Scientific name	Authority	First published in
Pinus kesiya subsp. yunnanensis	(Franch.) Businský	Acta Pruhon. 68: 24 (1999)
Pinus insularis var. yunnanensis	(Franch.) Silba	Phytologia Mem. 7: 52 (1984)
Pinus sinensis var. yunnanensis	(Franch.) Shaw	Pl. Wilson. 2: 17. 1914
Pinus tabuliformis var. yunnanensis	(Franch.) Dallim. & A.B.Jacks.	Handb. Conif. ed. 3: 563. 1948

Common names Top

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Filter by language:

Language	Common/alternative name
English	yunnan pine
Spanish	pino de yunnan
Arabic	صنوبر ينان
Esperanto	junana pino
Persian	کاج یوننانی
Hebrew	אורן יונאן
Croatian	yunnanski bor
Icelandic	yunnanfura
Japanese	ウンナンマツ
koi	Юньнанись пожум
mdf	Юньнанень пиче
udm	Юньнаньысь пужым
Chinese	雲南松
Chinese	地盘松球
Chinese	松笔头
Chinese	松叶
Chinese	飞松
Chinese	青松
Chinese	长毛松
Chinese	云南松
Chinese	松节
Chinese	松球

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Pinus yunnanensis var. pygmaea	(Hsueh ex C.Y.Cheng, W.C.Cheng & L.K.Fu) Hsueh	Fl. Reipubl. Popularis Sin. 7: 258 (1978)
Pinus yunnanensis var. yunnanensis

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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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 South-central
  - China Southeast

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000481591
Tropicos	24900663
KEW	urn:lsid:ipni.org:names:263419-1
The Plant List	kew-2562237
Open Tree Of Life	714289
NCBI Taxonomy	88732
IUCN Red List	42428
IPNI	263419-1
iNaturalist	135658
GBIF	5285783
Freebase	/m/02vt_gd
EPPO	PIUYU
EOL	1061744
USDA GRIN	28571
Wikipedia	Pinus_yunnanensis
CMAUP	NPO13294

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

Climate and soil stressed elevation patterns of plant species to determine the aboveground biomass distributions in a valley-type Savanna

He G, Shi Z, Fang H, Shi L, Wang Y, Yang H, Yan B, Yang C, Yu J, Liang Q, Zhao L, Jiang Q

Front Plant Sci

27-Mar-2024

PMCID:	PMC11004315
doi:	10.3389/fpls.2024.1324841
PMID:	38601315

Colonization of root endophytic fungus Serendipita indica improves drought tolerance of Pinus taeda seedlings by regulating metabolome and proteome

Wu C, Yang Y, Wang Y, Zhang W, Sun H

Front Microbiol

15-Mar-2024

PMCID:	PMC10978793
doi:	10.3389/fmicb.2024.1294833
PMID:	38559354

Environmental Controls on Evapotranspiration and Its Components in a Qinghai Spruce Forest in the Qilian Mountains

Gao G, Guo X, Feng Q, Xu E, Hao Y, Wang R, Jing W, Ren X, Liu S, Shi J, Wu B, Wang Y, Wen Y

Plants (Basel)

12-Mar-2024

PMCID:	PMC10974258
doi:	10.3390/plants13060801
PMID:	38592818

Responses of Three Pedicularis Species to Geological and Climatic Changes in the Qinling Mountains and Adjacent Areas in East Asia

Zhang Q, Lu Z, Guo M, Kang J, Li J, He X, Wu J, Liu R, Dang J, Li Z

Plants (Basel)

08-Mar-2024

PMCID:	PMC10974801
doi:	10.3390/plants13060765
PMID:	38592792

Population Structure and Genetic Diversity of the Toona ciliata (Meliaceae) Complex Assayed with Chloroplast DNA Markers

Wang ZY, Hu Y, Lv YW, Xiao Y, He ZH, Wu C, Hu XS

Genes (Basel)

28-Feb-2024

PMCID:	PMC10970150
doi:	10.3390/genes15030320
PMID:	38540379

Antioxidant Activity of Essential Oils from Pinaceae Species

Ancuceanu R, Anghel AI, Hovaneț MV, Ciobanu AM, Lascu BE, Dinu M

Antioxidants (Basel)

26-Feb-2024

PMCID:	PMC10967544
doi:	10.3390/antiox13030286
PMID:	38539820

Applicability analysis of flame height estimation based on Byram’s fireline intensity model under flat and windless conditions

Zhang Y, Luo A

Sci Rep

23-Feb-2024

PMCID:	PMC10891076
doi:	10.1038/s41598-024-55132-3
PMID:	38396250

Complete chloroplast genome sequence of Pinus tabuliformis var. henryi (Mast.) C.T.Kuan 1983 (Pinaceae)

Wang X, Zhao L, Yang XX, Liu ZL

Mitochondrial DNA B Resour

11-Jan-2024

PMCID:	PMC10786436
doi:	10.1080/23802359.2023.2301013
PMID:	38222979

Vertical distribution characteristics of soil organic carbon and vegetation types under different elevation gradients in Cangshan, Dali

Yang X, Xu J, Wang H, Quan H, Yu H, Luan J, Wang D, Li Y, Lv D

PeerJ

04-Jan-2024

PMCID:	PMC10771771
doi:	10.7717/peerj.16686
PMID:	38188153

A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes

Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B

Molecules

21-Dec-2023

PMCID:	PMC10780140
doi:	10.3390/molecules29010060
PMID:	38202643

Plastome phylogenomics and morphological traits analyses provide new insights into the phylogenetic position, species delimitation and speciation of Triplostegia (Caprifoliaceae)

Fu QL, Mo ZQ, Xiang XG, Milne RI, Jacquemyn H, Burgess KS, Sun YN, Yan H, Qiu L, Yang BY, Tan SL

BMC Plant Biol

15-Dec-2023

PMCID:	PMC10722739
doi:	10.1186/s12870-023-04663-4
PMID:	38097946

Morphology and Molecular Phylogeny Reveal Five New Species of Laccaria (Hydnangiaceae, Agaricales) from Southern China

Zhang M, Gao XL, Mu LQ, Deng WQ

J Fungi (Basel)

08-Dec-2023

PMCID:	PMC10744585
doi:	10.3390/jof9121179
PMID:	38132780

Phytohormone biosynthesis and transcriptional analyses provide insight into the main growth stage of male and female cones Pinus koraiensis

Li Y, Zhao M, Cai K, Liu L, Han R, Pei X, Zhang L, Zhao X

Front Plant Sci

11-Oct-2023

PMCID:	PMC10598626
doi:	10.3389/fpls.2023.1273409
PMID:	37885661

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Effects of geo‐climate factors on phenotypic variation in cone and seed traits of Pinus yunnanensis

Gao C, Liu F, Miao Y, Li J, Liu Z, Cui K

Ecol Evol

28-Sep-2023

PMCID:	PMC10534196
doi:	10.1002/ece3.10568
PMID:	37780092

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 / Cumenes
(1S,2R,3S)-3-hydroxy-1,3-dimethyl-2-[2-(3-propan-2-ylphenyl)ethyl]cyclohexane-1-carboxylic acid	162998739	Click to see CC(C)C1=CC=CC(=C1)CCC2C(CCCC2(C)O)(C)C(=O)O	318.40	unknown	https://doi.org/10.1002/HLCA.200900238
3-Hydroxy-1,3-dimethyl-2-[2-(3-propan-2-ylphenyl)ethyl]cyclohexane-1-carboxylic acid	162998738	Click to see CC(C)C1=CC=CC(=C1)CCC2C(CCCC2(C)O)(C)C(=O)O	318.40	unknown	https://doi.org/10.1002/HLCA.200900238
> 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 CC1(CCCC2(C1CC(C3=CC(=O)CCC32)O)C)CO	278.40	unknown	https://doi.org/10.1080/10286020.2011.565747
13-Oxopodocarp-8(14)-en-18-oic acid	26183540	Click to see CC12CCCC(C1CCC3=CC(=O)CCC23)(C)C(=O)O	276.40	unknown	https://doi.org/10.1515/ZNB-2010-0614
7,15-Dihydroxypodocarp-8(14)-en-13-one	10731307	Click to see CC1(CCCC2(C1CC(C3=CC(=O)CCC32)O)C)CO	278.40	unknown	https://doi.org/10.1080/10286020.2011.565747
CID 14705600	14705600	Click to see CC12CCCC(C1CCC3=CC(=O)CCC23)(C)C(=O)O	276.40	unknown	https://doi.org/10.1515/ZNB-2010-0614
> Lignans, neolignans and related compounds
3-[(1S,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]-5-(3-hydroxypropyl)benzene-1,2-diol	162985356	Click to see COC1=C(C=CC(=C1)C(C(CO)C2=C(C(=CC(=C2)CCCO)O)O)O)O	364.40	unknown	https://doi.org/10.1515/ZNB-2010-0614
> Lignans, neolignans and related compounds / Lignan lactones
(5R,5aS,8aR)-5-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one	134842228	Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(=O)C3CC4=CC5=C(C=C24)OCO5	398.40	unknown	https://doi.org/10.1002/HLCA.200900238
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl)methanol	107171	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C	286.50	unknown	https://doi.org/10.1080/10286020.2011.565747
(1R,4aR,4bR,10S,10aR)-10-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-6-oxo-3,4,4b,5,10,10a-hexahydro-2H-phenanthrene-1-carboxylic acid	46895239	Click to see CC12CCCC(C1C(C=C3C2CC(=O)C(=C3)C(C)(C)O)O)(C)C(=O)O	348.40	unknown	https://doi.org/10.1515/ZNB-2010-0614
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/10.1080/10286020.2011.565747
1-(Hydroxymethyl)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol	3838750	Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)CO	318.40	unknown	https://doi.org/10.1080/10286020.2011.565747
1-(hydroxymethyl)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	78297554	Click to see CC1(CCCC2(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)C)CO	316.40	unknown	https://doi.org/10.1080/10286020.2011.565747
1-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	78297552	Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)O	302.40	unknown	https://doi.org/10.1080/10286020.2011.565747
1,4a-Dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid	90895	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	https://doi.org/10.1515/ZNB-2010-0614
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/10.1080/10286020.2011.565747
12-Hydroxyabietic acid	52325853	Click to see CC(C)C1=CC2=CCC3C(C2CC1O)(CCCC3(C)C(=O)O)C	318.40	unknown	https://doi.org/10.1515/ZNB-2010-0614
12-Hydroxydehydroabietic Acid	13370050	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)O	316.40	unknown	https://doi.org/10.1002/HLCA.200900238
12alpha-12-Hydroxy-7,13-abietadien-18-oic acid	288368	Click to see CC(C)C1=CC2=CCC3C(C2CC1O)(CCCC3(C)C(=O)O)C	318.40	unknown	https://doi.org/10.1515/ZNB-2010-0614
12alpha-Methoxyabieta-7,13-diene-18-oic acid	49871253	Click to see CC(C)C1=CC2=CCC3C(C2CC1OC)(CCCC3(C)C(=O)O)C	332.50	unknown	https://doi.org/10.1515/ZNB-2010-0614
13-Hydroxy-8,11,13-podocarpatriene-18-oic acid	11558144	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)O)(C)C(=O)O	274.35	unknown	https://doi.org/10.1515/ZNB-2010-0614
15-Hydroxy-7-oxodehydroabietic acid	14017925	Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O	330.40	unknown	https://doi.org/10.1080/10286020.2011.565747
15-Hydroxydehydroabietic acid	14487943	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O	316.40	unknown	https://doi.org/10.1515/ZNB-2010-0614 https://doi.org/10.1080/10286020.2011.565747
15,18-Dihydroxyabieta-8,11,13-trien-7-one	3009631	Click to see CC1(CCCC2(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)C)CO	316.40	unknown	https://doi.org/10.1080/10286020.2011.565747
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/10.1080/10286020.2011.565747
18-Norabieta-8,11,13-trien-4-ol	15605917	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C	272.40	unknown	https://doi.org/10.1080/10286020.2011.565747
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/10.1080/10286020.2011.565747
18-Rabieta-8,11,13-triene-4,15-diol	73069324	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)O	288.40	unknown	https://doi.org/10.1080/10286020.2011.565747
19-Nor-4-hydroxyabieta-8,11,13-trien-7-one	91884799	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)O)C	286.40	unknown	https://doi.org/10.1080/10286020.2011.565747
19-r-4-Hydroxyabieta-8,11,13-trien-7-one	13392644	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)O)C	286.40	unknown	https://doi.org/10.1080/10286020.2011.565747
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/10.1080/10286020.2011.565747
4-[[7-(2-Hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]methoxy]-4-oxobutanoic acid	75179786	Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)COC(=O)CCC(=O)O	402.50	unknown	https://doi.org/10.1080/10286020.2011.565747
6-Hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	241938	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)O	316.40	unknown	https://doi.org/10.1002/HLCA.200900238
7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic Acid	9944781	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O	316.40	unknown	https://doi.org/10.1080/10286020.2011.565747 https://doi.org/10.1515/ZNB-2010-0614
7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-9-oxo-3,4,10,10a-tetrahydro-2H-phenanthrene-1-carboxylic acid	11724193	Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)O	330.40	unknown	https://doi.org/10.1080/10286020.2011.565747
7-(2-Methoxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	75179805	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)OC)(C)C(=O)O	330.50	unknown	https://doi.org/10.1080/10286020.2011.565747 https://doi.org/10.1002/HLCA.200900238
7-Oxo-12alpha,13beta-dihydroxyabietane-8(14)-ene-18-oic acid	101521440	Click to see CC(C)C1(C=C2C(CC1O)C3(CCCC(C3CC2=O)(C)C(=O)O)C)O	350.40	unknown	https://doi.org/10.1515/ZNB-2010-0614
7-Oxodehydroabietinol	15715176	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2=O)(C)CO)C	300.40	unknown	https://doi.org/10.1080/10286020.2011.565747
Abiesadine I	46230076	Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)COC(=O)CCC(=O)O	402.50	unknown	https://doi.org/10.1080/10286020.2011.565747
Abiesadine N	46230129	Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)OC)(C)C(=O)O	330.50	unknown	https://doi.org/10.1002/HLCA.200900238 https://doi.org/10.1080/10286020.2011.565747
Abieta-8,11,13-triene-7,15,18-triol	91895315	Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)CO	318.40	unknown	https://doi.org/10.1080/10286020.2011.565747
Abietic acid	10569	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	https://doi.org/10.1515/ZNB-2010-0614
Daturabietatriene	11392488	Click to see CC1(CCCC2(C1CCC3=C2C=CC(=C3)C(C)(C)O)C)CO	302.50	unknown	https://doi.org/10.1080/10286020.2011.565747
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/10.1080/10286020.2011.565747
Dehydroabietinol	15586718	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C	286.50	unknown	https://doi.org/10.1080/10286020.2011.565747
delta8(14)-Pimaric acid	10116	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	https://doi.org/10.1515/ZNB-2010-0614
Dihydroagathic acid	578152	Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CC(=O)O	336.50	unknown	https://doi.org/10.1002/HLCA.200900238
Junicedric acid	38347252	Click to see CC(CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)CC(=O)O	336.50	unknown	https://doi.org/10.1002/HLCA.200900238
Methyl 7,15-dihydroxydehydroabietate	91895316	Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)OC	346.50	unknown	https://doi.org/10.1080/10286020.2011.565747
Pimaric acid	220338	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	https://doi.org/10.1515/ZNB-2010-0614
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,6S)-6-[(3R,5S,8R,10R,13S,14R,17S)-3-methoxy-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-1,2,3-triol	163009861	Click to see CC(CCC(C(C)(CO)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C	490.80	unknown	https://doi.org/10.1002/HLCA.200900238
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-methoxy-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	162939471	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C	474.80	unknown	https://doi.org/10.1002/HLCA.200900238
6-(3-methoxy-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-1,2,3-triol	163009860	Click to see CC(CCC(C(C)(CO)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)OC)C)C)C	490.80	unknown	https://doi.org/10.1002/HLCA.200900238
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
6-Hydroxy-7-[5-[5-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-4b-methyl-2-(2-methylfuran-3-yl)-2,3,4,4a,5,6,7,8,10,10a-decahydrophenanthren-1-one	73241677	Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3C(OC(CC3OC)OC4CC5=CCC6C(C5(CC4O)C)CCC(C6=O)C7=C(OC=C7)C)C)C)OC)O	762.90	unknown	https://doi.org/10.1080/10286020.2011.565747
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Pinyunin A	46895238	Click to see CC1(C2C(O1)C3CCC4C(C3=CC2=O)(CCCC4(C)C(=O)O)C)C	332.40	unknown	https://doi.org/10.1515/ZNB-2010-0614
> Organoheterocyclic compounds / Benzofurans / Flavaglines
(1R)-1alpha-(Formyloxy)-3beta-phenyl-3abeta-(1,3-benzodioxol-5-yl)-6,8-dimethoxy-8bbeta-hydroxy-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]benzofuran-2alpha-carboxylic acid methyl ester	10721063	Click to see COC1=CC2=C(C(=C1)OC)C3(C(C(C(C3(O2)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)C(=O)OC)OC=O)O	534.50	unknown	via CMAUP database
(1R)-1alpha,8bbeta-Dihydroxy-3beta-phenyl-3abeta-(1,3-benzodioxol-5-yl)-6,8-dimethoxy-2,3,3a,8b-tetrahydro-1H-cyclopenta[b]benzofuran-2alpha-carboxylic acid methyl ester	390507	Click to see COC1=CC2=C(C(=C1)OC)C3(C(C(C(C3(O2)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)C(=O)OC)O)O	506.50	unknown	via CMAUP database
(1R)-2,3-Dihydro-1-(formyloxy)-8bbeta-hydroxy-3beta-phenyl-3abeta-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2alpha-carboxylic acid methyl ester	10650033	Click to see COC1=C(C=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC=O)C(=O)OC)C5=CC=CC=C5)O	536.50	unknown	via CMAUP database
(1R)-2,3-Dihydro-1,8bbeta-dihydroxy-3beta-phenyl-3abeta-(3,4-dimethoxyphenyl)-6,8-dimethoxy-1H-cyclopenta[b]benzofuran-2alpha-carboxylic acid methyl ester	10720804	Click to see COC1=C(C=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)OC)C5=CC=CC=C5)OC	522.50	unknown	via CMAUP database
3'-Hydroxyrocagloic acid methylester	10815498	Click to see COC1=C(C=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)OC)C5=CC=CC=C5)O	508.50	unknown	via CMAUP database
8bH-Cyclopenta[b]benzofuran-1,8b-diol, 3a-(1,3-benzodioxol-5-yl)-1,2,3,3a-tetrahydro-6,8-dimethoxy-3-phenyl-, (1R,3S,3aR,8bS)-	10623340	Click to see COC1=CC2=C(C(=C1)OC)C3(C(CC(C3(O2)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)O)O	448.50	unknown	via CMAUP database
Aglafoline	393601	Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C(=O)OC)C5=CC=CC=C5	492.50	unknown	via CMAUP database
methyl (1R,2R,3S,3aR,8bS)-1-acetyloxy-3a-(1,3-benzodioxol-5-yl)-8b-hydroxy-6,8-dimethoxy-3-phenyl-2,3-dihydro-1H-cyclopenta[b][1]benzofuran-2-carboxylate	10697870	Click to see CC(=O)OC1C(C(C2(C1(C3=C(O2)C=C(C=C3OC)OC)O)C4=CC5=C(C=C4)OCO5)C6=CC=CC=C6)C(=O)OC	548.50	unknown	via CMAUP database
Methyl 1-Formyloxyrocaglate	10839697	Click to see COC1=CC=C(C=C1)C23C(C(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)OC=O)C(=O)OC)C5=CC=CC=C5	520.50	unknown	via CMAUP database
Rocaglaol	393602	Click to see COC1=CC=C(C=C1)C23C(CC(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C5=CC=CC=C5	434.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Planchol E	53350155	Click to see CC12C(CC(=O)O1)C3C(O2)C(=O)C4=C(C=C(C=C4O3)O)O	292.24	unknown	https://doi.org/10.1080/10286020.2011.565747
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
12-(2-Hydroxypropan-2-yl)-2,6-dimethyl-13,14-dioxatetracyclo[10.2.2.01,10.02,7]hexadec-10-ene-6-carboxylic acid	85258492	Click to see CC1(CCCC2(C1CCC3=CC4(CCC32OO4)C(C)(C)O)C)C(=O)O	350.40	unknown	https://doi.org/10.1002/HLCA.200900238
Angustanoic acid D	10760330	Click to see CC1(CCCC2(C1CCC3=CC4(CCC32OO4)C(C)(C)O)C)C(=O)O	350.40	unknown	https://doi.org/10.1002/HLCA.200900238
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
N-[4-(2-Methyl-4-hydroxy-2-butenoylamino)butyl]cinnamamide	10980024	Click to see CC(=CCO)C(=O)NCCCCNC(=O)C=CC1=CC=CC=C1	316.40	unknown	via CMAUP database

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Pinus yunnanensis

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