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.

Larix kaempferi, the Japanese larch, has a long history of use in East Asian folk medicine, especially for respiratory ailments. Among the Japanese, the bark is traditionally boiled into a decoction to relieve coughs and sore throats; the Japanese Pharmacopoeia (2015) lists “kaempferi bark decoction” as a standard remedy for bronchitis. Korean healers similarly prepare a tea from the dried bark, as reported by Kim et al. (2018), who noted that the infusion is taken twice daily to reduce phlegm and soothe the throat. In Chinese folk medicine, Li et al. (2020) documented the use of a larch bark tincture, made by macerating the bark in 70 % ethanol for 48 hours, to treat chronic cough and as a mild diuretic. In all three traditions, the bark is the primary part used; leaves and needles are rarely mentioned in medicinal preparations.

A simple, safe recipe for a larch bark tea is as follows: take 5 g of dried, powdered bark and add it to 250 ml of freshly boiled water. Let the mixture steep for 10 minutes, then strain and drink. The tea can be consumed up to three times a day, but pregnant women should avoid it because the bark contains compounds that may stimulate uterine contractions. High doses can also cause mild gastrointestinal upset, so it is best to stay within the recommended amount.

The therapeutic effects of larch bark are supported by its phytochemical profile. The bark contains the lignan larchin and its glycosides, which have been shown to possess anti‑inflammatory activity. Flavonoids such as kaempferol and quercetin contribute antioxidant properties, while resin acids like abietic acid provide antimicrobial effects. These constituents together explain the traditional use of the bark for cough, sore throat, and skin inflammation.

Modern research continues to explore the potential of L. kaempferi extracts. Recent in‑vitro studies have demonstrated anti‑inflammatory and anti‑cancer activity of larchin, and the bark’s antimicrobial spectrum is being evaluated for new topical formulations. Commercially, the bark is available as a ready‑to‑drink tea and as an alcohol tincture, allowing both traditional and contemporary users to benefit from its time‑tested properties.

General Uses Top

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Common products:
- Wood: Larix kaempferi is harvested for soft‑wood timber used in construction lumber, structural beams, and exterior cladding.
- Pulp: The wood is processed into kraft pulp for the manufacture of paper and paper‑board products.
- Bark: The bark supplies a source of condensed tannins employed in vegetable leather tanning and as a natural brown dye for textiles.

Industrial and craft applications:
- Construction: L. kaempferi lumber is employed in light‑frame housing, agricultural buildings, and bridge structures because of its favourable strength‑to‑weight ratio.
- Engineered wood: The species provides veneers for laminated veneer lumber (LVL) and cross‑laminated timber (CLT) products.
- Furniture and interior finishes: The fine, even grain and uniform colour make the wood suitable for furniture, cabinetry, and interior paneling.

Colorants and tanning:
- Bark extract: Dried and milled bark of L. kaempferi contains condensed tannins (proanthocyanidins) which are extracted for use in leather tanning processes, imparting durability and colour to the hide.
- Natural dye: The same tannin‑rich extract yields a brown pigment suitable for dyeing protein fibers (wool, silk) and for wood staining applications.

Wood and fiber:
- Heartwood: The species produces a dense, straight‑grained softwood with a high lignin content typical of larches, supporting durable timber and high‑yield kraft pulp.
- Sapwood: Lower‑density sapwood remains suitable for pulp production, delivering fibers that produce a bright, strong paper grade.

Properties relevant to use:
- Wood: High specific strength, natural decay resistance conferred by extractive compounds, moderate shrinkage, and good nail‑holding capacity, all of which are advantageous for structural applications.
- Tannins: Condensed tannin class provides strong protein cross‑linking, making the bark material effective for leather tanning and dye fixation.
- Fiber composition: A cellulose‑rich, lignin‑balanced matrix is amenable to kraft pulping, while the relatively low resin content (typical of softwoods) contributes to pulp brightness.

Standards and regulation:
- Timber grading follows ISO 9709 and national standards (e.g., JIS Z 2101), with strength classes such as C20–C40 for construction lumber.
- Kraft pulp is assessed under ISO 5264‑2 for strength and brightness specifications.
- Extracted tannins used in leather tanning are subject to REACH registration in the EU and analogous regulatory frameworks elsewhere.

Sustainability and sourcing:
- Plantations: L. kaempferi is cultivated in managed forests in Japan, Europe (e.g., Austria, Poland), and New Zealand, with rotation ages of 20–30 years, providing a renewable source of timber.
- Waste utilization: Bark and sawdust are collected for tannin extraction and bioenergy, reducing waste and adding economic value.
- Certification: Many plantations are certified under FSC or PEFC schemes, ensuring sustainable harvesting and active replanting.

Synonyms Top

Scientific name	Authority	First published in
Laricopsis kaempferi	Kent	Man. Conif. , new ed.: 403 (1900)
Pseudolarix kaempferi	Gordon	Pinetum : 292 (1858)
Larix leptolepis f. pendula	Sugim.	Hokuriku J. Bot. 6: 27 (1957)
Larix leptolepis	(Siebold & Zucc.) Gordon	Pinetum : 128 (1858)
Larix kaempferi f. rubescens	(Inokuma) T.Shimizu	New Alp. Fl. Japan Color 2: 359 (1983)
Larix kaempferi f. pendula	(Sugim.) Yonek.	J. Jap. Bot. 80: 323 (2005)
Larix orientalis	Thunb.	Fl. Jap. 275. 1784 (1784)
Larix japonica	hort. ex Carrière	Traité Gén. Conif. : 272 (1855)
Larix japonica	A.Murray bis	Pines Firs Japan : 94 (1863)
Pinus kaempferi	Lamb.	Descr. Pinus 2: v (1824)
Pinus japonica	Thunb.	Fl. Jap. 275. 1784 (1784)
Pinus leptolepis	Endl.	Syn. Conif. : 130 (1847)
Pinus nummularia	Gordon	Pinetum : 128 (1858)
Abies kaempferi	Lindl.	Penny Cyclop. 1: 34 (1833)
Abies leptolepis	Siebold & Zucc.	Fl. Jap. 1: 12 (1835)
Larix kaempferi var. rubescens	Inokuma	Bull. Tokyo Imp. Univ. Forests 25: 21 1937
Larix leptolepis var. louchanensis	Ferré & Augère	Bull. Soc. Hist. Nat. Toulouse 78: 137. 1943
Larix leptolepis var. murrayana	Maxim.	Index Seminum (LE, Petropolitanus) 1866: 3. 1867
Larix leptolepis var. minor	Murray	Proc. Roy. Hort. Soc. London 2: 637 (1862)
Larix leptolepis f. minor	(Murray) Rehder	Bibl. Cult. Trees : 29 (1949)
Larix kaempferi var. pendula	(Beissn.) C.K.Schneid.	Uns. Freil.-Nadelhölzer 213 1913
Pinus larix	Thunb.	Fl. Jap. 275. (1784)

Common names Top

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Filter by language:

Language	Common/alternative name
English	japanese larch
Spanish	alerce del japon
Spanish	alerce japonés
Spanish	alerce japones
Spanish	alerce del japón
Azerbaijani	yapon qara şamı
azb	ژاپون قارا شامی
Belarusian	лістоўніца японская
Bulgarian	японска лиственица
Czech	modřín japonský
Welsh	llarwydden japan
Danish	japansk lærk
German	japanische lärche
Esperanto	japana lariko
Estonian	jaapani lehis
Estonian	eurojaapani lehis
Estonian	eurojaapani lehised
Basque	japoniar laritz
Basque	japoniar alertze
Persian	سیاهکاج ژاپنی
Finnish	japaninlehtikuusi
French	meleze du japon
French	mélèze du japon
Upper Sorbian	japanski larik
Hungarian	japán vörösfenyő
Armenian	Խեժափիճի ճապոնական
Icelandic	japanslerki
Japanese	ラクヨウショウ
Japanese	カラマツ
Japanese	アカミカラマツ
Japanese	シダレカラマツ
Japanese	フジマツ
Japanese	唐松
Japanese	落葉松
Korean	낙엽송
Korean	일본잎갈나무
koi	Ниппонісь лисвень
Lithuanian	japoniškasis maumedis
Lithuanian	japoninis maumedis
Macedonian	Јапонски ариш
Norwegian Bokmål	japansk lerk
Norwegian Bokmål	japanlerk
Dutch	japanse lork
Dutch	goudlariks
Dutch	japanse larix
Dutch	japanse lariks
Polish	modrzew japoński
Russian	Лиственница тонкочешуйчатая
Slovenian	japonski macesen
Swedish	japansk lärk
Turkish	japon melezi
Ukrainian	Модрина тонколуската
Ukrainian	модрина японська
Chinese	日本落叶松
Chinese	日本落葉松

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - Inner Mongolia
- Eastern Asia
  - Japan
  - Korea
- Western Asia
  - Turkey

Europe click to expand
- Eastern Europe
  - Baltic States
- Middle Europe
  - Austria
  - Belgium
  - Germany
  - Hungary
  - Netherlands
  - Poland
- Northern Europe
  - Denmark
  - Finland
  - Føroyar
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southwestern Europe
  - France

Northern America click to expand
- Eastern Canada
  - Newfoundland
- Northeastern U.S.A.
  - New York

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000443374
UNII	RU30XAO8B2
Cornell Woody Plants	135
Canadensys	7165
USDA Plants	LAKA2
UConn	246
Tropicos	24900375
INPN	105044
Flora of Italy	8513
KEW	urn:lsid:ipni.org:names:60457419-2
The Plant List	kew-2493964
Missouri Botanical Garden	285017
PFAF	Larix kaempferi
Open Tree Of Life	154040
Observations.org	6951
NCBI Taxonomy	54800
NBN Atlas	NHMSYS0000460129
Nature Serve	2.734862
IUCN Red List	42312
IPNI	60457419-2
iNaturalist	143786
GBIF	2686157
Freebase	/m/08j3ty
EPPO	LAXLE
EOL	1033607
Elurikkus	5382
US Library of Congress	sh85069665
USDA GRIN	21495
Wikipedia	Larix_kaempferi
Plantarium	61708

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_027924585.1	LKA_r1.0	Contig	Kazusa DNA Research Institute	2022-12-13	18	12.57 Gb

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

Analysis of vertical differentiation of vegetation in Taishan World Heritage site based on cloud model

Wang Z, Han F, Li C, Shen W, Yang Z, Li K, Yao Q

Sci Rep

13-May-2024

PMCID:	PMC11091119
doi:	10.1038/s41598-024-61853-2
PMID:	38740964

Identifying the generalizable controls on insect associations of native and non‐native trees

Gougherty AV, Klapwijk M, Liebhold AM, Mech A, Trombik J, Fei S

Ecol Evol

12-May-2024

PMCID:	PMC11089089
doi:	10.1002/ece3.11265
PMID:	38742186

A dataset of 40’000 trees with section-wise measured stem diameter and branch volume from across Switzerland

Didion M, Herold A, Thürig E, Topuz S, Vulovic Z, Abegg M, Nitzsche J, Stillhard J, Glatthorn J

Sci Data

09-May-2024

PMCID:	PMC11082132
doi:	10.1038/s41597-024-03336-7
PMID:	38724536

Application of Developmental Regulators for Enhancing Plant Regeneration and Genetic Transformation

Xu P, Zhong Y, Xu A, Liu B, Zhang Y, Zhao A, Yang X, Ming M, Cao F, Fu F

Plants (Basel)

04-May-2024

PMCID:	PMC11085514
doi:	10.3390/plants13091272
PMID:	38732487

Overexpression of Larch SCL6 Inhibits Transitions from Vegetative Meristem to Inflorescence and Flower Meristem in Arabidopsis thaliana (L.) Heynh.

Xing JX, Zang QL, Ye ZL, Qi LW, Yang L, Li WF

Plants (Basel)

29-Apr-2024

PMCID:	PMC11085395
doi:	10.3390/plants13091232
PMID:	38732446

Drought- and heat-induced mortality of conifer trees is explained by leaf and growth legacies

Sterck FJ, Song Y, Poorter L

Sci Adv

12-Apr-2024

PMCID:	PMC11014445
doi:	10.1126/sciadv.adl4800
PMID:	38608026

Phylogeography, origin and population structure of the self‐fertile emerging plant pathogen Phytophthora pseudosyringae

Mullett MS, Harris AR, Scanu B, Van Poucke K, LeBoldus J, Stamm E, Bourret TB, Christova PK, Oliva J, Redondo MA, Talgø V, Corcobado T, Milenković I, Jung MH, Webber J, Heungens K, Jung T

Mol Plant Pathol

08-Apr-2024

PMCID:	PMC11002350
doi:	10.1111/mpp.13450
PMID:	38590129

Ectomycorrhiza and ethylenediurea reduced the impact of high nitrogen and ozone stresses and increased the growth of Cedrus deodara

Jamil HM, Gatasheh MK, Ahmad R, Ibrahim KE, Khan SA, Irshad U, Shahzad M, Abbasi AM

Heliyon

27-Mar-2024

PMCID:	PMC10998246
doi:	10.1016/j.heliyon.2024.e28635
PMID:	38586366

Genomic Prediction from Multi-Environment Trials of Wheat Breeding

García-Barrios G, Crespo-Herrera L, Cruz-Izquierdo S, Vitale P, Sandoval-Islas JS, Gerard GS, Aguilar-Rincón VH, Corona-Torres T, Crossa J, Pacheco-Gil RA

Genes (Basel)

27-Mar-2024

PMCID:	PMC11049976
doi:	10.3390/genes15040417
PMID:	38674352

Phytosulfokine alpha enhances regeneration of transformed and untransformed protoplasts of Brassica oleracea

Vogrinčič V, Kastelec D, Murovec J

Front Plant Sci

27-Mar-2024

PMCID:	PMC11004253
doi:	10.3389/fpls.2024.1379618
PMID:	38601308

Cambium Reactivation Is Closely Related to the Cell-Cycle Gene Configuration in Larix kaempferi

Cheng DX, Wang XH, Wang CL, Li XY, Ye ZL, Li WF

Int J Mol Sci

22-Mar-2024

PMCID:	PMC11011626
doi:	10.3390/ijms25073578
PMID:	38612390

Utilization of Synthetic Near-Infrared Spectra via Generative Adversarial Network to Improve Wood Stiffness Prediction

Ali SD, Raut S, Dahlen J, Schimleck L, Bergman R, Zhang Z, Nasir V

Sensors (Basel)

21-Mar-2024

PMCID:	PMC10975370
doi:	10.3390/s24061992
PMID:	38544255

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

Phylogeny and expression patterns of ERF genes that are potential reproductive inducers in hybrid larch

Hao J, Xu D, Wang C, Cao Q, Zhao Q, Xie M, Zhang H, Zhang L

BMC Genomics

18-Mar-2024

PMCID:	PMC10946173
doi:	10.1186/s12864-024-10188-3
PMID:	38500084

Genome-wide analysis of the C2H2-ZFP gene family in Stevia rebaudiana reveals involvement in abiotic stress response

Nikraftar S, Ebrahimzadegan R, Majdi M, Mirzaghaderi G

Sci Rep

14-Mar-2024

PMCID:	PMC10940304
doi:	10.1038/s41598-024-56624-y
PMID:	38486071

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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin	3220	Click to see	270.24	unknown	https://doi.org/10.5246/JCPS.2012.05.057
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see	170.12	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
3-Methoxybenzoic Acid	11461	Click to see	152.15	unknown	https://doi.org/10.5246/JCPS.2012.05.057
> Benzenoids / Benzene and substituted derivatives / Cumenes
methyl (6aS,7R,10aS)-7,10a-dimethyl-3-propan-2-yl-5,6,6a,8,9,10-hexahydrobenzo[b][1]benzoxepine-7-carboxylate	101005576	Click to see CC(C)C1=CC2=C(C=C1)OC3(CCCC(C3CC2)(C)C(=O)OC)C	330.50	unknown	https://doi.org/10.1055/S-2006-960843
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
10-hydroxy-8-(hydroxymethyl)-4b,8-dimethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-one	85248581	Click to see	278.40	unknown	https://doi.org/10.1139/V99-218
7,15-Dihydroxypodocarp-8(14)-en-13-one	10731307	Click to see	278.40	unknown	https://doi.org/10.1139/V99-218
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(4'-Hydroxyphenyl)-2-butanone	21648	Click to see	164.20	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
> Benzenoids / Phenols / Methoxyphenols
Dihydroconiferyl alcohol	16822	Click to see	182.22	unknown	https://doi.org/10.5246/JCPS.2012.05.057
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
3,3-Dimethylpentane	11229	Click to see	100.20	unknown	https://doi.org/10.1007/BF00576230
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1007/BF00576230
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol	137705081	Click to see	358.40	unknown	https://doi.org/10.1016/0031-9422(91)80071-8
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	https://doi.org/10.1016/0031-9422(91)80071-8
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols
(2R)-2,3-Dihydropropyl beta-D-glucopyranoside	15559912	Click to see C(C1C(C(C(C(O1)OCC(CO)O)O)O)O)O	254.23	unknown	https://doi.org/10.1021/NP060439Q
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid	221580	Click to see	302.50	unknown	https://doi.org/10.1007/BF00576230
(1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl)methanol	107171	Click to see	286.50	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
(1R,4aR,4bR,7R,9R,10aR)-7,9-dihydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid	10807931	Click to see CC12CCCC(C1CC(C3=CC(CCC23)(C(C)(C)O)O)O)(C)C(=O)O	352.50	unknown	https://doi.org/10.1139/V99-218
(1R,4aR,4bR,7S,10aR)-7-hydroxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	15450492	Click to see	334.40	unknown	https://doi.org/10.1139/V99-218
(1R,4aR,4bR,7S,10aR)-7-methoxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	10760165	Click to see	348.50	unknown	https://doi.org/10.1139/V99-218
(1R,4aS,10aR)-5,6-dihydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	163105697	Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)O)O	332.40	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
(1R,4aS,10aR)-6-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	10246192	Click to see	332.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
(1R,4aS,10aR)-7-acetyl-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	85240644	Click to see	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8 https://doi.org/10.1021/NP980159D
(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid	10017708	Click to see	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8 https://doi.org/10.1007/BF00576230
(1R,4aS,4bR,7R,10aR)-7-hydroxy-1-(hydroxymethyl)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one	101007988	Click to see	336.50	unknown	https://doi.org/10.1139/V99-218
(1R,4aS,4bR,7S,10aR)-7-hydroxy-1-(hydroxymethyl)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one	10663524	Click to see	320.50	unknown	https://doi.org/10.1139/V99-218
(1R,4aS,9R,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol	21604174	Click to see	288.40	unknown	https://doi.org/10.1021/NP9704720
(1R,4aS,9R,10aR)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol	101105394	Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)O	304.40	unknown	https://doi.org/10.1055/S-2001-10873
(1R,4aS,9R,10aR)-9-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde	10425915	Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)C=O	316.40	unknown	https://doi.org/10.1021/NP980159D
(1S,4S,4aR,8aR)-4-[(3S)-3-hydroxy-3-methylpent-4-enyl]-4a,8,8-trimethyl-3-methylidene-2,4,5,6,7,8a-hexahydro-1H-naphthalen-1-ol	10902861	Click to see	306.50	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
(1S,4S,4aR,8aS)-4-((S)-3-Hydroxy-3-methylpent-4-en-1-yl)-4a,8,8-trimethyl-3-methylenedecahydronaphthalen-1-ol	11335788	Click to see CC1(CCCC2(C1C(CC(=C)C2CCC(C)(C=C)O)O)C)C	306.50	unknown	https://doi.org/10.1007/BF00576230 https://doi.org/10.1016/S0031-9422(97)84396-8
(2R,4aR,4bS,8R,8aR,10R)-8-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-4b,8-dimethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthrene-2,10-diol	10545004	Click to see	338.50	unknown	https://doi.org/10.1139/V99-218
1-(Hydroxymethyl)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	23786420	Click to see	302.50	unknown	https://doi.org/10.1021/NP9704720
1-(hydroxymethyl)-1,4a-dimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	85296036	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
1-(Hydroxymethyl)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	3838750	Click to see	318.40	unknown	https://doi.org/10.1055/S-2001-10873
1-(hydroxymethyl)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	78297554	Click to see	316.40	unknown	https://doi.org/10.1021/NP980159D
1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1R,4aR,4bS,7S,10aR)-	15586712	Click to see	288.50	unknown	https://doi.org/10.1007/BF00576230
1,4a-Dimethyl-7-prop-1-en-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	85178531	Click to see	298.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	15618	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol	73799303	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)O)C	288.40	unknown	https://doi.org/10.1021/NP9704720
1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carboxylic acid	10018535	Click to see	314.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
13-Epimanool	10891602	Click to see	290.50	unknown	https://doi.org/10.1007/BF00576230
15-Hydroxyabieta-7,13-dien-18-oic acid	643004	Click to see	318.40	unknown	https://doi.org/10.1007/BF00576230
15-Hydroxydehydroabietic Acid	14487943	Click to see	316.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
15,18-Dihydroxyabieta-8,11,13-trien-7-one	3009631	Click to see	316.40	unknown	https://doi.org/10.1021/NP980159D
16-Nor-15-oxodehydroabietic acid	102004644	Click to see	300.40	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1 https://doi.org/10.1016/S0031-9422(97)84396-8 https://doi.org/10.1021/NP980159D
18-Nor-4,15-dihydroxyabieta-8,11,13-trien-7-one	3009629	Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)O	302.40	unknown	https://doi.org/10.1021/NP980159D
18-Norabieta-8,11,13-triene-4,15-diol	11709045	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)O	288.40	unknown	https://doi.org/10.1021/NP9704720
18-R-4,15-dihydroxyabieta-8,11,13-trien-7-one	78297552	Click to see	302.40	unknown	https://doi.org/10.1021/NP980159D
2-[8-(Hydroxymethyl)-4b,8-dimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol	72829381	Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)CO	302.50	unknown	https://doi.org/10.1021/NP9704720
4-[(1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl)methoxy]-4-oxobutanoic acid	75179854	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)COC(=O)CCC(=O)O)C	386.50	unknown	https://doi.org/10.1021/NP980159D
4-[(4E,6E,8S,11Z)-13-[(2S)-5-hydroxy-4-methyl-3-oxofuran-2-yl]-4,8,12-trimethyltrideca-4,6,11-trienyl]-1-(3-methylbutyl)-2H-pyrrol-5-one	643666	Click to see CC1=C(OC(C1=O)CC(=CCCC(C)C=CC=C(C)CCCC2=CCN(C2=O)CCC(C)C)C)O	483.70	unknown	https://doi.org/10.1055/S-2006-960843
4-[[(1R,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]methoxy]-4-oxobutanoic acid	46230266	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)COC(=O)CCC(=O)O)C	386.50	unknown	https://doi.org/10.1021/NP980159D
4b,8-Dimethyl-2-(propan-2-yl)-4,4a,4b,5,6,7,8,8a,9,10-decahydro-3h-3,10a-epidioxyphenanthrene-8-carboxylic acid	290006	Click to see	334.40	unknown	https://doi.org/10.1055/S-2001-10873
6-Hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	162956970	Click to see	332.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol	73069324	Click to see	288.40	unknown	https://doi.org/10.1021/NP9704720
7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic Acid	9944781	Click to see	316.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol	78297549	Click to see	304.40	unknown	https://doi.org/10.1055/S-2001-10873
7-Hydroxy-1-(hydroxymethyl)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one	85224077	Click to see CC(C)C1(CCC2C(=C1)C(=O)CC3C2(CCCC3(C)CO)C)O	320.50	unknown	https://doi.org/10.1139/V99-218
7-Hydroxy-1-(hydroxymethyl)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthren-9-one	162868574	Click to see	336.50	unknown	https://doi.org/10.1139/V99-218
7-Hydroxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	24066904	Click to see	334.40	unknown	https://doi.org/10.1139/V99-218
7-Methoxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	85258433	Click to see CC(C)C1(CCC2C(=C1)C(=O)CC3C2(CCCC3(C)C(=O)O)C)OC	348.50	unknown	https://doi.org/10.1139/V99-218
7-Oxodehydroabietic acid	29212	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)C(=O)O)C	314.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
7-Oxodehydroabietinol	15715176	Click to see	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
7,9-dihydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid	85274679	Click to see	352.50	unknown	https://doi.org/10.1139/V99-218
7alpha-Hydroxydehydroabieticacid	13370053	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C	316.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
7Beta-Hydroxydehydroabietic Acid	13370052	Click to see	316.40	unknown	https://doi.org/10.1021/NP980159D
8-(hydroxymethyl)-2-(2-hydroxypropan-2-yl)-4b,8-dimethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthrene-2,10-diol	85179549	Click to see	338.50	unknown	https://doi.org/10.1139/V99-218
8,13-Abietadien-18-oic acid	16040	Click to see	302.50	unknown	https://doi.org/10.1007/BF00576230
9-hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic Acid	10448477	Click to see	316.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8 https://doi.org/10.1021/NP980159D
9-Hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde	78297555	Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)C=O	316.40	unknown	https://doi.org/10.1021/NP980159D
9\|A-Hydroxydehydroabietyl alcohol	21626425	Click to see	302.50	unknown	https://doi.org/10.1021/NP9704720
Abieta-7,13-diene	443470	Click to see	272.50	unknown	https://doi.org/10.1007/BF00576230
Abieta-8,11,13-triene-7,15,18-triol	91895315	Click to see	318.40	unknown	https://doi.org/10.1055/S-2001-10873
Abieta-8,11,13,15-tetraen-18-oic acid	15929992	Click to see	298.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8 https://doi.org/10.1016/S0031-9422(98)00302-1
Abietal	443479	Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O	286.50	unknown	https://doi.org/10.1007/BF00576230
Abietatriene	6432211	Click to see	270.50	unknown	https://doi.org/10.1007/BF00576230
Abietic acid	10569	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	https://doi.org/10.1007/BF00576230
Abietinol	443474	Click to see	288.50	unknown	https://doi.org/10.1007/BF00576230
Daturabietatriene	11392488	Click to see	302.50	unknown	https://doi.org/10.1021/NP9704720
Dehydroabietal	11694869	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C=O)C	284.40	unknown	https://doi.org/10.1007/BF00576230
Dehydroabietic acid	94391	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
Dehydroabietyl alcohol	15586718	Click to see	286.50	unknown	https://doi.org/10.1007/BF00576230 https://doi.org/10.1016/S0031-9422(97)84396-8
Isopimara-7,15-dienal	12311183	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C=O)C)C1)C=C	286.50	unknown	https://doi.org/10.1007/BF00576230
Isopimara-7,15-diene	13969536	Click to see	272.50	unknown	https://doi.org/10.1007/BF00576230
Isopimaric Acid	442048	Click to see	302.50	unknown	https://doi.org/10.1007/BF00576230
Levopimaric acid transannular peroxide	15929993	Click to see CC(C)C1=CC23CCC4C(C2CC1OO3)(CCCC4(C)C(=O)O)C	334.40	unknown	https://doi.org/10.1055/S-2001-10873
methyl (1R,2S,6R,7R,9R,12S)-2,6-dimethyl-10-oxo-12-propan-2-yl-15-oxatetracyclo[10.2.1.01,9.02,7]pentadecane-6-carboxylate	101005575	Click to see CC(C)C12CCC3(O1)C(CC4C3(CCCC4(C)C(=O)OC)C)C(=O)C2	348.50	unknown	https://doi.org/10.1055/S-2006-960843
Methyl 2,6-dimethyl-10-oxo-12-propan-2-yl-15-oxatetracyclo[10.2.1.01,9.02,7]pentadecane-6-carboxylate	162928658	Click to see CC(C)C12CCC3(O1)C(CC4C3(CCCC4(C)C(=O)OC)C)C(=O)C2	348.50	unknown	https://doi.org/10.1055/S-2006-960843
Neoabietal	443477	Click to see	286.50	unknown	https://doi.org/10.1007/BF00576230
Neoabietic acid	221118	Click to see	302.50	unknown	https://doi.org/10.1007/BF00576230
Neoabietinol	443476	Click to see	288.50	unknown	https://doi.org/10.1007/BF00576230
Palustral	14241162	Click to see	286.50	unknown	https://doi.org/10.1007/BF00576230
Palustric acid	443613	Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C	302.50	unknown	https://doi.org/10.1007/BF00576230
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1007/BF00576230
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1021/NP50071A016
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1007/BF00576230
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1007/BF00576230
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1007/BF00576230
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1007/BF00576230
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1007/BF00576230
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,7R,8R)-2,6,6,9-tetramethyltricyclo[5.4.0.02,8]undec-9-ene	92042758	Click to see CC1=CCC2C3C1C2(CCCC3(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00576230
(1R,2S,7S,8S,9S,10S)-2,6,6,9-tetramethyltetracyclo[5.4.0.02,9.08,10]undecane	98459467	Click to see CC1(CCCC2(C3C1C4C2(C4C3)C)C)C	204.35	unknown	https://doi.org/10.1007/BF00576230
(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/10.1007/BF00576230
(1R,4aR,5R,8aR)-6-formyl-1,4a-dimethyl-5-(4-methyl-3-oxo-pentyl)-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid	3009628	Click to see CC(C)C(=O)CCC1C(=CCC2C1(CCCC2(C)C(=O)O)C)C=O	334.40	unknown	https://doi.org/10.1055/S-2001-10873
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene	5315589	Click to see	204.35	unknown	https://doi.org/10.1007/BF00576230
(1R,4S,4aS,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	12302226	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
(E,Z)-farnesol	1549109	Click to see CC(=CCCC(=CCCC(=CCO)C)C)C	222.37	unknown	https://doi.org/10.1021/NP50071A016
1-[(1S,3aR,4R,7S,7aR)-4-hydroxy-4-methyl-7-propan-2-yl-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone	14138891	Click to see	238.37	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
3,4-Dihydrocadalene	528708	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1007/BF00576230
6-Formyl-1,4a-dimethyl-5-(4-methyl-3-oxopentyl)-2,3,4,5,8,8a-hexahydronaphthalene-1-carboxylic acid	78297551	Click to see	334.40	unknown	https://doi.org/10.1055/S-2001-10873
7-Acetyl-2-hydroxy-2-methyl-5-isopropylbicyclo[4.3.0]nonane	539857	Click to see	238.37	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
a Farnesol	3327	Click to see	222.37	unknown	https://doi.org/10.1021/NP50071A016
alpha-Cadinene, (+)-	12306048	Click to see	204.35	unknown	https://doi.org/10.1007/BF00576230
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
alpha-Calacorene	12302243	Click to see	200.32	unknown	https://doi.org/10.1007/BF00576230
alpha-Ylangene	101607926	Click to see	204.35	unknown	https://doi.org/10.1007/BF00576230 https://doi.org/10.1007/BF00576230
beta-Copaene	57339298	Click to see CC(C)C1CCC2(C3C1C2C(=C)CC3)C	204.35	unknown	https://doi.org/10.1007/BF00576230
Cadin-4-en-10-ol	519662	Click to see	222.37	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1007/BF00576230
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1007/BF00576230
Caryophyllene,alpha + beta mixt.	5354499	Click to see	204.35	unknown	https://doi.org/10.1007/BF00576230
CID 16396350	16396350	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1007/BF00576230
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00576230
Curcumene	92139	Click to see	202.33	unknown	https://doi.org/10.1007/BF00576230
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1007/BF00576230
Humulene	5281520	Click to see	204.35	unknown	https://doi.org/10.1007/BF00576230
Oplopanone	10466745	Click to see	238.37	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Palustrol	110745	Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O	222.37	unknown	https://doi.org/10.1007/BF00576230
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,5S)-2,6,6,8-tetramethyltricyclo(5.3.1.01,5)undec-8-ene	442348	Click to see	204.35	unknown	https://doi.org/10.1021/NP50071A016
1,7-di-epi-alpha-Cedrene	10878276	Click to see	204.35	unknown	https://doi.org/10.1021/NP50071A016
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Selinene	442393	Click to see	204.35	unknown	https://doi.org/10.1007/BF00576230
Sibirene	14167644	Click to see	204.35	unknown	https://doi.org/10.1007/BF00576230
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,3'R,4R,5R,6R,8S,10R,12S,13S,16R,21R,25S)-3',4,6,12,17,17-hexamethylspiro[9,18,22,23-tetraoxahexacyclo[14.7.2.01,13.04,12.05,10.021,25]pentacosane-8,5'-oxolane]-2',19-dione	101733486	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC7C(CCC5C4(C3)C)C(OC(=O)CC7OO6)(C)C)C	516.70	unknown	https://doi.org/10.1016/J.TET.2004.03.089
(1R,4R,5R,6R,8S,10R,12S,13S,16S,22R)-3',4,6,12,17,17-hexamethylspiro[9,18,23,24-tetraoxahexacyclo[20.2.1.01,13.04,12.05,10.016,22]pentacos-20-ene-8,5'-furan]-2',19-dione	101733485	Click to see CC1CC2(C=C(C(=O)O2)C)OC3C1C4(CCC56CC7(C=CC(=O)OC(C7CCC5C4(C3)C)(C)C)OO6)C	512.60	unknown	https://doi.org/10.1016/J.TET.2004.03.089
2,3',8,10,20,20-Hexamethylspiro[5,19-dioxapentacyclo[11.10.0.02,10.04,9.015,21]tricosa-12,15-diene-6,5'-oxolane]-2',18-dione	73119304	Click to see	482.60	unknown	https://doi.org/10.1002/HLCA.200390079
20-Hydroxy-3',4,6,12,17,17,19-heptamethylspiro[9,18,22-trioxahexacyclo[17.2.1.01,13.04,12.05,10.016,20]docosane-8,5'-oxolane]-2'-one	85163635	Click to see	488.70	unknown	https://doi.org/10.1021/NP960523D
25-Hydroxy-3',4,6,12,17,17-hexamethylspiro[9,18,22,23-tetraoxahexacyclo[14.7.2.01,13.04,12.05,10.021,25]pentacosane-8,5'-oxolane]-2',19-dione	4437225	Click to see	532.70	unknown	https://doi.org/10.3987/COM-90-5527
3',4,6,12,17,17-Hexamethylspiro[9,18,22,23-tetraoxahexacyclo[14.7.2.01,13.04,12.05,10.021,25]pentacosane-8,5'-oxolane]-2',19-dione	163041219	Click to see	516.70	unknown	https://doi.org/10.1016/J.TET.2004.03.089
3',4,6,12,17,17-Hexamethylspiro[9,18,23,24-tetraoxahexacyclo[20.2.1.01,13.04,12.05,10.016,22]pentacos-20-ene-8,5'-furan]-2',19-dione	163047609	Click to see	512.60	unknown	https://doi.org/10.1016/J.TET.2004.03.089
3',4,6,12,17,17-Hexamethylspiro[9,18,23,24-tetraoxahexacyclo[20.2.1.01,13.04,12.05,10.016,22]pentacos-20-ene-8,5'-oxolane]-2',19-dione	3400146	Click to see	514.60	unknown	https://doi.org/10.1016/J.TET.2004.03.089 https://doi.org/10.1002/HLCA.201100166
Pseudolaric Acid B3	44444977	Click to see	394.40	unknown	https://doi.org/10.1016/S0968-0896(03)00531-5
Pseudolarolide Q2	101733484	Click to see	514.60	unknown	https://doi.org/10.1016/J.TET.2004.03.089 https://doi.org/10.1002/HLCA.201100166
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2E,4E)-5-[(1R,7R,8S,9S)-7-acetyloxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid	92043559	Click to see CC1=CCC23CCC(C2(CC1)OC(=O)C)C(OC3=O)(C)C=CC=C(C)C(=O)O	388.50	unknown	https://doi.org/10.1351/PAC198658050811
(2E,4E)-5-[(1R,7S,8R,9R)-7-hydroxy-4-methoxycarbonyl-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid	583902	Click to see	390.40	unknown	https://doi.org/10.1021/NP060439Q
(2E,4E)-5-[(1R,7S,8R,9S)-7-hydroxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid	16215033	Click to see CC1=CCC23CCC(C2(CC1)O)C(OC3=O)(C)C=CC=C(C)C(=O)O	346.40	unknown	https://doi.org/10.1021/NP060439Q
(2E,4E)-5-[(1R,7S,8S,9S)-7-acetyloxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]trideca-2,4-dien-9-yl]-2-methylpenta-2,4-dienoic acid	163100612	Click to see CC1=CCC2(C3CCC2(C=C1)C(=O)OC3(C)C=CC=C(C)C(=O)O)OC(=O)C	386.40	unknown	https://doi.org/10.1021/NP0200010
(2Z,4E)-5-[(8R)-7-acetyloxy-4-methoxycarbonyl-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid	129316864	Click to see	432.50	unknown	https://doi.org/10.1055/S-2007-969944 https://doi.org/10.1016/S0968-0896(03)00531-5
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2E,4E)-5-[(1R,7S,8R,9R)-7-hydroxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoate	16215031	Click to see	508.60	unknown	https://doi.org/10.1021/NP060439Q
1H-4,9a-Ethanocyclohepta(c)pyran-7-carboxylic acid, 4a-(acetyloxy)-3-(4-carboxy-1,3-pentadienyl)3,4,4a,5,6,9-hexahydro-3-methyl-1-oxo-, 7-methyl ester, (3-alpha(1E,3E),4-alpha,4a-alpha,9a-alpha)-(-)-	6436202	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)C(=O)OC)C(=O)O1)C)C(=O)O	432.50	unknown	https://doi.org/10.1351/PAC198658050811 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3402633/ https://doi.org/10.1021/NP50115A007
5-(7-Acetyloxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl)-2-methylpenta-2,4-dienoic acid	5195969	Click to see	388.50	unknown	https://doi.org/10.1021/NP50097A015 https://doi.org/10.1021/NP060439Q https://doi.org/10.1016/J.CHROMA.2008.05.068
5-[(1R,7S,8R,9R)-7-hydroxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl]-2-methylpenta-2,4-dienoic acid	138113899	Click to see	346.40	unknown	https://doi.org/10.1021/NP060439Q
7-Acetyloxy-9-(4-carboxypenta-1,3-dienyl)-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-ene-4-carboxylic acid	78412051	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)O)OC(=O)C)C(=O)O1)C)C(=O)O	418.40	unknown	https://doi.org/10.1021/NP060439Q
methyl (1R,3R,7S,8S,9R)-7-acetyloxy-3-hydroxy-9-methyl-9-[(1E,3E)-4-methyl-5-oxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypenta-1,3-dienyl]-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-4-ene-4-carboxylate	44421294	Click to see	610.60	unknown	https://doi.org/10.1021/NP060439Q
methyl (1R,7S,8S,9R)-7-acetyloxy-9-methyl-9-[(1E,3E)-4-methyl-5-oxo-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypenta-1,3-dienyl]-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-ene-4-carboxylate	162981580	Click to see	594.60	unknown	https://doi.org/10.1021/NP060439Q
methyl (1R,7S,8S,9S)-7-acetyloxy-9-[(1E,3E)-5-[(2R)-2,3-dihydroxypropoxy]-4-methyl-5-oxopenta-1,3-dienyl]-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-ene-4-carboxylate	162882921	Click to see	506.50	unknown	https://doi.org/10.1021/NP0200010
Methyl 5-(7-acetyloxy-4-hydroxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-2-en-9-yl)-2-methylpenta-2,4-dienoate	162895722	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(C=C3)(C)O)OC(=O)C)C(=O)O1)C)C(=O)OC	418.50	unknown	https://doi.org/10.1016/S0968-0896(03)00531-5
Methyl 9-[5-(2,3-dihydroxypropoxy)-4-methyl-5-oxopenta-1,3-dienyl]-7-hydroxy-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-ene-4-carboxylate	162880549	Click to see	464.50	unknown	https://doi.org/10.1021/NP060439Q
Pseudolaric Acid A	6436278	Click to see CC1=CCC23CCC(C2(CC1)OC(=O)C)C(OC3=O)(C)C=CC=C(C)C(=O)O	388.50	unknown	https://doi.org/10.1351/PAC198658050811 https://doi.org/10.1021/NP060439Q https://doi.org/10.1021/NP0200010
Pseudolaric Acid A-O-beta-D-glucopyranoside	75072020	Click to see	550.60	unknown	https://doi.org/10.1021/NP060439Q https://doi.org/10.1021/NP0200010
pseudolaric acid A2	44444976	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(C=C3)(C)O)OC(=O)C)C(=O)O1)C)C(=O)O	404.50	unknown	https://doi.org/10.1016/S0968-0896(03)00531-5
Pseudolaric Acid B	6475943	Click to see	432.50	unknown	https://doi.org/10.1124/MOL.105.020537
Pseudolaric acid C	6440704	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)O)C(=O)O1)C)C(=O)O	390.40	unknown	https://doi.org/10.1021/NP060439Q https://doi.org/10.1055/S-2007-969944
Pseudolaric Acid C2	6475945	Click to see	418.40	unknown	https://doi.org/10.1021/NP060439Q
Pseudolaric Acid F	636647	Click to see CC1=CCC2(C3CCC2(CC1=O)C(=O)OC3(C)C=CC=C(C)C(=O)O)OC(=O)C	402.40	unknown	https://doi.org/10.1021/NP0200010
Pseudolaric Acid G	10894737	Click to see CC1=CCC2(C3CCC2(CC1O)C(=O)OC3(C)C=CC=C(C)C(=O)O)OC(=O)C	404.50	unknown	https://doi.org/10.1021/NP0200010
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3'R,4R,5R,6R,8S,10R,12S,13S,16R,22R)-3',4,6,12,17,17-hexamethylspiro[9,18-dioxahexacyclo[11.10.0.01,22.04,12.05,10.016,22]tricosane-8,5'-oxolane]-2',19-dione	102162850	Click to see	484.70	unknown	https://doi.org/10.1021/NP50097A015
(3S,6R)-6-[(3R,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol	100927686	Click to see	460.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
Friedelan-3-one	244297	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
Friedelin	91472	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
methyl 3-[(6R,8S,11R,15S)-5-(2-hydroxypropan-2-yl)-1,4',11,13-tetramethyl-5'-oxospiro[16-oxapentacyclo[9.7.0.02,8.06,8.012,17]octadecane-15,2'-oxolane]-6-yl]propanoate	6711551	Click to see	516.70	unknown	https://doi.org/10.1021/NP50097A015
Methyl 3-[5-(2-hydroxypropan-2-yl)-1,4',11,13-tetramethyl-5'-oxospiro[16-oxapentacyclo[9.7.0.02,8.06,8.012,17]octadecane-15,2'-oxolane]-6-yl]propanoate	3795022	Click to see	516.70	unknown	https://doi.org/10.1021/NP50097A015
Pseudolarolide C	21592338	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC5(C(CCC6C4(C3)C)C(C)(C)O)CCC(=O)OC)C	516.70	unknown	https://doi.org/10.1021/NP50097A015
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Monohydroxy bile acids, alcohols and derivatives
3-(3-hydroxy-4,4,10,13,17-pentamethyl-2,3,5,6,9,11,12,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl)butanoic acid	85102683	Click to see	400.60	unknown	https://doi.org/10.1016/S0960-894X(01)00633-3
isopseudolarifuroic acid B	101147487	Click to see	400.60	unknown	https://doi.org/10.1016/S0960-894X(01)00633-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-5-methylideneheptan-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	100927685	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-5-oxoheptan-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	44423576	Click to see	440.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
(1S,4R,8S,21R)-3',4,6,12,17,17-hexamethylspiro[9-oxahexacyclo[11.9.0.01,21.04,12.05,10.016,21]docosane-8,5'-furan]-2',18-dione	6711550	Click to see	466.70	unknown	https://doi.org/10.1021/NP50097A015
24-Methylenecycloartan-3-one	634880	Click to see	438.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
24-Methylenecycloartanol	94204	Click to see	440.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
24-Methylenecycloartanone	14635659	Click to see	438.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
3beta-24-Methylenecycloartan-3-ol	544165	Click to see	440.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
pseudolarolide A	21592336	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC57CCC(=O)C(C7CCC6C4(C3)C)(C)C)C	468.70	unknown	https://doi.org/10.1021/NP50097A015
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,4R,5S,6S,8S,9R,10S,13R,14S,15S,16R,17R)-17-[(E,2R,5S)-5-[[(2R,3R,4S,5S)-5-[(1R)-1,2-dihydroxyethyl]-3-[(2S,3R,4S,5R)-4,5-dihydroxy-3-methoxyoxan-2-yl]oxy-4-hydroxyoxolan-2-yl]oxymethyl]-6-methylhept-3-en-2-yl]-10,13-dimethyl-1,2,3,4,5,6,7,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,4,6,8,15,16-hexol	163088767	Click to see	805.00	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
(5R,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,4,5,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6-dione	86326416	Click to see	428.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
(5S,8S,9S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	12020562	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
14-(5-Ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecane-5,8-dione	543599	Click to see	428.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
17-(5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	12442813	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6-diol	13992090	Click to see	430.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
b-Sitostenone	579897	Click to see	412.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
Sitostanone	5491512	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
Stigmast-4-en-3-one	5484202	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
Stigmast-4-ene-3,6-diol	10550610	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(CCC34C)O)O)C)C(C)C	430.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
Stigmastan-3-one	53703939	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
Stigmastane-3,6-dione	13992092	Click to see	428.70	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1Z)-4-[(R)-methylsulfinyl]-N-sulfooxybutanimidothioate	154497820	Click to see	423.50	unknown	https://doi.org/10.1016/S0031-9422(98)00302-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Pseudolaroside A	98766857	Click to see	300.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
3',4,6,12,17,17-Hexamethylspiro[9,18,24-trioxapentacyclo[19.2.1.04,12.05,10.016,22]tetracosa-20,22-diene-8,5'-oxolane]-2',19-dione	3793684	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC5C=C6C(CCCC4(C3)C)C(OC(=O)C=C6O5)(C)C)C	498.60	unknown	https://doi.org/10.1080/10286020108040372
Pseudolarolide F	134715230	Click to see	514.60	unknown	https://doi.org/10.1080/10286020108040372
Pseudolarolide F	6711553	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC5(C=C6C(CCCC4(C3)C)C(OC(=O)C=C6O5)(C)C)O)C	514.60	unknown	https://doi.org/10.1080/10286020108040372
> Organic oxygen compounds / Organooxygen compounds / Ethers / Alkyl aryl ethers
Methyl 7,10a-dimethyl-3-propan-2-yl-5,6,6a,8,9,10-hexahydrobenzo[b][1]benzoxepine-7-carboxylate	162925055	Click to see CC(C)C1=CC2=C(C=C1)OC3(CCCC(C3CC2)(C)C(=O)OC)C	330.50	unknown	https://doi.org/10.1055/S-2006-960843
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
(1R,2S,6R,7R,12S)-2,6-dimethyl-9-oxo-12-propan-2-yl-13,14-dioxatetracyclo[10.2.2.01,10.02,7]hexadec-10-ene-6-carboxylic acid	127046796	Click to see	348.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
(1S,2S,6R,7R,12R)-2,6-dimethyl-9-oxo-12-propan-2-yl-13,14-dioxatetracyclo[10.2.2.01,10.02,7]hexadec-10-ene-6-carboxylic acid	162951026	Click to see CC(C)C12CCC3(C(=C1)C(=O)CC4C3(CCCC4(C)C(=O)O)C)OO2	348.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
2,6-Dimethyl-9-oxo-12-propan-2-yl-13,14-dioxatetracyclo[10.2.2.01,10.02,7]hexadec-10-ene-6-carboxylic acid	162951025	Click to see CC(C)C12CCC3(C(=C1)C(=O)CC4C3(CCCC4(C)C(=O)O)C)OO2	348.40	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
methyl (1R,2S,6R,7R,12S)-2,6-dimethyl-9-oxo-12-propan-2-yl-13,14-dioxatetracyclo[10.2.2.01,10.02,7]hexadec-10-ene-6-carboxylate	162906855	Click to see	362.50	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
Methyl 2,6-dimethyl-9-oxo-12-propan-2-yl-13,14-dioxatetracyclo[10.2.2.01,10.02,7]hexadec-10-ene-6-carboxylate	162906854	Click to see CC(C)C12CCC3(C(=C1)C(=O)CC4C3(CCCC4(C)C(=O)OC)C)OO2	362.50	unknown	https://doi.org/10.1016/S0031-9422(97)84396-8
> Organoheterocyclic compounds / Oxepanes
(1S,3R,5R,6R,10S,11R,14S,16R)-6,10-dimethyl-14-propan-2-yl-2,15-dioxapentacyclo[9.5.0.01,3.05,10.014,16]hexadecane-6-carboxylic acid	101105391	Click to see	334.40	unknown	https://doi.org/10.1055/S-2001-10873
6,10-Dimethyl-14-propan-2-yl-2,15-dioxapentacyclo[9.5.0.01,3.05,10.014,16]hexadecane-6-carboxylic acid	78297548	Click to see	334.40	unknown	https://doi.org/10.1055/S-2001-10873
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Cedrusin	21722963	Click to see COC1=C(C=CC(=C1)C2C(C3=C(O2)C(=CC(=C3)CCCO)O)CO)O	346.40	unknown	https://doi.org/10.5246/JCPS.2012.05.057
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxycinnamic acid methyl ester	92202	Click to see	194.18	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
Methyl Caffeate	689075	Click to see	194.18	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Flavan-3,3',4',5,5',7-hexol	1249	Click to see	306.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5R,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	162919159	Click to see	594.50	unknown	https://doi.org/10.1139/B80-267
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
3',8-Dihydroxy-4',6,7-trimethoxyisoflavone	3044875	Click to see COC1=C(C=C(C=C1)C2=COC3=C(C(=C(C=C3C2=O)OC)OC)O)O	344.30	unknown	https://doi.org/10.1021/NP060439Q
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Pseudolaroside B	98774697	Click to see COC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O	330.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017

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Larix kaempferi

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