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Delphinium semibarbatum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644016338436a623070423
Scientific name Delphinium semibarbatum
Authority Bien. ex Boiss.
First published in Fl. Orient. 1: 92 (1867)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Arabic عائق شبه ملتحي
Azerbaijani yarımsaqqal mahmızçiçək
Uzbek isparak
Chinese 染丝翠雀花

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
  • Asia-temperate
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000640707
KEW urn:lsid:ipni.org:names:710998-1
The Plant List kew-2760367
PFAF Delphinium semibarbatum
Open Tree Of Life 224726
Observations.org 143966
NCBI Taxonomy 1127188
IPNI 710998-1
GBIF 3927661
EPPO DELSE
Elurikkus 605042
USDA GRIN 13470

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
In vitro antimicrobial and antibiofilm screening of eighteen Iranian medicinal plants Hamidi M, Toosi AM, Javadi B, Asili J, Soheili V, Shakeri A BMC Complement Med Ther 28-Mar-2024
PMCID:PMC10976835
doi:10.1186/s12906-024-04437-x
PMID:38549139
Anticancer Activity of Delphinium semibarbatum Alkaloid Fractions against LNCaP, and DU 145 Human Prostate Cancer Cells through the Intrinsic Apoptotic Pathway Lotfaliani M, Ghanadian M, Ayatollahi SA, Aghaei M, Kobarfard F Iran J Pharm Res 01-Sep-2021
PMCID:PMC8842624
doi:10.22037/ijpr.2021.115462.15382
PMID:35194432
Iranian Medicinal Plants: From Ethnomedicine to Actual Studies Buso P, Manfredini S, Reza Ahmadi-Ashtiani H, Sciabica S, Buzzi R, Vertuani S, Baldisserotto A Medicina (Kaunas) 26-Feb-2020
PMCID:PMC7143749
doi:10.3390/medicina56030097
PMID:32110920
Traditional Yellow Dyes Used in the 21st Century in Central Iran: The Knowledge of Master Dyers Revealed by HPLC-DAD and UHPLC-HRMS/MS Sharif S, Nabais P, Melo MJ, Oliveira MC Molecules 18-Feb-2020
PMCID:PMC7070888
doi:10.3390/molecules25040908
PMID:32085515
Ethnobotanical investigation of traditional medicinal plants commercialized in the markets of Mashhad, Iran Amiri MS, Joharchi MR Avicenna J Phytomed 01-Jun-2013
PMCID:PMC4075713
PMID:25050282
LXII.—Colouring matter from the flowers of Delphinium Consolida Arthur George Perkin, Edward John Wilkinson Royal Society of Chemistry (RSC) 02-Apr-2004
doi:10.1039/CT9028100585
XXVI.—The colouring matters of the Indian dye stuff asbarg, Delphinium zalil Arthur George Perkin, Julius Aldred Pilgrim Royal Society of Chemistry (RSC) 02-Apr-2004
doi:10.1039/CT8987300267
Norditerpenoid alkaloids from seeds of Delphinium zalil Sun Fang, Michael Benn Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83485-H

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 / Acylaminobenzoic acid and derivatives
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13S,16S,17R,18S)-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-11-en-13-yl]methyl 2-[(3S)-3-methyl-2,5-dioxopyrrolidin-1-yl]benzoate 101631699 Click to see 652.70 unknown https://doi.org/10.1016/0031-9422(92)83485-H
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1S,2R,3R,4S,5S,6S,8R,9S,10S,13S,16S,17R,18S)-11-ethyl-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8,9-triol 92854545 Click to see 467.60 unknown https://doi.org/10.1016/0031-9422(92)83485-H
(1S,5R,6S,8R,9S,13S,16S)-11-ethyl-13-(hydroxymethyl)-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-8,9-diol 145994515 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1016/0031-9422(92)83485-H
(8,9-Dihydroxy-4,6,16,18-tetramethoxy-12-oxo-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl)methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 75069568 Click to see CC1CC(=O)N(C1=O)C2=CC=CC=C2C(=O)OCC34CCC(C56C3C(C(C5NC4=O)(C7(CC(C8CC6C7C8OC)OC)O)O)OC)OC 668.70 unknown https://doi.org/10.1016/0031-9422(92)83485-H
[(1S,2R,3R,4S,5R,6S,8R,9S,10S,13R,16S,17S,18S)-8,9-dihydroxy-4,6,16,18-tetramethoxy-12-oxo-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-[(3S)-3-methyl-2,5-dioxopyrrolidin-1-yl]benzoate 101631702 Click to see CC1CC(=O)N(C1=O)C2=CC=CC=C2C(=O)OCC34CCC(C56C3C(C(C5NC4=O)(C7(CC(C8CC6C7C8OC)OC)O)O)OC)OC 668.70 unknown https://doi.org/10.1016/0031-9422(92)83485-H
[(1S,4S,5R,6S,8R,9S,13S,16S)-11-ethyl-8,9-dihydroxy-4,6,16,18-tetramethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 139292146 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 682.80 unknown https://doi.org/10.1016/0031-9422(92)83485-H
[(5R,6S,8R,9S,13S)-4-acetyloxy-11-ethyl-8,9-dihydroxy-6,16,18-trimethoxy-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-13-yl]methyl 2-(3-methyl-2,5-dioxopyrrolidin-1-yl)benzoate 145994475 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC(=O)C)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 710.80 unknown https://doi.org/10.1016/0031-9422(92)83485-H
14-Deacetylnudicauline 441722 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7N8C(=O)CC(C8=O)C 668.80 unknown https://doi.org/10.1016/0031-9422(92)83485-H
Browniine 441714 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6O)OC)O)O)OC)OC)COC 467.60 unknown https://doi.org/10.1016/0031-9422(92)83485-H
CID 11972492 11972492 Click to see CCN1CC2(CCC(C34C2C(C(C31)(C5(CC(C6CC4C5C6OC)OC)O)O)OC)OC)CO 467.60 unknown https://doi.org/10.1016/0031-9422(92)83485-H
Ipwqjeoncufcor-rnnmqtrdsa- 441750 Click to see 710.80 unknown https://doi.org/10.1016/0031-9422(92)83485-H
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown https://doi.org/10.1039/CT8987300267
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1039/CT9028100585
https://doi.org/10.1039/CT8987300267

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