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Larix sibirica

Larix sibirica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Larix sibirica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ffd6a730c7773810057
Scientific name Larix sibirica
Authority Ledeb.
First published in Fl. Altaic. 4: 204 (1833)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

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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Language Common/alternative name
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 pinus larix
German sibirische lärche
German pinus ledebouri
German pinus intermedia
German abies ledebourii
Greek Λάριξ η σιβηρική
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 シベリアカラマツ
Japanese 西伯利亜落葉松
Georgian ციმბირული ლარიქსი
Kazakh Сібір балқарағайы
koi Сибирись лисвень
Lithuanian sibirinis maumedis
Norwegian Bokmål sibirsk lerk
Norwegian Bokmål sibirlerk
Norwegian Bokmål sibirske lerker
Norwegian Bokmål sibirisk lerk
Norwegian Nynorsk sibirlerk
Polish modrzew syberyjski
Russian Лиственница архангельская
Russian Лиственица сибирская
Russian Лиственница сибирская
Swedish sibirisk lärk
Ukrainian Модрина сибірська
Chinese 新疆落葉松
Chinese 俄国落叶松
Chinese 西伯利亚落叶松
Chinese 红杉皮
Chinese 新疆落叶松

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
  • Europe
    • 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
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
De novo assembly of the complete mitochondrial genome of pepino (Solanum muricatum) using PacBio HiFi sequencing: insights into structure, phylogenetic implications, and RNA editing Li Z, Liu J, Liang M, Guo Y, Chen X, Wu H, Jin S BMC Plant Biol 04-May-2024
PMCID:PMC11069145
doi:10.1186/s12870-024-04978-w
PMID:38702620
Dihydroquercetin regulates HIF-1α/AKT/NR2B signalling to improve impaired brain function in rats with metabolic syndrome Fu Y, Yuan P, Zeng M, Zhang Q, Hou Y, Gao L, Wei Y, Zheng Y, Feng W, Zheng X Heliyon 28-Apr-2024
PMCID:PMC11088260
doi:10.1016/j.heliyon.2024.e29807
PMID:38737244
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
Complete organelle genomes of Korean fir, Abies koreana and phylogenomics of the gymnosperm genus Abies using nuclear and cytoplasmic DNA sequence data Park S, Kwak M, Park S Sci Rep 01-Apr-2024
PMCID:PMC10985005
doi:10.1038/s41598-024-58253-x
PMID:38561351
New Methods in Digital Wood Anatomy: The Use of Pixel-Contrast Densitometry with Example of Angiosperm Shrubs in Southern Siberia Khudykh TA, Belokopytova LV, Yang B, Kholdaenko YA, Babushkina EA, Vaganov EA Biology (Basel) 28-Mar-2024
PMCID:PMC11048334
doi:10.3390/biology13040223
PMID:38666835
Potential of Unmanned Aerial Vehicle Red–Green–Blue Images for Detecting Needle Pests: A Case Study with Erannis jacobsoni Djak (Lepidoptera, Geometridae) Bai L, Huang X, Dashzebeg G, Ariunaa M, Yin S, Bao Y, Bao G, Tong S, Dorjsuren A, Davaadorj E Insects 04-Mar-2024
PMCID:PMC10971561
doi:10.3390/insects15030172
PMID:38535368
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
Complete mitochondrial genome of Syzygium samarangense reveals genomic recombination, gene transfer, and RNA editing events Lu G, Li Q Front Plant Sci 09-Jan-2024
PMCID:PMC10803518
doi:10.3389/fpls.2023.1301164
PMID:38264024
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
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

Phytochemical Profile Top

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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
(1S,4R)-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
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (2S)- 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
CID 44630107 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
(+)-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
(E,E)-1,4,4-Trimethyl-8-methylene-1,5-cycloundecadiene 5318102 Click to see CC1=CCC(C=CCC(=C)CCC1)(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
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
Cyclosativene 519960 Click to see CC(C)C1CCC2(C3C1C4C2(C4C3)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
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
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
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
3,4-Dihydroxy cinnamic 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
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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