Pseudolarix amabilis, also known as golden larch, is a deciduous coniferous tree native to eastern China. It is not a true larch, but is closely related to other conifer species such as Keteleeria, Abies, and Cedrus. It can reach heights of 30-40 meters and has a broad conic crown. The leaves are bright green and turn a brilliant golden yellow in the autumn, giving the tree its common name. The cones are distinctive and mature after 7 months, releasing winged seeds. This tree is popular for ornamental purposes in parks and gardens, and is tolerant of summer heat and humidity, making it suitable for regions where other larches and firs do not thrive. It has been awarded the Royal Horticultural Society's Award of Garden Merit.

Synonyms Top

Scientific name	Authority	First published in
Laricopsis fortunei	Mayr	Fremdländ. Wald-Parkbäume : 392 (1906)
Larix amabilis	J.Nelson	Pinaceae : 84 (1866)
Pseudolarix fortunei	Mayr	Monogr. Abietin. Japan. Reich. : 99 (1890)
Pseudolarix pourtetii	Ferré	Trav. Lab. Forest. Toulouse 1(4)4: 9 (1944)
Chrysolarix amabilis	(J.Nelson) H.E.Moore	Baileya 13: 133 (1965)

Common names Top

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Filter by language:

Language	Common/alternative name
English	golden larch
English	golden-larch
English	chinese golden-larch
English	chinese golden larch
Spanish	falso alerce dorado
Czech	pamodřín
Czech	pamodřín líbezný
Danish	guldlærk
German	goldlärche
German	goldlärchen
Estonian	ebalehis
Persian	سیاهکاجهای زرین
Finnish	kultalehtikuuset
Finnish	kultalehtikuusi
French	mélèze doré de chine
Croatian	zlatni ariš
Hungarian	kínai aranyfenyő
Icelandic	gullerki
Italian	pseudolarice
Italian	falso larice
Italian	falso lerice
Georgian	ცრულარიქსი
Korean	금전송
Macedonian	Златен ариш
Norwegian Bokmål	gullerk
Norwegian Bokmål	gull-lerk
Dutch	japanse goudlarix
Dutch	goudlarix
Polish	modrzewnik chiński
Russian	Золотая лиственница
Russian	Псевдолиственница
Russian	Лжелиственница
Chinese	金松
Chinese	金錢松
Chinese	水树
Chinese	金钱松叶
Chinese	金钱松
Chinese	土荆皮
Chinese	土槿皮

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

Asia-temperate click to expand
- China
  - China Southeast

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000479701
UNII	G2TMJ38TAU
Cornell Woody Plants	341
USDA Plants	PSAM4
UConn	368
Tropicos	24900395
KEW	urn:lsid:ipni.org:names:677125-1
The Plant List	kew-2559351
Missouri Botanical Garden	285032
PaleoBotany	7605
Open Tree Of Life	641107
NCBI Taxonomy	3355
IUCN Red List	34196
IPNI	677125-1
iNaturalist	135543
GBIF	2686287
Freebase	/m/04krw6
EPPO	PSLAM
EOL	1034860
USDA GRIN	314442
Wikipedia	Pseudolarix_amabilis

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

An update about beneficial effects of medicinal plants in aquaculture: A review

Dadras F, Velisek J, Zuskova E

Vet Med (Praha)

26-Dec-2023

PMCID:	PMC10828785
doi:	10.17221/96/2023-VETMED
PMID:	38303995

Pseudolaric acid B induces apoptosis associated with the mitochondrial and PI3K/AKT/mTOR pathways in triple‑negative breast cancer

Yang K, Wang JQ, Li K, Chen SN, Yu F

Oncol Rep

14-Sep-2023

PMCID:	PMC10535017
doi:	10.3892/or.2023.8630
PMID:	37711030

Pseudolaric Acid A: A Promising Antifungal Agent Against Prevalent Non-albicans Candida Species

Li Z, Zhu B, Chen W, Hu J, Xue Y, Yin H, Hu X, Liu W

Infect Drug Resist

07-Sep-2023

PMCID:	PMC10494979
doi:	10.2147/IDR.S419646
PMID:	37700797

Natural products modulate cell apoptosis: a promising way for treating endometrial cancer

Zhou X, Zeng Y, Zheng R, Wang Y, Li T, Song S, Zhang S, Huang J, Ren Y

Front Pharmacol

08-Jun-2023

PMCID:	PMC10285317
doi:	10.3389/fphar.2023.1209412
PMID:	37361222

Transcriptomic and metabolomic analysis of autumn leaf color change in Fraxinus angustifolia

Wang Y, Zhen J, Che X, Zhang K, Zhang G, Yang H, Wen J, Wang J, Wang J, He B, Yu A, Li Y, Wang Z

PeerJ

12-May-2023

PMCID:	PMC10184661
doi:	10.7717/peerj.15319
PMID:	37197583

Effect of dietary garlic (Allium sativum) on the zootechnical performance and health indicators of aquatic animals: A mini-review

Delgado DL, Caceres LL, Gómez SA, Odio AD

Vet World

11-May-2023

PMCID:	PMC10420702
doi:	10.14202/vetworld.2023.965-976
PMID:	37576751

Research progress of Traditional Chinese Medicine (TCM) in targeting inflammation and lipid metabolism disorder for arteriosclerosis intervention: A review

Xuan X, Zhang J, Fan J, Zhang S

Medicine (Baltimore)

05-May-2023

PMCID:	PMC10158879
doi:	10.1097/MD.0000000000033748
PMID:	37144986

A review on pathogenicity of Aeromonas hydrophila and their mitigation through medicinal herbs in aquaculture

Semwal A, Kumar A, Kumar N

Heliyon

28-Feb-2023

PMCID:	PMC10018484
doi:	10.1016/j.heliyon.2023.e14088
PMID:	36938468

Anticancer Therapeutic Effects of Green Tea Catechins (GTCs) When Integrated with Antioxidant Natural Components

Oh JW, Muthu M, Pushparaj SS, Gopal J

Molecules

24-Feb-2023

PMCID:	PMC10004647
doi:	10.3390/molecules28052151
PMID:	36903395

Phylotranscriptomics and evolution of key genes for terpene biosynthesis in Pinaceae

Jiang K, Du C, Huang L, Luo J, Liu T, Huang S

Front Plant Sci

17-Feb-2023

PMCID:	PMC9982022
doi:	10.3389/fpls.2023.1114579
PMID:	36875589

Pest categorisation of Matsucoccus massonianae

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

EFSA J

25-Nov-2022

PMCID:	PMC9692236
doi:	10.2903/j.efsa.2022.7643
PMID:	36447753

Integrated Chemical Characterization, Network Pharmacology and Transcriptomics to Explore the Mechanism of Sesquiterpenoids Isolated from Gynura divaricata (L.) DC. against Chronic Myelogenous Leukemia

Ye X, Wang L, Yang X, Yang J, Zhou J, Lan C, Kantawong F, Kumsaiyai W, Wu J, Zeng J

Pharmaceuticals (Basel)

19-Nov-2022

PMCID:	PMC9693606
doi:	10.3390/ph15111435
PMID:	36422564

Suppressive effect of pseudolaric acid B on Echinococcus multilocularis involving regulation of TGF-β1 signaling in vitro and in vivo

Gao H, Huo L, Mo X, Jiang B, Luo Y, Xu B, Li J, Ma X, Jing T, Feng Z, Zhang T, Hu W

Front Microbiol

11-Nov-2022

PMCID:	PMC9691991
doi:	10.3389/fmicb.2022.1008274
PMID:	36439797

Role of macrophage polarization in osteoarthritis (Review)

Chen B, Hong H, Sun Y, Chen C, Wu C, Xu G, Bao G, Cui Z

Exp Ther Med

09-Nov-2022

PMCID:	PMC9748658
doi:	10.3892/etm.2022.11693
PMID:	36561979

Targeting HIF-1α by Natural and Synthetic Compounds: A Promising Approach for Anti-Cancer Therapeutics Development

Ghosh R, Samanta P, Sarkar R, Biswas S, Saha P, Hajra S, Bhowmik A

Molecules

15-Aug-2022

PMCID:	PMC9413992
doi:	10.3390/molecules27165192
PMID:	36014432

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	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
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
> Benzenoids / Phenols / Methoxyphenols
Isovanillin	12127	Click to see COC1=C(C=C(C=C1)C=O)O	152.15	unknown	https://doi.org/10.5246/JCPS.2012.05.057
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Pseudolaric acid D	91895324	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C4)C(=O)O)C)CO	318.40	unknown	https://doi.org/10.1002/CHIN.200703163
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,2S,3'R,4R,6S,8R,9R,10R,12S,15R,20S,21R,23S)-21-hydroxy-2,3',8,10,19,19-hexamethylspiro[5,13,14,18-tetraoxahexacyclo[18.3.2.02,10.04,9.012,23.015,21]pentacosane-6,5'-oxolane]-2',17-dione	163038835	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CC5C6CC7(C(CCC6C4(C3)C)C(OC(=O)CC7OO5)(C)C)O)C	532.70	unknown	https://doi.org/10.3987/COM-90-5527
(1R,3'R,4R,5R,6R,8S,10R,12S,13S,16R,21R,25R)-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	21595102	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC7(C(CCC5C4(C3)C)C(OC(=O)CC7OO6)(C)C)O)C	532.70	unknown	https://doi.org/10.3987/COM-90-5527
(1S,3'R,4R,5R,6R,8S,10R,12S,13S,16S,22S)-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	162988340	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC7(C=CC(=O)OC(C7CCC5C4(C3)C)(C)C)OO6)C	514.60	unknown	https://doi.org/10.1002/HLCA.201100166
21-Hydroxy-2,3',8,10,19,19-hexamethylspiro[5,13,14,18-tetraoxahexacyclo[18.3.2.02,10.04,9.012,23.015,21]pentacosane-6,5'-oxolane]-2',16-dione	163194485	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CC5C6CC7(C(CCC6C4(C3)C)C(OCC(=O)C7OO5)(C)C)O)C	532.70	unknown	https://doi.org/10.3987/COM-90-5527
21-Hydroxy-2,3',8,10,19,19-hexamethylspiro[5,13,14,18-tetraoxahexacyclo[18.3.2.02,10.04,9.012,23.015,21]pentacosane-6,5'-oxolane]-2',17-dione	163038833	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CC5C6CC7(C(CCC6C4(C3)C)C(OC(=O)CC7OO5)(C)C)O)C	532.70	unknown	https://doi.org/10.3987/COM-90-5527
22-Hydroxy-3',4,6,12,17,17-hexamethylspiro[9,18,24-trioxahexacyclo[19.2.1.01,13.04,12.05,10.016,22]tetracosane-8,5'-oxolane]-2',19-dione	163192823	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC7(C(CCC5C4(C3)C)C(OC(=O)CC7O6)(C)C)O)C	516.70	unknown	https://doi.org/10.1080/10286029908039866
3-(7-Acetyloxy-4-methoxycarbonyl-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl)propanoic acid	162983300	Click to see CC(=O)OC12CCC(=CCC13CCC2C(OC3=O)(C)CCC(=O)O)C(=O)OC	394.40	unknown	https://doi.org/10.1016/S0968-0896(03)00531-5
3-(7-Hydroxy-4-methoxycarbonyl-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl)propanoic acid	163034187	Click to see CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)O)C(=O)O1)CCC(=O)O	352.40	unknown	https://doi.org/10.1016/S0968-0896(03)00531-5
3-[(1R,7S,8R,9R)-7-hydroxy-4-methoxycarbonyl-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl]propanoic acid	163034188	Click to see CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)O)C(=O)O1)CCC(=O)O	352.40	unknown	https://doi.org/10.1016/S0968-0896(03)00531-5
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 CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC7(C=CC(=O)OC(C7CCC5C4(C3)C)(C)C)OO6)C	514.60	unknown	https://doi.org/10.1016/S0040-4039(00)97410-0
Pseudolarolide I	6711555	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC7(C(CCC5C4(C3)C)C(OC(=O)CC7OO6)(C)C)O)C	532.70	unknown	https://doi.org/10.3987/COM-90-5527
Pseudolarolide O	11826970	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CC=C5CC6=CCC(=O)OC(C6CCC5C4(C3)C)(C)C)C	482.60	unknown	https://doi.org/10.1002/HLCA.200390079
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,7S,8R,9S)-9-[(1E,3E)-4-carboxypenta-1,3-dienyl]-7-hydroxy-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-ene-4-carboxylic acid	162923392	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)O)O)C(=O)O1)C)C(=O)O	376.40	unknown	https://doi.org/10.1021/NP980469W
(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/10.1021/NP060439Q https://doi.org/10.1021/NP0200010 https://doi.org/10.1055/S-2007-969944
(2E,4E)-5-[(1R,7S,8R,9S)-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	124396989	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/NP980469W
(2E,4E)-5-[(1R,7S,8S,9S)-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	6341786	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)O	432.50	unknown	https://doi.org/10.1021/NP0200010 https://doi.org/10.1021/NP980469W
[(2R)-2,3-dihydroxypropyl] (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	163061398	Click to see CC1=CCC23CCC(C2(CC1)O)C(OC3=O)(C)C=CC=C(C)C(=O)OCC(CO)O	420.50	unknown	https://doi.org/10.1021/NP060439Q
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2E,4E)-5-[(1R,3R,7S,8S,9R)-7-acetyloxy-3-hydroxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-4-en-9-yl]-2-methylpenta-2,4-dienoate	44421306	Click to see CC1=CCC2(C3CCC2(CC1O)C(=O)OC3(C)C=CC=C(C)C(=O)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C	566.60	unknown	https://doi.org/10.1021/NP060439Q
[(2S)-2,3-dihydroxypropyl] (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-dienoate	163061397	Click to see CC1=CCC23CCC(C2(CC1)O)C(OC3=O)(C)C=CC=C(C)C(=O)OCC(CO)O	420.50	unknown	https://doi.org/10.1021/NP060439Q
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 5-(7-acetyloxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-en-9-yl)-2-methylpenta-2,4-dienoate	75072020	Click to see CC1=CCC23CCC(C2(CC1)OC(=O)C)C(OC3=O)(C)C=CC=C(C)C(=O)OC4C(C(C(C(O4)CO)O)O)O	550.60	unknown	https://doi.org/10.1021/NP980469W
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/10.1021/NP060439Q https://doi.org/10.1021/NP0200010 https://doi.org/10.1055/S-2007-969944 https://doi.org/10.1016/J.CHROMA.2008.05.068 https://doi.org/10.1002/CHIN.200407159
5-(7-Acetyloxy-3-hydroxy-4,9-dimethyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-4-en-9-yl)-2-methylpenta-2,4-dienoic acid	85305846	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/NP060439Q
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-dienoic acid	163023791	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
5-(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	621355	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)O	432.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3402633/ https://doi.org/10.1021/NP50097A015 https://doi.org/10.1021/NP060439Q https://doi.org/10.1016/J.CHROMA.2008.05.068 https://doi.org/10.1124/MOL.105.020537 https://doi.org/10.1021/NP980469W
5-(7-Acetyloxy-4,9-dimethyl-3,11-dioxo-10-oxatricyclo[6.3.2.01,7]tridec-4-en-9-yl)-2-methylpenta-2,4-dienoic acid	78200678	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/NP060439Q
5-(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 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/NP980469W
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 CC1=CCC23CCC(C2(CC1)O)C(OC3=O)(C)C=CC=C(C)C(=O)O	346.40	unknown	https://doi.org/10.1021/NP0200010
deacetylpseudolaric acid A	11977243	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
Demethoxydeacetoxypseudolaric acid B	6475946	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)O)O)C(=O)O1)C)C(=O)O	376.40	unknown	https://doi.org/10.1021/NP980469W
methyl (1R,7S,8R,9R)-9-[(1E,3E)-5-[(2R)-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	162880550	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)O)C(=O)O1)C)C(=O)OCC(CO)O	464.50	unknown	https://doi.org/10.1021/NP060439Q
methyl (1R,7S,8S,9S)-7-acetyloxy-9-[(1E,3E)-5-methoxy-4-methyl-5-oxopenta-1,3-dienyl]-9-methyl-11-oxo-10-oxatricyclo[6.3.2.01,7]tridec-3-ene-4-carboxylate	162987641	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)OC	446.50	unknown	https://doi.org/10.1021/NP0200010
methyl (2E,4E)-5-[(1R,4S,7S,8S,9R)-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	163189488	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 (2E,4E)-5-[(1R,7S,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-dienoate	163034782	Click to see CC1=CCC23CCC(C2(CC1)OC(=O)C)C(OC3=O)(C)C=CC=C(C)C(=O)OC	402.50	unknown	https://doi.org/10.1021/NP0200010
Methyl 7-acetyloxy-9-methyl-9-[4-methyl-5-oxo-5-[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	85097919	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)OC4C(C(C(C(O4)CO)O)O)O	594.60	unknown	https://doi.org/10.1021/NP060439Q https://doi.org/10.1021/NP980469W https://doi.org/10.1016/S0968-0896(03)00531-5
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/10.1055/S-2007-969944 https://doi.org/10.1016/J.CHROMA.2008.05.068
Pseudolaric acid B	6475943	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)O	432.50	unknown	https://doi.org/10.1021/NP060439Q https://doi.org/10.1021/NP980469W
Pseudolaric acid B-beta-D-glucoside	6475958	Click to see CC(=CC=CC1(COC(=O)C23CCC1C2(CCC(=CC3)C(=O)OC)O)C)C(=O)OC4C(C(C(C(O4)CO)O)O)O	566.60	unknown	https://doi.org/10.1021/NP060439Q
Pseudolaric acid B-O-beta-D-glucopyranoside	10031398	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)OC4C(C(C(C(O4)CO)O)O)O	594.60	unknown	https://doi.org/10.1021/NP060439Q https://doi.org/10.1021/NP0200010 https://doi.org/10.1021/NP980469W
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/10.1351/PAC198658050811 https://doi.org/10.1508/CYTOLOGIA.26.213 https://doi.org/10.1016/S0968-0896(03)00531-5 https://doi.org/10.1021/NP980469W
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/NP060439Q https://doi.org/10.1002/CHIN.200407159 https://doi.org/10.1016/S0968-0896(03)00531-5
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/NP060439Q
Pseudolaric acid H	11783999	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 https://doi.org/10.1016/S0968-0896(03)00531-5
PseudolaricacidAbeta-D-glucoside	44566375	Click to see CC1=CCC23CCC(C2(CC1)OC(=O)C)C(OC3=O)(C)C=CC=C(C)C(=O)OC4C(C(C(C(O4)CO)O)O)O	550.60	unknown	https://doi.org/10.1021/NP060439Q https://doi.org/10.1021/NP980469W
Pseudolaricacidb	129316864	Click to see CC(=CC=CC1(C2CCC3(C2(CCC(=CC3)C(=O)OC)OC(=O)C)C(=O)O1)C)C(=O)O	432.50	unknown	https://doi.org/10.1351/PAC198658050811 https://doi.org/10.1508/CYTOLOGIA.26.213 https://doi.org/10.1021/NP060439Q https://doi.org/10.1021/NP0200010 https://doi.org/10.1021/NP50115A007
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3'R,4R,8S,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	6711552	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC56CC57CCC(=O)OC(C7CCC6C4(C3)C)(C)C)C	484.70	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
(2R,6R)-6-[(3R,4S,5R,10S,13R,14S,17R)-3-hydroxy-4,10,13-trimethyl-7,11-dioxo-2,3,4,5,6,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-3-methylideneheptanoic acid	163082421	Click to see CC1C(CCC2(C1CC(=O)C3=C2C(=O)CC4(C3CCC4C(C)CCC(=C)C(C)C(=O)O)C)C)O	470.60	unknown	https://doi.org/10.1021/NP060439Q
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Pseudolarolide B	21592337	Click to see CC1CC2(C=C(C(=O)O2)C)OC3C1C4(CCC56CC57CCC(=O)C(C7CCC6C4(C3)C)(C)C)C	466.70	unknown	https://doi.org/10.1021/NP50097A015
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-alpha-hydroxysteroids
5-[(2R)-2-[(3R,5R,9S,10R,13S,17S)-3-hydroxy-4,4,10,13,17-pentamethyl-2,3,5,6,9,11,12,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl]propyl]furan-3-carboxylic acid	101147486	Click to see CC(CC1=CC(=CO1)C(=O)O)C2(CC=C3C2(CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C)C	466.70	unknown	https://doi.org/10.1016/S0960-894X(01)00633-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-hydroxy delta-7-steroids
5-[2-(3-hydroxy-4,4,10,13,17-pentamethyl-2,3,5,6,9,11,12,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl)propyl]furan-3-carboxylic acid	85141957	Click to see CC(CC1=CC(=CO1)C(=O)O)C2(CC=C3C2(CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C)C	466.70	unknown	https://doi.org/10.1016/S0960-894X(01)00633-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
2-[(4aR,4bS,6aR,6bS,7R,11aR,13aR)-1,1,4a,6a,7,11a-hexamethyl-2,9-dioxo-4,4b,5,6,6b,7,8,11,13,13a-decahydro-3H-indeno[2,1-a]phenanthren-10-yl]acetic acid	57326819	Click to see CC1CC(=O)C(=C2C1C3(CCC4C(=CCC5C4(CCC(=O)C5(C)C)C)C3(C2)C)C)CC(=O)O	452.60	unknown	https://doi.org/10.1016/J.TETLET.2011.12.004
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-Hydroxybenzoic acid glucoside	3320872	Click to see C1=CC(=CC=C1C(=O)O)OC2C(C(C(C(O2)CO)O)O)O	300.26	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxyphenyl)propan-1-one	638759	Click to see C1=CC(=CC=C1C(=O)CCO)O	166.17	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(3'R,4R,5R,6R,8S,10R,12R)-3',4,6,12,17,17-hexamethylspiro[9,18,24-trioxapentacyclo[19.2.1.04,12.05,10.016,22]tetracosa-15,20,22-triene-8,5'-oxolane]-2',19-dione	101244786	Click to see CC1CC2(CC(C(=O)O2)C)OC3C1C4(CCC5C=C6C(=CCCC4(C3)C)C(OC(=O)C=C6O5)(C)C)C	496.60	unknown	https://doi.org/10.1002/HLCA.200390079
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/10.1039/C39900001113
> Organoheterocyclic compounds / Isobenzofurans
3-Butylidene-6,7-dihydroxy-4,5,6,7-tetrahydro-2-benzofuran-1-one	3025856	Click to see CCCC=C1C2=C(C(C(CC2)O)O)C(=O)O1	224.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
Senkyunolide I	11521428	Click to see CCCC=C1C2=C(C(C(CC2)O)O)C(=O)O1	224.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-[[2-(3,5-Dihydroxyphenyl)-1-benzofuran-6-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	76189500	Click to see C1=CC2=C(C=C1OC3C(C(C(C(O3)CO)O)O)O)OC(=C2)C4=CC(=CC(=C4)O)O	404.40	unknown	https://doi.org/10.1021/NP980469W
> Phenylpropanoids and polyketides / Aurone flavonoids / Auronols
(2R)-2-[(3,5-dihydroxy-4-methoxyphenyl)methyl]-2,4,6-trihydroxy-1-benzofuran-3-one	92298898	Click to see COC1=C(C=C(C=C1O)CC2(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	334.28	unknown	https://doi.org/10.1021/NP980469W
(2S)-2-[(3,5-dihydroxy-4-methoxyphenyl)methyl]-2,4,6-trihydroxy-1-benzofuran-3-one	92298899	Click to see COC1=C(C=C(C=C1O)CC2(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	334.28	unknown	https://doi.org/10.1021/NP980469W
(2S)-2,4,6-trihydroxy-2-[(3,4,5-trihydroxyphenyl)methyl]-1-benzofuran-3-one	92299930	Click to see C1=C(C=C(C(=C1O)O)O)CC2(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1021/NP980469W
Amaronol A	485521	Click to see C1=C(C=C(C(=C1O)O)O)CC2(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	https://doi.org/10.1508/CYTOLOGIA.26.213 https://doi.org/10.5246/JCPS.2012.05.057 https://doi.org/10.1021/NP980469W
Amaronol B	485522	Click to see COC1=C(C=C(C=C1O)CC2(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	334.28	unknown	https://doi.org/10.1508/CYTOLOGIA.26.213 https://doi.org/10.5246/JCPS.2012.05.057 https://doi.org/10.1021/NP980469W
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin	9882981	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.017
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1021/NP980469W https://doi.org/10.1508/CYTOLOGIA.26.213
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
2,6-dihydroxy-2-[(4-hydroxyphenyl)methyl]-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-3-one	133554286	Click to see C1=CC(=CC=C1CC2(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O	450.40	unknown	https://doi.org/10.5246/JCPS.2012.05.057
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-Methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid	14132336	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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Pseudolarix amabilis

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