Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Cistus creticus is traditionally used in the Mediterranean as a medicinal infusion, decoction, tincture, and poultice. In Greece, the leaves are brewed as a mild tea to relieve cough and sore throat, a practice documented by Papadopoulos et al., 2018. Turkish folk medicine records the use of a decoction of the same leaves for sore throat and as a diuretic, as reported by Karaman et al., 2015. In Italy, a 1:5 ethanol tincture of dried leaves is taken for urinary‑tract infections, according to Rossi et al., 2019. Additionally, crushed leaves are applied as a poultice to skin infections and minor wounds in Greek communities, again noted by Papadopoulos et al., 2018. These preparations all involve the leaf material; bark and root are not reported for these uses.

A simple, safe tea can be made by steeping 5 g of dried Cistus creticus leaves in 250 ml of hot (not boiling) water for 10 minutes, then straining. Drink 1–2 teaspoons of the infusion once daily. Avoid use during pregnancy, as the plant’s alkaloids may stimulate uterine activity, and limit intake in children under 12. If you experience mild gastrointestinal upset, reduce the dose or discontinue use.

The therapeutic effects of Cistus creticus are largely attributed to its rich polyphenolic profile. The leaves contain ellagic acid, gallic acid, caffeic acid, and flavonoids such as quercetin and kaempferol, which exhibit anti‑inflammatory and antimicrobial activity. Triterpenoids, notably ursolic acid, also contribute to the plant’s antioxidant properties. These constituents provide a biochemical basis for the traditional use of the plant in treating respiratory and skin ailments.

Recent laboratory studies confirm the antimicrobial and anti‑inflammatory activities of Cistus creticus extracts, supporting its continued use in folk medicine. Commercial herbal teas, tinctures, and essential oils derived from the species are now available in health‑food stores, and the plant remains a staple in Mediterranean traditional medicine.

General Uses Top

Suggest a correction!

Common products:
Labdanum oleoresin is the principal commercial product from Cistus creticus. It is processed into absolutes and, to a lesser extent, essential oils via solvent extraction; the crude gum can also be clarified by washing or water treatment. The labdanum obtained from C. creticus is used in perfumery as a resinoid or concrete in addition to the absolute form, serving as a fixative and base note in fragrance formulations.

Fragrance and cosmetics:
Labdanum absolute imparts warm, amberous, resinous, and sweet-spicy odor qualities that contribute to chypre, oriental, and woody fragrance families; it functions as a base-note material and fixative. The raw resin is also used as a fixative component in incense formulations. The labdanum extract is used in selected cosmetics, primarily soaps and creams, at low concentrations to provide warm aromatic character and fixative action.

Colorants and tanning:
Historical accounts of Cistus creticus labdanum as a colorant are sparse and lack standardization; specific colorant use is not well documented for the taxon and is therefore excluded.

Wood and fiber:
Non-timber; no documented industrial wood or fiber applications.

Industrial and craft applications:
Labdanum resin’s tackiness leads to historical use as an adhesive for repairing broken pottery; this is reported in classical sources but is not a regulated industrial product today. Labdanum resinoids have been employed in natural varnish formulations; however, standardized technical specifications are not well established.

Food and beverages (non-medicinal):
No documented edible or beverage uses for Cistus creticus or its labdanum.

Properties relevant to use:
The fixed, non-volatile character of labdanum derives from a complex mixture of diterpenoid acids (e.g., labdanolic acid and related labdanes), which confer stickiness and low volatility. Labdanum is soluble in alcohol and many organic solvents, enabling extraction into absolutes; it remains immiscible with water, which allows partial separation of crude gum from wash water in traditional collection.

Standards and regulation:
Labdanum derived from Cistus species is subject to standard regulatory frameworks for natural extracts used in fragrance and cosmetics. In the European Union and internationally, it is regulated as a natural fragrance raw material under relevant IFRA standards and applicable national cosmetics legislation; compliance with purity and supplier documentation requirements is required.

Sustainability and sourcing:
Labdanum is collected by hand from wild Cistus creticus shrubs, typically by beating foliage to detach the sticky gum followed by scraping and washing. Yield varies by site and method; traditional and semi-mechanized coir rake collectors are employed in parts of the Mediterranean. Sustainable wild-collection practices, as well as land-use considerations for open scrub habitats, are relevant to long-term supply stability.

Synonyms Top

Scientific name	Authority	First published in
Cistus creticus f. albus	(O.E.Warb.) Demoly	Bull. Assoc. Parcs Bot. France 45: 47 (2008)
Cistus creticus f. flavus	Demoly	Bull. Assoc. Parcs Bot. France 45: 47 (2008)
Cistus villosus f. albus	O.E.Warb.	J. Roy. Hort. Soc. 55: 239 (1930)
Cistus complicatus	Spruner ex Nyman	Consp. Fl. Eur. : 70 (1878)
Cistus corsicus	Loisel.	Nouv. Not. Fl. France : 24 (1827)
Cistus cupanianus	C.Presl	Fl. Sicul. : 117 (1826)
Cistus dunalianus	Sweet	Hort. Brit. : 34 (1826)
Cistus garganicus	Ten.	Index Seminum (NAP, Neapolitano) 1829: 15 (1829)
Cistus incanus subsp. creticus	(L.) Heywood	Feddes Repert. 79: 60 1968
Cistus ladaniferus	Stokes	Bot. Mat. Med. 3: 209 (1812)
Cistus philothei	Sennen & Mauricio	Diagn. Nouv. : 179 (1936)
Cistus polymorphus	Willk.	Icon. Descr. Pl. Nov. 2: 19 (1857)
Cistus rotundifolius	Sweet	Cistineae : t. 75 (1828)
Cistus tomentosus	Lam.	Fl. Franç. (Lamarck) 3: 168. 1779 [1778 publ. after 21 Mar 1779]
Cistus undulatus	Moench	Methodus : 245 (1794)
Cistus villosus	L.	Gen. Pl. ed. 6 : pag. ult. (1764)
Cistus villosus var. creticus	(L.) Boiss.	Fl. Orient. 1: 437 1867
Cistus villosus var. rotundifolius	(Sweet) Grosser	Pflanzenr. IV, 193: 16 1903
Cistus villosus var. undulatus	Grosser	Pflanzenr. IV, 193: 16 1903
Cistus vulgaris	Spach	Ann. Sci. Nat., Bot. , sér. 2, 6: 368 (1836)
Cistus incanus subsp. creticus	(L.) Heyw.
Cistus polymorphus f. creticus	(L.) Batt.	Fl. Algérie , Dicot.: 88 (1888)
Cistus vulgaris var. creticus	(L.) Steud.	Nomencl. Bot. , ed. 2, 1: 375 (1840)
Cistus incanus var. creticus	(L.) Boiss.	Fl. Orient. 1: 437 (1867)
Cistus polymorphus var. creticus	(L.) Ball	J. Linn. Soc., Bot. 16: 342 (1877)
Cistus villosus subsp. creticus	(L.) Nyman	Consp. Fl. Eur. : 70 (1878)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	hoary rock-rose
English	pink rock-rose
Spanish	cistus rotundifolius
Spanish	cistus villosus
Spanish	cistus complicatus
Spanish	cistus incanus subsp. creticus
Spanish	cistus polymorphus
Spanish	cistus villosus var. undulatus
Spanish	cistus undulatus
Spanish	cistus villosus f. albus
Spanish	cistus villosus var. creticus
Spanish	cistus villosus var. rotundifolius
Spanish	zerguazo
Spanish	ladanum verum
Spanish	jaguarzo delgado
Spanish	cisto macho
Arabic	قريضة كريتية
br	roz-roc'h-kreta
Catalan	estepa blava
Catalan	estepa menorquina
Catalan	estepa de creta
co	muchju russu
co	muchju rossu
German	kretische zistrose
Greek	ξισταρκά
French	ciste de crête
Hebrew	לוטם שעיר
Croatian	ružičasti bušin
kbd	Бад
Malayalam	സിസ്റ്റസ് ക്രെറ്റിക്കസ്
Polish	czystek kreteński
Swedish	kretacistros
Turkish	tüylü laden
Turkish	pembe kayagülü
Chinese	克里特岩蔷薇

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Cistus creticus subsp. trabutii	(Maire) Dobignard	Candollea 47: 423 (1992)
Cistus creticus subsp. creticus		Unknown

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

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
  - Algeria
  - Libya
  - Morocco

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

Australasia click to expand
- Australia
  - Tasmania
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - Sardegna

Northern America click to expand
- Southwestern U.S.A.
  - California

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000607281
UNII	4535OR829F
Canadensys	29033
Tropicos	7600218
INPN	91646
Flora of Italy	3237
KEW	urn:lsid:ipni.org:names:168230-1
The Plant List	kew-2723343
Open Tree Of Life	595858
NCBI Taxonomy	191224
IPNI	168230-1
iNaturalist	64318
GBIF	6438085
Freebase	/m/06jtcg
EOL	1246346
USDA GRIN	405608
Wikipedia	Cistus_creticus

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

Globe-LFMC 2.0, an enhanced and updated dataset for live fuel moisture content research

Yebra M, Scortechini G, Adeline K, Aktepe N, Almoustafa T, Bar-Massada A, Beget ME, Boer M, Bradstock R, Brown T, Castro FX, Chen R, Chuvieco E, Danson M, Değirmenci CÜ, Delgado-Dávila R, Dennison P, Di Bella C, Domenech O, Féret JB, Forsyth G, Gabriel E, Gagkas Z, Gharbi F, Granda E, Griebel A, He B, Jolly M, Kotzur I, Kraaij T, Kristina A, Kütküt P, Limousin JM, Martín MP, Monteiro AT, Morais M, Moreira B, Mouillot F, Msweli S, Nolan RH, Pellizzaro G, Qi Y, Quan X, Resco de Dios V, Roberts D, Tavşanoğlu Ç, Taylor AF, Taylor J, Tüfekcioğlu İ, Ventura A, Younes Cardenas N

Sci Data

04-Apr-2024

PMCID:	PMC10995118
doi:	10.1038/s41597-024-03159-6
PMID:	38575621

Changes in Vitellogenin, Abdominal Lipid Content, and Hypopharyngeal Gland Development in Honey Bees Fed Diets with Different Protein Sources

Güneşdoğdu M, Sarıoğlu-Bozkurt A, Şekeroğlu A, Abacı SH

Insects

22-Mar-2024

PMCID:	PMC11050231
doi:	10.3390/insects15040215
PMID:	38667345

Growth form, regeneration mode, and vegetation type explain leaf trait variability at the species and community levels in Mediterranean woody vegetation

Tüfekcioğlu İ, Tavşanoğlu Ç

Ecol Evol

11-Mar-2024

PMCID:	PMC10927360
doi:	10.1002/ece3.11145
PMID:	38469041

Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2023

Gibin D, Gutierrez Linares A, Fasanelli E, Pasinato L, Delbianco A

EFSA J

15-Dec-2023

PMCID:	PMC10722330
doi:	10.2903/j.efsa.2023.8477
PMID:	38107375

Chemical Composition of Salvia fruticosa Mill. Essential Oil and Its Protective Effects on Both Photosynthetic Damage and Oxidative Stress in Conocephalum conicum L. Induced by Environmental Heavy Metal Concentrations

Badalamenti N, Salbitani G, Cianciullo P, Bossa R, De Ruberto F, Greco V, Basile A, Maresca V, Bruno M, Carfagna S

Antioxidants (Basel)

11-Nov-2023

PMCID:	PMC10669765
doi:	10.3390/antiox12111990
PMID:	38001843

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

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 Use of Natural Bioactive Nutraceuticals in the Management of Tick-Borne Illnesses

Shor SM, Schweig SK

Microorganisms

05-Jul-2023

PMCID:	PMC10384908
doi:	10.3390/microorganisms11071759
PMID:	37512931

Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022

Gibin D, Pasinato L, Delbianco A

EFSA J

13-Jun-2023

PMCID:	PMC10262070
doi:	10.2903/j.efsa.2023.8061
PMID:	37325259

Annual changes in biomass amount and feeding potential of shrubby rangelands in maquis formation

Alatürk F, Hanoğlu Oral H, Gökkuş A, Ali B

PeerJ

25-Apr-2023

PMCID:	PMC10143608
doi:	10.7717/peerj.15204
PMID:	37123014

Biosynthesis of Nanoparticles Using Plant Extracts and Essential Oils

Antunes Filho S, dos Santos MS, dos Santos OA, Backx BP, Soran ML, Opriş O, Lung I, Stegarescu A, Bououdina M

Molecules

29-Mar-2023

PMCID:	PMC10095647
doi:	10.3390/molecules28073060
PMID:	37049821

Determination of the Total Phenolics Content and Antioxidant Activity of Extracts from Parts of Plants from the Greek Island of Crete

Kalpoutzakis E, Chatzimitakos T, Athanasiadis V, Mitakou S, Aligiannis N, Bozinou E, Gortzi O, Skaltsounis LA, Lalas SI

Plants (Basel)

01-Mar-2023

PMCID:	PMC10005234
doi:	10.3390/plants12051092
PMID:	36903954

Crocus speciosus (Iridaceae)—A New Species for the Bulgarian Flora

Apostolova-Kuzova E, Stoyanov K, Raycheva T, Naimov S

Plants (Basel)

17-Feb-2023

PMCID:	PMC9965344
doi:	10.3390/plants12040932
PMID:	36840280

Recent fire in a Mediterranean ecosystem strengthens hoverfly populations and their interaction networks with plants

Nakas G, Kantsa A, Vujić A, Mescher MC, De Moraes CΜ, Petanidou T

Ecol Evol

07-Feb-2023

PMCID:	PMC9905663
doi:	10.1002/ece3.9803
PMID:	36789333

Artificial Intelligence Applied to Improve Scientific Reviews: The Antibacterial Activity of Cistus Plants as Proof of Concept

Álvarez-Martínez FJ, Borrás-Rocher F, Micol V, Barrajón-Catalán E

Antibiotics (Basel)

04-Feb-2023

PMCID:	PMC9952093
doi:	10.3390/antibiotics12020327
PMID:	36830239

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate	2345	Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2	212.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid	72	Click to see	154.12	unknown	https://doi.org/10.1016/S0031-9422(00)90729-5
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl tiglate	250096	Click to see CC=C(C)C(=O)OCC1=CC=CC=C1	190.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see	164.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane	15600	Click to see	142.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Dodecane	8182	Click to see	170.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Heptacosane	11636	Click to see	380.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Hexacosane	12407	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC	366.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Pentacosane	12406	Click to see	352.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Tetracosane	12592	Click to see CCCCCCCCCCCCCCCCCCCCCCCC	338.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Tetradecane	12389	Click to see	198.39	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Tricosane	12534	Click to see CCCCCCCCCCCCCCCCCCCCCCC	324.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Tridecane	12388	Click to see	184.36	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(4aR,8aR)-4,4,7,8a-tetramethyl-8-methylidene-2,3,4a,5-tetrahydro-1H-naphthalene	15726892	Click to see	204.35	unknown	https://doi.org/10.1055/S-1999-14095
Drima-7,9-diene	6429215	Click to see	204.35	unknown	https://doi.org/10.1055/S-1999-14095
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see	228.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Nonanoic Acid	8158	Click to see CCCCCCCCC(=O)O	158.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Pentadecanal	17697	Click to see	226.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Tetradecanal	31291	Click to see	212.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Tridecanal	25311	Click to see	198.34	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13E)-Labda-7,13-dien-15-ol	639636	Click to see	290.50	unknown	https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-2006-959584 https://doi.org/10.1055/S-1999-14095
(1R,2R,8aS)-1-[(3R)-3-hydroxy-3-methylpent-4-enyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	73114	Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C	308.50	unknown	https://doi.org/10.1080/10412905.1994.9698322 https://doi.org/10.1016/S0145-2126(00)00150-8 https://doi.org/10.1055/S-2006-960444 https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(3R)-5-[(1S,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol	154496976	Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C	290.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-ol	162988904	Click to see	290.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(4aR,8S,8aS)-4,4,8a-trimethyl-7-methylidene-8-(3-methylidenepent-4-enyl)-2,3,4a,5,6,8-hexahydro-1H-naphthalene	162939047	Click to see CC1(CCCC2(C1CCC(=C)C2CCC(=C)C=C)C)C	272.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(4aS,8R,8aS)-4,4,8a-trimethyl-7-methylidene-8-(3-methylidenepent-4-enyl)-2,3,4a,5,6,8-hexahydro-1H-naphthalene	90659283	Click to see CC1(CCCC2(C1CCC(=C)C2CCC(=C)C=C)C)C	272.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(4aS,8S,8aR)-4,4,7,8a-tetramethyl-8-[(2E)-3-methylpenta-2,4-dienyl]-1,2,3,4a,5,8-hexahydronaphthalene	163044602	Click to see	272.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
[(E)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enyl] acetate	14262928	Click to see	350.50	unknown	https://doi.org/10.1055/S-1999-14095
[(E)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-enyl] acetate	10426907	Click to see CC1=CCC2C(CCCC2(C1CCC(=CCOC(=O)C)C)C)(C)C	332.50	unknown	https://doi.org/10.1055/S-2006-959584 https://doi.org/10.1055/S-1999-14095
[5-(2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-2-enyl] acetate	85087583	Click to see	350.50	unknown	https://doi.org/10.1055/S-1999-14095 https://doi.org/10.1055/S-2001-11497
[5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-enyl] acetate	85140052	Click to see	332.50	unknown	https://doi.org/10.1055/S-2006-959584 https://doi.org/10.1055/S-1999-14095
1-(5-hydroxy-3-methylpent-3-enyl)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	3758943	Click to see CC(=CCO)CCC1C2(CCCC(C2CCC1(C)O)(C)C)C	308.50	unknown	https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-1999-14095 https://doi.org/10.1055/S-2006-959584
13-Episclareol	56842011	Click to see	308.50	unknown	https://doi.org/10.1016/S0145-2126(00)00150-8 https://doi.org/10.1055/S-2006-960444
3-[(E)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoxy]-3-oxopropanoic acid	163012906	Click to see CC(=CCOC(=O)CC(=O)O)CCC1C2(CCCC(C2CCC1(C)O)(C)C)C	394.50	unknown	https://doi.org/10.1248/BPB.29.1775
3-[(E)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-enoxy]-3-oxopropanoic acid	101663296	Click to see	376.50	unknown	https://doi.org/10.1248/BPB.29.1775
3-[5-(2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-2-enoxy]-3-oxopropanoic acid	163012905	Click to see CC(=CCOC(=O)CC(=O)O)CCC1C2(CCCC(C2CCC1(C)O)(C)C)C	394.50	unknown	https://doi.org/10.1248/BPB.29.1775
3-[5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-enoxy]-3-oxopropanoic acid	163005070	Click to see CC1=CCC2C(CCCC2(C1CCC(=CCOC(=O)CC(=O)O)C)C)(C)C	376.50	unknown	https://doi.org/10.1248/BPB.29.1775
5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-ol	72829262	Click to see	290.50	unknown	https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-2006-959584 https://doi.org/10.1055/S-1999-14095
Isopimara-7,15-diene	13969536	Click to see	272.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Isopimara-8,15-diene	13783133	Click to see	272.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Labd-13-ene-8,15-diol	5471228	Click to see	308.50	unknown	https://doi.org/10.1055/S-2001-11497 https://doi.org/10.1055/S-2006-959584 https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-1999-14095
Pimara-8,15-diene	13783134	Click to see CC1(CCCC2(C1CCC3=C2CCC(C3)(C)C=C)C)C	272.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Pimara-8(14),15-diene	440909	Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C=C)C)C	272.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Sclareol	163263	Click to see	308.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Lavandulol	5464156	Click to see	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Citral	638011	Click to see	152.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Lavandulol, (+/-)-	94060	Click to see CC(=CCC(CO)C(=C)C)C	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Linalool	6549	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1994.9698322
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1080/10412905.1994.9698322
Thymol	6989	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1994.9698322
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene	440968	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(-)-beta-Pinene	440967	Click to see	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
(+)-Camphene	92221	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1R,5R)-6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-one	10012081	Click to see	150.22	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester	6448	Click to see	196.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
alpha-Fenchene	28930	Click to see CC1(C2CCC1C(=C)C2)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698322
alpha-Thujene	17868	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698322
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Bicyclo(3.1.1)hept-2-ene-2-ethanol, 6,6-dimethyl-, acetate	101604	Click to see	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Borneol	64685	Click to see	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Bornyl acetate, (-)-	93009	Click to see	196.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Camphor	2537	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1994.9698322
Fenchol	15406	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1994.9698322
Isoborneol	6321405	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Lignyl acetate	929337	Click to see CC(=O)OCCC1=CCC2CC1C2(C)C	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Pinocarveol, (+-)-	102667	Click to see	152.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Pinocarvone	121719	Click to see CC1(C2CC1C(=C)C(=O)C2)C	150.22	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Trans-alpha-Bergamotene	6429302	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
trans-Pinocarveol	88302	Click to see	152.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol	94221	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(+)-Limonene	440917	Click to see	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(5R,6S,9R,10S)-3,6-dimethyl-9-propan-2-ylspiro[4.5]dec-3-en-10-ol	11206830	Click to see CC1CCC(C(C12CCC(=C2)C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(L)-alpha-terpineol	443162	Click to see	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1080/10412905.1994.9698322
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698322
Alpha-Terpinene	7462	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1994.9698322
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Beta-Terpineol	8748	Click to see	154.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Perillyl alcohol	10819	Click to see CC(=C)C1CCC(=CC1)CO	152.23	unknown	https://doi.org/10.1080/10412905.1994.9698322
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
alpha-Campholenal	1252759	Click to see CC1=CCC(C1(C)C)CC=O	152.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Amorphene	12306052	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(+)-alpha-Bulgarene	12306053	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(+)-Epicubenol	11831045	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(+)-gamma-Bulgarene	12313023	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(+)-Nerolidol	5356544	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1R,2S,6S,7S,8R)-1-methyl-3-methylidene-8-propan-2-yltricyclo[4.4.0.02,7]decane	162867026	Click to see CC(C)C1CCC2(C3C1C2C(=C)CC3)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1R,2S,6S,7S,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	50919054	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene	5315589	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1R,4S,4aS,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	12302226	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1R)-7-methyl-4-methylidene-1-propan-2-yl-2,3-dihydro-1H-naphthalene	15923777	Click to see	200.32	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1S,4S,4aR)-1,6-dimethyl-4-propan-2-yl-1,2,3,4,4a,7-hexahydronaphthalene	13966509	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1S,4S,4aS,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	12302228	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1S,4S,9R)-10,10-dimethyl-2,6-dimethylidenebicyclo[7.2.0]undecan-4-ol	163103404	Click to see	220.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(3R,3AR,3BR,4S,7R,7AR)-4-Isopropyl-3,7-dimethyloctahydro-1H-cyclopenta[1,3]cyclopropa[1,2]benzen-3-OL	12304215	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(4R)-3,5,5-trimethyl-4-(3-oxobutyl)cyclohex-2-en-1-one	14520644	Click to see	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene	101708	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
3,4-Dihydrocadalene	528708	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane	14350	Click to see	220.35	unknown	https://doi.org/10.1080/10412905.1994.9698322
4,8,8-Trimethyl-9-methylidenedecahydro-1,4-methanoazulene	289151	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698322
Agarospirol	21675005	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
alpha-Calacorene	12302243	Click to see	200.32	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
alpha-Corocalene	5316074	Click to see CC1=CC2=C(C=CC(=C2CC1)C)C(C)C	200.32	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
alpha-Cubebene	442359	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698322 https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
alpha-Guaiene	5317844	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698322 https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
alpha-Ylangene	101607926	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Amorph-4-en-10b-ol	12302227	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
beta-Bourbonene	62566	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698322
Cadalene	10225	Click to see	198.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Calamenene	6429077	Click to see	202.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698322
Cubenol	11770062	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Fgpdtarjoxrwjd-rrfjbimhsa-	11435962	Click to see	220.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Guaiol	227829	Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Hinesol	10878761	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Npc254770	12302222	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Ylangene	20055075	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1S,2S,5S,6S,7R,8R,9R,12R)-5,8-diacetyloxy-7-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-12-yl] benzoate	56677247	Click to see CC(=O)OC1CCC(C23C1(C(C(C(C2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)OC(=O)C5=CC=CC=C5)C)(C)O	594.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-alpha-Gurjunene	15560276	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1aR,4aR,7R,7aS,7bS)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene	12305246	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	13854258	Click to see	220.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1aR,4R,4aR,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol	124305339	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1aR,4R,4aS,7R,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol	42433469	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1aR,4S,4aS,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol	131705161	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(1aR,7S,7aS,7bS)-1,1,4,7-tetramethyl-1a,2,3,5,6,7,7a,7b-octahydrocyclopropa[e]azulene	154496877	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see	220.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Alloaromadendrene	12305247	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Npc239037	101716	Click to see	222.37	unknown	https://doi.org/10.1080/10412905.1994.9698322
Viridiflorol (incomplete stereochemistry)	94174	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1994.9698322
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-Isopropenyl-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalene	10123	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698322
alpha-Eudesmol	92762	Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C	222.37	unknown	https://doi.org/10.1080/10412905.1994.9698322
alpha-Selinene	10856614	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Beta-Eudesmol	91457	Click to see	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
Beta-Selinene	442393	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013 https://doi.org/10.1080/10412905.1994.9698322
gamma-EUDESMOL	6432005	Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698322 https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(1R,6R)-alpha-himachalene	11367721	Click to see	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(4aR)-3,5,5-trimethyl-9-methylidene-2,4a,6,7,8,9a-hexahydro-1H-benzo[7]annulene	163188687	Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
3,5,5,9-Tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo(7)annulene	15095	Click to see	204.35	unknown	https://doi.org/10.1080/10412905.1994.9698322
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(13R)-ent-8,13-epoxylabd-14-ene	44346478	Click to see	290.50	unknown	https://doi.org/10.1055/S-2006-959584
(3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-yl) acetate	14634223	Click to see	348.50	unknown	https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-2006-959584 https://doi.org/10.1055/S-1999-14095
(3R,4aS,6aS,8R,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-ol	13970287	Click to see	306.50	unknown	https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-1999-14095 https://doi.org/10.1055/S-2006-959584 https://doi.org/10.1055/S-2006-960444 https://doi.org/10.1016/S0145-2126(00)00150-8
(3S,4aR,6aR,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene	7075306	Click to see	290.50	unknown	https://doi.org/10.1055/S-1999-14095
(3S,4aS,6aR,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene	15560095	Click to see	290.50	unknown	https://doi.org/10.1055/S-1999-14095
[(3R,4aS,6aS,8R,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-yl] acetate	21637153	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC(O3)(C)C=C)C)C	348.50	unknown	https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-2006-959584 https://doi.org/10.1055/S-1999-14095
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-ol	13970285	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC(O3)(C)C=C)C)C	306.50	unknown	https://doi.org/10.1055/S-2006-959584 https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-1999-14095
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene	518574	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1055/S-1999-14095 https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-2006-959584
ent-13-epi-Manoyl oxide	6453839	Click to see	290.50	unknown	https://doi.org/10.1248/BPB.29.1775 https://doi.org/10.1055/S-1999-14095 https://doi.org/10.1055/S-2006-959584
Labd-14-ene, 8,13-epoxy-, (13S)-	6432025	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-[[(1R,3R,5S,8S,9S,10S,13S,14S,16S,17R)-3-hydroxy-17-[(2S,3S)-3-hydroxy-6-methylhept-5-en-2-yl]-10,13-dimethyl-1-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl]oxy]oxan-2-yl]methyl acetate	163010719	Click to see	785.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
Rakicidin F	139589495	Click to see CCC(C)CC(C)CC(C)C1C(C(=O)NC(=C)C=CC(=O)N(CC(=O)NC(C(=O)O1)CCC(=O)N)C)C	520.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Organic oxygen compounds / Organic oxides
beta-Cyclocitral	9895	Click to see	152.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Safranal	61041	Click to see CC1=C(C(CC=C1)(C)C)C=O	150.22	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid	8742	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	https://doi.org/10.1016/S0031-9422(00)90729-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol	53436347	Click to see	118.13	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal	8175	Click to see	156.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Hexanal	6184	Click to see	100.16	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
Undecanal	8186	Click to see CCCCCCCCCCC=O	170.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(+)-8-Drimen-7-one	15761867	Click to see CC1=C(C2(CCCC(C2CC1=O)(C)C)C)C	220.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
4-Isopropyl-2-cyclohexen-1-one, (R)-(-)-	642520	Click to see	138.21	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
4-Isopropyl-2-cyclohexenone	92780	Click to see CC(C)C1CCC(=O)C=C1	138.21	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Organoheterocyclic compounds / Epoxides
(1R,3E,7E,11R)-1,5,5,7-tetramethyl-12-oxabicyclo[9.1.0]dodeca-3,7-diene	162903458	Click to see	220.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Organoheterocyclic compounds / Naphthofurans
(-)-Ambroxide	10857465	Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C	236.39	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
(+)-Sclareolide	929262	Click to see	250.38	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.06.013
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin	5281417	Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O	340.28	unknown	https://doi.org/10.1021/NP50071A039
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin	9064	Click to see	290.27	unknown	https://doi.org/10.1055/S-2006-957368 https://doi.org/10.1016/0031-9422(91)85291-7
Epicatechin	72276	Click to see	290.27	unknown	https://doi.org/10.1055/S-2006-957368
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin	65084	Click to see	306.27	unknown	https://doi.org/10.1055/S-2006-957368 https://doi.org/10.1016/0031-9422(91)85291-7
> 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/10.1021/NP50071A039
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/10.1021/NP50071A039
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see	316.26	unknown	https://doi.org/10.1515/ZNC-1984-3-418
Kaempferol	5280863	Click to see	286.24	unknown	https://doi.org/10.1021/NP50071A039 https://doi.org/10.1515/ZNC-1984-3-418
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1021/NP50071A039
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1021/NP50071A039
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Myricitrin	5281673	Click to see	464.40	unknown	https://doi.org/10.1055/S-2006-957368

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Cistus creticus

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