| AG 538 |
A potent, competitive inhibitor of IGF-1 receptor kinase (IC50 = 400 nM). Reaction is competitive with respect to IGF-1R substrate. Also inhibits the phosphorylation of PTK substrate poly(Glu,Tyr) by IGF-1R, IR, EGF-R, and Src (IC50 = 60 nM, 113 n... |
n/a |
658403 |
CALBIOCHEM/EMD BIOSCIENCES |
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| AG 555 |
A potent inhibitor of epidermal growth factor (EGF) receptor kinase autophosphorylation (IC50 = 700 nM). Exhibits opposite potency profiles with AG 527 (Cat. No. 658402) for EGF receptor autophosphorylation versus poly-GAT substrate phosphorylation. |
n/a |
658404 |
CALBIOCHEM/EMD BIOSCIENCES |
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| AG 556 |
Selectively inhibits epidermal growth factor receptor kinase autophosphorylation (IC50 = 5 µM) over HER1/2 autophosphorylation. Also blocks LPS-induced TNF-α production and attentuates LPS-induced hypotension in rats. |
n/a |
658415 |
CALBIOCHEM/EMD BIOSCIENCES |
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| AG 82 |
A cell-permeable, competitive inhibitor of substrate binding on protein tyrosine kinases. Inhibits epidermal growth factor receptor tyrosine kinase (IC50 = 3 µM) and the GTPase activity of transducin (IC50 = 7 µM). Inhibits neuromedin ... |
n/a |
658400 |
CALBIOCHEM/EMD BIOSCIENCES |
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| AG 825 |
A potent and selective inhibitor of HER2 (neu/ErbB2; IC50 = 0.35 µM) relative to HER1 (IC50 = 19 µM) autophosphorylation. The inhibition is competitive with respect to ATP binding. Enhances chemosensitivity in non-small cell lung cance... |
n/a |
121765 |
CALBIOCHEM/EMD BIOSCIENCES |
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| AG 879 |
Inhibits nerve growth factor (NGF)-dependent p140c-trk tyrosine phosphorylation (EC50 = 10 µM) as well as NGF-induced phospholipase C-γ1 phosphorylation. Also blocks NGF-induced neurite outgrowth in PC12 cells. Does not affect the tyro... |
n/a |
658460 |
CALBIOCHEM/EMD BIOSCIENCES |
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| AG 9 |
An inactive compound that can be used as a negative control for inhibition of EGFR (IC50 >1250 µM for EGFR kinase). Has been shown to inhibit IL-2 stimulated Tyk-2 phosphorylation in ConA-activated T cells. |
n/a |
658390 |
CALBIOCHEM/EMD BIOSCIENCES |
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| AG 957 |
A potent tyrosine kinase inhibitor. Selectively blocks the tyrosine kinase activity of human p210bcr-abl (Ki = 750 nM) over p140c-abl (Ki = 10 µM). Also decreases p210bcr-abl phosphorylation in viable K562 cells at concentrations and duratio... |
n/a |
121761 |
CALBIOCHEM/EMD BIOSCIENCES |
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| AG 99 |
Inhibits epidermal growth factor (EGF) receptor tyrosine kinase (IC50 = 10 µM) and EGF-dependent cell proliferation. Inhibits EGFR phosphorylation and ERK1 and ERK2 activities. |
n/a |
658430 |
CALBIOCHEM/EMD BIOSCIENCES |
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| AG 045572 |
Selective gonadotropin-releasing hormone (GnRH) receptor antagonist (Ki values are 2.2, 3.8 and 6.0 nM for mouse, rat and human receptors respectively). Suppresses testosterone and luteinising hormone (LH) levels in vivo. |
1mg, 10mg |
2730 |
TOCRIS BIOSCIENCE |
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| AG 18 |
Inhibitor of epidermal growth factor receptor (EGFR) and platelet-derived growth factor receptor (PDGFR) kinase (IC50 values are 35 and 25 μM respectively). Inhibits EGF-stimulated cell proliferation. |
10mg, 50mg |
0493 |
TOCRIS BIOSCIENCE |
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| AG 213 |
A potent inhibitor of epidermal growth factor receptor (EGFR) and platelet-derived growth factor receptor (PDGFR) kinase (IC50 values are 2.4 and 3 μM respectively). Also inhibits protein kinase C (IC50 = 60 μM). |
10mg, 50mg |
0503 |
TOCRIS BIOSCIENCE |
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| AG 490 |
Selective inhibitor of EGF receptor tyrosine kinase (IC50 values are 2 and 13.5 μM for EGFR and Her2-neu respectively). Inhibitor of Jak2, Jak3/STAT, Jak3/AP-1 and Jak3/MAPK pathways. |
10mg, 50mg |
0414 |
TOCRIS BIOSCIENCE |
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| AG 494 |
Potent inhibitor of epidermal growth factor receptor (EGFR) kinase (IC50 = 0.7 μM). Selective over Her2-neu, PDGFR and insulin receptor kinase (IC50 values are 42, 6 and > 100 μM respectively). |
10mg, 50mg |
0619 |
TOCRIS BIOSCIENCE |
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| AG 555 |
Potent epidermal growth factor receptor (EGFR) kinase (IC50 = 0.7 μM). Selective over Her2-neu and insulin receptor kinase (IC50 values are 35 and > 100 μM respectively). |
10mg, 50mg |
0618 |
TOCRIS BIOSCIENCE |
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| AG 556 |
Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 1.1 μM). Selective over Her2-neu (IC50 > 500 μM). |
10mg, 50mg |
0616 |
TOCRIS BIOSCIENCE |
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| AG 825 |
Epidermal growth factor receptor (EGFR) kinase inhibitor. Selective for Her2 over Her1 (IC50 values are 0.15 and 19 mM respectively). Preferentially triggers p38 MAP kinase-dependent apoptosis in androgen-independent prostate cancer cells. |
10mg, 50mg |
1555 |
TOCRIS BIOSCIENCE |
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| AG 99 |
Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 10 μM). Selective over insulin receptor kinase. |
10mg, 50mg |
0497 |
TOCRIS BIOSCIENCE |
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| AGAR |
n/a |
n/a |
n/a |
AMERICAN BIOANALYTICAL |
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| Agar |
Suitable for inclusion in culture media. |
n/a |
12177 |
CALBIOCHEM/EMD BIOSCIENCES |
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