NF-κB is important in regulating cellular responses because it belongs to the category of "rapid-acting" primary transcription factors, i.e., transcription factors that are present in cells in an inactive state and do not require new protein synthesis in order to become activated (other members of this family include transcription factors such as c-Jun, STATs, and nuclear hormone receptors). This allows NF-κB to be a first responder to harmful cellular stimuli. Known inducers of NF-κB activity are highly variable and include reactive oxygen species (ROS), tumor necrosis factor alpha (TNFα), interleukin 1-beta (IL-1β), bacterial lipopolysaccharides (LPS), isoproterenol, cocaine, and ionizing radiation.
L-755,507 enhances CRISPR-mediated homology-directed repair (HDR) efficiency in human induced pluripotent stem cells (iPSCs). L-755,507 is also a very potent and selective β3-AR adrenergic receptor partial agonist, selective over both β1-AR and β2-AR adrenoceptor binding.
MoreBTZ043是DprE1的抑制剂,它在结核杆菌中有低浓度的抗菌活性。
MoreL-Epinephrine Bitartrate是α和β肾上腺素受体刺激剂,是一种激素和神经递质。
MoreIvabradine是新的If抑制剂,IC50为2.9μM。
MoreLY-2584702甲苯磺酸盐是p70S6K信号转导口服性抑制剂,能抑制和阻止核糖体S6亚基的磷酸化。
MoreL-755,507 enhances CRISPR-mediated homology-directed repair (HDR) efficiency in human induced pluripotent stem cells (iPSCs). L-755,507 is also a very potent and selective β3-AR adrenergic receptor partial agonist, selective over both β1-AR and β2-AR adrenoceptor binding.
MoreBTZ043是DprE1的抑制剂,它在结核杆菌中有低浓度的抗菌活性。
MoreL-Epinephrine Bitartrate是α和β肾上腺素受体刺激剂,是一种激素和神经递质。
MoreIvabradine是新的If抑制剂,IC50为2.9μM。
MoreLY-2584702甲苯磺酸盐是p70S6K信号转导口服性抑制剂,能抑制和阻止核糖体S6亚基的磷酸化。
More