Scientific name	Authority	First published in
Picea intercedens var. glabra	Uyeki	J. Korean Pl. Forest. Soc. 206: ?. 1942
Picea koyamae var. koraiensis	(Nakai) Liou & Z.Wang	Ill. Fl. Lign. Pl. N. E. China 88 1955
Picea pungsanensis var. intercedens	(Nakai) T.Lee	Ill. Woody Pl. Korea 234 1966

Common names Top

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Filter by language:

Language	Common/alternative name
English	korean spruce
Arabic	تنوب كوري
Arabic	راتنج كوري
Bulgarian	корейски смърч
Czech	smrk korejský
Estonian	korea kuusk
Finnish	koreankuusi
Icelandic	kóreugreni
Italian	peccio coreano
Korean	종비나무
koi	Кореяись кӧз
Lithuanian	korėjinė eglė
Dutch	korean spruce
Russian	Ель корейская
udm	Кореяысь кыз
Ukrainian	Ялина корейська
vep	koreine kuz'
Chinese	紅皮雲杉
Chinese	高丽云杉
Chinese	针松
Chinese	虎尾松
Chinese	红皮臭
Chinese	溪云杉
Chinese	带岭云杉
Chinese	岛内云杉
Chinese	小片鳞松
Chinese	丰山云杉
Chinese	红皮云杉
Chinese	沙树

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Picea koraiensis var. pungsanensis	(Uyeki ex Nakai) Schmidt-Vogt ex Farjon	Pinaceae [Farjon] 231 (1990):.
Picea koraiensis var. tonaiensis	(Nakai) T.Lee	Ill. Woody Pl. Korea 234 1966

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
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Korea
- Russian Far East
  - Primorye

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000482447
Tropicos	24900103
INPN	611375
KEW	urn:lsid:ipni.org:names:676960-1
The Plant List	kew-2563377
Open Tree Of Life	262757
Observations.org	130574
NCBI Taxonomy	308680
IUCN Red List	42326
IPNI	676960-1
iNaturalist	135796
GBIF	5284854
Freebase	/m/0bj_xy
EOL	1061640
Elurikkus	6226
USDA GRIN	28300
Wikipedia	Picea_koraiensis

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

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

Effects of continuous monoculture on rhizosphere soil nutrients, growth, physiological characteristics, hormone metabolome of Casuarina equisetifolia and their interaction analysis

Wang Y, Wang Y, Li J, Cai Y, Hu M, Lin W, Wu Z

Heliyon

13-Feb-2024

PMCID:	PMC10878944
doi:	10.1016/j.heliyon.2024.e26078
PMID:	38384578

Effect of forest planting patterns on the formation of soil organic carbon during litter lignocellulose degradation from a microbial perspective

Wu D, Yin C, Fan Y, Chi H, Liu Z, Jin G

Front Microbiol

22-Dec-2023

PMCID:	PMC10771852
doi:	10.3389/fmicb.2023.1327481
PMID:	38188580

Changes in Soil Properties, Microbial Quantity and Enzyme Activities in Four Castanopsis hystrix Forest Types in Subtropical China

Wang R, Ma J, Liang H, Zhang Y, Yang J, Chen F, Wang Y, Yan W

Plants (Basel)

22-Jun-2023

PMCID:	PMC10347116
doi:	10.3390/plants12132411
PMID:	37446972

Transcriptome Analysis of Embryogenic and Non-Embryogenic Callus of Picea Mongolica

Wang Y, Wang H, Bao W, Sui M, Bai Y

Curr Issues Mol Biol

21-Jun-2023

PMCID:	PMC10378709
doi:	10.3390/cimb45070332
PMID:	37504248

Species asynchrony stabilizes productivity over 20 years in Northeast China

Jia B, He J, Wang X

Ecol Evol

03-May-2023

PMCID:	PMC10156448
doi:	10.1002/ece3.9991
PMID:	37153024

Effects of thinning on soil nutrient availability and fungal community composition in a plantation medium-aged pure forest of Picea koraiensis

Caihong Z, Nier S, Hao W, Honglin X, Hailong S, Ling Y

Sci Rep

13-Feb-2023

PMCID:	PMC9925727
doi:	10.1038/s41598-023-29498-9
PMID:	36781913

New insights into the cortex-to-stele ratio show it to effectively indicate inter- and intraspecific function in the absorptive roots of temperate trees

Liu X, Du Y, Ren Y, Wang S, Wang Y, Li Z, Wang W

Front Plant Sci

20-Jan-2023

PMCID:	PMC9895863
doi:	10.3389/fpls.2023.1061503
PMID:	36743504

Is the Lesser Khingan Suitable for the Amur Tiger Restoration? Perspectives with the Current State of the Habitat and Prey Base

Yachmennikova A, Zhu S, Kotlov I, Sandlersky R, Yi Q, Rozhnov V

Animals (Basel)

30-Dec-2022

PMCID:	PMC9818025
doi:	10.3390/ani13010155
PMID:	36611763

Effects of aspect on phenology of Larix gmelinii forest in Northeast China

Dong C, Qiao R, Chang X

Sci Rep

22-Dec-2022

PMCID:	PMC9780224
doi:	10.1038/s41598-022-26712-y
PMID:	36550181

Composition and diversity of soil bacterial communities under identical vegetation along an elevational gradient in Changbai Mountains, China

Li M, Dai G, Mu L

Front Microbiol

01-Dec-2022

PMCID:	PMC9751831
doi:	10.3389/fmicb.2022.1065412
PMID:	36532438

Development of Native Essential Oils from Forestry Resources in South Korea

Park C, Woo H

Life (Basel)

29-Nov-2022

PMCID:	PMC9785413
doi:	10.3390/life12121995
PMID:	36556360

Morphological and Transcriptional Characteristics of the Symbiotic Interaction between Pinus massoniana and Suillus bovinus

Feng W, Sun X, Ding G

J Fungi (Basel)

03-Nov-2022

PMCID:	PMC9699607
doi:	10.3390/jof8111162
PMID:	36354929

Mixed conifer-broadleaf trees on arbuscular mycorrhizal and ectomycorrhizal communities in rhizosphere soil of different plantation stands in the temperate zone, Northeast China

Zhang Y, Wang Q, Xu L, Ma S, Cui D, Zhu K, Feng W

Front Microbiol

27-Sep-2022

PMCID:	PMC9551461
doi:	10.3389/fmicb.2022.986515
PMID:	36238594

Pathophysiology and transcriptomic analysis of Picea koraiensis inoculated by bark beetle-vectored fungus Ophiostoma bicolor

Liu Y, Zhou Q, Wang Z, Wang H, Zheng G, Zhao J, Lu Q

Front Plant Sci

19-Jul-2022

PMCID:	PMC9345248
doi:	10.3389/fpls.2022.944336
PMID:	35928703

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/10.1007/BF00564022
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1007/BF00564022
> 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/10.1007/BF00564022
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1007/BF00579987
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
3,3-Dimethylpentane	11229	Click to see CCC(C)(C)CC	100.20	unknown	https://doi.org/10.1007/BF00570218
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1007/BF00570218
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol, (+)-	160521	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1007/BF00563906
> Lignans, neolignans and related compounds / Furanoid lignans
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/10.1007/BF00563906
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Olivile; Vladinol C	129317076	Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O	376.40	unknown	https://doi.org/10.1007/BF00563906
Lariciresinol	332427	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1007/BF00563906
> Lignans, neolignans and related compounds / Lignan lactones
(3aR,9aR)-7-hydroxy-9-(4-hydroxy-3-methoxyphenyl)-6-methoxy-3a,4,9,9a-tetrahydro-1H-benzo[f][2]benzofuran-3-one	12303843	Click to see COC1=C(C=C2C(C3COC(=O)C3CC2=C1)C4=CC(=C(C=C4)O)OC)O	356.40	unknown	https://doi.org/10.1007/BF00563906
CID 369613	369613	Click to see COC1=C(C=C2C(C3COC(=O)C3CC2=C1)C4=CC(=C(C=C4)O)OC)O	356.40	unknown	https://doi.org/10.1007/BF00563906
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Abietal	443479	Click to see CC(C)C1=CC2=CCC3C(CCCC3(C2CC1)C)(C)C=O	286.50	unknown	https://doi.org/10.1007/BF00569584
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/BF00569584
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1007/BF00570218
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-Isopropyl-5-methylanisole	14104	Click to see CC1=CC(=C(C=C1)C(C)C)OC	164.24	unknown	https://doi.org/10.1007/BF00570218
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1007/BF00570218
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,4S,5R)-4-Thujanol	12315154	Click to see CC(C)C12CCC(C1C2)(C)O	154.25	unknown	https://doi.org/10.1007/BF00579987
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1007/BF00579987 https://doi.org/10.1007/BF00570218
2,6,6-Trimethyl-bicyclo[3.1.1]heptanol	22833381	Click to see CC1CCC2CC1(C2(C)C)O	154.25	unknown	https://doi.org/10.1007/BF00579987
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1007/BF00570218 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264755/
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1007/BF00570218
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1007/BF00570218
Borneol	6552009	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1007/BF00579987
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1007/BF00579987 https://doi.org/10.1007/BF00570218
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1007/BF00570218
cis-Sabinene hydrate	11744854	Click to see CC(C)C12CCC(C1C2)(C)O	154.25	unknown	https://doi.org/10.1007/BF00579987
Sabinene hydrate	62367	Click to see CC(C)C12CCC(C1C2)(C)O	154.25	unknown	https://doi.org/10.1007/BF00579987
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1007/BF00579987
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1007/BF00579987
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1007/BF00579987
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1007/BF00570218
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1007/BF00570218
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1007/BF00570218
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Cyclosativene	519960	Click to see CC(C)C1CCC2(C3C1C4C2(C4C3)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
(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/BF00570218
(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/BF00570218
(1R,4aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene	5315589	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
(1R,4S,6R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]decan-4-ol	11543111	Click to see CC1CCC(C2C13C2C(CC3)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1007/BF00579987
(3R,6E)-nerolidol	11241545	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1007/BF00579987
(3S,6E)-Nerolidol	5281525	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1007/BF00579987
(4R,6R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]decan-4-ol	101410488	Click to see CC1CCC(C2C13C2C(CC3)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1007/BF00579987
(R)-beta-bisabolene	68128	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane	5317024	Click to see CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C	218.38	unknown	https://doi.org/10.1007/BF00570218
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
1,6-Dimethyl-4-isopropyltetralin	10224	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1007/BF00570218
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane	6432312	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
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/BF00570218
alpha-Cadinene, (+)-	12306048	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
alpha-Calacorene	12302243	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1007/BF00570218
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
Ar-Curcumene	3083834	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C	202.33	unknown	https://doi.org/10.1007/BF00570218
beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
beta-Copaene	57339298	Click to see CC(C)C1CCC2(C3C1C2C(=C)CC3)C	204.35	unknown	https://doi.org/10.1007/BF00570218
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/BF00570218
Calamenene	6429077	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1007/BF00570218
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
CID 16396350	16396350	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
Cubebol	11276107	Click to see CC1CCC(C2C13C2C(CC3)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1007/BF00579987
epi-Cubenol	519857	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	https://doi.org/10.1007/BF00579987
Epicubenol	12046149	Click to see CC1CCC(C2C1(CCC(=C2)C)O)C(C)C	222.37	unknown	https://doi.org/10.1007/BF00579987
epsilon-Muurolene	520461	Click to see CC(C)C1CCC(=C)C2C1CC(=C)CC2	204.35	unknown	https://doi.org/10.1007/BF00570218
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
gamma-Muurolene	12313020	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
Longicyclene	564934	Click to see CC1(CCCC2(C3C1C4C2(C4C3)C)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
Longifolene	289151	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
Nerolidol	8888	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1007/BF00579987
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1007/BF00570218
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,2R,4aS,8S,8aR)-4a,8-dimethyl-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,8-diol	162965423	Click to see CC(C)C1CCC2(CCCC(C2C1O)(C)O)C	240.38	unknown	https://doi.org/10.1007/BF00579987
(1S,2S,4aR,8S,8aS)-4a,8-dimethyl-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,8-diol	101596820	Click to see CC(C)C1CCC2(CCCC(C2C1O)(C)O)C	240.38	unknown	https://doi.org/10.1007/BF00579987
4a,8-Dimethyl-2-propan-2-yl-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,8-diol	5256741	Click to see CC(C)C1CCC2(CCCC(C2C1O)(C)O)C	240.38	unknown	https://doi.org/10.1007/BF00579987
7-epi-alpha-Selinene	10123	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
alpha-Selinene	10856614	Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1007/BF00570218
Sibirene	14167644	Click to see CC(C)C1=CC2C(=C)CCCC2(CC1)C	204.35	unknown	https://doi.org/10.1007/BF00570218
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
2,7-Cyclodecadien-1-ol, 1,7-dimethyl-4-(1-methylethyl)-	522445	Click to see CC1=CCCC(C=CC(CC1)C(C)C)(C)O	222.37	unknown	https://doi.org/10.1007/BF00579987
Germacra-1(10),5-dien-4beta-ol	11148775	Click to see CC1=CCCC(C=CC(CC1)C(C)C)(C)O	222.37	unknown	https://doi.org/10.1007/BF00579987
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1007/BF00564022
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1007/BF00564022
> Phenylpropanoids and polyketides / Stilbenes
Isorhapontigenin	5318650	Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O	258.27	unknown	https://doi.org/10.1007/BF00564001
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
Isorhapontin	5281716	Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O	420.40	unknown	https://doi.org/10.1007/BF00564001

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Picea koraiensis

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