Respiratory Disease Research

The respiratory system consists of the lungs, airways, diaphragm, trachea (windpipe) and pharynx (throat) and its primary function is the exchange of oxygen and carbon dioxide- breathing in and out. Between 6 and 10 liters of air are brought in and out of the lungs and 0.3 liters of oxygen are transferred from the alveoli to the blood per minute.

Respiratory Disease Research Products Areas

Products for Respiratory Disease Research - Page 21

  1. Cat.No. Product Name Information/Activity
  2. BCC3878 LY335979 (Zosuquidar 3HCL) Zosuquidar trihydrochloride is an inhibitor of P-glycoprotein with a Ki value of 59 nM. LY335979 (Zosuquidar 3HCL) chemical structure
  3. 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
  4. 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
  5. 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
  6. BCC8084 cGMP Dependent Kinase Inhibitor Peptide 82801-73-8 cGMP Dependent Kinase Inhibitor Peptide chemical structure
  7. 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
  8. 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
  9. BCC1042 PKA inhibitor fragment (6-22) amide Potent protein kinase A inhibitor PKA inhibitor fragment (6-22) amide chemical structure
  10. BCC8087 PKI 14-22 amide, myristoylated Cell-permeable protein kinase A inhibitor PKI 14-22 amide, myristoylated chemical structure
  11. BCC8081 cAMPS-Sp, triethylammonium salt 93602-66-5 cAMPS-Sp, triethylammonium salt chemical structure

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