Cell Signaling & Oncology
The signaling pathways controlling cell growth and differentiation are almost invariably altered in cancer. During the course of tumor progression, cancer cells acquire a number of characteristic alterations. These include the capacities to proliferate independently of exogenous growth-promoting or growth-inhibitory signals, to invade surrounding tissues and metastasize to distant sites, to elicit an angiogenic response, and to evade mechanisms that limit cell proliferation, such as apoptosis and replicative senescence. These properties reflect alterations in the cellular signaling pathways that in normal cells control cell proliferation, motility, and survival. These interconnected pathways are being deciphered, but understanding the alterations that lead to cancer and correcting them is a substantial challenge. Among the key pathways are those controlling cell proliferation, which coordinate a response to the cellular environment, with the mTOR kinase as a critical node. Tumour development is influenced by infections and inflammation, and the complex role of the nuclear factor-B transcription factors is being unravelled. Expansion of tumour cells depends on nutrient supply and vascularization, which is orchestrated by the transcription factor known as HIF. And the metastatic spread of primary tumours to other organs is facilitated by many signaling pathways[1],[2].
Cell Signaling and Oncology products Library
For your convenience, you can order a library of all of our Cell Signaling and Oncology research related products. Make your personal library by cherry picking products of your interest from our comprehensive list (>800 products), or order all together not to miss any. The libraries will be shipped as 10 mM solutions (in DMSO, 250 µL of each selected Axon Ligand™) on a 96-well microtiter plate with a clear map of its contents.
Simply download our comprehensive list of epigenetics products below (Microsoft Excel (.xls)), check the products to be included, and return your list to order the library of your preference.
 Axon 5051 - Cell signaling and Oncology Library.xls |
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[1] A. Eccleston, R. Dhand. Signalling in cancer. Nature 441, 423, editorial note
[2] G.S. Martin. Cell signaling and cancer. Cancer Cell. 2003 Sep;4(3):167-74.
| Axon ID | Name | Description | From price | |
|---|---|---|---|---|
| 3408 | AKI603 | Inhibitor of Aurora A kinase | €145.00 | |
| 2540 | Akt Inhibitor VIII | Inhibitor of Akt1 and 2 with significant off-side effects (CaMKIα and AhR) | €95.00 | |
| 3834 | Alantolactone | STAT3 inhibitor; NLRP3 inhibitor | €90.00 | |
| 2551 | Alda 1 | Small molecule activator of ALDH2 | €65.00 | |
| 1884 | Alectinib | Orally available and selective ALK inhibitor | €70.00 | |
| 2930 | Alofanib | Allosteric inhibitor of FGFR2 | €90.00 | |
| 3549 | Aloperine | Potent multifunctional anti-tumor agent | €50.00 | |
| 2925 | Alpelisib | PI3K inhibitor (p110-α specific) | €90.00 | |
| 2062 | Alprostadil | Prostaglandin EP (1-4) receptor antagonist | €125.00 | |
| N0001 | Altemicidin | Small bioactive molecule with acaricidal and antitumor activity | Inquire | |
| 3946 | Altiratinib | Balanced inhibitor for MET, TIE2 (TEK), and VEGFR2 (KDR) kinases | Inquire | |
| 2948 | AM 580 | RAR-α agonist | €95.00 | |
| 2971 | Amcasertib | First-in-class stemness kinase inhibitor | €145.00 | |
| 1738 | AMD 3100 | CXCR4 antagonist | €90.00 | |
| 1930 | AMD 3465 hexahydrobromide | Potent and selective CXCR4 antagonist | €85.00 | |
| 1916 | AMG 208 | Inhibitor of c-MET receptor tyrosine kinase (RTK) | €95.00 | |
| 2639 | AMG 232 | Potent, selective, and orally bioavailable MDM2-p53 inhibitor | €120.00 | |
| 1768 | AMG 706 | Multiple receptor tyrosine kinase inhibitor | €105.00 | |
| 2405 | AMG 837 calcium | Orally bioavailable partial agonist of GPR40 (FFA1) | €90.00 | |
| 1783 | AMG 900 | Aurora inhibitor (non-specific) | €110.00 | |
| 3686 | AMG-176 | Potent and selective Mcl-1 inhibitor | €490.00 | |
| 3945 | AMG-337 | Potent and exquisitely selective inhibitor of wild-type and some mutant forms of c-Met | Inquire | |
| 3827 | AMG-511 | Orally bioavailable, highly potent and selective pan-class I phosphatidylinositol-3 kinase (PI3K) inhibitor | Inquire | |
| 4071 | AMG-925 | Potent, selective, and orally available FLT3/CDK4 dual inhibitor | Inquire | |
| 3575 | AMG510 | Highly potent, selective, and orally bioavailable KRAS-G12C inhibitor | €90.00 | |
| 2863 | AMI-1 | Inhibitor of PRMT | €99.00 | |
| 2368 | Amuvatinib | RTK inhibitor which effectively inhibits PDGFR, c-Kit and c-Met | €105.00 | |
| 2468 | ANA 12 | Selective TrkB antagonist with anxiolytic and antidepressant activity in mice | €90.00 | |
| 1490 | Anacardic acid A | HAT inhibitor | €60.00 | |
| 3316 | Anastrozole | Potent, highly selective, and orally active aromatase inhibitor | €50.00 | |