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

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

The Stimulatory Effect of Purine-Type Cytokinins on Proliferation and Polyphenolic Compound Accumulation in Shoot Culture of Salvia viridis

Grzegorczyk-Karolak I, Hnatuszko-Konka K, Zarzycka M, Kuźma Ł

Biomolecules

24-Jan-2020

PMCID:	PMC7072693
doi:	10.3390/biom10020178
PMID:	31991557

Recent insights into natural product inhibitors of matrix metalloproteinases

Kumar GB, Nair BG, Perry JJ, Martin DB

Medchemcomm

07-Oct-2019

PMCID:	PMC7451072
doi:	10.1039/c9md00165d
PMID:	32904148

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

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 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
(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 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
(1S,2R,4aS,6aS,6bR,10S,12aR,12bR,14bS)-10-Hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carbaldehyde	14423519	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O	440.70	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 CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)CO)C)C)(C)C)O)C	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 CC1CCC2(CCC3(C4(CCC5C(C(CCC5(C4CC6C3(C2C1C)O6)C)O)(C)C)C)C)O	444.70	unknown	https://doi.org/10.1002/HLCA.200690271
11alpha, 12alpha-Epoxyoleanolic lactone	177092	Click to see CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1)OC3=O)O7)C)O)(C)C)C)C)C	470.70	unknown	https://doi.org/10.1002/HLCA.200690271
28-Norurs-12-ene-3beta-ol	44583863	Click to see CC1CCC2CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C	412.70	unknown	https://doi.org/10.1002/HLCA.200690271
3-Hydroxy-11-ursen-28,13-olide	21606663	Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C	454.70	unknown	https://doi.org/10.1002/HLCA.200690271
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	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 CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)CO)C)C)(C)C)O)C	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 CC1CCC2(CCC3(C4(CCC5C(C(CCC5(C4CC6C3(C2C1C)O6)C)O)(C)C)C)C)O	444.70	unknown	https://doi.org/10.1002/HLCA.200690271
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	2371	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	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 CC1(CCC23CCC4(C5(CCC6C(C(CCC6(C5C7C(C4(C2C1)OC3=O)O7)C)O)(C)C)C)C)C	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 CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1002/HLCA.200690271
CID 4450096	4450096	Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C	454.70	unknown	https://doi.org/10.1002/HLCA.200690271
Lup-20(29)-ene-3beta,28-diol	221023	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
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1002/HLCA.200690271
Ursolic aldehyde	14423521	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O	440.70	unknown	https://doi.org/10.1002/HLCA.200690271
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Artonin K	15340661	Click to see CC1(C2CC3=C(C4=C2C(=C(C=C4O)O)O1)OC5=CC(=CC(=C5C3=O)O)OC)C	382.40	unknown	https://doi.org/10.1002/HLCA.200690271

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Dracocephalum forrestii

Table of Contents

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Subspecies (abbr. subsp./ssp.) Top

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Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

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