DOC2A inhibitors belong to a specific class of chemical compounds designed to target and modulate the activity of DOC2A, a protein of significance in cellular processes. DOC2A, short for Double C2-like Domain-Containing Protein Alpha, is a member of the DOC2 protein family, which is known for its involvement in regulating calcium-dependent vesicle trafficking and neurotransmitter release within nerve cells. These proteins play a crucial role in the exocytosis of synaptic vesicles at neuronal synapses, a fundamental process in the transmission of nerve signals. In particular, DOC2A is implicated in the facilitation of vesicle fusion with the plasma membrane, an essential step for neurotransmitter release and subsequent neuronal communication. Inhibitors of DOC2A are designed to interact with this protein, potentially modulating its activity and thereby influencing vesicle trafficking and neurotransmitter release processes within neurons.
Structurally, DOC2A inhibitors are engineered to interact with specific regions or binding sites on the DOC2A protein. By doing so, they may disrupt the normal functioning of DOC2A, affecting its ability to mediate vesicle fusion and neurotransmitter release. The precise mechanisms by which these inhibitors act can vary, but their overarching goal is to provide researchers with a valuable tool for investigating the intricacies of vesicle trafficking and synaptic transmission at the molecular level. Understanding the role of DOC2A in these processes and its modulation by inhibitors can offer insights into the fundamental biology of neurons and their communication, which can be crucial for advancing our understanding of neurological function and potentially informing future research directions in this field.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
BAPTA/AM | 126150-97-8 | sc-202488 sc-202488A | 25 mg 100 mg | $138.00 $458.00 | 61 | |
BAPTA-AM is a cell-permeable calcium chelator. By affecting calcium dynamics, it could potentially interfere with DOC2A's calcium-dependent functions. | ||||||
2-APB | 524-95-8 | sc-201487 sc-201487A | 20 mg 100 mg | $28.00 $53.00 | 37 | |
2-APB modulates intracellular calcium release. Changes in calcium signaling might indirectly influence DOC2A-mediated processes. | ||||||
Nifedipine | 21829-25-4 | sc-3589 sc-3589A | 1 g 5 g | $59.00 $173.00 | 15 | |
As a calcium channel blocker, Nifedipine might alter calcium-dependent processes involving DOC2A. | ||||||
EGTA | 67-42-5 | sc-3593 sc-3593A sc-3593B sc-3593C sc-3593D | 1 g 10 g 100 g 250 g 1 kg | $21.00 $65.00 $120.00 $251.00 $815.00 | 23 | |
EGTA is another calcium chelator. By sequestering calcium, it could potentially impact DOC2A functions. | ||||||
Dantrolene | 7261-97-4 | sc-500165 | 25 mg | $350.00 | 7 | |
This compound inhibits ryanodine receptors, affecting calcium release from the endoplasmic reticulum, which could indirectly influence DOC2A-mediated processes. | ||||||
Verapamil | 52-53-9 | sc-507373 | 1 g | $374.00 | ||
Being a calcium channel blocker, Verapamil might affect calcium-dependent functions of DOC2A. | ||||||
TMB-8 • HCl | 53464-72-5 | sc-3522 sc-3522A | 10 mg 50 mg | $43.00 $129.00 | 10 | |
This compound inhibits calcium release from intracellular stores, potentially affecting DOC2A functions. | ||||||
Ryanodine | 15662-33-6 | sc-201523 sc-201523A | 1 mg 5 mg | $223.00 $799.00 | 19 | |
By modulating ryanodine receptors and altering calcium dynamics, Ryanodine might indirectly affect DOC2A-mediated processes. | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $136.00 $446.00 | 114 | |
This compound depletes calcium stores from the endoplasmic reticulum, potentially influencing DOC2A functions. | ||||||
Nimodipine | 66085-59-4 | sc-201464 sc-201464A | 100 mg 1 g | $61.00 $307.00 | 2 | |
As another calcium channel blocker, Nimodipine might interfere with calcium-dependent activities of DOC2A. | ||||||