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Search Results for " Fgr "

ターゲット

12

阻害剤

1

天然化合物

2

リコンビナントタンパク質

カタログ番号 製品名 別名 ターゲット
T13186 TL02-59 Apoptosis , Src , Hck
T6078 Saracatinib AZD0530 EGFR , Src , BTK , Autophagy
Saracatinib (AZD0530) (AZD0530) is an effective Src inhibitor (IC50: 2.7 nM), and effective to Lck, Fyn, Lyn, Blk, Fgr and c-Yes.
T2640 Rebastinib DCC2036,DCC 2036,DCC-2036 Apoptosis , FLT , Bcr-Abl , Src
DCC-2036 (Rebastinib (DCC-2036)) is a conformational control Bcr-Abl inhibitor for Abl1(WT, IC50: 0.8 nM) and Abl1(T315I, IC50: 4 nM), also inhibits LYN, SRC, HCK, FGR, FLT3, KDR, and Tie-2, and low activity to c-Kit. Re...
T3211 Midostaurin N-Benzoylstaurosporine,PKC412,CGP41231,CGP 41251 Others , PKC
PKC412(Midostaurin (PKC412); CGP41231; CGP41251) is a broad spectrum protein kinase inhibitor. Midostaurin inhibits protein kinase C alpha (PKCalpha), vascular endothelial growth factor receptor 2 (VEGFR2), c-kit, platel...
T13186L TL02-59 dihydrochloride Src
TL02-59 dihydrochloride is an orally active inhibitor of Src-family kinase Fgr (IC50: 0.03 nM).
T39129 BMS-986143
BMS-986143, an orally active, reversible BTK inhibitor with an IC50 value of 0.26 nM, is designed for autoimmune disease research. Additionally, it targets TEC, BLK, BMX, TXK, FGR, YES1, and ITK, exhibiting IC50s of 3 nM...
T13157L TG 100801 Hydrochloride VEGFR
TG 100801 Hydrochloride is a prodrug to treat age-related macular degeneration. TG 100572 is a inhibitor of multi-targeted kinase(IC50s of 2, 7, 2, 16, 13, 5, 0.5, 6, 0.1, 0.4, 1, 0.2 for VEGFR1, VEGFR2, FGFR1, FGFR2, PD...
T13156 TG 100572 VEGFR
T13156L TG 100572 Hydrochloride VEGFR , FGFR , PDGFR , Src
T2696 PRT062607 hydrochloride PRT062607 (P505-15, BIIB057) HCl,P505-15 Hydrochloride MLK , Syk , Src
PRT062607 hydrochloride (P505-15 Hydrochloride) is a selective inhibitor of Syk (IC50: 1 nM). It displays at least 80-fold selectivity for Syk over other kinases.
T2709 TAK-901 TAK901 JAK , CDK , Src , Aurora Kinase
TAK-901 has been used in trials studying the treatment of Lymphoma, Myelofibrosis, Multiple Myeloma, Myeloid Metaplasia, and Advanced Solid Tumors, among others.
T1835 Ibrutinib PCI-32765 Tyrosine Kinases , Src , BTK , Ligands for Target Protein for PROTAC
Ibrutinib (PCI-32765) is an irreversible inhibitor of BTK (IC50: 0.5 nM) that selectively blocks B cell activation.
カタログ番号 製品名 別名 ターゲット
T6680 Staurosporine Antibiotic AM-2282,AM-2282,CGP 41251 Apoptosis , PKA , Antibacterial , Antibiotic , Src , PKC , Antifungal
Staurosporine (AM-2282) is a protein kinase inhibitor with ATP-competitive and non-selective inhibitory activity (IC50=6/15/2/3/3000 nM) against PKC, PKA, c-Fgr, phosphorylase kinase and TAOK2. Staurosporine also induces...

Recombinant Proteins

カタログ番号 製品名 Species Expression System
TMPY-01782 FGFR1 Protein, Mouse, Recombinant (hFc) Mouse HEK293 Cells
FGFR1 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 66.5 kDa and the accession number is P16092-1.
TMPY-01781 FGFR1 Protein, Mouse, Recombinant (His) Mouse HEK293 Cells
FGFR1 Protein, Mouse, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 40.9 kDa and the accession number is P16092-1.