Date published: 2025-12-24

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OR1F1 Inhibitors

OR1F1 inhibitors represent a targeted chemical class designed to specifically inhibit the activity of the OR1F1 protein, an entity involved in cellular signaling pathways or molecular processes. The purpose of these inhibitors is to bind directly to the OR1F1 protein, thereby blocking its interaction with other molecules or substrates and effectively reducing its functional activity within the cell. This direct inhibition can lead to alterations in the cellular processes governed by OR1F1, providing insights into the protein's role and the biological pathways it influences. The development of OR1F1 inhibitors is based on a deep understanding of the protein's structure and function, aiming to identify molecules that can specifically and effectively bind to OR1F1, impeding it from fulfilling its normal biological roles. By inhibiting OR1F1, researchers can study the downstream effects on cellular signaling pathways, gene expression, and other cellular functions to better understand the protein's contributions to cellular physiology. The identification and characterization of OR1F1 inhibitors involve a multifaceted approach that combines computational, biochemical, and cellular techniques. Computational methods such as molecular docking and virtual screening are first employed to predict inhibitors based on their structural compatibility with OR1F1. These computational predictions are then validated through in vitro biochemical assays, which may include competitive binding assays, fluorescence resonance energy transfer (FRET) assays, or enzyme-linked immunosorbent assays (ELISA) to assess the binding affinity and specificity of these molecules to OR1F1. Following the in vitro validation, cell-based assays are conducted to observe the physiological effects of OR1F1 inhibition, such as changes in signaling pathway activation, alterations in gene expression profiles, and impacts on cell proliferation or apoptosis. Techniques like quantitative PCR (qPCR) for measuring gene expression changes, Western blotting for detecting protein levels, and immunofluorescence microscopy for visualizing cellular localization of proteins are utilized to understand the consequences of inhibiting OR1F1.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

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)

Nonspecific GPCR antagonist, may influence olfactory receptor signaling indirectly.

Propranolol

525-66-6sc-507425
100 mg
$180.00
(0)

Beta-adrenergic receptor antagonist, could affect GPCR-mediated pathways, indirectly influencing OR1F1.

Carvedilol

72956-09-3sc-200157
sc-200157A
sc-200157B
sc-200157C
sc-200157D
100 mg
1 g
10 g
25 g
100 g
$122.00
$235.00
$520.00
$979.00
$1500.00
2
(1)

Beta-blocker with alpha-1 blocking activity, may have an indirect effect on GPCR signaling.

Nifedipine

21829-25-4sc-3589
sc-3589A
1 g
5 g
$58.00
$170.00
15
(1)

Calcium channel blocker, could indirectly influence GPCR signaling pathways.

Verapamil

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

Calcium channel antagonist, may indirectly affect GPCR-related signaling.

Diltiazem

42399-41-7sc-204726
sc-204726A
1 g
5 g
$209.00
$464.00
4
(1)

A calcium channel blocker, potentially impacting signaling pathways of GPCRs.

Itraconazole

84625-61-6sc-205724
sc-205724A
50 mg
100 mg
$76.00
$139.00
23
(1)

Inhibits cytochrome P450 enzymes, potentially affecting GPCR signaling indirectly.

Ketoconazole

65277-42-1sc-200496
sc-200496A
50 mg
500 mg
$62.00
$260.00
21
(1)

Similar to Itraconazole, may influence GPCR pathways indirectly.

Amiodarone

1951-25-3sc-480089
5 g
$312.00
(1)

Affects multiple ion channels, potentially influencing GPCR signaling pathways.

Lidocaine

137-58-6sc-204056
sc-204056A
50 mg
1 g
$50.00
$128.00
(0)

Sodium channel blocker, could indirectly influence GPCR-mediated signaling.