Santolina chamaecyparissus, commonly known as cotton lavender or lavender-cotton, is a species of flowering plant in the family Asteraceae. It is native to the western and central Mediterranean and is a small evergreen shrub growing to 50 cm tall and broad. It produces masses of yellow, button-like composite flowerheads in summer, and its aromatic, grey-green leaves can be maintained by cutting back in spring. Cultivars of this plant have been produced, and 'Nana', a dwarf form growing to 25 cm, has gained the Royal Horticultural Society's Award of Garden Merit. In cosmetics, it is used as a tonic and as an effective fumigant. It is susceptible to Phytophthora tentaculata.

Synonyms Top

Scientific name	Authority	First published in
Santolina ericoides	hort. ex Poir.	Encycl. 6: 504 (1805)
Santolina brevifolia	Jord. & Fourr.	Icon. Fl. Eur. 2: 11 (1869)
Santolina microcephala	Jord. & Fourr.	Icon. Fl. Eur. 2: 11 (1869)
Santolina lobata	Jord.	Icon. Fl. Eur. 2: 12 (1869)
Santolina provincialis	Jord. & Fourr.	Icon. Fl. Eur. 2: 9 (1869)
Santolina pallida	Salisb.	Prodr. Stirp. Chap. Allerton : 189 (1796)
Santolina ruscinonensis	Rouy	Fl. France 8: 225, in syn. (1903)
Santolina rigidula	Jord. & Fourr.	Icon. Fl. Eur. 2: 10 (1869)
Santolina marchii	Arrigoni	Webbia 32(1): 131 (1977)
Santolina pecten	Rouy	Fl. France 8: 224 (1903)
Abrotanum foemina	Garsault	Fig. Pl. Med. 2: t. 120. 1764 , nom. inval., opus utique oppressum; Descr. Pl. Anim. 89. 1767; Thell. in Bull. Herb. Boiss. Ser. II. viii. 786
Santolina homophylla	Jord. & Fourr.	Icon. Fl. Eur. 2: 8 (1869)
Santolina linearifolia	Jord. & Fourr.	Icon. Fl. Eur. 2: 12 (1869)
Santolina dentata	Moench	Methodus : 580 (1794)
Santolina intricata	Jord. & Fourr.	Icon. Fl. Eur. 2: 11 (1869)
Santolina sericea	Jord. & Fourr.	Icon. Fl. Eur. 2: 13 (1869)
Santolina valida	Jord. & Fourr.	Icon. Fl. Eur. 2: 9 (1869)
Santolina glabrescens	Jord. & Fourr.	Icon. Fl. Eur. 2: 11 (1869)
Santolina brevicaulis	Jord.	Icon. Fl. Eur. 2: 10 (1869)
Santolina squarrosa	Willd.	Sp. Pl., ed. 4 , 3: 1798 (1803)
Santolina brevidentata	Stokes	Bot. Mat. Med. iv. 172 (1812)
Santolina diversifolia	Jord. & Fourr.	Icon. Fl. Eur. 2: 9 (1869)
Santolina villosissima	Poir.	Encycl. 6: 505 (1805)
Santolina chamaecyparissus var. mariolensis	O.Bolòs & Vigo	Collect. Bot. (Barcelona) 17(1): 90 (1988)
Santolina chamaecyparissus var. teucrietorum	O.Bolòs & Vigo	Collect. Bot. (Barcelona) 17(1): 90 (1988)

Common names Top

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Filter by language:

Language	Common/alternative name
English	lavender cotton
English	algodón lavanda
English	santolina gris
Spanish	abrótano hembra
Spanish	papú
Spanish	santolina chamaecyparissus subsp. chamaecyparissus
Spanish	abrótamo hembra
Spanish	abrotano filigranado
Spanish	abrotano labrado
Spanish	abrotano montesino
Spanish	abrótano montesino
Spanish	abrotano montrino
Spanish	abrótano montrino
Spanish	abrotano serrano
Spanish	bocha basta
Spanish	bocha conejera
Spanish	bocha de cabezeta
Spanish	bocha pudenca
Spanish	bocheta
Spanish	bojetá
Spanish	boleta de san juan
Spanish	botano hembra
Spanish	boxa sanxuanera
Spanish	brotano
Spanish	cabezeta (inflorescencia)
Spanish	caja sanjuanera
Spanish	centonicon
Spanish	ciprés bajo
Spanish	cipresilla
Spanish	coscoxú
Spanish	escobas mujeriegas
Spanish	guarda ropa
Spanish	guarda-ropa
Spanish	hierba cupresillo
Spanish	hierba lombriguera hembra
Spanish	lombriguera española
Spanish	manzanilla de mahon
Spanish	manzanilla de mahón
Spanish	manzanilla del pirineo
Spanish	manzanilla mahon
Spanish	manzanilla mahón
Spanish	manzanilla salvaje
Spanish	manzanillera
Spanish	ontina
Spanish	ontina de cabeceta
Spanish	ontina de cabezetas
Spanish	ontina de cabezuelas
Spanish	pacencia
Spanish	pudidera
Spanish	salbaje de manzanilla
Spanish	sanchuanera
Spanish	santolina chamaecyparissus subespecie pecten
Spanish	santolina chamaecyparissus subsp chamaecyparissus
Spanish	santolina chamaecyparissus subsp insularis
Spanish	santolina chamaecyparissus subsp squarrosa
Spanish	santolina chamaecyparissus subsp tomentosa
Spanish	santolina chamaecyparissus subsp. insularis
Spanish	santolina chamaecyparissus subsp. pecten
Spanish	santolina chamaecyparissus subsp. squarrosa
Spanish	santolina chamaecyparissus subsp. tomentosa
Spanish	santolina chamaecyparissus var insularis
Spanish	santolina chamaecyparissus var. insularis
Spanish	santolina pinata
Spanish	te de aragón
Spanish	té de aragón
Spanish	untina
Spanish	untina de cabezuelas
Spanish	yerba cupresillo
Spanish	yerba lombriguera hembra
Arabic	قيصوم جبلي
Arabic	قيسون
Arabic	عشب بري
Arabic	بابوني
Arabic	سنطونية
Arabic	ضطرلينة
Arabic	عشب دود
Arabic	اللافر
Azerbaijani	sərvəoxşar santolina
Bulgarian	кипарисова сантолина
Catalan	espernallac
Catalan	botxes de sant joan
Catalan	camamilla de la mola
Catalan	cordonet
Catalan	esparnellac
Catalan	espernellac
Catalan	groga camamilla
Czech	svatolina cypřišová
Czech	svatolína cypřiškovitá
Welsh	hen wraig
German	graues heiligenkraut
German	heiligenblume
German	santolina ericoides
German	santolina incana
German	silberblättriges heiligenkraut
German	zypressen-heiligenkraut
German	zypressenkraut
Basque	astakamamila
Finnish	nyhähopeayrtti
French	santoline petit-cyprès
Galician	herba da loba
Galician	hierba loba
Galician	santalina común
Galician	santolina brava
Galician	gei quien lea
io	santolino
Dutch	cypressenkruid
Dutch	heiligenbloem
Polish	santolina cyprysikowata
Russian	Сантолина кипарисовидная
Chinese	绵杉菊
Chinese	银香菊

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
- South Tropical Africa
  - Zimbabwe

Asia-temperate click to expand
- Western Asia
  - Turkey

Europe click to expand
- Eastern Europe
  - Krym
  - Ukraine
- Middle Europe
  - Germany
  - Poland
  - Switzerland
- Northern Europe
  - Great Britain
  - Ireland
- Southeastern Europe
  - Bulgaria
  - Italy
  - Sicilia
  - Yugoslavia
- Southwestern Europe
  - Portugal
  - Sardegna

Northern America click to expand
- Northeastern U.S.A.
  - Massachusetts
  - New York
- Southeastern U.S.A.
  - Arkansas
  - Georgia
  - Louisiana
  - North Carolina
  - South Carolina
- Southwestern U.S.A.
  - California

Southern America click to expand
- Central America
  - Costa Rica
- Western South America
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000045085
Cornell Woody Plants	413
USDA Plants	SACH2
Tropicos	2701201
INPN	120785
Flora of Italy	5590
KEW	urn:lsid:ipni.org:names:241927-1
The Plant List	gcc-143604
Missouri Botanical Garden	277227
PFAF	Santolina chamaecyparissus
Open Tree Of Life	944231
Observations.org	121753
NCBI Taxonomy	41644
NBN Atlas	NBNSYS0000004457
Nature Serve	2.158078
IPNI	241927-1
iNaturalist	53778
GBIF	3125933
Freebase	/m/02vmdwn
EPPO	SNTCH
EOL	509719
Elurikkus	244571
Calflora (Californian flora)	7342
Wikipedia	Santolina_chamaecyparissus

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

Correction: Velasco-Amo et al. Use of traC Gene to Type the Incidence and Distribution of pXFAS_5235 Plasmid-Bearing Strains of Xylella fastidiosa subsp. fastidiosa ST1 in Spain. Plants 2022, 11, 1562

Velasco-Amo MP, Arias-Giraldo LF, Olivares-García C, Denancé N, Jacques MA, Landa BB

Plants (Basel)

11-Jan-2024

PMCID:	PMC10819106
doi:	10.3390/plants13020200
PMID:	38256851

Morphology, Molecular Phylogeny, and Fungicide Sensitivity of Phytophthora nagaii and P. tentaculata in Korea

Lee SH, Nam B, Lee DJ, Choi YJ

Mycobiology

16-Oct-2023

PMCID:	PMC10621251
doi:	10.1080/12298093.2023.2265579
PMID:	37929005

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

The role of plant growth promoting rhizobacteria in plant drought stress responses

Chieb M, Gachomo EW

BMC Plant Biol

25-Aug-2023

PMCID:	PMC10464363
doi:	10.1186/s12870-023-04403-8
PMID:	37626328

Developing Sustainable Agriculture Systems in Medicinal and Aromatic Plant Production by Using Chitosan and Chitin-Based Biostimulants

Sun W, Shahrajabian MH, Petropoulos SA, Shahrajabian N

Plants (Basel)

28-Jun-2023

PMCID:	PMC10346470
doi:	10.3390/plants12132469
PMID:	37447031

Update of the Xylella spp. host plant database – systematic literature search up to 31 December 2022

Gibin D, Pasinato L, Delbianco A

EFSA J

13-Jun-2023

PMCID:	PMC10262070
doi:	10.2903/j.efsa.2023.8061
PMID:	37325259

Essential Oils for a Sustainable Control of Honeybee Varroosis

Bava R, Castagna F, Palma E, Marrelli M, Conforti F, Musolino V, Carresi C, Lupia C, Ceniti C, Tilocca B, Roncada P, Britti D, Musella V

Vet Sci

23-Apr-2023

PMCID:	PMC10221473
doi:	10.3390/vetsci10050308
PMID:	37235392

Ecological drivers of fine-scale distribution of arbuscular mycorrhizal fungi in a semiarid Mediterranean scrubland

López-Angulo J, Matesanz S, Illuminati A, Pescador DS, Sánchez AM, Pías B, Chacón-Labella J, de la Cruz M, Escudero A

Ann Bot

28-Mar-2023

PMCID:	PMC10457037
doi:	10.1093/aob/mcad050
PMID:	36976581

Therapeutic Potential of Dopamine and Related Drugs as Anti-Inflammatories and Antioxidants in Neuronal and Non-Neuronal Pathologies

Bandala C, Cárdenas-Rodríguez N, Mendoza-Torreblanca JG, Contreras-García IJ, Martínez-López V, Cruz-Hernández TR, Carro-Rodríguez J, Vargas-Hernández MA, Ignacio-Mejía I, Alfaro-Rodriguez A, Lara-Padilla E

Pharmaceutics

18-Feb-2023

PMCID:	PMC9966027
doi:	10.3390/pharmaceutics15020693
PMID:	36840015

Anti-Trypanosomatidae Activity of Essential Oils and Their Main Components from Selected Medicinal Plants

Bailén M, Illescas C, Quijada M, Martínez-Díaz RA, Ochoa E, Gómez-Muñoz MT, Navarro-Rocha J, González-Coloma A

Molecules

02-Feb-2023

PMCID:	PMC9920086
doi:	10.3390/molecules28031467
PMID:	36771132

Chemical Profile, Anti-Microbial and Anti-Inflammaging Activities of Santolina rosmarinifolia L. Essential Oil from Portugal

Alves-Silva JM, Gonçalves MJ, Silva A, Cavaleiro C, Cruz MT, Salgueiro L

Antibiotics (Basel)

15-Jan-2023

PMCID:	PMC9854695
doi:	10.3390/antibiotics12010179
PMID:	36671380

Chitosan Edible Films and Coatings with Added Bioactive Compounds: Antibacterial and Antioxidant Properties and Their Application to Food Products: A Review

Muñoz-Tebar N, Pérez-Álvarez JA, Fernández-López J, Viuda-Martos M

Polymers (Basel)

12-Jan-2023

PMCID:	PMC9864592
doi:	10.3390/polym15020396
PMID:	36679276

Update of the Xylella spp. host plant database – systematic literature search up to 30 June 2022

Delbianco A, Gibin D, Pasinato L, Boscia D, Morelli M

EFSA J

09-Jan-2023

PMCID:	PMC9827234
doi:	10.2903/j.efsa.2023.7726
PMID:	36628332

A Morphometric Analysis of the Santolina chamaecyparissus Complex (Asteraceae)

Giacò A, De Giorgi P, Astuti G, Caputo P, Serrano M, Carballal R, Sáez L, Bacchetta G, Peruzzi L

Plants (Basel)

09-Dec-2022

PMCID:	PMC9785004
doi:	10.3390/plants11243458
PMID:	36559569

Phylogenetic affiliation of endophytic actinobacteria associated with selected orchid species and their role in growth promotion and suppression of phytopathogens

Saikia J, Mazumdar R, Thakur D

Front Plant Sci

07-Dec-2022

PMCID:	PMC9769409
doi:	10.3389/fpls.2022.1058867
PMID:	36570961

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Artemisiatriene	5320377	Click to see CC(=C)C=CC(C)(C)C=C	136.23	unknown	https://doi.org/10.1002/FFJ.2730070109
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A037
Santolina triene	519872	Click to see CC(=CC(C=C)C(=C)C)C	136.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.04.027
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[5-[(E)-4-(furan-2-yl)but-3-en-1-ynyl]thiophen-2-yl]methyl 3-methylbutanoate	14465017	Click to see CC(C)CC(=O)OCC1=CC=C(S1)C#CC=CC2=CC=CO2	314.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
[5-[4-(Furan-2-yl)but-3-en-1-ynyl]thiophen-2-yl]methyl 3-methylbutanoate	163064140	Click to see CC(C)CC(=O)OCC1=CC=C(S1)C#CC=CC2=CC=CO2	314.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
> 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/10.1002/FFJ.2730070109
Linalyl acetate	8294	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	https://doi.org/10.1002/FFJ.2730070109
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1021/NP50048A037 https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1080/10412905.1991.9697907 https://doi.org/10.1016/S0031-9422(00)86318-9
> 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/10.1021/NP50048A037
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1021/NP50048A037 https://doi.org/10.1002/FFJ.2730070109
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)86318-9
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)86318-9
(+)-Isoborneol	6973640	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730070109
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one	6973628	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1002/FFJ.2730070109
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane	6429260	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1021/NP50048A037
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/10.1002/FFJ.2730070109 https://doi.org/10.1016/S0031-9422(97)00891-1 https://doi.org/10.1021/NP50048A037
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A037
3-Thujanone	11027	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1021/NP50048A037
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A037 https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1016/S0031-9422(00)86318-9
alpha-Thujone	12304613	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1021/NP50048A037
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1021/NP50048A037 https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1016/S0031-9422(00)86318-9
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1 https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1021/NP50048A037
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1021/NP50048A037 https://doi.org/10.1002/FFJ.2730070109
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1021/NP50048A037 https://doi.org/10.1080/10412905.2000.9712173
Fenchone	14525	Click to see CC1(C2CCC(C2)(C1=O)C)C	152.23	unknown	https://doi.org/10.1021/NP50048A037
Isoborneol	6321405	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
Isoborneol, acetate	637531	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
Myrtanol	521314	Click to see CC1(C2CCC(C1C2)CO)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730070109
Myrtenal	61130	Click to see CC1(C2CC=C(C1C2)C=O)C	150.22	unknown	https://doi.org/10.1021/NP50048A037
Myrtenol	10582	Click to see CC1(C2CC=C(C1C2)CO)C	152.23	unknown	https://doi.org/10.1002/FFJ.2730070109
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1021/NP50048A037
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1021/NP50048A037
Verbenone	29025	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	unknown	https://doi.org/10.1002/FFJ.2730070109
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1021/NP50048A037
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A037
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50048A037
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/NP50048A037 https://doi.org/10.1002/FFJ.2730070109
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1021/NP50048A037 https://doi.org/10.1080/10412905.2000.9712173
beta-Terpineol	8748	Click to see CC(=C)C1CCC(CC1)(C)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730070109
Carveol	7438	Click to see CC1=CCC(CC1O)C(=C)C	152.23	unknown	https://doi.org/10.1002/FFJ.2730070109
Carvyl acetate	7335	Click to see CC1=CCC(CC1OC(=O)C)C(=C)C	194.27	unknown	https://doi.org/10.1002/FFJ.2730070109
Dihydrocarveol	12072	Click to see CC1CCC(CC1O)C(=C)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730070109
gamma-Terpineol	11467	Click to see CC(=C1CCC(CC1)(C)O)C	154.25	unknown	https://doi.org/10.1002/FFJ.2730070109
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1021/NP50048A037
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1021/NP50048A037
> 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/10.1002/FFJ.2730070109 https://doi.org/10.1021/NP50048A037
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730070109
(+)-T-Cadinol	91752279	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1021/NP50048A037
(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/10.1021/NP50048A037
(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/10.1002/FFJ.2730070109
(1S,2S,6S,7R,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	101607926	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50048A037 https://doi.org/10.1021/NP50048A037
(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/10.1021/NP50048A037
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol	6506009	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
(3R,6E)-nerolidol	11241545	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
(4aR,5S,8R,8aS)-8-hydroxy-3,8-dimethyl-5-propan-2-yl-1,4a,5,6,7,8a-hexahydronaphthalen-2-one	10014358	Click to see CC1=CC2C(CCC(C2CC1=O)(C)O)C(C)C	236.35	unknown	https://doi.org/10.1002/FFJ.2730070109
1-[(1S,3aS,4R,7S,7aR)-4-hydroxy-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone	162972359	Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O	238.37	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
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/10.1021/NP50048A037
3-Cyclohexen-1-ol, 1-(1,5-dimethyl-4-hexenyl)-4-methyl-	27208	Click to see CC1=CCC(CC1)(C(C)CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
6-Epi-beta-bisabolol	12300148	Click to see CC1=CCC(CC1)(C(C)CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane	539857	Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O	238.37	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
alpha-Bisabolol	10586	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
alpha-Cubebene	442359	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A037
alpha-Curcumene	92139	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C	202.33	unknown	https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1016/0031-9422(90)80181-F
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50048A037
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730070109 https://doi.org/10.1021/NP50048A037
Cadinol	6428423	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1021/NP50048A037
Caryophylladienol	91747928	Click to see CC1(CC2C1CCC(=C)CC(CC2=C)O)C	220.35	unknown	https://doi.org/10.1002/FFJ.2730070109
Cedrelanol	160799	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50048A037
Cubenol	11770062	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
gamma-Bisabolene, (Z)-	3033866	Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1	204.35	unknown	https://doi.org/10.1016/0031-9422(90)80181-F
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1002/FFJ.2730070109
Isocaryophyllene	5281522	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/NP50048A037
Nerolidol	8888	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
Oplopenone	6429350	Click to see CC(C)C1CCC(=C)C2C1C(CC2)C(=O)C	220.35	unknown	https://doi.org/10.1002/FFJ.2730070109
Ylangenol	179519	Click to see CC(C)C1CCC2(C3C1C2C(=CC3)CO)C	220.35	unknown	https://doi.org/10.1002/FFJ.2730070109
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/S0024-3205(99)00578-0 https://doi.org/10.1002/FFJ.2730070109
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/S0024-3205(99)00578-0 https://doi.org/10.1002/FFJ.2730070109
Alloaromadendren	91746537	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	https://doi.org/10.1021/NP50048A037 https://doi.org/10.1002/FFJ.2730070109
alpha-Gurjunene	15560276	Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C	204.35	unknown	https://doi.org/10.1021/NP50048A037
beta-Gurjunene	6450812	Click to see CC1CCC2C(C2(C)C)C3C1CCC3=C	204.35	unknown	https://doi.org/10.1021/NP50048A037
Ledum camphor	22297324	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	44583886	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	https://doi.org/10.1016/0031-9422(90)80181-F
Bicyclogermacrene	5315347	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	https://doi.org/10.1016/0031-9422(90)80181-F
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-ol	547972	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1R,2R,4S)-rel-	10583	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1002/FFJ.2730070109
Elemol	92138	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(5,6-Dihydroxy-4a-methyl-8-methylidene-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl) acetate	14681604	Click to see CC(C)C1CCC2(C(C1OC(=O)C)C(=C)CC(C2O)O)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
[(1R,2S,4aS,5R,6R,8aR)-5,6-dihydroxy-4a-methyl-8-methylidene-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalen-1-yl] acetate	14681603	Click to see CC(C)C1CCC2(C(C1OC(=O)C)C(=C)CC(C2O)O)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1002/FFJ.2730070109
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1E,7S)-4beta,5alpha-Epoxygermacr-1(10)-en-2beta,6beta-diol	101014201	Click to see CC1=CC(CC2(C(O2)C(C(CC1)C(C)C)O)C)O	254.36	unknown	https://doi.org/10.1016/0031-9422(91)83205-Y
(1R,2E,5R,6E,10S)-3,7-dimethyl-10-propan-2-ylcyclodeca-2,6-diene-1,5-diol	15699877	Click to see CC1=CC(CC(=CC(C(CC1)C(C)C)O)C)O	238.37	unknown	https://doi.org/10.1016/0031-9422(91)83205-Y
(1R,2R,4S,6R,7R,8S,11S)-4,11-dimethyl-8-propan-2-yl-5,12-dioxatricyclo[9.1.0.04,6]dodecane-2,7-diol	163185225	Click to see CC(C)C1CCC2(C(O2)C(CC3(C(C1O)O3)C)O)C	270.36	unknown	https://doi.org/10.1016/0031-9422(91)83205-Y
(1R,2R,5R,6E,10S)-7-methyl-3-methylidene-10-propan-2-ylcyclodec-6-ene-1,2,5-triol	162915562	Click to see CC1=CC(CC(=C)C(C(C(CC1)C(C)C)O)O)O	254.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
(1R,2R,5R,6R,10S)-3,7-dimethylidene-10-propan-2-ylcyclodecane-1,2,5,6-tetrol	162974517	Click to see CC(C)C1CCC(=C)C(C(CC(=C)C(C1O)O)O)O	270.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
(1R,2R,5R,6R,7Z,10S)-7-methyl-3-methylidene-10-propan-2-ylcyclodec-7-ene-1,2,5,6-tetrol	44583979	Click to see CC1=CCC(C(C(C(=C)CC(C1O)O)O)O)C(C)C	270.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
(1R,2S,3R,6R,7R,8S)-1-methyl-5-methylidene-8-propan-2-yl-11-oxabicyclo[4.4.1]undecane-2,3,7-triol	101739999	Click to see CC(C)C1CCC2(C(C(CC(=C)C(C1O)O2)O)O)C	270.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
(1S,2R,4S,6R,7R,8S,11R)-4,11-dimethyl-8-propan-2-yl-5,12-dioxatricyclo[9.1.0.04,6]dodecane-2,7-diol	162947835	Click to see CC(C)C1CCC2(C(O2)C(CC3(C(C1O)O3)C)O)C	270.36	unknown	https://doi.org/10.1016/0031-9422(91)83205-Y
(1S,4S,7S,8E,10S)-7-methyl-3-methylidene-10-propan-2-ylcyclodec-8-ene-1,4,7-triol	163016716	Click to see CC(C)C1C=CC(CCC(C(=C)CC1O)O)(C)O	254.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
(2E,6S,7R,8R)-7,8-dihydroxy-3-methyl-9-methylidene-6-propan-2-ylcyclodec-2-en-1-one	162874854	Click to see CC1=CC(=O)CC(=C)C(C(C(CC1)C(C)C)O)O	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
(5-Hydroxy-3,7-dimethyl-10-propan-2-ylcyclodeca-2,6-dien-1-yl) acetate	162918499	Click to see CC1=CC(CC(=CC(C(CC1)C(C)C)OC(=O)C)C)O	280.40	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
(5,6-Dihydroxy-3-methyl-7-methylidene-10-propan-2-ylcyclodec-2-en-1-yl) acetate	163048916	Click to see CC1=CC(C(CCC(=C)C(C(C1)O)O)C(C)C)OC(=O)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
(5,6-Dihydroxy-3,7-dimethyl-10-propan-2-ylcyclodeca-2,7-dien-1-yl) acetate	162982287	Click to see CC1=CC(C(CC=C(C(C(C1)O)O)C)C(C)C)OC(=O)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
(7,8-Dihydroxy-3-methyl-9-methylidene-6-propan-2-ylcyclodec-2-en-1-yl) acetate	72801528	Click to see CC1=CC(CC(=C)C(C(C(CC1)C(C)C)O)O)OC(=O)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
(9-Hydroxy-1,5-dimethyl-8-propan-2-yl-11-oxabicyclo[8.1.0]undec-4-en-3-yl) acetate	75051827	Click to see CC1=CC(CC2(C(O2)C(C(CC1)C(C)C)O)C)OC(=O)C	296.40	unknown	https://doi.org/10.1016/0031-9422(91)83205-Y
(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(90)80181-F
[(1R,2E,5R,6E,10S)-5-hydroxy-3,7-dimethyl-10-propan-2-ylcyclodeca-2,6-dien-1-yl] acetate	15381634	Click to see CC1=CC(CC(=CC(C(CC1)C(C)C)OC(=O)C)C)O	280.40	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
[(1R,2E,5R,6R,10S)-5,6-dihydroxy-3-methyl-7-methylidene-10-propan-2-ylcyclodec-2-en-1-yl] acetate	15381630	Click to see CC1=CC(C(CCC(=C)C(C(C1)O)O)C(C)C)OC(=O)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
[(1R,2E,5R,6R,7Z,10S)-5,6-dihydroxy-3,7-dimethyl-10-propan-2-ylcyclodeca-2,7-dien-1-yl] acetate	162982288	Click to see CC1=CC(C(CC=C(C(C(C1)O)O)C)C(C)C)OC(=O)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
[(1R,2E,6S,7R,8R)-7,8-dihydroxy-3-methyl-9-methylidene-6-propan-2-ylcyclodec-2-en-1-yl] acetate	11323939	Click to see CC1=CC(CC(=C)C(C(C(CC1)C(C)C)O)O)OC(=O)C	296.40	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
[(1S,3R,4E,8S,9R,10R)-9-hydroxy-1,5-dimethyl-8-propan-2-yl-11-oxabicyclo[8.1.0]undec-4-en-3-yl] acetate	162983528	Click to see CC1=CC(CC2(C(O2)C(C(CC1)C(C)C)O)C)OC(=O)C	296.40	unknown	https://doi.org/10.1016/0031-9422(91)83205-Y
1-Methyl-5-methylidene-8-propan-2-yl-11-oxabicyclo[4.4.1]undecane-2,3,7-triol	73047591	Click to see CC(C)C1CCC2(C(C(CC(=C)C(C1O)O2)O)O)C	270.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
3,7-Dimethyl-10-propan-2-ylcyclodeca-2,6-diene-1,5-diol	75051828	Click to see CC1=CC(CC(=CC(C(CC1)C(C)C)O)C)O	238.37	unknown	https://doi.org/10.1016/0031-9422(91)83205-Y
3,7-Dimethylidene-10-propan-2-ylcyclodecane-1,2,5,6-tetrol	162974516	Click to see CC(C)C1CCC(=C)C(C(CC(=C)C(C1O)O)O)O	270.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
4,11-Dimethyl-8-propan-2-yl-5,12-dioxatricyclo[9.1.0.04,6]dodecane-2,7-diol	85446360	Click to see CC(C)C1CCC2(C(O2)C(CC3(C(C1O)O3)C)O)C	270.36	unknown	https://doi.org/10.1016/0031-9422(91)83205-Y
6,10-Dimethyl-3-propan-2-yl-11-oxabicyclo[8.1.0]undec-6-ene-2,8-diol	75051826	Click to see CC1=CC(CC2(C(O2)C(C(CC1)C(C)C)O)C)O	254.36	unknown	https://doi.org/10.1016/0031-9422(91)83205-Y
7-Methyl-3-methylidene-10-propan-2-ylcyclodec-6-ene-1,2,5-triol	75051825	Click to see CC1=CC(CC(=C)C(C(C(CC1)C(C)C)O)O)O	254.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
7-Methyl-3-methylidene-10-propan-2-ylcyclodec-7-ene-1,2,5,6-tetrol	75051829	Click to see CC1=CCC(C(C(C(=C)CC(C1O)O)O)O)C(C)C	270.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
7-Methyl-3-methylidene-10-propan-2-ylcyclodec-8-ene-1,4,7-triol	163016715	Click to see CC(C)C1C=CC(CCC(C(=C)CC1O)O)(C)O	254.36	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
7,8-Dihydroxy-3-methyl-9-methylidene-6-propan-2-ylcyclodec-2-en-1-one	162874852	Click to see CC1=CC(=O)CC(=C)C(C(C(CC1)C(C)C)O)O	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	https://doi.org/10.1021/NP50048A037
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(90)80181-F
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(2S)-5-[(S)-hydroxy-[(2S)-4-methylidene-5-oxooxolan-2-yl]methyl]-2-propan-2-ylhex-5-enoic acid	162991788	Click to see CC(C)C(CCC(=C)C(C1CC(=C)C(=O)O1)O)C(=O)O	282.33	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
5-[Hydroxy-(4-methylidene-5-oxooxolan-2-yl)methyl]-2-propan-2-ylhex-5-enoic acid	162991787	Click to see CC(C)C(CCC(=C)C(C1CC(=C)C(=O)O1)O)C(=O)O	282.33	unknown	https://doi.org/10.1016/S0031-9422(00)90844-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	https://doi.org/10.1016/0031-9422(90)80181-F
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/PTR.2650030513
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/PTR.2650030513
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
8alpha-Tigloyloxyhirsutinolide 13-O-acetate	10002209	Click to see CC=C(C)C(=O)OC1CC(C2(CCC(O2)(C=C3C1=C(C(=O)O3)COC(=O)C)C)O)C	420.50	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol	53436347	Click to see C12C3C4C1C5(C2C3=C45)O	118.13	unknown	https://doi.org/10.1002/FFJ.2730070109
Yomogi alcohol	5315406	Click to see CC(C)(C=C)C=CC(C)(C)O	154.25	unknown	https://doi.org/10.1002/FFJ.2730070109
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
3,3,6-Trimethylhepta-1,5-dien-4-one	68346	Click to see CC(=CC(=O)C(C)(C)C=C)C	152.23	unknown	https://doi.org/10.1080/10412905.2000.9712173 https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799 https://doi.org/10.1080/10412905.1991.9697907 https://doi.org/10.1021/NP50048A037 https://doi.org/10.1002/FFJ.2730070109
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2-Hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl) acetate	327392	Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C	256.25	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
(2E,5R,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-ol	162897102	Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)O	214.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
(5R)-2-[(E)-2,4-Hexadiyne-1-ylidene]-1,6-dioxaspiro[4.4]nona-3,7-diene	44575221	Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2	198.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
(5R)-2-[(Z)-2,4-Hexadiyne-1-ylidene]-1,6-dioxaspiro[4.4]nona-3,7-diene	44575223	Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2	198.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
[(2E,5R,9S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate	162983961	Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C	256.25	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
[(2Z,5R,9S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate	162983963	Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C	256.25	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
2-Hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene	327390	Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2	198.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
> Organoheterocyclic compounds / Dihydrofurans
(2R)-2-[(E)-hept-1-en-3,5-diynyl]-2,3-dihydrofuran	162854164	Click to see CC#CC#CC=CC1CC=CO1	158.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
2-Hept-1-en-3,5-diynyl-2,3-dihydrofuran	162854162	Click to see CC#CC#CC=CC1CC=CO1	158.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
> Organoheterocyclic compounds / Dithiins
2-[4-(Dithiin-3-yl)but-1-en-3-ynyl]furan	162884586	Click to see C1=COC(=C1)C=CC#CC2=CC=CSS2	232.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
> Organoheterocyclic compounds / Heteroaromatic compounds
(Z)-1-(2-Furyl)-4-(2-thienyl)-1-buten-3-yne	5317432	Click to see C1=COC(=C1)C=CC#CC2=CC=CS2	200.26	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
2-(4-Thiophen-2-ylbut-1-en-3-ynyl)furan	78384933	Click to see C1=COC(=C1)C=CC#CC2=CC=CS2	200.26	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
2-[(E)-4-thiophen-2-ylbut-1-en-3-ynyl]furan	12811065	Click to see C1=COC(=C1)C=CC#CC2=CC=CS2	200.26	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
2-[(E)-hept-1-en-3,5-diynyl]furan	11019107	Click to see CC#CC#CC=CC1=CC=CO1	156.18	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
2-Hept-1-en-3,5-diynylfuran	85369169	Click to see CC#CC#CC=CC1=CC=CO1	156.18	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
> Organoheterocyclic compounds / Naphthopyrans
5,13,13-Trimethyl-9,18-dioxapentacyclo[8.6.2.12,6.01,12.010,19]nonadeca-2(19),3,5-trien-14-ol	162851735	Click to see CC1=C2CCOC34C2=C(C=C1)C5(CCC(C(C5C3)(C)C)O)CO4	314.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
> Organoheterocyclic compounds / Quinolidines
CID 3524402	3524402	Click to see CC1CC2CC3=NC(CCC3C4CC2C(C1)N(C4)C)CC5CC(CC6C5CCCN6C(=O)C)C	467.70	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
[5-[(E)-4-(furan-2-yl)but-3-en-1-ynyl]thiophen-2-yl]methyl acetate	14465015	Click to see CC(=O)OCC1=CC=C(S1)C#CC=CC2=CC=CO2	272.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
[5-[(Z)-4-(furan-2-yl)but-3-en-1-ynyl]thiophen-2-yl]methyl acetate	14465016	Click to see CC(=O)OCC1=CC=C(S1)C#CC=CC2=CC=CO2	272.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
[5-[4-(Furan-2-yl)but-3-en-1-ynyl]thiophen-2-yl]methanol	85768599	Click to see C1=COC(=C1)C=CC#CC2=CC=C(S2)CO	230.28	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
1-(2-Furyl)-4-(5-acetoxymethyl-2-thienyl)-1-buten-3-yne	72731781	Click to see CC(=O)OCC1=CC=C(S1)C#CC=CC2=CC=CO2	272.30	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
5-[(E)-4-(furan-2-yl)but-3-en-1-ynyl]thiophene-2-carbaldehyde	14465013	Click to see C1=COC(=C1)C=CC#CC2=CC=C(S2)C=O	228.27	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
5-[4-(Furan-2-yl)but-3-en-1-ynyl]thiophene-2-carbaldehyde	162926166	Click to see C1=COC(=C1)C=CC#CC2=CC=C(S2)C=O	228.27	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.43-0799
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	https://doi.org/10.1016/0031-9422(90)80181-F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Axillaroside	101243893	Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O	508.40	unknown	https://doi.org/10.1055/S-0028-1097749
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	https://doi.org/10.1016/0031-9422(90)80181-F
Isokaempferide	5280862	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	300.26	unknown	https://doi.org/10.1016/S0031-9422(97)00891-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin	5317284	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	https://doi.org/10.1016/S0024-3205(99)00578-0
Jaceosidin	5379096	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O	330.29	unknown	https://doi.org/10.1055/S-2008-1074873
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin	73571	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O	286.28	unknown	https://doi.org/10.1016/0031-9422(90)80181-F

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Santolina chamaecyparissus

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