Cistus monspeliensis

Details Top

Internal ID UUID64401183d38eb083896683
Scientific name Cistus monspeliensis
Authority L.
First published in Sp. Pl. : 524 (1753)

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • 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 monspeliensis has long been valued across parts of the Mediterranean as a simple tea and poultice plant. In the eastern Iberian Peninsula, people have used infusions of the aerial parts for colds and coughs, and fresh leaves macerated in water for mouthwash, the latter recorded among locals in Valencia by Cardenas et al., 2007. Across southern Spain, Cistus infusions were a household remedy for colds and throat complaints (González‑Coloma et al., 2013). In Portugal, the same plant is still found on market stalls, where herbalists sell dried material for tea to improve the season’s symptoms, as reported by Codesido, 2014. These practices concentrate on the leaves and flowering tops; no bark or root uses are documented for this species.

To make a mild everyday tea, place 4–6 g of dried leaves and flowering tops in 250 ml of just‑boiled water and let it stand, covered, for 5–7 minutes; strain and drink one cup up to twice daily. A gentle 1:5 tincture for on‑the‑go use can be prepared with 20 g of dried leaves in 100 ml of 40% alcohol, shaking twice daily for 2 weeks before straining. Safety notes are sensible: use the tincture sparingly (1–2 ml), avoid long high‑dose courses without supervision, and avoid during pregnancy and in people on anticoagulant therapy. For topical macerations, cool the liquid before use to prevent irritation.

The leaves and aerial parts contain well‑studied phenolics that plausibly underpin these uses: flavone and flavonol glycosides (myricetin, quercetin, kaempferol and their methyl ethers), labdane diterpenes (particularly carnosol and carnosolic acid), essential‑oil monoterpenes (1,8‑cineole and α‑pinene), and polymeric tannins; these constituents show antibacterial, anti‑inflammatory and antioxidant activity and help explain the cold‑relief, mouthwash and wound‑support traditions (Dutra et al., 2016; Greff et al., 2017; Luna et al., 2018).

Commercial interest has increased as research evaluates Cistus extracts for cold‑symptom relief and oral care, while herbal suppliers now sell dried Cistus leaves—including C. monspeliensis—for teas, a revival of the old market‑stall practice reported by Codesido, 2014.

General Uses Top

Suggest a correction!

Common products:
The species yields a fragrant resin (labdanum) and an essential oil, both harvested for commercial use; it is also cultivated as an ornamental shrub for landscaping.

Industrial and craft applications:
The essential oil is employed by the fragrance industry in perfume bases, soaps, and detergents; the labdanum resin serves as a fixative in incense and as a natural adhesive in certain craft processes; dried foliage provides a brown natural dye for wool and silk; and its aerial parts contain tannins used in leather‑tanning.

Fragrance and cosmetics:
The essential oil, rich in monoterpenes such as α‑pinene, 1,8‑cineole, and sesquiterpenes, is incorporated into perfume compositions, aftershaves, and cosmetic creams; the resin is added to incense blends and serves as a fixative in fragrance formulations.

Colorants and tanning:
The aerial parts contain condensed tannins (proanthocyanidins) and flavonoids that yield a reddish‑brown dye when mordanted on protein fibers; the same tannins provide the astringent properties employed in traditional leather‑tanning processes.

Properties relevant to use:
The labdanum resin is rich in labdane‑type diterpenes (e.g., labdanolic acid) that impart sticky, water‑repellent characteristics suitable for fixatives; the essential oil’s high monoterpene content gives a fresh, resinous aroma desirable in fragrance blends; tannin concentrations typically range from about 10 % to 20 % dry weight, providing strong astringency useful for leather tanning.

Standards and regulation:
The International Fragrance Association (IFRA) lists Cistus‑derived labdanum and essential oil as natural fragrance materials with recommended usage limits; EU cosmetic regulation (EC No 1223/2009) permits their use in cosmetics when labeling complies with the INCI requirements for “Cistus monspeliensis extract/oil”.

Sustainability and sourcing:
The species occurs widely in Mediterranean macchie and maquis and is harvested both from wild populations and from cultivated ornamental plantations; sustainable harvest practices such as limiting cutting to mature shrubs and encouraging regrowth are promoted by regional botanical societies to prevent overharvest; the plant’s drought tolerance makes it suitable for low‑input cultivation, reducing environmental impact compared with more water‑intensive aromatic crops.

Synonyms Top

Scientific name Authority First published in
Stephanocarpus monspeliensis Spach Ann. Sci. Nat., Bot. , sér. 2, 6: 369 (1836)
Cistus affinis Bertol. ex Guss. Fl. Sicul. Prodr. 2: 12 (1828)
Cistus collinus Salisb. Prodr. Stirp. Chap. Allerton : 368 (1796)
Cistus feredjensis Batt. Bull. Soc. Bot. France 30: 263 (1883)
Cistus olbiensis A.Huet & Hanry Bull. Soc. Bot. France 7: 346 (1860)
Cistus oleifolius Mill. Gard. Dict. ed. 8 : n.º 10 (1768)
Cistus valentinus Pourr. ex Nyman Consp. Fl. Eur. : 71 (1878)
Cistus monspeliensis subsp. canariensis Rivas Mart., Martín Osorio & Wildpret Itinera Geobot. 18: 482 (2011)
Cistus monspeliensis var. feredjensis (Batt.) Batt. Fl. Algérie , Dicot.: 90 (1888)
Cistus monspeliensis var. vulgaris Willk. Icon. Descr. Pl. Nov. 2: 30 (1856)
Cistus monspeliensis var. minor Willk. Icon. Descr. Pl. Nov. 2: 30 (1856)
Cistus monspeliensis f. flavescens Briq. Prodr. Fl. Corse 2(2): 174 (1936)
Cistus monspeliensis prol. affinis (Bertol. ex Guss.) Rouy & Foucaud Fl. France 2: ? (1895)
Cistus monspeliensis f. albiflorus Briq. Prodr. Fl. Corse 2(2): 174 (1935)
Cistus monspeliensis var. densifolius Sennen Monde Pl. 32: 38 (1931)
Cistus monspeliensis var. major Rouy & Foucaud Fl. France 2: 263 (1895)
Cistus monspeliensis var. parviflorus Sennen Mem. Primer Congr. Naturalistas Esp. : 280 (1909)
Cistus monspeliensis f. typicus Dans. Boissiera 4: 66 (1939)
Cistus monspeliensis var. flavescens Briq. Prodr. Fl. Corse 2(2): 175 (1936)
Cistus monspeliensis prol. affinis (Bertol. ex Guss.) Rouy & Foucaud Fl. France 2: 264 (1895)
Cistus monspeliensis var. affinis (Bertol. ex Guss.) P.Fourn. Quatre Fl. France : 438 (1936)
Cistus monspeliensis subsp. affinis (Bertol. ex Guss.) Sennen Monde Pl. 32: 38 (1931)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English montpelier cistus
Spanish jaguarzo
Arabic قريضة متوسطية
br roz-roc'h-montpelher
Catalan estepa negra
co muchju biancu
German montpellier-zistrose
Finnish kaitakistus
French ciste de montpellier
Kabyle tuzzalt
Norwegian Bokmål montpellier-solrose
oc moja negra
Portuguese sargação
Chinese 白岩蔷薇

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

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
    • Macaronesia
      • Canary Islands
      • Madeira
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
  • Europe
    • 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-0000607465
UNII T2OG06826L
USDA Plants CIMO7
Tropicos 7600023
INPN 91692
Flora of Italy 3233
KEW urn:lsid:ipni.org:names:168375-1
The Plant List kew-2723524
PaleoBotany 57044
Open Tree Of Life 177675
Observations.org 105135
NCBI Taxonomy 335184
IUCN Red List 73094084
IPNI 168375-1
iNaturalist 76363
GBIF 2874030
Freebase /m/05p3txc
EPPO CSTMO
EOL 483190
Calflora (Californian flora) 2154
USDA GRIN 10643
Wikipedia Cistus_monspeliensis

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
Vertebrate Pollination of Angiosperms in the Mediterranean Area: A Review Valdés B Plants (Basel) 20-Mar-2024
PMCID:PMC10976121
doi:10.3390/plants13060895
PMID:38592907
Origins of the central Macaronesian psyllid lineages (Hemiptera; Psylloidea) with characterization of a new island radiation on endemic Convolvulus floridus (Convolvulaceae) in the Canary Islands Bastin S, Reyes-Betancort JA, Siverio de la Rosa F, Percy DM PLoS One 26-Jan-2024
PMCID:PMC10817144
doi:10.1371/journal.pone.0297062
PMID:38277393
Fungal Planet description sheets: 1550–1613 Crous PW, Costa MM, Kandemir H, Vermaas M, Vu D, Zhao L, Arumugam E, Flakus A, Jurjević Ž, Kaliyaperumal M, Mahadevakumar S, Murugadoss R, Shivas RG, Tan YP, Wingfield MJ, Abell SE, Marney TS, Danteswari C, Darmostuk V, Denchev CM, Denchev TT, Etayo J, Gené J, Gunaseelan S, Hubka V, Illescas T, Jansen GM, Kezo K, Kumar S, Larsson E, Mufeeda KT, Piątek M, Rodriguez-Flakus P, Sarma PV, Stryjak-Bogacka M, Torres-Garcia D, Vauras J, Acal DA, Akulov A, Alhudaib K, Asif M, Balashov S, Baral HO, Baturo-Cieśniewska A, Begerow D, Beja-Pereira A, Bianchinotti MV, Bilański P, Chandranayaka S, Chellappan N, Cowan DA, Custódio FA, Czachura P, Delgado G, De Silva NI, Dijksterhuis J, Dueñas M, Eisvand P, Fachada V, Fournier J, Fritsche Y, Fuljer F, Ganga KG, Guerra MP, Hansen K, Hywel-Jones N, Ismail AM, Jacobs CR, Jankowiak R, Karich A, Kemler M, Kisło K, Klofac W, Krisai-Greilhuber I, Latha KP, Lebeuf R, Lopes ME, Lumyong S, Maciá-Vicente JG, Maggs-Kölling G, Magistà D, Manimohan P, Martín MP, Mazur E, Mehrabi-Koushki M, Miller AN, Mombert A, Ossowska EA, Patejuk K, Pereira OL, Piskorski S, Plaza M, Podile AR, Polhorský A, Pusz W, Raza M, Ruszkiewicz-Michalska M, Saba M, Sánchez RM, Singh R, Śliwa L, Smith ME, Stefenon VM, Strasiftáková D, Suwannarach N, Szczepańska K, Telleria MT, Tennakoon DS, Thines M, Thorn RG, Urbaniak J, van der Vegte M, Vasan V, Vila-Viçosa C, Voglmayr H, Wrzosek M, Zappelini J, Groenewald JZ Persoonia 30-Dec-2023
PMCID:PMC11041897
doi:10.3767/persoonia.2023.51.08
PMID:38665977
Mediterranean Shrub Species as a Source of Biomolecules against Neurodegenerative Diseases Chaves N, Nogales L, Montero-Fernández I, Blanco-Salas J, Alías JC Molecules 16-Dec-2023
PMCID:PMC10745362
doi:10.3390/molecules28248133
PMID:38138621
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
Myrmecia, Not Asterochloris, Is the Main Photobiont of Cladonia subturgida (Cladoniaceae, Lecanoromycetes) Pino-Bodas R, Blázquez M, de los Ríos A, Pérez-Ortega S J Fungi (Basel) 02-Dec-2023
PMCID:PMC10744234
doi:10.3390/jof9121160
PMID:38132761
Effects of Chloride and Sulfate Salts on Seed Germination and Seedling Growth of Ballota hirsuta Benth. and Myrtus communis L. Dadach M, Ahmed MZ, Bhatt A, Radicetti E, Mancinelli R Plants (Basel) 20-Nov-2023
PMCID:PMC10675368
doi:10.3390/plants12223906
PMID:38005803
Wild Avian Gut Microbiome at a Small Spatial Scale: A Study from a Mediterranean Island Population of Alectoris rufa Guerrini M, Tanini D, Vannini C, Barbanera F Animals (Basel) 27-Oct-2023
PMCID:PMC10648672
doi:10.3390/ani13213341
PMID:37958097
Zoonotic Microparasites in Invasive Black Rats (Rattus rattus) from Small Islands in Central Italy Zanet S, Occhibove F, Capizzi D, Fratini S, Giannini F, Hoida AD, Sposimo P, Valentini F, Ferroglio E Animals (Basel) 20-Oct-2023
PMCID:PMC10603634
doi:10.3390/ani13203279
PMID:37894002
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 with Antimicrobial Activity against Staphylococcus aureus, a Meta-Analysis for Green Veterinary Pharmacology Applications Oppedisano F, De Fazio R, Gugliandolo E, Crupi R, Palma E, Abbas Raza SH, Tilocca B, Merola C, Piras C, Britti D Microorganisms 09-Sep-2023
PMCID:PMC10534841
doi:10.3390/microorganisms11092264
PMID:37764109
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 Therapeutic Potential of Natural Dietary Flavonoids against SARS-CoV-2 Infection Wang Z, Yang L Nutrients 03-Aug-2023
PMCID:PMC10421531
doi:10.3390/nu15153443
PMID:37571380
Bioclimatic and Landscape Factors drive the Potential Distribution of Philaenus spumarius, Neophilaenus campestris and N. lineatus (Hemiptera, Aphrophoridae) in Southeastern Iberian Peninsula Gallego D, Sabah SC, Lencina JL, Carrillo AF Insects 30-Jun-2023
PMCID:PMC10380695
doi:10.3390/insects14070592
PMID:37504597

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dodecane 8182 Click to see 170.33 unknown https://doi.org/10.1515/ZNC-1984-7-802
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://doi.org/10.1515/ZNC-1984-7-802
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown https://doi.org/10.1515/ZNC-1984-7-802
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown https://doi.org/10.1515/ZNC-1984-7-802
Octacosane 12408 Click to see 394.80 unknown https://doi.org/10.1515/ZNC-1984-7-802
Pentacosane 12406 Click to see 352.70 unknown https://doi.org/10.1515/ZNC-1984-7-802
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown https://doi.org/10.1515/ZNC-1984-7-802
Tetradecane 12389 Click to see 198.39 unknown https://doi.org/10.1515/ZNC-1984-7-802
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1515/ZNC-1984-7-802
Tridecane 12388 Click to see 184.36 unknown https://doi.org/10.1515/ZNC-1984-7-802
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
alpha-Acoradiene 90351 Click to see 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Carbocyclic fatty acids
(3R)-5-[(1S,2S,4aS,8aR)-4a-(hydroxymethyl)-1,2-dimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 162884799 Click to see 308.50 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
5-[4a-(Hydroxymethyl)-1,2-dimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 162884798 Click to see CC1CCC2(C=CCCC2C1(C)CCC(C)CC(=O)O)CO 308.50 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3S)-5-[(1S,2S,4aS,8aR)-4a-(hydroxymethyl)-1,2-dimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentan-1-ol 162909041 Click to see 294.50 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
(4aS,7S,8S,8aR)-8-[(3S)-5-hydroxy-3-methylpentyl]-7,8-dimethyl-1,2,5,6,7,8a-hexahydronaphthalene-4a-carboxylic acid 162937567 Click to see 308.50 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
5-[4a-(Hydroxymethyl)-1,2-dimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentan-1-ol 162909040 Click to see 294.50 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
8-(5-Hydroxy-3-methylpentyl)-7,8-dimethyl-1,2,5,6,7,8a-hexahydronaphthalene-4a-carboxylic acid 162937566 Click to see 308.50 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4R)-6-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-4-methylhexanoic acid 162845489 Click to see 338.50 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
[(3S)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentyl] acetate 21681319 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCOC(=O)C 352.60 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
6-(2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-4-methylhexanoic acid 162845488 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCC(=O)O 338.50 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
NCGC00380376-01_C22H40O3_1-Naphthalenepentanol, decahydro-2-hydroxy-gamma,2,5,5,8a-pentamethyl-, alpha-acetate 56776325 Click to see 352.60 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(3R)-5-[(1S,2R,4aS,8aR)-1,2,4a-trimethyl-5-(2-oxopropyl)-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 162887899 Click to see 348.50 unknown https://doi.org/10.1055/S-2001-11497
(3R)-5-[(1S,2R,4aS,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 21626056 Click to see 306.50 unknown https://doi.org/10.1021/NP0204388
(3R)-5-[(1S,2R,4aS,8aR)-5-(acetyloxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 10406487 Click to see 364.50 unknown https://doi.org/10.1021/NP0204388
(3R)-5-[(1S,2R,4aS,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 21626051 Click to see 322.50 unknown https://doi.org/10.1021/NP0204388
(3R)-5-[(1S,2R,4aS,8aS)-5-(acetyloxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 162915903 Click to see 364.50 unknown https://doi.org/10.1016/S0031-9422(00)97359-X
(3S)-5-[(1S,2R,4aS,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 101235636 Click to see 306.50 unknown https://doi.org/10.1248/BPB.29.1775
(3S)-5-[(1S,2R,4aS,8aR)-5-(acetyloxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 44380735 Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)O)CCC=C2COC(=O)C)C 364.50 unknown https://doi.org/10.1248/BPB.29.1775
https://doi.org/10.1021/NP0204388
(3S)-5-[(1S,2R,4aS,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentan-1-ol 101235639 Click to see 308.50 unknown https://doi.org/10.1021/NP0204388
https://doi.org/10.1248/BPB.29.1775
(3S)-5-[(1S,2R,4aS,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 44380441 Click to see CC1CCC2(C(C1(C)CCC(C)CC(=O)O)CCC=C2CO)C 322.50 unknown https://doi.org/10.1021/NP0204388
(4aR,5S,6R,8aS)-5-[(3S)-5-acetyloxy-3-methylpentyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 101235637 Click to see 364.50 unknown https://doi.org/10.1248/BPB.29.1775
https://doi.org/10.1021/NP0204388
(4aR,5S,6R,8aS)-5-[(3S)-5-hydroxy-3-methylpentyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carbaldehyde 101235638 Click to see CC1CCC2(C(C1(C)CCC(C)CCO)CCC=C2C=O)C 306.50 unknown https://doi.org/10.1021/NP0204388
https://doi.org/10.1248/BPB.29.1775
(4aR,5S,6R,8aS)-5-[(3S)-5-hydroxy-3-methylpentyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 101235634 Click to see 322.50 unknown https://doi.org/10.1021/NP0204388
[(3S)-5-[(1S,2R,4aS,8aR)-5-(acetyloxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl] acetate 101235632 Click to see 392.60 unknown https://doi.org/10.1248/BPB.29.1775
https://doi.org/10.1021/NP0204388
[(3S)-5-[(1S,2R,4aS,8aR)-5-(hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl] acetate 101235633 Click to see 350.50 unknown https://doi.org/10.1021/NP0204388
https://doi.org/10.1248/BPB.29.1775
[(3S)-5-[(1S,2R,4aS,8aR)-5-formyl-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl] acetate 637193 Click to see 348.50 unknown https://doi.org/10.1248/BPB.29.1775
https://doi.org/10.1021/NP0204388
[(4aR,5S,6R,8aS)-5-[(3S)-5-hydroxy-3-methylpentyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl acetate 101235635 Click to see CC1CCC2(C(C1(C)CCC(C)CCO)CCC=C2COC(=O)C)C 350.50 unknown https://doi.org/10.1021/NP0204388
https://doi.org/10.1248/BPB.29.1775
[5-(5-Formyl-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpentyl] acetate 22297633 Click to see 348.50 unknown https://doi.org/10.1021/NP0204388
https://doi.org/10.1248/BPB.29.1775
[5-(5-Hydroxy-3-methylpentyl)-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]methyl acetate 73155219 Click to see 350.50 unknown https://doi.org/10.1248/BPB.29.1775
https://doi.org/10.1021/NP0204388
[5-[5-(Acetyloxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl] acetate 73812996 Click to see 392.60 unknown https://doi.org/10.1248/BPB.29.1775
https://doi.org/10.1021/NP0204388
[5-[5-(Hydroxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentyl] acetate 73812997 Click to see CC1CCC2(C(C1(C)CCC(C)CCOC(=O)C)CCC=C2CO)C 350.50 unknown https://doi.org/10.1021/NP0204388
https://doi.org/10.1248/BPB.29.1775
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/10.1248/BPB.29.1775
https://doi.org/10.1021/NP0204388
5-(5-Acetyloxy-3-methylpentyl)-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 73812999 Click to see 364.50 unknown https://doi.org/10.1248/BPB.29.1775
https://doi.org/10.1021/NP0204388
5-(5-Hydroxy-3-methylpentyl)-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carbaldehyde 73813000 Click to see 306.50 unknown https://doi.org/10.1021/NP0204388
https://doi.org/10.1248/BPB.29.1775
5-(5-Hydroxy-3-methylpentyl)-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid 73812998 Click to see 322.50 unknown https://doi.org/10.1021/NP0204388
5-[(1S,2R,4aR)-5-(acetyloxymethyl)-1,2,4a-trimethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 74177094 Click to see 364.50 unknown https://doi.org/10.1021/NP0204388
https://doi.org/10.1248/BPB.29.1775
https://doi.org/10.1016/S0031-9422(00)97359-X
5-[1,2,4a-Trimethyl-5-(2-oxopropyl)-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpentanoic acid 162887898 Click to see 348.50 unknown https://doi.org/10.1055/S-2001-11497
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
Tricyclene 79035 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Isopropenylcyclohexene-1-carboxylic acid 2724160 Click to see CC(=C)C1CCC(=CC1)C(=O)O 166.22 unknown https://doi.org/10.1248/BPB.29.1775
https://doi.org/10.1021/NP0204388
alpha-PHELLANDRENE 7460 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,6R,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 84690 Click to see 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1S,2S,6S,7S,9R,13S,15R,16S,17S)-15,16-dihydroxy-4-methoxy-2,6,17-trimethyl-14-methylidene-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11-dione 11740247 Click to see 376.40 unknown https://doi.org/10.1021/NP0204388
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see 498.70 unknown https://doi.org/10.1248/BPB.29.1775
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-2001-11497
3-O-Acetyloleanolic Acid 151202 Click to see 498.70 unknown https://doi.org/10.1248/BPB.29.1775
ent-13-epi-Manoyl oxide 6453839 Click to see 290.50 unknown https://doi.org/10.1055/S-2001-11497
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1515/ZNC-1984-3-418
Rhamnazin 5320945 Click to see 330.29 unknown https://doi.org/10.1515/ZNC-1984-3-418
Rhamnetin 5281691 Click to see 316.26 unknown https://doi.org/10.1515/ZNC-1984-3-418
Rhamnocitrin 5320946 Click to see 300.26 unknown https://doi.org/10.1515/ZNC-1984-3-418
> 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/10.1515/ZNC-1984-3-418
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-7-hydroxy-3,5-dimethoxy-4H-1-benzopyran-4-one 5489501 Click to see 330.29 unknown https://doi.org/10.1515/ZNC-1984-3-418
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',5-Dihydroxy-3,4',5',7-tetramethoxyflavone 5748580 Click to see 374.30 unknown https://doi.org/10.1016/S0305-1978(00)00071-5
https://doi.org/10.1016/0040-4020(67)80066-8

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.