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 10

  1. Cat.No. Product Name Information/Activity
  2. BCC7764 Reversan Reversan (CBLC4H10) is a potent and nontoxic multidrug resistance-associated protein 1 (MRP1) and P-glycoprotein (Pgp) inhibitor. Reversan chemical structure
  3. BCC3878 LY335979 (Zosuquidar 3HCL) Zosuquidar trihydrochloride is an inhibitor of P-glycoprotein with a Ki value of 59 nM. LY335979 (Zosuquidar 3HCL) chemical structure
  4. BCN2961 Ingenol 3-Angelate Ingenol Mebutate is an active ingredient in Euphorbia peplus, acts as a potent PKC modulator, with Kis of 0.3, 0.105, 0.162, 0.376, and 0.171 nM for PKC-α, PKC-β, PKC-γ, PKC-δ, and PKC-ε, respectively, and has antiinflammatory and antitumor activity. Ingenol 3-Angelate chemical structure
  5. BCC8082 cAMPS-Rp, triethylammonium salt Rp-cAMPS triethylammonium salt is an analog of cAMP which acts as a potent, competitive and cell-permeable antagonist of cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 6.05 µM and 9.75 µM, respectively). Rp-cAMPS triethylammonium salt is resistant to hydrolysis by phosphodiesterases. cAMPS-Rp, triethylammonium salt chemical structure
  6. BCC2542 Fasudil (HA-1077) HCl Fasudil Hydrochloride (HA-1077 Hydrochloride; AT877 Hydrochloride), is a nonspecific ROCK inhibitor and also has inhibitory effect on protein kinases, with an Ki of 0.33 μM for ROCK1, IC50s of 0.158 μM and 4.58 μM, 12.30 μM, 1.650 μM for ROCK2 and PKA, PKC, PKG, respectively. Fasudil Hydrochloride is also a potent Ca2+ channel antagonist and vasodilator. Fasudil (HA-1077) HCl chemical structure
  7. BCC8084 cGMP Dependent Kinase Inhibitor Peptide 82801-73-8 cGMP Dependent Kinase Inhibitor Peptide chemical structure
  8. BCC4997 H 89 2HCl H-89 dihydrochloride is a potent and selective inhibitor of protein kinase A (PKA) with an IC50 of 48 nM and has weak inhibition on PKG, PKC, Casein Kinase. H 89 2HCl chemical structure
  9. BCC8080 KT 5720 KT5720 is a cell-permeable, potent, specific, reversible, ATP-competitive inhibitor of protein kinase A (PKA), with a Ki of 60 nM. KT 5720 chemical structure
  10. BCC1042 PKA inhibitor fragment (6-22) amide Potent protein kinase A inhibitor PKA inhibitor fragment (6-22) amide chemical structure
  11. BCC8087 PKI 14-22 amide, myristoylated Cell-permeable protein kinase A inhibitor PKI 14-22 amide, myristoylated chemical structure

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