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inosine monophosphate

compound / compound-inosine-monophosphate

イノシン一リン酸

Inosine monophosphate (IMP), a umami-related substance used in hTAS2R16 cell assays.

On this page (6 sections)
  1. Overview
  2. Sources for this overview (1)
  3. Topic hubs
  4. Follow the connections
  5. Related entries (10)
  6. Mechanism and receptors (1)
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Reading the bitterness

Inosine monophosphate (IMP) is one of the umami-related substances. A 2020 study used cells expressing TAS2R16, one of the human bitter taste receptors (hTAS2R16), to examine how IMP acts on this receptor's response to bitter ligands. As a result, IMP was reported to act as partial non-surmountable antagonism (response inhibition that cannot be overcome competitively) on hTAS2R16 wild-type bitter ligand response.

The full text of the same study showed a dose-response curve using salicin as a bitter agonist. When IMP was added, salicin's EC50 (half-maximal effective concentration) increased 2- to 3-fold, and at the highest concentration, IMP 30 mM, the maximum response decreased 50% compared to salicin alone. However, this result derives from an in vitro experimental system using hTAS2R16-expressing cells, and does not confirm in human sensory tests that umami substances weaken bitter taste perception.

Sources for this overview

  1. Suppression of hTAS2R16 Signaling by Umami Substances

    Rhyu Mee-Ra; Kim Yiseul; Misaka Takumi / 2020 / journal article / full text checked

    Checked for this overview: Adoption of qualitative findings of antagonistic action. / Adoption of numerical values for EC50 shift and maximum response decrease rate.

Follow the connections

inosine monophosphate →antagonizes→ TAS2R16

Structured claims — open a section to read each claim's confidence, evidence and limits

Mechanism and receptors (1)

inosine monophosphate antagonizes TAS2R16preliminary

Scope: The same hTAS2R16-expressing cell system

Note: Reported as partial, non-surmountable antagonism. Not extrapolated to human sensory perception.

IMP was reported to act as a partial, non-surmountable antagonist of the bitter-ligand response of wild-type hTAS2R16.
Limitations: No human sensory testing.
Source: Suppression of hTAS2R16 Signaling by Umami Substances (Rhyu Mee-Ra; Kim Yiseul; Misaka Takumi, 2020) · full text checked
Adding IMP raised salicin's EC50 by 2-3 fold, and at the highest concentration (IMP 30 mM) the maximal response to salicin alone decreased by 50%. Verbatim: "the maximal response of salicin alone was gradually decreased by... 50%... at the highest concentration of... IMP (30 mM)".
Limitations: The abstract gave only the qualitative classification "partial insurmountable antagonist", but the full text confirmed quantitative values — the percentage decrease in maximal response and the fold shift in EC50. Not a human sensory test.
Source: Suppression of hTAS2R16 Signaling by Umami Substances (Rhyu Mee-Ra; Kim Yiseul; Misaka Takumi, 2020) · full text checked
Show datacompound-inosine-monophosphate —antagonizes→ receptor-tas2r16
claim: clm-imp-antagonizes-tas2r16 / type: mechanism / updated: 2026-08-31

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