Src

TL02-59 is an orally active inhibitor of Src-family kinase Fgr (IC50: 0.03 nM), and potently …

Inulicin, an active compound isolated from Inula Britannica L, inhibits VEGF-mediated activation of Src and …

TL02-59 dihydrochloride is an orally active inhibitor of Src-family kinase Fgr (IC50: 0.03 nM).

A 419259 is a pyrrolo-pyrimidine inhibitor, designed to enhance selectivity towards the Src family (IC50s: …

A 419259 trihydrochloride is an Src family kinases inhibitor (IC50s: 9 nM, 3 nM and …

1-Naphthyl PP1 is a selective src inhibitor(v-Src and c-Fyn, c-Abl, CDK2 and CAMK II with …

PP 3 is a Negative control for the Src kinase inhibitor PP 2

RK-24466 is a selective and potent inhibitor of Lck, inhibits Lck (64-509) and LckCD isoforms …

AMG-47a is a potent inhibitor of Lck and T cell proliferation. AMG-47a could promote the …

Tirbanibulin is an inhibitor of Src that targets the peptide substrate site of Src (GI50: …

Dasatinib is a potent inhibitor of the Bcr-Abl and Src family (IC50s: 0.6, 0.8, 79 …

Benidipine HCl, a hydrochloride salt form of benidipine, is used as a blocker of dihydropyridine …

Bafetinib (INNO-406) is an effective and specific dual Bcr-Abl/Lyn inhibitor (IC50: 5.8/19 nM), and no …

NCGC00262650 is an inhibitor of AMA1-RON2 interaction and c-Src tyrosine kinase activity.

squarunkinA is a novel modulator of the UNC119-Cargo Interaction, potently and selectively inhibiting the binding …

Spebrutinib is an orally bioavailable, selective inhibitor of Bruton's agammaglobulinemia tyrosine kinase (BTK), with potential …

Tirbanibulin Mesylate is an inhibitor of Src that targets the peptide substrate site of Src …

Ibrutinib is an irreversible inhibitor of BTK (IC50: 0.5 nM) that selectively blocks B cell …

Bosutinib D8 is a deuterium-labeled Bosutinib. Bosutinib (SKI-606) is a dual Src/Abl inhibitor (IC50s: 1.2 …

eCF506 is a potent and selective inhibitor of SRC (IC50 < 0.5 nM)

SU 6656 is a selective inhibitor of Src family kinases, with IC50 of 280 nM, …

CH6953755 is a potent, orally active and selective inhibitor of YES1 kinase (IC50: 1.8 nM). …

Saracatinib (AZD0530) is an effective Src inhibitor (IC50: 2.7 nM), and effective to Lck, Fyn, …

Bosutinib is a synthetic quinolone derivative and dual kinase inhibitor that targets both Abl (IC50: …

1-Naphthyl PP1 hydrochloride is a selective inhibitor of src family kinases v-Src

Src Inhibitor 1 is a potent and selective dual site Src tyrosine kinase inhibitor.

WH-4-023 is a potent and orally active Lck/Src inhibitor. It also potently inhibits SIK.

MLR-1023 is a chemical compound which inhibits acid secretion in animal models and also acts …

ZM 306416, a VEGFR1 inhibitor (IC50: 0.33 μM), can also inhibit EGFR (IC50<10 nM).

Scutellarein reduces inflammatory responses by inhibiting Src kinase activity.

Dasatinib is an orally bioavailable synthetic small molecule-inhibitor of SRC-family protein-tyrosine kinases. Dasatinib binds to …

PP1, a specific and effective Src inhibitor, is with IC50 for Lck/Fyn is 5 nM/ …

PD173955 is src family-selective tyrosine kinase inhibitor with IC50 of ~22 nM for Src, Yes …

WAY-303290 inhibits the pY binding site of tyrosine kinase p56lck SH2 domain.

PF-477736 is a specifc, effective and ATP-competitive Chk1 inhibitor (Ki: 0.49 nM ) and also …

KX1-004, a potential protective drug for NIHL, is an effective small molecule inhibitor of Src-PTK.

A-770041 is selective and orally active Src-family Lck inhibitor, and the other Src family kinase …

KX2-391 is a highly selective Src kinase inhibitor that has demonstrated efficacy in pre-Clinicalal animal …

UM-164 is a highly potent inhibitor of c-Src with a Kd of 2.7 nM. UM-164 …

Keap1-Nrf2 IN-1 activates Nrf2-regulated cytoprotective response and antagonizes acetaminophen-induced liver injury both in cellular and …

7-Hydroxychromone is a Src kinase inhibitor (IC50 of <300 μM).

MCB-613 is an effective steroid receptor coactivator (SRC) stimulator.