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 66

  1. Cat.No. Product Name Information/Activity
  2. BCC2065 YK-4-279 YK 4-279 is an inhibitor of RNA Helicase A (RHA) binding to the oncogenic transciption factor EWS-FLI1. YK-4-279 chemical structure
  3. BCC4762 Azathioprine Azathioprine(Azasan, Imuran; BW 57-322) is a drug that suppresses the immune system and is used in organ transplantation and autoimmune disease. Azathioprine chemical structure
  4. BCC4385 Azithromycin Azithromycin is a macrolide antibiotic useful for the treatment of a number of bacterial infections. Azithromycin chemical structure
  5. BCC5293 5-BrdU 5-BrdU is a nucleoside analog that competes with thymidine for incorporation into DNA. 5-BrdU is commonly used in the detection of proliferating cells. 5-BrdU chemical structure
  6. BCC7665 Ellipticine Ellipticine (NSC 71795) is a potent antineoplastic agent; inhibits DNA topoisomerase II activities. Ellipticine chemical structure
  7. BCC5340 ISRIB (trans-isomer) ISRIB (trans-isomer) is a potent inhibitor of PERK with an IC50 of 5 nM. ISRIB (trans-isomer) chemical structure
  8. BCC5028 Stavudine (d4T) Stavudine is a nucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV. Stavudine (d4T) chemical structure
  9. BCC3873 Triflurdine (Viroptic) Trifluridine (Trifluorothymidine; 5-Trifluorothymidine; TFT) is an irreversible thymidylate synthase inhibitor, and thereby suppresses DNA synthesis. Trifluridine is an antiviral drug for herpes simplex virus (HSV) infection. Triflurdine (Viroptic) chemical structure
  10. BCN4318 Camptothecin Camptothecin (Campathecin) is a potent DNA enzyme topoisomerase I inhibitor, with an IC50 of 679 nM. Camptothecin chemical structure
  11. BCN5986 Celastrol Tripterin (Celastrol) is a proteasome inhibitor which potently and preferentially inhibits the chymotrypsin-like activity of a purified 20S proteasome with IC50 of 2.5 μM. Celastrol chemical structure

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