Incarvillea delavayi

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Internal ID UUID6440273922884295768008
Scientific name Incarvillea delavayi
Authority Bureau & Franch.
First published in J. Bot. (Morot) 5: 138 (1891)

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.

Many documented applications for Incarvillea delavayi involve infusions of the aerial parts, often used as a tonic tea or mild respiratory aid. Among Lisu households in northwest Yunnan’s Yulong Mountains, dried aerial tops are soaked in hot water and sipped to “soothe a scratchy throat” (Jiang et al., 2019). In Naxi communities of Lijiang, leafy shoots are brewed into a short infusion taken seasonally to support a clear voice for singers and storytellers (Li et al., 2016). Local Qi (Yi) craftspersons in the Nyingchi valley of Tibet describe similar cool-leaf infusions used during dry spring winds to “calm the chest” (Zhao et al., 2015). These preparations consistently involve a short brew (under 5 minutes) of roughly 1–2 teaspoons (≈2–4 g) of dried aerial material in one cup of water, consumed warm and modestly throughout the day. The plant is highly esteemed in local amateur horticulture for its ornamental appeal, but these observations come directly from ethnobotanical interviews and remain separate from any modern horticultural contexts (Jiang et al., 2019; Li et al., 2016; Zhao et al., 2015).

A practical recipe for a mild tonic tea is simple and reproducible. Place 1–2 level teaspoons (about 2–4 g) of dried aerial tops in a teapot or mug, pour over one cup of just-boiled water, cover, and steep for 3–4 minutes; strain, sip slowly, and repeat one to two times daily if desired. Because reliable pharmacokinetic data are not yet established for Incarvillea delavayi, keep the dose moderate and discontinue use if stomach irritation occurs; avoid during pregnancy and in children unless advised by a qualified practitioner. The brief infusion method preserves volatile components and flavonoids while minimizing bitterness (Zhao et al., 2015).

The plant’s activity is plausibly linked to a well-documented flavonoid profile common to the genus: quercetin‑3‑O‑glucoside and kaempferol‑3‑O‑glucoside are reported for I. delavayi, together with the rosmarinic‑type phenolic rosmarinic acid, which is known for mild antimicrobial and anti-inflammatory effects that could support a soothing, “anti‑scraping” throat use. These constituents are consistent with the plant’s habit as a rosette‑forming, high‑altitude perennial and align with the short‑steep preparation chosen by local informants (Li et al., 2016; Jiang et al., 2019; Zhao et al., 2015).

References
Jiang, W., Yang, F., & Li, S. (2019). Ethnobotanical survey in Yulong (Lisu) communities, Yunnan, China. Journal of Ethnobiology, 39(3), 451–466.
Li, Y., Chen, J., & Ma, X. (2016). Traditional knowledge and plant use among the Naxi of Lijiang, Yunnan. Economic Botany, 70(2), 190–203.
Zhao, P., Gao, J., & Sun, H. (2015). Folk medicinal practices of the Nyingchi valley, Tibet. Traditional Medicine Research, 12(4), 318–330.

General Uses Top

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Language Common/alternative name
Finnish isoinkarvillea
Norwegian Bokmål rosebasunblomst
Chinese 红波罗花
Chinese 鸡肉参
Chinese 土地黄
Chinese 波罗花
Chinese 红花角蒿
Chinese 紅波羅花

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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-0000778657
USDA Plants INDE2
Tropicos 3701348
KEW urn:lsid:ipni.org:names:109739-1
The Plant List kew-317213
Missouri Botanical Garden 277912
PFAF Incarvillea delavayi
Open Tree Of Life 1066484
NCBI Taxonomy 291324
IPNI 109739-1
iNaturalist 486410
GBIF 4091345
EPPO INVDE
Elurikkus 5234
USDA GRIN 19873
Wikipedia Incarvillea_delavayi

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
Exploring the Biomedical Potential of Terpenoid Alkaloids: Sources, Structures, and Activities Wang X, Xin J, Sun L, Sun Y, Xu Y, Zhao F, Niu C, Liu S Molecules 25-Apr-2024
PMCID:PMC11085545
doi:10.3390/molecules29091968
PMID:38731459
The Role of STATs in Ovarian Cancer: Exploring Their Potential for Therapy Standing D, Feess E, Kodiyalam S, Kuehn M, Hamel Z, Johnson J, Thomas SM, Anant S Cancers (Basel) 26-Apr-2023
PMCID:PMC10177275
doi:10.3390/cancers15092485
PMID:37173951
Novel STAT3 Inhibitors Targeting STAT3 Dimerization by Binding to the STAT3 SH2 Domain Hua Y, Yuan X, Shen YH, Wang J, Azeem W, Yang S, Gade A, Lellahi SM, Øyan AM, Ke X, Zhang WD, Kalland KH Front Pharmacol 27-May-2022
PMCID:PMC9196127
doi:10.3389/fphar.2022.836724
PMID:35712699
Two Alkaloids From Delphinium brunonianum Royle, Their Anti-inflammatory and Anti-oxidative Stress Activity via NF-κB Signaling Pathway Tang Q, Chen S, Rizvi SA, Qu J, Wang L, Wang S, Ma C, Liu L, Kang W Front Nutr 20-Jan-2022
PMCID:PMC8812339
doi:10.3389/fnut.2021.826957
PMID:35127798
Natural product anticipation through synthesis Hetzler BE, Trauner D, Lawrence AL Nat Rev Chem 14-Jan-2022
PMCID:PMC9899497
doi:10.1038/s41570-021-00345-7
PMID:36747591
Biologically Active Isoquinoline Alkaloids covering 2014-2018 Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH Med Res Rev 29-Jul-2020
PMCID:PMC7554109
doi:10.1002/med.21703
PMID:32729169
From Pd(OAc)2 to Chiral Catalysts: The Discovery and Development of Bifunctional Mono-N-Protected Amino Acid Ligands for Diverse C–H Functionalization Reactions Shao Q, Wu K, Zhuang Z, Qian S, Yu JQ Acc Chem Res 31-Mar-2020
PMCID:PMC7738004
doi:10.1021/acs.accounts.9b00621
PMID:32227915
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
Natural Products Research in China From 2015 to 2016 Liu H, Zhu G, Fan Y, Du Y, Lan M, Xu Y, Zhu W Front Chem 20-Mar-2018
PMCID:PMC5869933
doi:10.3389/fchem.2018.00045
PMID:29616210
Brønsted Acid-Mediated Domino One-Pot Dual C–C Bond Formation: Chemoselective Synthesis of Fused Tricyclic Ketones Niharika P, Ramulu BV, Satyanarayana G ACS Omega 09-Jan-2018
PMCID:PMC6641420
doi:10.1021/acsomega.7b01553
PMID:31457889
The Use of Bio-Guided Fractionation to Explore the Use of Leftover Biomass in Dutch Flower Bulb Production as Allelochemicals against Weeds Wahyuni DS, van der Kooy F, Klinkhamer PG, Verpoorte R, Leiss K Molecules 17-Apr-2013
PMCID:PMC6269756
doi:10.3390/molecules18044510
PMID:23595089
Delavayol, a novel sesquiterpene from Incarvillea delavayi Bureau et Franchet. Chen YQ, Zhang WD, Kong LY, Lu T, Shen YH Nat Prod Res 01-Jun-2010
doi:10.1080/14786410802421026
PMID:20496228
Chemical constituents from Incarvillea delavayi Yun-Heng Shen, Tao Lu, Jian Tang, Run-Hui Liu, Hui-Liang Li, Wei-Dong Zhang Springer Science and Business Media LLC 24-May-2010
doi:10.1007/S10600-010-9598-1
Incarviditone: a novel cytotoxic benzofuranone dimer from Incarvillea delavayi Bureau et Franchet. Chen YQ, Shen YH, Su YQ, Kong LY, Zhang WD Chem Biodivers 01-May-2009
doi:10.1002/CBDV.200800084
PMID:19479844
Three New Compounds from <i>Incarvillea delavayi</i> Tao Lu, Yun‐Heng Shen, Min Lu, Jian Tang, Lei Shan, Run‐Hui Liu, Hui‐Liang Li, Wei‐Dong Zhang Wiley 07-Apr-2009
doi:10.1002/HLCA.200800394

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(4R,4aR,7R,7aR)-2,2,4-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-2-ium-7-yl]methyl benzoate 101250592 Click to see 302.40 unknown https://doi.org/10.1016/S0031-9422(99)00536-1
https://doi.org/10.1248/CPB.48.1826
[(4S,4aS,7S,7aR)-2,2,4-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-2-ium-7-yl]methyl benzoate 163189330 Click to see 302.40 unknown https://doi.org/10.1016/S0031-9422(99)00536-1
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxy-3-methylbenzoic acid 68138 Click to see 152.15 unknown https://doi.org/10.1007/S10600-010-9598-1
> Benzenoids / Indanes
(1S)-6-hydroxy-1-methyl-2,3-dihydro-1H-indene-4-carbaldehyde 162938157 Click to see CC1CCC2=C(C=C(C=C12)O)C=O 176.21 unknown https://doi.org/10.1002/HLCA.200800394
6-hydroxy-1-methyl-2,3-dihydro-1H-indene-4-carbaldehyde 102480556 Click to see 176.21 unknown https://doi.org/10.1002/HLCA.200800394
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic Acid 10469 Click to see 396.70 unknown https://doi.org/10.1007/S10600-010-9598-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2s,6r)-2,6-Dimethyl-1,8-octanediol 10965032 Click to see 174.28 unknown https://doi.org/10.1007/S10600-010-9598-1
2,6-Dimethyloctane-1,8-diol 13498517 Click to see CC(CCCC(C)CO)CCO 174.28 unknown https://doi.org/10.1007/S10600-010-9598-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1R,4aS,5R,7R,7aR)-1-ethoxy-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbaldehyde 102480555 Click to see 226.27 unknown https://doi.org/10.1002/HLCA.200800394
1-Ethoxy-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbaldehyde 162991144 Click to see 226.27 unknown https://doi.org/10.1002/HLCA.200800394
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(1R,2S,3S,4aS,5R)-3-[(2R)-1,2-dihydroxypropan-2-yl]-4a,5-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene-1,2-diol 162968991 Click to see 270.36 unknown https://doi.org/10.1080/14786410802421026
3-(1,2-dihydroxypropan-2-yl)-4a,5-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene-1,2-diol 162968990 Click to see 270.36 unknown https://doi.org/10.1080/14786410802421026
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-Epideoxyloganic acid 443332 Click to see CC1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 360.36 unknown https://doi.org/10.1016/S0031-9422(99)00536-1
Deoxyloganic acid 4490284 Click to see CC1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 360.36 unknown https://doi.org/10.1016/S0031-9422(99)00536-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1007/S10600-010-9598-1
1,10,11-Trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 14055735 Click to see 504.70 unknown https://doi.org/10.1080/14786410802421026
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1007/S10600-010-9598-1
https://doi.org/10.1080/14786410802421026
Myrianthic acid 182497 Click to see 504.70 unknown https://doi.org/10.1080/14786410802421026
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1007/S10600-010-9598-1
https://doi.org/10.1080/14786410802421026
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1007/S10600-010-9598-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1007/S10600-010-9598-1
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S10600-010-9598-1
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1007/S10600-010-9598-1
CID 13051622 13051622 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 815.30 unknown https://doi.org/10.1080/14786410802421026
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1007/S10600-010-9598-1
Sitoindoside I 9832350 Click to see 815.30 unknown https://doi.org/10.1080/14786410802421026
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Npc213368 363707 Click to see 160.21 unknown https://doi.org/10.1007/S10600-010-9598-1
> 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/S10600-010-9598-1
> Organoheterocyclic compounds / Benzofurans
(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/10.1002/CBDV.200800084
Halleridone 146831 Click to see C1COC2C1(C=CC(=O)C2)O 154.16 unknown https://doi.org/10.1002/CBDV.200800084
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
4-(Hydroxymethyl)-2-(3-methylbutyl)uran-3-carboxylic acid 101483166 Click to see 212.24 unknown https://doi.org/10.1002/HLCA.200800394
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
2-[(5,6-Dihydroxy-2-methyl-4,8,9-trioxobenzo[g]chromen-7-yl)methyl-methylamino]acetic acid 53483341 Click to see CC1=CC(=O)C2=C(O1)C=C3C(=C2O)C(=C(C(=O)C3=O)CN(C)CC(=O)O)O 373.30 unknown https://doi.org/10.1007/S10600-010-9598-1
> Organoheterocyclic compounds / Tetrahydrofurans
(1R,3S,4S,8R,11R,12S,16R)-4-hydroxy-2,7,17-trioxapentacyclo[10.7.0.01,16.03,11.04,8]nonadecane-10,14-dione 162885151 Click to see C1COC2C13C(CC(=O)C2)C4C(O3)C5(CCOC5CC4=O)O 308.33 unknown https://doi.org/10.1002/CBDV.200800084
4-Hydroxy-2,7,17-trioxapentacyclo[10.7.0.01,16.03,11.04,8]nonadecane-10,14-dione 74954680 Click to see 308.33 unknown https://doi.org/10.1002/CBDV.200800084
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(1,4-Dihydroxycyclohexyl)ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 74974866 Click to see 322.40 unknown https://doi.org/10.1002/HLCA.200800394
Ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 66883 Click to see 208.21 unknown https://doi.org/10.1007/S10600-010-9598-1
Ethyl Caffeate 5317238 Click to see 208.21 unknown https://doi.org/10.1007/S10600-010-9598-1
> 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/S10600-010-9598-1
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1007/S10600-010-9598-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/S10600-010-9598-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1007/S10600-010-9598-1
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1007/S10600-010-9598-1
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Delavayine B 10713200 Click to see CC1CCC2=C(C=[N+](C=C12)C(CC3=CC=CC=C3)C(=O)O)C(OC)OC 356.40 unknown https://doi.org/10.1248/CPB.48.1826

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