Cancer Research

Cancer is a term used to define a group of diseases in which abnormal cells divide without control, are able to invade neighboring tissues/organs and metastasize. Cancer has been characterized by six hallmarks; self sufficiency in proliferative growth signals, insensitivity to growth inhibitors, evasion of apoptosis, limitless replicative potential, ability to develop blood vessels (angiogenesis), and tissue invasion and metastasis.

Cancer Research Products Areas

Products for Cancer Research - Page 102

  1. Cat.No. Product Name Information/Activity
  2. BCC6718 (±)-Palmitoylcarnitine chloride Palmitoylcarnitine chloride is a fatty acid-derived mitochondrial substrate, and selectively decreases cell survival in colorectal and prostate cancer cells by affecting on pro-inflammatory pathways, Ca2+ influx, and DHT-like effects. (±)-Palmitoylcarnitine chloride chemical structure
  3. BCC5350 Midostaurin (PKC412) Midostaurin (PKC412; CGP 41251) is a multi-targeted protein kinase inhibitor which inhibits PKCα/β/γ, Syk, Flk-1, Akt, PKA, c-Kit, c-Fgr, c-Src, FLT3, PDFRβ and VEGFR1/2 with IC50 ranging from 22-500 nM. Midostaurin (PKC412) chemical structure
  4. BCC5811 PKC β pseudosubstrate 172308-76-8 PKC β pseudosubstrate chemical structure
  5. BCC7122 Ro 32-0432 hydrochloride 151342-35-7 Ro 32-0432 hydrochloride chemical structure
  6. BCC7127 Rottlerin Rottlerin, a natural product purified from Mallotus Philippinensis, is a specific PKC inhibitor, with IC50 values for PKCδ of 3-6 μM, PKCα,β,γ of 30-42 μM, PKCε,η,ζ of 80-100 μM. Rottlerin acts as a direct mitochondrial uncoupler, and stimulates autophagy by targeting a signaling cascade upstream of mTORC1. Rottlerin induces apoptosis via caspase 3 activation. Rottlerin chemical structure
  7. BCC6729 D-erythro-Sphingosine (synthetic) D-erythro-Sphingosine (Erythrosphingosine) is a very potent activator of p32-kinase with an EC50 of 8 μM, and inhibits protein kinase C (PKC). D-erythro-Sphingosine (Erythrosphingosine) is also a PP2A activator. D-erythro-Sphingosine (synthetic) chemical structure
  8. BCC4003 ZIP Cell-permeable inhibitor of atypical PKC isozyme PKM<span class='symbol'>&zeta;</span> ZIP chemical structure
  9. BCC7343 Bryostatin 1 Bryostatin 1 is a natural macrolide isolated from the bryozoan Bugula neritina and is a potent and central nervous system (CNS)-permeable PKC modulator. Bryostatin 1 binds to the isolated C1 domain of Munc13-1 and the full-length Munc13-1 protein with Kis of 8.07 nM and 0.45 nM, respectively. Bryostatin 1 has anti-cancer, anti-inflammatory, neuroprotective, anti-HIV-1 infection properties. Bryostatin 1 chemical structure
  10. BCC5619 Bryostatin 2 87745-28-6 Bryostatin 2 chemical structure
  11. BCC5620 Bryostatin 3 143370-84-7 Bryostatin 3 chemical structure

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