Date published: 2025-9-22

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Vmn1r114 Inhibitors

The chemical class known as Vmn1r114 inhibitors encompasses a variety of compounds that can indirectly suppress the function of the vomeronasal 1 receptor 114 by modulating the signaling pathways and cellular processes upon which the receptor relies. These inhibitors target a broad spectrum of molecular mechanisms, including calcium signaling, kinase activity, and cytoskeletal dynamics, all of which are integral to the function of the Vmn1r114 receptor. For instance, compounds like BAPTA-AM act by chelating intracellular calcium, thereby dampening the receptor's calcium-dependent responses, while inhibitors such as U73122 and LY294002 disrupt the production or action of second messengers pivotal to Vmn1r114-associated pathways.

Moreover, these inhibitors influence the phosphorylation state of proteins that are critical for the receptor's signaling cascade. By inhibiting kinases like Src, JNK, p38 MAPK, MEK, and PKC with chemicals such as PP2, SP600125, SB203580, PD98059, GF109203X, Chelerythrine chloride, and Gö6976, the compounds can alter the phosphorylation and thereby modulate the activity of proteins downstream of the Vmn1r114 receptor. ML-7 and NSC 23766, by inhibiting myosin light chain kinase and Rac1 GTPase respectively, can affect the actin cytoskeleton organization and cell motility. These actions are crucial for the proper trafficking and signaling of the receptor.

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