Trk receptors are a family of three receptor tyrosine kinases (TrkA, TrkB, and TrkC), each of which can be activated by one or more of the four neurotrophins nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and neurotrophins 3 and 4 (NT3 and NT4).
The TRK receptor family is made up of the transmembrane proteins TrkA, TrkB, and TrkC. These receptor tyrosine kinases are expressed in human neuronal tissue and are crucial for the physiology of nervous system development and function. Neurotrophins (NTs) activate these receptor tyrosine kinases. For TrkA, BDGF, NT-4/5, and TrkB and TrkC, respectively, these latter substances are specific ligands known as NGF and NT-3.
When a ligand binds to a receptor, the receptors begin to oligomerize and certain tyrosine residues in the intracytoplasmic kinase domain become phosphorylated. As a result of this action, signal transduction pathways that promote proliferation, differentiation, and survival in both healthy and malignant neuronal cells are activated.
Structure | Cat No. | Product Name | CAS No. | Product Description |
---|---|---|---|---|
V69585 | LPM4870108 | 2803679-07-2 | LPM4870108 is a potent and orally bioactive pan-Trk (WT/MT) inhibitor (antagonist) with IC50s of 0.2 nM, 2.4 nM, 3.5 nM and 2.3 nM for TrkC, TrkA, TrkAG595R and TrkAG667C, respectively. | |
V80204 | Multi-kinase-IN-6 | Multi-kinase-IN-6 (compound 10e) is a multi-kinase inhibitor that shows good enzyme inhibitory effect against TrkA, ALK2, c-KIT, EGFR, PIM1, CK2α, CHK1 and CDK2. | ||
V69582 | paltimatrectinib | 2353522-15-1 | Paltimatrectinib (compound I-147) is a potent tyrosine kinase inhibitor (antagonist) with IC50 of <10 nM for myosin-related kinase A (TrkA). | |
V69597 | Pan-Trk-IN-3 | 2763637-66-5 | Pan-Trk-IN-3 (Compound 11g) is a potent broad-spectrum inhibitor of Trk and its drug-resistant mutants. | |
V2756 | PF-06273340 | 1402438-74-7 | PF-06273340 is a potent, selective, and well-tolerated pan-Trk inhibitor with IC50 of 6, 4, 3 nM for TrkA, TrkB, Trk C respectively. | |
V69599 | Protein kinase inhibitor 5 | 2278204-94-5 | Protein kinase inhibitor 5 is a potent TRK-A inhibitor (antagonist) with IC50 of 1.8 nM. | |
V81238 | Protein kinase inhibitor 5 sulfate hydrate | Protein kinase inhibitor 5 sulfate hydrate is a potent TRK-A inhibitor (antagonist) with IC50 of 1.8 nM. | ||
V2684 | Selitrectinib (BAY 2731954; LOXO-195) | 2097002-61-2 | Selitrectinib (also known as BAY-2731954;LOXO-195) is a 2nd generation, potent and selective TRK TKI (tyrosine kinase inhibitor) designed to overcome acquired resistance mediated by recurrent kinase domain (solvent front and xDFG) mutations identified in multiple patients who have developed resistance to other TRK TKIs such aslarotrectinib (LOXO-101). | |
V69595 | TIY-7 | 2846435-83-2 | TIY-7 is a selective and orally bioactive tropomyosin receptor kinase (TRK) inhibitor. | |
V69589 | TRK-IN-12 | 2823342-34-1 | TRK-IN-12 (Compound 9e) is a potent TRK inhibitor (TRKG595R IC50 = 13.1 nM). | |
V81625 | TRK-IN-22 | TRK-IN-22 (compound 11) is an inhibitor (blocker/antagonist) of TRK. | ||
V69594 | TRK-IN-24 | 2937544-01-7 | TRK-IN-24 (compound 10g) is a Trk receptor blocker/inhibitor (antagonist) with IC50s of 5.21, 4.51, 6.77, 1.42 and 6.13 nM for TRKA, TRKC, TRKAG595R, TRKAG667C and TRKAF589L respectively. | |
V85512 | TRK-IN-25 | 2412309-60-3 | ||
V85733 | TRK-IN-26 | 2412309-52-3 | ||
V84359 | TRK-IN-27 | |||
V69596 | Trk-IN-6 | 2489327-43-5 | Trk-IN-6 has excellent potency against TRK mutants in vitro (IC50 = 0.2-0.7 nM). | |
V69603 | Trk-IN-7 | 2383011-61-6 | Trk-IN-7 (compound I-6) is a potent Trk inhibitor (antagonist) with IC50 of 0.25-10 nM for TRKA, TRKB and TRKC respectively. | |
V69591 | Trk-IN-8 | 2762200-57-5 | Trk-IN-8 is a potent TRKA inhibitor (antagonist) with IC50 of 0.42, 0.89 and 1.5 nM for TRKAa, TRKA(G595R) and TRKC(G623R) respectively (WO2021115401A1, compound 3). | |
V69584 | TrkA-IN-1 | 1680179-43-4 | TrkA-IN-1 is a potent and specific inhibitor of myosin-related kinase A (TrkA) with IC50 of 99 nM in a cell-based assay. | |
V76395 | TrkA-IN-3 | TrkA-IN-3 is a potent and subselective allosteric inhibitor of TrkA with IC50 of 22.4 nM. |