Autophagy

Autophagy is a process by which a cell breaks down macromolecules in response to starvation or stress signals. While it is closely linked with apoptosis, autophagy is primarily characterized as a catabolic mechanism by which cellular energy homeostasis is maintained.

Products for Autophagy - Page 3

  1. Cat.No. Product Name Information/Activity
  2. BCC4378 Carbamazepine Carbamazepine, a sodium channel blocker, is an anticonvulsant drug. Carbamazepine chemical structure
  3. BCC4325 Clonidine HCl Clonidine hydrochloride is an agonist of α2-adrenoceptor and potent antihypertensive agent. Clonidine HCl chemical structure
  4. BCC1184 Dexamethasone (DHAP) Dexamethasone (Hexadecadrol) is a glucocorticoid receptor agonist. Dexamethasone also significantly decreases CD11b, CD18, and CD62L expression on neutrophils, and CD11b and CD18L expression on monocytes. Dexamethasone (DHAP) chemical structure
  5. BCC4361 Dorsomorphin 2HCl Dorsomorphin dihydrochloride (Compound C dihydrochloride) is a potent, selective and ATP-competitive AMPK inhibitor, with a Ki of 109 nM. Dorsomorphin dihydrochloride inhibits BMP pathway by targeting the type I receptors ALK2, ALK3, and ALK6. Dorsomorphin dihydrochloride induces autophagy. Dorsomorphin 2HCl chemical structure
  6. BCC1944 Seocalcitol Seocalcitol is a vitamin D analog, binds vitamin D receptor protein from human osteosarcoma MG-63 cells with Kd of 0.27 nM. Seocalcitol chemical structure
  7. 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
  8. BCC5666 L-690,330 L-690330 is a competitive inhibitor of inositol monophosphatase (IMPase) with Kis of 0.27 and 0.19 μM for recombinant human and bovine IMPase, 0.30 and 0.42 μM for human and bovine frontal cortex IMPase, respectively. L-690330 exhibits 10-fold more sensitive than mouse and rat IMPase. L-690,330 chemical structure
  9. BCC7043 NF 449 Highly selective P2X<sub>1</sub> antagonist NF 449 chemical structure
  10. BCC5081 Niclosamide Niclosamide (BAY2353) is an orally bioavailable chlorinated salicylanilide, with anthelmintic and potential antineoplastic activity. Niclosamide (BAY2353) inhibits STAT3 with IC50 of 0.25 μM in HeLa cells and inhibits DNA replication in a cell-free assay. Niclosamide chemical structure
  11. BCC3823 Nimodipine Nimodipine(Nimotop) is a dihydropyridine derivative and an analogue of the calcium channel blocker nifedipine, with antihypertensive activity. Nimodipine chemical structure

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