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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

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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

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Language Common/alternative name
Chinese 鸡肉参
Chinese 山羊参
Chinese 鷄肉蔘

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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

Links to other databases Top

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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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Community-wide patterns in pollen and ovule production, their ratio (P/O), and other floral traits along an elevation gradient in southwestern China Nepal S, Trunschke J, Ren ZX, Burgess KS, Wang H BMC Plant Biol 14-Sep-2023
PMCID:PMC10500814
doi:10.1186/s12870-023-04433-2
PMID:37710175
Genomic and Metabolomic Analysis of the Potato Common Scab Pathogen Streptomyces scabiei Liu J, Nothias LF, Dorrestein PC, Tahlan K, Bignell DR ACS Omega 20-Apr-2021
PMCID:PMC8153979
doi:10.1021/acsomega.1c00526
PMID:34056303
Research Progress of Therapeutic Enzymes and Their Derivatives: Based on Herbal Medicinal Products in Rheumatoid Arthritis Cai M, Ni WJ, Han L, Chen WD, Peng DY Front Pharmacol 16-Mar-2021
PMCID:PMC8008143
doi:10.3389/fphar.2021.626342
PMID:33796022
Synthesis of the Hexahydropyrrolo-[3,2-c]-quinoline Core Structure and Strategies for Further Elaboration to Martinelline, Martinellic Acid, Incargranine B, and Seneciobipyrrolidine Haarr MB, Sydnes MO Molecules 11-Jan-2021
PMCID:PMC7827258
doi:10.3390/molecules26020341
PMID:33440776
Do annual and perennial populations of an insect-pollinated plant species differ in mating system? Ma Y, Barrett SC, Wang FY, Deng JC, Bai WN Ann Bot 09-Oct-2020
PMCID:PMC8225283
doi:10.1093/aob/mcaa178
PMID:33035305
Phytochemical Analysis, Antioxidant and Analgesic Activities of Incarvillea compacta Maxim from the Tibetan Plateau Guo J, Zhang D, Yu C, Yao L, Chen Z, Tao Y, Cao W Molecules 30-Apr-2019
PMCID:PMC6539126
doi:10.3390/molecules24091692
PMID:31052248
LOX inhibitor HOEC interfered arachidonic acid metabolic flux in collagen-induced arthritis rats Yang W, Wang X, Xu L, Li H, Wang R Am J Transl Res 15-Aug-2018
PMCID:PMC6129533
PMID:30210691
Discovery of Natural Products as Novel and Potent FXR Antagonists by Virtual Screening Diao Y, Jiang J, Zhang S, Li S, Shan L, Huang J, Zhang W, Li H Front Chem 30-Apr-2018
PMCID:PMC5936786
doi:10.3389/fchem.2018.00140
PMID:29761098
Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol Giomi D, Ceccarelli J, Brandi A ACS Omega 15-Mar-2018
PMCID:PMC6641500
doi:10.1021/acsomega.8b00167
PMID:31458576
Seasonal variation in the mating system of a selfing annual with large floral displays Yin G, Barrett SC, Luo YB, Bai WN Ann Bot 31-Dec-2015
PMCID:PMC4765542
doi:10.1093/aob/mcv186
PMID:26721904
(+)-2-(1-Hydroxyl-4-oxocyclohexyl) ethyl caffeate suppresses solar UV-induced skin carcinogenesis by targeting PI3-K, ERK1/2 and p38 Lim DY, Lee MH, Shin SH, Chen H, Ryu J, Shan L, Li H, Bode AM, Zhang WD, Dong Z Cancer Prev Res (Phila) 20-May-2014
PMCID:PMC4125463
doi:10.1158/1940-6207.CAPR-13-0286
PMID:24845061
The reproductive strategy of a pollinator-limited Himalayan plant, Incarvillea mairei (Bignoniaceae) Ai H, Zhou W, Xu K, Wang H, Li D BMC Plant Biol 01-Dec-2013
PMCID:PMC4219382
doi:10.1186/1471-2229-13-195
PMID:24289097
A Unique Indolo‐[1,7]naphthyridine Alkaloid from <i>Incarvillea mairei</i> var. <i>grandiflora</i> (<scp>Wehrh.</scp>) <scp>Grierson</scp> Yun‐Heng Shen, Yong‐Qing Su, Jun‐Mian Tian, Sheng Lin, Hui‐Liang Li, Jian Tang, Wei‐Dong Zhang Wiley 15-Dec-2010
doi:10.1002/HLCA.201000092
Three New Monoterpene Alkaloids and a New Caffeic Acid Ester from <i>Incarvillea mairei</i> var. <i>multifoliolata</i> Ai‐Ting Xing, Jun‐Mian Tian, Chun‐Mei Liu, Hui‐Liang Li, Wei‐Dong Zhang, Lei Shan Wiley 15-Apr-2010
doi:10.1002/HLCA.200900284
Chemical constituents of Incarvillea mairei var. grandiflora Yong-Qing Su, Yun-Heng Shen, Jian Tang, Wei-Dong Zhang Springer Science and Business Media LLC 22-Mar-2010
doi:10.1007/S10600-010-9540-6

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

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