Scientific name	Authority	First published in
Larix archangelica	Laws.	Agric. Man. : 389 (1836)
Larix altaica	Fisch. ex Gordon	Pinetum : 127 (1858)
Larix russica	(Endl.) Sabine ex Trautv.	Encyc. Trees 1054.
Larix pseudolarix	Lodd. ex Gordon	Pinetum : 127 (1858)
Larix sibirica var. hybrida	Y.N.Lee	Bull. Korea Pl. Res. 3: 22 (2003)
Larix sibirica var. viridis	Y.N.Lee	Bull. Korea Pl. Res. 3: 20 (2003)
Pinus pseudolarix	Steud.	Nomencl. Bot. , ed. 2, 2: 338 (1841)
Larix europaea var. sibirica	(Ledeb.) Loudon	Arbor. Frutic. Brit. 4: 2352. 1838
Larix decidua var. sibirica	(Ledeb.) Regel	Gartenflora 20: 101. 1871
Larix decidua subsp. sibirica	(Ledeb.) Domin	Acta Bot. Bohem. 10: 6. 1931 (1931)
Larix sukaczewii	Dylis	Dokl. Akad. Nauk S.S.S.R. 50: 489. 1946 [dt. 1945; publ. 1946]
Pinus larix var. russica	Endl.	Syn. Conif. 134. 1847
Larix decidua var. russica	(Endl.) Henkel & W.Hochst.	Syn. Nadelhölz. 132 1865
Larix europaea var. russica	(Endl.) Beissn.	Ziergehloze Gart. Park. ed. 2: 469 1884
Larix sibirica f. pendula	Schelle	Winterh. Nadelh. 169 1909
Pinus larix var. intermedia	Antoine	Coniferen 52. 1840
Larix altaica	Fisch. ex Parl.	Pinaceae# 84 1866
Larix decidua var. rossica	Henk. & Hochst.	Syn. Nadelh. 132 1865

Common names Top

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Filter by language:

Language	Common/alternative name
English	larix siberica
English	siberian larch
Spanish	alerce de siberia
Spanish	alerce siberiano
Arabic	أرزية سيبيرية
Azerbaijani	sibir qara şamı
azb	سیبیر قارا شامی
Belarusian	Лістоўніца сібірская
Bulgarian	сибирска лиственица
Catalan	làrix siberià
Czech	modřín sibiřský
German	sibirische lärche
German	pinus larix var. russica
German	pinus larix
German	pinus intermedia
German	larix sukaczewii
German	larix russica
German	larix intermedia
German	larix decidua var. sibirica
German	larix decidua var. russica
German	abies ledebourii
German	pinus ledebouri
Esperanto	siberia lariko
Estonian	siberi lehis
Persian	سیاهکاج سیبری
Finnish	arkangelinlehtikuusi
Finnish	siperianlehtikuusi
French	mélèze de sibérie
Hungarian	szibériai vörösfenyő
Armenian	խեժափիճի սիբիրական
Icelandic	síberíulerki
Japanese	西伯利亜落葉松
Japanese	シベリアカラマツ
Georgian	ციმბირული ლარიქსი
Kazakh	Сібір балқарағайы
koi	Сибирись лисвень
Lithuanian	sibirinis maumedis
Norwegian Bokmål	sibirlerk
Norwegian Bokmål	sibirske lerker
Norwegian Bokmål	sibirsk lerk
Norwegian Bokmål	sibirisk lerk
Polish	modrzew syberyjski
Russian	Лиственица сибирская
Russian	Лиственница сибирская
Russian	Лиственница архангельская
Swedish	sibirisk lärk
Ukrainian	Модрина сибірська
Chinese	新疆落叶松
Chinese	红杉皮
Chinese	西伯利亚落叶松
Chinese	俄国落叶松
Chinese	新疆落葉松

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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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
  - Xinjiang
- Mongolia
  - Mongolia
- Siberia
  - Altay
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia

Europe click to expand
- Eastern Europe
  - Central European Russia
  - East European Russia
  - North European Russia
- Northern Europe
  - Finland
  - Iceland
  - Norway
  - Sweden

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000443388
UNII	EJS4OPA4YI
USDA Plants	LASI3
Tropicos	24900099
KEW	urn:lsid:ipni.org:names:262455-1
The Plant List	kew-2493981
Plantarium	22096
PFAF	Larix sibirica
PaleoBotany	34187
Open Tree Of Life	814107
Observations.org	144648
NCBI Taxonomy	62751
IUCN Red List	42317
IPNI	262455-1
iNaturalist	135893
GBIF	2686276
Freebase	/m/08tkjr
EPPO	LAXSI
EOL	1033611
Elurikkus	5386
US Library of Congress	sh85122216
USDA GRIN	21507
Wikipedia	Larix_sibirica

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_004151065.3	LarixSibirica0.16	Scaffold	Siberian Federal University	2024-03-05	90.0x	11.41 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

Assembly and comparative analysis of the complete multichromosomal mitochondrial genome of Cymbidium ensifolium, an orchid of high economic and ornamental value

Shen B, Shen A, Liu L, Tan Y, Li S, Tan Z

BMC Plant Biol

09-Apr-2024

PMCID:	PMC11003039
doi:	10.1186/s12870-024-04962-4
PMID:	38594641

The influence of tree genus, phylogeny, and richness on the specificity, rarity, and diversity of ectomycorrhizal fungi

Tedersoo L, Drenkhan R, Abarenkov K, Anslan S, Bahram M, Bitenieks K, Buegger F, Gohar D, Hagh‐Doust N, Klavina D, Makovskis K, Zusevica A, Pritsch K, Padari A, Põlme S, Rahimlou S, Rungis D, Mikryukov V

Environ Microbiol Rep

04-Apr-2024

PMCID:	PMC10994715
doi:	10.1111/1758-2229.13253
PMID:	38575147

The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered

Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O

Stud Mycol

22-Feb-2024

PMCID:	PMC11003443
doi:	10.3114/sim.2024.107.03
PMID:	38600960

The Diversity of Parasitoids and Their Role in the Control of the Siberian Moth, Dendrolimus sibiricus (Lepidoptera: Lasiocampidae), a Major Coniferous Pest in Northern Asia

Kirichenko NI, Ageev AA, Astapenko SA, Golovina AN, Kasparyan DR, Kosheleva OV, Timokhov AV, Tselikh EV, Zakharov EV, Musolin DL, Belokobylskij SA

Life (Basel)

17-Feb-2024

PMCID:	PMC10890493
doi:	10.3390/life14020268
PMID:	38398777

RNA editing events and expression profiles of mitochondrial protein-coding genes in the endemic and endangered medicinal plant, Corydalis saxicola

Li C, Liu H, Qin M, Tan YJ, Ou XL, Chen XY, Wei Y, Zhang ZJ, Lei M

Front Plant Sci

06-Feb-2024

PMCID:	PMC10876856
doi:	10.3389/fpls.2024.1332460
PMID:	38379941

Comprehensive Analysis of the Complete Mitochondrial Genome of Rehmannia chingii: An Autotrophic Species in the Orobanchaceae Family

Han Y, Feng YL, Wang J, Zhu SS, Jin XJ, Wu ZQ, Zhang YH

Genes (Basel)

15-Jan-2024

PMCID:	PMC10815111
doi:	10.3390/genes15010098
PMID:	38254987

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

Transport of Nanoparticles into Plants and Their Detection Methods

Sembada AA, Lenggoro IW

Nanomaterials (Basel)

05-Jan-2024

PMCID:	PMC10819755
doi:	10.3390/nano14020131
PMID:	38251096

Simulating long-term wildfire impacts on boreal forest structure in Central Yakutia, Siberia, since the Last Glacial Maximum

Glückler R, Gloy J, Dietze E, Herzschuh U, Kruse S

Fire Ecol

04-Jan-2024

PMCID:	PMC10766680
doi:	10.1186/s42408-023-00238-8
PMID:	38186675

H2O2 Significantly Affects Larix kaempferi × Larix olgensis Somatic Embryogenesis

Zhu J, Zhang K, Xiong H, Xie Y, Li R, Wu X, Yang Y, Wu H, Hao Z, Sun X, Chen J

Int J Mol Sci

04-Jan-2024

PMCID:	PMC10779820
doi:	10.3390/ijms25010669
PMID:	38203839

Soil Microbiome in Conditions of Oil Pollution of Subarctic Ecosystems

Melekhina EN, Belykh ES, Kanev VA, Taskaeva AA, Tarabukin DV, Zinovyeva AN, Velegzhaninov IO, Rasova EE, Baturina OA, Kabilov MR, Markarova MY

Microorganisms

30-Dec-2023

PMCID:	PMC10820038
doi:	10.3390/microorganisms12010080
PMID:	38257907

Special Issue on “Plant Biology and Biotechnology: Focus on Genomics and Bioinformatics 2.0”

Orlov YL, Chen M

Int J Mol Sci

18-Dec-2023

PMCID:	PMC10743833
doi:	10.3390/ijms242417588
PMID:	38139417

Analysis of Softwood Lignans by Comprehensive Two-Dimensional Liquid Chromatography

Falev DI, Voronov IS, Onuchina AA, Faleva AV, Ul’yanovskii NV, Kosyakov DS

Molecules

15-Dec-2023

PMCID:	PMC10745517
doi:	10.3390/molecules28248114
PMID:	38138599

Multispectral Remote Sensing Data Application in Modelling Non-Extensive Tsallis Thermodynamics for Mountain Forests in Northern Mongolia

Sandlersky R, Petrzhik N, Jargalsaikhan T, Shironiya I

Entropy (Basel)

13-Dec-2023

PMCID:	PMC10742449
doi:	10.3390/e25121653
PMID:	38136533

The Distribution Characteristics of Vegetation in the Subrange of the Altai Mountains, Xinjiang

Cao Q, Wei Y, Li W, Feng Y, Abduraimov OS

Plants (Basel)

20-Nov-2023

PMCID:	PMC10675357
doi:	10.3390/plants12223915
PMID:	38005812

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
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1007/S10600-008-9041-Z
> 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/S10600-008-9041-Z
> 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/BF00580452
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
(1R,4S)-2,3-Dimethylbicyclo[2.2.1]hept-2-ene	11457687	Click to see CC1=C(C2CCC1C2)C	122.21	unknown	https://doi.org/10.1007/BF00629870
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1007/BF00580452 https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00629870
Santene	10720	Click to see CC1=C(C2CCC1C2)C	122.21	unknown	https://doi.org/10.1007/BF00629870
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
2,3-bis(4-Hydroxy-3-methoxybenzyl)butane-1,4-diol	586372	Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O	362.40	unknown	https://doi.org/10.1007/BF00567947
meso-Secoisolariciresinol	11552274	Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O	362.40	unknown	https://doi.org/10.1007/BF00567947
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
3,4-Divanillyltetrahydrofuran	182210	Click to see COC1=C(C=CC(=C1)CC2COCC2CC3=CC(=C(C=C3)O)OC)O	344.40	unknown	https://doi.org/10.1007/BF00567947
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
15-Hydroxy-9-oxoprosta-8(12),13-dien-1-oic acid	4954	Click to see CCCCCC(C=CC1=C(C(=O)CC1)CCCCCCC(=O)O)O	336.50	unknown	https://doi.org/10.1007/BF00598571
7-[2-(3-Hydroxyoct-1-enyl)-5-oxocyclopent-3-en-1-yl]hept-5-enoic acid	4953	Click to see CCCCCC(C=CC1C=CC(=O)C1CC=CCCCC(=O)O)O	334.40	unknown	https://doi.org/10.1007/BF00598571
7-[2-(3-Hydroxyoct-1-enyl)-5-oxocyclopent-3-en-1-yl]heptanoic acid	4952	Click to see CCCCCC(C=CC1C=CC(=O)C1CCCCCCC(=O)O)O	336.50	unknown	https://doi.org/10.1007/BF00598571
7-[2-(3-Hydroxyoct-1-enyl)-5-oxocyclopenten-1-yl]hept-5-enoic acid	4955	Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)O)O	334.40	unknown	https://doi.org/10.1007/BF00598571
8-iso Prostaglandin E1	214	Click to see CCCCCC(C=CC1C(CC(=O)C1CCCCCCC(=O)O)O)O	354.50	unknown	https://doi.org/10.1007/BF00598571
8-iso PROSTAGLANDIN E2	158	Click to see CCCCCC(C=CC1C(CC(=O)C1CC=CCCCC(=O)O)O)O	352.50	unknown	https://doi.org/10.1007/BF00598571
Alprostadil	5280723	Click to see CCCCCC(C=CC1C(CC(=O)C1CCCCCCC(=O)O)O)O	354.50	unknown	https://doi.org/10.1007/BF00598571
Dinoprost	5280363	Click to see CCCCCC(C=CC1C(CC(C1CC=CCCCC(=O)O)O)O)O	354.50	unknown	https://doi.org/10.1007/BF00598571
Dinoprostone	5280360	Click to see CCCCCC(C=CC1C(CC(=O)C1CC=CCCCC(=O)O)O)O	352.50	unknown	https://doi.org/10.1007/BF00598571
PGD2;11-Dehydroprostaglandin F2-alpha	4956	Click to see CCCCCC(C=CC1C(C(CC1=O)O)CC=CCCCC(=O)O)O	352.50	unknown	https://doi.org/10.1007/BF00598571
prostaglandin A1	5281912	Click to see CCCCCC(C=CC1C=CC(=O)C1CCCCCCC(=O)O)O	336.50	unknown	https://doi.org/10.1007/BF00598571
prostaglandin A2	5280880	Click to see CCCCCC(C=CC1C=CC(=O)C1CC=CCCCC(=O)O)O	334.40	unknown	https://doi.org/10.1007/BF00598571
prostaglandin B1	5280388	Click to see CCCCCC(C=CC1=C(C(=O)CC1)CCCCCCC(=O)O)O	336.50	unknown	https://doi.org/10.1007/BF00598571
prostaglandin B2	5280881	Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)O)O	334.40	unknown	https://doi.org/10.1007/BF00598571
prostaglandin D2	448457	Click to see CCCCCC(C=CC1C(C(CC1=O)O)CC=CCCCC(=O)O)O	352.50	unknown	https://doi.org/10.1007/BF00598571
prostaglandin F1a	4957	Click to see CCCCCC(C=CC1C(CC(C1CCCCCCC(=O)O)O)O)O	356.50	unknown	https://doi.org/10.1007/BF00598571
Prostaglandin f1alpha	5280939	Click to see CCCCCC(C=CC1C(CC(C1CCCCCCC(=O)O)O)O)O	356.50	unknown	https://doi.org/10.1007/BF00598571
Prostaglandin F2a;PGF2alpha	160	Click to see CCCCCC(C=CC1C(CC(C1CC=CCCCC(=O)O)O)O)O	354.50	unknown	https://doi.org/10.1007/BF00598571
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Tetracosanol	10472	Click to see CCCCCCCCCCCCCCCCCCCCCCCCO	354.70	unknown	https://doi.org/10.1007/BF00630226 https://doi.org/10.1007/BF00630093
Docosanol	12620	Click to see CCCCCCCCCCCCCCCCCCCCCCO	326.60	unknown	https://doi.org/10.1007/BF00630226 https://doi.org/10.1007/BF00630093
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
13-Epimanool	10891602	Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C	290.50	unknown	https://doi.org/10.1007/BF00630226 https://doi.org/10.1007/BF00630093
13-Epitorulosol	12444402	Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)CO	306.50	unknown	https://doi.org/10.1007/BF00630226 https://doi.org/10.1007/BF00630093
Methyl abieta-7,13-dien-18-oate	516981	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)OC)C	316.50	unknown	https://doi.org/10.1007/BF00630226
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids
Isolongifolene	102562	Click to see CC1(CCC=C2C13CCC(C3)C2(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00580452 https://doi.org/10.1007/BF00567053
> 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/BF00567053 https://doi.org/10.1007/BF00580452
> 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/BF00567053
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1007/BF00629870 https://doi.org/10.1007/BF00567053
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1007/BF00629870
(-)-Camphene	440966	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1007/BF00629870
(+)-3-Carene	443156	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1007/BF00629870
(+)-alpha-Pinene	82227	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1007/BF00629870
(+)-Isoborneol	6973640	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1007/BF00580452
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/BF00580452 https://doi.org/10.1007/BF00567053
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1007/BF00629870 https://doi.org/10.1007/BF00580452 https://doi.org/10.1007/BF00567053
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1007/BF00629870 https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00580452
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1007/BF00629870 https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00580452
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1007/BF00580452
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1007/BF00629870 https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00580452
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1007/BF00580452
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1007/BF00580452 https://doi.org/10.1007/BF00567053
Tricyclene	79035	Click to see CC1(C2CC3C1(C3C2)C)C	136.23	unknown	https://doi.org/10.1007/BF00629870
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-beta-Phellandrene	442484	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1007/BF00629870
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1007/BF00567053
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1007/BF00567053
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1007/BF00629870
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00580452
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1007/BF00580452 https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00629870
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1007/BF00629870
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1007/BF00629870 https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00580452
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1007/BF00580452 https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00629870
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Isolongifolene	11127402	Click to see CC1(CCC=C2C13CCC(C3)C2(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00580452 https://doi.org/10.1007/BF00567053
(+)-Cyclosativene	519960	Click to see CC(C)C1CCC2(C3C1C4C2(C4C3)C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
(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/BF00580452
(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/BF00567053
(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/BF00567053
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315594	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1007/BF00580452
(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/BF00567053
(1S,2R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	145994486	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00580452
(1S,2S,6S,7R,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	101607926	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00567053
(1S,2S,7R,9R)-3,3,7-trimethyl-8-methylidenetricyclo[5.4.0.02,9]undecane	1797732	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1007/BF00580452
(1S,6R,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	84690	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00580452
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/BF00567053
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/BF00580452 https://doi.org/10.1007/BF00567053
1,4,4-Trimethyl-8-methylenecycloundeca-1,5-diene	24798692	Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C	204.35	unknown	https://doi.org/10.1007/BF00580452
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/BF00567053
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/BF00567053
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/BF00567053
alpha-Cadinene, (+)-	12306048	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
alpha-Calacorene	12302243	Click to see CC1=CCC(C2=C1C=CC(=C2)C)C(C)C	200.32	unknown	https://doi.org/10.1007/BF00567053
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00580452
beta-Cadinene	10657	Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
beta-Copaene	57339298	Click to see CC(C)C1CCC2(C3C1C2C(=C)CC3)C	204.35	unknown	https://doi.org/10.1007/BF00567053
beta-Humulene	5318102	Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C	204.35	unknown	https://doi.org/10.1007/BF00580452
Calamenene	6429077	Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C	202.33	unknown	https://doi.org/10.1007/BF00567053
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00580452
Caryophyllene,alpha + beta mixt.	5354499	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1007/BF00580452 https://doi.org/10.1007/BF00567053
CID 16396350	16396350	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)-	89316	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1007/BF00580452
delta-Elemene	12309449	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
epsilon-Bulgarene	12302128	Click to see CC(C)C1CCC(=C)C2C1CC(=C)CC2	204.35	unknown	https://doi.org/10.1007/BF00567053
epsilon-Cadinene	12302130	Click to see CC(C)C1CCC(=C)C2C1CC(=C)CC2	204.35	unknown	https://doi.org/10.1007/BF00567053
epsilon-Muurolene	520461	Click to see CC(C)C1CCC(=C)C2C1CC(=C)CC2	204.35	unknown	https://doi.org/10.1007/BF00567053
gamma-Bisabolene, (Z)-	3033866	Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1	204.35	unknown	https://doi.org/10.1007/BF00580452
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
gamma-Muurolene	12313020	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
Longicyclene	564934	Click to see CC1(CCCC2(C3C1C4C2(C4C3)C)C)C	204.35	unknown	https://doi.org/10.1007/BF00567053
Longifolene	289151	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	https://doi.org/10.1007/BF00567053 https://doi.org/10.1007/BF00580452
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Sibirene	14167644	Click to see CC(C)C1=CC2C(=C)CCCC2(CC1)C	204.35	unknown	https://doi.org/10.1007/BF00580452 https://doi.org/10.1007/BF00567053
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1007/BF00630093 https://doi.org/10.1007/BF00630226
22,23-Dihydrobrassicasterol	5283637	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1007/BF00630093
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1007/BF00630093 https://doi.org/10.1007/BF00630226
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-[[(1R,3R,5S,8S,9S,10S,13S,14S,16S,17R)-3-hydroxy-17-[(2S,3S)-3-hydroxy-6-methylhept-5-en-2-yl]-10,13-dimethyl-1-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl]oxy]oxan-2-yl]methyl acetate	163010719	Click to see CC1C(C(C(C(O1)OC2CC(CC3C2(C4CCC5(C(C4CC3)CC(C5C(C)C(CC=C(C)C)O)OC6C(C(C(C(O6)COC(=O)C)O)O)O)C)C)O)O)O)O	785.00	unknown	https://doi.org/10.1007/BF00629870
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1007/BF00630226 https://doi.org/10.1007/BF00601286 https://doi.org/10.1007/BF00630093
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/BF00630093 https://doi.org/10.1007/BF00630226
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/BF00630093
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(E,4R)-4-hydroxy-N-(2-methylpropyl)hex-2-enamide	163044166	Click to see CCC(C=CC(=O)NCC(C)C)O	185.26	unknown	https://doi.org/10.1007/BF00567053
> Organoheterocyclic compounds / Heteroaromatic compounds
Longifolin	5372204	Click to see CC1=C(OC=C1)CC=C(C)CC2=CC(=CO2)C	230.30	unknown	https://doi.org/10.1007/BF00580452
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1007/S10600-008-9041-Z
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid	709	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1007/S10600-008-9041-Z
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1007/S10600-008-9041-Z https://doi.org/10.1007/BF00630226
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1007/S10600-008-9041-Z https://doi.org/10.1007/BF00630226
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin	471	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1007/BF00565363
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	https://doi.org/10.1007/BF00565363
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Tricetin	5281701	Click to see C1=C(C=C(C(=C1O)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	302.23	unknown	https://doi.org/10.1007/BF00564355
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	https://doi.org/10.1007/BF00564355
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1007/BF00567999
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxy-5-methoxyphenyl)-6,8-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162846202	Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(O2)C(=CC(=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	494.40	unknown	https://doi.org/10.1007/BF00563605
2-(3,4-Dihydroxy-5-methoxyphenyl)-6,8-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162846201	Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(O2)C(=CC(=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	494.40	unknown	https://doi.org/10.1007/BF00563605
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00564611
3-(beta-D-Arabinopyranosyloxy)-5,7-dihydroxy-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one	21722017	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1007/BF00565363
3-[(2R,3S,4R,5S)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	162957574	Click to see CC(C1C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF00565363
3-[(2R,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	92468677	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1007/BF00565363
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	12308704	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1007/BF00565363
3-[3,4-Dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	78385433	Click to see CC(C1C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF00565363
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF00564466
5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	124488029	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1007/BF00564611
6,8-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	163009918	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=C(C3=O)C=C(C=C4O)O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O)O)O)O	654.60	unknown	https://doi.org/10.1007/BF00563605
6,8-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	163009917	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=C(C3=O)C=C(C=C4O)O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O)O)O)O	654.60	unknown	https://doi.org/10.1007/BF00563605
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF00564466
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1007/BF00564611
Isorhamnetin 3-galactoside	13245586	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1007/BF00564611
isorhamnetin 3-O-glucoside	5318645	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1007/BF00564611
Myricetin 3-beta-D-glucopyranoside	12311099	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	https://doi.org/10.1007/BF00564611
Reynoutrin	5878729	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1007/BF00565363

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Larix sibirica

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