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Non-antibody Products (Kits, Proteins, Microbial Antigens, Tissues, Services, etc.) - Page 9 of 6,058
| Name |
Description |
Size |
Catalog # |
Supplier |
|
| AG-490 |
AG 490 is a potent epidermal growth factor receptor kinase autophosphorylation inhibitor with an IC50 of 100 nM and 56.8 ?M for EGFR and JAK, respectively. Purity is greater than 99%. |
25 mg |
orb60171 |
 BIORBYT LTD. |
More Info
|
| AG 1478 |
Cell-permeable. A potent EGFR Tyrosine Kinase (TK) inhibitor with an IC50 of 3 nM. Only weakly inhibits PDGFR and HER2-NEU kinases (IC50 >100 µM). |
5 mg |
1800-5 |
 BIOVISION, INC. |
More Info
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| AG 1478 |
Cell-permeable. A potent EGFR Tyrosine Kinase (TK) inhibitor with an IC50 of 3 nM. Only weakly inhibits PDGFR and HER2-NEU kinases (IC50 >100 µM). |
25 mg |
1800-25 |
 BIOVISION, INC. |
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| AG 045572 |
GnRH Receptor Antagonist |
1 mg |
2730/1 |
 R&D SYSTEMS, INC. |
More Info
|
| AG 045572 |
GnRH Receptor Antagonist |
10 mg |
2730/10 |
 R&D SYSTEMS, INC. |
More Info
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| AG 18 |
EGF Receptor Inhibitor |
10 mg |
0493/10 |
 R&D SYSTEMS, INC. |
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| AG 18 |
EGF Receptor Inhibitor |
50 mg |
0493/50 |
 R&D SYSTEMS, INC. |
More Info
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| AG 213 |
EGF Receptor Inhibitor |
10 mg |
0503/10 |
 R&D SYSTEMS, INC. |
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| AG 213 |
EGF Receptor Inhibitor |
50 mg |
0503/50 |
 R&D SYSTEMS, INC. |
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| AG 490 |
EGF Receptor Inhibitor |
10 mg |
0414/10 |
 R&D SYSTEMS, INC. |
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| AG 490 |
EGF Receptor Inhibitor |
50 mg |
0414/50 |
 R&D SYSTEMS, INC. |
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| AG 494 |
EGF Receptor Inhibitor |
10 mg |
0619/10 |
 R&D SYSTEMS, INC. |
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| AG 494 |
EGF Receptor Inhibitor |
50 mg |
0619/50 |
 R&D SYSTEMS, INC. |
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| AG 555 |
EGF Receptor Inhibitor |
10 mg |
0618/10 |
 R&D SYSTEMS, INC. |
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| AG 555 |
EGF Receptor Inhibitor |
50 mg |
0618/50 |
 R&D SYSTEMS, INC. |
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| AG 556 |
EGF Receptor Inhibitor |
10 mg |
0616/10 |
 R&D SYSTEMS, INC. |
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| AG 556 |
EGF Receptor Inhibitor |
50 mg |
0616/50 |
 R&D SYSTEMS, INC. |
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|
| AG 825 |
EGF Receptor Inhibitor |
10 mg |
1555/10 |
 R&D SYSTEMS, INC. |
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| AG 825 |
EGF Receptor Inhibitor |
50 mg |
1555/50 |
 R&D SYSTEMS, INC. |
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| AG 879 |
Trk Receptor Inhibitor |
10 mg |
2617/10 |
 R&D SYSTEMS, INC. |
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| AG 99 |
EGF Receptor Inhibitor |
10 mg |
0497/10 |
 R&D SYSTEMS, INC. |
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| AG 99 |
EGF Receptor Inhibitor |
50 mg |
0497/50 |
 R&D SYSTEMS, INC. |
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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. Minimum Purity: > 98% |
1mg |
2730 |
 TOCRIS BIOSCIENCE |
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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. Minimum Purity: > 98% |
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. Also acts as a mitochondrial uncoupler t... |
10mg |
0493 |
 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. Also acts as a mitochondrial uncoupler t... |
50mg |
0493 |
 TOCRIS BIOSCIENCE |
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|
| AG 213 |
Epidermal growth factor receptor (EGFR) and platelet-derived growth factor receptor (PDGFR) kinase inhibitor (IC50 values are 2.4 and 3 µM respectively). Stimulates microtubule polymerization and promotes neurite outgrowth > 17-fold over bas... |
10mg |
0503 |
 TOCRIS BIOSCIENCE |
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|
| AG 213 |
Epidermal growth factor receptor (EGFR) and platelet-derived growth factor receptor (PDGFR) kinase inhibitor (IC50 values are 2.4 and 3 µM respectively). Stimulates microtubule polymerization and promotes neurite outgrowth > 17-fold over bas... |
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 ErbB2 respectively). Inhibitor of JAK2, JAK3/STAT, JAK3/AP-1 and JAK3/MAPK pathways and potently inhibits cytokine-independent cell growth in vit... |
10mg |
0414 |
 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 ErbB2 respectively). Inhibitor of JAK2, JAK3/STAT, JAK3/AP-1 and JAK3/MAPK pathways and potently inhibits cytokine-independent cell growth in vit... |
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 ErbB2, PDGFR and insulin receptor kinase (IC50 values are 42, 6 and > 100 µM respectively). Minimum Purity: > 98% |
10mg |
0619 |
 TOCRIS BIOSCIENCE |
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| AG 494 |
Potent inhibitor of epidermal growth factor receptor (EGFR) kinase (IC50 = 0.7 µM). Selective over ErbB2, PDGFR and insulin receptor kinase (IC50 values are 42, 6 and > 100 µM respectively). Minimum Purity: > 98% |
50mg |
0619 |
 TOCRIS BIOSCIENCE |
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|
| AG 555 |
Potent epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 0.7 µM) that displays 50-fold and >140-fold selectivity over ErbB2 and insulin receptor kinase respectively. Induce G1 growth arrest selectively in transformed cells (IC... |
10mg |
0618 |
 TOCRIS BIOSCIENCE |
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| AG 555 |
Potent epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 0.7 µM) that displays 50-fold and >140-fold selectivity over ErbB2 and insulin receptor kinase respectively. Induce G1 growth arrest selectively in transformed cells (IC... |
50mg |
0618 |
 TOCRIS BIOSCIENCE |
More Info
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| AG 556 |
Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 1.1 µM). Selective over ErbB2 (IC50 > 500 µM). Minimum Purity: > 99% |
10mg |
0616 |
 TOCRIS BIOSCIENCE |
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| AG 556 |
Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 1.1 µM). Selective over ErbB2 (IC50 > 500 µM). Minimum Purity: > 99% |
50mg |
0616 |
 TOCRIS BIOSCIENCE |
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| AG 825 |
Selective ErbB2 inhibitor (IC50 values are 0.15 and 19 µM at ErbB2 and ErbB1 respectively). Preferentially triggers p38 MAP kinase-dependent apoptosis in androgen-independent prostate cancer cells. Minimum Purity: > 98% |
10mg |
1555 |
 TOCRIS BIOSCIENCE |
More Info
|
| AG 825 |
Selective ErbB2 inhibitor (IC50 values are 0.15 and 19 µM at ErbB2 and ErbB1 respectively). Preferentially triggers p38 MAP kinase-dependent apoptosis in androgen-independent prostate cancer cells. Minimum Purity: > 98% |
50mg |
1555 |
 TOCRIS BIOSCIENCE |
More Info
|
| AG 879 |
Inhibitor of the tyrosine kinase activity of nerve growth factor (NGF) TrkA. Decreases cellular proliferation in human muscular sarcoma cell lines. Also inhibits ErbB2 and VEGFR-2 (IC50 values are approximately 1 µM for both). Minimum Purity... |
10mg |
2617 |
 TOCRIS BIOSCIENCE |
More Info
|
| AG 99 |
Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 10 µM) that is selective over insulin receptor kinase. Blocks tyrosine phosphorylation of p145met and promotes cell death of normal and cancer cells via activation of caspase-l... |
10mg |
0497 |
 TOCRIS BIOSCIENCE |
More Info
|
| AG 99 |
Epidermal growth factor receptor (EGFR) kinase inhibitor (IC50 = 10 µM) that is selective over insulin receptor kinase. Blocks tyrosine phosphorylation of p145met and promotes cell death of normal and cancer cells via activation of caspase-l... |
50mg |
0497 |
 TOCRIS BIOSCIENCE |
More Info
|
| AG-014699 |
MW: 421.36 Da. CAS number: [459868-92-9]. Formula: C19H18FN3O. Store at or below -20 °. For research use only. |
5 mg |
orb61207 |
 BIORBYT LTD. |
More Info
|
| AG 1024 |
Molecular Weight: 305.2. Off-white to yellow solid. Packaged under inert gas. |
1 mg |
121767-1MG |
 EMD MILLIPORE |
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| AG 126 |
Molecular Weight: 215.2. Yellow solid. |
5 mg |
658452-5MG |
 EMD MILLIPORE |
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|
| AG 1295 |
Molecular Weight: 234.3. White solid. |
5 mg |
658550-5MG |
 EMD MILLIPORE |
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|
| AG 1296 |
Molecular Weight: 266.3. White solid. |
5 mg |
658551-5MG |
 EMD MILLIPORE |
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|
| AG 1433 |
Molecular Weight: 302.8. Pale brown solid. Packaged under inert gas. |
5 mg |
658553-5MG |
 EMD MILLIPORE |
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|
| AG 1478 |
Molecular Weight: 315.8. Pale yellow solid. |
5 mg |
658552-5MG |
 EMD MILLIPORE |
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|
| AG 17 |
Molecular Weight: 282.4. Pale yellow solid. |
5 mg |
658425-5MG |
 EMD MILLIPORE |
More Info
|
| AG 18 |
Molecular Weight: 186.2. Yellow solid. |
5 mg |
658395-5MG |
 EMD MILLIPORE |
More Info
|
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