Date published: 2025-10-30

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TPCN1 Inhibitors

TPCN1 inhibitors constitute a well-defined chemical class that demonstrates a remarkable ability to modulate a specific cellular function. Within this class, compounds are meticulously crafted to exert their effects on the TPCN1 protein, a pivotal member of the two-pore channel family localized within cellular membranes. The intricate role of TPCN1 revolves around its capacity to orchestrate the flux of ions, notably calcium and sodium ions, across these membranes. This ion transportation is of paramount importance in upholding the delicate balance of ion concentrations within cells and is crucial for various cellular signaling pathways. The structural configuration of TPCN1 inhibitors is meticulously engineered to enable interactions with distinct binding sites on the TPCN1 protein.

Through this interaction, the inhibitors induce alterations in the three-dimensional conformation of the protein, subsequently modulating its ion channel activity. This process occurs without necessitating the inhibitors to partake in any chemical transformations themselves. Instead, they act as regulatory switches, influencing the flow of ions across the membrane. The specificity exhibited by TPCN1 inhibitors towards this particular protein underscores their significance in advancing the understanding of cellular physiology. By selectively targeting TPCN1, these inhibitors offer a unique tool to unravel the intricacies of ion homeostasis, cellular signaling, and other vital cellular processes influenced by ion flux. Their mechanism of action and their capacity to perturb intracellular ion concentrations position TPCN1 inhibitors as invaluable agents for investigating the underlying mechanisms of cellular responses.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Imatinib

152459-95-5sc-267106
sc-267106A
sc-267106B
10 mg
100 mg
1 g
$25.00
$117.00
$209.00
27
(1)

Imatinib inhibits tyrosine kinases, particularly the BCR-ABL fusion protein in chronic myeloid leukemia (CML). It also targets c-KIT and PDGFR kinases, leading to reduced cell proliferation and survival.

Sunitinib, Free Base

557795-19-4sc-396319
sc-396319A
500 mg
5 g
$150.00
$920.00
5
(0)

Sunitinib inhibits multiple receptor tyrosine kinases including VEGFR, PDGFR, and c-KIT, interfering with angiogenesis and tumor growth pathways.

Dasatinib

302962-49-8sc-358114
sc-358114A
25 mg
1 g
$47.00
$145.00
51
(1)

Dasatinib inhibits BCR-ABL, c-KIT, and other kinases. It's used for CML and Ph+ ALL by blocking aberrant signaling pathways.

Erlotinib Hydrochloride

183319-69-9sc-202154
sc-202154A
10 mg
25 mg
$74.00
$119.00
33
(1)

Erlotinib targets the epidermal growth factor receptor (EGFR), impeding downstream signaling in cancer cells, commonly used in non-small cell lung carcinoma.

Lapatinib

231277-92-2sc-353658
100 mg
$412.00
32
(1)

Lapatinib inhibits both EGFR and HER2/neu receptors, reducing their activation and downstream signaling in breast and other cancers.

ABT-199

1257044-40-8sc-472284
sc-472284A
sc-472284B
sc-472284C
sc-472284D
1 mg
5 mg
10 mg
100 mg
3 g
$116.00
$330.00
$510.00
$816.00
$1632.00
10
(0)

Venetoclax targets BCL-2 proteins, promoting apoptosis and approved for certain leukemias.