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Aloysia citrodora

Aloysia citrodora - 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 UUID6440397f9a90e994356315
Scientific name Aloysia citrodora
Authority Paláu
First published in Parte Práct. Bot. 1: 768 (1784)

Description Top

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Aloysia citrodora, also known as lemon verbena, is a flowering plant native to South America and brought to Europe in the 17th century by the Spanish and Portuguese. It is a perennial shrub with glossy, lemon-scented leaves and small purple or white flowers. Lemon verbena has many culinary uses, including adding flavor to dishes and beverages, and is also used in traditional medicine. Its oil was historically used in perfumes, but is now prohibited in the European Union due to its skin-sensitizing properties. Lemon verbena is also known for its chemical compounds, including citral and verbascoside, which may interact with certain medications. It was first introduced to Europe by French botanist Philibert Commerson and has since become popular in horticulture, earning the Royal Horticultural Society's Award of Garden Merit.

Synonyms Top

Scientific name Authority First published in
Lippia citrodora (Paláu) Kunth Nov. Gen. Sp. 2: 269 (1818)
Lippia triphylla Kuntze Revis. Gen. Pl. 3(2): 253 (1898)
Verbena citrodora (Paláu) Cav. Descr. Pl. : 68 (1801)
Verbena fragrans Salisb. Prodr. Stirp. Chap. Allerton : 71 (1796)
Verbena triphylla L'Hér. Stirp. Nov. 21.
Zappania citriodora (Paláu) Lam. Tabl. Encycl. 1: 59 (1791)
Cordia microcephala Willd. in Roem. & Schult. Syst. Veg. 4: 801 1819
Aloysia sleumeri Moldenke Phytologia 10: 170 (1964)
Aloysia triphylla Britton Bot. Porto Rico 6: 140 (1925)
Aloysia triphylla f. serrulata Moldenke Phytologia 50: 308 (1982)
Aloysia triphylla Royle Ill. Bot. Himal. Mts. [Royle] 299. 1836 [Apr 1835 publ. May 1836]

Common names Top

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Language Common/alternative name
Afrikaans sitroenverbena
Arabic لويزة ليمونية
ary لويزة
Bulgarian лимонова върбинка
Bengali লেবু ভারবেনা
Catalan reina lluïsa
Catalan marialluïsa
Catalan herba lluïsa
Catalan herba de la princesa
Catalan berbena de nucs florits
Catalan maria lluïsa
Czech aloisie citronová
Danish citron-aloysia
Danish citronverbena
German zitronenstrauch
Greek Λουΐζα
Esperanto citronverbeno
Basque berbena limoiusain
Persian بهلیمو
Finnish sitruunaverbena
French verveine odorante
French verveine citronnelle
French verveine du pérou
Galician herba luísa
gn cedron
Hebrew לואיזה לימונית
Hungarian citromverbéna
Indonesian kerinyu limau
Italian erba luigia
Italian verbena odorosa
Japanese レモンバーベナ
Georgian ვერბენა ლიმონისა
Kazakh Лимон нарқайсары
Korean 레몬버베나
Lithuanian citrininė aloyzija
Dutch citroenverbena
Polish lippia trójlistna
Portuguese lúcia-lima
Romanian lămâie verbină
Romanian verbină parfumată
Russian Алоизия трёхлистная
Chinese 柠檬橙香木
Chinese 柠檬马鞭草
Chinese 檸檬馬鞭草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000950712
Tropicos 100433373
INPN 639101
Flora of Italy 4393
KEW urn:lsid:ipni.org:names:1015994-1
Missouri Botanical Garden 291522
Open Tree Of Life 862761
Observations.org 913418
NCBI Taxonomy 925377
IPNI 330575-2
iNaturalist 332455
GBIF 5667503
Freebase /m/037vn2
EPPO ALYTR
Elurikkus 639196
USDA GRIN 317750
Wikipedia Aloysia_citrodora
CMAUP NPO21046
Tropicos 50069454
The Plant List kew-6894
IPNI 861051-1

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
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
Plant-Origin Components: New Players to Combat Antibiotic Resistance in Klebsiella pneumoniae Luna-Pineda VM, Rodríguez-Martínez G, Salazar-García M, Romo-Castillo M Int J Mol Sci 10-Feb-2024
PMCID:PMC10888558
doi:10.3390/ijms25042134
PMID:38396811
Use of Essential Oils to Counteract the Phenomena of Antimicrobial Resistance in Livestock Species Lupia C, Castagna F, Bava R, Naturale MD, Zicarelli L, Marrelli M, Statti G, Tilocca B, Roncada P, Britti D, Palma E Antibiotics (Basel) 07-Feb-2024
PMCID:PMC10885947
doi:10.3390/antibiotics13020163
PMID:38391549
Disclosing the potential of Cupressus leylandii A.B. Jacks & Dallim, Eucalyptus globulus Labill., Aloysia citrodora Paláu, and Melissa officinalis L. hydrosols as eco-friendly antimicrobial agents Almeida HH, Crugeira PJ, Amaral JS, Rodrigues AE, Barreiro MF Nat Prod Bioprospect 02-Jan-2024
PMCID:PMC10758378
doi:10.1007/s13659-023-00417-9
PMID:38163838
Verbascoside-Rich Plant Extracts in Animal Nutrition Rossi R, Mainardi E, Vizzarri F, Corino C Antioxidants (Basel) 24-Dec-2023
PMCID:PMC10812750
doi:10.3390/antiox13010039
PMID:38247465
Exploring the Sustainable Exploitation of Bioactive Compounds in Pelargonium sp.: Beyond a Fragrant Plant Roman S, Voaides C, Babeanu N Plants (Basel) 10-Dec-2023
PMCID:PMC10748180
doi:10.3390/plants12244123
PMID:38140450
Essential Oil Molecules Can Break the Loop of Oxidative Stress in Neurodegenerative Diseases Spisni E, Valerii MC, Massimino ML Biology (Basel) 07-Dec-2023
PMCID:PMC10740714
doi:10.3390/biology12121504
PMID:38132330
Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A Saudi J Biol Sci 26-Nov-2023
PMCID:PMC10749906
doi:10.1016/j.sjbs.2023.103877
PMID:38148949
Development of a Holistic In Vitro Cell-Free Approach to Determine the Redox Bioactivity of Agricultural Products Skaperda Z, Tekos F, Vardakas P, Nechalioti PM, Kourti M, Patouna A, Makri S, Gkasdrogka M, Kouretas D Int J Mol Sci 17-Nov-2023
PMCID:PMC10671064
doi:10.3390/ijms242216447
PMID:38003634
Organic Medicinal and Aromatic Plants: Consumption Profile of a Portuguese Consumer Sample Mendes A, Oliveira A, Lameiras J, Mendes-Moreira P, Botelho G Foods 16-Nov-2023
PMCID:PMC10670743
doi:10.3390/foods12224145
PMID:38002202
Mechanisms and Applications of Citral’s Antimicrobial Properties in Food Preservation and Pharmaceuticals Formulations Gutiérrez-Pacheco MM, Torres-Moreno H, Flores-Lopez ML, Velázquez Guadarrama N, Ayala-Zavala JF, Ortega-Ramírez LA, López-Romero JC Antibiotics (Basel) 09-Nov-2023
PMCID:PMC10668791
doi:10.3390/antibiotics12111608
PMID:37998810
Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ Foods 08-Nov-2023
PMCID:PMC10671036
doi:10.3390/foods12224066
PMID:38002124
Deciphering morphological and biochemical responses of Salvia leriifolia to seed cold plasma treatment, priming, and foliar spraying with nano-salicylic acid Ghodsimaab SP, Ghasimi Hagh Z, Makarian H, Gholipoor M Sci Rep 31-Oct-2023
PMCID:PMC10618475
doi:10.1038/s41598-023-45823-8
PMID:37907628
The complete chloroplast genome of Phyla nodiflora (Linnaeus) Greene (1899) from the Verbenaceae family and its phylogenetic analysis Sharmishtha R, Tanuja T, Balaji R, Parani M Mitochondrial DNA B Resour 18-Oct-2023
PMCID:PMC10588534
doi:10.1080/23802359.2023.2266877
PMID:37869568
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

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
> Benzenoids / Phenol ethers / Anisoles
Ethyleugenol 6429690 Click to see CCOC1=C(C=C(C=C1)CC=C)OC 192.25 unknown https://doi.org/10.1055/S-0028-1099422
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Hexyl 2-methylbutanoate 24838 Click to see CCCCCCOC(=O)C(C)CC 186.29 unknown https://doi.org/10.1080/10412905.1994.9698440
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1994.9698440
Geranyl isobutyrate 6086514 Click to see CC(C)C(=O)OCC=C(C)CCC=C(C)C 224.34 unknown https://doi.org/10.1080/10412905.1994.9698440
Geranyl propionate 5355853 Click to see CCC(=O)OCC=C(C)CCC=C(C)C 210.31 unknown https://doi.org/10.1080/10412905.1994.9698440
Neryl acetate 1549025 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1994.9698440
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1080/10412905.1994.9698440
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1080/10412905.1994.9698440
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(2E,6E)-3,7-dimethylnona-2,6-dienoic acid 21561550 Click to see CCC(=CCCC(=CC(=O)O)C)C 182.26 unknown https://doi.org/10.1080/10412905.1994.9698440
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1055/S-0028-1099422
3,7-Dimethyl-2,6-octadien-1-al 8843 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1055/S-0028-1099422
https://doi.org/10.1021/NP50017A018
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698409
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1055/S-0028-1099422
https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1016/S0367-326X(98)00016-1
Citronellal 7794 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown https://doi.org/10.1055/S-0028-1099422
Geranic acid 5275520 Click to see CC(=CCCC(=CC(=O)O)C)C 168.23 unknown https://doi.org/10.1080/10412905.1994.9698440
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
Ipsdienone 6430826 Click to see CC(=CC(=O)CC(=C)C=C)C 150.22 unknown https://doi.org/10.1080/10412905.1994.9698409
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1055/S-0028-1099422
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1055/S-0028-1099422
Methyl geranate 5365910 Click to see CC(=CCCC(=CC(=O)OC)C)C 182.26 unknown https://doi.org/10.1080/10412905.1994.9698440
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698409
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1016/S0367-326X(98)00016-1
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.1994.9698440
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
https://doi.org/10.1055/S-0028-1099422
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1055/S-0028-1099422
(-)-Verbenone 92874 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1055/S-0028-1099422
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698409
(1S,3R,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol 12314318 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698440
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1080/10412905.1994.9698440
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1055/S-0028-1099422
https://doi.org/10.1080/10412905.1994.9698409
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698409
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
https://doi.org/10.1055/S-0028-1099422
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
https://doi.org/10.1055/S-0028-1099422
beta-Thujone 91456 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698409
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698409
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1055/S-0028-1099422
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1994.9698409
Bornyl butyrate 97897 Click to see CCCC(=O)OC1CC2CCC1(C2(C)C)C 224.34 unknown https://doi.org/10.1080/10412905.1994.9698440
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698409
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698409
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698409
Fenchone 14525 Click to see CC1(C2CCC(C2)(C1=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698440
Myrtenal 61130 Click to see CC1(C2CC=C(C1C2)C=O)C 150.22 unknown https://doi.org/10.1080/10412905.1994.9698440
Myrtenol 10582 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698409
Pinocarveol 102667 Click to see CC1(C2CC1C(=C)C(C2)O)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698440
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
Thujone 261491 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698409
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698409
https://doi.org/10.1080/10412905.1994.9698440
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1055/S-0028-1099422
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1055/S-0028-1099422
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
https://doi.org/10.1055/S-0028-1099422
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1055/S-0028-1099422
Carveol 7438 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
Carvone, (+/-)- 7439 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
Piperitenone 381152 Click to see CC1=CC(=O)C(=C(C)C)CC1 150.22 unknown https://doi.org/10.1080/10412905.1994.9698409
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1080/10412905.1994.9698440
(-)-beta-Bourbonene 324224 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
(+)-Gamma-cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
(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/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698440
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
(E)-alpha-bisabolene 5315468 Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698409
(Z)-alpha-Bisabolene 5352653 Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698409
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene 519346 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown https://doi.org/10.1080/10412905.1994.9698440
alpha-Curcumene 92139 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1080/10412905.1994.9698440
beta-Bourbonene 62566 Click to see CC(C)C1CCC2(C1C3C2CCC3=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
beta-Cubebene 93081 Click to see CC1CCC(C2C13C2C(=C)CC3)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698440
CID 16396350 16396350 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
Cuparene 86895 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown https://doi.org/10.1080/10412905.1994.9698440
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698409
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698440
delta-Elemene 12309449 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698409
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698409
Isocaryophyllene 5281522 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
Isocaryophyllene oxide 1742211 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698440
Longifolene 289151 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
Isospathulenol 14038848 Click to see CC1=C2CCC(C2C3C(C3(C)C)CC1)(C)O 220.35 unknown https://doi.org/10.1080/10412905.1994.9698409
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698440
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698440
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698409
Bicyclogermacrene 5315347 Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698409
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
1,7-di-epi-alpha-Cedrene 10878276 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
alpha-Cederene 442348 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698440
https://doi.org/10.1080/10412905.1994.9698409
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698409
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698409
> 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/10.1080/10412905.1994.9698409
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698409
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
Lippifoli-1(6)-en-5-one 91750065 Click to see CC1CCC2=C(C1=O)C(CC3C2(C3)C)(C)C 218.33 unknown https://doi.org/10.1080/10412905.1994.9698409
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Geniposide 107848 Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/0305-1978(86)90106-7
Geniposidic Acid 443354 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 374.34 unknown https://doi.org/10.1016/0305-1978(86)90106-7
methyl (4aR,7aS)-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 137706142 Click to see COC(=O)C1=COC(C2C1CC=C2CO)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/0305-1978(86)90106-7
Mussaenoside 182423 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/0305-1978(86)90106-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
beta-Citraurin 9845703 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C 432.60 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one 9862 Click to see CC(=CCCC(=O)C)C 126.20 unknown https://doi.org/10.1080/10412905.1994.9698440
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(4E,7E)-1,5,9,9-Tetramethyl-12-oxabicyclo[9.1.0]dodeca-4,7-diene 22559443 Click to see CC1=CCCC2(C(O2)CC(C=CC1)(C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698409
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(1S,7S,9R,10S)-1,9-Dimethyl-4-methylidene-6,13-dioxatricyclo[8.4.0.03,7]tetradecane-5,12-dione 10400578 Click to see CC1CC2C(CC3(C1CC(=O)OC3)C)C(=C)C(=O)O2 264.32 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
Rose oxide 27866 Click to see CC1CCOC(C1)C=C(C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698440
> Organoheterocyclic compounds / Oxepanes
(1S,2S,5S,8S)-1,4,4,8-tetramethyl-12-oxatricyclo[6.3.1.02,5]dodecane 162910564 Click to see CC1(CC2C1CCC3(CCCC2(O3)C)C)C 222.37 unknown https://doi.org/10.1002/HLCA.19760590537
Limonene-1,2-epoxide 441245 Click to see CC(=C)C1CCC2(C(C1)O2)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698409
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1248/CPB.45.499
Acteoside;Kusaginin;TJC160 354009 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1248/CPB.45.499
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1016/S0367-326X(98)00016-1
https://doi.org/10.1248/CPB.45.499
> Phenylpropanoids and polyketides / Flavonoids / Flavones
6-Hydroxyluteolin 5281642 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O)O 302.23 unknown https://doi.org/10.1055/S-2006-962505
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/10.1055/S-2006-962505
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/JF990444I
https://doi.org/10.1055/S-2006-962505
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Flavone base + 4O, O-HexA-HexA 74413803 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O 638.50 unknown https://doi.org/10.1055/S-2006-958152
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-962505
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1055/S-2006-962505
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1055/S-2006-962505
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1021/JF990444I
https://doi.org/10.1055/S-2006-962505
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1055/S-2006-962505
https://doi.org/10.1021/JF990444I
Jaceosidin 5379096 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1021/JF990444I
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1055/S-2006-962505
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1055/S-2006-962505
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1021/JF990444I
https://doi.org/10.1055/S-2006-962505
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1021/JF990444I
https://doi.org/10.1055/S-2006-962505
Fastigenin 162464 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1021/JF990444I
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1055/S-2006-962505

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