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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Filter by language:

Language	Common/alternative name
English	cassidony
English	stœchas
English	stoechas
English	french lavender
English	stechados
English	stickadove
Spanish	tomillo de cantueso
Spanish	tomillo cantuoso
Spanish	cantueso
Spanish	tomillo salvaje
Spanish	astecados
Spanish	cantrueso
Spanish	cantueso basto
Spanish	cantueso comun
Spanish	cantueso común
Spanish	cantueso fino
Spanish	cantueso montés
Spanish	tomillo del señor
Spanish	tomillo mielero
Spanish	tomillo basto
Spanish	galanita
Spanish	cantueso real de espana
Spanish	cantueso purpúreo
Spanish	cantueso purpureo
Spanish	cantueso montes
Arabic	خزامى مكورة
Azerbaijani	yunan lavandası
azb	یونان لاوانداسی
br	lavand-kêr
Catalan	cap d'ase
Catalan	caps d'ase
Catalan	tomaní
co	piumbonu
co	piumbone
co	arba dritta
Czech	levandule smilovitá
Czech	levandule ouškatá
Czech	levandule klasnatá
Czech	levandule hlávkovitá
Czech	levandule francouzská
Czech	levandule korunkatá
Danish	sommerfugle-lavendel
German	schopflavendel
German	schopf-lavendel
Basque	izpiliku min
Persian	اسطوخودوس
Persian	لاواند حقیقی
Persian	اسطوقودوس
Persian	اسطوقدوس
Persian	استوقودوس
Persian	اسطو خودوس
Persian	اسطقودوس
Persian	اسطخودوس
Persian	استخدوس
Persian	استخودوس
Persian	استقدوس
Persian	استقودوس
Persian	استوخدوس
Persian	استو خودوس
Persian	استوقدوس
Persian	اسطخدوس
Persian	اسطقدوس
Finnish	tupsulaventeli
Galician	cantroxo
Hebrew	אזוביון דגול
Hungarian	bóbitás levendula
Hungarian	füzéres 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

Suggest others/fix!

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

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

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

The Role of Polyphenols in Modulating PON1 Activity Regarding Endothelial Dysfunction and Atherosclerosis

Sirca TB, Mureșan ME, Pallag A, Marian E, Jurca T, Vicaș LG, Tunduc IP, Manole F, Ștefan L

Int J Mol Sci

04-Mar-2024

PMCID:	PMC10931629
doi:	10.3390/ijms25052962
PMID:	38474211

Chitosan-Based Nanoencapsulated Essential Oils: Potential Leads against Breast Cancer Cells in Preclinical Studies

Tan WN, Samling BA, Tong WY, Chear NJ, Yusof SR, Lim JW, Tchamgoue J, Leong CR, Ramanathan S

Polymers (Basel)

08-Feb-2024

PMCID:	PMC10891598
doi:	10.3390/polym16040478
PMID:	38399856

Phenolic Content Analysis of Two Species Belonging to the Lamiaceae Family: Antioxidant, Anticholinergic, and Antibacterial Activities

Ndhlala AR, Işık M, Kavaz Yüksel A, Dikici E

Molecules

18-Jan-2024

PMCID:	PMC10821218
doi:	10.3390/molecules29020480
PMID:	38257392

Evaluation of the Potential Effect of Postbiotics Obtained from Honey Bees against Varroa destructor and Their Combination with Other Organic Products

García-Vicente EJ, Benito-Murcia M, Martín M, Rey-Casero I, Pérez A, González M, Alonso JM, Risco D

Insects

17-Jan-2024

PMCID:	PMC10816111
doi:	10.3390/insects15010067
PMID:	38249073

Aromatic oil from lavender as an atopic dermatitis suppressant

Sato H, Kato K, Koreishi M, Nakamura Y, Tsujino Y, Satoh A

PLoS One

05-Jan-2024

PMCID:	PMC10769034
doi:	10.1371/journal.pone.0296408
PMID:	38181031

Chemical Composition and Biological Properties of New Romanian Lavandula Species

Marchidan IG, Ortan A, Marcu Spinu S, Avramescu SM, Avram I, Fierascu RC, Babeanu N

Antioxidants (Basel)

16-Dec-2023

PMCID:	PMC10741150
doi:	10.3390/antiox12122127
PMID:	38136246

Mediterranean Shrub Species as a Source of Biomolecules against Neurodegenerative Diseases

Chaves N, Nogales L, Montero-Fernández I, Blanco-Salas J, Alías JC

Molecules

16-Dec-2023

PMCID:	PMC10745362
doi:	10.3390/molecules28248133
PMID:	38138621

Macaronesian Plants as Promising Biopesticides against the Crop Pest Ceratitis capitata

Tavares WR, Jiménez IA, Oliveira L, Kuhtinskaja M, Vaher M, Rosa JS, Seca AM, Bazzocchi IL, Barreto MD

Plants (Basel)

10-Dec-2023

PMCID:	PMC10747946
doi:	10.3390/plants12244122
PMID:	38140449

Linking functional composition moments of the sub-Mediterranean ecotone with environmental drivers

de Tomás Marín S, Galán Díaz J, Rodríguez-Calcerrada J, Prieto I, de la Riva EG

Front Plant Sci

08-Dec-2023

PMCID:	PMC10748396
doi:	10.3389/fpls.2023.1303022
PMID:	38143583

Tick infestation in spur-thighed tortoise population: a pilot study for unraveling epidemiological patterns and demographic consequences

Segura A, Rafael M, Vaz-Rodrigues R, Rodríguez O, Gortázar C, de la Fuente J

Exp Appl Acarol

16-Nov-2023

PMCID:	PMC10689538
doi:	10.1007/s10493-023-00863-7
PMID:	37973690

Enhanced Natural Strength: Lamiaceae Essential Oils and Nanotechnology in In Vitro and In Vivo Medical Research

Kowalczyk T, Merecz-Sadowska A, Ghorbanpour M, Szemraj J, Piekarski J, Bijak M, Śliwiński T, Zajdel R, Sitarek P

Int J Mol Sci

17-Oct-2023

PMCID:	PMC10607815
doi:	10.3390/ijms242015279
PMID:	37894959

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

Antihyperglycemic potential of the Lavandula stoechas aqueous extract via inhibition of digestive enzymes and reduction of intestinal glucose absorption

Elrherabi A, Bouhrim M, Abdnim R, Berraaouan A, Ziyyat A, Mekhfi H, Legssyer A, Bnouham M

J Ayurveda Integr Med

06-Sep-2023

PMCID:	PMC10492212
doi:	10.1016/j.jaim.2023.100795
PMID:	37683576

Comparative Evaluation between Lavender Essential Oil and Patchouli Essential Oil in Aromatherapy and Its Effect on Dental Anxiety in Children

Tripathy S, Kohli A, Sharma K, Katyayan R, Bhatnagar P, Sahar N

Int J Clin Pediatr Dent

01-Sep-2023

PMCID:	PMC10753106
doi:	10.5005/jp-journals-10005-2674
PMID:	38162239

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
4-Phenyl-1-butanol	76889	Click to see C1=CC=C(C=C1)CCCCO	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
2-(4-Methylphenyl)propan-2-ol	14529	Click to see CC1=CC=C(C=C1)C(C)(C)O	150.22	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
> Hydrocarbons / Polycyclic hydrocarbons
Apopinene	244024	Click to see CC1(C2CC=CC1C2)C	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 CC1=CCC(=CC1)C(C)C	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 CCCCCC(C=C)O	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 CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Linalyl acetate	8294	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	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 CC1=CC=C(C=C1)C(C)C	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
(1R,2R,5R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hexan-2-ol	439727	Click to see CC(C)C12CCC(C1C2)(C)O	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)-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/10.1016/0305-1978(96)00023-3
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/10.1016/0305-1978(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
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/0305-1978(96)00023-3 https://doi.org/10.1515/ZNC-2002-9-1007
beta-Fenchyl alcohol	6973643	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1515/ZNC-2002-9-1007 https://doi.org/10.1016/0305-1978(96)00023-3
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
cis-Verbenol	164888	Click to see CC1=CC(C2CC1C2(C)C)O	152.23	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Fenchone	14525	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	https://doi.org/10.1016/0305-1978(96)00023-3 https://doi.org/10.1016/J.FOODCHEM.2013.05.055
Myrtenal	61130	Click to see CC1(C2CC=C(C1C2)C=O)C	150.22	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	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
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
trans-Verbenol	89664	Click to see CC1=CC(C2CC1C2(C)C)O	152.23	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
(+)-Menthone	443159	Click to see CC1CCC(C(=O)C1)C(C)C	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 CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	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 CC(=C)C1CCC(CC1)(C)O	154.25	unknown	https://doi.org/10.1515/ZNC-2002-9-1007
Carveol	7438	Click to see CC1=CCC(CC1O)C(=C)C	152.23	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
Carvone, (+/-)-	7439	Click to see CC1=CCC(CC1=O)C(=C)C	150.22	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1515/ZNC-2002-9-1007
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 CC1CCC(C(C1)O)C(C)C	156.26	unknown	https://doi.org/10.1515/ZNC-2002-9-1007
p-Menthan-3-one	6986	Click to see CC1CCC(C(=O)C1)C(C)C	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 CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
(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 CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	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 CC1=CC(=O)C2C3C1C2(C(CC(C3(C)C)O)O)C	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 CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	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 CC1CCC(C2C13C2C(=CC3)C)C(C)C	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 CC1=CC(=O)C2C3C1C2(CCC3C(C)C)C	218.33	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Copaborneol	101289803	Click to see CC(C)C1CCC2(C3C1C(C2(CC3)C)O)C	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
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
> 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 CC1CCC2C1C3C(C3(C)C)CCC2(C)O	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 CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1016/0305-1978(96)00023-3
Globulol	101716	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	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
beta-Elemol	20057139	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	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 CC1=C(C(=O)OC(C1)C(C)(C2(C(CC3(C2(CCC4C3CC5C6(C4(C(=O)CC(C6)OC)C)O5)C)O)O)O)O)C	534.60	unknown	https://doi.org/10.1016/0031-9422(88)83056-5

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Lavandula stoechas

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