Scientific name	Authority	First published in
Ledonia populifolia	Spach	Ann. Sci. Nat., Bot. , sér. 2, 6: 369 (1836)
Libanotis populifolius	Raf.	Sylva Tellur. 132. 1838
Cistus cordifolius	Moench	Methodus (Moench) 245. 1794 [4 May 1794]
Cistus latifolius	Sweet	Cistineae : t. 15 (1825)
Cistus populifolius f. marianus	Willk.	Icon. Descr. Pl. Nov. 2: 40 1856
Cistus populifolius f. narbonnensis	Willk.	Icon. Descr. Pl. Nov. 2: 40 1856

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	ledonia populifolia var longifolia
Spanish	ledonia populifolia
Spanish	cistus populifolius f. marianus
Spanish	cistus latifolius
Spanish	cistus cordifolius
Spanish	libanotis populifolius
Spanish	ogarzo
Spanish	ledonia populifolia var. longifolia
Spanish	ledonia populifolia var. cordifolia
Spanish	ledonia populifolia var cordifolia
Spanish	jarón
Spanish	jaranzo
Spanish	jara-jarguna
Spanish	jara jarguna
Spanish	jara jaguana
Spanish	jara con hoja de laurel
Spanish	jara cervuna
Spanish	jara cerval
Spanish	estevâo
Spanish	estevao
Spanish	jaron
Arabic	قريضة حورية الأوراق
Catalan	estepa populifòlia
Galician	estevón
Galician	xara macho
Galician	carpaza macho

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Cistus populifolius subsp. populifolius		Unknown

Varieties (abbr. var.) Top

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Name	Authority	First published in
Cistus populifolius var. major	(Dunal) Heywood	Feddes Repert. 79: 61 (1968)

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
- Northern Africa
  - Morocco

Europe click to expand
- Southwestern Europe
  - France
  - Portugal
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000607532
Tropicos	7600150
INPN	91707
KEW	urn:lsid:ipni.org:names:168435-1
The Plant List	kew-2723588
Open Tree Of Life	752029
Observations.org	139271
NCBI Taxonomy	335177
IPNI	168435-1
iNaturalist	333978
GBIF	7331314
Freebase	/m/012z8gq0
EPPO	CSTPO
Elurikkus	589635
USDA GRIN	402756
Wikipedia	Cistus_populifolius

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

Mediterranean Plants as Potential Source of Biopesticides: An Overview of Current Research and Future Trends

Fragkouli R, Antonopoulou M, Asimakis E, Spyrou A, Kosma C, Zotos A, Tsiamis G, Patakas A, Triantafyllidis V

Metabolites

22-Aug-2023

PMCID:	PMC10535963
doi:	10.3390/metabo13090967
PMID:	37755247

The genus Gautieria (Gomphales) in Europe and the Mediterranean Basin: a morphological and phylogenetic taxonomic revision

Vidal JM, Cseh P, Merényi Z, Bóna L, Rudnóy S, Bratek Z, Paz A, Mleczko P, Kozak M, Chachuła P, Assyov B, Slavova M, Kaounas V, Konstantinidis G, Rodríguez F, Cabero J, García-Verdugo F, García-Alonso F, Mahiques R, Fantini P, States JS

Persoonia

12-May-2023

PMCID:	PMC10983841
doi:	10.3767/persoonia.2023.50.03
PMID:	38567262

Adaptations to the stressful combination of serpentine soils and Mediterranean climate drive plant functional groups and trait richness

Hidalgo-Triana N, Pérez-Latorre AV, Adomou AC, Rudner M, Thorne JH

Front Plant Sci

13-Mar-2023

PMCID:	PMC10040603
doi:	10.3389/fpls.2023.1040839
PMID:	36993858

Parasiticides: Weapons for Controlling Microbial Vector-Borne Diseases in Veterinary Medicine; The Potential of Ethnobotanic/Phytoparasiticides: An Asset to One Health

Carvalho da Silva R, Meisel L, Farinha N, Póvoa O, De Mello-Sampayo C

Antibiotics (Basel)

06-Feb-2023

PMCID:	PMC9952419
doi:	10.3390/antibiotics12020341
PMID:	36830252

A Review on Cistus sp.: Phytochemical and Antimicrobial Activities

Zalegh I, Akssira M, Bourhia M, Mellouki F, Rhallabi N, Salamatullah AM, Alkaltham MS, Khalil Alyahya H, Mhand RA

Plants (Basel)

15-Jun-2021

PMCID:	PMC8232106
doi:	10.3390/plants10061214
PMID:	34203720

Comparative Metabolite and Gene Expression Analyses in Combination With Gene Characterization Revealed the Patterns of Flavonoid Accumulation During Cistus creticus subsp. creticus Fruit Development

Aničić N, Patelou E, Papanikolaou A, Kanioura A, Valdesturli C, Arapitsas P, Skorić M, Dragićević M, Gašić U, Koukounaras A, Kostas S, Sarrou E, Martens S, Mišić D, Kanellis A

Front Plant Sci

26-Mar-2021

PMCID:	PMC8034662
doi:	10.3389/fpls.2021.619634
PMID:	33841455

Secondary Metabolites of Plants as Modulators of Endothelium Functions

Bartáková A, Nováková M

Int J Mol Sci

03-Mar-2021

PMCID:	PMC7959468
doi:	10.3390/ijms22052533
PMID:	33802468

RETRACTED ARTICLE: Fire and summer temperatures work together breaking physical seed dormancy

Luna B

Sci Rep

07-Apr-2020

PMCID:	PMC7138829
doi:	10.1038/s41598-020-62909-9
PMID:	32265565

Biological Control of Citrus Postharvest Phytopathogens

Moraes Bazioli J, Belinato JR, Costa JH, Akiyama DY, Pontes JG, Kupper KC, Augusto F, de Carvalho JE, Fill TP

Toxins (Basel)

06-Aug-2019

PMCID:	PMC6723504
doi:	10.3390/toxins11080460
PMID:	31390769

Cistus incanus from Strandja Mountain as a Source of Bioactive Antioxidants

Dimcheva V, Karsheva M

Plants (Basel)

26-Jan-2018

PMCID:	PMC5874597
doi:	10.3390/plants7010008
PMID:	29373566

Impact of an Educational Hands-on Project on the Antimicrobial, Antitumor and Anti-Inflammatory Properties of Plants on Portuguese Students’ Awareness, Knowledge, and Competences

Azevedo MM, Pinheiro C, Dias AC, Pinto-Ribeiro F, Baltazar F

Int J Environ Res Public Health

23-Feb-2015

PMCID:	PMC4377910
doi:	10.3390/ijerph120302437
PMID:	25711362

Adaptive Radiation in Mediterranean Cistus (Cistaceae)

Guzmán B, Lledó MD, Vargas P

PLoS One

23-Jul-2009

PMCID:	PMC2719431
doi:	10.1371/journal.pone.0006362
PMID:	19668338

Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects

BENNETT MD, LEITCH IJ

Ann Bot

01-Jan-2005

PMCID:	PMC4246708
doi:	10.1093/aob/mci003
PMID:	15596457

2α,3β-dihydroxy-4(18)-neo-cleroden-15-oic acid from cistus populifolius

Julio G. Urones, Isidro S. Marcos, Pilar Basabe, Alicia Jimenez, Antonio Gomez, Anna M. Lithgow

Elsevier BV

30-Apr-2003

doi:	10.1016/0031-9422(94)00709-3

Ring a functionalized Neo-clerodane diterpenoids from Cistus populifolius

Julio G. Urones, Pilar Basabe, Isidro S. Marcos, Alicia Jiménez, Anna M. Lithgow, Margarita López, Rosalina F. Moro, Antonio Gómez

Elsevier BV

25-Jul-2002

doi:	10.1016/S0040-4020(01)89271-1

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 / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
methyl (3R)-5-[(1S,2R,4aR,8aR)-1,2,4a-trimethyl-5-methylidene-3,4,8,8a-tetrahydro-2H-naphthalen-1-yl]-3-methylpentanoate	163191062	Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)OC)CC=CC2=C)C	318.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl (3R)-5-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,8a-tetrahydronaphthalen-1-yl]-3-methylpentanoate	163025308	Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)OC)C=CC=C2C)C	318.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl 5-(1,2,4a-trimethyl-5-methylidene-3,4,8,8a-tetrahydro-2H-naphthalen-1-yl)-3-methylpentanoate	73826663	Click to see	318.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
Methyl 5-(1,2,4a,5-tetramethyl-2,3,4,8a-tetrahydronaphthalen-1-yl)-3-methylpentanoate	73826662	Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)OC)C=CC=C2C)C	318.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2R,9S,14Z,20Z)-tricosa-14,20-dien-3,5,10,12,22-pentayne-1,2,9-triol	163071479	Click to see	348.40	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
5-(1,2,4a,5-Tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpentanoic acid	13918481	Click to see	306.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl (3R)-5-[(1S,2R,4aR,5R,6R,8aR)-5,6-dihydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-3-methylpentanoate	162961993	Click to see	354.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl (3R)-5-[(1S,2R,4aR,5R,8aR)-5-hydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-3-methylpentanoate	162851120	Click to see	338.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl (3R)-5-[(1S,2R,4aR,6R,7R,8aR)-6,7-dihydroxy-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl]-3-methylpentanoate	15276147	Click to see	352.50	unknown	https://doi.org/10.1016/0031-9422(94)00709-3
methyl (3R)-5-[(1S,2R,4aR,7R,8aR)-7-acetyloxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoate	15215473	Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)OC)CC(C=C2C)OC(=O)C)C	378.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl (3R)-5-[(1S,2R,4aR,7R,8aR)-7-hydroxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoate	15276149	Click to see	336.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl (3R)-5-[(1S,2R,4aR,7S,8aR)-7-hydroxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoate	15276150	Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)OC)CC(C=C2C)O)C	336.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl (3R)-5-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoate	162897320	Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)OC)CCC=C2C)C	320.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl (3R)-5-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalen-1-yl]-3-methylpentanoate	13918489	Click to see	334.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl (3S)-5-[(1S,2R,4aR,7R,8aR)-7-methoxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoate	162855972	Click to see	350.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl 5-(1,2,4a,5-tetramethyl-7-oxo-3,4,8,8a-tetrahydro-2H-naphthalen-1-yl)-3-methylpentanoate	13918490	Click to see	334.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl 5-(5-hydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)-3-methylpentanoate	73826666	Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)OC)CCCC2(C)O)C	338.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl 5-(5,6-dihydroxy-1,2,4a,5-tetramethyl-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)-3-methylpentanoate	14733557	Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)OC)CCC(C2(C)O)O)C	354.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
methyl 5-(6,7-dihydroxy-1,2,4a-trimethyl-5-methylidene-3,4,6,7,8,8a-hexahydro-2H-naphthalen-1-yl)-3-methylpentanoate	163095753	Click to see	352.50	unknown	https://doi.org/10.1016/0031-9422(94)00709-3
Methyl 5-(7-acetyloxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpentanoate	73826665	Click to see	378.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
Methyl 5-(7-hydroxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpentanoate	73826667	Click to see	336.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
Methyl 5-(7-methoxy-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpentanoate	73826664	Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)OC)CC(C=C2C)OC)C	350.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
> Organoheterocyclic compounds / Oxepanes
methyl (3R)-5-[(1aR,3aR,4S,5R,7aR,7bR)-4,5,7a,7b-tetramethyl-2-oxo-1a,3,3a,5,6,7-hexahydronaphtho[1,2-b]oxiren-4-yl]-3-methylpentanoate	163054984	Click to see	350.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1
Methyl 5-(4,5,7a,7b-tetramethyl-2-oxo-1a,3,3a,5,6,7-hexahydronaphtho[1,2-b]oxiren-4-yl)-3-methylpentanoate	73826668	Click to see	350.50	unknown	https://doi.org/10.1016/S0040-4020(01)89271-1

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Cistus populifolius

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top