Date published: 2025-9-17

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SPEM1 Inhibitors

SPEM1 inhibitors LY294002 and Rapamycin target the PI3K/AKT/mTOR signaling axis, a pathway integral to cell growth, proliferation, and survival. Inhibition of this pathway by these chemicals may result in reduced activity of proteins regulated by this signaling cascade, including the SPEM1. Other inhibitors, such as PD98059, SB203580, and SP600125, target the MAPK signaling pathways. These pathways are pivotal in the control of cellular responses to growth signals, stress, and inflammatory cytokines. Inhibition of these kinases can lead to alterations in gene expression, cell differentiation, or apoptosis, affecting the functional state of proteins like SPEM1 that may be downstream effectors.

Compounds like BAPTA-AM and Thapsigargin can alter intracellular calcium levels, a signaling ion that modulates numerous cellular functions, including enzyme activity, gene transcription, and muscle contraction. If SPEM1 is sensitive to calcium levels, these agents can modulate its activity by altering the calcium signaling within the cell. Kinase inhibitors such as Go6983 and Y-27632 are known to impact a variety of signaling pathways by inhibiting protein kinases involved in cell proliferation, apoptosis, and cytoskeletal organization. Through their broad-spectrum activity, these inhibitors can affect the signaling pathways that SPEM1 is part of, leading to changes in its activity.

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