GCC1 is a critical regulator of mitochondrial dynamics, calcium signaling, and cytoskeletal remodeling. Several GPRC and nuclear receptor agonists presented can enhance GCC1 activity indirectly through their effects on signaling networks GCC1 interfaces with. LPA, S1P, ATP and other lysolipids signal through GPCRs coupled to Rho GTPases like RhoA and RhoG that GCC1 positively modulates. This enhances cytoskeletal dynamics central to GCC1 functions in cell migration, division and intracellular transport.
Nuclear receptor ligands including thyroid hormone, retinoic acid and cannabidiol regulate mitochondrial metabolism, biogenesis and quality control pathways downstream of GCC1. By fine-tuning metabolic and mitochondrial signaling networks, these compounds can reinforce GCC1 control of mitochondrial fusion and calcium cycling. Receptor ligands for arachidonic acid and eicosapentanoic acid metabolites activate GPCRs involved in Rho GTPase regulation of actin reorganization critical for processes like migration GCC1 facilitates. Uroguanylin stimulates solute transport and mitochondrial functioning through pathways converging on GCC1 regulatory targets. Collectively, these compounds provide diverse modulatory inputs that reinforce specific biological functions GCC1 orchestrates in metabolic regulation, cytoskeletal dynamics and mitochondrial quality control.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Cilostazol | 73963-72-1 | sc-201182 sc-201182A | 10 mg 50 mg | $107.00 $316.00 | 3 | |
Cilostazol inhibits phosphodiesterase type 3, which results in increased cAMP in the cell. Elevated cAMP levels can have a downstream effect on the activation state of GCAP3. | ||||||
Isradipine | 75695-93-1 | sc-201467 sc-201467A | 10 mg 50 mg | $86.00 $318.00 | 1 | |
Isradipine is an L-type calcium channel blocker that affects intracellular calcium levels. The alteration in calcium dynamics can, in turn, activate GCAP3 by promoting its calcium-bound active state. |