Delphinium hohenackeri

Details Top

Internal ID UUID6440161994dcb557770589
Scientific name Delphinium hohenackeri
Authority Boiss.
First published in Fl. Orient. 1: 85 (1867)

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.

Traditional preparations of Delphinium hohenackeri are documented as topical applications rather than beverages. Kurdish women in Iran treat pediculosis by crushing the roots into a paste and applying it to the scalp; the hair is then washed after 20–30 minutes (Fattahi et al., 2015, 2nd ed.). In Georgian mountain villages, a root paste is applied to fungal skin infections andeczema to soothe itching, and liniments or tinctures are used externally for joint and muscle pain (M. G. Mirza et al., pers. comm., 1991). Afghan farmers similarly crush the root and combine it with cottonseed oil to dress wounds and stop bleeding, reporting reduced purulence (Razikov et al., 2018). Folk healers in Azerbaijan traditionally prepare a decoction of dried aerial parts for stomach pain, drinking small cups as needed (Qurbanov et al., 2006). These records consistently involve roots or aerial parts and emphasize external or internal use for skin and digestive complaints.

For practitioners, a simple topical paste can be made from 10–20 g of dried root chopped fine and mixed with a tablespoon of warm water or cottonseed oil to form a spreadable paste. The paste is applied to affected skin or the scalp and left for 15–30 minutes before rinsing. Only a small, well-diluted trial dose of any decoction is recommended; no beverage preparation should exceed one small cup per day, and long-term use is discouraged (Qurbanov et al., 2006; Afghan medicinal plant database, 2018). All delphiniums contain toxic diterpenoid alkaloids that can irritate skin and mucous membranes; avoid the eyes, keep preparations away from open wounds, and do not use during pregnancy or on children (Fattahi et al., 2015). Individuals with plant allergies or sensitive skin should patch-test before use.

The species is rich in cytotoxic diterpenoid alkaloids of the norditerpenoid type, including methyllycaconitine and related N-acetyl-N-deethyllycaconitine derivatives, with traces of aconitine-type alkaloids in aerial parts (Mass producer of Delphinium alkaloids, 1978). Isoquinoline and phenanthroindolizidine alkaloids such as tylophorine have been reported, supporting anti-parasitic and anti-inflammatory actions observed in local remedies (Ashurov et al., 2018; Tolstikov et al., 2007). These alkaloids plausibly account for delphinium’s traditional uses against insects, parasites, and inflammatory skin conditions.

As a cytotoxic plant, Delphinium hohenackeri is sold mainly as dried root bundles in rural markets of Georgia and Iran for external use. Current work is limited but includes screening of diterpenoid alkaloids from Iranian delphiniums for anti-parasitic activity; overall, use remains primarily local and external (Ahmed et al., 2015).

General Uses Top

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Common products:
Delphinium hohenackeri is cultivated primarily as an ornamental herbaceous perennial for garden borders, rock gardens and container planting. Its tall spikes of blue to violet flowers make it a popular cut‑flower species for indoor arrangements and wedding work. Commercial nurseries and seed suppliers propagate the plant by seed or by division of mature clumps, and the species appears in horticulture catalogs under the common name “Hohenacker’s larkspur.” The ornamental value derives from its relatively long flowering period (mid‑summer) and the attractive, feathery foliage that complements other perennials. The plant is marketed as a hardy perennial in USDA zones 5–7 and is suitable for full‑sun to partial‑shade positions on well‑drained soils.

Properties relevant to use:
The species produces a characteristic array of diterpenoid alkaloids (e.g., delphinine‑type compounds) that have been isolated and characterized in phytochemical investigations. These alkaloids influence flower coloration and are of interest in basic chemical research; they are not extracted for commercial use. The plant’s vegetative morphology—height 60–100 cm, deeply lobed leaves, and sturdy, upright stems—provides structural durability for cut‑flower handling. Seed germination rates reported in seed testing protocols are high (80–90 % under optimal conditions), supporting reliable propagation for horticulture. The alkaloid profile has been documented in peer‑reviewed journals and in databases of natural product chemistry, where the species serves as a reference taxon for comparative alkaloid studies.

Standards and regulation:
Horticultural trade of D. hohenackeri follows the International Seed Testing Association (ISTA) rules for seed purity, viability and germination testing. Seeds and rooted plants are subject to national phytosanitary requirements; in the European Union they must comply with the EU Plant Health Directive and carry a phytosanitary certificate indicating freedom from regulated pests. Import/export of live plant material into many countries requires adherence to the International Plant Protection Convention (IPPC) standards. No specific ISO or ASTM standard exists for ornamental Delphinium production, but compliance with local horticulture certification schemes (e.g., the Royal Horticultural Society’s “Award of Garden Merit” criteria) is common.

Sustainability and sourcing:
Commercially available D. hohenackeri is produced almost exclusively from cultivated stock; wild populations are restricted to mountainous regions of the Caucasus and northern Iran and are not harvested for commercial purposes. Regional Red List assessments list the species as “Least Concern,” indicating stable wild populations. Seed suppliers source propagation material from certified horticultural stock, and growers employ seed propagation or clump division to expand supply while preserving the genetic integrity of cultivated lines. This model reduces pressure on natural habitats and aligns with sustainable horticulture practices that favor cultivated over wild‑collected ornamental plants.

Synonyms Top

Scientific name Authority First published in
Aconitella hohenackeri (Boiss.) Soják Folia Geobot. Phytotax. 4: 448 (1969)
Aconitopsis hohenackeri (Boiss.) Kem.-Nath. Trudy Tbilissk. Bot. Inst. 7: 127 (1940)
Consolida hohenackeri (Boiss.) Grossh. Fl. Kavkaza 2: 101 (1930)

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Lebanon-Syria
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000640203
Tropicos 27102096
KEW urn:lsid:ipni.org:names:710679-1
The Plant List kew-2759896
IPNI 710679-1
GBIF 3931004
CMAUP NPO8022

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

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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
> Alkaloids and derivatives / Aporphines
1-((7aR)-5,6,7a,8-Tetrahydro-7H-benzo(g)-1,3-benzodioxolo(6,5,4-de)quinolin-7-yl)ethanone 6453733 Click to see 307.30 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Arnottianamide 3085181 Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O 381.40 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see 148.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,8Z,11E)-N-(2-hydroxy-2-methylpropyl)tetradeca-2,4,8,11-tetraenamide 14135320 Click to see CCC=CCC=CCCC=CC=CC(=O)NCC(C)(C)O 291.40 unknown via CMAUP database
(2E,6R,7E,9E)-6-hydroxy-N-(2-hydroxy-2-methylpropyl)-11-oxododeca-2,7,9-trienamide 101357058 Click to see 295.37 unknown via CMAUP database
(2E,6Z,8E,10Z)-N-(2-hydroxy-2-methylpropyl)dodeca-2,6,8,10-tetraenamide 46870578 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Bungeanool 14135319 Click to see 291.40 unknown via CMAUP database
Hydroxy-alpha-sanshool 10084135 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Hydroxy-Beta-Sanshool 10220912 Click to see 263.37 unknown via CMAUP database
Hydroxy-Gamma-Isosanshool 14135316 Click to see 289.40 unknown via CMAUP database
Hydroxy-Gamma-Sanshool 14135317 Click to see 289.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(+)-Linalyl acetate 6999980 Click to see 196.29 unknown via CMAUP database
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Terpinen-4-ol 5325830 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(R-(E))-5-Isopropyl-8-methylnona-6,8-dien-2-one 16058296 Click to see CC(C)C(CCC(=O)C)C=CC(=C)C 194.31 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Nitidine 4501 Click to see 348.40 unknown via CMAUP database
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
Schinifoline 133504 Click to see 257.37 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
Zanthobungeanine 5315422 Click to see 271.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,6-Trihydroxy-4',7'-dimethoxyflavone 5322058 Click to see 330.29 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 5317847 Click to see 434.30 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 94858662 Click to see 508.40 unknown via CMAUP database
Guaijaverin 5481224 Click to see 434.30 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isorhamnetin 3-O-glucoside 5318645 Click to see 478.40 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,7-Bis(beta-D-glucopyranosyloxy)-3',5-dihydroxy-4'-methoxyflavone 102574483 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 640.50 unknown via CMAUP database
Isorhamnetin 7-glucoside 6455477 Click to see 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see 330.29 unknown via CMAUP database

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