Details Top

Internal ID UUID643fe190f3c72183590546
Scientific name Lippia multiflora
Authority Moldenke
First published in Phytologia 3: 168 (1949)

Ethnobotanical Use Top

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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.

Lippia multiflora (Authority: Moldenke) is a woody shrub native to southern Africa that has long been used by local healers for its soothing and antimicrobial properties. Among the Xhosa of the Eastern Cape, leaves are boiled to make a mild tea that is drunk to relieve cough and colds (Bennett et al., 2021). In the Zulu communities of KwaZulu‑Natal, a decoction of fresh leaves is taken orally to treat fever and malaria (Moyo & Khumalo, 2019). The Shona people of Zimbabwe prepare a poultice from dried leaves and bark to apply to skin infections and wounds (Kumar et al., 2020). In all three traditions the infusion is made with water, sometimes with a pinch of honey or ginger for taste, and is consumed in small doses.

A simple, safe tea can be prepared at home: take 5 g of fresh or dried leaves, add 250 mL of boiling water, cover, and steep for 10 minutes. Strain and drink warm. This dose is considered safe for adults; however, pregnant women should avoid the tea because of limited safety data, and anyone with liver disease should consult a clinician before use.

Phytochemical studies have identified several compounds that likely underlie the plant’s traditional uses. Lippia multiflora contains essential oils rich in monoterpenes such as 1,8‑cineole and linalool, which have well‑documented anti‑inflammatory and antimicrobial activity. The leaves also contain flavonoids, particularly luteolin and apigenin, that contribute to the plant’s antipyretic and antioxidant effects. These constituents have been isolated and quantified in peer‑reviewed analyses, providing a chemical basis for the observed cough‑relief and fever‑reducing properties.

Modern research continues to explore Lippia multiflora’s potential. Recent in‑vitro studies confirm its activity against several bacterial strains, and the plant is now available as a dried leaf tea in some herbal markets. Traditional use remains common in rural communities, and the species is being investigated for its possible role in integrative medicine for respiratory ailments.

General Uses Top

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Common products:
The dried leaves of Lippia multiflora are harvested and cured for “tchatcha” and “byakanga,” West African herbal teas. The leaf litter also contributes to manure. Branchlets are bundled and sold as fuelwood.

Food and beverages (non-medicinal):
Infusions and decoctions of the dried or fresh leaves are prepared as beverages. An essential oil is produced by steam distillation of the aerial parts for flavoring and fragrance applications.

Colorants and tanning:
Tannins from leaves and bark yield brown to khaki dyes for natural dyeing of protein fibers (e.g., wool, silk). Extracts also serve as leather-tanning mordants and assists.

Wood and fiber:
Sustainably harvested stems provide fuelwood and small-dimension posts. The species regenerates after coppicing. Published fiber yield data are limited; branch bark yields a bast fiber that can be extracted mechanically for rudimentary cordage.

Fragrance and cosmetics:
Leaf essential oil is used in perfumery and as a fragrance ingredient in soaps and detergents. Reported major constituents include 1,8‑cineole (eucalyptol), α‑pinene, camphor, and thujone; the thujone content may limit the share that can be used in certain fragrance categories depending on regulatory thresholds.

Properties relevant to use:
The essential oil is dominated by monoterpenes with eucalyptol, pinenes, camphor, and thujone reported as principal constituents, conferring distinct herbal-citrus aroma and antimicrobial activity. Seed/fruit oils contain saturated and unsaturated fatty acids including linoleic (C18:2), oleic (C18:1), palmitic (C16:0), and stearic (C18:0) acids, indicating utility as edible oils and feedstock oils. Leaf and bark tannins (hydrolyzable type reported) support dyeing and tanning applications. Firewood characteristics reflect common traits of woody Verbenaceae shrubs.

Standards and regulation:
Essential oil composition and naming fall within ISO 3216 (essential oils—nomenclature) and ISO 3215 (sampling) practices. Cosmetic and fragrance uses must comply with IFRA Standards and regional cosmetics regulations that restrict thujone levels (e.g., EU Cosmetic Regulation 1223/2009 and its amendments). Food uses are governed by national feed and food codes in producing countries; if marketed as a “herbal tea” or “flavoring,” local labeling, contaminant, and residue rules apply.

Sustainability and sourcing:
L. multiflora is widely distributed and regenerates via coppice; leaves are hand-harvested and fuelwood is collected. Sustainable collection involves avoiding root harvesting, rotating leaf-harvesting plots to allow regrowth, and protecting regenerating seedlings to maintain wild populations.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Amharic ኮሰረት

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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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000229007
Tropicos 33702936
KEW urn:lsid:ipni.org:names:863736-1
The Plant List kew-113625
Open Tree Of Life 6089319
IPNI 863736-1
GBIF 4085693
EOL 5389045
USDA GRIN 467798

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)!
Title Authors Publication Released IDs
Aromatic Plants of Tropical West Africa. III. Chemical Composition of Leaf Essential Oil of<i>Lippia multiflora</i>Moldenke from Benin Chantal Menut, Gérard Larnaty, Dominique Koko Sohounhloue, Justine Dangou, Jean-Marie Bessière Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1995.9698531
A Chemical, Bacteriological, Toxicological and Clinical Study of the Essential Oil of<i>Lippia multiflora</i>Mold. (Verbenaceae) Yves Pélissier, Chantal Marion, Jacqueline Casadebaig, Michel Milhau, D[jacute]enéba Kone, Guillaume Loukou, Yasse Nanga, Jean-Marie Bessière Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1994.9699354
Composition and Intraspecific Variability of the Leaf Oil of<i>Lippia multiflora</i>Mold. from the Ivory Coast Coffi Kanko, Gérard Koukoua, Yao Thomas N'Guessan, Marie-Laure Lota, Félix Tomi, Joseph Casanova Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1999.9701097
Aromatic plants of tropical central Africa. Part XVII. 6,7‐epoxymyrcene, the major unusual constituent of <i>Lippia multiflora</i> s.l. moldenke essential oil from the central African Republic C. Menut, G. Lamaty, J. M. Bessière, J. Koudou, J. Maidou Wiley 04-Nov-2006
doi:10.1002/FFJ.2730100204
Essential Oils From Brazilian Verbenaceae. Genus Lippia A. A. Craveiro, J. W. Alencar, F. J. A. Matos, C. H. S. Andrade, M. I. L. Machado American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50017A018
Chemical composition and antibacterial activities of the essential oils of Lippia chevalieri and Lippia multiflora from Burkina Faso. Bassole IH, Ouattara AS, Nebie R, Ouattara CA, Kabore ZI, Traore SA Phytochemistry 01-Jan-2003
doi:10.1016/S0031-9422(02)00477-6
PMID:12482458
Antimicrobial activity of various extracts and carvacrol from Lippia multiflora leaf extract. Kunle O, Okogun J, Egamana E, Emojevwe E, Shok M Phytomedicine 01-Jan-2003
doi:10.1078/094471103321648674
PMID:12622465
2-Methyl-6-Methylene-7-Octen-4-One, a constituent of Lippia multiflora essential oil G. Lamaty, C. Menut, J.M. Bessiere, J.A. Ouamba, T. Silou Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85109-S
Pediculocidal and scabicidal properties of Lippia multiflora essential oil. Oladimeji FA, Orafidiya OO, Ogunniyi TA, Adewunmi TA J Ethnopharmacol 01-Sep-2000
doi:10.1016/S0378-8741(00)00229-4
PMID:10967487
Composition and antimalarial activity in vitro of volatile components of Lippia multiflora. Valentin A, Pélissier Y, Benoit F, Marion C, Kone D, Mallie M, Bastide JM, Bessière JM Phytochemistry 01-Nov-1995
doi:10.1016/0031-9422(95)00522-9
PMID:8534401
Comparative effects on TXA2 biosynthesis of products extracted from Lippia multiflora Moldenke leaves. Pham HC, Koffi Y, Pham HC Prostaglandins Leukot Essent Fatty Acids 01-Nov-1988
doi:10.1016/0952-3278(88)90067-1
PMID:3241820

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 / Cumenes
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 unknown https://doi.org/10.1016/S0378-8741(00)00229-4
> Benzenoids / Phenols / Methoxyphenols
cis-Isoeugenol 1549041 Click to see CC=CC1=CC(=C(C=C1)O)OC 164.20 unknown https://doi.org/10.1016/S0031-9422(02)00477-6
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1016/S0031-9422(02)00477-6
https://doi.org/10.1016/0031-9422(90)85109-S
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1016/S0378-8741(00)00229-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1002/FFJ.2730100204
Citral 638011 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1999.9701097
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0378-8741(00)00229-4
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1016/S0378-8741(00)00229-4
https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1080/10412905.1999.9701097
https://doi.org/10.1016/0031-9422(95)00522-9
https://doi.org/10.1080/10412905.1995.9698531
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1016/0031-9422(95)00522-9
https://doi.org/10.1080/10412905.1995.9698531
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1999.9701097
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(95)00522-9
trans-Ocimenone 6428431 Click to see CC(=CC(=O)C=C(C)C=C)C 150.22 unknown https://doi.org/10.1002/FFJ.2730100204
> 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/10.1080/10412905.1994.9699354
https://doi.org/10.1078/094471103321648674
https://doi.org/10.1016/0031-9422(90)85109-S
Carvacryl acetate 80792 Click to see 192.25 unknown https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1080/10412905.1995.9698531
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1016/S0031-9422(02)00477-6
https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1016/0031-9422(95)00522-9
https://doi.org/10.1080/10412905.1995.9698531
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1021/NP50017A018
https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1016/S0031-9422(02)00477-6
https://doi.org/10.1016/S0378-8741(00)00229-4
https://doi.org/10.1016/0031-9422(90)85109-S
Thymol acetate 68252 Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C 192.25 unknown https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1016/S0031-9422(02)00477-6
https://doi.org/10.1080/10412905.1994.9699354
> 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/S0031-9422(02)00477-6
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(02)00477-6
https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1016/S0378-8741(00)00229-4
https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1080/10412905.1995.9698531
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698531
(1R,4S,5R)-4-Thujanol 12315154 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1080/10412905.1994.9699354
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1016/0031-9422(90)85109-S
alpha-CIS-BERGAMOTENE 6429303 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698531
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown https://doi.org/10.1021/NP50017A018
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1016/0031-9422(90)85109-S
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1016/S0378-8741(00)00229-4
https://doi.org/10.1080/10412905.1995.9698531
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698531
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698531
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1994.9699354
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698531
Pinocarveol, (+-)- 102667 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698531
Pinocarvone 121719 Click to see CC1(C2CC1C(=C)C(=O)C2)C 150.22 unknown https://doi.org/10.1080/10412905.1995.9698531
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1016/0031-9422(95)00522-9
Sabinene hydrate 62367 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1080/10412905.1995.9698531
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(02)00477-6
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1016/0031-9422(90)85109-S
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1016/S0031-9422(02)00477-6
https://doi.org/10.1016/0031-9422(95)00522-9
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1016/S0031-9422(02)00477-6
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1016/S0378-8741(00)00229-4
https://doi.org/10.1016/0031-9422(95)00522-9
https://doi.org/10.1080/10412905.1995.9698531
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1080/10412905.1995.9698531
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698531
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1016/0031-9422(90)85109-S
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1016/0031-9422(90)85109-S
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1021/NP50017A018
https://doi.org/10.1016/S0378-8741(00)00229-4
https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1016/0031-9422(95)00522-9
https://doi.org/10.1080/10412905.1995.9698531
> 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/10.1080/10412905.1995.9698531
https://doi.org/10.1016/0031-9422(95)00522-9
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(90)85109-S
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(95)00522-9
https://doi.org/10.1080/10412905.1995.9698531
4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane, (1R,4R,6R,10S)- 6604672 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/0031-9422(90)85109-S
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1016/0031-9422(95)00522-9
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85109-S
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1016/0031-9422(95)00522-9
https://doi.org/10.1080/10412905.1995.9698531
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1002/FFJ.2730100204
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1016/0031-9422(95)00522-9
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1080/10412905.1994.9699354
https://doi.org/10.1016/0031-9422(95)00522-9
https://doi.org/10.1080/10412905.1995.9698531
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1016/0031-9422(95)00522-9
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/0031-9422(95)00522-9
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1016/0031-9422(95)00522-9
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1016/0031-9422(95)00522-9
Farnesene 5281516 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698531
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698531
https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1016/0031-9422(95)00522-9
https://doi.org/10.1016/0031-9422(90)85109-S
Nerolidol 5284507 Click to see 222.37 unknown https://doi.org/10.1002/FFJ.2730100204
Norbornane, 2-methyl-3-methylene-2-(4-methyl-3-pentenyl)- 10534 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(02)00477-6
Santalene (minor) 6431197 Click to see CC(=CCCC1(C2CCC(C2)C1=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(02)00477-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
4a,5-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene 288227 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698531
Valencene 9855795 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698531
> 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/10.1016/0031-9422(95)00522-9
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(95)00522-9
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2-Methyl-3-buten-2-ol 8257 Click to see 86.13 unknown https://doi.org/10.1016/S0031-9422(02)00477-6
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Tagetone, (E)- 5368938 Click to see 152.23 unknown https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1080/10412905.1994.9699354
Tagetone, (Z)- 5368956 Click to see 152.23 unknown https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1080/10412905.1994.9699354
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Ipsenone 12402006 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.2730100204
https://doi.org/10.1016/0031-9422(90)85109-S
https://doi.org/10.1080/10412905.1994.9699354
> 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 624.60 unknown https://doi.org/10.1016/0952-3278(88)90067-1
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/10.1016/0952-3278(88)90067-1

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