Signaling Pathways
A basic property of living systems is the ability to respond to extracellular signals by evoking an internal response. Signal-transduction cascades mediate the sensing and processing of these stimuli. These molecular circuits detect, amplify, and integrate diverse external signals to generate responses such as changes in enzyme activity, gene expression, phenotypic alterations, or ion-channel activity. Signal-transduction pathways follow a broadly similar course that can be viewed as a molecular circuit. Upon an environmental signal, Membrane receptors transfer information from the environment to the cell's interior. Subsequently, second messengers relay information from the receptor-ligand complex into the cell's interior. Particularly important second messengers include cyclic AMP and cyclic GMP, calcium ion, inositol 1,4,5-trisphosphate, (IP3), and diacylglycerol. While these second messengers are free to move, they can easily diffuse to other compartments of the cell, such as the nucleus, where they can influence gene expression and other processes. Interestingly, signal transduction may be amplified significantly in the generation of second messengers, since initial stimulation may lead to the generation of many second messengers within the cell. Thus, a low concentration of signal in the environment, even as little as a single molecule, can yield a large intracellular signal and response. Besides this phenomenon, cross-talk between two or more signaling cascades may occur, which permits more finely tuned regulation of cell activity than would the action of individual independent pathways[1]
[1] Signal-Transduction Pathways: An Introduction to Information Metabolism. Biochemistry. 5th edition. J.M. Berg, J.L.Tymoczko, L. Stryer.New York, 2002.
Axon ID | Name | Description | From price | |
---|---|---|---|---|
3039 | ACY-241 | Selective and orally available HDAC6 inhibitor | €120.00 | |
2269 | AK 1 | Potent inhibitor of SIRT with good selectivity for SIRT2 over SIRT1 and SIRT3 | €90.00 | |
2270 | AK 7 | Potent, brain-permeable and selective inhibitor of SIRT2 | €90.00 | |
2394 | AR-42 | HDAC inhibitor | €125.00 | |
5052 | Axon Ligands™ Epigenetic compound library | Axon Ligands™ Epigenetic compound library | Inquire | |
3115 | Belinostat | HDAC inhibitor | €70.00 | |
3397 | BG45 | HDAC inhibitor (1, 2, 3 Selective) | €80.00 | |
3399 | BML-210 | HDAC inhibitor | €80.00 | |
2471 | BRD 73954 | Dual HDAC 6/8 inhibitor with excellent selectivity over the other HDACs | €85.00 | |
2803 | Cambinol | Inhibitor of SIRT1 and SIRT2 | €95.00 | |
2250 | CHR 6494 trifluoroacetate | Specific, first-in-class inhibitor of histone kinase Haspin | €120.00 | |
2014 | CI 994 | HDAC inhibitor that causes histone hyperacetylation in living cells | €70.00 | |
3038 | CXD101 | HDAC inhibitor (1, 2, 3 Selective) | €125.00 | |
2568 | EML 425 | Potent reversible dual inhibitor of CBP and p300 (HAT/KAT3) | €95.00 | |
3769 | FHD-286 | Selective inhibitor of the BAF chromatin remodeling complex ATPases (BRG1/BRM) | Inquire | |
2208 | Gallic acid | Multi-affinity drug. Antioxidant. | €50.00 | |
1645 | HDAC6 inhibitor ISOX | HDAC6 Inhibitor | €110.00 | |
2529 | JNJ 26481585 dihydrochloride | Potent, orally available second-generation pan-HDAC inhibitor | €125.00 | |
2319 | L 002 | Inhibitor of p300 HAT (KAT3B) and p53 acetylation | €80.00 | |
1548 | LBH 589 | HDAC1 Inhibitor | €90.00 | |
2430 | LW 479 | HDAC inhibitor with cytotoxicity in a panel of breast cancer cell lines. | €135.00 | |
1707 | MC 1568 | HDAC inhibitor (class IIA selective) | €85.00 | |
2505 | Mocetinostat | Class I selective HDAC inhibitor with broad spectrum antitumor activity | €80.00 | |
1803 | MS 275 | Inhibitor of HDAC (1 and 3 Selective) | €60.00 | |
2359 | Nexturastat A | HDAC6 inhibitor with good selectivity over HDAC1 and HDAC8 | €90.00 | |
3409 | NKL 22 | HDAC inhibitor | €80.00 | |
2843 | OSS-128167 | Selective SIRT6 inhibitor | €125.00 | |
1853 | PCI 34051 | HDAC8 Inhibitor | €90.00 | |
1801 | Pyroxamide | HDAC1 Inhibitor | €90.00 | |
2299 | Remodelin | Potent NAT 10 inhibitor that mediates nuclear shape rescue in laminopathic cells via microtubule reorganization | €90.00 |