Details Top

Internal ID UUID643ff763d23e8985441608
Scientific name Pimpinella anisum
Authority L.
First published in Sp. Pl. : 264 (1753)

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.

Across the eastern Mediterranean, Pimpinella anisum is best known as a gentle tea made from its seeds. Turkish healers grind the seeds and steep one teaspoon in 200 ml of boiling water for five to ten minutes to ease flatulence and cough, recorded by Güner and Yilmaz (2006). Greek folk practitioners brew anise seed infusions for colic and menstrual cramps, described by Pyrgioti et al. (2004). In Iran, a decoction of the seeds—two teaspoons simmered ten minutes—stimulates lactation and relieves dyspepsia, noted in Zargaran et al. (2012). Each tradition cites the seed as the plant part.

Across the Levant, crushed anise leaves are used as a poultice for abdominal pain, recorded by Haddad and Al‑Khatib (2008). In North‑African Maghreb communities, a macerated tincture of whole anise flowers in 40 % ethanol is taken in drops for bronchial congestion, described by Benabdallah and Boudia (2015). In Indian Ayurvedic practice, Shatapushpa (the Sanskrit name for anise) is prepared by soaking powdered seeds in water for an hour to make a decoction taken before meals to aid digestion, as summarized by Sharma (2015). These preparations rely on the seed or aerial parts, showing the plant's versatility as an herbal remedy.

To make a traditional tea, place two teaspoons (about 3 g) of lightly crushed anise seeds in a tea infuser, pour 250 ml of boiling water over them, cover, and steep for 7–10 minutes before removing the seeds. Drink the warm infusion up to three times a day. Safety note: the essential oil contains trans‑anethole, which in high doses can stimulate uterine activity, so pregnant women should limit intake to no more than one cup a day and avoid it in the first trimester. Do not give anise tea to infants under six months, and stop use if irritation occurs.

The therapeutic actions of anise are largely due to its essential‑oil profile, dominated by trans‑anethole (often 70‑90 % of the oil) with secondary compounds such as estragole, limonene, and p‑anisic acid. The seed also contains coumarins like scopoletin and flavonoids such as quercetin, which together provide antispasmodic, carminative, and expectorant effects documented in pharmacological studies (Mills & Bone, 2000). Today, anise is a common culinary spice and a commercial herbal ingredient; its essential oil and dried seeds are sold in health‑food stores, and modern clinical trials are evaluating its impact on gastrointestinal motility and respiratory health. This blend of longstanding folk tradition and contemporary scientific interest keeps Pimpinella anisum valuable in both kitchen and apothecary.

General Uses Top

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Common products:
The seed yields anise essential oil (distilled) and oleoresins used as flavoring agents. Processed forms include powdered spice, ground seed, crushed seed, and tinctures/bitters formulations for beverage flavoring. The major constituent is trans-anethole (typically 80–95%), with minor components such as estragole, p-anisaldehyde, and limonene.

Industrial and craft applications:
Essential oil is used in flavor compositions for alcoholic beverages (e.g., ouzo- and sambuca-style spirits), liqueurs, and nonalcoholic syrups. It also functions as a fragrance in soaps, detergents, and cleaning products. Oleoresins are employed as standard flavoring ingredients in food processing.

Food and beverages (non-medicinal):
Seeds are used whole or ground as a culinary spice in breads, cakes, confectionery, and savory dishes. Oil and oleoresins are standard flavoring components in beverage bases, syrups, and bakery formulations; standardized solutions of eugenol or estragole derived from anise are used as analytical standards in gas chromatography–mass spectrometry (GC–MS) flavor profiling.

Colorants and tanning:
No documented use as a dye, ink, or tanning agent is established for this taxon.

Wood and fiber:
No documented timber or fiber use is established for this taxon.

Fragrance and cosmetics:
Anise oil imparts a characteristic sweet-spicy note used in perfumes and soaps, and as a scenting agent in household products.

Properties relevant to use:
The seed essential oil is rich in phenylpropene trans-anethole, which confers a high odor activity value and stability under neutral-to-alkaline conditions. Density and refractive index are consistent with published specifications for Pimpinella anisum oil; the oil is soluble in ethanol and used at low concentrations due to its potency.

Standards and regulation:
Aniseed oil conforms to international standards for essential oils; the International Organization for Standardization (ISO) specifies limits for trans-anethole and related physicochemical parameters (ISO 3475). Flavoring use in foods and beverages is governed by regional additive regulations (e.g., EU Flavouring Regulation (EC) No 1334/2008 and FEMA GRAS listings in the United States).

Sustainability and sourcing:
Global production is concentrated in Mediterranean and Near Eastern countries. Sustainable practices emphasize maintained seed quality (oil content and anethole levels), avoidance of admixture with other Pimpinella species, and traceability to minimize adulteration with oils from Illicium verum (star anise). Cultivation is not reported as threatened.

Scientific/model use:
The draft genome sequence of Pimpinella anisum has been published, providing reference genomic resources for Apiaceae phylogeny and studies of essential-oil biosynthesis pathways.

Synonyms Top

Scientific name Authority First published in
Ptychotis vargasiana DC. Prodr. 4: 109 (1830)
Anisum odoratum Raf. Good Book : 52 (1840)
Anisum officinale DC. Prodr. 4: 122 (1830)
Anisum officinarum Moench Methodus : 100 (1794)
Anisum vulgare Gaertn. Fruct. Sem. Pl. 1: 23 (1788)
Apium anisum Crantz Cl. Umbell. Emend. : 101 (1767)
Carum anisum Baill. Hist. Pl. 7: 119, 178 (1879)
Selinum anisum E.H.L.Krause Deutschl. Fl. Abbild. , ed. 2, 12: 56 (1904)
Sison anisum Spreng. Mag. Neuesten Entdeck. Gesammten Naturk. Ges. Naturf. Freunde Berlin 6: 260 (1812)
Tragium anisum Link Enum. Hort. Berol. Alt. 1: 285 (1821)
Pimpinele anisa St.-Lag. Ann. Soc. Bot. Lyon vii. (1880) 131.
Pimpinella palmetorum Steud. Nomencl. Bot. [Steudel], ed. 2. 2: 335. 1841
Tragium palmetorum Hochst. & Steud. ex Steud. Nomencl. Bot. , ed. 2, 2: 696 (1841)
Pimpinella anisum var. cultum Alef. Landw. Fl. : 154 (1866)

Common names Top

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Language Common/alternative name
English anise burnet saxifrage
English anise
English the anise plant
Spanish anís
Spanish anis verde
Spanish anís verde
Spanish matalahuga
Spanish matalahúga
Spanish matalahuva
Spanish matalahúva
Spanish matalauva
Spanish matalaúva
Spanish saunf
Afrikaans anys
Arabic آنسون
Arabic أنيسون
Arabic ينسون
Arabic اليانسون
Arabic كَمُّونُ الحُلْوُ
Arabic يانسسسون
Arabic الأنيسون
Arabic حبة حلوة
Arabic نيسوون
Arabic يانسون
Azerbaijani adi xırdazirə
Azerbaijani adi cirəgülü
azb جیره
ba Әнис үләне
bcl anis
Belarusian Аніс
Bulgarian анасон
Tibetan དྲི་ཞིམ་སོན་ཅན་
Tibetan དྲི་ཞིམ་སོན་ཅན།
Bosnian anis
Catalan matafaluga
Catalan anís verd
Catalan anisada
Catalan anís
Czech bedrník anýz
Czech anýz
cv Анис
Welsh anise
Welsh aniseed
Welsh anis
Danish anis
German anis
Greek Άνισο
Greek Γλυκάνισος
Esperanto anizo
Estonian harilik aniis
Basque anis
Persian انیسون
Finnish anisruoho
Finnish anis
French anis
French anis vert
frr anis
Galician anís
Manx anis
Manx lus anis
Manx lus yn anis
Hausa anise
Hebrew כמנון האניס
Hebrew כמנון ירוק
Hebrew אניס
Croatian anis
Upper Sorbian anis
Hungarian édeskömény
Hungarian ánizs
Armenian անիսոն
Indonesian adas manis
io anizo
Icelandic anís
Italian anice comune
Italian anice
Italian anice verde
Italian anice volgare
Japanese アニシード
Japanese アニス
jv adas legi
Georgian ანისული
Kabyle Ḥeb leḥlawa
Kazakh Анис
Kazakh Бәден
Korean 아니스
ku anason
ku anîs
ku anix
ku sorê
ku anesûn
Cornish anis
lb anäis
lld ciuites
Lithuanian anyžius
Lithuanian paprastasis anyžius
Lithuanian anyžinė ožiažolė
Latvian anīss
Latvian parastais anīss
Malagasy anisy
Macedonian анасон
mrj Анис
Malay jintan manis
nap annese
nap airella
nap pempinella
Norwegian Bokmål anis
Dutch anijs
Norwegian Nynorsk anis
oc anís
os Хорнæмыгон
pcd anis
pcd anéte
pcd an·nisse
Polish anyżek
Polish biedrzeniec anyż
Portuguese anis
Quechua anís
Quechua anis
Romanian anason
Russian анис
Russian бедренец анисовый
Russian анис обыкновенный
sc anis
scn zammù
sd پلاجيري
Samogitian anėžė
Serbo-Croatian Анис
Slovak bedrovník anízový
Slovenian janež
Slovenian sladki janež
Slovenian bedrenec
Slovenian laški janež
Albanian anasoni
Serbian Аниш
Serbian Анасон
Serbian Аниж
Serbian Слатки јанеж
Serbian Слатки коморац
Serbian Слатки копар
Serbian Слатки кумин
Serbian анис
Swedish anis
Tamil சோம்பு
Telugu కుప్పి సోపు నూనె
tg Анис
Thai เทียนสัตตบุษย์
Turkish anason
tt Гади әнис
udm Анис
udm Калямпер
Ukrainian Аніс звичайний
Ukrainian Ганус
Ukrainian Аніс
Urdu انیسوں
Uzbek arpabodiyon
vec àneze
Vietnamese tiểu hồi hương
Vietnamese tiểu hồi
Vietnamese tiểu hồi cần
Chinese 羊洪膻
Chinese 洋茴香
Chinese 茴芹
Chinese 茴芹*(突蕨茴芹、茴香、洋茴香)
Chinese 西洋茴香
Chinese 茴香
Chinese 突蕨茴芹

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Arabian Peninsula
      • Oman
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
    • Indo-China
      • Laos
  • Europe
    • Eastern Europe
      • Belarus
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
    • Northern Europe
      • Denmark
      • Norway
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France
      • Portugal
      • Spain
  • Southern America
    • Brazil
      • Brazil South
    • Caribbean
      • Leeward Islands
      • Trinidad-Tobago
    • Central America
      • Guatemala
    • Northern South America
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000390925
UNII HO63CL229O
USDA Plants PIAN3
Tropicos 1700194
INPN 113554
Flora of Italy 3479
KEW urn:lsid:ipni.org:names:846658-1
The Plant List kew-2402426
Open Tree Of Life 700330
Observations.org 7189
NCBI Taxonomy 271192
NBN Atlas NBNSYS0200002887
Nature Serve 2.154075
IPNI 846658-1
iNaturalist 166878
GBIF 5371877
Freebase /m/0hyn4
EPPO PIMAN
EOL 581422
Elurikkus 6272
US Library of Congress sh85005298
USDA GRIN 28395
Wikipedia Anise
PFAF Pimpinella anisum

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
Impact of silver nanoparticles on secondary metabolite composition and toxicity in anise (Pimpinella anisum L.) callus culture Ulusoy E, Bozkurt A, Durmaz S, Servi H, Vardar F, Erisen S BMC Plant Biol 04-May-2024
PMCID:PMC11069286
doi:10.1186/s12870-024-05067-8
PMID:38702604
Chemical composition and biological activities of essential oils of seven Cultivated Apiaceae species Önder S, Periz ÇD, Ulusoy S, Erbaş S, Önder D, Tonguç M Sci Rep 02-May-2024
PMCID:PMC11066118
doi:10.1038/s41598-024-60810-3
PMID:38698117
An overwinter protocol for detecting wolverines and other carnivores at camera traps paired with automated scent dispensers Long RA, MacKay P, Sauder JD, Sinclair M, Aubry KB, Raley CM Ecol Evol 02-May-2024
PMCID:PMC11066567
doi:10.1002/ece3.11290
PMID:38706935
Effect of Maternal Flavour Conditioning Combined with Organic and Inorganic Iron-Supplemented Creep Feed on Piglet Performance and Haemoglobin Status Kristen R, Bathgate R, Cronin GM, Hall E, Possell M, O’Shea CJ Animals (Basel) 23-Apr-2024
PMCID:PMC11082972
doi:10.3390/ani14091263
PMID:38731271
Petroselinum crispum L., essential oil as promising source of bioactive compounds, antioxidant, antimicrobial activities: In vitro and in silico predictions Nouioura G, El fadili M, El Hachlafi N, Abuelizz HA, Elidrissi AE, Ferioun M, Soulo N, Er-rahmani S, Lyoussi B, Derwich E Heliyon 16-Apr-2024
PMCID:PMC11040043
doi:10.1016/j.heliyon.2024.e29520
PMID:38660278
Ethnobotanical survey on herbal remedies for the management of type 2 diabetes in the Casablanca-Settat region, Morocco Arraji M, Al Wachami N, Boumendil K, Chebabe M, Mochhoury L, Laamiri FZ, Barkaoui M, Chahboune M BMC Complement Med Ther 15-Apr-2024
PMCID:PMC11017650
doi:10.1186/s12906-024-04468-4
PMID:38622669
Anthriscus sylvestris—Noxious Weed or Sustainable Source of Bioactive Lignans? Berežni S, Mimica-Dukić N, Domina G, Raimondo FM, Orčić D Plants (Basel) 12-Apr-2024
PMCID:PMC11053937
doi:10.3390/plants13081087
PMID:38674496
Obtaining Microbiologically Safe Hatching Eggs from Hatcheries: Using Essential Oils for Integrated Sanitization Strategies in Hatching Eggs, Poultry Houses and Poultry Oliveira GD, McManus C, Vale IR, dos Santos VM Pathogens 18-Mar-2024
PMCID:PMC10974541
doi:10.3390/pathogens13030260
PMID:38535603
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
Heavy Metal Bioaccumulation in Peruvian Food and Medicinal Products Tejada-Purizaca TR, Garcia-Chevesich PA, Ticona-Quea J, Martínez G, Martínez K, Morales-Paredes L, Romero-Mariscal G, Arenazas-Rodríguez A, Vanzin G, Sharp JO, McCray JE Foods 29-Feb-2024
PMCID:PMC10931273
doi:10.3390/foods13050762
PMID:38472875
Adulticidal synergy of two plant essential oils and their major constituents against the housefly Musca domestica and bioassay on non-target species Soonwera M, Moungthipmalai T, Puwanard C, Sittichok S, Sinthusiri J, Passara H Heliyon 27-Feb-2024
PMCID:PMC10920383
doi:10.1016/j.heliyon.2024.e26910
PMID:38463861
Safety and efficacy of a polyherbal formulation from traditional Persian medicine in patients with calcium kidney stones: A randomized, double-blinded clinical trial Ansari R, Karimzade I, Nimrouzi M, Ezatzadegan S, Hosseini MM, Zarshenas MM J Res Med Sci 23-Feb-2024
PMCID:PMC10956567
doi:10.4103/jrms.jrms_670_22
PMID:38524751
Plants in Menstrual Diseases: A Systematic Study from Italian Folk Medicine on Current Approaches Mazzei R, Genovese C, Magariello A, Patitucci A, Russo G, Tagarelli G Plants (Basel) 22-Feb-2024
PMCID:PMC10935160
doi:10.3390/plants13050589
PMID:38475436
A survey into the utilization of probiotics and medicinal plants among individuals afflicted with gastrointestinal disorders in healthcare institutions in Saïda, Algeria Tazi LA, Benabdesslem Y, Amara S, Hachem K Libyan J Med 18-Feb-2024
PMCID:PMC10878339
doi:10.1080/19932820.2024.2317492
PMID:38369815
Exploring the Efficacy of Four Apiaceae Essential Oils against Nine Stored-Product Pests in Wheat Protection Kavallieratos NG, Eleftheriadou N, Boukouvala MC, Skourti A, Filintas CS, Gidari DL, Maggi F, Rossi P, Drenaggi E, Morshedloo MR, Ferrati M, Spinozzi E Plants (Basel) 15-Feb-2024
PMCID:PMC10893152
doi:10.3390/plants13040533
PMID:38498519

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1021/JF040083T
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown https://doi.org/10.1007/BF00629778
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methoxybenzaldehyde 31244 Click to see 136.15 unknown https://doi.org/10.1007/BF00629778
Benzaldehyde 240 Click to see 106.12 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
1-(4-Methoxyphenyl)propane-1,2-diol 3016654 Click to see CC(C(C1=CC=C(C=C1)OC)O)O 182.22 unknown https://doi.org/10.1248/CPB.50.1460
1-(p-Methoxyphenyl)-2-propanone 31231 Click to see 164.20 unknown https://doi.org/10.1021/JF9708958
Erythro Anethole Glycol 9799166 Click to see 182.22 unknown https://doi.org/10.1248/CPB.50.1460
> Benzenoids / Phenol esters
[4-methoxy-2-[(2S,3R)-3-methyloxiran-2-yl]phenyl] (2R)-2-methylbutanoate 162948610 Click to see CCC(C)C(=O)OC1=C(C=C(C=C1)OC)C2C(O2)C 264.32 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
[4-methoxy-2-[(2S,3S)-3-methyloxiran-2-yl]phenyl] (2R)-2-methylbutanoate 162948609 Click to see 264.32 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
[4-methoxy-2-[(E)-prop-1-enyl]phenyl] (2R)-2-methylbutanoate 102340671 Click to see 248.32 unknown https://doi.org/10.1515/ZNB-1976-0233
https://doi.org/10.1016/S0031-9422(98)00022-3
4-Methoxy-2-(prop-1-en-1-yl)phenyl 2-methylbutanoate 69864932 Click to see 248.32 unknown https://doi.org/10.1515/ZNB-1976-0233
https://doi.org/10.1016/S0031-9422(98)00022-3
Thellungianin G 545130 Click to see 264.32 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Benzenoids / Phenol ethers / Anisoles
1-Methoxy-4-Prop-1-Enylbenzene 7703 Click to see 148.20 unknown https://doi.org/10.1515/ZNC-1988-1-211
https://doi.org/10.1055/S-2004-827203
https://doi.org/10.1016/S0031-9422(98)00022-3
https://doi.org/10.1021/JF00034A048
https://doi.org/10.1021/JF9708958
Anethole 637563 Click to see 148.20 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
https://doi.org/10.1007/BF00629778
https://doi.org/10.1021/JF9708958
https://doi.org/10.1515/ZNC-1988-1-211
https://doi.org/10.1055/S-2004-827203
https://doi.org/10.1021/JF00034A048
https://doi.org/10.1021/ED077P361
Anethole, (Z)- 1549040 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1007/BF00629778
https://doi.org/10.1016/S0031-9422(98)00022-3
Estragole 8815 Click to see 148.20 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
https://doi.org/10.1007/BF00629778
> Benzenoids / Phenols / Cresols / Meta cresols
M-Cresol 342 Click to see 108.14 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Benzenoids / Phenols / Methoxyphenols
(e)-3-Hydroxyanethole 18539717 Click to see 164.20 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1007/BF00629778
Guaiacol 460 Click to see 124.14 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane 15600 Click to see 142.28 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
CID 555328 555328 Click to see 162.27 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Pregeijerene 21160126 Click to see 162.27 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Lipids and lipid-like molecules / Endocannabinoids
1,3-Dihydroxypropan-2-yl 3,8-diacetyloxyicosanoate 163021367 Click to see 502.70 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
CID 14484636 14484636 Click to see CC(=CCCC(C)(C=C)O)COC1C(C(C(C(O1)CO)O)O)O 332.39 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Lauryl Alcohol 8193 Click to see 186.33 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> 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/10.1016/S0031-9422(98)00022-3
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1007/BF00629778
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1007/BF00629778
(+)-Sabinene 10887971 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1007/BF00629778
alpha-Bergamotene 86608 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
alpha-CIS-BERGAMOTENE 6429303 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1007/BF00629778
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1007/BF00629778
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> 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(98)00022-3
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
(L)-alpha-terpineol 443162 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
https://doi.org/10.1007/BF00629778
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
https://doi.org/10.1007/BF00629778
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(3S,4S)-4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexene 12310053 Click to see 162.27 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
(3S,4S)-4-ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexene 10607083 Click to see CC(=C)C1C=CCCC1(C)C=C 162.27 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene 442360 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
(+)-beta-Sesquiphellandrene 11106487 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene 403919 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
2-Methyl-5-(6-methylhept-5-en-2-yl)cyclohexa-1,3-diene 521253 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
7-Epizingiberene 21729595 Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene 10407 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Sesquiphellandrene 519764 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-(prop-1-en-2-yl)cyclohexyl)propan-2-ol 547972 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Elemol 92138 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Chamazulene 10719 Click to see 184.28 unknown https://doi.org/10.1007/BF00629778
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-Deoxy-D-threitol 6398419 Click to see 106.12 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
1-Deoxy-l-erythritol 12241264 Click to see CC(C(CO)O)O 106.12 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-[2-(4-methoxyphenyl)ethoxy]oxane-3,4,5-triol 584315 Click to see 314.33 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
Benzyl-beta-d-glucopyranoside 13254166 Click to see 270.28 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Isotachioside 15098566 Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
Tachioside 11962143 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
Vanilloloside 44577222 Click to see COC1=C(C=CC(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown https://doi.org/10.1016/S0031-9422(03)00179-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Heptanal 8130 Click to see 114.19 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
Octanal 454 Click to see 128.21 unknown https://doi.org/10.1016/S0031-9422(98)00022-3
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives
Benzyle aminopurine 53445306 Click to see 225.25 unknown https://doi.org/10.1007/BF00397528
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines / 6-alkylaminopurines
Isopentenyladenine 92180 Click to see 203.24 unknown https://doi.org/10.1007/BF00397528
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1139/B91-065
https://doi.org/10.1055/S-2006-959644
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1055/S-2006-959644
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1055/S-2006-959644
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin 68229 Click to see 228.24 unknown https://doi.org/10.1007/BF00993733
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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/JF040083T

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