Date published: 2026-4-1

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Olfr370 Activators

Or10k2 is an olfactory receptor in Mus musculus (house mouse), classified within the G-protein-coupled receptor (GPCR) family. These receptors, characterized by their 7-transmembrane domain structure, are responsible for the detection of odorant molecules and the initiation of neuronal responses that culminate in the perception of smell. The olfactory receptor gene family, noted for its extensive diversity, underscores the complexity of odor recognition and the nuanced mechanisms of signal transduction that these receptors employ. Or10k2, like its counterparts, operates within this sophisticated framework, translating chemical signals into a biological response that is fundamental to the organism's interaction with its environment. The activation of Or10k2, akin to other GPCRs, begins with the binding of an odorant molecule, leading to a conformational change in the receptor. This change is pivotal as it facilitates the interaction between the receptor and G-proteins. Subsequent to this interaction, the G-proteins dissociate into their respective subunits, with the Gα subunit playing a central role in activating downstream effectors like adenylyl cyclase. The activation of adenylyl cyclase catalyzes the conversion of ATP to cyclic AMP (cAMP), a secondary messenger of paramount importance in cellular signaling. The rise in cAMP levels triggers the activation of protein kinase A (PKA), which phosphorylates various proteins, thereby generating a neuronal signal interpreted as a specific odor.

This activation pathway is modulated by various factors, both intrinsic and extrinsic to the cell. Chemical compounds that can elevate cAMP levels, whether by stimulating adenylyl cyclase directly or inhibiting the enzymes that degrade cAMP, represent potential indirect activators of Or10k2. Moreover, the dynamic nature of GPCR signaling means that the activation state of Or10k2 can be influenced by the activity of neighboring receptors and the overall cellular signaling milieu. For instance, compounds that affect the signaling of adjacent GPCRs can indirectly modify the activation threshold or efficacy of Or10k2, thereby influencing its response to odorant stimuli. In summary, the activation of Or10k2 is a multi-faceted process, intricately linked to the broader context of GPCR signaling and cellular response mechanisms. Understanding these complex interactions and the potential for modulation through various chemical compounds offers valuable insights into the olfactory system. This knowledge not only enhances our comprehension of olfaction but also illuminates the broader principles governing GPCR function and regulation 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)

As a beta-adrenergic agonist, Isoproterenol raises intracellular cAMP through adenylyl cyclase activation. This cAMP increase can indirectly enhance Or10k2 activity by promoting G-protein coupling and receptor responsiveness, critical for effective odorant signaling.

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 broad-spectrum phosphodiesterase inhibitor, prevents cAMP degradation, maintaining high cAMP levels. This sustained cAMP elevation can indirectly aid Or10k2 activation by stabilizing GPCR conformations that are more receptive to odorant molecules.

Rolipram

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

Rolipram selectively inhibits phosphodiesterase-4, leading to increased cAMP in relevant cells. Elevated cAMP levels may indirectly facilitate Or10k2 activation by improving GPCR signaling efficiency, which is crucial in olfactory signal transduction.

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), through its EP receptors, raises cAMP levels. This cAMP surge might indirectly stimulate Or10k2 by enhancing the GPCR's readiness for signal transduction, thus improving olfactory response.

Dopamine

51-61-6sc-507336
1 g
$290.00
(0)

Dopamine acts on its GPCRs, potentially modulating cAMP levels. This modulation can indirectly influence Or10k2 activation, potentially altering the receptor's responsiveness to odorant signals through changes in GPCR signaling dynamics.

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 influence cAMP levels. This effect might indirectly impact Or10k2, potentially modifying its activation state in response to odorants by altering the GPCR signaling environment.

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 affects cAMP levels via its GPCRs. This action might indirectly affect Or10k2 by modulating GPCR signaling, potentially making the receptor more responsive to 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, antagonizing adenosine receptors, indirectly influences cAMP levels and thus GPCR signaling. This might affect Or10k2 activation by modifying the GPCR signaling landscape, potentially impacting the receptor's response 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, influences cAMP levels via various GPCRs. This might indirectly enhance Or10k2 activity by altering GPCR signaling, potentially affecting the receptor's sensitivity to odorant molecules.

Zaprinast (M&B 22948)

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

Zaprinast, by inhibiting phosphodiesterases, increases cAMP levels, which might indirectly enhance Or10k2 activation by stabilizing GPCR conformations favorable for odorant signal transduction, especially in olfactory neurons.