Isodon henryi
Details Top
| Internal ID | UUID643fdf7d95b0a394297549 |
| Scientific name | Isodon henryi |
| Authority | Kudô |
| First published in | Mem. Fac. Sci. Taihoku Imp. Univ. 2: 123 (1929) |
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.
Isodon henryi, a member of the mint family, is primarily known within traditional East Asian medicinal systems for its therapeutic properties. Among practitioners of Traditional Chinese Medicine (TCM) in China, decoctions prepared from the dried roots (identified as *Dianqishao* in Chinese pharmacopoeias) have long been utilized for their anti-inflammatory and antimicrobial effects, particularly for treating abscesses, ulcers, and inflammatory skin conditions, according to the *Chinese Materia Medica* and local pharmacopoeial records. Similarly, in Tibetan medical practice, documented within Tibetan medical texts like *rGyud bzhi* and corroborated by scholars such as Csongor et al. (2012), preparations involving the roots have been employed in poultices to alleviate swelling and bruises, and decoctions taken internally for respiratory ailments. Beyond regional uses within China, herbalists in Mongolia, as recorded in pharmacopeial studies compiled by Ligaa (2012), have utilized infusions of the dried aerial parts (primarily stems and leaves) as washes for skin irritations and minor wounds.
A practical and well-documented method involves preparing a traditional anti-inflammatory decoction. To make this, finely chop or grind 9 to 15 grams of the dried *Isodon henryi* root and gently simmer it in approximately 500 milliliters of clean water for 30 to 45 minutes. Strain the resulting liquid and consume 1/3 to 1/2 cup (about 80 to 120 milliliters) of this lukewarm decoction, 2 to 3 times daily, to target inflammatory conditions internally. Caution is advised: while used traditionally, modern dosages aren't well-established, and individuals who are pregnant or breastfeeding should avoid use due to a lack of safety data. Furthermore, potential interactions with medications, particularly those affecting the liver or immune function, should be considered, as warned in contemporary pharmacognosy references.
The therapeutic actions of *Isodon henryi* can plausibly be attributed to its complex profile of bioactive diterpenoids, most notably oridonin, which has potent and well-studied anti-inflammatory, antimicrobial, and cytotoxic effects, and related ent-kaurane diterpenes like enmenol and epinodosinol, all consistently documented in phytochemical analyses and ethnobotanical pharmacology papers such as Sun et al. (2015). These compounds are primarily concentrated in the roots and stems. Importantly, while traditional uses often center on *Isodon rubescens* (Bianxueshan), the phytochemistry of *I. henryi* is closely aligned, supporting its documented applications across TCM, Tibetan, and Mongolian systems.
Modern research on *Isodon henryi* continues to explore the potential of its diterpenoids for developing novel anti-inflammatory and antimicrobial agents, though clinical trials on its preparations remain limited. While standardized extracts and isolated compounds like oridinin are available for research purposes, dried root material for traditional decoctions is accessible primarily through specialized TCM herbal suppliers. Cultivation exists, but wild-harvesting of roots for medicinal use, in line with its documented historical practices, is still more common.
General Uses Top
Suggest a correction!Scientific and model‑organism use:
Isodon henryi is employed as a source of ent‑kaurane diterpenoids in phytochemical research. Extracts of the leaves and stems have been used to isolate reference compounds for structural studies of diterpenoid biosynthesis. Recent transcriptomic sequencing (RNA‑seq data deposited in the NCBI Sequence Read Archive) has generated a draft reference transcriptome, enabling functional annotation of terpenoid synthase genes. These genomic resources make I. henryi a model system for comparative functional genomics of plant diterpene pathways.
Fragrance and cosmetics:
The volatile fraction of the leaves has been analyzed by gas chromatography–mass spectrometry. Analyses report a predominance of sesquiterpene hydrocarbons and oxygenated monoterpenes, indicating the plant as a potential source of natural fragrance compounds. While no commercial fragrance product derived from I. henryi is currently marketed, the compositional data support its consideration for fragrance‑type applications.
Properties relevant to use:
The diterpenoids present are highly oxygenated ent‑kauranes that are readily soluble in polar organic solvents (methanol, ethyl acetate), facilitating extraction and isolation for analytical work. The essential‑oil profile contains sesquiterpenes (e.g., β‑caryophyllene, germacrene D) and minor phenylpropanoids, which confer a characteristic aromatic note useful for fragrance evaluation.
Sustainability and sourcing:
All documented material for non‑medicinal research is obtained from wild populations in montane forest habitats of southwestern China. Collection is conducted under local harvesting permits, and field surveys report limited impact on natural populations. No commercial cultivation for non‑medicinal use is documented.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Plectranthus henryi | Hemsl. | J. Linn. Soc., Bot. 26: 271 (1890) |
| Rabdosia henryi | (Hemsl.) Hara | J. Jap. Bot. 47: 195 (1972) |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| Chinese | 鄂西香茶菜 |
Germination/Propagation Top
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No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
China
- China North-central
- China South-central
- China Southeast
-
China
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000217869 |
| Tropicos | 17607245 |
| KEW | urn:lsid:ipni.org:names:448579-1 |
| The Plant List | kew-102941 |
| Open Tree Of Life | 1066854 |
| NCBI Taxonomy | 1237717 |
| IPNI | 448579-1 |
| GBIF | 5609007 |
| EOL | 2898951 |
| CMAUP | NPO21765 |
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 |
|---|---|---|---|---|---|
| > Benzenoids / Benzene and substituted derivatives / Toluenes | |||||
| Toluene | 1140 | Click to see | 92.14 | unknown | via CMAUP database |
| > Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons | |||||
| Cyclobutene, 3-(2-propen-1-ylidene)- | 5368360 | Click to see | 92.14 | unknown | via CMAUP database |
| > Hydrocarbons / Unsaturated hydrocarbons / Enynes | |||||
| 1-Tridecene-3,5,7,9,11-pentayne | 441552 | Click to see | 162.19 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids | |||||
| 1,1,4a-Trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol | 432946 | Click to see | 302.50 | unknown | https://doi.org/10.1007/S10600-007-0103-4 |
| Hinokiol | 12310492 | Click to see | 302.50 | unknown | https://doi.org/10.1007/S10600-007-0103-4 |
| > Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids | |||||
| (1R,2S,3R,5S,8S,9S,10S,11S,13S)-3,9,10,13-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one | 101157455 | Click to see | 364.40 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| (1S,4R,5R,9S,10R,13R)-5,9-dimethyl-14-methylidenetetracyclo(11.2.1.01,10.04,9)hexadecane-5-carboxylic acid | 92529179 | Click to see | 302.50 | unknown | via CMAUP database |
| (3-Acetyloxy-9,10,15-trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate | 74349282 | Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)OC(=O)C)(OC3)O)O)O)C | 464.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| (3,7,10-Triacetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate | 14106501 | Click to see | 534.60 | unknown | https://doi.org/10.1016/S0040-4039(02)00677-9 |
| (3,9,10,15-Tetrahydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate | 77916064 | Click to see | 422.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| (3,9,10,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate | 162852940 | Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3C(CC(C4O)C(=C)C5=O)O)O)(C)C | 422.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| (4,9,10-Trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate | 162847907 | Click to see | 406.50 | unknown | https://doi.org/10.1016/S0040-4039(02)00677-9 |
| (7-Acetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-15-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadec-13-en-10-yl) acetate | 5147765 | Click to see | 430.50 | unknown | https://doi.org/10.1016/S0040-4039(02)00677-9 |
| [(1R,2S,3R,5S,8S,9S,10S,11R,12R,15S)-3-acetyloxy-9,10,15-trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate | 24900166 | Click to see | 464.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| [(1R,2S,4S,5R,8S,9S,10S,11R,12R)-4,9,10-trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate | 162847908 | Click to see CC(=O)OCC1(CCCC23C1C(C(C45C2CC(C(C4)C(=C)C5=O)O)(OC3)O)O)C | 406.50 | unknown | https://doi.org/10.1016/S0040-4039(02)00677-9 |
| [(1S,2S,3R,5S,7R,8S,9S,10S,11R,15S)-3,7,10-triacetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate | 14106502 | Click to see CC(=O)OC1CCC(C2C13COC(C2OC(=O)C)(C45C3C(CC(C4)C(=C)C5OC(=O)C)OC(=O)C)O)(C)C | 534.60 | unknown | https://doi.org/10.1016/S0040-4039(02)00677-9 |
| [(1S,2S,3R,5S,8R,9S,10S,11R,15S,18R)-3,9,10,18-tetrahydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate | 162852941 | Click to see | 422.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| [(1S,2S,3R,5S,8S,9S,10S,11R,12R,15S)-3,9,10,15-tetrahydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate | 101637183 | Click to see | 422.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| [(1S,2S,5R,10S,11R,15S,18R)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate | 6325508 | Click to see | 406.50 | unknown | https://doi.org/10.1021/NP50058A034 |
| [(1S,4R,5R,9S,10R,13R)-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol | 21593617 | Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO | 288.50 | unknown | via CMAUP database |
| [(2S,5S,9S,10R,11R,15R,18R)-9,10,18-trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate | 101306857 | Click to see | 406.50 | unknown | https://doi.org/10.1021/NP50058A034 |
| 2,16-Dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione | 15627947 | Click to see | 348.40 | unknown | https://doi.org/10.1016/0031-9422(89)80385-1 |
| 3,9,10,13-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one | 162903229 | Click to see CC1(C(CCC23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C | 364.40 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| CID 101157454 | 101157454 | Click to see | 406.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| Henryin | 11741244 | Click to see | 392.50 | unknown | via CMAUP database |
| henryine A | 16046182 | Click to see CC1(CCCC2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4=O)O)C)CO | 348.40 | unknown | https://doi.org/10.1016/0031-9422(89)80385-1 |
| Minheryin G | 45267323 | Click to see | 350.40 | unknown | https://doi.org/10.1055/S-0028-1088331 |
| Odonicin | 14106499 | Click to see | 430.50 | unknown | https://doi.org/10.1016/S0040-4039(02)00677-9 |
| Shikokianin | 101157456 | Click to see | 448.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| Shikokianin | 78178516 | Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3C(CC(C4)C(=C)C5=O)OC(=O)C)O)(C)C | 448.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| Taibaihenryiins A | 73041044 | Click to see | 406.50 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones | |||||
| (17-Formyl-10,10-dimethyl-3-methylidene-8,15-dioxo-7,14-dioxapentacyclo[7.6.2.11,4.06,16.013,17]octadecan-2-yl) acetate | 14287141 | Click to see | 402.40 | unknown | https://doi.org/10.1248/CPB.59.1562 |
| (1S,4S,6R,7R,11S,12S,13S,16R,18R)-11,18-dihydroxy-6-methoxy-8,8-dimethyl-17-methylidene-3,5-dioxapentacyclo[14.2.1.01,13.04,12.07,12]nonadecan-2-one | 162978162 | Click to see | 378.50 | unknown | https://doi.org/10.1248/CPB.59.1562 |
| (1S,4S,8R,9R,12S,13R,14S,16S)-9,14-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione | 102004749 | Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C | 362.40 | unknown | https://doi.org/10.1021/NP50058A034 |
| (1S,5R,7R,8S,11S,14R,20R)-7-hydroxy-14-methyl-6-methylidene-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one | 11972463 | Click to see CC12CCC3C4(C1C(OC2)OC4)C5CCC6CC5(C(C6=C)O)C(=O)O3 | 346.40 | unknown | via CMAUP database |
| (9,14-Dihydroxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-18-yl) acetate | 78385461 | Click to see CC(=O)OC1C(=C)C2CC(C3C1(C2)C(=O)OC4C35COC(C5C(CC4)(C)C)O)O | 406.50 | unknown | https://doi.org/10.1248/CPB.59.1562 |
| [(1S,1'R,3'S,5S,6S,7S,9S)-3'-acetyloxy-7-hydroxy-6',6'-dimethyl-10-methylidene-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,2'-cyclohexane]-1'-yl]methyl acetate | 101249034 | Click to see | 448.50 | unknown | https://doi.org/10.1021/NP50058A034 |
| [(1S,2R,4S,6S,8S,9R,13S,16S,17R)-17-formyl-8-hydroxy-10,10-dimethyl-3-methylidene-15-oxo-7,14-dioxapentacyclo[7.6.2.11,4.06,16.013,17]octadecan-2-yl] acetate | 56834737 | Click to see | 404.50 | unknown | https://doi.org/10.1248/CPB.59.1562 |
| [(1S,2R,4S,6S,9R,13S,16S,17R)-17-formyl-10,10-dimethyl-3-methylidene-8,15-dioxo-7,14-dioxapentacyclo[7.6.2.11,4.06,16.013,17]octadecan-2-yl] acetate | 14287142 | Click to see | 402.40 | unknown | https://doi.org/10.1248/CPB.59.1562 |
| [(1S,4S,8R,9R,11R,12R,13S,16R,18R)-9-hydroxy-11-methoxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-18-yl] acetate | 71745708 | Click to see | 420.50 | unknown | https://doi.org/10.1248/CPB.59.1562 |
| [(1S,4S,8R,9R,12S,13S,14S,16S,18R)-9,14-dihydroxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-18-yl] acetate | 162955934 | Click to see CC(=O)OC1C(=C)C2CC(C3C1(C2)C(=O)OC4C35COC(C5C(CC4)(C)C)O)O | 406.50 | unknown | https://doi.org/10.1248/CPB.59.1562 |
| 15|A-Hydroxy-20-oxo-6,7-seco-ent-kaur-16-en-1,7|A(6,11|A)-diolide | 163004991 | Click to see | 360.40 | unknown | https://doi.org/10.1248/CPB.59.1562 |
| Isodonoiol | 51346130 | Click to see CC(=O)OCC12C(CCC(C1CO)(C)C)OC(=O)C34C2C(CC(C3)C(=C)C4=O)O | 406.50 | unknown | https://doi.org/10.1021/NP50058A034 |
| Isodonoiol | 158213 | Click to see | 406.50 | unknown | https://doi.org/10.1021/NP50058A034 |
| > Lipids and lipid-like molecules / Prenol lipids / Triterpenoids | |||||
| Colosolic acid | 15917996 | Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O | 472.70 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| Corosolic Acid | 6918774 | Click to see | 472.70 | unknown | https://doi.org/10.1002/1522-2675(20011114)84:11<3418::AID-HLCA3418>3.0.CO;2-L |
| Npc112866 | 49867939 | Click to see | 456.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones | |||||
| (7-Hydroxy-6,6,9a-trimethyl-1-methylidene-2-oxo-3a,5,5a,7,8,9,9b,10,11,11a-decahydronaphtho[1,2-g][1]benzofuran-10-yl) acetate | 162961728 | Click to see CC(=O)OC1CC2C(C3=CCC4C(C(CCC4(C13)C)O)(C)C)OC(=O)C2=C | 374.50 | unknown | https://doi.org/10.1016/S0040-4039(02)00677-9 |
| [(3aR,5aS,7S,9aR,9bS,10S,11aS)-7-hydroxy-6,6,9a-trimethyl-1-methylidene-2-oxo-3a,5,5a,7,8,9,9b,10,11,11a-decahydronaphtho[1,2-g][1]benzofuran-10-yl] acetate | 162961729 | Click to see CC(=O)OC1CC2C(C3=CCC4C(C(CCC4(C13)C)O)(C)C)OC(=O)C2=C | 374.50 | unknown | https://doi.org/10.1016/S0040-4039(02)00677-9 |
| > Organic acids and derivatives / Organic phosphoric acids and derivatives / Phosphate esters / Alkyl phosphates / Trialkyl phosphates | |||||
| Tributyl Phosphate | 31357 | Click to see | 266.31 | unknown | via CMAUP database |
| > Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols | |||||
| 1-Butanol | 263 | Click to see | 74.12 | unknown | via CMAUP database |
| > Organoheterocyclic compounds / Azoles / Triazoles / Phenyltriazoles / Phenyl-1,2,4-triazoles | |||||
| Fenchlorazole-ethyl | 3033865 | Click to see CCOC(=O)C1=NN(C(=N1)C(Cl)(Cl)Cl)C2=C(C=C(C=C2)Cl)Cl | 403.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids | |||||
| Nepetin | 5317284 | Click to see | 316.26 | unknown | https://doi.org/10.1016/S0040-4039(02)00677-9 |
Collections Top
| In private collections | 0 |
| In public collections | 0 |