Date published: 2025-12-24

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OR2A25 Inhibitors

OR2A25 inhibitors pertain to a specialized class of chemical compounds that interact with the OR2A25 receptor, a type of olfactory receptor. Olfactory receptors are a group of G-protein-coupled receptors (GPCRs) that are primarily located in the sensory epithelium of the olfactory system and are responsible for the detection of odor molecules. Each receptor in this family is encoded by a distinct gene and can bind to a variety of odorant molecules. The OR2A25 receptor belongs to this extensive family, and inhibitors targeting this receptor are designed to bind selectively, reducing or preventing its normal action. By doing so, these inhibitors can modulate the receptor's function, leading to a change in the signaling pathways that are activated upon the binding of specific odorant molecules. The molecular design of OR2A25 inhibitors is based on the structural understanding of the receptor and the chemical properties that govern ligand-receptor interactions within the olfactory system. These inhibitors typically exhibit high affinity for the OR2A25 receptor, showing specificity in their binding to prevent the usual ligand-receptor interactions. The development of such inhibitors involves intricate medicinal chemistry approaches to ensure that the molecules possess the necessary characteristics to interact with the receptor's binding site effectively. This includes considerations of the molecule's size, shape, and electronic distribution, which are all crucial for the inhibitor to achieve the desired level of interaction with the receptor. Moreover, the stability of the inhibitor, its metabolic profile, and its selectivity for the OR2A25 receptor over other olfactory receptors are key factors in its design. The inhibitors are usually the result of extensive structure-activity relationship (SAR) studies, which help in refining their molecular features to enhance their inhibitory activity.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Amiloride • HCl

2016-88-8sc-3578
sc-3578A
25 mg
100 mg
$22.00
$56.00
6
(2)

Amiloride serves as an inhibitor of epithelial sodium channels. Given that OR2A25 is an olfactory receptor, the ionic balance modulated by sodium channels may be critical for receptor activity, and altering it could indirectly inhibit OR2A25 signaling.

Ruthenium red

11103-72-3sc-202328
sc-202328A
500 mg
1 g
$184.00
$245.00
13
(1)

This compound is a polycationic dye that blocks certain ion channels. By blocking calcium channels, it may influence the signaling cascade that olfactory receptors like OR2A25 rely upon for initiating a cellular response.

Verapamil

52-53-9sc-507373
1 g
$367.00
(0)

Verapamil is a calcium channel blocker that could inhibit the calcium-mediated signaling pathways that are potentially involved in the function of OR2A25, thus indirectly reducing its activity.

BAPTA, Free Acid

85233-19-8sc-201508
sc-201508A
100 mg
500 mg
$67.00
$262.00
10
(1)

BAPTA is a calcium chelator that could prevent calcium-dependent processes within the cellular signaling cascades, potentially affecting OR2A25 function indirectly by disrupting downstream signaling.

Capsazepine

138977-28-3sc-201098
sc-201098A
5 mg
25 mg
$145.00
$450.00
11
(1)

Capsazepine is a TRPV1 antagonist and by modulating this receptor, it may influence the intracellular calcium levels and thus indirectly affect the signaling pathways associated with OR2A25.

Suramin sodium

129-46-4sc-507209
sc-507209F
sc-507209A
sc-507209B
sc-507209C
sc-507209D
sc-507209E
50 mg
100 mg
250 mg
1 g
10 g
25 g
50 g
$149.00
$210.00
$714.00
$2550.00
$10750.00
$21410.00
$40290.00
5
(1)

Suramin is a polysulfonated naphthylurea that inhibits various growth factor receptors and enzymes. It may indirectly influence the signaling environment of OR2A25 by altering the activities of these proteins.

Thapsigargin

67526-95-8sc-24017
sc-24017A
1 mg
5 mg
$94.00
$349.00
114
(2)

This sesquiterpene lactone acts as a SERCA pump inhibitor, leading to an increase in cytosolic calcium. Elevated calcium levels could desensitize OR2A25 or alter its signaling mechanism indirectly.