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Dracocephalum forrestii

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 UUID644038a91157a334932960
Scientific name Dracocephalum forrestii
Authority W.W.Sm.
First published in Trans. Bot. Soc. Edinburgh 27: 90 (1916)

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
Chinese 白花甜蜜蜜
Chinese 傅氏青兰
Chinese 松叶青兰

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000945337
Tropicos 17606203
KEW urn:lsid:ipni.org:names:446421-1
The Plant List kew-63783
Open Tree Of Life 6082229
Observations.org 450911
NCBI Taxonomy 2054469
IPNI 446421-1
GBIF 3902894
Elurikkus 436983

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
Optimization of Plant Growth Regulators for In Vitro Mass Propagation of a Disease-Free ‘Shine Muscat’ Grapevine Cultivar Kim SH, Zebro M, Jang DC, Sim JE, Park HK, Kim KY, Bae HM, Tilahun S, Park SM Curr Issues Mol Biol 22-Sep-2023
PMCID:PMC10605919
doi:10.3390/cimb45100487
PMID:37886931
Meta-Topolin-induced mass shoot multiplication and biosynthesis of valuable secondary metabolites in Stevia rebaudiana Bertoni bioreactor culture Ptak A, Szewczyk A, Simlat M, Błażejczak A, Warchoł M Sci Rep 19-Sep-2023
PMCID:PMC10509197
doi:10.1038/s41598-023-42619-8
PMID:37726319
Synergistic Combination of NAPROC-13 and NMR 13C DFT Calculations: A Powerful Approach for Revising the Structure of Natural Products Sánchez-Martínez HA, Morán-Pinzón JA, del Olmo Fernández E, Eguiluz DL, Adserias Vistué JF, López-Pérez JL, De León EG J Nat Prod 07-Sep-2023
PMCID:PMC10616860
doi:10.1021/acs.jnatprod.3c00437
PMID:37675572
Effect of Light Conditions on Polyphenol Production in Transformed Shoot Culture of Salvia bulleyana Diels Krzemińska M, Hnatuszko-Konka K, Weremczuk-Jeżyna I, Owczarek-Januszkiewicz A, Ejsmont W, Olszewska MA, Grzegorczyk-Karolak I Molecules 07-Jun-2023
PMCID:PMC10302416
doi:10.3390/molecules28124603
PMID:37375158
Phenolic Acids and Amaryllidaceae Alkaloids Profiles in Leucojum aestivum L. In Vitro Plants Grown under Different Light Conditions Morańska E, Simlat M, Warchoł M, Skrzypek E, Waligórski P, Laurain-Mattar D, Spina R, Ptak A Molecules 04-Feb-2023
PMCID:PMC9958804
doi:10.3390/molecules28041525
PMID:36838512
The Effect of the Stress-Signalling Mediator Triacontanol on Biochemical and Physiological Modifications in Dracocephalum forrestii Culture Weremczuk-Jeżyna I, Hnatuszko-Konka K, Lebelt L, Piotrowska DG, Grzegorczyk-Karolak I Int J Mol Sci 02-Dec-2022
PMCID:PMC9735700
doi:10.3390/ijms232315147
PMID:36499476
In Vitro Strategy for the Enhancement of the Production of Bioactive Polyphenols in Transformed Roots of Salvia bulleyana Krzemińska M, Owczarek A, Olszewska MA, Grzegorczyk-Karolak I Int J Mol Sci 14-Jul-2022
PMCID:PMC9322094
doi:10.3390/ijms23147771
PMID:35887119
A Temporary Immersion System to Improve Cannabis sativa Micropropagation Rico S, Garrido J, Sánchez C, Ferreiro-Vera C, Codesido V, Vidal N Front Plant Sci 23-Jun-2022
PMCID:PMC9262383
doi:10.3389/fpls.2022.895971
PMID:35812929
Effect of LED Lighting on Physical Environment and Microenvironment on In Vitro Plant Growth and Morphogenesis: The Need to Standardize Lighting Conditions and Their Description Barceló-Muñoz A, Barceló-Muñoz M, Gago-Calderon A Plants (Basel) 25-Dec-2021
PMCID:PMC8747321
doi:10.3390/plants11010060
PMID:35009064
Effects of Light on Secondary Metabolite Biosynthesis in Medicinal Plants Zhang S, Zhang L, Zou H, Qiu L, Zheng Y, Yang D, Wang Y Front Plant Sci 10-Dec-2021
PMCID:PMC8702564
doi:10.3389/fpls.2021.781236
PMID:34956277
Precursor-Boosted Production of Metabolites in Nasturtium officinale Microshoots Grown in Plantform Bioreactors, and Antioxidant and Antimicrobial Activities of Biomass Extracts Klimek-Szczykutowicz M, Dziurka M, Blažević I, Đulović A, Miazga-Karska M, Klimek K, Ekiert H, Szopa A Molecules 31-Jul-2021
PMCID:PMC8348939
doi:10.3390/molecules26154660
PMID:34361814
The Protective Function and Modification of Secondary Metabolite Accumulation in Response to Light Stress in Dracocephalum forrestii Shoots Weremczuk-Jeżyna I, Hnatuszko-Konka K, Lebelt L, Grzegorczyk-Karolak I Int J Mol Sci 26-Jul-2021
PMCID:PMC8347274
doi:10.3390/ijms22157965
PMID:34360728
Transformed Shoots of Dracocephalum forrestii W.W. Smith from Different Bioreactor Systems as a Rich Source of Natural Phenolic Compounds Weremczuk-Jeżyna I, Lisiecki P, Gonciarz W, Kuźma Ł, Szemraj M, Chmiela M, Grzegorczyk-Karolak I Molecules 03-Oct-2020
PMCID:PMC7583972
doi:10.3390/molecules25194533
PMID:33022943
Plant In Vitro Systems as a Sustainable Source of Active Ingredients for Cosmeceutical Application Marchev AS, Georgiev MI Molecules 25-Apr-2020
PMCID:PMC7248771
doi:10.3390/molecules25092006
PMID:32344812
Exogenous Kinetin Promotes the Nonenzymatic Antioxidant System and Photosynthetic Activity of Coffee (Coffea arabica L.) Plants Under Cold Stress Conditions Acidri R, Sawai Y, Sugimoto Y, Handa T, Sasagawa D, Masunaga T, Yamamoto S, Nishihara E Plants (Basel) 21-Feb-2020
PMCID:PMC7076472
doi:10.3390/plants9020281
PMID:32098166

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4aR,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bR)-4a-(hydroxymethyl)-1,2,6a,6b,9,9,12a-heptamethyl-1,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-tetradecahydropicene-2,10-diol 163083989 Click to see 458.70 unknown https://doi.org/10.1002/HLCA.200690271
(1R,3aR,5aR,5bR,6S,7aR,9S,11aS,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydro-1H-cyclopenta[a]chrysene-6,9-diol 162907034 Click to see 428.70 unknown https://doi.org/10.1002/HLCA.200690271
(1S,2S,4aR,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bS)-4a-(hydroxymethyl)-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-2,10-diol 102513124 Click to see 460.70 unknown https://doi.org/10.1002/HLCA.200690271
(1S,3R,5R,6R,9S,11R,14R,15S,18S,21R,22S,23R)-6,10,10,14,15,21,22-heptamethyl-2-oxahexacyclo[13.8.0.01,3.05,14.06,11.018,23]tricosane-9,18-diol 162856367 Click to see 444.70 unknown https://doi.org/10.1002/HLCA.200690271
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,11,12,14b-heptamethyl-1,2,3,4a,5,6,7,8,8a,9,10,11,12,12a,14,14a-hexadecahydropicen-3-ol 44583863 Click to see 412.70 unknown https://doi.org/10.1002/HLCA.200690271
10-Hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-23-one 4450096 Click to see 454.70 unknown https://doi.org/10.1002/HLCA.200690271
11alpha, 12alpha-Epoxyoleanolic lactone 177092 Click to see 470.70 unknown https://doi.org/10.1002/HLCA.200690271
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.200690271
3|A-Hydroxyurs-11-en-28,13|A-olide 21606663 Click to see 454.70 unknown https://doi.org/10.1002/HLCA.200690271
4a-(Hydroxymethyl)-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-2,10-diol 162866112 Click to see 460.70 unknown https://doi.org/10.1002/HLCA.200690271
4a-(Hydroxymethyl)-1,2,6a,6b,9,9,12a-heptamethyl-1,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-tetradecahydropicene-2,10-diol 163083988 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(C=CC1(C)O)CO)C)C)(C)C)O)C 458.70 unknown https://doi.org/10.1002/HLCA.200690271
5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydro-1H-cyclopenta[a]chrysene-6,9-diol 162907033 Click to see CC(=C)C1CCC2C1C3CCC4C5(CCC(C(C5CC(C4(C3(CC2)C)C)O)(C)C)O)C 428.70 unknown https://doi.org/10.1002/HLCA.200690271
6,10,10,14,15,21,22-Heptamethyl-2-oxahexacyclo[13.8.0.01,3.05,14.06,11.018,23]tricosane-9,18-diol 162856366 Click to see 444.70 unknown https://doi.org/10.1002/HLCA.200690271
9-Hydroxy-6,10,10,14,15,21,21-heptamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 15598275 Click to see 470.70 unknown https://doi.org/10.1002/HLCA.200690271
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1002/HLCA.200690271
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.200690271
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.200690271
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1002/HLCA.200690271
Npc86422 14423519 Click to see 440.70 unknown https://doi.org/10.1002/HLCA.200690271
Oleanoaldehyde 14423521 Click to see 440.70 unknown https://doi.org/10.1002/HLCA.200690271
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1002/HLCA.200690271
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Artonin K 15340661 Click to see 382.40 unknown https://doi.org/10.1002/HLCA.200690271

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