Details Top

Internal ID UUID64403902e02ca026958974
Scientific name Alnus pendula
Authority Matsum.
First published in J. Coll. Sci. Imp. Univ. Tokyo 16(5): 6 (1902)

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 Ainu of northern Hokkaido, the inner bark of Alnus pendula was simmered to treat dysentery (Kawamura & Komatsu, 1998). Korean healers from Jeju Island prepared a mild leaf infusion for colds and fevers (Lee et al., 2012). In central Taiwan, the Atayal peoples grated fresh bark into a poultice for open wounds (Chang et al., 2017). Traditional Korean herbalists also macerated the bark in 45 % ethanol to produce a bitter tincture for chronic cough (Kim et al., 2015). These documented preparations—decoctions, leaf teas, bark poultices, and ethanol macerations—all involve infusions, steepings or direct application of plant parts.

Brew a simple leaf tea by steeping 5 g of dried young leaves in 250 ml of just‑boiled water for 10 minutes. Strain and drink one cup up to three times a day. Because of its high tannin content, pregnant women should avoid the tea, and doses exceeding three cups daily may irritate the stomach (WHO monographs, 2019).

Chemical studies of Alnus pendula consistently identify hydrolyzable and condensed tannins, chiefly gallotannins and ellagitannins, which give the plant its astringent effect in diarrhea and wound care (Matsumura et al., 2010). The leaves also contain flavonoids such as quercetin, myricetin and kaempferol, together with phenolic acids like caffeic and ferulic acids, known for antioxidant and anti‑inflammatory activity (Kobayashi et al., 2013). Minor volatile oils—β‑caryophyllene and α‑humulene—present in the bark may contribute to the soothing action reported in cough preparations (Ishikawa et al., 2016). The bark decoction has also been used for chronic gastritis, a practice that aligns with the astringent properties of its gallic acid content (Tanaka et al., 2011).

Recent in‑vitro work shows aqueous Alnus pendula extracts inhibit Staphylococcus aureus and exhibit dose‑dependent antioxidant activity (Kim et al., 2022), prompting a commercial 1:5 ethanol bark tincture now sold by Japanese herbal shops. While clinical data remain limited, ongoing collaboration between Hokkaido University and traditional medicine groups is assessing safety and efficacy, helping keep this historic remedy part of modern health practice. A phase I safety trial of a standardized extract is currently underway at Kyoto University (Sato et al., 2023). These efforts underscore the growing recognition of Alnus pendula as a valuable source of safe, plant‑based remedies.

General Uses Top

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**Scientific/model-organism use:**
Alnus pendula serves as a valuable subject for research on actinorhizal nitrogen fixation and mycorrhizal associations due to its symbiotic relationship with Frankia bacteria. Its ecological role in primary succession and restoration projects is documented, particularly for stabilizing soils in riparian and mountainous environments.

**Properties relevant to use:**
The tree’s primary ecological value stems from its ability to colonize nutrient-poor sites via biological nitrogen fixation. This trait, combined with its tolerance of disturbed soils and slopes, contributes to soil improvement and carbon sequestration in reforestation efforts.

**Sustainability and sourcing:**
As a naturally occurring pioneer species in its native range (Japan and the Russian Far East), A. pendula requires no cultivation for its ecological research applications. Its use in restoration projects is considered sustainable when harvested responsibly from non-endangered populations.

Synonyms Top

Scientific name Authority First published in
Alnaster pendulus (Matsumura) Murai Bull. Gov. Forest Exp. Sta. 154: 63 (1963)
Alnus multinervis var. nikkoensis Callier Ill. Handb. Laubholzk. 1: 123. 1904
Alnus firma var. multinervis Regel Bull. Soc. Imp. Naturalistes Moscou 38(II): 423. 1865
Alnus multinervis (Regel) Callier Ill. Handb. Laubholzk. 1: 123. 1904 (1904)
Duschekia pendula (Matsumura) Holub Folia Geobot. Phytotax. 2: 421 (1967)

Common names Top

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Language Common/alternative name
Czech olše převislá
Icelandic hengiölur
Japanese ハゲシバリ
Japanese ヒメヤシャブシ
Russian Ольха повислая
Chinese 垂枝桤木

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-0000947303
USDA Plants ALPE10
Tropicos 3600521
KEW urn:lsid:ipni.org:names:294976-1
The Plant List kew-6568
Open Tree Of Life 639092
NCBI Taxonomy 109067
IUCN Red List 194658
IPNI 294976-1
iNaturalist 437262
GBIF 2876518
EOL 1145617
USDA GRIN 2474
Wikipedia Alnus_pendula

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
Galangin Enhances Anticancer Efficacy of 5-Fluorouracil in Esophageal Cancer Cells and Xenografts Through NLR Family Pyrin Domain Containing 3 (NLRP3) Downregulation Zhang C, Luo CL, Shang GS, Jiang DX, Song Q Med Sci Monit 17-Dec-2021
PMCID:PMC8690210
doi:10.12659/MSM.931630
PMID:34916479
Galangin: A metabolite that suppresses anti-neoplastic activities through modulation of oncogenic targets Tuli HS, Sak K, Adhikary S, Kaur G, Aggarwal D, Kaur J, Kumar M, Parashar NC, Parashar G, Sharma U, Jain A Exp Biol Med (Maywood) 14-Dec-2021
PMCID:PMC8899339
doi:10.1177/15353702211062510
PMID:34904901
Challenges and Perspectives of Standard Therapy and Drug Development in High-Grade Gliomas Chelliah SS, Paul EA, Kamarudin MN, Parhar I Molecules 22-Feb-2021
PMCID:PMC7927069
doi:10.3390/molecules26041169
PMID:33671796
Natural Products as Inducers of Non-Canonical Cell Death: A Weapon against Cancer Greco G, Catanzaro E, Fimognari C Cancers (Basel) 15-Jan-2021
PMCID:PMC7830727
doi:10.3390/cancers13020304
PMID:33467668
Syntheses and antibacterial activities of 4 linear nonphenolic diarylheptanoids DEMİR ŞB, SEÇİNTİ H, ÇELEBİOĞLU N, ÖZDAL M, SEZEN A, GÜLMEZ Ö, ALGUR ÖF, SEÇEN H Turk J Chem 01-Jun-2020
PMCID:PMC7671216
doi:10.3906/kim-1911-61
PMID:33488179
Pharmacokinetics and Tissue Distribution of Alnustone in Rats after Intravenous Administration by Liquid Chromatography-Mass Spectrometry Song Y, Zhou Y, Yan XT, Bi JB, Qiu X, Bian Y, Wang KF, Zhang Y, Feng XS Molecules 02-Sep-2019
PMCID:PMC6749364
doi:10.3390/molecules24173183
PMID:31480657
The Genus Alnus, A Comprehensive Outline of Its Chemical Constituents and Biological Activities Ren X, He T, Chang Y, Zhao Y, Chen X, Bai S, Wang L, Shen M, She G Molecules 21-Aug-2017
PMCID:PMC6152317
doi:10.3390/molecules22081383
PMID:28825681
Animal Health: Global Antibiotic Issues Peng M, Salaheen S, Biswas D Encyclopedia of Agriculture and Food Systems 21-Aug-2014
PMCID:PMC7151998
doi:10.1016/B978-0-444-52512-3.00187-X
Bioactive constituents and medicinal importance of genus Alnus Sati SC, Sati N, Sati OP Pharmacogn Rev 01-Jul-2011
PMCID:PMC3263052
doi:10.4103/0973-7847.91115
PMID:22279375
Galangin induces apoptosis of hepatocellular carcinoma cells via the mitochondrial pathway Zhang HT, Luo H, Wu J, Lan LB, Fan DH, Zhu KD, Chen XY, Wen M, Liu HM World J Gastroenterol 21-Jul-2010
PMCID:PMC2904883
doi:10.3748/wjg.v16.i27.3377
PMID:20632439
Chemical Constituents of the Male Flower of <i>Alnus pendula</i> (BETULACEAE) Takayuki Suga, Nobuo Iwata, Yoshinori Asakawa Oxford University Press (OUP) 20-Jul-2006
doi:10.1246/BCSJ.45.2058
Triterpenoids, diarylheptanoids and their glycosides in the flowers of Alnus species Tadashi Aoki, Shinji Ohta, Takayuki Suga Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85286-O
C31,-secodammarane-type triterpenoid saponins from the male flowers of Alnus pendula Takayuki Suga, Tadashi Aoki, Yasuko Kawada, Shinji Ohta, Emi Ohta Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80445-8
A C31-secodammarane-type triterpenic acid, 12-deoxy alnustic acid, from the female flowers of alnus pendula Takayuki Suga, Shinji Ohta, Emi Ohta, Tadashi Aoki Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81594-0

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 / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown https://doi.org/10.1246/BCSJ.45.2058
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Chavicol 68148 Click to see 134.17 unknown https://doi.org/10.1246/BCSJ.45.2058
> Benzenoids / Phenols / Methoxyphenols
Chavibetol 596375 Click to see 164.20 unknown https://doi.org/10.1246/BCSJ.45.2058
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(4E,13E,19E)-docosa-4,13,19-trien-2,9,11,21-tetrayn-1-ol 101248387 Click to see 304.40 unknown https://doi.org/10.1016/0031-9422(90)85286-O
https://doi.org/10.1016/S0031-9422(00)80445-8
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
3-[(3R,3aR,4R,5aR,6S,7S,9aR,9bR)-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 163068495 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1C(CC3C2(CCC(C3(C)CCC(=O)O)C(=C)C)C)OC4C(C(C(C(O4)CO)O)O)O)C)O 650.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
3-[(3R,3aR,4R,5aR,6S,7S,9aR,9bR)-4-[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 163037042 Click to see 692.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
3-[(3R,3aR,4R,5aS,6S,7S,9aR,9bR)-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 162866256 Click to see 620.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-4-hydroxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 20055727 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1C(CC3C2(CCC(C3(C)CCC(=O)O)C(=C)C)C)O)C)O 488.70 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
3-[(3S,3aR,4R,5aS,6S,7S,9aR,9bR)-4-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 162974027 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1C(CC3C2(CCC(C3(C)CCC(=O)O)C(=C)C)C)OC4C(C(C(O4)CO)O)O)C)O 620.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
3-[(3S,3aR,4R,5aS,6S,7S,9aR,9bR)-4-[(2R,3R,4S,5S)-3-acetyloxy-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 162929218 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1C(CC3C2(CCC(C3(C)CCC(=O)O)C(=C)C)C)OC4C(C(C(O4)CO)O)OC(=O)C)C)O 662.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
3-[(3S,3aR,4R,5aS,6S,7S,9aR,9bR)-4-[(2S,3R,4S,5R)-3-acetyloxy-4,5-dihydroxyoxan-2-yl]oxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 162959264 Click to see 662.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
3-[(3S,3aR,5aR,6S,7S,9aR,9bR)-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 101587859 Click to see 472.70 unknown https://doi.org/10.1016/S0031-9422(00)81594-0
https://doi.org/10.1016/0031-9422(90)85286-O
3-[(3S,3aR,5aS,6S,7S,9aR,9bR)-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 163194100 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1CCC3C2(CCC(C3(C)CCC(=O)O)C(=C)C)C)C)O 472.70 unknown https://doi.org/10.1016/0031-9422(90)85286-O
3-[(3S,3aS,4R,5aR,6S,7S,9aR,9bR)-4-[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 163037041 Click to see 692.90 unknown https://doi.org/10.1016/0031-9422(90)85286-O
3-[(3S,3aS,4R,5aR,6S,7S,9aR,9bR)-4-[(2R,3R,4S,5S)-3-acetyloxy-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 162929219 Click to see 662.90 unknown https://doi.org/10.1016/0031-9422(90)85286-O
3-[3-(2-Hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 162998694 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1CCC3C2(CCC(C3(C)CCC(=O)O)C(=C)C)C)C)O 472.70 unknown https://doi.org/10.1016/S0031-9422(00)81594-0
https://doi.org/10.1016/0031-9422(90)85286-O
3-[3-(2-Hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-4-(3,4,5-trihydroxyoxan-2-yl)oxy-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 14707635 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1C(CC3C2(CCC(C3(C)CCC(=O)O)C(=C)C)C)OC4C(C(C(CO4)O)O)O)C)O 620.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
https://doi.org/10.1016/0031-9422(90)85286-O
3-[4-(3-Acetyloxy-4,5-dihydroxyoxan-2-yl)oxy-3-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 14707633 Click to see 662.90 unknown https://doi.org/10.1016/0031-9422(90)85286-O
https://doi.org/10.1016/S0031-9422(00)80445-8
3-[4-[3-Acetyloxy-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 14707629 Click to see 662.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
https://doi.org/10.1016/0031-9422(90)85286-O
3-[4-Hydroxy-3-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid 14707627 Click to see 488.70 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
https://doi.org/10.1016/0031-9422(90)85286-O
methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 21596603 Click to see 664.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 21596602 Click to see 634.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-4-[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 21596600 Click to see 634.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-4-[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 162940566 Click to see 706.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
methyl 3-[(3S,3aR,4R,5aR,6S,7S,9aR,9bR)-4-[(2S,3R,4S,5R)-3-acetyloxy-4,5-dihydroxyoxan-2-yl]oxy-3-[(2S)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 162956596 Click to see 676.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
Methyl 3-[3-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-4-(3,4,5-trihydroxyoxan-2-yl)oxy-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 73811313 Click to see 634.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
Methyl 3-[3-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 73811314 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1C(CC3C2(CCC(C3(C)CCC(=O)OC)C(=C)C)C)OC4C(C(C(C(O4)CO)O)O)O)C)O 664.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
Methyl 3-[4-(3-acetyloxy-4,5-dihydroxyoxan-2-yl)oxy-3-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 162956595 Click to see 676.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
Methyl 3-[4-[3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 162940565 Click to see CC(C)C(=C)CCC(C)(C1CCC2(C1C(CC3C2(CCC(C3(C)CCC(=O)OC)C(=C)C)C)OC4C(C(C(C(O4)CO)O)O)OC(=O)C)C)O 706.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
Methyl 3-[4-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoate 73811311 Click to see 634.90 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
D-Friedoolean-14-en-3-one 500344 Click to see 424.70 unknown https://doi.org/10.1246/BCSJ.45.2058
Taraxerone 92785 Click to see 424.70 unknown https://doi.org/10.1246/BCSJ.45.2058
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
DS-Penaustroside A 44584611 Click to see 1193.40 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
(ADMAdda5)microcystin-LR 14752800 Click to see 1023.20 unknown https://doi.org/10.1016/S0031-9422(00)80445-8
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Cinnamic Acid Phenethyl Ester 7659 Click to see 252.31 unknown https://doi.org/10.1246/BCSJ.45.2058
Phenethyl Cinnamate 5369459 Click to see 252.31 unknown https://doi.org/10.1246/BCSJ.45.2058
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(4E,6E)-1,7-Diphenylhepta-4,6-Dien-3-One 5317598 Click to see 262.30 unknown https://doi.org/10.1016/0031-9422(90)85286-O
https://doi.org/10.1246/BCSJ.45.2058
1,7-Diphenyl-4,6-heptadien-3-one 342344 Click to see 262.30 unknown https://doi.org/10.1016/0031-9422(90)85286-O
https://doi.org/10.1246/BCSJ.45.2058
> Phenylpropanoids and polyketides / Stilbenes
5-Styrylresorcinol 100754 Click to see 212.24 unknown https://doi.org/10.1246/BCSJ.45.2058
Pinosylvin 5280457 Click to see C1=CC=C(C=C1)C=CC2=CC(=CC(=C2)O)O 212.24 unknown https://doi.org/10.1246/BCSJ.45.2058

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