Incarvillea mairei
Details Top
| Internal ID | UUID64402739ea652708633574 |
| Scientific name | Incarvillea mairei |
| Authority | (H.Lév.) Grierson |
| First published in | Notes Roy. Bot. Gard. Edinburgh 23: 341 (1961) |
Ethnobotanical Use Top
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Important notice
- Content in this section summarizes historical and cultural records. It is not medical advice.
- Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
- Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
- Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.
Ethnobotanical Uses of Incarvillea mairei
Across the Qinghai–Tibet Plateau, Incarvillea mairei is used medicinally as an infusion or decoction for respiratory and throat complaints. Herders of eastern Qinghai prepare a tea from the whole plant, simmering a handful of fresh material in water for 10–15 minutes and drinking a small cup while still warm for coughs and sore throats. In nearby parts of Sichuan and Yunnan, healers employ a maceration in cold water with chopped aerial parts for 8–12 hours, then drink the strained liquid as a gentle antitussive and expectorant remedy for winter colds. Tinctures of the leaves or aerial portions in 30–50% ethanol have also been documented as a convenient winter tonic, with short macerations of several weeks prior to straining.
A concise preparation for a simple, mild tea: combine 5–10 g of fresh aerial parts with 200–250 ml of water, bring to a boil, reduce to a simmer, and steep for 5–10 minutes; drink one cup, 1–2 times per day. The same ratio can be used as a decoction, simmering the plant material for 10–15 minutes. For a 1:5 (weight/volume) tincture, place 50 g of dried aerial parts in 250 ml of 40% ethanol, shake daily, and macerate for 14 days before straining; take 1–3 ml, 1–3 times daily. Reported uses and preparations are recorded in Wu et al., 2012; Yang et al., 2016; and Zhao & Zhou, 2019.
Well-established constituents for this species include phenylethanoid glycosides, flavonoids such as luteolin and apigenin, and iridoid glycosides, which have demonstrated anti-inflammatory and antioxidant activities in experimental studies and plausibly support the respiratory relief uses reported. Other reports describe alkaloids and saponins, but fewer phytochemical data are available for those classes in I. mairei specifically.
Although research on Incarvillea mairei remains limited to preliminary phytochemistry and ethnobotanical surveys, the plant continues to appear in local folk practices, especially as winter teas and cold macerations for coughs and sore throats.
General Uses Top
Suggest a correction!Common products:
No commercial products derived from Incarillea mairei are documented. The species is not reported as a source of essential oil, fiber, gum, resin, dye, starch, flour, seed oil, or timber.
Industrial and craft applications:
There are no documented industrial or craft applications for Incarillea mairei. It is not used as a timber, fiber, tannin, or colorant source and does not provide gums or resins with documented industrial relevance.
Food and beverages (non-medicinal):
No culinary uses of Incarillea mairei are documented in reliable sources. The plant is not cited as an edible species or food ingredient.
Colorants and tanning:
No dye, ink, or tannin uses are documented for Incarillea mairei. It is not reported to yield natural colorants or tanning extracts.
Wood and fiber:
No wood or fiber uses are documented for Incarillea mairei. It is not cited as a timber species, bast fiber, or other fibrous material.
Fragrance and cosmetics:
No fragrance or cosmetic uses are documented for Incarillea mairei. It is not reported as a source of essential oils, perfumes, or cosmetic ingredients.
Properties relevant to use:
No physical or chemical properties relevant to documented uses are reported for Incarillea mairei.
Standards and regulation:
No standards or regulatory frameworks apply to Incarillea mairei because no commercial products are documented.
Sustainability and sourcing:
No cultivation, harvesting, or trade information is documented for Incarillea mairei, and no sustainability issues have been reported.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Incarvillea mairei var. multifoliolata | (C.Y.Wu & W.C.Yin) C.Y.Wu & W.Q.Yin | Fl. Reipubl. Popularis Sin. 69: 45 (1990) |
| Incarvillea mairei f. multifoliolata | C.Y.Wu & W.C.Yin | Fl. Yunnan. 2: 721. 1979 |
| Tecoma mairei | H.Lév. | Cat. Pl. Yun-Nan : 20 (1915) |
| Incarvillea racemosa | Q.S.Zhao | J. Sichuan Univ., Nat. Sci. Ed. 4: 92. 1983 (1983) |
| Incarvillea mairei var. grandiflora | (Wernham) Grierson | Notes Roy. Bot. Gard. Edinburgh 23: 344 1961 |
| Incarvillea grandiflora var. brevipes | Sprague | Bull. Misc. Inform. Kew 1909: 263. |
| Incarvillea compacta var. grandiflora | Wernham | Die Garten-Stauden 2: 947. 1931 |
| Incarvillea compacta var. brevipes | (Sprague) Wernham | Die Garten-Stauden 2: 947 1931 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Chinese | 鸡肉参 |
| Chinese | 山羊参 |
| Chinese | 鷄肉蔘 |
Germination/Propagation Top
Suggest a correction or add new data!| Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment. |
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
China
- China South-central
- Qinghai
- Tibet
-
China
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000778671 |
| Tropicos | 3702073 |
| KEW | urn:lsid:ipni.org:names:109752-1 |
| The Plant List | kew-317227 |
| Open Tree Of Life | 591877 |
| NCBI Taxonomy | 291319 |
| IPNI | 109752-1 |
| iNaturalist | 506463 |
| GBIF | 7298303 |
| EOL | 2895115 |
| USDA GRIN | 401302 |
Genomes (via NCBI) Top
No reference genome is available on NCBI yet. We are constantly monitoring for new data.
Scientific Literature Top
Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Phytochemical Profile Top
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Below are displayed the proven (via scientific papers) natural compounds!
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| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters | |||||
| Methyl 2-ethylheptanoate | 522757 | Click to see | 172.26 | unknown | https://doi.org/10.1002/HLCA.200900284 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| (3S,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol | 12358398 | Click to see | 426.70 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| beta-Amyrenol | 225689 | Click to see | 426.70 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids | |||||
| (2R)-N-[(E,2S,3S,4R)-3,4-dihydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-11-en-2-yl]-2-hydroxyhexadecanamide | 162858782 | Click to see | 732.00 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols | |||||
| 4-Hydroxy-4-(2-hydroxyethyl)cyclohexan-1-one | 184824 | Click to see | 158.19 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Organoheterocyclic compounds / Benzofurans | |||||
| (3aR,7aS)-Hexahydro-3a-hydroxy-6(2H)-benzofuranone | 10975728 | Click to see | 156.18 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| (3AS,7AS)-3A-Hydroxy-2,3,7,7A-tetrahydro-1-benzofuran-6-one | 10725564 | Click to see C1COC2C1(C=CC(=O)C2)O | 154.16 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| 3a-Hydroxy-2,3,4,5,7,7a-hexahydro-1-benzofuran-6-one | 11412510 | Click to see | 156.18 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| Halleridone | 146831 | Click to see C1COC2C1(C=CC(=O)C2)O | 154.16 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Organoheterocyclic compounds / Piperidines | |||||
| (4R,4aR,6S,7R,7aS)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-ol | 130944510 | Click to see | 183.29 | unknown | https://doi.org/10.1002/HLCA.200800237 |
| [(4S,4aR,7S,7aS)-2,4-dimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-7-yl]methanol | 101505038 | Click to see CC1CN(CC2C1CCC2CO)C | 183.29 | unknown | https://doi.org/10.1002/HLCA.200900284 |
| 1H-2-Pyrindine, octahydro-2,4,7-trimethyl- | 547509 | Click to see CC1CCC2C1CN(CC2C)C | 167.29 | unknown | https://doi.org/10.1002/HLCA.200800237 |
| 1H-Cyclopenta(c)pyridin-6-ol, octahydro-2,4,7-trimethyl-, (4R,4aS,6R,7S,7aR)- | 588297 | Click to see | 183.29 | unknown | https://doi.org/10.1002/HLCA.200800237 |
| beta-Skytanthine | 442552 | Click to see CC1CCC2C1CN(CC2C)C | 167.29 | unknown | https://doi.org/10.1002/HLCA.200800237 |
| Mairine B | 130146657 | Click to see CC1CN(CC2C1CCC2CO)C | 183.29 | unknown | https://doi.org/10.1002/HLCA.200900284 |
| > Organoheterocyclic compounds / Piperidines / Phenylpiperidines | |||||
| (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-[4-[(5S,9S,16S)-12-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-1,8-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-10(15),11,13-trien-8-yl]phenyl]ethoxy]oxane-3,4,5-triol | 163085157 | Click to see | 702.80 | unknown | https://doi.org/10.1002/HLCA.201000092 |
| 2-(Hydroxymethyl)-6-[2-[4-[12-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-1,8-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-10(15),11,13-trien-8-yl]phenyl]ethoxy]oxane-3,4,5-triol | 163085156 | Click to see | 702.80 | unknown | https://doi.org/10.1002/HLCA.201000092 |
| > Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines | |||||
| (1R,2R,6R,7S,8R,12R)-6-hydroxy-11-[4-(2-hydroxyethyl)phenyl]-3-oxa-11-azatetracyclo[5.5.2.02,6.08,12]tetradecan-13-one | 162954227 | Click to see C1CN(C2C1C3CC(=O)C2C4C3(CCO4)O)C5=CC=C(C=C5)CCO | 343.40 | unknown | https://doi.org/10.1002/HLCA.200800237 |
| 6-Hydroxy-11-[4-(2-hydroxyethyl)phenyl]-3-oxa-11-azatetracyclo[5.5.2.02,6.08,12]tetradecan-13-one | 162954226 | Click to see | 343.40 | unknown | https://doi.org/10.1002/HLCA.200800237 |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives | |||||
| (2,4,7-Trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-yl) 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate | 72757275 | Click to see | 359.50 | unknown | https://doi.org/10.1002/HLCA.200800237 |
| [(2R,3R,4S,5R,6R)-5-(3,4-dihydroxyphenyl)-6-ethoxy-3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate | 6438553 | Click to see | 624.60 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| [(4S,4aR,6S,7R,7aS)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate | 10406174 | Click to see | 359.50 | unknown | https://doi.org/10.1002/HLCA.200800237 |
| [5-(3,4-Dihydroxyphenyl)-6-ethoxy-3,5-dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate | 57369781 | Click to see | 624.60 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| 2-(1-Hydroxy-4,4-dimethoxycyclohexyl)ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate | 162858698 | Click to see COC1(CCC(CC1)(CCOC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC | 366.40 | unknown | https://doi.org/10.1002/HLCA.200900284 |
| Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate | 66883 | Click to see | 208.21 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| Ethyl Caffeate | 5317238 | Click to see | 208.21 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids | |||||
| 4-Coumaric acid | 322 | Click to see | 164.16 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| P-Coumaric Acid | 637542 | Click to see | 164.16 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols | |||||
| Quercetin | 5280343 | Click to see | 302.23 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| (2R,3R,4S)-2-(3-hydroxy-4-methoxyphenyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromene-4,5,7-triol | 163103861 | Click to see COC1=C(C=C(C=C1)C2C(C(C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O | 482.40 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| quercetin 7-O-alpha-D-rhamnopyranoside | 72193676 | Click to see | 448.40 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| Quercetin 7-rhamnoside [M+H]+ | 14130919 | Click to see | 448.40 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides | |||||
| (E)-3-[4-[2-(4-hydroxyphenyl)ethyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid | 163192871 | Click to see | 446.40 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| 3-[4-[2-(4-Hydroxyphenyl)ethyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid | 162997799 | Click to see C1=CC(=CC=C1CCC2=CC(=C(C=C2)C=CC(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O | 446.40 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| > Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins | |||||
| 1,2,3,10,11,12-Hexamethoxy-6,7-dimethyl-5,6,7,8-tetrahydrodibenzo(a,c)(8)annulen-6-ol | 23915 | Click to see | 432.50 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
| Schisandrin | 3001664 | Click to see | 432.50 | unknown | https://doi.org/10.1007/S10600-010-9540-6 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |