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Torreya nucifera

Torreya nucifera - 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 UUID643ff94297486137191411
Scientific name Torreya nucifera
Authority Siebold & Zucc.
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 234 (1846)

Description Top

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Synonyms Top

Scientific name Authority First published in
Torreya nucifera var. sphaerica Kimura Jap. J. Bot. 13: 519 (1948)
Torreya nucifera f. sphaerica (Kimura) Yonek. J. Jap. Bot. 80: 323 (2005)
Tumion nuciferum Greene Pittonia 2: 194 (1891)
Taxus nucifera L. Sp. Pl. : 1040 (1753)
Torreya macrosperma Miyoshi Rep. Nat. Monum. Invest. Pl. 32: 2 (1922)
Torreya igaensis Doi & Morikawa Bot. Mag. (Tokyo) 42: 536 (1928)
Torreya ascendens Nakai ex Uyeki Sci. Rep. Matsuyama Agric. Coll. 10(2): 3 (1953)
Torreya fruticosa Nakai Tyosen Sanrin Kaiho 158: 26 (1938)
Taxodium nuciferum (L.) Brongn. ex Voigt Hort. Suburb. Calcutt. : 559 (1845)
Podocarpus nuciferus Loudon Hort. Brit. [Loudon] 388. 1830
Caryotaxus nucifera Zucc. ex Endl. Syn. Conif. 241. 1847 [May-Jun 1847]
Foetataxus nucifera J.Nelson Pinaceae : 168 (1866)
Torreya unda Miyoshi Bot. Mag. (Tokyo) 34: 236. 1925 (1925)
Torreya nucifera var. articulata Miyoshi Tennenkinen-butsu-chosahakoku 3: 19. 1926
Torreya nucifera var. radicans Nakai Bot. Mag. (Tokyo) 33: 194. 1919
Torreya nucifera var. macrosperma (Miyoshi) Koidz.
Torreya nucifera var. igaensis (Doi & Morikawa) Ohwi

Common names Top

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Language Common/alternative name
English japanese nutmeg tree
English japanese nutmeg-yew
English japanese torreya
Spanish kaya
Arabic تورية جوزة الطيب
German japanische nusseibe
German japanische stinkeibe
Hungarian kajamag
Hungarian kajafa
Hungarian kaya
Hungarian japán nagymagvú tiszafa
Japanese カヤノキ
Japanese カヤ
Korean 비자나무
Norwegian Bokmål japansk nøttebarlind
Polish torreja orzechowa
Portuguese kaya
Russian Торрея орехоносная
Russian Кая
Chinese 日榧
Chinese 日本榧
Chinese 日本榧树

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000409013
UNII 91Z68135ZV
USDA Plants TONU3
Tropicos 31200002
INPN 611613
KEW urn:lsid:ipni.org:names:263999-1
The Plant List kew-2434734
Missouri Botanical Garden 287299
Open Tree Of Life 238588
NCBI Taxonomy 50189
IUCN Red List 42552
IPNI 263999-1
iNaturalist 55197
GBIF 5284492
Freebase /m/05ph3b
EPPO TOYNU
EOL 1033659
USDA GRIN 36767
Wikipedia Torreya_nucifera
CMAUP NPO28466

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
Worldwide forest surveys reveal forty-three new species in Phytophthora major Clade 2 with fundamental implications for the evolution and biogeography of the genus and global plant biosecurity Jung T, Milenković I, Balci Y, Janoušek J, Kudláček T, Nagy ZÁ, Baharuddin B, Bakonyi J, Broders KD, Cacciola SO, Chang TT, Chi NM, Corcobado T, Cravador A, Đorđević B, Durán A, Ferreira M, Fu CH, Garcia L, Hieno A, Ho HH, Hong C, Junaid M, Kageyama K, Kuswinanti T, Maia C, Májek T, Masuya H, Magnano di San Lio G, Mendieta-Araica B, Nasri N, Oliveira LS, Pane A, Pérez-Sierra A, Rosmana A, Sanfuentes von Stowasser E, Scanu B, Singh R, Stanivuković Z, Tarigan M, Thu PQ, Tomić Z, Tomšovský M, Uematsu S, Webber JF, Zeng HC, Zheng FC, Brasier CM, Horta Jung M Stud Mycol 27-Feb-2024
PMCID:PMC11003442
doi:10.3114/sim.2024.107.04
PMID:38600961
Effects of Natural Products on Enzymes Involved in Ferroptosis: Regulation and Implications Zuo HL, Huang HY, Lin YC, Liu KM, Lin TS, Wang YB, Huang HD Molecules 04-Dec-2023
PMCID:PMC10708253
doi:10.3390/molecules28237929
PMID:38067658
Mechanisms of ferroptosis and targeted therapeutic approaches in lymphoma Yu T, Xu-Monette ZY, Yu L, Li Y, Young KH Cell Death Dis 25-Nov-2023
PMCID:PMC10676406
doi:10.1038/s41419-023-06295-w
PMID:38007476
Functional characterisation of twelve terpene synthases from actinobacteria Chhalodia AK, Xu H, Tabekoueng GB, Gu B, Taizoumbe KA, Lauterbach L, Dickschat JS Beilstein J Org Chem 15-Sep-2023
PMCID:PMC10509563
doi:10.3762/bjoc.19.100
PMID:37736393
TCM “medicine and food homology” in the management of post-COVID disorders Ng CY, Bun HH, Zhao Y, Zhong LL Front Immunol 31-Aug-2023
PMCID:PMC10500073
doi:10.3389/fimmu.2023.1234307
PMID:37720220
Phylogenetic Relationships and Next-Generation Barcodes in the Genus Torreya Reveal a High Proportion of Misidentified Cultivated Plants Mo ZQ, Wang J, Möller M, Yang JB, Gao LM Int J Mol Sci 25-Aug-2023
PMCID:PMC10487542
doi:10.3390/ijms241713216
PMID:37686021
Four new species of Phyllosticta from China based on morphological and phylogenetic characterization Sui XN, Guo MJ, Zhou H, Hou CL Mycology 04-Jul-2023
PMCID:PMC10424619
doi:10.1080/21501203.2023.2225552
PMID:37583457
Plausibility of natural immunomodulators in the treatment of COVID-19–A comprehensive analysis and future recommendations Akter R, Rahman MR, Ahmed ZS, Afrose A Heliyon 21-Jun-2023
PMCID:PMC10284624
doi:10.1016/j.heliyon.2023.e17478
PMID:37366526
The Liverwort and Hornwort Flora of Jeju Island, Republic of Korea: A Volcanic Island with a Unique Mixture of Subtropical, Temperate, Boreal, and Arctomontane Taxa Choi SS, Bakalin VA, Bum HM, Park SJ, Kim DS, Ahn US, Moon MO Plants (Basel) 20-Jun-2023
PMCID:PMC10301385
doi:10.3390/plants12122384
PMID:37376013
Herbal medicine use in Republic of Korea to alleviate side effects of COVID-19 vaccines: A cross-sectional study Yoon HC J Integr Med 08-Jun-2023
PMCID:PMC10249366
doi:10.1016/j.joim.2023.06.002
PMID:37349213
In-silico study for the identification of potential destabilizers between the spike protein of SARS-CoV-2 and human ACE-2 Medina-Barandica J, Contreras-Puentes N, Tarón-Dunoyer A, Durán-Lengua M, Alviz-Amador A Inform Med Unlocked 05-Jun-2023
PMCID:PMC10241490
doi:10.1016/j.imu.2023.101278
PMID:37305192
An overview on medicinal plants used for combating coronavirus: Current potentials and challenges Abou Baker DH, Hassan EM, El Gengaihi S J Agric Food Res 20-May-2023
PMCID:PMC10198795
doi:10.1016/j.jafr.2023.100632
PMID:37251276
A Brief Review on Medicinal Plants-At-Arms against COVID-19 Srivastava S, He F, Huang Y, Niu M, Adholeya A, Peng WK Interdiscip Perspect Infect Dis 24-Apr-2023
PMCID:PMC10151152
doi:10.1155/2023/7598307
PMID:37139479
Role of Cytochrome P450 2C9 in COVID-19 Treatment: Current Status and Future Directions Lim SY, Al Bishtawi B, Lim W Eur J Drug Metab Pharmacokinet 24-Apr-2023
PMCID:PMC10123480
doi:10.1007/s13318-023-00826-8
PMID:37093458
Ferroptosis in Haematological Malignancies and Associated Therapeutic Nanotechnologies Mynott RL, Habib A, Best OG, Wallington-Gates CT Int J Mol Sci 21-Apr-2023
PMCID:PMC10146166
doi:10.3390/ijms24087661
PMID:37108836

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 / Biphenyls and derivatives
Honokiol 72303 Click to see C=CCC1=CC(=C(C=C1)O)C2=CC(=C(C=C2)O)CC=C 266.30 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3R,4R)-3-(4-Hydroxy-3-methoxy-benzyl)-4-(4-hydroxy-3,5-dimethoxybenzyl)dihydrofuran-2(3H)-one 10249666 Click to see COC1=CC(=CC(=C1O)OC)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC 388.40 unknown https://doi.org/10.1055/S-2001-15804
4-[(4-Hydroxy-3,5-dimethoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 163046461 Click to see COC1=CC(=CC(=C1O)OC)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC 388.40 unknown https://doi.org/10.1055/S-2001-15804
5-O-methylthujaplicatin 11406596 Click to see COC1=CC(=CC(=C1O)OC)CC2C(COC2=O)CC3=CC(=C(C=C3)O)OC 388.40 unknown https://doi.org/10.1248/BPB.26.1202
https://doi.org/10.1055/S-2001-15804
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/S1567-5769(01)00153-9
https://doi.org/10.1055/S-2001-15804
https://doi.org/10.1248/BPB.26.1202
l-Arctigenin 230232 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1055/S-2001-15804
Traxillagenin 10069677 Click to see COC1=CC(=CC(=C1OC)OC)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC 402.40 unknown https://doi.org/10.1248/BPB.26.1202
https://doi.org/10.1055/S-2001-15804
> Lignans, neolignans and related compounds / Lignan glycosides
3-[[3-Methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl]-4-[(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one 85097674 Click to see COC1=CC(=CC(=C1OC)OC)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC 564.60 unknown https://doi.org/10.1055/S-2001-15804
Arctii;NSC 315527;Arctigenin-4-glucoside 3660596 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1055/S-2001-15804
Arctiin 100528 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1055/S-2001-15804
Traxillaside 10030789 Click to see COC1=CC(=CC(=C1OC)OC)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC 564.60 unknown https://doi.org/10.1055/S-2001-15804
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aS,10aS)-2,5-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 162911446 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(C3(C)C)O)C)O)OC 346.50 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
(2S,4aS,10aS)-2,5,8-trihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 163028933 Click to see CC(C)C1=C(C2=C(C(=C1OC)O)C3(CCC(C(C3CC2=O)(C)C)O)C)O 362.50 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
(3R)-5-[(1S,4aR,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol 12444400 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)CO 306.50 unknown https://doi.org/10.1080/00021369.1971.10860025
(3S)-5-[(1S,4aR,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol 101277957 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)CO 306.50 unknown https://doi.org/10.1080/00021369.1971.10860025
(3S)-5-[(1S,4aS,5R,8aR)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol 6560267 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)CO 306.50 unknown via CMAUP database
(4aS,10aS)-5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione 163010400 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
(4aS,9R,10aS)-5-hydroxy-6,9-dimethoxy-1,1,4a-trimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 163016545 Click to see CC(C)C1=C(C(=C2C(=C1)C(CC3C2(CCC(=O)C3(C)C)C)OC)O)OC 360.50 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
(E)-5-[(1S,4aR,5R,8aS)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-en-1-ol 163193362 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)CO)C 306.50 unknown https://doi.org/10.1080/00021369.1971.10860025
(Z)-5-[(1S,4aR,5R,8aS)-5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-en-1-ol 162958284 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)CO)C 306.50 unknown https://doi.org/10.1080/00021369.1971.10860025
[(4bS,8R,8aR)-8-(hydroxymethyl)-4b,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl] acetate 52945977 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)CO)C)OC(=O)C 344.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
[8-(Hydroxymethyl)-4b,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-yl] acetate 75969603 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)CO)C)OC(=O)C 344.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
1,1,4a-Trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol 432946 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://doi.org/10.1016/S0031-9422(01)00390-9
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
1,2,3,4,4a,9,10,10a-Octahydro-6-hydroxy-7-isopropyl-1,4a-dimethyl-1-phenanthrenemethanol 240051 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)CO)C)O 302.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
https://doi.org/10.1016/S0031-9422(00)82385-7
12-Hydroxyabieta-8,11,13-triene-18-oic acid methyl ester 14132237 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(=O)OC)C)O 330.50 unknown https://doi.org/10.1021/JF060896C
18-Dimethoxyferruginol 11359963 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(OC)OC)C)O 346.50 unknown https://doi.org/10.1021/JF060896C
18-Hydroxyferruginol 21582568 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)CO)C)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
18-Oxoferruginol 52946772 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C=O)C)O 300.40 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
2,5-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 162911445 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(C3(C)C)O)C)O)OC 346.50 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
2,5,6-trihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 13970370 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(C3(C)C)O)C)O)O 332.40 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
2,5,8-trihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 22297197 Click to see CC(C)C1=C(C2=C(C(=C1OC)O)C3(CCC(C(C3CC2=O)(C)C)O)C)O 362.50 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
5-[5-(hydroxymethyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-en-1-ol 557177 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)CO)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
5-Hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione 163010399 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
5-hydroxy-6,9-dimethoxy-1,1,4a-trimethyl-7-propan-2-yl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 163016544 Click to see CC(C)C1=C(C(=C2C(=C1)C(CC3C2(CCC(=O)C3(C)C)C)OC)O)OC 360.50 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
6-Hydroxy-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde 14323964 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C=O)C)O 300.40 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 267302 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
8-(Dimethoxymethyl)-4b,8-dimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol 72816212 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(OC)OC)C)O 346.50 unknown https://doi.org/10.1021/JF060896C
Abieta-9(11),8(14),12-trien-12-ol 521330 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://doi.org/10.1016/S0031-9422(01)00390-9
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
acs.jmedchem.1c00409_ST.766 101297733 Click to see CC(=CCO)CCC1C(=C)CCC2C1(CCCC2(C)CO)C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
Dehydroabietinol 15586718 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C 286.50 unknown via CMAUP database
ent-8(17),13(16),14-Labdatrien-18-oic acid 72780956 Click to see CC12CCCC(C1CCC(=C)C2CCC(=C)C=C)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
Ferruginol 442027 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O 286.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
https://doi.org/10.1016/S0031-9422(01)00390-9
https://doi.org/10.1016/S0031-9422(00)82385-7
Hinokiol 12310492 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://doi.org/10.1016/S0031-9422(01)00390-9
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
Isocommunic acid 11278066 Click to see CC12CCCC(C1CCC(=C)C2CCC(=C)C=C)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
Isopimaric acid 442048 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
Methyl 12-hydroxyabieta-8(14),9(11),12-trien-18-oate 241939 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C(=O)OC)C)O 330.50 unknown https://doi.org/10.1021/JF060896C
Methyl abieta-8,11,13-trien-18-oate 247581 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)OC)C 314.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
Methyl dehydroabietate 14697 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)OC)C 314.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
Sandaracopimaric acid 221580 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Taiwanin F 13970371 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(C3(C)C)O)C)O)O 332.40 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
Taxusabietane A 76330776 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O)OC 344.40 unknown https://doi.org/10.1016/S0031-9422(01)00390-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(2E,6E)-9-(furan-3-yl)-2,6-dimethylnona-2,6-dien-1-ol 12444395 Click to see CC(=CCCC1=COC=C1)CCC=C(C)CO 234.33 unknown https://doi.org/10.1246/BCSJ.38.381
3-(4,8-Dimethylnona-3,7-dienyl)furan 90049 Click to see CC(=CCCC(=CCCC1=COC=C1)C)C 218.33 unknown https://doi.org/10.1246/BCSJ.38.381
9-(Furan-3-yl)-2,6-dimethylnona-2,6-dien-1-ol 71435590 Click to see CC(=CCCC1=COC=C1)CCC=C(C)CO 234.33 unknown https://doi.org/10.1246/BCSJ.38.381
9-(Furan-3-yl)-2,6-dimethylnona-2,6-dienal 85955177 Click to see CC(=CCCC1=COC=C1)CCC=C(C)C=O 232.32 unknown https://doi.org/10.1246/BCSJ.38.381
Dendrolasin 5316534 Click to see CC(=CCCC(=CCCC1=COC=C1)C)C 218.33 unknown https://doi.org/10.1246/BCSJ.38.381
Torreyal 12444394 Click to see CC(=CCCC1=COC=C1)CCC=C(C)C=O 232.32 unknown https://doi.org/10.1246/BCSJ.38.381
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
6-Chromanol, 2,8-dimethyl-2-(4,8,12-trimethyltridecyl)- 586537 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
delta-Tocopherol 92094 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,4aR,8S,8aS)-2,5-dimethyl-8-propan-2-yl-3,4,4a,7,8,8a-hexahydro-1H-naphthalen-2-ol 57634663 Click to see CC1=CCC(C2C1CCC(C2)(C)O)C(C)C 222.37 unknown https://doi.org/10.1246/BCSJ.36.1261
(S,Z)-2-Methyl-6-(p-tolyl)hept-2-en-1-ol 67178146 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)CO 218.33 unknown https://doi.org/10.1246/BCSJ.38.381
2-Hepten-1-ol, 2-methyl-6-(4-methylphenyl)-, (E)- 577141 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)CO 218.33 unknown https://doi.org/10.1246/BCSJ.38.381
2-Methyl-6-(4-methylphenyl)hept-2-enal 71348610 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C=O 216.32 unknown https://doi.org/10.1246/BCSJ.38.381
2,5-dimethyl-8-propan-2-yl-3,4,4a,7,8,8a-hexahydro-1H-naphthalen-2-ol 288207 Click to see CC1=CCC(C2C1CCC(C2)(C)O)C(C)C 222.37 unknown https://doi.org/10.1246/BCSJ.36.1261
Farnesol 3327 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
Nuciferal 10900058 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C=O 216.32 unknown https://doi.org/10.1246/BCSJ.38.381
trans,trans-Farnesol 445070 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(1R,2S,4aS,10aR)-1-(hydroxymethyl)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol 163003074 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)O 318.40 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
1-(Hydroxymethyl)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol 163003073 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)O 318.40 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Lys-Thr-Trp-Tyr 71464642 Click to see CC(C(C(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)NC(CC3=CC=C(C=C3)O)C(=O)O)NC(=O)C(CCCCN)N)O 596.70 unknown https://doi.org/10.1016/S0031-9422(00)82385-7
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
Bilobetin 5315459 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 552.50 unknown via CMAUP database
Ginkgetin 5271805 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 566.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/
Kayaflavone 9894522 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)OC 580.50 unknown via CMAUP database
Sciadopitysin 5281696 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)OC 580.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126309/

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