Lavandula stoechas

Details Top

Internal ID UUID643fe09383e1e696500182
Scientific name Lavandula stoechas
Authority L.
First published in Sp. Pl. : 573 (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.

Lavandula stoechas, the “Spanish lavender”, has long been part of Mediterranean folk medicine. In the dry hills of Andalusia in southern Spain, the aerial parts—fresh leaves and flowers—are routinely infused as a tea to relieve cold‑related chest discomfort and to act as a mild carminative (Pardo‑de‑Santayana et al., 2007). On the island of Crete, women traditionally steep the same plant material for ten minutes to obtain a calming infusion used to ease menstrual cramps and to soothe coughs, a practice recorded by Stavropoulou et al., 2008. Across the Aegean coast of Turkey, healers boil stems and flower clusters for fifteen minutes to produce a decoction taken as a diuretic and to treat abdominal pain, an ethnobotanical survey of the region noted (Yilmaz et al., 2015). In addition to teas, the crushed leaves are sometimes macerated in warm water to make a poultice for minor skin irritations, a preparation documented in the Sardinian island communities (Cazzola et al., 2010).

A simple, safe preparation that reflects these historical customs is a mild tea. Place 1–2 teaspoons (≈2–3 g) of dried leaves and flowers into a cup, pour 250 ml of freshly boiled water over them, cover and steep for 5–10 minutes. The infusion is then strained and can be drunk up to three times a day. Because the plant contains essential‑oil components that may stimulate uterine muscles, it is not recommended for pregnant women, and large doses should be avoided by children under two; individuals with known allergies to Lamiaceae should test a small amount first.

The activity of this herbal tea is linked to well‑characterised phytochemicals. The aerial parts yield an essential oil rich in linalool, camphor, 1,8‑cineole (eucalyptol) and borneol, all documented by Da Porto et al., 2009, which together provide antispasmodic and mild sedative effects. In addition, flavonoids such as luteolin and apigenin, together with phenolic acids like rosmarinic acid, have been isolated from the plant and contribute antioxidant and anti‑inflammatory actions. These constituents align closely with the traditional therapeutic actions observed in the three cultural contexts.

Modern interest in Lavandula stoechas remains strong: recent laboratory work (Miller et al., 2022) confirms antimicrobial activity against common respiratory pathogens, while commercial herb retailers continue to sell dried L. stoechas for tea blends and essential‑oil aromatherapy, sustaining a living tradition that bridges ethnobotany and contemporary health markets.

General Uses Top

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Common products:
Lavandula stoechas yields an essential oil (≈0.5–2 % of fresh flower weight) by steam distillation of the flowering tops; the oil is marketed as “Spanish lavender oil”. The dried flower spikes are also a commercial product, sold for potpourri, sachets, and decorative bundles.

Industrial and craft applications:
The essential oil is used as a fragrance component in soaps, detergents, cleaning products, air‑fresheners and as a principal note in fine perfumery. Dried spikes are employed in craft items such as lavender wands, aromatic sachets and potpourri mixtures.

Food and beverages (non‑medicinal):
Lavender oil is listed as a GRAS flavoring in the United States (under the generic “lavender oil” category) and is authorized by the EU Flavouring Regulation (EC No 1334/2008). It is added to confectionery, baked goods, ice‑cream, syrups and to alcoholic beverages such as gin and floral liqueurs, typically at 0.01–0.05 % of product weight. Lavender honey, produced when bees forage on L. stoechas flowers, is marketed as a specialty honey with a distinctive floral aroma and amber colour. The dried flowers themselves are used as a culinary garnish and to flavour sugar, sauces and desserts.

Fragrance and cosmetics:
The oil’s aroma is characterized by a high camphor content (≈15–30 %), notable 1,8‑cineole (≈5–15 %) and lower levels of linalool/linalyl acetate than English lavender, giving a fresh, camphoraceous‑sweet profile suitable for fine fragrance, toiletries and personal‑care formulations.

Properties relevant to use:
- The monoterpene profile confers strong volatility and rapid scent diffusion, desirable in fragrance applications.
- Camphor and 1,8‑cineole are soluble in ethanol and most fragrance carriers, ensuring stable incorporation into alcohol‑based products.
- Lavender honey’s sugar composition (≈70 % glucose/fructose) and retained volatile compounds make it a natural flavour‑enhancing sweetener.

Standards and regulation:
- Food‑grade use must meet U.S. FDA GRAS status and EU Flavouring Regulation limits on added lavender oil.
- Cosmetic and fragrance use is governed by IFRA Standards for “lavender oil” and the EU Cosmetic Regulation (EC No 1223/2009); the oil must be listed as a fragrance allergen when present at ≥0.001 % in leave‑on products.
- Lavender honey sold as a food product must comply with national honey standards (e.g., Codex Alimentarius CXS 12‑1981).

Sustainability and sourcing:
Commercial L. stoechas is cultivated across the Mediterranean basin; harvest of flowering tops is performed before full bloom to maximise oil yield. The species thrives on well‑drained, limestone soils with modest irrigation, reducing environmental impact. Sustainable management includes pruning to maintain productivity and a growing shift toward certified organic production in line with EU organic regulations (EU 2018/848).

Synonyms Top

Scientific name Authority First published in
Lavandula stoechadensis St.-Lag. Ann. Soc. Bot. Lyon 7: 128 (1880)
Stoechas arabica Garsault Fig. Pl. Méd. : t. 45 (1764)
Stoechas officinarum Mill. Gard. Dict. ed. 8 : n.º 1 (1768)
Lavandula stoechas var. brachystachya Ging. Hist. Nat. Lavand. 130. 1826
Lavandula stoechas var. macrostachya Ging. Hist. Nat. Lavand. 130. 1826
Lavandula stoechas var. platyloba Briq. Lab. Alp. Mar. 463. 1895
Lavandula stoechas var. stenoloba Briq. Lab. Alp. Mar. 464. 1895
Lavandula stoechas f. microstachya Font Quer Trab. Mus. Ci. Nat. Barcelona 5: 220 1920
Lavandula stoechas f. macrostachya Font Quer Trab. Mus. Ci. Nat. Barcelona 5: 220 1920
Lavandula stoechas f. purpurea Emb. & Maire Bull. Soc. Hist. Nat. Afrique N. 24: 223 1933
Lavandula stoechas var. brevibracteolata Sennen Diagn. Nouv. 113. 1936
Lavandula stoechas f. parvibracteata Sennen Diagn. Nouv. 26 1936
Lavandula stoechas var. heterophylla Sennen Diagn. Nouv. 75. 1936
Lavandula stoechas f. rosea Maire Bull. Soc. Hist. Nat. Afrique N. 25: 314 1934

Common names Top

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Language Common/alternative name
English cassidony
English french lavender
English stechados
English stickadove
English stœchas
English stoechas
Spanish cantueso montes
Spanish cantueso común
Spanish cantueso comun
Spanish cantueso basto
Spanish cantrueso
Spanish astecados
Spanish tomillo salvaje
Spanish cantueso
Spanish cantueso fino
Spanish cantueso montés
Spanish cantueso purpureo
Spanish cantueso purpúreo
Spanish cantueso real de espana
Spanish galanita
Spanish tomillo basto
Spanish tomillo cantuoso
Spanish tomillo de cantueso
Spanish tomillo del señor
Spanish tomillo mielero
Arabic شاة أسبرم رومي
Arabic خزامى فرنسي
Arabic خزامى بحرية كتاعة
Arabic اسطوخودوس
Arabic البري الحلحال
Arabic الضرم
Arabic خزامى مكورة
Azerbaijani yunan lavandası
azb یونان لاوانداسی
br lavand-kêr
Catalan cap d'ase
Catalan caps d'ase
Catalan tomaní
co arba dritta
co piumbone
co piumbonu
Czech levandule korunkatá
Czech levandule francouzská
Czech levandule hlávkovitá
Czech levandule klasnatá
Czech levandule ouškatá
Czech levandule smilovitá
Danish sommerfugle-lavendel
German schopf-lavendel
German schopflavendel
Basque izpiliku min
Persian اسطوقدوس
Persian اسطوخودوس
Persian لاواند حقیقی
Persian اسطوقودوس
Persian اسطو خودوس
Persian استخدوس
Persian استخودوس
Persian استقدوس
Persian استقودوس
Persian استو خودوس
Persian استوخدوس
Persian استوقدوس
Persian استوقودوس
Persian اسطخدوس
Persian اسطخودوس
Persian اسطقودوس
Persian اسطقدوس
Finnish tupsulaventeli
Galician cantroxo
Hebrew אזוביון דגול
Hungarian füzéres levendula
Hungarian bóbitás levendula
Japanese フレンチラベンダー
Kabyle amezzir
Dutch franse lavendel
Dutch vlinderlavendel
Dutch kuiflavendel
Portuguese rosmaninho
Russian Лаванда стэхадская
Slovak levanduľa hlávkovitá
Turkish karabaş otu
Urdu اسطو خودوس فرانسیسی
Chinese 法国熏衣草
Chinese 法国薰衣草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Lavandula stoechas subsp. luisieri (Rozeira) Rozeira Agron. Lusit. 24: 173 (1964)
Lavandula stoechas subsp. stoechas Unknown

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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Start at 20°C; if no germination occurs within 3 months, cool seeds to 4°C for 1-2 months, then return to 20°C.

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

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Database ID/link to page
World Flora Online wfo-0000224244
UNII MTZ2ZA34ZV
USDA Plants LAST9
Tropicos 17600106
INPN 105321
KEW urn:lsid:ipni.org:names:449089-1
The Plant List kew-109094
PFAF Lavandula stoechas
Open Tree Of Life 355949
Observations.org 145953
NCBI Taxonomy 39333
IPNI 113972-3
iNaturalist 61904
GBIF 2927303
Freebase /m/054vlz
EPPO LAVST
EOL 483849
Calflora (Californian flora) 8616
USDA GRIN 21685
Wikipedia Lavandula_stoechas

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_056592055.1 ASM5659205v1 Scaffold Iridian Genomes 2026-04-05 60 413.48 Mb

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
Natural products for managing metabolic syndrome: a scoping review Abdulghani MF, Al-Fayyadh S Front Pharmacol 30-Apr-2024
PMCID:PMC11091304
doi:10.3389/fphar.2024.1366946
PMID:38746011
Insect floral visitors of thermo-Mediterranean shrubland maquis (Ajaccio, Corsica, France) Maestracci PY, Plume L, Gibernau M Biodivers Data J 25-Apr-2024
PMCID:PMC11079593
doi:10.3897/BDJ.12.e118614
PMID:38726024
Re‐evaluation of certain aspects of the EFSA Scientific Opinion of April 2010 on risk assessment of parasites in fishery products, based on new scientific data. Part 1: ToRs1–3 Koutsoumanis K, Allende A, Alvarez‐Ordóñez A, Bover‐Cid S, Chemaly M, De Cesare A, Herman L, Hilbert F, Lindqvist R, Nauta M, Nonno R, Peixe L, Ru G, Simmons M, Skandamis P, Suffredini E, Buchmann K, Careche M, Levsen A, Mattiucci S, Mladineo I, Santos MJ, Barcia‐Cruz R, Broglia A, Chuzhakina K, Goudjihounde SM, Guerra B, Messens W, Guajardo IM, Bolton D EFSA J 22-Apr-2024
PMCID:PMC11033839
doi:10.2903/j.efsa.2024.8719
PMID:38650612
Design of three-component essential oil extract mixture from Cymbopogon flexuosus, Carum carvi, and Acorus calamus with enhanced antioxidant activity Assaggaf H, Jeddi M, Mrabti HN, Ez-zoubi A, Qasem A, Attar A, Goh BH, Tan SL, Bouyahya A, Goh KW, Hachlafi NE Sci Rep 22-Apr-2024
PMCID:PMC11035653
doi:10.1038/s41598-024-59708-x
PMID:38649707
Clove Essential Oil: Chemical Profile, Biological Activities, Encapsulation Strategies, and Food Applications Liñán-Atero R, Aghababaei F, García SR, Hasiri Z, Ziogkas D, Moreno A, Hadidi M Antioxidants (Basel) 19-Apr-2024
PMCID:PMC11047511
doi:10.3390/antiox13040488
PMID:38671935
Influence of Maqian essential oil on gut microbiota and immunoresponses in type 1 diabetes: In silico study Dahab M, Idris H, Zhang P, Aladhadh M, Alatawi EA, Ming LC, Goh KW, Ser HL Heliyon 15-Apr-2024
PMCID:PMC11035065
doi:10.1016/j.heliyon.2024.e29490
PMID:38655301
The Repellent Capacity against Sitophilus zeamais (Coleoptera: Curculionidae) and In Vitro Inhibition of the Acetylcholinesterase Enzyme of 11 Essential Oils from Six Plants of the Caribbean Region of Colombia Muñoz-Acevedo A, González MC, Alonso JE, Flórez KC Molecules 12-Apr-2024
PMCID:PMC11051817
doi:10.3390/molecules29081753
PMID:38675573
Phytochemical Composition and Antimicrobial Properties of New Lavandula angustifolia Ecotypes Betlej I, Andres B, Cebulak T, Kapusta I, Balawejder M, Żurek N, Jaworski S, Lange A, Kutwin M, Pisulewska E, Kidacka A, Krochmal-Marczak B, Boruszewski P, Borysiuk P Molecules 11-Apr-2024
PMCID:PMC11052340
doi:10.3390/molecules29081740
PMID:38675563
Exploring the multifaceted bioactivities of Lavandula pinnata L. essential oil: promising pharmacological activities Haddou M, Elbouzidi A, Taibi M, Baraich A, Loukili EH, Bellaouchi R, Saalaoui E, Asehraou A, Salamatullah AM, Bourhia M, Nafidi HA, Addi M, Guerrouj BE, Chaabane K Front Chem 08-Apr-2024
PMCID:PMC11041020
doi:10.3389/fchem.2024.1383731
PMID:38660570
Biogeochemical prospecting of metallic critical raw materials: soil to plant transfer in SW Ciudad Real Province, Spain Barquero JI, Lorenzo S, Rivera S, González-Valoys AC, García-Ordiales E, Esbrí JM, Higueras P Environ Sci Pollut Res Int 06-Apr-2024
PMCID:PMC11058908
doi:10.1007/s11356-024-33097-0
PMID:38580874
Nanoformulated herbal compounds: enhanced antibacterial efficacy of camphor and thymol-loaded nanogels Abdollahi A, Fereydouni N, Moradi H, Karimivaselabadi A, Zarenezhad E, Osanloo M BMC Complement Med Ther 02-Apr-2024
PMCID:PMC10985855
doi:10.1186/s12906-024-04435-z
PMID:38566054
Comparative study of the chemical composition, antioxidant, and antimicrobial activity of the essential oils extracted from Lavandula abrialis and Lavandula stoechas: in vitro and in silico analysis Radi M, Eddardar Z, Drioiche A, Remok F, Hosen ME, Zibouh K, Ed-Damsyry B, Bouatkiout A, Amine S, Touijer H, Salamatullah AM, Bourhia M, Ibenmoussa S, Zair T Front Chem 25-Mar-2024
PMCID:PMC10999623
doi:10.3389/fchem.2024.1353385
PMID:38591060
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
The High Pressure Preservation of Honey: A Comparative Study on Quality Changes during Storage Scepankova H, Majtan J, Estevinho LM, Saraiva JA Foods 24-Mar-2024
PMCID:PMC11011302
doi:10.3390/foods13070989
PMID:38611294
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

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
Benzenebutanol 76889 Click to see 150.22 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Hydrocarbons / Polycyclic hydrocarbons
Apopinene 244024 Click to see 122.21 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Linalyl Acetate 8294 Click to see 196.29 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1016/0305-1978(96)00023-3
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1515/ZNC-2002-9-1007
https://doi.org/10.1016/0305-1978(96)00023-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-2002-9-1007
https://doi.org/10.1016/0305-1978(96)00023-3
(+-)-Fenchone 14525 Click to see 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
https://doi.org/10.1016/J.FOODCHEM.2013.05.055
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
(+)-cis-Verbenol 164888 Click to see 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
(1R,2R,5R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hexan-2-ol 439727 Click to see 154.25 unknown https://doi.org/10.1016/0305-1978(96)00023-3
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
(1S,3R,5S)-2(10)-Pinen-3-ol 12314318 Click to see 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1016/0305-1978(96)00023-3
alpha-Fenchene 28930 Click to see CC1(C2CCC1C(=C)C2)C 136.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
beta-Fenchyl alcohol 6973643 Click to see 154.25 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
https://doi.org/10.1515/ZNC-2002-9-1007
Bicyclo(3.1.1)hept-3-en-2-ol, 4,6,6-trimethyl-, (1R,2S,5R)-rel- 89664 Click to see 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Myrtenal 61130 Click to see 150.22 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Pinocarveol, (+-)- 102667 Click to see 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Sabinene hydrate 62367 Click to see CC(C)C12CCC(C1C2)(C)O 154.25 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Verbenene 6427476 Click to see CC1(C2CC1C(=C)C=C2)C 134.22 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.1515/ZNC-2002-9-1007
(+)-Menthone 443159 Click to see 154.25 unknown https://doi.org/10.1515/ZNC-2002-9-1007
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Beta-Terpineol 8748 Click to see 154.25 unknown https://doi.org/10.1515/ZNC-2002-9-1007
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Menthol 1254 Click to see 156.26 unknown https://doi.org/10.1515/ZNC-2002-9-1007
p-Menthan-3-one 6986 Click to see 154.25 unknown https://doi.org/10.1515/ZNC-2002-9-1007
Pulegone 442495 Click to see CC1CCC(=C(C)C)C(=O)C1 152.23 unknown https://doi.org/10.1515/ZNC-2002-9-1007
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> 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/10.1016/0305-1978(96)00023-3
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1016/0305-1978(96)00023-3
(1S,2R,3R,5R,7S,8S)-3,5-dihydroxy-2,6,6,11-tetramethyltricyclo[5.4.0.02,8]undec-10-en-9-one 162925839 Click to see 250.33 unknown https://doi.org/10.1016/0031-9422(88)83056-5
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene 134779875 Click to see 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0305-1978(96)00023-3
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
CID 24816380 24816380 Click to see 218.33 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Copaborneol 101289803 Click to see 222.37 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see 222.37 unknown https://doi.org/10.1016/0305-1978(96)00023-3
(1aR,4S,4aR,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 137704583 Click to see 222.37 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1016/0305-1978(96)00023-3
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-[(1R,3R,4S)-4-ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl]propan-2-ol 20057139 Click to see 222.37 unknown https://doi.org/10.1016/0305-1978(96)00023-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(1S,2R,5R,7S,9R,11R,12R,14S,15R,16S)-15-[(1R)-1-[(2R)-4,5-dimethyl-6-oxo-2,3-dihydropyran-2-yl]-1-hydroxyethyl]-12,14,15-trihydroxy-5-methoxy-2,16-dimethyl-8-oxapentacyclo[9.7.0.02,7.07,9.012,16]octadecan-3-one 162876539 Click to see 534.60 unknown https://doi.org/10.1016/0031-9422(88)83056-5

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