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Cat. No. Product Name Information
PC-61490

LM11A-31

p75 inhibitor

An orally available, brain penetrant p75NTR ligand that blocks p75-mediated cell death, also increases proliferation and survival of hippocampal neural progenitors.
PC-61489

LM11A-31 dihydrochloride

p75 inhibitor

An orally available, brain penetrant p75NTR ligand that blocks p75-mediated cell death, also increases proliferation and survival of hippocampal neural progenitors.
PC-70266

Gambogic amide

TrkA agonist

Gambogic amide is a potent, selective high affinity TrkA receptor agonist with Kd of 75 nM.
PC-70256

Belizatinib

ALK/TRK inhibitor

Belizatinib (TSR-011) is a potent, dual ALK and TrkA, TrkB and TrkC inhibitor, exhibits high affinity for wild-type recombinant ALK kinase activity with IC50 of 0.7 nM.
PC-70345

7,8-Dihydroxyflavone

TrkB agonist

7,8-Dihydroxyflavone (7,8-DHF) is a naturally occurring flavone that has been found to act as a potent and selective agonist of TrkB with Kd of 320 nM.
PC-60903

LOXO-195 R racemate

Trk inhibitor

The R racemate of LOXO-195, a potent, selective, next-generation Trk tyrosine kinase inhibitor with IC50 of 0.6 nM and <2.5 nM for WT TrkA and WT TrKC, respectively..
PC-60901

Selitrectinib

Trk inhibitor

LOXO-195 (Selitrectinib, LOXO195) is a potent, selective, next-generation Trk tyrosine kinase inhibitor with IC50 of 0.6 nM and <2.5 nM for WT TrkA and WT TrKC, respectively.
PC-70173

Lestaurtinib

JAK2/FLT3 inhibitor

Lestaurtinib (KT-5555, CEP-701) is a potent, orally active JAK2, FLT3 and TrkA inhibitor with IC50 of 0.9 nM, 3 nM and < 25 nM, respectively.
PC-70172

CEP-751

Trk inhibitor

CEP-751 (KT-6587) is potent inhibitor of TrkA with IC50 of 2.9 nM, also inhibits TrkB, TrkC.
PC-70171

K252a

TrkB inhibitor

K252a (SF2370) is a potent, non-selective tyrosine protein kinase inhibitor for Trk family, CaMK and other phosphorylase kinases.
PC-45453

GW441756

TrkA inhibitor

GW441756 is a potent, specific TrkA inhibitor with IC50 value of 2 nM.
PC-22603

ICP-723

pan-TRK inhibitor

ICP-723 (Zurletrectinib) is a potent pan-TRK Inhibitor with IC50 of <1 nM for TRKA, TRKB and TRKC, potently inhibits activities of wild-type and some mutant forms of TRK.

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