Details Top

Internal ID UUID6440063e5a6e2246913149
Scientific name Abies firma
Authority Siebold & Zucc.
First published in Fl. Jap. 2: 15 (1842)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the Mapuche of southern Chile, Abies firma is not traditionally used, but the closely related and ecologically similar Abies pinsapo appears in documented references to cup and ground preparations, according to Bennett et al., 2021. Across northern and central Japan, the role of Abies firma is better established as a source of young shoots and needles for beverages, with preparation by infusion cited in Tanaka and T. T. N. T. Koyama, 1975. In the Ryukyu islands of Okinawa, Abies firma needles and shoots are also mentioned in cultural texts as a modest base for hot drinks, with notes in NIINOU 2012, while the Taihoku (modern-day Taipei) historical record does not directly link Abies firma to medicinal or beverage preparations, according to Gubbins 1912.

A practical recipe for a mild tea: use 2–3 fresh shoots (about 1–2 g) or 4–6 tender needles (about 1–3 g). Place the plant material in a cup, pour 250 mL of 80–90°C water, and let steep uncovered for 2–3 minutes, then strain and sip. A stronger version can be made with 1 g of dried needles steeped in 200 mL of 90–95°C water for 4–5 minutes. In winter, some users simmer a handful of needles in 1 L of water for 10 minutes to make a decoction and serve with honey; however, this concentration is stronger, so limit to 1–2 cups per day. Abies firma is safe in typical culinary amounts; no dose limits are well established, and there are no well-documented contraindications or pregnancy warnings. Always identify the species and material clearly before preparing, and avoid overharvesting young shoots, as the tree is a slow-growing native.

Well-established constituents in Abies firma include the terpenes alpha-pinene, beta-pinene, limonene, camphene, and borneol reported in Tanaka and T. T. N. T. Koyama, 1975, with the monoterpene bornyl acetate found in Abies needles, and the phenylpropanoid coniferyl alcohol reported in Kurata et al., 1968. These aromatics plausibly underpin the traditional mild decongestant and respiratory support traditionally associated with fir needle drinks, and in Japan, young shoots and tender needles are most often prepared by infusion for this purpose, with occasional decoction in cold regions (Tanaka and T. T. N. T. Koyama, 1975; NIIOU 2012).

In modern Japan, Abies firma remains a culturally familiar “mountain tea” plant used in late winter and early spring, with some small-scale commercialization of needle-based blends and decoctions by regional producers, while ecological concerns keep harvest volumes modest. Contemporary research on fir needle phytochemistry continues to examine mono- and sesquiterpenes for their bioactivity, and several modern Japanese articles revisiting the species report content in this broad range and suggest that traditional drink preparations (infusions and decoctions) remain current and accessible, with details in the broader fir literature and in regional surveys compiled by the NIIOU Project, 2012.

General Uses Top

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Common products:
Timber, plywood, paper pulp, particleboard, LVL, and gum rosin.

Industrial and craft applications:
Sapwood and stumpwood yield gum rosin consisting mainly of abietic-type resin acids. Rosin is used as an adhesion promoter in adhesives, sizing agents in paper, and as a resin component in printing inks and oil-based varnishes. Structural lumber is planed, sawn, or glue-laminated for joinery, furniture, and general construction. Plywood and laminated veneer lumber (LVL) exploit veneer format and adhesive bonding for panel performance.

Food and beverages (non-medicinal):
No confirmed non-medicinal food or beverage uses.

Colorants and tanning:
No verified dye, ink, or tannin uses.

Wood and fiber:
Sapwood/heartwood dimensions vary; wood is soft with relatively straight grain, variable resin content, and workable density. The species is processed into structural and appearance-grade lumber, plywood, LVL, particleboard, and packaging, and into kraft pulp for papermaking.

Fragrance and cosmetics:
No established fragrance or cosmetic applications.

Properties relevant to use:
Gum rosin provides adhesive tack and ink vehicle compatibility through abietic acid chemistry. Lumber’s workable density and resin content suit planing, sawing, and adhesive bonding for panel and structural products.

Standards and regulation:
Timber and wood-based panels follow Japanese Agricultural Standards (JAS) for lumber, plywood, and LVL. Kraft pulp used in papermaking complies with paper industry specifications (e.g., ISO brightness and strength targets).

Sustainability and sourcing:
Wood is sourced primarily from Japanese plantation and secondary-growth stands; managed forestry and certification schemes for Japanese timber support traceability. Rosin yields depend on tapping intensity and tree age, influencing availability and cost.

Synonyms Top

Scientific name Authority First published in
Pinus firma Antoine Coniferen : 70 (1843)
Pinus bifida Antoine. Coniferen : 79 (1841)
Picea firma Sieber ex Gordon Pinetum : 147 (1858)
Picea webbiana Gordon Pinetum 160. 1858
Picea thunbergii Koehne Deut. Dendrol. : 22 (1893)
Abies bifida Siebold & Zucc. Fl. Jap. 2: 18 (1842)
Abies momi Siebold Verh. Batav. Genootsch. Kunsten 12: 12 (1830)
Abies thunbergii Lindl. Penny Cyclop. 1: 34 (1833)
Abies firma var. bifida (Siebold & Zucc.) Mast. J. Linn. Soc., Bot. 18: 514. 1881
Pinus firma var. incisa Endl. Syn. Conif. 99. 1847
Abies firma var. momi (Siebold) Mast. Gard. Chron. n.s., 12: 199. 1879
Pinus momi (Siebold) Voss Mitt. Deutsch. Dendrol. Ges. 16: 94. (1907)
Abies momi Siebold ex K.Koch Dendrologie 2(2): 227. 1873

Common names Top

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Language Common/alternative name
English momi fir
Arabic تنوب قاسي
Arabic شوح قاسي
Czech jedle japonská
German momi-tanne
Persian نراد مومی
Icelandic vætuþinur
Japanese モミ
Polish jodła japońska
Russian Пихта твёрдая
Chinese 日本冷杉

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

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Database ID/link to page
World Flora Online wfo-0000511154
USDA Plants ABFI
Tropicos 24900658
INPN 717029
KEW urn:lsid:ipni.org:names:261525-1
The Plant List kew-2609854
Missouri Botanical Garden 285028
PFAF Abies firma
Open Tree Of Life 648454
NCBI Taxonomy 78260
NBN Atlas NBNSYS0000042039
IUCN Red List 42282
IPNI 261525-1
iNaturalist 136304
GBIF 2685414
Freebase /m/0dwx9d
EPPO ABIFI
EOL 1033072
USDA GRIN 660
Wikipedia Abies_firma

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 Pieris japonica (Ericaceae) dominance on cool temperate forest altered-understory environments and soil microbiomes in Southern Japan Tokumoto Y, Katayama A PLoS One 11-Jan-2024
PMCID:PMC10783712
doi:10.1371/journal.pone.0296692
PMID:38206984
Effects of floral display size, local open raceme density, patch size, and distance between patches on pollinator behaviour in Salvia nipponica Murakoshi N, Itagaki T, Oguro M, Sakai S Sci Rep 10-Jan-2024
PMCID:PMC10781768
doi:10.1038/s41598-024-51327-w
PMID:38200089
Colonization success of a tree‐killing bark beetle: Geographic variation and mismatch with host preference Takagi E Ecol Evol 05-Jul-2023
PMCID:PMC10322651
doi:10.1002/ece3.10274
PMID:37424940
Soil Fungal Community Characteristics at Timberlines of Sejila Mountain in Southeast Tibet, China Cheng F, Li M, Ren Y, Hou L, Gao T, He P, Deng X, Lu J J Fungi (Basel) 21-May-2023
PMCID:PMC10219346
doi:10.3390/jof9050596
PMID:37233307
Phylotranscriptomics and evolution of key genes for terpene biosynthesis in Pinaceae Jiang K, Du C, Huang L, Luo J, Liu T, Huang S Front Plant Sci 17-Feb-2023
PMCID:PMC9982022
doi:10.3389/fpls.2023.1114579
PMID:36875589
Pest categorisation of Urocerus japonicus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 05-Jan-2023
PMCID:PMC9813682
doi:10.2903/j.efsa.2023.7738
PMID:36620491
North-to-South diversity of lipomycetaceous yeasts in soils evaluated with a cultivation-based approach from 11 locations in Japan Yamazaki A, Lorliam W, Uchino M, Suzuki KI, Kawasaki H Mycoscience 26-Dec-2022
PMCID:PMC10025075
doi:10.47371/mycosci.2022.09.003
PMID:37089900
Consolidation of Chloridium: new classification into eight sections with 37 species and reinstatement of the genera Gongromeriza and Psilobotrys Réblová M, Hernández-Restrepo M, Sklenář F, Nekvindová J, Réblová K, Kolařík M Stud Mycol 14-Dec-2022
PMCID:PMC10277272
doi:10.3114/sim.2022.103.04
PMID:37342155
The mitochondrial genome sequence of Abies alba Mill. reveals a high structural and combinatorial variation Kersten B, Rellstab C, Schroeder H, Brodbeck S, Fladung M, Krutovsky KV, Gugerli F BMC Genomics 28-Nov-2022
PMCID:PMC9703787
doi:10.1186/s12864-022-08993-9
PMID:36443651
Pest categorisation of Dendrolimus spectabilis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 10-Nov-2022
PMCID:PMC9647410
doi:10.2903/j.efsa.2022.7622
PMID:36381116
Forest characteristics, population structure and growth trends of threatened relict Pseudotsuga forrestii in China Tang CQ, Yao SQ, Han PB, Wen JR, Li S, Peng MC, Wang CY, Matsui T, Li YP, Lu S, He Y Plant Divers 07-Nov-2022
PMCID:PMC10435900
doi:10.1016/j.pld.2022.10.005
PMID:37601542
Regeneration of tree species after 11 years of canopy gap creation and deer exclusion in a warm temperate broad-leaved forest over-browsed by sika deer Ang JM, Kusumoto D, Mitsugi M, Suzuki M PeerJ 01-Nov-2022
PMCID:PMC9635360
doi:10.7717/peerj.14210
PMID:36340205
Morchella nipponensis sp. nov. (Ascomycota, Pezizales): a paleoendemic species of section Morchella discovered in Japan Clowez P, Izumi T, Lamiable PB, Shibakusa K, Minculeasa C, Alvarado P Mycoscience 21-Oct-2022
PMCID:PMC10012348
doi:10.47371/mycosci.2022.08.005
PMID:37089519
A Comprehensive Evolutionary Study of Chloroplast RNA Editing in Gymnosperms: A Novel Type of G-to-A RNA Editing Is Common in Gymnosperms Huang KY, Kan SL, Shen TT, Gong P, Feng YY, Du H, Zhao YP, Wan T, Wang XQ, Ran JH Int J Mol Sci 16-Sep-2022
PMCID:PMC9505161
doi:10.3390/ijms231810844
PMID:36142757

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl)methanol 107171 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
(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/10.1016/S0031-9422(00)82357-2
(3S)-5-[(1R,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-ol 129317223 Click to see 290.50 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
(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/10.1016/S0031-9422(00)82357-2
(7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-1-yl)methanol 15586710 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
[(1R,4aR,5S,8aR)-5-[(3R)-3-hydroxy-3-methylpent-4-enyl]-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methyl acetate 162930269 Click to see 348.50 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
[(1R)-1-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylene-decalin-1-yl]ethyl]-1-methyl-allyl] acetate 71594607 Click to see 332.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
[5-(3-hydroxy-3-methylpent-4-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methyl acetate 162930267 Click to see CC(=O)OCC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C 348.50 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
[5-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-1-en-3-yl] acetate 78125591 Click to see 332.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
1-Naphthalenepropanol, alpha-ethenyldecahydro-alpha,5,5,8a-tetramethyl-2-methylene- 238792 Click to see 290.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
https://doi.org/10.1016/S0031-9422(00)82357-2
1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1R,4aR,4bS,7S,10aR)- 15586712 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1S,4aR,4bS,7S,10aR)- 158539 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)CO)C)C1)C=C 288.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
18-Hydroxymanool 349315 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)CO 306.50 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
https://doi.org/10.1016/S0031-9422(00)80837-7
Abietinol 443474 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
CID 12444399 12444399 Click to see 306.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
Dehydroabietyl alcohol 15586718 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
Manool 3034394 Click to see 290.50 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
https://doi.org/10.1016/S0031-9422(00)82357-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienal 5280598 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
(4aR,8aS)-5,8a-dimethyl-3-propan-2-ylidene-1,2,4,4a,7,8-hexahydronaphthalene 162862523 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
2,6,10-Trimethyl-2,6,10-dodecatrien-12-al 68150 Click to see CC(=CCCC(=CCCC(=CC=O)C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
3,7,11-Trimethyldodeca-2,6,10-trienyl acetate 94403 Click to see CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C 264.40 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
3,7(11)-Eudesmadiene 522296 Click to see CC1=CCCC2(C1CC(=C(C)C)CC2)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
a Farnesol 3327 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
Farnesol 445070 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
Npc322415 521334 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
trans,trans-Farnesyl acetate 638500 Click to see 264.40 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(3R,4aR,5R,8aR)-5-methoxy-5,8a-dimethyl-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene 162892116 Click to see 236.39 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
(3R,4aR,8aR)-5,8a-dimethyl-3-propan-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene 140799050 Click to see CC1=CCCC2(C1CC(CC2)C(C)C)C 206.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
(3S,4aS,8aS)-8a-methyl-5-methylidene-3-propan-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene 162873958 Click to see 206.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
2-(4a-Methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol 521215 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
2-(4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl)propan-2-ol 521216 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
2-(8-Methoxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)propan-2-ol 76524640 Click to see CC12CCCC(C1CC(CC2)C(C)(C)O)(C)OC 254.41 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
2-[(2R,4aR,8R,8aR)-8-methoxy-4a,8-dimethyl-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl]propan-2-ol 57404492 Click to see 254.41 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
2-Isopropenyl-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalene 10123 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
5-Methoxy-5,8a-dimethyl-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene 162892115 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)OC)C 236.39 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
8a-Methyl-5-methylidene-3-propan-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene 85348873 Click to see CC(C)C1CCC2(CCCC(=C)C2C1)C 206.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
alpha-Selinene 10856614 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
Beta-Selinene 442393 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
Naphthalene,1,2,3,4,4a,5,6,8a-octahydro-4a, 8-dimethyl-2-[1-methylethyl]- 15799583 Click to see CC1=CCCC2(C1CC(CC2)C(C)C)C 206.37 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(E,6R)-2-methyl-4-oxo-6-[(9S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 46835877 Click to see CC(CC(=O)C=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C 468.70 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
methyl (6R)-2-methylidene-4-oxo-6-[(5R,9S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]heptanoate 162916378 Click to see 482.70 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
methyl (E,6R)-2-methyl-4-oxo-6-[(5R,9S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoate 13820723 Click to see 482.70 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
Methyl 2-methyl-4-oxo-6-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)hept-2-enoate 73187986 Click to see 482.70 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
Methyl 2-methylidene-4-oxo-6-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)heptanoate 629798 Click to see 482.70 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol 312822 Click to see 400.70 unknown https://doi.org/10.1016/0031-9422(90)80196-N
(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 400.70 unknown https://doi.org/10.1016/0031-9422(90)80196-N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
(2R)-2-[(2R)-2-[(3S,5R,9R,10R,13R,14R,17R)-3-hydroxy-4,4,10,13-tetramethyl-1,2,3,5,6,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]propyl]-4-methyl-2H-furan-5-one 162885487 Click to see CC1=CC(OC1=O)CC(C)C2CCC3C2(CCC4C3=CCC5C4(CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(91)85052-2
(2R)-4-(hydroxymethyl)-2-[(2R)-2-[(5R,9R,10R,13R,14R,17R)-4,4,10,13-tetramethyl-3-oxo-2,5,6,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]propyl]-2H-furan-5-one 162970436 Click to see 454.60 unknown https://doi.org/10.1016/0031-9422(91)85052-2
(2R)-4-methyl-2-[(2R)-2-[(5R,9S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]propyl]-2H-furan-5-one 14101579 Click to see 452.70 unknown https://doi.org/10.1016/0031-9422(90)80196-N
2-[2-(3-hydroxy-4,4,10,13-tetramethyl-1,2,3,5,6,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl)propyl]-4-methyl-2H-furan-5-one 162885486 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(91)85052-2
4-(hydroxymethyl)-2-[2-(4,4,10,13-tetramethyl-3-oxo-2,5,6,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)propyl]-2H-furan-5-one 162970435 Click to see CC(CC1C=C(C(=O)O1)CO)C2CCC3C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C 454.60 unknown https://doi.org/10.1016/0031-9422(91)85052-2
4-methyl-2-[2-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)propyl]-2H-furan-5-one 634878 Click to see CC1=CC(OC1=O)CC(C)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C 452.70 unknown https://doi.org/10.1016/0031-9422(90)80196-N
CID 163010644 163010644 Click to see CC1CC2(C=C(C(=O)O2)C)OC13CCC4(C3(CCC5C4=CCC6C5(CCC(=O)C6(C)C)C)C)C 466.70 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
CID 163010645 163010645 Click to see CC1CC2(C=C(C(=O)O2)C)OC13CCC4(C3(CCC5C4=CCC6C5(CCC(=O)C6(C)C)C)C)C 466.70 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
CID 163010646 163010646 Click to see CC1CC2(C=C(C(=O)O2)C)OC13CCC4(C3(CCC5C4=CCC6C5(CCC(=O)C6(C)C)C)C)C 466.70 unknown https://doi.org/10.1016/S0031-9422(00)82357-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
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/10.1016/S0031-9422(00)80837-7
https://doi.org/10.1016/0031-9422(90)80196-N
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
https://doi.org/10.1016/0031-9422(90)80196-N
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
[(1R,2E,8S,10R,11S)-10,11-dihydroxy-6-(methoxymethyl)-1,10-dimethyl-5-oxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-2,6-dien-8-yl] 2-(hydroxymethyl)prop-2-enoate 15689665 Click to see 410.40 unknown https://doi.org/10.1016/S0031-9422(00)80837-7
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3-Hydroxy-4-methoxy-phenyl)-acrylic acid 92126 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/0031-9422(90)80196-N
Isoferulic Acid 736186 Click to see 194.18 unknown https://doi.org/10.1016/0031-9422(90)80196-N

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