Scientific name	Authority	First published in
Dicoma gnaphaloides	Mattei	Boll. Reale Orto Bot. Palermo 7: 112. 1908 [Jan-Sep 1908]
Acilepis lanata	Spreng. ex DC.	Prodr. 7(1): 36 (1838)
Schaffnera carduoides	Sch.Bip.	Flora 24(1, Intelligenzbl.): 42. 1841
Dicoma lanuginosa	DC.	Prodr. 7(1): 36 (1838)
Xeropappus lanuginosus	Wall.	Numer. List : n.° 2980 (1831)
Onopordum lanatum	Herb.Madr. ex DC.	Prodr. 7(1): 36 (1838)

Common names Top

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Language	Common/alternative name
Arabic	نبات مرار

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Chad
  - Eritrea
  - Ethiopia
  - Socotra
  - Somalia
  - Sudan
- South Tropical Africa
  - Angola
  - Malawi
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Botswana
  - Cape Provinces
  - Namibia
  - Northern Provinces
  - Swaziland
- West Tropical Africa
  - Benin
  - Burkina
  - Mali
  - Mauritania
  - Niger
  - Nigeria
  - Senegal
  - Togo
- West-central Tropical Africa
  - Cameroon

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
  - Yemen

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Pakistan
- Indo-China
  - Myanmar

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000004304
Tropicos	2722690
KEW	urn:lsid:ipni.org:names:201373-1
The Plant List	gcc-104145
Open Tree Of Life	1046697
NCBI Taxonomy	1184229
IPNI	201373-1
iNaturalist	507107
GBIF	3103375
EPPO	DMATO
EOL	6268649

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

Green Synthesis of Bioinspired Nanoparticles Mediated from Plant Extracts of Asteraceae Family for Potential Biological Applications

Jaison JP, Balasubramanian B, Gangwar J, James N, Pappuswamy M, Anand AV, Al-Dhabi NA, Valan Arasu M, Liu WC, Sebastian JK

Antibiotics (Basel)

08-Mar-2023

PMCID:	PMC10044610
doi:	10.3390/antibiotics12030543
PMID:	36978410

Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches

Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF

Plants (Basel)

02-Mar-2023

PMCID:	PMC10005506
doi:	10.3390/plants12051145
PMID:	36904005

Local perception of ecosystem services and their conservation in Sudanian savannas of Burkina Faso (West Africa)

Nabaloum A, Goetze D, Ouédraogo A, Porembski S, Thiombiano A

J Ethnobiol Ethnomed

19-Feb-2022

PMCID:	PMC8858500
doi:	10.1186/s13002-022-00508-w
PMID:	35183193

Influence of Elicitation and Drying Methods on Anti-Metabolic Syndrome, and Antimicrobial Properties of Extracts and Hydrolysates Obtained from Elicited Lovage (Levisticum officinale Koch)

Jakubczyk A, Złotek U, Rybczyńska-Tkaczyk K

Nutrients

04-Dec-2021

PMCID:	PMC8708861
doi:	10.3390/nu13124365
PMID:	34959917

Studies on Activities and Chemical Characterization of Medicinal Plants in Search for New Antimalarials: A Ten Year Review on Ethnopharmacology

Ceravolo IP, Aguiar AC, Adebayo JO, Krettli AU

Front Pharmacol

22-Sep-2021

PMCID:	PMC8493299
doi:	10.3389/fphar.2021.734263
PMID:	34630109

Antiplasmodial, antimalarial activities and toxicity of African medicinal plants: a systematic review of literature

Tajbakhsh E, Kwenti TE, Kheyri P, Nezaratizade S, Lindsay DS, Khamesipour F

Malar J

25-Aug-2021

PMCID:	PMC8390284
doi:	10.1186/s12936-021-03866-0
PMID:	34433465

Antiplasmodial natural products: an update

Tajuddeen N, Van Heerden FR

Malar J

05-Dec-2019

PMCID:	PMC6896759
doi:	10.1186/s12936-019-3026-1
PMID:	31805944

Zingiber Officinale Roscoe and Echinops Kebericho Mesfin Showed Antiplasmodial Activities against Plasmodium Berghei in a Dose-dependent Manner in Ethiopia

Biruksew A, Zeynudin A, Alemu Y, Golassa L, Yohannes M, Debella A, Urge G, De Spiegeleer B, Suleman S

Ethiop J Health Sci

01-Sep-2018

PMCID:	PMC6308778
doi:	10.4314/ejhs.v28i5.17
PMID:	30607081

Ethnobotanical investigation on medicinal plants in Algoz area (South Kordofan), Sudan

Issa TO, Mohamed YS, Yagi S, Ahmed RH, Najeeb TM, Makhawi AM, Khider TO

J Ethnobiol Ethnomed

27-Apr-2018

PMCID:	PMC5921783
doi:	10.1186/s13002-018-0230-y
PMID:	29699576

Antiparasitic activity in Asteraceae with special attention to ethnobotanical use by the tribes of Odisha, India

Panda SK, Luyten W

Parasite

12-Mar-2018

PMCID:	PMC5847338
doi:	10.1051/parasite/2018008
PMID:	29528842

Plant-derived antimicrobials to fight against multi-drug-resistant human pathogens

Subramani R, Narayanasamy M, Feussner KD

3 Biotech

29-Jun-2017

PMCID:	PMC5489455
doi:	10.1007/s13205-017-0848-9
PMID:	28660459

Antidiabetic Medicinal Plants Used by the Basotho Tribe of Eastern Free State: A Review

Balogun FO, Tshabalala NT, Ashafa AO

J Diabetes Res

29-Jun-2016

PMCID:	PMC4942634
doi:	10.1155/2016/4602820
PMID:	27437404

Effect of crude leaf extract of Osyris quadripartita on Plasmodium berghei in Swiss albino mice

Girma S, Giday M, Erko B, Mamo H

BMC Complement Altern Med

16-Jun-2015

PMCID:	PMC4467072
doi:	10.1186/s12906-015-0715-3
PMID:	26077462

The potential of anti-malarial compounds derived from African medicinal plants, part I: a pharmacological evaluation of alkaloids and terpenoids

Amoa Onguéné P, Ntie-Kang F, Lifongo LL, Ndom JC, Sippl W, Mbaze LM

Malar J

13-Dec-2013

PMCID:	PMC3878730
doi:	10.1186/1475-2875-12-449
PMID:	24330395

Anti-plasmodial activity of Dicoma tomentosa (Asteraceae) and identification of urospermal A-15-O-acetate as the main active compound

Jansen O, Tits M, Angenot L, Nicolas JP, De Mol P, Nikiema JB, Frédérich M

Malar J

21-Aug-2012

PMCID:	PMC3483198
doi:	10.1186/1475-2875-11-289
PMID:	22909422

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 / Diterpenoids
2-(6-ethenyl-6-formyl-4-hydroxy-3-methylidene-2-oxo-4,5,7,7a-tetrahydro-3aH-1-benzofuran-7-yl)prop-2-enyl acetate	163034333	Click to see CC(=O)OCC(=C)C1C2C(C(CC1(C=C)C=O)O)C(=C)C(=O)O2	320.30	unknown	https://doi.org/10.1016/0031-9422(90)89034-7
2-[(3aR,4S,6R,7S,7aR)-6-ethenyl-6-formyl-4-hydroxy-3-methylidene-2-oxo-4,5,7,7a-tetrahydro-3aH-1-benzofuran-7-yl]prop-2-enyl acetate	101872087	Click to see CC(=O)OCC(=C)C1C2C(C(CC1(C=C)C=O)O)C(=C)C(=O)O2	320.30	unknown	https://doi.org/10.1016/0031-9422(90)89034-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
[(1R,2R,6S,7S,8R,10S,12R,14S,16S,17R,18R)-6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-5-oxo-16-prop-1-en-2-yl-14-[(1E,3E)-undeca-1,3-dienyl]-9,13,15,19-tetraoxahexacyclo[12.4.1.01,11.02,6.08,10.012,16]nonadec-3-en-17-yl] acetate	101949524	Click to see CCCCCCCC=CC=CC12OC3C4C5C(O5)(C(C6(C(C4(O1)C(C(C3(O2)C(=C)C)OC(=O)C)C)C=C(C6=O)C)O)O)CO	614.70	unknown	https://doi.org/10.1016/0031-9422(82)83062-8 https://doi.org/10.1016/0031-9422(90)89034-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,4S,11aR)-4-hydroxy-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carbaldehyde	163187604	Click to see C=C1C2C(CC(=CCCC(=CC2OC1=O)CO)C=O)O	278.30	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
(3aR,4S,6Z,10Z,11aR)-4-hydroxy-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carbaldehyde	100854253	Click to see C=C1C2C(CC(=CCCC(=CC2OC1=O)CO)C=O)O	278.30	unknown	https://doi.org/10.1016/0031-9422(90)89034-7
(3aS,11aR)-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carbaldehyde	163192920	Click to see C=C1C2CCC(=CCCC(=CC2OC1=O)CO)C=O	262.30	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
(3aS,6E,10E,11aR)-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carbaldehyde	162993488	Click to see C=C1C2CCC(=CCCC(=CC2OC1=O)CO)C=O	262.30	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
(3S,4S)-4-hydroxy-10-(hydroxymethyl)-3-methyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-6-carbaldehyde	163194757	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C=O)O	280.32	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[(3aR,4S,6E,10E,11aR)-4-hydroxy-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl]methyl acetate	163042077	Click to see CC(=O)OCC1=CCCC(=CC2C(C(C1)O)C(=C)C(=O)O2)CO	322.40	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[(3aR,4S,6Z,10Z,11aR)-6-(acetyloxymethyl)-4-hydroxy-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate	14466092	Click to see CC(=O)OCC1=CC2C(C(CC(=CCC1)COC(=O)C)O)C(=C)C(=O)O2	364.40	unknown	https://doi.org/10.1016/0031-9422(90)89034-7 https://doi.org/10.1016/0031-9422(82)83062-8
[(3aS,11aR)-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl]methyl acetate	163185790	Click to see CC(=O)OCC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)CO	306.40	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[(3aS,11aR)-6-formyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate	163189883	Click to see CC(=O)OCC1=CC2C(CCC(=CCC1)C=O)C(=C)C(=O)O2	304.34	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[(3aS,6E,10E,11aR)-6-formyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate	101872089	Click to see CC(=O)OCC1=CC2C(CCC(=CCC1)C=O)C(=C)C(=O)O2	304.34	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[(3aS,6Z,10Z,11aR)-10-(acetyloxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl]methyl acetate	14262541	Click to see CC(=O)OCC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)COC(=O)C	348.40	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[(3aS,6Z,10Z,11aR)-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl]methyl acetate	14466097	Click to see CC(=O)OCC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)CO	306.40	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[(3aS,6Z,10Z,11aR)-6-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate	14466090	Click to see CC(=O)OCC1=CC2C(CCC(=CCC1)CO)C(=C)C(=O)O2	306.40	unknown	https://doi.org/10.1016/0031-9422(90)89034-7
[(3aS,6Z,10Z,11aR)-6-formyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate	14466088	Click to see CC(=O)OCC1=CC2C(CCC(=CCC1)C=O)C(=C)C(=O)O2	304.34	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[(3aS,6Z,10Z,11aS)-6-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate	162890176	Click to see CC(=O)OCC1=CC2C(CCC(=CCC1)CO)C(=C)C(=O)O2	306.40	unknown	https://doi.org/10.1016/0031-9422(90)89034-7
[10-(Acetyloxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl]methyl acetate	163046975	Click to see CC(=O)OCC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)COC(=O)C	348.40	unknown	https://doi.org/10.1016/0031-9422(90)89034-7 https://doi.org/10.1016/0031-9422(82)83062-8
[10-(Hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl]methyl acetate	72833944	Click to see CC(=O)OCC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)CO	306.40	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[4-Hydroxy-10-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-yl]methyl acetate	163042076	Click to see CC(=O)OCC1=CCCC(=CC2C(C(C1)O)C(=C)C(=O)O2)CO	322.40	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
[6-(Acetyloxymethyl)-4-hydroxy-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate	163093347	Click to see CC(=O)OCC1=CC2C(C(CC(=CCC1)COC(=O)C)O)C(=C)C(=O)O2	364.40	unknown	https://doi.org/10.1016/0031-9422(90)89034-7 https://doi.org/10.1016/0031-9422(82)83062-8
[6-(Hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-10-yl]methyl acetate	72731790	Click to see CC(=O)OCC1=CC2C(CCC(=CCC1)CO)C(=C)C(=O)O2	306.40	unknown	https://doi.org/10.1016/0031-9422(90)89034-7
10-(Hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carbaldehyde	72819966	Click to see C=C1C2CCC(=CCCC(=CC2OC1=O)CO)C=O	262.30	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
Urospermal	14287067	Click to see C=C1C2C(CC(=CCCC(=CC2OC1=O)CO)C=O)O	278.30	unknown	https://doi.org/10.1016/0031-9422(90)89034-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Eupatin	5317287	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)O	360.30	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
Eupatolitin	5317291	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O)OC	346.30	unknown	https://doi.org/10.1016/0031-9422(82)83062-8
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/10.1016/0031-9422(82)83062-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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	https://doi.org/10.4314/GJPAS.V7I2.16244

Biological Material Top

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Dicoma tomentosa

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