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mozambioside

compound / compound-mozambioside

モザンビオシド

Mozambioside is a bitter furanocumarin glycoside found uniquely in Arabica coffee beans. During roasting it decomposes into a group of degradation products with lower bitterness thresholds.

On this page (8 sections)
  1. Overview
  2. Sources for this overview (4)
  3. Topic hubs
  4. Related entries (10)
  5. Measured values (2)
  6. Composition and content (1)
  7. Sensory (1)
  8. How processing and cooking change it (1)
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Reading the bitterness

Mozambioside is a bitter furanocumarin glycoside found uniquely in Arabica coffee beans. It exists concentrated in Arabica during the green bean stage, and transforms into a group of degradation products with lower bitterness thresholds during roasting—this transformation is why this compound is studied at this bitterness research lab.

Quantification by UPLC-HDMS showed a concentration difference large enough to distinguish species: approximately 396–1188 nmol/g in Arabica green beans, versus less than 5 nmol/g in Robusta. In roasted Arabica beans, the concentration declined to 232±37 nmol/g, and extraction recovery was reported at 86–98%.

Regarding the recognition threshold for bitterness, one 2015 study reported 60±10 µmol/L in aqueous solution, while a 2025 study reported the same compound's threshold at 132 µM—a gap of approximately 2.2-fold. Both reports trace to roughly the same research lineage; panel differences, compound purity, and methodological differences have been proposed as possible causes, but they cannot be pinned down within the scope of abstracts alone. This is an example demonstrating that a threshold cannot be treated as a single value.

The thermal decomposition products that form as mozambioside breaks down during roasting include glucosyl cafestol-type derivatives, several of which show lower human thresholds (27–80 µM) than the parent compound (132 µM). Measured from actual roasted coffee powder at 21.0–170.4 nmol/g with extraction recovery of approximately 41–128%, a mixture at this concentration in coffee was reported to be recognized as bitter by 80% of a panel. Sensitivity correlated with an intact TAS2R43 locus.

On the receptor side, that a pair of bitter taste receptors—TAS2R43 and TAS2R46—responds to mozambioside with sensitivity far exceeding that to caffeine was previously shown using cultured cells and functional calcium imaging. Structurally related compounds cafestol and kawheol are reported to also activate this receptor pair more strongly than caffeine; when kawheol is given simultaneously with mozambioside, it has been reported to act as a weak partial agonist with inhibitory effect. This finding, in prior form, supports the explanation that roasting-derived products transmit bitterness through the same receptor pair.

Sources for this overview

  1. Mozambioside Is an Arabica-Specific Bitter-Tasting Furokaurane Glucoside in Coffee Beans

    Lang R; Klade S; Beusch A; Dunkel A; Hofmann T / 2015 / journal article / abstract checked

    Checked for this overview: Confirmed as a bitter furanocumarin glycoside specific to Arabica. / Confirmed concentration values in green and roasted beans and extraction recovery rates. / Confirmed 2015 report threshold of 60±10 µM.

  2. Contribution of mozambioside roasting products to coffee's bitter taste

    Bichlmaier C; Froehlich SM; Brychcy V; Grassl A; Behrens M; Lang R / 2025 / journal article / abstract checked

    Checked for this overview: Confirmed 2025 report threshold of 132 µM and discrepancy. / Confirmed concentration of degradation products in coffee, human thresholds, and genetic correlation.

  3. Identification of mozambioside roasting products and their bitter taste receptor activation

    Czech C; Lang T; Grassl A; Steuer A; Di Pizio A; Behrens M; Lang R / 2024 / journal article / abstract checked

    Checked for this overview: Confirmed structure of 5 degradation products and their thresholds lower than the parent compound.

  4. Numerous Compounds Orchestrate Coffee's Bitterness

    Lang T; Lang R; Di Pizio A; Mittermeier VK; Schlagbauer V; Hofmann T; Behrens M / 2020 / journal article / abstract checked

    Checked for this overview: Confirmed high-sensitivity response of TAS2R43/46 and action of structurally related compounds.

Measured values (2)

KindCompoundTargetValueConditionsSource
human recognition thresholdmozambioside—60±10 µMaqueous solution (132 µM (2025), under dispute)Lang R, 2015
human recognition thresholdmozambioside—132 µMaqueous solution (60±10 µM (2015), under dispute)Bichlmaier C, 2025

Values are the reported values of each source (with units and conditions). Thresholds and EC50 depend on the panel and method; they are not single true values.

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

Composition and content (1)

mozambioside is a marker for Arabica (396-1188 nmol/g in green beans; robusta is <5 nmol/g)supported

Scope: Quantified by UPLC-HDMS. Decreases to 232±37 nmol/g in roasted beans; extraction rate 86-98%

Arabica green beans: 396-1188 nmol/g; robusta: <5 nmol/g. Roasted arabica: 232±37 nmol/g; extraction rate 86-98%.
Limitations: Abstract only checked. Number of samples unknown.
Source: Mozambioside Is an Arabica-Specific Bitter-Tasting Furokaurane Glucoside in Coffee Beans (Lang R; Klade S; Beusch A; Dunkel A; Hofmann T, 2015) · abstract checked
Show datacompound-mozambioside —is_marker_for→ "Arabica (396-1188 nmol/g in green beans; robusta is <5 nmol/g)"
claim: clm-mozambioside-arabica-marker / type: composition / updated: 2026-08-30

Sensory (1)

mozambioside — bitter recognition threshold: 60±10 µM (2015) and 132 µM (2025) — roughly a 2-fold discrepancy within the same lineage of laboratoriescontested

Scope: Human recognition threshold in aqueous solution

Note: NIGAMI LAB's first contested claim. The threshold is panel- and method-dependent, an example that it cannot be treated as a single fixed value.

Mozambioside's bitterness recognition threshold is 60±10 µmol/L.
Limitations: Only the abstract was checked.
Source: Mozambioside Is an Arabica-Specific Bitter-Tasting Furokaurane Glucoside in Coffee Beans (Lang R; Klade S; Beusch A; Dunkel A; Hofmann T, 2015) · abstract checked
Contradicts: Reports the threshold of the same compound as 132 µM — about 2.2 times the 60±10 µM reported in 2015. Panel, purity, and methodological differences are candidate causes.
Limitations: Only the abstract was checked. The cause of the discrepancy cannot be identified from either abstract alone.
Source: Contribution of mozambioside roasting products to coffee's bitter taste (Bichlmaier C; Froehlich SM; Brychcy V; Grassl A; Behrens M; Lang R, 2025) · abstract checked
Show datacompound-mozambioside —has_bitter_recognition_threshold→ "60±10 µM (2015) and 132 µM (2025) — roughly a 2-fold discrepancy within the same lineage of laboratories"
claim: clm-mozambioside-threshold / type: sensory / updated: 2026-08-30

How processing and cooking change it (1)

mozambioside degrades into more potently bitter compounds via Roasting-derived breakdown products (glucosylated cafestol derivatives, bengalensol, and others) have a lower bitterness threshold than the parent compound (27–80 µM vs 132 µM) and activate TAS2R43/46supported

Scope: HEK293T cell assay plus human threshold measurement. A mixture at coffee-level concentrations was recognized as bitter by 80% of the panel. Sensitivity correlated with whether the TAS2R43 gene locus was intact

Note: That chicory bitterness is received by the same TAS2R43/46 connects to Research Note 002.

The structures of 5 heat-degradation products were determined by NMR/UHPLC-ToF-MS. Of these, 3 had a lower receptor-activation threshold than the parent compound. Docking analysis examined the binding mode to TAS2R43/46. The compounds were also detected in actual roasted-coffee extracts.
Limitations: Abstract only checked. This is a cultured-cell system, not human perception itself.
Source: Identification of mozambioside roasting products and their bitter taste receptor activation (Czech C; Lang T; Grassl A; Steuer A; Di Pizio A; Behrens M; Lang R, 2024) · abstract checked
21.0–170.4 nmol/g in ground coffee, with an extraction rate of about 41–128%. The human threshold of the main breakdown products was 27–80 µM (parent compound 132 µM). A mixture of 1–8 at coffee-level concentrations was recognized as bitter by 80% of the panel. Sensitivity correlated with an intact TAS2R43 gene locus.
Limitations: Abstract only checked. Panel size is unknown. This is only at the stage of 「寄与を示唆」 (in translation: "suggesting a contribution"), not a quantification of the contribution rate.
Source: Contribution of mozambioside roasting products to coffee's bitter taste (Bichlmaier C; Froehlich SM; Brychcy V; Grassl A; Behrens M; Lang R, 2025) · abstract checked
In functional calcium imaging, TAS2R43/46 responded to mozambioside with far higher sensitivity than to caffeine. The structurally related compounds bengalensol, cafestol, and kahweol also activated the same receptor pair more strongly than caffeine did. Kahweol is a weak partial agonist of TAS2R43 and showed a suppressive effect when co-applied with mozambioside. This lends prior support to the receptor assignment reported by Czech 2024 and Bichlmaier 2025, that 「モザンビオシド系化合物の受け手は TAS2R43/46」 (in translation: "the receptors for mozambioside-class compounds are TAS2R43/46").
Limitations: Abstract only checked. This is receptor data for the parent compound and structurally related compounds, not the roasting breakdown products themselves (glucosylated cafestol derivatives, etc.). This is research from the Leibniz/TUM cluster with personnel overlap with Czech 2024 and Bichlmaier 2025, so it is not a fully independent-lab replication.
Source: Numerous Compounds Orchestrate Coffee's Bitterness (Lang T; Lang R; Di Pizio A; Mittermeier VK; Schlagbauer V; Hofmann T; Behrens M, 2020) · abstract checked
The formal names of the 5 mozambioside heat-degradation products: 17-O-β-D-glucosyl-11-hydroxycafestol-2-one, 11-O-β-D-glucosyl-16-deoxycafestol-2-one, 11-O-β-D-glucosyl-(S)-16-deoxy-17-oxocafestol-2-one, 11-O-β-D-glucosyl-15,16-dehydrocafestol-2-one, and 11-O-β-D-glucosyl-(R)-16-deoxy-17-oxocafestol-2-one. Of these, the (S)-form, the 15,16-dehydro form, and the (R)-form (3 compounds) showed a lower receptor-activation threshold than the parent compound, and 2 of these 3 (the 15,16-dehydro form and the (R)-form) were also detected by UHPLC-ToF-MS in actual roasted-coffee extracts.
Limitations: This information was extracted from the structured abstract (JSON-LD metadata); the Materials and Methods/Results body of the full text was not reached. This is a cultured-cell assay, not human perception itself.
Source: Identification of mozambioside roasting products and their bitter taste receptor activation (Czech C; Lang T; Grassl A; Steuer A; Di Pizio A; Behrens M; Lang R, 2024) · abstract checked
Show datacompound-mozambioside —degrades_into_more_potent_bitter_compounds_via→ "Roasting-derived breakdown products (glucosylated cafestol derivatives, bengalensol, and others) have a lower bitterness threshold than the parent compound (27–80 µM vs 132 µM) and activate TAS2R43/46"
claim: clm-mozambioside-roasting-products / type: processing / updated: 2026-08-30

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