Date published: 2025-12-24

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BAIAP3 Inhibitors

BAIAP3 Inhibitors target various components of the vesicle trafficking system and related cellular processes, potentially influencing the functional context of BAIAP3. Given BAIAP3's involvement in synaptic vesicle trafficking, modulation of these pathways could indirectly impact its activity. Compounds such as Brefeldin A, Tetanus Toxin, and Botulinum Toxin target key aspects of vesicle trafficking and neurotransmitter release. Brefeldin A disrupts the Golgi apparatus, a crucial organelle in the sorting and transport of vesicles, which could affect processes where BAIAP3 is involved. Tetanus Toxin, by affecting the SNARE complex involved in vesicle docking and fusion, might indirectly influence the role of BAIAP3 in synaptic vesicle dynamics. Inhibitors like Dynamin Inhibitor I, Dynasore, which targets the GTPase dynamin, and Clathrin Inhibitors, affecting clathrin-mediated endocytosis, provide insights into the endocytic pathways crucial for synaptic vesicle recycling and trafficking. These processes are essential for the proper functioning of synaptic transmission, where BAIAP3 might play a role.

Furthermore, compounds like N-Ethylmaleimide, Monensin Sodium Salt, and Tunicamycin, which affect various aspects of vesicle fusion and protein trafficking, can have implications for BAIAP3 function. The disruption of microtubule dynamics by agents like Colchicine and Nocodazole also provides an indirect approach to study the role of BAIAP3 in intracellular transport mechanisms. Wortmannin's inhibition of PI3K, a key player in intracellular signaling, underscores the interconnected nature of signaling pathways and vesicle trafficking processes. The modulation of these pathways provides a broader understanding of how synaptic vesicle trafficking and associated proteins like BAIAP3 are regulated. These compounds, while not directly targeting BAIAP3, are crucial for exploring the complex processes of synaptic vesicle trafficking and neuronal communication. They offer valuable tools for research into the roles of proteins involved in these processes.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Brefeldin A

20350-15-6sc-200861C
sc-200861
sc-200861A
sc-200861B
1 mg
5 mg
25 mg
100 mg
$30.00
$52.00
$122.00
$367.00
25
(3)

Brefeldin A disrupts the Golgi apparatus and can affect vesicle trafficking, potentially impacting BAIAP3-related processes in neurons.

Dynamin Inhibitor I, Dynasore

304448-55-3sc-202592
10 mg
$87.00
44
(2)

Dynasore inhibits dynamin, a GTPase involved in vesicle scission, potentially impacting BAIAP3's role in vesicle trafficking.

N-Ethylmaleimide

128-53-0sc-202719A
sc-202719
sc-202719B
sc-202719C
sc-202719D
1 g
5 g
25 g
100 g
250 g
$22.00
$68.00
$210.00
$780.00
$1880.00
19
(1)

N-Ethylmaleimide inhibits NSF (N-ethylmaleimide-sensitive factor), which is involved in SNARE complex disassembly, potentially impacting BAIAP3's role in vesicle fusion.

Monensin A

17090-79-8sc-362032
sc-362032A
5 mg
25 mg
$152.00
$515.00
(1)

Monensin, a Na+/H+ ionophore, affects intracellular transport and pH regulation, potentially influencing BAIAP3-related vesicle trafficking.

Tunicamycin

11089-65-9sc-3506A
sc-3506
5 mg
10 mg
$169.00
$299.00
66
(3)

Tunicamycin inhibits N-linked glycosylation, impacting protein folding and trafficking, potentially affecting BAIAP3.

Colchicine

64-86-8sc-203005
sc-203005A
sc-203005B
sc-203005C
sc-203005D
sc-203005E
1 g
5 g
50 g
100 g
500 g
1 kg
$98.00
$315.00
$2244.00
$4396.00
$17850.00
$34068.00
3
(2)

Colchicine disrupts microtubule dynamics, which can affect intracellular transport mechanisms relevant to BAIAP3's function.

Nocodazole

31430-18-9sc-3518B
sc-3518
sc-3518C
sc-3518A
5 mg
10 mg
25 mg
50 mg
$58.00
$83.00
$140.00
$242.00
38
(2)

Nocodazole, a microtubule-depolymerizing agent, may influence vesicle trafficking and indirectly impact BAIAP3.

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$66.00
$219.00
$417.00
97
(3)

Wortmannin inhibits PI3K, affecting various signaling pathways, potentially impacting BAIAP3-related synaptic processes.