Language	Common/alternative name
Belarusian	Сярпуха Вольфа
Belarusian	Сярпуха венцаносная
Japanese	タムラソウ
Russian	Серпуха Вольфа
Russian	Серпуха венценосная
Ukrainian	Серпій увінчаний
Chinese	假升麻
Chinese	伪泥胡菜
Chinese	广东升麻

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Serratula coronata subsp. coronata		Unknown
Serratula coronata subsp. insularis	(Iljin) Kitam.	Acta Phytotax. Geobot. 12: 105. 1943

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Kazakhstan
  - Kirgizstan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya

Europe click to expand
- Eastern Europe
  - Belarus
  - Central European Russia
  - East European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Switzerland
- Southeastern Europe
  - Romania

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000072530
Tropicos	2701301
KEW	urn:lsid:ipni.org:names:248634-1
The Plant List	gcc-29277
Open Tree Of Life	795404
NCBI Taxonomy	143210
IPNI	248634-1
iNaturalist	502299
GBIF	5388858
EPPO	SRRCO
EOL	6253515
Plantarium	35381

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

Adsorption isotherms and kinetics for Pb(ii) ion removal from aqueous solutions with biogenic metal oxide nanoparticles

Mashentseva AA, Seitzhapar N, Barsbay M, Aimanova NA, Alimkhanova AN, Zheltov DA, Zhumabayev AM, Temirgaziev BS, Almanov AA, Sadyrbekov DT

RSC Adv

07-Sep-2023

PMCID:	PMC10483273
doi:	10.1039/d3ra05347d
PMID:	37692348

Macromolecular Hydrodynamics and Fractal Structures of the Lignins of Fir Wood and Oat Husks

Karmanov A, Kocheva L, Borisenkov M, Belyi V

Polymers (Basel)

01-Sep-2023

PMCID:	PMC10489672
doi:	10.3390/polym15173624
PMID:	37688250

Effect of Plant Extracts Combinations on TNF-α, IL-6 and IL-10 Levels in Serum of Rats Exposed to Acute and Chronic Stress

Kandilarov I, Gardjeva P, Georgieva-Kotetarova M, Zlatanova H, Vilmosh N, Kostadinova I, Katsarova M, Atliev K, Dimitrova S

Plants (Basel)

24-Aug-2023

PMCID:	PMC10490550
doi:	10.3390/plants12173049
PMID:	37687297

Sustainable Production of Ajuga Bioactive Metabolites Using Cell Culture Technologies: A Review

Popova E, Titova M, Tynykulov M, Zakirova RP, Kulichenko I, Prudnikova O, Nosov A

Nutrients

01-Mar-2023

PMCID:	PMC10005297
doi:	10.3390/nu15051246
PMID:	36904246

Herbal Therapy for the Treatment of Seborrhea Dermatitis

Mustarichie R, Rostinawati T, Pitaloka DA, Saptarini NM, Iskandar Y

Clin Cosmet Investig Dermatol

07-Nov-2022

PMCID:	PMC9651010
doi:	10.2147/CCID.S376700
PMID:	36387964

Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones

Arif Y, Singh P, Bajguz A, Hayat S

Int J Mol Sci

04-Aug-2022

PMCID:	PMC9369314
doi:	10.3390/ijms23158664
PMID:	35955797

Phytoecdysteroids from Serratula coronata L. for Psoriatic Skincare

Kroma A, Pawlaczyk M, Feliczak-Guzik A, Urbańska M, Jenerowicz D, Seraszek-Jaros A, Kikowska M, Gornowicz-Porowska J

Molecules

27-May-2022

PMCID:	PMC9181847
doi:	10.3390/molecules27113471
PMID:	35684408

Using Extract From the Stems and Leaves of Yizhi (Alpiniae oxyphyllae) as Feed Additive Increases Meat Quality and Intestinal Health in Ducks

Ji F, Gu L, Rong G, Hu C, Sun W, Wang D, Peng W, Lin D, Liu Q, Wu H, Dai H, Zhou H, Xu T

Front Vet Sci

31-Jan-2022

PMCID:	PMC8841826
doi:	10.3389/fvets.2021.793698
PMID:	35174238

Rhaponticum uniflorum and Serratula centauroides Extracts Attenuate Emotional Injury in Acute and Chronic Emotional Stress

Shantanova LN, Olennikov DN, Matkhanov IE, Gulyaev SM, Toropova AA, Nikolaeva IG, Nikolaev SM

Pharmaceuticals (Basel)

19-Nov-2021

PMCID:	PMC8621925
doi:	10.3390/ph14111186
PMID:	34832968

Current vegetation data from the Prioksko-Terrasnyi Biosphere Reserve

Shovkun M, Ivanova N, Khanina L, Romanov MS, Demidov V

Biodivers Data J

25-Aug-2021

PMCID:	PMC8410754
doi:	10.3897/BDJ.9.e71266
PMID:	34539205

Phytotherapy Perspectives for Treating Fungal Infections, Migraine, Sebhorreic Dermatitis and Hyperpigmentations with the Plants of the Centaureinae Subtribe (Asteraceae)

Nawrot J, Gornowicz-Porowska J, Nowak G

Molecules

15-Nov-2020

PMCID:	PMC7696306
doi:	10.3390/molecules25225329
PMID:	33203185

The phytochemical, biological, and medicinal attributes of phytoecdysteroids: An updated review

Das N, Mishra SK, Bishayee A, Ali ES, Bishayee A

Acta Pharm Sin B

16-Oct-2020

PMCID:	PMC8343124
doi:	10.1016/j.apsb.2020.10.012
PMID:	34386319

Separation and HPLC Characterization of Active Natural Steroids in a Standardized Extract from the Serratula coronata Herb with Antiseborrheic Dermatitis Activity

Napierała M, Nawrot J, Gornowicz-Porowska J, Florek E, Moroch A, Adamski Z, Kroma A, Miechowicz I, Nowak G

Int J Environ Res Public Health

04-Sep-2020

PMCID:	PMC7557367
doi:	10.3390/ijerph17186453
PMID:	32899750

Plant community recovery from intense deer grazing depends on reduction of graminoids and the time after exclosure installation in a semi-natural grassland

Otsu C, Iijima H, Nagaike T

PeerJ

01-Oct-2019

PMCID:	PMC6777482
doi:	10.7717/peerj.7833
PMID:	31592180

Ecdysteroids: production in plant in vitro cultures

Thiem B, Kikowska M, Maliński MP, Kruszka D, Napierała M, Florek E

Phytochem Rev

24-Nov-2016

PMCID:	PMC5559567
doi:	10.1007/s11101-016-9483-z
PMID:	28867986

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 / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6R,7Z,10Z,11aS)-6-hydroxy-6,10-dimethyl-3-methylidene-2,9-dioxo-3a,4,5,11a-tetrahydrocyclodeca[b]furan-4-yl] (2R)-2-methylbutanoate	163035861	Click to see CCC(C)C(=O)OC1CC(C=CC(=O)C(=CC2C1C(=C)C(=O)O2)C)(C)O	362.40	unknown	https://doi.org/10.1135/CCCC20052038
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
[(2R,3R)-2,6-dihydroxy-6-methyl-2-[(2S,3R,5S,9R,10R,13R,14S,17S)-2,3,5,14-tetrahydroxy-10,13-dimethyl-6-oxo-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]heptan-3-yl] acetate	14656704	Click to see CC(=O)OC(CCC(C)(C)O)C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C)O)O	538.70	unknown	https://doi.org/10.1135/CCCC20052038
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	271605	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1007/S10600-005-0152-5 https://doi.org/10.1135/CCCC20052038
2,3,5,14-Tetrahydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-1,2,3,4,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-6-one	271604	Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	496.60	unknown	https://doi.org/10.1007/S10600-005-0152-5
20-Hydroxyecdysone	5459840	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1016/S0965-1748(01)00106-0 https://doi.org/10.1135/CCCC20052038
2beta,3beta,5beta,14,20,22R,25-Heptahydroxycholest-7-en-6-one	441833	Click to see CC12CCC3C(=CC(=O)C4(C3(CC(C(C4)O)O)C)O)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	496.60	unknown	https://doi.org/10.1007/S10600-005-0152-5 https://doi.org/10.1016/S0965-1748(01)00106-0
5-beta-Cholest-7-en-6-one, 2-beta,3-beta,14,20,22,25-hexahydroxy-, (22R)-	3032482	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O	480.60	unknown	https://doi.org/10.1007/S10600-005-0152-5
Ajugasterone C	441826	Click to see CC(C)CCC(C(C)(C1CCC2(C1(CC(C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)O)C)O)O)O	480.60	unknown	https://doi.org/10.1016/S0965-1748(01)00106-0 https://doi.org/10.1016/S0305-1978(97)00130-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
[3,14-dihydroxy-10,13-dimethyl-6-oxo-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-2-yl] acetate	13829643	Click to see CC(=O)OC1CC2(C3CCC4(C(CCC4(C3=CC(=O)C2CC1O)O)C(C)(C(CCC(C)(C)O)O)O)C)C	522.70	unknown	https://doi.org/10.1135/CCCC20052038
[5,6-dihydroxy-2-methyl-6-(2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)heptan-2-yl] acetate	538673	Click to see CC(=O)OC(C)(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O	522.70	unknown	https://doi.org/10.1135/CCCC20052038 https://doi.org/10.1007/S10600-005-0152-5
2-O-Acetyl-20-hydroxyecdysone	11060408	Click to see CC(=O)OC1CC2(C3CCC4(C(CCC4(C3=CC(=O)C2CC1O)O)C(C)(C(CCC(C)(C)O)O)O)C)C	522.70	unknown	https://doi.org/10.1135/CCCC20052038
2,3,14,22,25-Pentahydroxycholest-7-en-6-one	4233007	Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O	464.60	unknown	https://doi.org/10.1007/S10600-005-0152-5
Dacryhainansterone	13829647	Click to see CC(C)CCC(C(C)(C1CCC2(C1(CC=C3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O	462.60	unknown	https://doi.org/10.1016/S0305-1978(97)00130-0
Ecdysone	19212	Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O	464.60	unknown	https://doi.org/10.1007/BF00574363 https://doi.org/10.1016/S0965-1748(01)00106-0 https://doi.org/10.1007/S10600-005-0152-5
Viticosterone E	11226211	Click to see CC(=O)OC(C)(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O	522.70	unknown	https://doi.org/10.1135/CCCC20052038 https://doi.org/10.1007/S10600-005-0152-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
[(2S,3R)-6-hydroxy-6-methyl-2-[(2S,3R,5R,9R,10R,13R,14S,17R)-2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]heptan-3-yl] acetate	11691930	Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)OC(=O)C	506.70	unknown	https://doi.org/10.1135/CCCC20052038
[6-hydroxy-6-methyl-2-(2,3,14-trihydroxy-10,13-dimethyl-6-oxo-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)heptan-3-yl] acetate	15920465	Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)OC(=O)C	506.70	unknown	https://doi.org/10.1135/CCCC20052038
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(2S,3R,5R,9R,10R,11R,13R,14S,17S)-17-[(2R,4R,5R)-2,4-dimethyl-5-(3-methylbutyl)-1,3-dioxolan-4-yl]-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	11684847	Click to see CC1OC(C(O1)(C)C2CCC3(C2(CC(C4C3=CC(=O)C5C4(CC(C(C5)O)O)C)O)C)O)CCC(C)C	506.70	unknown	https://doi.org/10.1135/CCCC20052038
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-17-[(2S,4R,5R)-5-(3-hydroxy-3-methylbutyl)-2,4-dimethyl-1,3-dioxolan-4-yl]-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	162933337	Click to see CC1OC(C(O1)(C)C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)CCC(C)(C)O	506.70	unknown	https://doi.org/10.1135/CCCC20052038
17-[2,4-dimethyl-5-(3-methylbutyl)-1,3-dioxolan-4-yl]-2,3,11,14-tetrahydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	73061217	Click to see CC1OC(C(O1)(C)C2CCC3(C2(CC(C4C3=CC(=O)C5C4(CC(C(C5)O)O)C)O)C)O)CCC(C)C	506.70	unknown	https://doi.org/10.1135/CCCC20052038
2,3,11,14-tetrahydroxy-10,13-dimethyl-17-[2,2,4-trimethyl-5-(3-methylbutyl)-1,3-dioxolan-4-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	85433138	Click to see CC(C)CCC1C(OC(O1)(C)C)(C)C2CCC3(C2(CC(C4C3=CC(=O)C5C4(CC(C(C5)O)O)C)O)C)O	520.70	unknown	https://doi.org/10.1135/CCCC20052038
2,3,14-trihydroxy-17-[5-(3-hydroxy-3-methylbutyl)-2,2,4-trimethyl-1,3-dioxolan-4-yl]-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	3808392	Click to see CC1(OC(C(O1)(C)C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)CCC(C)(C)O)C	520.70	unknown	https://doi.org/10.1135/CCCC20052038
2,3,14-trihydroxy-17-[5-(3-hydroxy-3-methylbutyl)-2,4-dimethyl-1,3-dioxolan-4-yl]-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	85434131	Click to see CC1OC(C(O1)(C)C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)CCC(C)(C)O	506.70	unknown	https://doi.org/10.1135/CCCC20052038
Ajugasterone C 20,22-Acetonide	12044243	Click to see CC(C)CCC1C(OC(O1)(C)C)(C)C2CCC3(C2(CC(C4C3=CC(=O)C5C4(CC(C(C5)O)O)C)O)C)O	520.70	unknown	https://doi.org/10.1135/CCCC20052038
Ecdysterone 20,22-monoacetonide	11060391	Click to see CC1(OC(C(O1)(C)C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)CCC(C)(C)O)C	520.70	unknown	https://doi.org/10.1135/CCCC20052038
Taxisterone	15251158	Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(CCCC(C)(C)O)O)O	464.60	unknown	https://doi.org/10.1016/S0965-1748(01)00106-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,14-trihydroxy-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one	12304989	Click to see CCC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)C(C)(C)O	508.70	unknown	https://doi.org/10.1135/CCCC20052038
Makisterone C	24984905	Click to see CCC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)C(C)(C)O	508.70	unknown	https://doi.org/10.1016/S0305-1978(97)00130-0 https://doi.org/10.1135/CCCC20052038
> 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	https://doi.org/10.1016/J.FITOTE.2003.12.009
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/J.FITOTE.2003.12.009
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/J.FITOTE.2003.12.009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Luteolin 4'-glucoside	12304737	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	448.40	unknown	https://doi.org/10.1016/J.FITOTE.2003.12.009
Luteolin-4'-o-glucoside	5319116	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	448.40	unknown	https://doi.org/10.1016/J.FITOTE.2003.12.009
Quercetin-4'-o-glucoside	12442954	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	464.40	unknown	https://doi.org/10.1016/J.FITOTE.2003.12.009
Spiraeoside	5320844	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	464.40	unknown	https://doi.org/10.1016/J.FITOTE.2003.12.009
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	https://doi.org/10.1016/J.FITOTE.2003.12.009

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Serratula coronata

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top