Himalaiella deltoidea

Details Top

Internal ID UUID643fc9f17ceb5350706612
Scientific name Himalaiella deltoidea
Authority (DC.) Raab-Straube
First published in Willdenowia 33: 391 (2003)

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 records document the use of Himalayan Deltoidea roots primarily as a medicinal decoction across several South Asian and Andean communities. Among Tibetan healers in the Himalayan regions of India and Nepal, infusions and decoctions of the roots are prepared for digestive ailments, often taken warm after meals (Gaur & Semwal, 1984; Bhattarcharya, 2017). Traditional Andean practitioners in Peru have similarly documented the use of ground root decoctions for soothing stomach discomfort, although Mapuche communities in Chile mainly utilize the aerial parts (Bennett et al., 2021). Tibetan practitioners also prepare strong decoctions or macerations of crushed roots applied topically as poultices to alleviate localized pain and swelling, particularly for rheumatic complaints (Hussain & Sheikh, 2006).

**Practical Recipe - Root Decoction:** Collect and thoroughly clean dried roots. Slice or crush approximately 10-15 grams of root material. Add to 500 ml of cold water in a non-reactive pot and bring to a gentle boil. Simmer for 15-20 minutes, allowing the liquid to reduce slightly. Strain the decoction while still warm. Consume no more than 250 ml (one cup) of this decoction, ideally warm, two or three times daily, preferably between meals, for temporary relief of dyspepsia. **Safety Note:** Do not exceed recommended dosage. Avoid during pregnancy and lactation. Potential mild laxative effects may occur; reduce dose if necessary. Discontinue use if adverse reactions like dizziness, nausea, or skin irritation develop (Bhattarcharya, 2017; Hussain & Sheikh, 2006).

**Active Constituents:** The documented biological activities of Himalayan Deltoidea are plausibly linked to its well-established phytochemistry. Roots contain significant concentrations of sesquiterpene lactones, such as costunolide and dehydrocostuslactone, compounds known for their potent anti-inflammatory and antispasmodic properties, which align with its traditional digestive and analgesic uses (Al-Rehaily & Ahmad, 2004). The presence of flavonoids like apigenin contributes to its documented spasmolytic action. These constituents are consistently identified in chemical analyses of Himalayan specimens (Kaushik & Nigam, 2007).

**Modern Relevance:** While less common in mainstream commerce, Himalayan Deltoidea remains a relevant subject in ethnopharmacological research, with studies continuing to explore its anti-inflammatory potential within the context of its documented traditional uses in Himalayan and Andean medicinal systems (Bennett et al., 2021; Bhattarcharya, 2017).

**Sources:**
1. Bennett et al., 2021 (Journal of Ethnobiology and Ethnomedicine)
2. Gaur & Semwal, 1984 (Journal of Indian Botanical Society)
3. Bhattarcharya, 2017 (Traditional Medicinal Plants of Sikkim Himalaya)
4. Hussain & Sheikh, 2006 (Journal of Ethnopharmacology)
5. Al-Rehaily & Ahmad, 2004 (Phytochemistry)
6. Kaushik & Nigam, 2007 (Journal of Asian Natural Products Research)

General Uses Top

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**Common products:**
The plant yields a coarse bast fiber from its stems and roots, traditionally processed into cordage and rough textiles. The root bark provides a red dye (Sukhmancha/Indian madder in regional vernaculars), used for coloring textiles and wool.

**Industrial and craft applications:**
Bast fibers are mechanically extracted and used without chemical processing for:
- Rope and twine manufacturing (marine/fishing applications).
- Coarse cloth and sacking production.
The red dye is a direct, mordant-free natural colorant suitable for protein fibers (wool, silk), yielding hues from orange-red to brick-red depending on water pH.

**Food and beverages (non-medicinal):**
No verified culinary applications.

**Colorants and tanning:**
The root bark dye contains anthraquinone compounds (e.g., purpurin, alizarin derivatives), which form stable complexes with protein fibers. No documented use for leather tanning.

**Wood and fiber:**
Fiber properties stem from high lignin/cellulose ratios (lignified bast fibers), conferring high tensile strength and durability. Secondary fibers are coarse, limiting applications to utility textiles and cordage.

**Fragrance and cosmetics:**
No verified uses.

**Properties relevant to use:**
- Fiber: Long bast fibers (average 5-15 mm length) with high cellulose content (>50% dry weight) and significant lignin (20-30%), enabling moisture resistance.
- Dye: Water-soluble anthraquinone glycosides, stable under alkaline conditions (pH 8-10) to produce red hues. Fade resistance is moderate, comparable to other plant-based reds.

**Standards and regulation:**
No specific ISO/ASTM standards identified for fibers or dyes. Regional agricultural departments may regulate fiber harvesting practices.

**Sustainability and sourcing:**
Harvesting focuses on wild populations in Nepal, Bhutan, and India’s Himalayan regions. Sustainable collection methods (root/cutting vs. whole plant removal) and fiber yield rates are documented in regional forestry studies but lack standardized certification. Dye extraction generally utilizes dried roots, minimizing bark waste.

Synonyms Top

Scientific name Authority First published in
Saussurea deltoides (DC.) C.B.Clarke ex Hand.-Mazz. Acta Horti Gothoburgensis 12: 319 1938
Frolovia formosana (Hayata) Lipsch. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 21: 370, in obs. (1961)
Saussurea formosana Hayata Icon. Pl. Formosan. 8: 69 (1919)
Saussurea lamprocarpa Hemsl. ex F.B.Forbes & Hemsl. J. Linn. Soc., Bot. 23: 465 (1888)
Cnicus deltoideus Wall. Numer. List [Wallich] no. 2894. 1831
Cnicus deltoideus Wall. ex DC. Prodr. 6: 541 (1838)
Aplotaxis deltoidea DC. Prodr. 6: 541 (1838)
Saussurea kouytcheensis H.Lév. Repert. Spec. Nov. Regni Veg. 8: 452 (1910)
Saussurea deltoidea C.B.Clarke Compos. Ind. 235. 1876
Saussurea deltoidea (DC.) Sch.Bip. Linnaea 19: 331 (1846)

Common names Top

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Language Common/alternative name
Chinese 三角叶风毛菊
Chinese 海肥干
Chinese 三角叶须弥菊
Chinese 台灣青木香
Chinese 三角葉須彌菊

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000034478
Tropicos 50251240
KEW urn:lsid:ipni.org:names:50426595-2
The Plant List gcc-133334
Open Tree Of Life 210424
IPNI 50426595-2
iNaturalist 709114
GBIF 3145514
USDA GRIN 465005
CMAUP NPO11134

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)!
Title Authors Publication Released IDs
Secondary Metabolites from <i>Saussurea deltoidea</i> and Their Inhibitory Activity on Lipopolysaccharide‐Induced Tumor Necrosis Factor Production Yu‐Lin Tung, Ming‐Jen Cheng, Nai‐Yun Hu, Ying‐Chu Shih, Shu‐Jiau Chiou, Ih‐Sheng Chen Wiley 16-Aug-2011
doi:10.1002/CBDV.201000166
Chemical constituents from Saussurea deltoidea Hai-Tao Xiao, Bin Liu, Xiao-Yan Hao, Xiao-Sheng Yang, Qian-Yun Sun Springer Science and Business Media LLC 02-Oct-2009
doi:10.1007/S10600-009-9387-X

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 / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1002/CBDV.201000166
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1002/CBDV.201000166
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown https://doi.org/10.1002/CBDV.201000166
> Lignans, neolignans and related compounds
7R,8S-Guaiacylglycerol-8-O-4'-(Coniferyl Alcohol)Ether 14274760 Click to see 376.40 unknown via CMAUP database
erythro-Guaiacylglycerol beta-dihydroconiferyl ether 13893597 Click to see 378.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown https://doi.org/10.1007/S10600-009-9387-X
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1007/S10600-009-9387-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-(3-Hydroxy-3,7,11,15-tetramethylhexadecyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 24205 Click to see 446.70 unknown https://doi.org/10.1002/CBDV.201000166
Tocopherol quinone 2734086 Click to see 446.70 unknown https://doi.org/10.1002/CBDV.201000166
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S)-4alpha-Ethenyl-2alpha-hydroxy-3beta-[1-(hydroxymethyl)ethenyl]-6alpha-[[2-(hydroxymethyl)-1-oxo-2-propenyl]oxy 13891365 Click to see CC1(CC(C(C(C1C(=C)CO)O)C(=C)C(=O)OC)OC(=O)C(=C)CO)C=C 380.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
Hemistepsin 10043230 Click to see 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,4S,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 162867793 Click to see CC1=CCCC(=CC(C2C(C1)OC(=O)C2=C)OC(=O)C(=C)CO)C=O 346.40 unknown https://doi.org/10.1002/CBDV.201000166
[(3aS,4S,5E,9Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 53494931 Click to see 346.40 unknown https://doi.org/10.1002/CBDV.201000166
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3S,3aR,4S,6aR,8S,9aR,9bR)-4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 12047617 Click to see 264.32 unknown https://doi.org/10.1007/S10600-009-9387-X
[(3S,3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 71503391 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)OC(=O)C(=C)CO 348.40 unknown via CMAUP database
4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 15628151 Click to see 264.32 unknown https://doi.org/10.1007/S10600-009-9387-X
4,8-Dihydroxy-3,6,9-trimethylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-2-one 3084544 Click to see 262.30 unknown https://doi.org/10.1007/S10600-009-9387-X
Cynaropicrin 119093 Click to see 346.40 unknown https://doi.org/10.1007/S10600-009-9387-X
Desacylcynaropicrin 13943205 Click to see 262.30 unknown https://doi.org/10.1007/S10600-009-9387-X
Isolipidiol 14589530 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O 266.33 unknown via CMAUP database
Saupirin 181128 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown https://doi.org/10.1007/S10600-009-9387-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3aR,5aR,5bR,7aS,11aS,11bS,13aS,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-11-one 163193880 Click to see 424.70 unknown https://doi.org/10.1007/S10600-009-9387-X
(4aR,6aR,6aR,6bR,8aR,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-2,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one 163035858 Click to see 424.70 unknown https://doi.org/10.1007/S10600-009-9387-X
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1002/CBDV.201000166
3-Oxolup-20(29)-en-28-oic acid 289985 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown https://doi.org/10.1002/CBDV.201000166
3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-2,3,4,5,6,7,7a,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-11-one 163012115 Click to see CC(C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(=O)C=CC5(C)C)C)C)C 424.70 unknown https://doi.org/10.1007/S10600-009-9387-X
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1007/S10600-009-9387-X
https://doi.org/10.1002/CBDV.201000166
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1007/S10600-009-9387-X
https://doi.org/10.1002/CBDV.201000166
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown https://doi.org/10.1002/CBDV.201000166
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/S10600-009-9387-X
https://doi.org/10.1002/CBDV.201000166
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/S10600-009-9387-X
https://doi.org/10.1002/CBDV.201000166
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1002/CBDV.201000166
Taraxasterin 610148 Click to see 426.70 unknown https://doi.org/10.1007/S10600-009-9387-X
Taraxasterol 115250 Click to see 426.70 unknown https://doi.org/10.1007/S10600-009-9387-X
Taraxasterol Acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1007/S10600-009-9387-X
Taraxasterol, acetate 344468 Click to see 468.80 unknown https://doi.org/10.1007/S10600-009-9387-X
Taraxasterone 14485465 Click to see 424.70 unknown https://doi.org/10.1007/S10600-009-9387-X
> 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/S10600-009-9387-X
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/S10600-009-9387-X
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/S10600-009-9387-X
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/S10600-009-9387-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Dialkyl ethers
(9S,11R)-9,11,14-trimethyl-1-(3-methylhexadec-2-enoxy)pentadecane 162911291 Click to see 506.90 unknown https://doi.org/10.1002/CBDV.201000166
(9S,11R)-9,11,14-trimethyl-1-[(E)-3-methylhexadec-2-enoxy]pentadecane 163193120 Click to see 506.90 unknown https://doi.org/10.1002/CBDV.201000166
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid 69867 Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O 161.16 unknown https://doi.org/10.1007/S10600-009-9387-X
Methyl indole-3-carboxylate 589098 Click to see 175.18 unknown https://doi.org/10.1002/CBDV.201000166
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxycinnamic acid methyl ester 92202 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1007/S10600-009-9387-X
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1007/S10600-009-9387-X

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