c-RET
The c-RET proto-oncogene, which was originally identified as a transforming gene by transfection of T-cell lymphoma DNA into NIH3T3 cells, is a member of the receptor tyrosine kinase (RTK) gene superfamily that encodes a receptor tyrosine kinase involved in the regulation of glial cell line-derived neurotrophic factor (GDNF) signaling. Signaling proteins, such as Grb7/Grb10, PLCγ, Shc/Enigma and Grb2, are recruited by activated c-RET protein through binding to the phosphorylated tyrosine residues in c-RET protein’s COOH-terminal sequence, Y905, Y1015, Y1062 and Y1096 respectively. Moreover, results of in vivo studies suggest mutations of c-RET have been implicated in tumorigenesis, in which c-RET mRNA and/or protein have been found in tumors of neuroectodermal origin as well as in human neuroblastoma cell lines.
Products for c-RET
- Cat.No. Nombre del producto Información
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GC16362
AD57 (hydrochloride)
polypharmacological cancer therapeutic that inhibits RET.
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GC16391
Amuvatinib (MP-470, HPK 56)
HPK56, MP470
A multi-targeted RTK inhibitor -
GC15217
Danusertib (PHA-739358)
PHA-739358
A pan-Aurora kinase and Abl inhibitor -
GC14606
Regorafenib hydrochloride
A multi-kinase inhibitor
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GC14534
Regorafenib monohydrate
A multi-kinase inhibitor
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GC13194
RPI-1
RPI-1 es un inhibidor especÍfico de la tirosina cinasa de 2-indolinona Ret disponible por vÍa oral. RPI-1 inhibe la proliferaciÓn, la fosforilaciÓn de tirosina Ret, la expresiÓn de proteÍna Ret y la activaciÓn de PLCgamma, ERK y AKT en células TT de carcinoma medular de tiroides humano. Actividad antitumoral.
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GC15307
SU5416
NSC 696819, Semaxinib, Sugen 5416, VEGFR 2 Kinase Inhibitor
SU5416 is a potent small molecule vascular endothelial growth factor receptor (VEGFR) inhibitor. -
GC10035
TG101209
An inhibitor of JAK2, FLT3, RET, and JAK3