Cystic Fibrosis Research

Cystic fibrosis (CF) is a common inherited disease that mostly affects the lungs and airways of a sufferer. One of the main pathological characteristics of CF is the failure of airway defence against bacterial infection, leading to frequent chest infection and progressive lung damage.

Cystic Fibrosis Research Products Targets

Products for Cystic Fibrosis Research - Page 9

  1. Cat.No. Product Name Information/Activity
  2. BCC6717 17-ODYA Alkynyl Stearic Acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs. 17-ODYA chemical structure
  3. BCC7882 CP 100356 hydrochloride 142715-48-8 CP 100356 hydrochloride chemical structure
  4. BCC1547 Elacridar hydrochloride Elacridar hydrochloride (GF120918A) is a P-glycoprotein inhibitor, and has been used both in vitro and in vivo as a tool inhibitor of P-glycoprotein (Pgp) to investigate the role of transporters in the disposition of various test molecules. Elacridar hydrochloride chemical structure
  5. BCC7719 Estropipate Estropipate is a form of estrogen, used to treat symptoms of menopause, also used to prevent osteoporosis. Estropipate chemical structure
  6. BCC7507 Fumitremorgin C Fumitremorgin C is a potent and selective ABCG2/BRCP inhibitor. Fumitremorgin C chemical structure
  7. BCC1684 Ko 143 Ko 143 is a potent and selective ATP-binding cassette subfamily G member 2 (ABCG2/BCRP) inhibitor. Ko 143 displays >200-fold selectivity over P-gp and MRP-1 transporters. Ko 143 chemical structure
  8. BCC7874 KS 176 KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BCRP) multidrug transporter (IC50 values are 0.59 and 1.39 μM in Pheo A and Hoechst 33342 assays respectively). Displays no inhibitory activity against P-gp or MRP1. KS 176 chemical structure
  9. BCC4832 Probenecid Probenecid is a potent and selective agonist of transient receptor potential vanilloid 2 (TRPV2) channels. Probenecid also inhibits pannexin 1 channels. Probenecid chemical structure
  10. BCC2027 Valspodar Valspodar is a selective P-glycoprotein inhibitor that has been used as an experimental cancer treatment and chemosensitizer. Valspodar chemical structure
  11. BCC2307 Pyrimethamine Pyrimethamine(RP4753) is a medication used for protozoal infections; interferes with tetrahydrofolic acid synthesis from folic acid by inhibiting the enzyme dihydrofolate reductase (DHFR). Pyrimethamine chemical structure

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