日本語版

tea catechins

compound class / compound-catechins

茶カテキン類

Flavan-3-ols found in tea.

On this page (9 sections)
  1. Overview
  2. Sources for this overview (6)
  3. Topic hubs
  4. Follow the connections
  5. Related entries (10)
  6. Composition and content (7)
  7. Sensory (2)
  8. Mechanism and receptors (3)
  9. How processing and cooking change it (4)
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Reading the bitterness

A 2022 study examining astringency differences between 8 tea catechins and flavonol glycosides quantified astringency using aggregation and floating of artificial oil bodies coated with histatin-3-fused caleosin as the index. The astringency ranking of the 8 catechins showed galloylated forms stronger than non-galloylated: epicatechin gallate > epigallocatechin gallate > gallocatechin gallate > catechin gallate > epigallocatechin > epicatechin > gallocatechin > catechin. AFM/SEM observation showed the EGCG complex surface as rough and the rutinose (flavonol glycoside) complex as smooth; the authors attributed these to differences between puckering and velvety astringency. However, this is an in vitro physical model and does not directly demonstrate human perceptual subqualities.

A 2004 taste dilution analysis of black tea infusion reported that flavan-3-ol glycosides induced 『velvety and mouth-coating』 (in translation: "velvety and mouth-coating") astringency at an extremely low threshold, with quercetin glycoside threshold 0.001 µmol/L stated as 1/190,000 of the EGCG threshold. In contrast, a 2018 study targeting green tea infusion reported catechins as major contributing compounds to astringency and bitterness, with astringency highly correlated (R2 = 0.7878) to ECG and flavonol glycoside concentrations. For the same question 『茶カテキンは渋味に寄与するか』 (in translation: "does tea catechin contribute to astringency?"), green tea findings were supportive, whereas black tea taste dilution research identified flavonol glycosides as dominant, and conclusions diverged by tea type and method.

A 2011 cell assay examining green tea catechin TAS2R39 activation showed hTAS2R39-expressing cells displaying clear responses to 300 µM galloylated ECg and EGCg, with ECg strongest followed by EGCg, while non-galloylated EC and EGC responses were far weaker. An independent retest in 2013 derived threshold and EC50 from dose-response, reporting ECG and EGCG threshold 32 µM, EC 250 µM, EGC 500 µM, an ordering where galloylated forms show lower thresholds (stronger activation) consistent with the 2011 result. Co-authored work from University of Porto and DIfE also reported that non-galloylated (-)-epicatechin activates TAS2R4, TAS2R5, and TAS2R39, positioning galloylation not as an obligate requirement for receptor activation but as a factor affecting response strength.

The same 2013 study further reported that catechins act as agonists activating not only TAS2R39 but also hTAS2R14, noting 『これまではhTAS2R39の活性化のみが報告されていた』 (in translation: "hitherto only TAS2R39 activation had been reported"). Responses to hTAS2R14 were positive for (+)-catechin, ECG, and EGCG (thresholds 500, 125, 250 µM respectively), weak and uncertain for EC, and negative for EGC. A separate quantitative study using green tea infusion showed bitterness highly correlated (R2 = 0.7769) with galloylated catechin EGCG and ECG concentrations, with the cell assay relationship between galloylation and activation strength corresponding to actual infusion-based and sensory bitterness data.

Sources for this overview

  1. Exploring The Relative Astringency of Tea Catechins and Distinct Astringent Sensation of Catechins and Flavonol Glycosides via an In Vitro Assay Composed of Artificial Oil Bodies

    Liu CT; Tzen JTC / 2022 / journal article / full text checked

    Checked for this overview: Confirmed the 8-catechin astringency ranking in the AOB model and AFM/SEM observation descriptions

  2. Identification of the astringent taste compounds in black tea infusions by combining instrumental analysis and human bioresponse

    Scharbert S; Holzmann N; Hofmann T / 2004 / journal article / abstract checked

    Checked for this overview: Confirmed black tea glycoside velvety astringency and 1/190,000 threshold description / Confirmed black tea flavonol glycoside as major astringency contributor—countervailing result

  3. Quantitative analyses of the bitterness and astringency of catechins from green tea

    Xu YQ; Zhang YN; Chen JX; Wang F; Du QZ; Yin JF / 2018 / journal article / abstract checked

    Checked for this overview: Confirmed green tea astringency and EGCG/ECG concentration correlation R2=0.7878 / Confirmed green tea infusion bitterness and galloylated catechin correlation R2=0.7769

  4. Evaluation of the bitterness of green tea catechins by a cell-based assay with the human bitter taste receptor hTAS2R39

    Narukawa M; Noga C; Ueno Y; Sato T; Misaka T; Watanabe T / 2011 / journal article / abstract checked

    Checked for this overview: Confirmed 300 µM ECg and EGCg responses and weak EC and EGC responses

  5. Bitter taste receptor activation by flavonoids and isoflavonoids: modeled structural requirements for activation of hTAS2R14 and hTAS2R39

    Roland WS; van Buren L; Gruppen H; Driesse M; Gouka RJ; Smit G; Vincken JP / 2013 / journal article / full text checked

    Checked for this overview: Confirmed Verbatim: 4-catechin thresholds 32/32/250/500 µM / Confirmed hTAS2R14 novel activation and threshold and negative results by compound

  6. Different phenolic compounds activate distinct human bitter taste receptors

    Soares S; Kohl S; Thalmann S; Mateus N; Meyerhof W; De Freitas V / 2013 / journal article / abstract checked

    Checked for this overview: Confirmed non-galloylated EC activation of TAS2R4/5/39—independent replication

Follow the connections

tea catechins →are main contributors to→ astringency →is not synonymous with→ bitterness

tea catechins →activates→ TAS2R39

tea catechins →— galloylation strengthens→ bitterness →can be measured separately …→ astringency

Hypotheses and recipe candidates for this entry are on the Japanese page.

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

Composition and content (7)

Kudingcha contains tea catechinssupported

Scope: Large-leaved kudingcha (Ilex latifolia, Ilex kudingcha)

Note: This review groups them under the term "flavones", but the compounds in the table are actually flavan-3-ols (catechins) (EC/EGCG/ECG). A new cross-entity connection showing these are compounds shared with green tea (ingredient-green-tea). The review does not state the content or contribution to bitterness. The primary isolation literature is citation [61], not data from this review itself.

Verbatim: "Compounds 90–92 and 119–121 were the main flavones isolated from the large-leaved Kudingcha. They are also the primary constituents in the popular green tea." Compound table: No. 119 Epicatechin (EC) [61], No. 120 Epigallocatechin gallate (EGCG) [61], No. 121 Epicatechin gallate (ECG) [61]. As a supplement, later in the text: "Catechins... are the highest in green tea, followed by the large-leaved Kudingcha and Yerba maté tea [32, 62, 63]."
Limitations: Based on citation [61] rather than the review's own primary analysis. The content comparison is only an ordering — "highest in green tea, followed by kudingcha and yerba mate" — with no numbers given. The classificatory term "flavones" may be a conventional misnomer for catechins. The text collectively calls compounds 119–121 "flavones", but Fig. 1's compound table identifies them individually as EC, EGCG, and ECG (the looseness of the classificatory term comes from the original; catechins are flavan-3-ols). The integrator confirmed this by directly viewing the Fig. 1d image (2026-09-01).
Show dataingredient-kuding-tea —contains→ compound-catechins
claim: clm-kudingcha-contains-tea-catechins / type: composition / updated: 2026-09-01
tea catechins — concentration declines during development because of: Second-flush bud growth and hardening. In 2 periods—early growth (6/28 to 7/7) when bud weight surged and leaf-opening increased sharply, and after 7/19 when leaf-opening reached 100% and hardening progressed—catechin content decline (EGC+EC+EGCG+ECG sum, % dry weight) was large. Between 7/7–7/19 when growth slowed, decline was smaller.supported

Scope: Shiga Prefecture Agricultural Technology Promotion Center Tea Industry Extension Office research field, Yabukita cultivar, second flush from June 28 to August 9, 2000, n=7 timepoints, 2 replicates

Note: Temporal change within the same second-flush window, distinct from the colloquial 「一番茶より二番茶の方がカテキンが多い」 (in translation: "second flush contains more catechins than first flush")—a different scale. Catechin yield (g/m²) rose until 7/19 then plateaued; concentration decline and yield dynamics require separate treatment.

Verbatim: (Table 1, catechin content percent dry matter, EGC+EC+EGCG+ECG sum): 2000/6/28=15.6, 7/3=14.1, 7/7=12.9, 7/12=12.4, 7/19=12.2, 7/24=11.2, 8/9=8.8. Main text: 「6月28日から7月7日にかけて,二番茶芽のカテキン類含有率は非常に低下し,同時に,摘芽重は顕著に増加し,出開き度は大幅に上昇した.その後,7月7日から19日にかけて,二番茶芽の生長はやや緩慢になり,カテキン類含有率の低下程度は小さくなった.7月19日以降,二番茶芽は出開き度が100%に達して硬化が進み,カテキン類含有率は再び非常に低下した」(in translation: "From June 28 to July 7, second-flush bud catechin content declined sharply, simultaneously with marked increase in bud weight and large rise in leaf-opening degree. Subsequently, from July 7 to 19, second-flush growth became somewhat slower and catechin content decline was smaller. After July 19, second-flush buds reached 100% leaf-opening with progressive hardening, and catechin content declined sharply again"). Catechin yield (g/m²) increased through July 19 then remained stable. Individual catechins showed EGC rising with growth then slightly declining after 7/19; EC constant 0.7–0.9%; EGCG and ECG declining during early growth then stabilizing.
Limitations: Single-year, single-cultivar, single location (Shiga Prefecture) trial. Limited to second flush; the same paper notes that autumn flush did not show similar sharp changes.
Show datacompound-catechins —shows_developmental_concentration_decline_due_to→ "Second-flush bud growth and hardening. In 2 periods—early growth (6/28 to 7/7) when bud weight surged and leaf-opening increased sharply, and after 7/19 when leaf-opening reached 100% and hardening progressed—catechin content decline (EGC+EC+EGCG+ECG sum, % dry weight) was large. Between 7/7–7/19 when growth slowed, decline was smaller."
claim: clm-w37h-tea-nibancha-catechin-decline-within-flush / type: composition / updated: 2026-09-02
tea catechins — composition: Second-flush layer-by-layer catechin content (measured 1 cm intervals from height above first-flush heading line, 1999 July 1 harvest) showed non-monotonic distribution: 2–3 cm layer 10.7%, 7–8 cm layer 10.9% (high), and 4–5 cm, 5–6 cm layers 9.1% (low). EGCG content showed the same pattern (2–3 cm layer 5.7% highest, 0–1 cm layer 4.4% lowest). Lower harvest position increased fresh leaf yield and catechin yield per unit area, but content percent showed no monotonic trend.observation

Scope: Same as above second-flush layer survey (July 1, 1999 harvest, no replicates, trial unit 4.32 m²)

Note: Records position-dependent differences within a single flush (corresponding to node position). Authors did not explain the physiological mechanism of the non-monotonic pattern, and no replicates preclude generalization.

Verbatim: 「EGCGでは4.4〜5.7%と層の差がやや見られたが,他のカテキンでは差がほとんど見られなかった.EGCG含有率は,2〜3cm層が5.7%と最も高く,次いで1〜2cm層,3〜4cm層,および7〜8cm層が5.4〜5.6%と高くなり,0〜1cm層が4.4%と最も低く,5〜6cm層も4.5%と低かった.また,カテキン類含有率は,EGCG含有率の変化に応じて同様の傾向を呈し,2〜3cm層および7〜8cm層でそれぞれ10.7%,10.9%と高く,4〜5cm層および5〜6cm層で9.1%と低かった」(in translation: "For EGCG, small layer differences 4.4-5.7% were observed, but other catechins showed almost no difference. EGCG content was highest at 5.7% in the 2–3 cm layer, followed by 1–2 cm, 3–4 cm, and 7–8 cm layers at 5.4–5.6%, with 0–1 cm lowest at 4.4% and 5–6 cm also low at 4.5%. Total catechin content showed the same trend as EGCG variation, high at 10.7% and 10.9% in 2–3 cm and 7–8 cm layers respectively, and low at 9.1% in 4–5 cm and 5–6 cm layers"). Fresh leaf yield by layer showed 3–4 cm greatest at 90 kg/10a with declining yield at higher layers.
Limitations: Single-year, no-replicate data. Layer position corresponds to node position within a single flush, but authors did not explain the physiological mechanism of the non-monotonic pattern.
Show datacompound-catechins —has_composition→ "Second-flush layer-by-layer catechin content (measured 1 cm intervals from height above first-flush heading line, 1999 July 1 harvest) showed non-monotonic distribution: 2–3 cm layer 10.7%, 7–8 cm layer 10.9% (high), and 4–5 cm, 5–6 cm layers 9.1% (low). EGCG content showed the same pattern (2–3 cm layer 5.7% highest, 0–1 cm layer 4.4% lowest). Lower harvest position increased fresh leaf yield and catechin yield per unit area, but content percent showed no monotonic trend."
claim: clm-w37h-tea-layer-position-nonmonotonic / type: composition / updated: 2026-09-02
tea catechins — concentration declines during development because of: Tea harvest progression. The review states 「カテキンは一番茶に多く,二番茶,三番茶になると減少し」 (in translation: "catechins abundant in first flush, decrease in second and third flushes").preliminary

Scope: Generalization by review author affiliated with Shizuoka Prefecture University Tea Comprehensive Research Center (individual primary studies and regions within the review are not specified)

Verbatim: 「カテキンは一番茶に多く,二番茶,三番茶になると減少し,成熟した葉(3、4葉目)よりも若い芽(1、2葉目)に多く含まれている.また,茶葉中のカテキンの生成は栽培条件に影響され,日光の照射時間の増加と気温の上昇により促進される.」(in translation: "Catechins are abundant in first flush and decrease in second and third flushes, with higher content in young buds (first–second leaf) than in mature leaves (third–fourth leaf). Catechin formation in tea leaves is affected by cultivation conditions and promoted by increased sunlight duration and temperature rise.")
Limitations: Review generalization without identifying primary studies (replicates, cultivar, region). The text also states 「日光照射時間の増加でカテキン生成が促進される」 (in translation: "increased sunlight promotes catechin generation"), yet the relationship between this and lower second-flush catechin (which typically receives longer daylight) is not explicitly resolved.
Source: 茶カテキンの特性とその有効利用 (斎藤貴江子, 2018) · full text checked
Show datacompound-catechins —shows_developmental_concentration_decline_due_to→ "Tea harvest progression. The review states 「カテキンは一番茶に多く,二番茶,三番茶になると減少し」 (in translation: "catechins abundant in first flush, decrease in second and third flushes")."
claim: clm-w37h-tea-flush-order-review / type: composition / updated: 2026-09-02
tea catechins — concentration declines during development because of: Tea leaf position. The review states 「成熟した葉(3・4葉目)よりも若い芽(1・2葉目)に多く含まれている」 (in translation: "more catechins in young buds (1st–2nd leaf) than mature leaves (3rd–4th leaf)").preliminary

Scope: Same review-level generalization

Verbatim: 「成熟した葉(3、4葉目)よりも若い芽(1、2葉目)に多く含まれている.」(in translation: "Higher content in young buds (first–second leaf) than in mature leaves (third–fourth leaf).")
Limitations: Individual primary studies (replicate number, cultivar, region) not identified.
Source: 茶カテキンの特性とその有効利用 (斎藤貴江子, 2018) · full text checked
Show datacompound-catechins —shows_developmental_concentration_decline_due_to→ "Tea leaf position. The review states 「成熟した葉(3・4葉目)よりも若い芽(1・2葉目)に多く含まれている」 (in translation: "more catechins in young buds (1st–2nd leaf) than mature leaves (3rd–4th leaf)")."
claim: clm-w37h-tea-leaf-position-review / type: composition / updated: 2026-09-02
hojicha roasting reduces tea catechinssupported

Scope: Kochi Prefectural Agricultural Technology Center Tea Experiment Station; crude teas of first flush, cut-leaf, and second flush with a 50-second steaming time. Roasted 2 times with an automatic continuous hojicha roaster (exhaust temperature 90 C for the 1st roast, 100 C for the 2nd roast, with drum rotation speed adjusted for each flush and roasting degree).

Note: Direct quantification by HPLC (JASCO X-LC system). Only 1 sample per condition; the number of replicates is not stated.

For first flush, cut-leaf, and second flush alike, total catechins decreased as roasting deepened. Some individual catechins increased from crude tea to light roast before decreasing at deep roast.
Limitations: 1 sample analyzed per condition; the number of replicates and statistical testing are not stated.
Source: 焙煎程度とほうじ茶の品質 (高知県農業技術センター茶業試験場) · full text checked
Show dataprocess-hojicha-roasting —reduces→ compound-catechins
claim: clm-hojicha-catechin-decrease-degree / type: composition / updated: 2026-09-02
Tieguanyin oolong tea infusion — composition: tea catechinssupported

Scope: Layer: Food. LC-MS metabolite quantification. Oolong tea 2 cultivars (Tieguanyin and Jinguanyin) compared across processing stages.

"the contents of catechin and catechin gallate in each stage of JGY were significantly greater than those in TGY. Specifically, the average content of catechins was approximately 15 times greater." "Catechins play a crucial role in determining the bitterness of tea due to their relatively low threshold values."
Limitations: Comparison limited to 2 specific cultivars under specific processing conditions.
Source: Insights into "Yin Rhyme": Analysis of nonvolatile components in Tieguanyin oolong tea during the manufacturing process (Li Q; Hu Q; Ou X; He J; Yu X; Hao Y; Zheng Y; Sun Y, 2024) · full text checked
Show dataingredient-tieguanyin-infusion —has_composition→ compound-catechins
claim: clm-w71b2-tieguanyin-catechin-lower-than-jinguanyin / type: composition / updated: 2026-09-07

Sensory (2)

tea catechinsRough, puckering astringency vs smooth, velvety astringency may differ from flavonol glycosides in: supported

Scope: Artificial oil body in vitro assay

Note: This model does not provide direct human demonstration of independent astringency subqualities.

Aggregation and floating (emulsion layer thickness) of histatin-3-fused-caleosin-coated artificial oil bodies (AOB) quantified astringency. The 8-catechin astringency ranking was "epicatechin gallate > epigallocatechin gallate > gallocatechin gallate > catechin gallate > epigallocatechin > epicatechin > gallocatechin > catechin" (in translation: "epicatechin gallate > epigallocatechin gallate > gallocatechin gallate > catechin gallate > epigallocatechin > epicatechin > gallocatechin > catechin") with galloylated > non-galloylated. AFM/SEM showed the EGCG (catechin) complex AOB surface as rough and the rutinose (flavonol glycoside) complex as smooth, with the authors corresponding these to rough (puckering) and smooth (velvety) astringency respectively, with the statement "In accordance with sensory evaluation" (in translation: "In accordance with sensory evaluation") explicitly marking alignment with sensory assessment.
Limitations: In vitro physical model not directly demonstrating human perceptual subqualities. Coating used only histatin-3; the authors themselves note the need for modification adding saliva proteins (mucin, etc.). EC50 and other quantitative thresholds were not reported.
Taste dilution analysis of black tea infusion explicitly stated in the abstract that flavan-3-ol glycosides induce "velvety and mouth-coating" (in translation: "velvety and mouth-coating") astringency at extremely low thresholds (quercetin glycoside 0.001 µmol/L stated as 1/190,000 of EGCG threshold). This human sensory account of differential astringency quality and threshold range between catechins and glycosides provides perceptual support for the rough/velvety binary division of the Liu 2022 artificial oil body model.
Limitations: Abstract only examined. Results from black tea, not green tea. The abstract confirms only the velvety side of the description; the catechin side as rough/puckering was not explicitly stated in the abstract (indirect support from threshold and quality contrast).
Show datacompound-catechins —may_differ_from_flavonol_glycosides_in→ "Rough, puckering astringency vs smooth, velvety astringency"
claim: clm-tea-subqualities-model / type: sensory / updated: 2026-08-30
tea catechins are main contributors to astringencycontested

Scope: Tea infusions. Asserted for green tea; contradicted for black tea.

Note: The green tea literature regards catechins as the main contributor to astringency, but a taste-dilution study on black tea found flavonol glycosides to be dominant instead. The matrix (green tea vs. black tea) and the method (correlation vs. dilution-to-threshold) differ.

States that catechins are the main contributors to the bitterness and astringency of green tea infusions, and that astringency correlates strongly with ECG and flavonol glycosides (R2 = 0.7878).
Limitations: Correlational only; the same abstract also suggests a role for flavonol glycosides.
Source: Quantitative analyses of the bitterness and astringency of catechins from green tea (Xu YQ; Zhang YN; Chen JX; Wang F; Du QZ; Yin JF, 2018) · abstract checked
Contradicts: In black tea, taste dilution identified 14 flavon-3-ol glycosides -- not catechins or theaflavins -- as the main contributors to astringency; the glycosides' thresholds were up to 190,000 times lower than EGCG's.
Limitations: The matrix (black tea vs. green tea) and method (dilution-to-threshold vs. correlation) differ, so the contradiction may partly reflect matrix and methodology rather than a true conflict.
Show datacompound-catechins —are_main_contributors_to→ sensation-astringent
claim: clm-catechins-main-tea-astringency / type: sensory / updated: 2026-08-30

Mechanism and receptors (3)

tea catechinsTAS2R39 activates supported

Scope: A cultured-cell assay. A clear response to 300 uM ECg and EGCg. ECg is strongest, followed by EGCg, with EC and EGC far weaker

Note: The abstract reports only a single concentration (300 uM). The receptor is broadly tuned (many flavonoids also activate TAS2R39).

Cells expressing hTAS2R39 showed a clear response to 300 uM of both ECg and EGCg. Among the catechins tested, the response to ECg was strongest, followed by EGCg, with the responses to EC and EGC far weaker.
Limitations: The reported concentration is a single value (300 uM). This is an in vitro receptor response, not a direct measurement of bitterness.
Source: Evaluation of the bitterness of green tea catechins by a cell-based assay with the human bitter taste receptor hTAS2R39 (Narukawa M; Noga C; Ueno Y; Sato T; Misaka T; Watanabe T, 2011) · abstract checked
Context: Of a large set of structurally related (iso)flavonoids, 70 activated hTAS2R39, with activation thresholds spanning 0.12-500 uM, showing the receptor's broad tuning. The abstract does not name individual tea catechins.
Limitations: Catechin-specific values are not visible at the abstract level. Used only as contextual information on tuning.
Source: Bitter taste receptor activation by flavonoids and isoflavonoids: modeled structural requirements for activation of hTAS2R14 and hTAS2R39 (Roland WS; van Buren L; Gruppen H; Driesse M; Gouka RJ; Smit G; Vincken JP, 2013) · abstract checked
In an independent assay by the University of Porto and DIfE, (-)-epicatechin activated 3 receptors: TAS2R4, TAS2R5, and TAS2R39. This confirms, from a lab lineage independent of Narukawa 2011 (Shizuoka) and Roland 2013 (Wageningen), that a catechin-scaffold compound is an agonist of TAS2R39.
Limitations: Confirmed at abstract level only. The compound tested was the non-galloylated EC, not a re-measurement of ECg or EGCg themselves. EC50 is stated to vary 100-fold across compounds, but the value for EC is not given in the abstract.
Source: Different phenolic compounds activate distinct human bitter taste receptors (Soares S; Kohl S; Thalmann S; Mateus N; Meyerhof W; De Freitas V, 2013) · abstract checked
Context: The primary full text of Narukawa 2011 has not been obtained, but the full-text Discussion of Roland 2013 (a different source), which independently re-tested the same receptor (hTAS2R39), directly quotes Narukawa's values: "Previously reported thresholds were between 10 and 30 µM for all four catechins (14)", and gives EC50 values of ECG 88.2 µM, EGCG 181.6 µM, EGC 395.5 µM, and EC 417.7 µM. Compared with Roland's own values (thresholds: ECG/EGCG 32 µM, EC 250 µM, EGC 500 µM; EC50: ECG 150.6 µM, EGCG 161.2 µM), it reports thresholds about 10 times higher for the non-galloylated catechins (EC and EGC), and explicitly notes the difference between assays.
Limitations: This line is a secondary citation from the full-text source record for Roland 2013 on TAS2R39 flavonoids, not from Narukawa 2011's own source record. It is not treated as a correction to Narukawa's own evidence row, but as supporting context drawn from a different source.
Source: Bitter taste receptor activation by flavonoids and isoflavonoids: modeled structural requirements for activation of hTAS2R14 and hTAS2R39 (Roland WS; van Buren L; Gruppen H; Driesse M; Gouka RJ; Smit G; Vincken JP, 2013) · full text checked
In a heterologous-expression receptor assay independent of Narukawa 2011 (a single concentration of 300 µM), dose-response thresholds and EC50 for 4 catechins against hTAS2R39 were quantified. Verbatim: "we identified thresholds of ECG, EGCG, EC, and EGC, to be 32, 32, 250, and 500 µM, respectively". EC50 was ECG 150.6 µM and EGCG 161.2 µM (EC and EGC could not be calculated). The ordering, in which the galloylated catechins (ECG, EGCG) have lower thresholds than the non-galloylated catechins (EC, EGC) -- meaning stronger activation -- is consistent with Narukawa.
Limitations: These are receptor-assay values, not a direct measurement of human sensory perception. Compared with Narukawa, thresholds about 10 times higher are reported for the non-galloylated catechins, so absolute values differ between assays (though the trend is the same).
Source: Bitter taste receptor activation by flavonoids and isoflavonoids: modeled structural requirements for activation of hTAS2R14 and hTAS2R39 (Roland WS; van Buren L; Gruppen H; Driesse M; Gouka RJ; Smit G; Vincken JP, 2013) · full text checked
Show datacompound-catechins —activate→ receptor-tas2r39
claim: clm-galloylated-catechins-activate-tas2r39 / type: mechanism / updated: 2026-08-30
tea catechins — galloylation strengthens bitternesssupported

Scope: The role of the galloyl group is inferred from the hTAS2R39 response order (ECg, EGCg >> EC, EGC), described as resembling human taste-intensity observations.

Note: A direct human dose-response is not part of this assay. The human comparison in the receptor study is a citation, not something the study itself carried out.

Because the cellular response to EC and EGC was far weaker than to ECg and EGCg, the galloyl group was strongly inferred to be involved in bitterness intensity; the finding is described as resembling taste-intensity observations from human sensory studies.
Limitations: The comparison with human sensory data is a citation, not something carried out in this study; the direction of the effect relies on the amplitude of the receptor response.
Source: Evaluation of the bitterness of green tea catechins by a cell-based assay with the human bitter taste receptor hTAS2R39 (Narukawa M; Noga C; Ueno Y; Sato T; Misaka T; Watanabe T, 2011) · abstract checked
In a quantitative analysis of green tea infusions, bitterness correlated strongly with the concentration of the galloylated catechins EGCG and ECG (R2 = 0.7769, p < 0.01). Independent of the receptor assay (Narukawa 2011), this supports the link between galloylation and bitterness on an actual-infusion, sensory basis.
Limitations: Abstract only. This is a correlation and does not directly demonstrate the galloyl group's causal contribution (a paired comparison on the same backbone). Panel details are not given in the abstract.
Source: Quantitative analyses of the bitterness and astringency of catechins from green tea (Xu YQ; Zhang YN; Chen JX; Wang F; Du QZ; Yin JF, 2018) · abstract checked
Limits: Reports that the non-galloylated (-)-epicatechin also activates TAS2R4/5/39. This shows that galloylation is a factor that enhances the response but is not a requirement for receptor activation, and sets a boundary for reading the statement "EC and EGC are far weaker" (Narukawa 2011) as weaker but not zero.
Limitations: Abstract only. Without EC's response threshold or EC50, a quantitative comparison with Narukawa's "much weaker" is not possible. This is a limit on scope, not a contradiction.
Source: Different phenolic compounds activate distinct human bitter taste receptors (Soares S; Kohl S; Thalmann S; Mateus N; Meyerhof W; De Freitas V, 2013) · abstract checked
The statement that shading cultivation reduces the weakly bitter-astringent EGC, while the strongly bitter-astringent EGCG shows almost no reduction from shading, is an independent mention -- in the food matcha -- consistent with the generalization that galloylated catechins (such as EGCG) are more bitter-astringent than non-galloylated catechins (such as EGC).
Limitations: Evidence newly added in this round of research. Note that it is a different kind of evidence (a background statement in a food-science conference abstract) from the existing claim's subject (the hTAS2R39 cell assay).
Source: 抹茶の点て方に関する化学的考察 (Chemical research on the preparation of matcha) (Horie H; Ema K; Nomura S; Monobe M, 2018) · full text checked
Show datacompound-catechins —have_bitterness_increased_by_galloylation→ sensation-bitter
claim: clm-galloylation-increases-catechin-bitterness / type: mechanism / updated: 2026-08-30
tea catechinsTAS2R14 activates supported

Scope: A heterologous-expression cell receptor assay (cultured cells expressing hTAS2R14)

Verbatim: "We identified catechins as agonists of two bitter receptors, hTAS2R14 and hTAS2R39. Previously, only activation of hTAS2R39 was reported (14)." Compound table (hTAS2R14 column): (+)-catechin active (+), threshold 500 µM / EC weakly active (+/-), threshold 500 µM / ECG active (+), threshold 125 µM / EGC not active (-) / EGCG active (+), threshold 250 µM. EC50 could not be calculated for any of them (n.d.).
Limitations: EGC did not activate hTAS2R14 (-). Activation by EC was weak and uncertain (+/-). EC50 values could not be calculated (a limitation of the concentration range). This is a receptor assay, not a direct measurement of human sensory perception.
Source: Bitter taste receptor activation by flavonoids and isoflavonoids: modeled structural requirements for activation of hTAS2R14 and hTAS2R39 (Roland WS; van Buren L; Gruppen H; Driesse M; Gouka RJ; Smit G; Vincken JP, 2013) · full text checked
Show datacompound-catechins —activate→ receptor-tas2r14
claim: clm-catechins-activate-tas2r14 / type: mechanism / updated: 2026-09-01

How processing and cooking change it (4)

tea shading cultivation reduces tea catechinscontextual

Scope: Layer: Food. Summary table of tea-plant buds (showing qualitative increase/decrease/no-change classification, not numeric values).

Summary table (component/form—change—notes) Verbatim: 「カフェイン 増加する 苦味・機能性」「カテキン類 EGCG EGC 減少する 変化しない 減少する 苦渋味成分、機能性」(in translation: "Caffeine: increases—bitterness and bioactivity" and "Catechins—EGCG—EGC: decrease—no change—decrease—bitter-astringent components and bioactivity").
Limitations: Qualitative increase/decrease/no-change classification only; numeric values (% or concentration) not provided. Specific shading ratio and duration conditions not noted in the table.
Source: 被覆茶安定生産マニュアル (農食研究推進事業27015Cコンソーシアム(「実需者需要に応える簡易な樹体診断法と効率的被覆作業による高品位安定生産技術の確立」研究チーム), 2018) · full text checked
Show dataprocess-tea-shading-cultivation —reduces→ compound-catechins
claim: clm-w71c2-shading-catechins-bitter-astringent-decrease / type: processing / updated: 2026-09-07
goishi-cha two-stage fermentation reduces tea catechinssupported

Scope: Layer: Food. Green tea (unfermented, control) and Goishicha (two-stage fermented) extracted under identical conditions (hot water 100 mL, 1.5 g leaf, 5 minutes), n=5 comparison.

Table 1 (mg/100 mL extract, n=5, superscript letters indicate p<0.05 significance groups): Green tea (unfermented): caffeine 43.7a, EGC 24.5a, EGCg 45.9a, EC 9.5a, GCg 0.9a, ECg 6.9a, total catechin 87.8a. Goishicha (two-stage fermented): caffeine 11.6b, EGC 6.5c, EGCg 0.4b, EC 0.2b, GCg trace, ECg trace, total catechin 7.1c. Main text: "Compared with green tea as a control unfermented tea, caffeine content of postfermented tea was low. Catechin content of postfermented tea was also lower than that of green tea."
Limitations: Quantitative method (HPLC etc.) details not in main text. Goishicha noted as 「一部の生産者の茶葉をブレンドした一つの製品」 (in translation: "a single product blended from tea leaves of some producers"), not a single-lot before–after comparison.
Source: Comparison of antioxidant activities among four kinds of Japanese traditional fermented tea (Horie M; Nara K; Sugino S; Umeno A; Yoshida Y, 2017) · full text checked
Show dataprocess-goishi-cha-fermentation —reduces→ compound-catechins
claim: clm-w71c2-goishicha-caffeine-catechin-reduced-vs-greentea / type: processing / updated: 2026-09-07
ishizuchi kurocha two-stage fermentation reduces tea catechinssupported

Scope: Layer: Food. Green tea (unfermented, control) and Ishizuchi-kurocha (2 samples from different producers) extracted under identical conditions (hot water 100 mL, 1.5 g leaf, 5 minutes), n=5 comparison.

Table 1: Ishizuchi-kurocha 1: caffeine 13.9b, EGC 16.0b, EGCg 2.0b, EC 1.9b, GCg 0.1a, ECg 0.1b, total catechin 20.1b. Ishizuchi-kurocha 2: caffeine 15.7b, EGC 19.5b, EGCg 1.0b, EC 4.8ab, GCg 0.1a, ECg trace, total catechin 25.3b. Main text: "Among the postfermented teas, the concentration of all catechins was the highest in Ishizuchi-kurocha. In particular, the concentration of EGC in Ishizuchi-kurocha was high."
Limitations: Authors note small 2-producer differences, but the comparison uses separate green tea lots (control) rather than a single lot's before–after fermentation.
Source: Comparison of antioxidant activities among four kinds of Japanese traditional fermented tea (Horie M; Nara K; Sugino S; Umeno A; Yoshida Y, 2017) · full text checked
Show dataprocess-ishizuchi-kurocha-fermentation —reduces→ compound-catechins
claim: clm-w71c2-ishizuchikurocha-caffeine-catechin-reduced-vs-greentea / type: processing / updated: 2026-09-07
awa bancha boil-then-lactic fermentation reduces tea catechinssupported

Scope: Layer: Food. Green tea (unfermented, control) and Awa-bancha (2 samples from different producers) extracted under identical conditions (hot water 100 mL, 1.5 g leaf, 5 minutes), n=5 comparison.

Table 1: Awa-bancha 1 (anaerobic fermentation): caffeine 6.1bc, EGC 7.0c, EGCg trace, EC 0.6b, GCg 0.2a, ECg 0.1b, total catechin 7.9c. Awa-bancha 2: caffeine 3.8c, EGC 7.8c, EGCg 0.2b, EC 1.1b, GCg 0.1a, ECg 0.5b, total catechin 9.7c. Main text: "The concentration of catechins was the lowest in Awa-bancha [among the postfermented teas]."
Limitations: Authors note small 2-producer differences, but the comparison uses separate green tea lots (control) rather than a single lot's before–after fermentation.
Source: Comparison of antioxidant activities among four kinds of Japanese traditional fermented tea (Horie M; Nara K; Sugino S; Umeno A; Yoshida Y, 2017) · full text checked
Show dataprocess-awa-bancha-fermentation —reduces→ compound-catechins
claim: clm-w71c2-awabancha-caffeine-catechin-reduced-vs-greentea / type: processing / updated: 2026-09-07

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