Date published: 2026-4-1

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Olfr368 Activators

Or5c1, belonging to the olfactory receptor family 5 subfamily C member 1 in Mus musculus (house mouse), plays a crucial role in the perception of smell. As a member of the G-protein-coupled receptor (GPCR) superfamily, Or5c1 exhibits a characteristic 7-transmembrane domain structure. This structural feature is shared with many neurotransmitter and hormone receptors, underscoring the versatility and significance of GPCRs in cellular signaling. The activation of Or5c1, like other olfactory receptors, is initiated by the binding of odorant molecules, which triggers a cascade of intracellular events leading to neuronal responses. The olfactory receptor family, notably the largest in the genome, underlines the complexity and diversity of odor detection and the subsequent signal transduction processes. The mechanism of activation of Or5c1 involves several key steps. Initially, the binding of an odorant molecule to Or5c1 induces a conformational change in the receptor, facilitating its interaction with G-proteins. This interaction leads to the dissociation of the G-protein subunits, primarily the Gα subunit, which in turn activates adenylyl cyclase. The activation of adenylyl cyclase catalyzes the conversion of ATP to cyclic AMP (cAMP), a critical second messenger in cellular signaling. The increase in intracellular cAMP levels further activates protein kinase A (PKA), which phosphorylates various target proteins, leading to the generation of a neuronal signal that is perceived as a smell.

The activation of Or5c1 and similar GPCRs is finely tuned and can be influenced by various extracellular and intracellular factors. Chemicals that can elevate intracellular cAMP levels, either by direct activation of adenylyl cyclase or by inhibition of phosphodiesterases (which degrade cAMP), are potential indirect activators of Or5c1. Additionally, compounds that modulate the activity of other GPCRs in the vicinity can also influence the activation state of Or5c1. This indirect modulation occurs through the intricate network of GPCR signaling, where the activation of one receptor can impact the signaling dynamics of another. In summary, the activation of Or5c1 is a complex process involving the orchestration of multiple signaling components. The ability to modulate this process, either directly or indirectly, through various chemical compounds highlights the intricate interplay of cellular signaling pathways in the olfactory system. The understanding of these mechanisms provides insights into the fundamental aspects of olfaction and the broader implications of GPCR signaling in various physiological contexts.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Isoproterenol Hydrochloride

51-30-9sc-202188
sc-202188A
100 mg
500 mg
$28.00
$38.00
5
(0)

Isoproterenol, a synthetic catecholamine, functions as a non-selective beta-adrenergic agonist, raising intracellular cAMP levels via adenylyl cyclase activation. This cAMP upsurge can indirectly augment Or5c1 activity by promoting G-protein subunit association with the receptor.

IBMX

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

IBMX, a non-selective inhibitor of phosphodiesterases, prevents cAMP degradation, sustaining enhanced intracellular cAMP concentrations. This maintained elevation in cAMP may indirectly support Or5c1 activation by stabilizing active GPCR conformations conducive to signal transduction.

Rolipram

61413-54-5sc-3563
sc-3563A
5 mg
50 mg
$77.00
$216.00
18
(1)

Rolipram, a selective phosphodiesterase-4 inhibitor, specifically augments intracellular cAMP in cells expressing this enzyme. Elevated cAMP levels could indirectly facilitate Or5c1 activation by enhancing GPCR signaling efficiency, particularly in olfactory sensory neurons.

PGE2

363-24-6sc-201225
sc-201225C
sc-201225A
sc-201225B
1 mg
5 mg
10 mg
50 mg
$57.00
$159.00
$275.00
$678.00
37
(1)

Prostaglandin E2 (PGE2) operates through its G-protein-coupled EP receptors, elevating intracellular cAMP levels. This increase in cAMP might indirectly stimulate Or5c1 by promoting a more receptive state of the GPCR for signal transduction, enhancing olfactory response.

Histamine, free base

51-45-6sc-204000
sc-204000A
sc-204000B
1 g
5 g
25 g
$94.00
$283.00
$988.00
7
(1)

Histamine, interacting with its GPCRs, can modulate intracellular signaling pathways, including cAMP levels. Such modulation may have an indirect effect on Or5c1, potentially altering its activation state in response to odorants by influencing the overall GPCR signaling milieu.

Adenosine

58-61-7sc-291838
sc-291838A
sc-291838B
sc-291838C
sc-291838D
sc-291838E
sc-291838F
1 g
5 g
100 g
250 g
1 kg
5 kg
10 kg
$34.00
$48.00
$300.00
$572.00
$1040.00
$2601.00
$4682.00
1
(0)

Adenosine, through its GPCRs, primarily modulates cAMP levels. This action could indirectly affect Or5c1 by altering the balance of GPCR signaling, potentially making the olfactory receptor more responsive to activation by odorant molecules.

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, a non-selective adenosine receptor antagonist, indirectly affects cAMP levels and thus GPCR signaling. This could influence Or5c1 by modifying the GPCR signaling environment, potentially affecting the receptor's responsiveness to odorants.

(−)-Epinephrine

51-43-4sc-205674
sc-205674A
sc-205674B
sc-205674C
sc-205674D
1 g
5 g
10 g
100 g
1 kg
$41.00
$104.00
$201.00
$1774.00
$16500.00
(1)

Epinephrine, a hormone and neurotransmitter, acts on various GPCRs, influencing cAMP levels. This action could indirectly enhance Or5c1 activity by modulating GPCR signaling dynamics, potentially affecting the receptor's sensitivity to odorant signals.

Zaprinast (M&B 22948)

37762-06-4sc-201206
sc-201206A
25 mg
100 mg
$105.00
$250.00
8
(2)

Zaprinast, a phosphodiesterase inhibitor, increases cAMP levels by preventing its breakdown. Elevated cAMP might indirectly enhance Or5c1 activation by stabilizing GPCR conformations favorable for odorant signal transduction, especially in olfactory sensory neurons.