS inhibitor that blocks signaling via both the GDP(off)- and GTP(on)-bound states of KRAS, potently bind to a diverse set of common oncogenic KRAS mutants with IC50 of 2-10 nM in NanoBRET KRAS target engagement assay, also potently bind to KRAS WT (IC50=2 nM).
PC-27036

JMKX1899

KRAS G12C inhibitor

JMKX1899 is a potent and selective, covalent, BBB-penetrating KRAS G12C inhibitor.
PC-26521

SOS1 inhibitor SL43

SOS1 inhibitor

SOS1 inhibitor SL43 is a potent, selective and orally bioavailable SOS1 inhibitor with binding KD of 0.16 uM, potently disrupts the SOS1-KRASG12C interaction with IC50 of 13 nM, broadly inhibits SOS1-mediated nucleotide exchange on multiple KRAS mutants (G12C, G12V and G12D; IC50 = 13.4-29.1 nM).
PC-26395

XMU-MP-9

K-RAS mutants degrader

XMU-MP-9 is bifunctional, specific small molecule K-RAS mutants degrader, facilitates NEDD4-1-mediated ubiquitination and degradation of various oncogenic K-RAS mutants.
PC-26309

BI-1830

KRAS G12D inhibitor

BI-1830 is a specific small molecule KRAS(G12D)-D92C binder, binds to D92-adjacent pocket stabilizes KRAS and inhibits signaling, inhibits phospho-ERK levels in KRAS(G12D)-D92C cells.
PC-25991

KRAS G12C inhibitor compound 8

KRAS G12C inhibitor

KRAS G12C inhibitor compound 8 is a potent, specific KRAS G12C dual inhibitor with IC50 of 10 nM (GDP Exchange Inhibition) and 133 nM (RAS/RAF Disruption), covalently modifies both KRAS G12C inactive and active states.
PC-25960

PDE6δ-IN-2

PDEδ inhibitor

PDE6δ-IN-2 is a potent, small molecule PDE6δ (PDE6delta, PDE6D) inhibitor with KD of <30 nM in displacement assays, inibits binding of PDE6δ to farnesylated Ras proteins and inhibits oncogenic Ras signaling in cells.
PC-25959

PDE6δ-IN-1

PDEδ inhibitor

PDE6δ-IN-1 is a potent, small molecule PDE6δ (PDE6delta, PDE6D) inhibitor with KD of <30 nM in displacement assays, inibits binding of PDE6δ to farnesylated Ras proteins and inhibits oncogenic Ras signaling in cells.

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