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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-73005

TH-Z835

KRAS G12D inhibitor

TH-Z835 is a potent, mutant selective KRAS (G12D) inhibitor with IC50 of 1.6 uM.
PC-72978

PHT-7.3

Cnksr1 (Cnk1) inhibitor

PHT-7.3 (Cnksr1 (Cnk1) inhibitor PHT-7.3) is a selective inhibitor of connector enhancer of kinase suppressor of Ras 1 (Cnk1) pleckstrin homology (PH) domain (Kd=4.7 μM).
PC-72963

KRA-533

KRAS agonist

KRA-533 (NSC112533, KRA533) is a small molecule KRAS agonist that binds the GTP/GDP-binding pocket of KRAS.
PC-72958

ASP2453

KRAS G12C inhibitor

ASP2453 (ASP-2453) is a novel potent, selective and covalent KRAS G12C inhibitor, inhibits SOS-mediated interaction between KRAS G12C and Raf with IC50 of 40 nM.
PC-72897

JDQ443

KRAS G12C inhibitor

JDQ443 (Opnurasib, NVP-JDQ443) is a potent, mutant-selective, covalent KRAS G12C inhibitor.
PC-72832

NSC290956

Kras inhibitor

NSC290956 (Spiclomazine, Clospirazine) is a small molecule inhibitor of KRas with Kd of 21.3 uM.
PC-72332

BI-2852

KRAS inhibitor

BI-2852 (BI 2852) is a potent pan-Ras inhibitor, targets GTP-bound KRAS, binds to KRASG12D with a KD of 740 nM (ITC), inhibits GTP-KRAS G12D binding to effectors like SOS1, CRAF and PI3Kα with an IC50 of 490, 770 and 500 nM.
PC-72331

MRTX1133

KRAS G12D inhibitor

MRTX-1133 (MRTX1133) is a potent, selective and noncovalent inhibitor KRAS G12D with SPR Kd of 0.2 nM, AlphaLISA IC50 of 5 nM.
PC-72314

KRAS G12C Pipetide LVVVGACGVGK

KRAS G12C Pipetide (LVVVGACGVGK) is a KRas4B G12C allele-specific N-terminal mutant tryptic peptide.
PC-72313

LY-3537982

KRAS-G12C inhibitor

LY-3537982 (LY3537982) is a highly selective and potent KRAS-G12C inhibitor, selectively inhibits growth of KRAS G12C mutant cells (IC50=1-60 nM).
PC-72227

MRTX849

KRAS G12C inhibitor

MRTX849 (Adagrasib, MRTX-849) is a potent, selective, and covalent KRAS G12C inhibitor, inhibits KRAS-dependent signaling.
PC-72222

Chelidonine

STK19 inhibitor

Chelidonine (Stylophorin, (+)-Chelidonine) is a potent, selective, ATP-competitive inhibitor of STK19 kinase activity, inhibits STK19-mediated NRAS S89 phosphorylation with IC50 of 125 nM, inhibits NRAS-mediated signaling.

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