Scientific name	Authority	First published in
Asphodelus albus subsp. microcarpus	(Viv.) Bonnier & Layens	Tabl. Syn. Pl. Vasc. France 301. 1894 (1894)
Asphodelus albus subsp. ramosus	(L.) Bonnier & Layens	Tabl. Syn. Pl. Vasc. France 301. 1894 (1894)
Asphodelus jacobi	Sennen & Mauricio	Cat. Fl. Rif Orient. : 119 (1933)
Asphodelus microcarpus subsp. affinis	(Parl.) Arcang.	Comp. Fl. Ital. 704. 1882 (1882)
Asphodelus microcarpus var. africanus	Maire & Weiller	Fl. Afrique N. 5: 29. 1958
Asphodelus microcarpus var. audibertii	(Req. ex Schult. & Schult.f.) Briq.	Prodr. Fl. Corse 1: 278 1910
Asphodelus microcarpus f. crinipes	(Jord.) Asch. & Graebn.	Syn. Mitteleur. Fl. 3: 33 1905
Asphodelus microcarpus var. jacobi	Maire & Weiller	Bull. Soc. Hist. Nat. Afrique N. 26: 230. 1935
Asphodelus microcarpus f. littoralis	(Jord.) Asch. & Graebn.	Syn. Mitteleur. Fl. 3: 33 1905
Asphodelus microcarpus subsp. nervosus	(Pomel) Batt. & Trab.	Fl. Algérie Monocot.: 55. 1895 (1895)
Asphodelus microcarpus var. nervosus	(Pomel) Maire	Cat. Pl. Maroc 1: 117. 1931
Asphodelus ramosus var. aestivus	Fiori	Nuov. Fl. Italia 1: 276. 1923
Asphodelus ramosus var. microcarpus	(Viv.) Duby	Bot. Gall. ed. 2, 2: 1034. 1830
Asphodelus ramosus subsp. microcarpus	(Viv.) Baker	J. Linn. Soc., Bot. 15: 270. 1876 (1876)
Asphodelus albus var. littoralis	(Jord.) Nyman	Consp. Fl. Eur. 719. 1882
Asphodelus albus subsp. morisianus	(Parl.) K.Richt.	Pl. Eur. 1: 192. 1890 (1890)

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	بروق متفرع
ceb	asphodelus aestivus
Czech	asfodyl větvený
Czech	červená horská lilie, žlutý kořen
Czech	afodel větévnatý
German	Ästiger affodill
Greek	Ασφόδελος ο πολύκλαδος
French	asphodèle ramifié
Hebrew	עירית גדולה
Polish	asfodel gałęzisty
Portuguese	abrótea (botânica)
war	asphodelus aestivus

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Asphodelus albus subsp. albus		Unknown
Asphodelus ramosus subsp. distalis	Z.Díaz & Valdés	Boissiera 52: 61 (1996)
Asphodelus ramosus subsp. ramosus		Unknown

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!

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
- Macaronesia
  - Canary Islands
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Europe click to expand
- Southeastern Europe
  - Albania
  - Greece
  - Italy
  - Kriti
  - Sicilia
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000637103
Tropicos	18400529
INPN	84372
KEW	urn:lsid:ipni.org:names:531548-1
The Plant List	kew-275588
Open Tree Of Life	41518
Observations.org	140861
NCBI Taxonomy	221659
NBN Atlas	NBNSYS0200001836
IPNI	531548-1
iNaturalist	82906
GBIF	2778478
Freebase	/m/01kwyz
EPPO	ASHRA
EOL	991197
USDA GRIN	5577
Wikipedia	Asphodelus_ramosus

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

A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics

Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B

J Ethnopharmacol

25-Mar-2024

PMCID:	PMC7615571
doi:	10.1016/j.jep.2023.117622
PMID:	38128894

The hidden order of Turing patterns in arid and semi‐arid vegetation ecosystems

Ge Z

Proc Natl Acad Sci U S A

10-Oct-2023

PMCID:	PMC10589663
doi:	10.1073/pnas.2306514120
PMID:	37816060

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Bioguided Identification of Active Antimicrobial Compounds from Asphodelus bento-rainhae and Asphodelus macrocarpus Root Tubers

Malmir M, Lima K, Camões SP, Manageiro V, Duarte MP, Miranda JP, Serrano R, da Silva IM, Lima BS, Caniça M, Silva O

Pharmaceuticals (Basel)

01-Jun-2023

PMCID:	PMC10301023
doi:	10.3390/ph16060830
PMID:	37375777

An overview on medicinal plants used for combating coronavirus: Current potentials and challenges

Abou Baker DH, Hassan EM, El Gengaihi S

J Agric Food Res

20-May-2023

PMCID:	PMC10198795
doi:	10.1016/j.jafr.2023.100632
PMID:	37251276

Identification of Marker Compounds and In Vitro Toxicity Evaluation of Two Portuguese Asphodelus Leaf Extracts

Malmir M, Lima K, Póvoas Camões S, Manageiro V, Duarte MP, Paiva Miranda J, Serrano R, Moreira da Silva I, Silva Lima B, Caniça M, Silva O

Molecules

04-Mar-2023

PMCID:	PMC10005749
doi:	10.3390/molecules28052372
PMID:	36903618

An Ethnobotanical Investigation into the Traditional Uses of Mediterranean Medicinal and Aromatic Plants: The Case of Troodos Mountains in Cyprus

Savvides AM, Stavridou C, Ioannidou S, Zoumides C, Stylianou A

Plants (Basel)

02-Mar-2023

PMCID:	PMC10005048
doi:	10.3390/plants12051119
PMID:	36903979

HPTLC-based fingerprinting: An alternative approach for fructooligosaccharides metabolism profiling

Salomé-Abarca LF, Márquez-López RE, Santiago-García PA, López MG

Curr Res Food Sci

31-Jan-2023

PMCID:	PMC9925861
doi:	10.1016/j.crfs.2023.100451
PMID:	36798949

Xylella fastidiosa in Europe: From the Introduction to the Current Status

Trkulja V, Tomić A, Iličić R, Nožinić M, Milovanović TP

Plant Pathol J

01-Dec-2022

PMCID:	PMC9742796
doi:	10.5423/PPJ.RW.09.2022.0127
PMID:	36503185

Quantitative Real-Time PCR Based on SYBR Green Technology for the Identification of Philaenus italosignus Drosopoulos & Remane (Hemiptera Aphrophoridae)

Rizzo D, Bracalini M, Campigli S, Nencioni A, Porcelli F, Marchi G, Da Lio D, Bartolini L, Rossi E, Sacchetti P, Panzavolta T

Plants (Basel)

30-Nov-2022

PMCID:	PMC9741283
doi:	10.3390/plants11233314
PMID:	36501353

Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview

Motti R, Paura B, Cozzolino A, de Falco B

Plants (Basel)

28-Nov-2022

PMCID:	PMC9736219
doi:	10.3390/plants11233272
PMID:	36501312

From Biodiversity to Musketry: Detection of Plant Diversity in Pre-Industrial Peloponnese during the Flora Graeca Expedition

Chimona C, Papadopoulou S, Kolyva F, Mina M, Rhizopoulou S

Life (Basel)

23-Nov-2022

PMCID:	PMC9785030
doi:	10.3390/life12121957
PMID:	36556322

Monographic Quality Parameters and Genotoxicity Assessment of Asphodelus bento-rainhae and Asphodelus macrocarpus Root Tubers as Herbal Medicines

Malmir M, Serrano R, Lima K, Duarte MP, Moreira da Silva I, Silva Lima B, Caniça M, Silva O

Plants (Basel)

20-Nov-2022

PMCID:	PMC9692987
doi:	10.3390/plants11223173
PMID:	36432902

Ethnopharmacobotany and Diversity of Mediterranean Endemic Plants in Marmilla Subregion, Sardinia, Italy

Cocco E, Maccioni D, Sanjust E, Falconieri D, Farris E, Maxia A

Plants (Basel)

18-Nov-2022

PMCID:	PMC9695302
doi:	10.3390/plants11223165
PMID:	36432894

Biodiversity in Urban Areas: The Extraordinary Case of Appia Antica Regional Park (Rome, Italy)

Iamonico D

Plants (Basel)

15-Aug-2022

PMCID:	PMC9414419
doi:	10.3390/plants11162122
PMID:	36015425

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
> Benzenoids / Anthracenes
(10R)-1,8,10-trihydroxy-6-methyl-2-[(9S)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]-10-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]anthracen-9-one	163187164	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(CO4)O)O)O)O)C=CC(=C3O)C5(C6=C(C(=CC=C6)O)C(=O)C7=C5C=C(C=C7O)C)O	642.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
(10S)-1,8,10-trihydroxy-6-methyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2-[(9R)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]anthracen-9-one	162964916	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)O)O)O)O)C=CC(=C3O)C5(C6=C(C(=CC=C6)O)C(=O)C7=C5C=C(C=C7O)C)O	672.60	unknown	https://doi.org/10.1016/0031-9422(89)85063-0
(10S)-10-[(10R)-1,8-dihydroxy-6-methyl-9-oxo-10-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-2-yl]-1,8,10-trihydroxy-3-methylanthracen-9-one	162932989	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(C(O4)CO)O)O)O)C=CC(=C3O)C5(C6=C(C(=CC=C6)O)C(=O)C7=C5C=C(C=C7O)C)O	656.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
(10S)-10-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-1,8,10-trihydroxy-6-methyl-2-[(9R)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]anthracen-9-one	162964258	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)C=CC(=C3O)C6(C7=C(C(=CC=C7)O)C(=O)C8=C6C=C(C=C8O)C)O	834.80	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
1,8,10-Trihydroxy-6-methyl-2-(4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl)-10-(3,4,5-trihydroxyoxan-2-yl)anthracen-9-one	14584818	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(CO4)O)O)O)O)C=CC(=C3O)C5(C6=C(C(=CC=C6)O)C(=O)C7=C5C=C(C=C7O)C)O	642.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
10-[1,8-dihydroxy-6-methyl-9-oxo-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-10H-anthracen-2-yl]-1,8,10-trihydroxy-3-methylanthracen-9-one	14584820	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(C(O4)CO)O)O)O)C=CC(=C3O)C5(C6=C(C(=CC=C6)O)C(=O)C7=C5C=C(C=C7O)C)O	656.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
10-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]-1,8,10-trihydroxy-6-methyl-2-(4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl)anthracen-9-one	14584822	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)C=CC(=C3O)C6(C7=C(C(=CC=C7)O)C(=O)C8=C6C=C(C=C8O)C)O	834.80	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
Ramosin	363268	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)CO)O)O)O)O)C=CC(=C3O)C5(C6=C(C(=CC=C6)O)C(=O)C7=C5C=C(C=C7O)C)O	672.60	unknown	https://doi.org/10.1016/0031-9422(89)85063-0
> Benzenoids / Anthracenes / Anthraquinones
1-[(10R)-1,8-dihydroxy-6-methyl-9-oxo-10-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]-10H-anthracen-2-yl]-4,5-dihydroxy-2-methylanthracene-9,10-dione	102153707	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(CO4)O)O)O)C=CC(=C3O)C5=C6C(=C(C=C5C)O)C(=O)C7=C(C6=O)C=CC=C7O	624.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
1-[(10S)-1,8-dihydroxy-6-methyl-9-oxo-10-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]-10H-anthracen-2-yl]-4,5-dihydroxy-2-methylanthracene-9,10-dione	162991942	Click to see CC1C(C(C(C(O1)C2C3=C(C(=C(C=C3)C4=C5C(=C(C=C4C)O)C(=O)C6=C(C5=O)C=CC=C6O)O)C(=O)C7=C2C=C(C=C7O)C)O)O)O	638.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
1-[(10S)-1,8-dihydroxy-6-methyl-9-oxo-10-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]-10H-anthracen-2-yl]-4,5-dihydroxy-2-methylanthracene-9,10-dione	162991940	Click to see CC1C(C(C(C(O1)C2C3=C(C(=C(C=C3)C4=C5C(=C(C=C4C)O)C(=O)C6=C(C5=O)C=CC=C6O)O)C(=O)C7=C2C=C(C=C7O)C)O)O)O	638.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
1-[(10S)-1,8-dihydroxy-6-methyl-9-oxo-10-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]-10H-anthracen-2-yl]-4,5-dihydroxy-2-methylanthracene-9,10-dione	162991941	Click to see CC1C(C(C(C(O1)C2C3=C(C(=C(C=C3)C4=C5C(=C(C=C4C)O)C(=O)C6=C(C5=O)C=CC=C6O)O)C(=O)C7=C2C=C(C=C7O)C)O)O)O	638.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
1-[(10S)-1,8-dihydroxy-6-methyl-9-oxo-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]-10H-anthracen-2-yl]-4,5-dihydroxy-2-methylanthracene-9,10-dione	162882528	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(CO4)O)O)O)C=CC(=C3O)C5=C6C(=C(C=C5C)O)C(=O)C7=C(C6=O)C=CC=C7O	624.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
1-[1,8-dihydroxy-6-methyl-9-oxo-10-(3,4,5-trihydroxy-6-methyloxan-2-yl)-10H-anthracen-2-yl]-4,5-dihydroxy-2-methylanthracene-9,10-dione	73825287	Click to see CC1C(C(C(C(O1)C2C3=C(C(=C(C=C3)C4=C5C(=C(C=C4C)O)C(=O)C6=C(C5=O)C=CC=C6O)O)C(=O)C7=C2C=C(C=C7O)C)O)O)O	638.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
1-[1,8-dihydroxy-6-methyl-9-oxo-10-(3,4,5-trihydroxyoxan-2-yl)-10H-anthracen-2-yl]-4,5-dihydroxy-2-methylanthracene-9,10-dione	73825288	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(CO4)O)O)O)C=CC(=C3O)C5=C6C(=C(C=C5C)O)C(=O)C7=C(C6=O)C=CC=C7O	624.60	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
1,8-dihydroxy-6-methyl-2-[(9R)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]anthracene-9,10-dione	163007814	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC(=C3O)C4(C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)C)O	508.50	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
Kstmmfcurgnhnw-uhfffaoysa-	14584824	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC(=C3O)C4(C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)C)O	508.50	unknown	https://doi.org/10.1016/S0040-4020(01)87112-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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/10.1139/B97-921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isocytisoside	44257871	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1139/B97-921
Isoorientin	114776	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1139/B97-921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
2-(3,4-Dihydroxyphenyl)-8-beta-D-glucopyranosyl-5-hydroxy-7-methoxy-4H-1-benzopyran-4-one	73829966	Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1139/B97-921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1139/B97-921
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1139/B97-921

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Asphodelus ramosus

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