Tetraclinis is a genus of evergreen coniferous trees in the cypress family, with only one species, Tetraclinis articulata. This tree is also known as arar, araar, Sictus tree, Thuja articulata, sandarac, sandarac tree, or Barbary thuja. It is found in the western Mediterranean region and is known for its distinctive appearance and medicinal properties.

Synonyms Top

Scientific name	Authority	First published in
Juniperus cunninghamii	hort. ex Carrière	Traité Gén. Conif. : 71 (1855)
Thuja articulata	Vahl	Symb. Bot. 2: 96 (1791)
Callitris articulata	H.Karst.	Deut. Fl. : 319 (1881)
Callitris macrostachya	hort. ex Steud.	Nomencl. Bot. , ed. 2, 1: 260 (1840)
Callitris quadrivalvis	Vent.	Comm. Bot. Conif. Cycad. : 46 (1826)
Callitris triquetra	hort. ex Loudon	Encycl. Trees Shrubs : 1072 (1842)
Cupressus articulata	J.Forbes	Pinet. Woburn. : 191 (1839)
Cupressus triquetra	Jacques	Ann. Fl. Pomone 5: 259 (1837)
Callitris articulata	Murb.	Contrib. Fl. Nord-Ouest Afr. Ser. 1. iv. 29 (1890) (Act. Reg Soc. Physiogr. Lund, xi.).

Common names Top

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Filter by language:

Language	Common/alternative name
English	sandarac
English	arar tree
English	sandarac gum tree
Spanish	alerce
Arabic	سندروس رباعي المصاريع
Czech	sandarakovník článkovaný
German	sandarakbaum
Esperanto	tetraklino
Persian	سندروس
Finnish	atlassypressi
French	cyprès de l'atlas
French	thuya de barbarie
French	bois de citre
Hebrew	טטרקליניס מפריק
Kabyle	thuya
koi	Тетраклинис
kv	Тетраклинис
mrj	Тетраклинис
mt	siġra tal-għargħar
mt	għargħar
Norwegian Bokmål	sandaraksypress
Polish	cyprzyk czteroklapowy
Russian	Тетраклинис
sd	چندرس
Turkish	sandarak agaci
udm	Тетраклинис
Ukrainian	Тетраклініс зчленований
Chinese	香漆柏
Chinese	四鳞柏属
Chinese	四鱗柏屬

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Western Asia
  - Palestine

Europe click to expand
- Southeastern Europe
  - Sicilia
- Southwestern Europe
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000456325
UNII	CQC5UZI50Z
USDA Plants	TEAR7
Tropicos	9400144
INPN	611328
KEW	urn:lsid:ipni.org:names:677193-1
The Plant List	kew-2516538
Open Tree Of Life	194278
Observations.org	122871
NCBI Taxonomy	13717
IUCN Red List	30318
IPNI	677193-1
iNaturalist	135549
GBIF	2684184
Freebase	/m/06_m8g
EPPO	TEIAR
EOL	1034862
USDA GRIN	310517
Wikipedia	Tetraclinis_articulata

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_046118435.1	ASM4611843v1	Scaffold	Iridian Genomes	2024-12-16	60.0x	591.17 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

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

In vitro micropropagation and conservation of endangered medicinal plant Nepeta asterotricha Rech.f. (Lamiaceae): genetic fidelity, phytochemical and biological assessment

Zamani M, Sonboli A, Goldansaz M, Mirjalili MH

Physiol Mol Biol Plants

23-Feb-2024

PMCID:	PMC10901756
doi:	10.1007/s12298-024-01416-x
PMID:	38435858

Tetraclinis articulata (Vahl) Mast.: Volatile constituents, antioxidant, antidiabetic and wound healing activities of its essential oil

Khatib S, Mahdi I, Drissi B, Fahsi N, Bouissane L, Sobeh M

Heliyon

17-Jan-2024

PMCID:	PMC10839871
doi:	10.1016/j.heliyon.2024.e24563
PMID:	38317922

Fungal Planet description sheets: 1550–1613

Crous PW, Costa MM, Kandemir H, Vermaas M, Vu D, Zhao L, Arumugam E, Flakus A, Jurjević Ž, Kaliyaperumal M, Mahadevakumar S, Murugadoss R, Shivas RG, Tan YP, Wingfield MJ, Abell SE, Marney TS, Danteswari C, Darmostuk V, Denchev CM, Denchev TT, Etayo J, Gené J, Gunaseelan S, Hubka V, Illescas T, Jansen GM, Kezo K, Kumar S, Larsson E, Mufeeda KT, Piątek M, Rodriguez-Flakus P, Sarma PV, Stryjak-Bogacka M, Torres-Garcia D, Vauras J, Acal DA, Akulov A, Alhudaib K, Asif M, Balashov S, Baral HO, Baturo-Cieśniewska A, Begerow D, Beja-Pereira A, Bianchinotti MV, Bilański P, Chandranayaka S, Chellappan N, Cowan DA, Custódio FA, Czachura P, Delgado G, De Silva NI, Dijksterhuis J, Dueñas M, Eisvand P, Fachada V, Fournier J, Fritsche Y, Fuljer F, Ganga KG, Guerra MP, Hansen K, Hywel-Jones N, Ismail AM, Jacobs CR, Jankowiak R, Karich A, Kemler M, Kisło K, Klofac W, Krisai-Greilhuber I, Latha KP, Lebeuf R, Lopes ME, Lumyong S, Maciá-Vicente JG, Maggs-Kölling G, Magistà D, Manimohan P, Martín MP, Mazur E, Mehrabi-Koushki M, Miller AN, Mombert A, Ossowska EA, Patejuk K, Pereira OL, Piskorski S, Plaza M, Podile AR, Polhorský A, Pusz W, Raza M, Ruszkiewicz-Michalska M, Saba M, Sánchez RM, Singh R, Śliwa L, Smith ME, Stefenon VM, Strasiftáková D, Suwannarach N, Szczepańska K, Telleria MT, Tennakoon DS, Thines M, Thorn RG, Urbaniak J, van der Vegte M, Vasan V, Vila-Viçosa C, Voglmayr H, Wrzosek M, Zappelini J, Groenewald JZ

Persoonia

30-Dec-2023

PMCID:	PMC11041897
doi:	10.3767/persoonia.2023.51.08
PMID:	38665977

Thymoquinone: A Promising Therapeutic Agent for the Treatment of Colorectal Cancer

Kurowska N, Madej M, Strzalka-Mrozik B

Curr Issues Mol Biol

23-Dec-2023

PMCID:	PMC10814900
doi:	10.3390/cimb46010010
PMID:	38248312

Phytochemical study on the essential oils of Callitris glaucophylla Joy Thomps. & L.A.S. Johnson, and assessment of their antioxidant, anti-enzymatic and allelopathic effects

Kochti O, Polito F, Caputo L, Marwa K, Mabrouk Y, Hamrouni L, Amri I, De Feo V

Heliyon

13-Dec-2023

PMCID:	PMC10770506
doi:	10.1016/j.heliyon.2023.e23656
PMID:	38187260

Essential Oil Molecules Can Break the Loop of Oxidative Stress in Neurodegenerative Diseases

Spisni E, Valerii MC, Massimino ML

Biology (Basel)

07-Dec-2023

PMCID:	PMC10740714
doi:	10.3390/biology12121504
PMID:	38132330

Tetraclinis articulata (Vahl) Mast. essential oil as a promising source of bioactive compounds with antimicrobial, antioxidant, anti-inflammatory and dermatoprotective properties: In vitro and in silico evidence

El Hachlafi N, Fikri-Benbrahim K, Al-Mijalli SH, Elbouzidi A, Jeddi M, Abdallah EM, Assaggaf H, Bouyahya A, Alnasser SM, Attar A, Goh KW, Ming LC, Ong SK, Mrabti HN, Chahdi FO

Heliyon

02-Dec-2023

PMCID:	PMC10758745
doi:	10.1016/j.heliyon.2023.e23084
PMID:	38169772

Inhibitory effects of Jasminum grandiflorum L. essential oil on lipopolysaccharide-induced microglia activation-integrated characteristic analysis of volatile compounds, network pharmacology, and BV-2 cell

Lu J, Zeng X, Feng Y, Li S, Wang Y, Liu Y, Chen F, Guan Z, Chen T, Wei F

Front Pharmacol

04-Aug-2023

PMCID:	PMC10436289
doi:	10.3389/fphar.2023.1180618
PMID:	37601063

Overview of the European species of the genus Clitocella (Entolomataceae, Agaricales) with notes on extralimital taxa

Vizzini A, Consiglio G, Marchetti M

Persoonia

20-Jun-2023

PMCID:	PMC10983838
doi:	10.3767/persoonia.2023.50.04
PMID:	38567261

Variation in Yield, Chemical Composition and Biological Activities of Essential Oil of Three Curcuma Species: A Comparative Evaluation of Hydrodistillation and Solvent-Free Microwave Extraction Methods

Mohanty S, Ray A, Naik PK, Sahoo A, Jena S, Das PK, Patnaik J, Panda PC, Nayak S

Molecules

30-May-2023

PMCID:	PMC10254477
doi:	10.3390/molecules28114434
PMID:	37298910

Therapeutic potential of aromatic plant extracts in Alzheimer's disease: Comprehensive review of their underlying mechanisms

Ma Y, Li Y, Yin R, Guo P, Lei N, Li G, Xiong L, Xie Y

CNS Neurosci Ther

30-Apr-2023

PMCID:	PMC10352876
doi:	10.1111/cns.14234
PMID:	37122144

Descriptive and Geometric Morphometry of the Wings of Phlebotomus sergenti Populations in Central Morocco

Abou-Elaaz FZ, Sereno D, Himmi O, Ghamizi M, Guernaoui S

J Arthropod Borne Dis

31-Mar-2023

PMCID:	PMC10440493
doi:	10.18502/jad.v17i1.13200
PMID:	37609567

Natural essential oils derived from herbal medicines: A promising therapy strategy for treating cognitive impairment

Shi A, Long Y, Ma Y, Yu S, Li D, Deng J, Wen J, Li X, Wu Y, He X, Hu Y, Li N, Hu Y

Front Aging Neurosci

16-Mar-2023

PMCID:	PMC10060871
doi:	10.3389/fnagi.2023.1104269
PMID:	37009463

Feeding Ecology of the Cuvier’s Gazelle (Gazella cuvieri, Ogilby, 1841) in the Sahara Desert

Herrera-Sánchez FJ, López O, Rodríguez-Siles J, Díaz-Portero MÁ, Arredondo Á, Sáez JM, Álvarez B, Cancio I, de Lucas J, Pérez J, Valenzuela G, Martínez-Valderrama J, Sánchez-Cerdá M, Qninba A, Virgós E, Calleja JA, Bartolomé J, Albanell E, Serrano E, Abáigar T, Gil-Sánchez JM

Animals (Basel)

06-Feb-2023

PMCID:	PMC9951649
doi:	10.3390/ani13040567
PMID:	36830354

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 / Diphenylethers
4-Methoxy-2-(4-methoxy-5-methyl-2-propan-2-ylphenoxy)-3-methyl-6-propan-2-ylphenol	251511	Click to see CC1=CC(=C(C=C1OC)C(C)C)OC2=C(C(=CC(=C2C)OC)C(C)C)O	358.50	unknown	https://doi.org/10.1021/NP0204949
> Hydrocarbon derivatives / Tropones / Tropolones
gamma-Thujaplicin	12649	Click to see CC(C)C1=CC=C(C(=O)C=C1)O	164.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
> Lignans, neolignans and related compounds / Lignan lactones
(-)-Deoxypodophyllotoxin	2203	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	https://doi.org/10.1021/NP0204949
(5aR,8aS,9R)-4-methoxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one	101618921	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC)COC3=O	428.40	unknown	https://doi.org/10.1021/NP0204949
4-methoxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one	3581045	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC)COC3=O	428.40	unknown	https://doi.org/10.1021/NP0204949
beta-Peltatin	92122	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O	414.40	unknown	https://doi.org/10.1021/NP0204949
Deoxypodophyllotoxin	345501	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	https://doi.org/10.1021/NP0204949
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(10aR)-7-hydroxy-1,1,4a-trimethyl-8-propan-2-yl-10,10a-dihydro-9H-phenanthren-2-one	162978563	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(C=CC(=O)C3(C)C)C)O	298.40	unknown	https://doi.org/10.1021/NP0204949
(1R,4aS,4bR,7S,8aR,10S)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-8a,10-diol	10958252	Click to see CC1(CCC2C3(CCCC(C3C(CC2(C1)O)O)(C)CO)C)C=C	322.50	unknown	https://doi.org/10.1021/NP0204949
(1R,4aS,4bR,7S,8aS)-7-ethenyl-8a-hydroxy-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-1-carbaldehyde	10881268	Click to see CC1(CCC2C3(CCCC(C3CCC2(C1)O)(C)C=O)C)C=C	304.50	unknown	https://doi.org/10.1021/NP0204949
(1S,4aR,4bS,7R,8aR,10aS)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-8a-ol	163074963	Click to see CC1(CCC2C3(CCCC(C3CCC2(C1)O)(C)CO)C)C=C	306.50	unknown	https://doi.org/10.1021/NP0204949
(1S,4aR,4bS,7R,8aR,10aS)-7-ethenyl-8a-hydroxy-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-1-carbaldehyde	162850775	Click to see CC1(CCC2C3(CCCC(C3CCC2(C1)O)(C)C=O)C)C=C	304.50	unknown	https://doi.org/10.1021/NP0204949
(1S,4aS,4bR,6S,7S,10aS)-7-ethenyl-6-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid	162897574	Click to see CC12CCCC(C1CCC3=CC(C(CC23)O)(C)C=C)(C)C(=O)O	318.40	unknown	https://doi.org/10.1021/NP0204949
(2S,4bS,8R,9S)-2-ethenyl-8-(hydroxymethyl)-2,4b,8-trimethyl-3,4,5,6,7,8a,9,10-octahydro-1H-phenanthren-9-ol	10859689	Click to see CC1(CCC2=C(C1)CC(C3C2(CCCC3(C)CO)C)O)C=C	304.50	unknown	https://doi.org/10.1021/NP0204949
(2S,4S,4aS,10aS)-1,1,4a-trimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,4,7-triol	21577157	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(C(CC(C3(C)C)O)O)C)O	318.40	unknown	https://doi.org/10.1021/NP0204949
(2S,4S,4aS)-1,1,4a-trimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,4,7-triol	10936061	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(C(CC(C3(C)C)O)O)C)O	318.40	unknown	https://doi.org/10.1021/NP0204949
(4aS,10aR)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one	11700871	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(=O)C3(C)C)C)O	300.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
(4aS,10aS)-7-hydroxy-1,1,4a-trimethyl-8-propan-2-yl-10,10a-dihydro-9H-phenanthren-4-one	10334865	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(C(=O)C=CC3(C)C)C)O	298.40	unknown	https://doi.org/10.1021/NP0204949
(4aS,10aS)-7-hydroxy-1,1,4a-trimethyl-8-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one	162902861	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCC(=O)C3(C)C)C)O	300.40	unknown	https://doi.org/10.1021/NP0204949
(7-Ethenyl-8a-hydroxy-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-1-yl)methyl acetate	73802947	Click to see CC(=O)OCC1(CCCC2(C1CCC3(C2CCC(C3)(C)C=C)O)C)C	348.50	unknown	https://doi.org/10.1021/NP0204949
[(1R,4aS,4bR,7S,8aS)-7-ethenyl-8a-hydroxy-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-1-yl]methyl acetate	11013502	Click to see CC(=O)OCC1(CCCC2(C1CCC3(C2CCC(C3)(C)C=C)O)C)C	348.50	unknown	https://doi.org/10.1021/NP0204949
[(1S,4aR,4bS,7R,8aR,10aS)-7-ethenyl-8a-hydroxy-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-1-yl]methyl acetate	163033782	Click to see CC(=O)OCC1(CCCC2(C1CCC3(C2CCC(C3)(C)C=C)O)C)C	348.50	unknown	https://doi.org/10.1021/NP0204949
1-Phenanthrenecarboxylic acid, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-6-hydroxy-1,4a,7-trimethyl-	577913	Click to see CC12CCCC(C1CCC3=CC(C(CC23)O)(C)C=C)(C)C(=O)O	318.40	unknown	https://doi.org/10.1021/NP0204949
1,1,4a-Trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol	432946	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O	302.50	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
1,1,4a-Trimethyl-8-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,4,7-triol	73802951	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(C(CC(C3(C)C)O)O)C)O	318.40	unknown	https://doi.org/10.1021/NP0204949
13-epi-Pimar-16-en-6alpha,8alpha,18-triol	21577150	Click to see CC1(CCC2C3(CCCC(C3C(CC2(C1)O)O)(C)CO)C)C=C	322.50	unknown	https://doi.org/10.1021/NP0204949
14-Isopropylpodocarpa-8,11,13-triene-3,13-diol	622898	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCC(C3(C)C)O)C)O	302.50	unknown	https://doi.org/10.1021/NP0204949
15-Isopimarene-8,18-diol	543955	Click to see CC1(CCC2C3(CCCC(C3CCC2(C1)O)(C)CO)C)C=C	306.50	unknown	https://doi.org/10.1021/NP0204949
7-Ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-8a,10-diol	73802945	Click to see CC1(CCC2C3(CCCC(C3C(CC2(C1)O)O)(C)CO)C)C=C	322.50	unknown	https://doi.org/10.1021/NP0204949
7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid	267302	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C	302.50	unknown	https://doi.org/10.1021/NP0204949
7-Ethenyl-8a-hydroxy-1,4a,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-1-carbaldehyde	73802948	Click to see CC1(CCC2C3(CCCC(C3CCC2(C1)O)(C)C=O)C)C=C	304.50	unknown	https://doi.org/10.1021/NP0204949
7-hydroxy-1,1,4a-trimethyl-8-propan-2-yl-10,10a-dihydro-9H-phenanthren-2-one	162978562	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(C=CC(=O)C3(C)C)C)O	298.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
7-hydroxy-1,1,4a-trimethyl-8-propan-2-yl-10,10a-dihydro-9H-phenanthren-4-one	85113858	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(C(=O)C=CC3(C)C)C)O	298.40	unknown	https://doi.org/10.1021/NP0204949
7-hydroxy-1,1,4a-trimethyl-8-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one	625254	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCC(=O)C3(C)C)C)O	300.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.14-1852 https://doi.org/10.1021/NP0204949 https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
7-Hydroxy-8-isopropyl-1,1,4a-trimethyl-4a,9,10,10a-tetrahydro-phenanthren-2(1H)-one	139080817	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(C=CC(=O)C3(C)C)C)O	298.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1021/NP0204949
Hinokiol	12310492	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O	302.50	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
Isopimaric Acid	442048	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C	302.50	unknown	https://doi.org/10.1021/NP0204949
methyl (1R,4aR,4bR,7R,9S,10aR)-7-ethenyl-9-methoxy-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	162816998	Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)C(=O)OC)C)OC)C=C	346.50	unknown	https://doi.org/10.1021/NP0204949
methyl (1R,4aR,4bS,6R,7R,10aR)-7-ethenyl-6-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	162994130	Click to see CC12CCCC(C1CCC3=CC(C(CC23)O)(C)C=C)(C)C(=O)OC	332.50	unknown	https://doi.org/10.1021/NP0204949
methyl (1R,4aR,4bS,6R,7R)-7-ethenyl-6-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	162994129	Click to see CC12CCCC(C1CCC3=CC(C(CC23)O)(C)C=C)(C)C(=O)OC	332.50	unknown	https://doi.org/10.1021/NP0204949
methyl (1R,4aR,4bS,6R,7S,10aR)-6-acetyloxy-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylate	21577156	Click to see CC(=O)OC1CC2C(=CCC3C2(CCCC3(C)C(=O)OC)C)CC1(C)C=C	374.50	unknown	https://doi.org/10.1021/NP0204949
methyl (1R,4aR,4bS,6R,7S,10aR)-7-ethenyl-6-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylate	21577155	Click to see CC12CCCC(C1CC=C3C2CC(C(C3)(C)C=C)O)(C)C(=O)OC	332.50	unknown	https://doi.org/10.1021/NP0204949
methyl (1R,4aR,4bS,6R,7S)-6-acetyloxy-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylate	11025168	Click to see CC(=O)OC1CC2C(=CCC3C2(CCCC3(C)C(=O)OC)C)CC1(C)C=C	374.50	unknown	https://doi.org/10.1021/NP0204949
methyl (1R,4aR,4bS,6R,7S)-7-ethenyl-6-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylate	11034960	Click to see CC12CCCC(C1CC=C3C2CC(C(C3)(C)C=C)O)(C)C(=O)OC	332.50	unknown	https://doi.org/10.1021/NP0204949
methyl 6-acetyloxy-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylate	73802950	Click to see CC(=O)OC1CC2C(=CCC3C2(CCCC3(C)C(=O)OC)C)CC1(C)C=C	374.50	unknown	https://doi.org/10.1021/NP0204949
methyl 7-ethenyl-6-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylate	73802949	Click to see CC12CCCC(C1CC=C3C2CC(C(C3)(C)C=C)O)(C)C(=O)OC	332.50	unknown	https://doi.org/10.1021/NP0204949
methyl 7-ethenyl-6-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylate	162994128	Click to see CC12CCCC(C1CCC3=CC(C(CC23)O)(C)C=C)(C)C(=O)OC	332.50	unknown	https://doi.org/10.1021/NP0204949
NSC 299936; trans-Totarol;Totarol	326995	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
Pimar-8(14)-en-18-oic acid	220339	Click to see CCC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C	304.50	unknown	https://doi.org/10.1021/NP0204949
Podocarpa-8,11,13-trien-3-one, 12-hydroxy-13-isopropyl-	627190	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(=O)C3(C)C)C)O	300.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
Sandaracopimaric Acid	221580	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	https://doi.org/10.1021/NP0204949
Totaradiol	9995105	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCC(C3(C)C)O)C)O	302.50	unknown	https://doi.org/10.1021/NP0204949
Totarol	92783	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCCC3(C)C)C)O	286.50	unknown	https://doi.org/10.1021/NP0204949 https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
Totarolone	22295782	Click to see CC(C)C1=C(C=CC2=C1CCC3C2(CCC(=O)C3(C)C)C)O	300.40	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.14-1852 https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291 https://doi.org/10.1021/NP0204949
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-Isopropyl-4-methoxy-5-methyl-phenol	251510	Click to see CC1=CC(=C(C=C1OC)C(C)C)O	180.24	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291 https://doi.org/10.1021/NP0204949
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
Thymohydroquinone	95779	Click to see CC1=CC(=C(C=C1O)C(C)C)O	166.22	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
Cedran-8-ol	522667	Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O	222.37	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291 https://doi.org/10.1021/NP0204949
Cedrol	65575	Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O	222.37	unknown	https://doi.org/10.1021/NP0204949 https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,2R,5S,7R,9S,12R,16R)-5-ethenyl-7-hydroxy-1,5,12-trimethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadecan-11-one	21577149	Click to see CC1(CCC2C3(CCCC4(C3C(CC2(C1)O)OC4=O)C)C)C=C	318.40	unknown	https://doi.org/10.1021/NP0204949
(1S,2R,5S,7R,9S,12R)-5-ethenyl-7-hydroxy-1,5,12-trimethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadecan-11-one	11130956	Click to see CC1(CCC2C3(CCCC4(C3C(CC2(C1)O)OC4=O)C)C)C=C	318.40	unknown	https://doi.org/10.1021/NP0204949
5-Ethenyl-7-hydroxy-1,5,12-trimethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadecan-11-one	73802944	Click to see CC1(CCC2C3(CCCC4(C3C(CC2(C1)O)OC4=O)C)C)C=C	318.40	unknown	https://doi.org/10.1021/NP0204949
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(-)-alpha-Acorenol	101306697	Click to see CC1CCC(C12CCC(=CC2)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1021/NP0204949
2-(1,8-Dimethylspiro[4.5]dec-8-en-4-yl)propan-2-ol	14105905	Click to see CC1CCC(C12CCC(=CC2)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1021/NP0204949
2-[(1R)-1,8-dimethylspiro[4.5]dec-8-en-4-yl]propan-2-ol	5316231	Click to see CC1CCC(C12CCC(=CC2)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1021/NP0204949
alpha-Acorenol	11972555	Click to see CC1CCC(C12CCC(=CC2)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1021/NP0204949
beta-Acorenol	14105907	Click to see CC1CCC(C12CCC(=CC2)C)C(C)(C)O	222.37	unknown	https://doi.org/10.1021/NP0204949
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
Thymoquinone	10281	Click to see CC1=CC(=O)C(=CC1=O)C(C)C	164.20	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.16-1291
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone	5281600	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	https://doi.org/10.1016/0031-9422(83)85032-8
Bilobetin	5315459	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O	552.50	unknown	https://doi.org/10.1016/0031-9422(83)85032-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Hinokiflavone	5281627	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	https://doi.org/10.1016/0031-9422(83)85032-8

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Tetraclinis articulata

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