Date published: 2026-5-30

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V1RE11 Activators

V1RE11 activators comprise a chemical class of compounds that can influence the signaling pathways of the V1RE11 protein, a member of the G protein-coupled receptor (GPCR) family. These activators encompass a diverse array of chemical entities, each with a unique mode of action on the cellular mechanisms that can engage V1RE11. Some compounds in this class function by increasing the intracellular concentration of second messengers like cAMP, which plays a pivotal role in the signaling cascade of GPCRs. By elevating cAMP levels, these activators can enhance the receptor's signaling efficiency. Other molecules in this class are designed to modulate protein kinase activity, which can subsequently lead to the phosphorylation of proteins associated with V1RE11 signaling. This phosphorylation can alter the receptor's conformation or its interaction with other cellular components, thereby modulating its activity.

Additionally, the chemical class of V1RE11 activators includes compounds that alter intracellular calcium levels, either by sequestering calcium ions or facilitating their influx into the cell. Calcium ions serve as crucial secondary messengers in GPCR signaling and, therefore, fluctuations in calcium concentrations can have a significant impact on V1RE11 activity. Some activators target specific proteins involved in the breakdown or synthesis of signaling molecules, thereby affecting the receptor's signaling pathway. These modulators either prevent the degradation of signaling molecules, allowing them to exert their effects for a prolonged period, or inhibit enzymes that participate in the signaling cascade, thus altering the receptor's response. Collectively, the chemicals within the V1RE11 activators class act on various components of the cellular machinery to regulate the activity of this receptor without directly binding to the receptor itself.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

PMA

16561-29-8sc-3576
sc-3576A
sc-3576B
sc-3576C
sc-3576D
1 mg
5 mg
10 mg
25 mg
100 mg
$41.00
$132.00
$214.00
$500.00
$948.00
119
(6)

PMA activates protein kinase C (PKC), which could activate Vmn1r66 by phosphorylating related proteins and potentially altering receptor activity.

IBMX

28822-58-4sc-201188
sc-201188B
sc-201188A
200 mg
500 mg
1 g
$260.00
$350.00
$500.00
34
(1)

IBMX is a phosphodiesterase inhibitor that prevents the breakdown of cAMP, which could result in enhanced signaling through Vmn1r66.

Ionomycin

56092-82-1sc-3592
sc-3592A
1 mg
5 mg
$78.00
$270.00
80
(4)

Ionomycin is a calcium ionophore that increases intracellular calcium levels, which could activate Vmn1r66 by affecting calcium-dependent signaling pathways.

BAPTA/AM

126150-97-8sc-202488
sc-202488A
25 mg
100 mg
$138.00
$458.00
61
(2)

BAPTA-AM is a calcium chelator that could activate Vmn1r66 by modulating intracellular calcium levels and affecting downstream signaling.

Pertussis Toxin (islet-activating protein)

70323-44-3sc-200837
50 µg
$451.00
3
(1)

Pertussis toxin inhibits G(i/o) proteins and could alter Vmn1r66 signaling by changing the regulatory context of the receptor’s activity.

Caffeine

58-08-2sc-202514
sc-202514A
sc-202514B
sc-202514C
sc-202514D
50 g
100 g
250 g
1 kg
5 kg
$33.00
$67.00
$97.00
$192.00
$775.00
13
(1)

Caffeine, as a phosphodiesterase inhibitor, could activate Vmn1r66 by raising cAMP levels within the cell, affecting the receptor’s signaling.

2-APB

524-95-8sc-201487
sc-201487A
20 mg
100 mg
$28.00
$53.00
37
(1)

2-ApB modulates IP3 receptors and could activate Vmn1r66 by altering calcium signaling pathways in the cell.