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Cistus ladanifer

Cistus ladanifer - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Cistus ladanifer - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644011823ad0f213578118
Scientific name Cistus ladanifer
Authority L.
First published in Sp. Pl. : 523 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Ladanium officinarum Spach Ann. Sci. Nat., Bot. , sér. 2, 6: 67 (1836)
Ladanum verum Raf. Sylva Tellur. : 131 (1838)
Cistus grandiflorus Pourr. ex Willk. & Lange Prodr. Fl. Hispan. 3(3): 712. 1878 [Jul 1878]
Cistus ladanifer var. albiflorus Dunal Prodr. 1: 266 1824
Cistus ladanifer f. bicolor Demoly Bull. Soc. Bot. Centre-Ouest, n.s. 16: 93 (1985).
Cistus ladanifer var. maculatus Dunal Prodr. 1: 266 1824
Cistus ladanifer var. stenophyllus (Link) Grosser Pflanzenr. IV, 193: 24 1903
Cistus ladanifer var. sulcatus Demoly Bull. Soc. Bot. Centre-Ouest, n.s. 16: 93 (1985).
Cistus ladanifer f. sulcatus Demoly Bull. Soc. Bot. Centre-Ouest , n.s., 16: 93 (1985)
Cistus ladanifer subsp. sulcatus (Demoly) P.Monts. Anales Jard. Bot. Madrid 49: 152 (1991)
Cistus ladanifer f. immaculatus Dans. Monogr. Cistus : 80 (1939)
Cistus ladanosma Hoffmanns. Verz. Pfl.-Kult. : 51 (1824)
Cistus viscosus Stokes Bot. Mat. Med. 3: 209 (1812)
Cistus ladanifer subsp. subcatus (Dunal) P.Monts. Anales Jard. Bot. Madrid 49(1): 152 1991

Common names Top

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Language Common/alternative name
English common gum cistus
Spanish pringe
Spanish jara melosa
Spanish jara mora
Spanish jara pegajosa
Spanish jara pegantosa
Spanish jara sabia
Spanish jaracepa
Spanish lada ladon
Spanish lada ladón
Spanish mángala
Spanish manguila
Spanish mánguila
Spanish estepa de ládano
Spanish repipion
Spanish repipión
Spanish ripion
Spanish ripión
Spanish rosa de la jara
Spanish ládano
Spanish ladano
Spanish xara
Spanish ledo
Spanish jara pringosa
Spanish mangala
Spanish jara ladanifera
Spanish estepa de ladano
Spanish estepa del ladan
Spanish estepa del ladán
Spanish estepa ladanifera
Spanish estepa ladanífera
Spanish gallarin
Spanish gallarín
Spanish jara comun
Spanish jara común
Spanish jara de flor manchada
Spanish jara de hornos
Spanish jara de ladano
Spanish jara de ládano
Spanish jara de las cinco llagas
Spanish jara de laudano
Spanish jara de laúdano
Spanish jara de sierra morena
Spanish jara del ladano
Spanish jara del ládano
Spanish jara estepa y pegajosa
Spanish jara gomosa
Spanish jara manchega
Arabic قريضة عنبرية
Arabic قريضة لاذنية
Azerbaijani ladan burxurkolu
azb لادان بورخورکولو
Catalan estepa ladanífera
Czech cist ladanový
Czech cist ladanonosný
German lack-zistrose
Galician xara
Galician estepa
Hungarian balzsamos szuhar
Portuguese esteva
Swedish ladanumcistros
Swedish ladanumklippros
Swedish ladanum
Swedish labdanumklippros
Swedish hartsklippros
Chinese 膠薔樹
Chinese 岩蔷薇

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Cistus ladanifer subsp. mauritanicus (Thibaud ex Dunal) Pau & Sennen Diagn. Nouv. 178. 1936 [Jul 1936] (as ladaniferus)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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
    • Macaronesia
      • Canary Islands
      • Madeira
    • Northern Africa
      • Algeria
      • Morocco

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000607397
UNII 3Q78QJ6QP2
USDA Plants CILA10
Tropicos 7600228
INPN 91680
KEW urn:lsid:ipni.org:names:168325-1
The Plant List kew-2723459
Open Tree Of Life 752021
Observations.org 131096
NCBI Taxonomy 335173
NBN Atlas NBNSYS0200003566
Nature Serve 2.154713
IPNI 168325-1
iNaturalist 76362
GBIF 6437976
Freebase /m/06jtdh
EPPO CSTLA
EOL 488251
Elurikkus 3761
Calflora (Californian flora) 2153
USDA GRIN 10639
Wikipedia Cistus_ladanifer

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
Revised taxon definition in European Cortinarius subgenus Dermocybe based on phylogeny, chemotaxonomy, and morphology Huymann LR, Hannecker A, Giovanni T, Liimatainen K, Niskanen T, Probst M, Peintner U, Siewert B Mycol Prog 05-Apr-2024
PMCID:PMC10997704
doi:10.1007/s11557-024-01959-z
PMID:38585620
Alternative Approaches to Feeding Small Ruminants and Their Potential Benefits Boudalia S, Smeti S, Dawit M, Senbeta EK, Gueroui Y, Dotas V, Bousbia A, Symeon GK Animals (Basel) 14-Mar-2024
PMCID:PMC10967440
doi:10.3390/ani14060904
PMID:38540002
Using Analytic Hierarchy Process to Assess Beekeeping Suitability in Portuguese Controlled Areas: A First Approach Roque N, Fernandez P, Silveira C, Vilas-Boas M, Anjos O Insects 29-Jan-2024
PMCID:PMC10888816
doi:10.3390/insects15020091
PMID:38392511
A Study on E-Nose System in Terms of the Learning Efficiency and Accuracy of Boosting Approaches Chang IS, Byun SW, Lim TB, Park GM Sensors (Basel) 04-Jan-2024
PMCID:PMC10781315
doi:10.3390/s24010302
PMID:38203164
Keep the ball rolling: sexual differences in conglobation behavior of a terrestrial isopod under different degrees of perceived predation pressure Zamora-Camacho FJ PeerJ 19-Dec-2023
PMCID:PMC10740659
doi:10.7717/peerj.16696
PMID:38144184
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
Polyphenol Fingerprint, Biological Activities, and In Silico Studies of the Medicinal Plant Cistus parviflorus L. Extract El-Shibani FA, Sulaiman GM, Abouzied AS, Al Ali A, Abdulkarim AK, Alamami AD, Asiri M, Mohammed HA ACS Omega 04-Dec-2023
PMCID:PMC10733917
doi:10.1021/acsomega.3c07545
PMID:38144113
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
The biocontrol agent Lactiplantibacillus plantarum AMBP214 is dispersible to plants via bumblebees Temmermans J, Legein M, Zhao Y, Kiekens F, Smagghe G, de Coninck B, Lebeer S Appl Environ Microbiol 26-Oct-2023
PMCID:PMC10686056
doi:10.1128/aem.00950-23
PMID:37882529
Plant Extracts as Skin Care and Therapeutic Agents Michalak M Int J Mol Sci 22-Oct-2023
PMCID:PMC10607442
doi:10.3390/ijms242015444
PMID:37895122
Technosols Derived from Mining, Urban, and Agro-Industrial Waste for the Remediation of Metal(loid)-Polluted Soils: A Microcosm Assay Aguilar-Garrido A, Romero-Freire A, Paniagua-López M, Martínez-Garzón FJ, Martín-Peinado FJ, Sierra-Aragón M Toxics 12-Oct-2023
PMCID:PMC10610840
doi:10.3390/toxics11100854
PMID:37888704
Searching for new antifungals for the treatment of cryptococcosis de Sousa NS, de Almeida JD, Frickmann H, Lacerda MV, de Souza JV Rev Soc Bras Med Trop 24-Jul-2023
PMCID:PMC10367226
doi:10.1590/0037-8682-0121-2023
PMID:37493736
A Green Solution for the Rehabilitation of Marginal Lands: The Case of Lablab purpureus (L.) Sweet Grown in Technosols Aguilar-Garrido A, Reyes-Martín MP, Vidigal P, Abreu MM Plants (Basel) 18-Jul-2023
PMCID:PMC10385650
doi:10.3390/plants12142682
PMID:37514296
Fungal Planet description sheets: 1478–1549 Crous PW, Osieck ER, Shivas RG, Tan YP, Bishop-Hurley SL, Esteve-Raventós F, Larsson E, Luangsa-ard JJ, Pancorbo F, Balashov S, Baseia IG, Boekhout T, Chandranayaka S, Cowan DA, Cruz RH, Czachura P, De la Peña-Lastra S, Dovana F, Drury B, Fell J, Flakus A, Fotedar R, Jurjević Ž, Kolecka A, Mack J, Maggs-Kölling G, Mahadevakumar S, Mateos A, Mongkolsamrit S, Noisripoom W, Plaza M, Overy DP, Piątek M, Sandoval-Denis M, Vauras J, Wingfield MJ, Abell SE, Ahmadpour A, Akulov A, Alavi F, Alavi Z, Altés A, Alvarado P, Anand G, Ashtekar N, Assyov B, Banc-Prandi G, Barbosa KD, Barreto GG, Bellanger JM, Bezerra JL, Bhat DJ, Bilański P, Bose T, Bozok F, Chaves J, Costa-Rezende DH, Danteswari C, Darmostuk V, Delgado G, Denman S, Eichmeier A, Etayo J, Eyssartier G, Faulwetter S, Ganga KG, Ghosta Y, Goh J, Góis JS, Gramaje D, Granit L, Groenewald M, Gulden G, Gusmão LF, Hammerbacher A, Heidarian Z, Hywel-Jones N, Jankowiak R, Kaliyaperumal M, Kaygusuz O, Kezo K, Khonsanit A, Kumar S, Kuo CH, Læssøe T, Latha KP, Loizides M, Luo SM, Maciá-Vicente JG, Manimohan P, Marbach PA, Marinho P, Marney TS, Marques G, Martín MP, Miller AN, Mondello F, Moreno G, Mufeeda KT, Mun HY, Nau T, Nkomo T, Okrasińska A, Oliveira JP, Oliveira RL, Ortiz DA, Pawłowska J, Pérez-De-Gregorio MÀ, Podile AR, Portugal A, Privitera N, Rajeshkumar KC, Rauf I, Rian B, Rigueiro-Rodríguez A, Rivas-Torres GF, Rodriguez-Flakus P, Romero-Gordillo M, Saar I, Saba M, Santos CD, Sarma PV, Siquier JL, Sleiman S, Spetik M, Sridhar KR, Stryjak-Bogacka M, Szczepańska K, Taşkın H, Tennakoon DS, Thanakitpipattana D, Trovão J, Türkekul İ, van Iperen AL, van ’t Hof P, Vasquez G, Visagie CM, Wingfield BD, Wong PT, Yang WX, Yarar M, Yarden O, Yilmaz N, Zhang N, Zhu YN, Groenewald JZ Persoonia 29-Jun-2023
PMCID:PMC10983837
doi:10.3767/persoonia.2023.50.05
PMID:38567263
Proposal of a New System for Essential Oil Classification Based on Low-Cost Gas Sensor and Machine Learning Techniques Viciano-Tudela S, Parra L, Navarro-Garcia P, Sendra S, Lloret J Sensors (Basel) 22-Jun-2023
PMCID:PMC10347007
doi:10.3390/s23135812
PMID:37447662

Phytochemical Profile Top

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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
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown https://doi.org/10.1515/ZNC-1984-7-802
Eicosane 8222 Click to see CCCCCCCCCCCCCCCCCCCC 282.50 unknown https://doi.org/10.1515/ZNC-1984-7-802
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown https://doi.org/10.1515/ZNC-1984-7-802
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1515/ZNC-1984-7-802
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown https://doi.org/10.1515/ZNC-1984-7-802
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1515/ZNC-1984-7-802
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown https://doi.org/10.1515/ZNC-1984-7-802
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown https://doi.org/10.1515/ZNC-1984-7-802
Pentadecane 12391 Click to see CCCCCCCCCCCCCCC 212.41 unknown https://doi.org/10.1515/ZNC-1984-7-802
Triacontane 12535 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 422.80 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4As,8aS)-1-[(3S)-5-hydroxy-3-methylpentyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 11130717 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCO 310.50 unknown https://doi.org/10.1016/S0040-4020(01)88343-5
1-(5-hydroxy-3-methylpentyl)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 14239431 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCO 310.50 unknown https://doi.org/10.1016/S0040-4020(01)88343-5
Labd-7-en-15-oic acid, 6-oxo-, methyl ester 630546 Click to see CC1=CC(=O)C2C(CCCC2(C1CCC(C)CC(=O)OC)C)(C)C 334.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
Labdanolic acid 11186394 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O 324.50 unknown https://doi.org/10.1039/JR9560004262
methyl (3R)-5-[(1R,2R,4aR,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoate 162849957 Click to see CC(CCC1C2(CCCC(C2C=CC1(C)O)(C)C)C)CC(=O)OC 336.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl (3R)-5-[(1R,2R,4aR,8aS)-2-methoxy-2,5,5,8a-tetramethyl-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoate 163067794 Click to see CC(CCC1C2(CCCC(C2C=CC1(C)OC)(C)C)C)CC(=O)OC 350.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl (3R)-5-[(1R,3R,4aS,8aS)-3-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoate 163022788 Click to see CC(CCC1C(=C)C(CC2C1(CCCC2(C)C)C)O)CC(=O)OC 336.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl (3R)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoate 163039848 Click to see CC1=CC(=O)C2C(CCCC2(C1CCC(C)CC(=O)OC)C)(C)C 334.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl (3R)-5-[(1S,4aS,8aR)-5,5,8a-trimethyl-2-methylidene-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoate 162924263 Click to see CC(CCC1C(=C)C=CC2C1(CCCC2(C)C)C)CC(=O)OC 318.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl (3R)-5-[(4aR,8aS)-2,5,5,8a-tetramethyl-3-oxo-4a,6,7,8-tetrahydro-4H-naphthalen-1-yl]-3-methylpentanoate 162884825 Click to see CC1=C(C2(CCCC(C2CC1=O)(C)C)C)CCC(C)CC(=O)OC 334.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl (3R)-5-[(4S,4aR,8aS)-4-acetyloxy-2,5,5,8a-tetramethyl-3-oxo-4a,6,7,8-tetrahydro-4H-naphthalen-1-yl]-3-methylpentanoate 162922617 Click to see CC1=C(C2(CCCC(C2C(C1=O)OC(=O)C)(C)C)C)CCC(C)CC(=O)OC 392.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl (E)-5-[(1R,2R,4aR,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate 162893419 Click to see CC(=CC(=O)OC)CCC1C2(CCCC(C2C=CC1(C)O)(C)C)C 334.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl 5-(2-hydroxy-2,5,5,8a-tetramethyl-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl)-3-methylpent-2-enoate 162893418 Click to see CC(=CC(=O)OC)CCC1C2(CCCC(C2C=CC1(C)O)(C)C)C 334.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl 5-(2-hydroxy-2,5,5,8a-tetramethyl-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl)-3-methylpentanoate 162849956 Click to see CC(CCC1C2(CCCC(C2C=CC1(C)O)(C)C)C)CC(=O)OC 336.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl 5-(2-methoxy-2,5,5,8a-tetramethyl-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl)-3-methylpentanoate 163067793 Click to see CC(CCC1C2(CCCC(C2C=CC1(C)OC)(C)C)C)CC(=O)OC 350.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl 5-(2,5,5,8a-tetramethyl-3-oxo-4a,6,7,8-tetrahydro-4H-naphthalen-1-yl)-3-methylpentanoate 162884824 Click to see CC1=C(C2(CCCC(C2CC1=O)(C)C)C)CCC(C)CC(=O)OC 334.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl 5-(3-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpentanoate 163022786 Click to see CC(CCC1C(=C)C(CC2C1(CCCC2(C)C)C)O)CC(=O)OC 336.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl 5-(4-acetyloxy-2,5,5,8a-tetramethyl-3-oxo-4a,6,7,8-tetrahydro-4H-naphthalen-1-yl)-3-methylpentanoate 162922616 Click to see CC1=C(C2(CCCC(C2C(C1=O)OC(=O)C)(C)C)C)CCC(C)CC(=O)OC 392.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
methyl 5-(5,5,8a-trimethyl-2-methylidene-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl)-3-methylpentanoate 162924261 Click to see CC(CCC1C(=C)C=CC2C1(CCCC2(C)C)C)CC(=O)OC 318.50 unknown https://doi.org/10.1016/0031-9422(82)80089-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
beta-Thujene 520384 Click to see CC1C=CC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
(1S,2R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 145994486 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 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
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1515/ZNC-1984-7-802
> Organoheterocyclic compounds / Naphthofurans
(3aS,5aR,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran 12838593 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown https://doi.org/10.1016/S0031-9422(00)97701-X
8,12-Epoxy-13,14,15,16-tetranorlabdane 11861328 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown https://doi.org/10.1016/S0031-9422(00)97701-X
Ambrox 107166 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown https://doi.org/10.1016/S0031-9422(00)97701-X
> 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/10.1515/ZNC-1984-3-418
https://doi.org/10.1016/S0031-9422(00)80359-3
https://doi.org/10.1016/S0021-9673(97)01042-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(92)80355-I
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/10.1016/0031-9422(92)80355-I
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/0031-9422(92)80355-I
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(92)80355-I
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 129354321 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5315208 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 162926525 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
3-[(6-O-alpha-L-arabinopyranosyl-beta-D-glucopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one 13887800 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
3-[(6-O-beta-D-Xylopyranosyl-beta-D-glucopyranosyl)oxy]-4',5,7-trihydroxy-3'-methoxyflavone 102148697 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
3-[[6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-galactopyranosyl]oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one 73803273 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 14185727 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162884589 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(92)80355-I
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12313332 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Calendoflavobioside 14034827 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Isorhamnetin 3-galactoside 13245586 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Isorhamnetin 3-O-[b-D-xylopyranosyl-(1->6)-b-D-glucopyranoside] 74977613 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Myricetin 3-beta-D-glucopyranoside 12311099 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1016/0031-9422(92)80355-I
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Myricetin-3-O-rutinoside 21577860 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Quercetin 3-sophoroside 44259144 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 163194179 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
2-(3,4-dihydroxyphenyl)-5-hydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 163062784 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Quercetin 3-galactoside 7-rhamnoside 14130922 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
Quercetin 3-galactoside-7-rhamnoside 44259104 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(92)80355-I
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)80359-3
https://doi.org/10.1515/ZNC-1984-3-418
https://doi.org/10.1016/S0021-9673(97)01042-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://doi.org/10.1515/ZNC-1984-3-418
https://doi.org/10.1016/S0021-9673(97)01042-X
https://doi.org/10.1016/S0031-9422(00)80359-3
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown https://doi.org/10.1016/S0031-9422(00)80359-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(00)80359-3
https://doi.org/10.1515/ZNC-1984-3-418
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown https://doi.org/10.1515/ZNC-1984-3-418
https://doi.org/10.1016/S0031-9422(00)80359-3

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