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 22

  1. Cat.No. Product Name Information/Activity
  2. BCC8078 8-Bromo-cAMP, sodium salt 8-Bromo-cAMP sodium salt (8-Br-Camp sodium salt), a cyclic AMP analog, is an activator of cyclic AMP-dependent protein kinase (PKA). 8-Bromo-cAMP, sodium salt chemical structure
  3. BCC7868 Bisindolylmaleimide II 137592-45-1 Bisindolylmaleimide II chemical structure
  4. BCC6687 C-1 HA-100 is an inhibitor of cGMP-dependent protein kinase (PKG), cAMP-dependent protein kinase (PKA), protein kinase C (PKC) and MLC-kinase with IC50s of 4, 8, 12 and 240 μM, respectively. C-1 chemical structure
  5. BCC7131 Calphostin C 121263-19-2 Calphostin C chemical structure
  6. BCC7363 CGP 53353 145915-60-2 CGP 53353 chemical structure
  7. BCC6778 Dihydrosphingosine 3102-56-5 Dihydrosphingosine chemical structure
  8. BCC1100 Enzastaurin (LY317615) Enzastaurin is a potent and selective PKCβ inhibitor with an IC50 of 6 nM, showing 6- to 20-fold selectivity over PKCα, PKCγ and PKCε. Enzastaurin (LY317615) chemical structure
  9. BCC3704 GF 109203X Bisindolylmaleimide I (GF109203X) is a highly selective, cell-permeable, and reversible protein kinase C (PKC) inhibitor with a Ki of 14 nM. GF 109203X chemical structure
  10. BCC3705 Go 6983 Go 6983 is a pan-PKC inhibitor against for PKCα, PKCβ, PKCγ, PKCδ and PKCζ with IC50 of 7 nM, 7 nM, 6 nM, 10 nM and 60 nM, respectively. Go 6983 chemical structure
  11. BCC3706 K-252c K-252c, a staurosporine analog isolated from Nocardiopsis sp., is a cell-permeable PKC inhibitor, with an IC50 of 2.45 µM. K-252c induces apoptosis in human chronic myelogenous leukemia cancer cells. K-252c also inhibits β-lactamase, chymotrypsin, and malate dehydrogenase. K-252c chemical structure

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