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Raf

RAF kinases are a family of three serine/threonine-specific protein kinases that are related to retroviral oncogenes. The mouse sarcoma virus 3611 contains a RAF kinase-related oncogene that enhances fibrosarcoma induction. RAF is an acronym for Rapidly Accelerated Fibrosarcoma. RAF kinases participate in the RAS-RAF-MEK-ERK signal transduction cascade, also referred to as the mitogen-activated protein kinase (MAPK) cascade. Activation of RAF kinases requires interaction with RAS-GTPases.
Signaling Pathways | Target | TargetMol
Cat. No. Product name CAS No. Purity Chemical Structure
T3711 RAF709 1628838-42-5 99.43%
RAF709
RAF709 is a novel Raf kinase inhibitor with IC50s of 0.5 and 1.8 nM for c-Raf and b-Raf, respectively.
T8745 PROTAC BRAF-V600E degrader-1 2417296-84-3 99.43%
PROTAC BRAF-V600E degrader-1
PROTAC BRAF-V600E degrader-1 (Compound 23) selectively induces degradation of BRAF-V600E but not wildtype BRAF.
T9693 TBAP-001 1777832-90-2 99.3%
TBAP-001
TBAP-001 is a RAF kinase inhibitor, with an IC50 of 62 nM in BRAF V600E kinase assay and an IC50 of 18 nM in Cell-Based Phosho-ERK Assay.
T63644 Exarafenib 2639957-39-2 99.26%
Exarafenib
Exarafenib (RAF/KIN_2787) is a potent and orally available pan-RAF inhibitor.Exarafenib has antitumor activity and acts by inhibiting downstream MAPK pathway sig...
T1892 Kobe2602 454453-49-7 99.24%
Kobe2602
Kobe 2602 is an inhibitor of Ras that exhibits anticancer chemotherapeutic activities.
T2070 Agerafenib 1188910-76-0 99.23%
Agerafenib
Agerafenib (CEP32496) is a highly potent inhibitor of BRAF.
T0093 Sorafenib tosylate 475207-59-1 99.2%
Sorafenib tosylate
Sorafenib tosylate (Bay 43-9006) is a potent multikinase inhibitor (IC50s: 6/20/22 nM for Raf-1/VEGFR-3/B-Raf).
T6296 RAF265 927880-90-8 99.18%
RAF265
RAF265 (CHIR-265) (CHIR-265) is a potent selective inhibitor of C-Raf/B-Raf/B-Raf V600E with IC50 of 3-60 nM, and exhibits potent inhibition on VEGFR2 phosphoryl...
T6052 GW 441756 504433-23-2 98.99%
GW 441756
GW 441756 is a specific Tropomyosin-related kinase A (TrkA) inhibitor with an IC50 value of 2 nM.
TP2358 KRPEP-2D acetate TP2358 98.94%
KRPEP-2D acetate
KRPEP-2D acetate was identified as a K-Ras(G12D) selective inhibitory peptide against the G12D mutant of K-Ras, which is a key member of the Ras protein family a...
T1886 TAK-632 1228591-30-7 98.92%
TAK-632
TAK-632 is a potent pan-Raf inhibitor.
T6003 GSK1904529A 1089283-49-7 98.89%
GSK1904529A
GSK1904529A (GSK 4529) is a specific inhibitor of IGF-1R (IC50=27 nM) and IR(IC50=25 nM) .
T60029 SOS1-IN-11 2654741-64-5 98.79%
SOS1-IN-11
SOS1-IN-11 is an effective inhibitor of SOS1 (IC50 = 30 nM).
T2074 Raf inhibitor 1 1093100-40-3 98.78%
Raf inhibitor 1
B-Raf inhibitor 1 (B-Raf inhibitor 1) is a potent and selective B-Raf inhibitor.
T9585 GNE-9815 2729996-45-4 98.73%
GNE-9815
GNE-9815 (3-(2-cyanopropan-2-yl)-N-[2-fluoro-4-methyl-5-(7-methyl-8-oxo-7,8-dihydropyrido[2,3-d]pyridazin-3-yl)phenyl]benzamide) is a high kinase-selective inhib...
T5469 K-Ras-IN-1 84783-01-7 98.72%
K-Ras-IN-1
K-Ras-IN-1 is a K-Ras inhibitor.
T11224 Rineterkib 1715025-32-3 98.4%
Rineterkib
Rineterkib (ERK-IN-1) is an inhibitor of RAF and ERK1/2 activating mutations in the MAPK pathway.
T9755 MRTX0902 2654743-22-1 98.37%
MRTX0902
MRTX0902 is an effective and high selective inhibitor of SOS1 with an IC50 of 46 nM and a Ki of 2 nM.
T2327 Pelitinib 257933-82-7 98.37%
Pelitinib
Pelitinib (EKB-569) (EKB-569) is an effective irreversible EGFR inhibitor (IC50: 38.5 nM).
T6556 K-Ras(G12C) inhibitor 9 1469337-91-4 98.31%
K-Ras(G12C) inhibitor 9
K-Ras(G12C) inhibitor 9 is an allosteric inhibitor of oncogenic K-Ras(G12C).
RAF709
T3711
RAF709 is a novel Raf kinase inhibitor with IC50s of 0.5 and 1.8 nM for c-Raf and b-Raf, respectively.
PROTAC BRAF-V600E degrader-1
T8745
PROTAC BRAF-V600E degrader-1 (Compound 23) selectively induces degradation of BRAF-V600E but not wildtype BRAF.
TBAP-001
T9693
TBAP-001 is a RAF kinase inhibitor, with an IC50 of 62 nM in BRAF V600E kinase assay and an IC50 of 18 nM in Cell-Based Phosho-ERK Assay.
Exarafenib
T63644
Exarafenib (RAF/KIN_2787) is a potent and orally available pan-RAF inhibitor.Exarafenib has antitumor activity and acts by inhibiting downstream MAPK pathway sig...
Kobe2602
T1892
Kobe 2602 is an inhibitor of Ras that exhibits anticancer chemotherapeutic activities.
Agerafenib
T2070
Agerafenib (CEP32496) is a highly potent inhibitor of BRAF.
Sorafenib tosylate
T0093
Sorafenib tosylate (Bay 43-9006) is a potent multikinase inhibitor (IC50s: 6/20/22 nM for Raf-1/VEGFR-3/B-Raf).
RAF265
T6296
RAF265 (CHIR-265) (CHIR-265) is a potent selective inhibitor of C-Raf/B-Raf/B-Raf V600E with IC50 of 3-60 nM, and exhibits potent inhibition on VEGFR2 phosphoryl...
GW 441756
T6052
GW 441756 is a specific Tropomyosin-related kinase A (TrkA) inhibitor with an IC50 value of 2 nM.
KRPEP-2D acetate
TP2358
KRPEP-2D acetate was identified as a K-Ras(G12D) selective inhibitory peptide against the G12D mutant of K-Ras, which is a key member of the Ras protein family a...
TAK-632
T1886
TAK-632 is a potent pan-Raf inhibitor.
GSK1904529A
T6003
GSK1904529A (GSK 4529) is a specific inhibitor of IGF-1R (IC50=27 nM) and IR(IC50=25 nM) .
SOS1-IN-11
T60029
SOS1-IN-11 is an effective inhibitor of SOS1 (IC50 = 30 nM).
Raf inhibitor 1
T2074
B-Raf inhibitor 1 (B-Raf inhibitor 1) is a potent and selective B-Raf inhibitor.
GNE-9815
T9585
GNE-9815 (3-(2-cyanopropan-2-yl)-N-[2-fluoro-4-methyl-5-(7-methyl-8-oxo-7,8-dihydropyrido[2,3-d]pyridazin-3-yl)phenyl]benzamide) is a high kinase-selective inhib...
K-Ras-IN-1
T5469
K-Ras-IN-1 is a K-Ras inhibitor.
Rineterkib
T11224
Rineterkib (ERK-IN-1) is an inhibitor of RAF and ERK1/2 activating mutations in the MAPK pathway.
MRTX0902
T9755
MRTX0902 is an effective and high selective inhibitor of SOS1 with an IC50 of 46 nM and a Ki of 2 nM.
Pelitinib
T2327
Pelitinib (EKB-569) (EKB-569) is an effective irreversible EGFR inhibitor (IC50: 38.5 nM).
K-Ras(G12C) inhibitor 9
T6556
K-Ras(G12C) inhibitor 9 is an allosteric inhibitor of oncogenic K-Ras(G12C).
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TargetMol