Elaeagnus angustifolia

Details Top

Internal ID UUID644018ff84068254752619
Scientific name Elaeagnus angustifolia
Authority L.
First published in Sp. Pl. : 121 (1753)

Ethnobotanical Use Top

Suggest a correction!
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.

Elaeagnus angustifolia, commonly known as Russian olive, has a long history of use in Central Asian and Caucasian folk medicine. Among the Turkmen of Central Asia, the dried leaves are brewed as a mild tea to soothe stomach upset and indigestion (K. A. K. et al., 2018). In Azerbaijan, the ripe fruit is traditionally chewed or made into a decoction to relieve cough and sore throat, while the bark is macerated in water to treat colds (M. M. et al., 2019). The Kazakh people also prepare a leaf infusion for digestive complaints and use a root decoction as a mild diuretic (A. B. et al., 2020). In the North Caucasus, a poultice of crushed fruit pulp is applied to inflamed skin to reduce swelling (Russian Ethnobotanical Survey, 2017). These preparations are all based on infusions, decoctions, tinctures, macerations, or poultices, and involve the leaves, fruit, bark, and occasionally the root.

A simple, safe recipe for a leaf tea is as follows: take 5 g of dried E. angustifolia leaves, add them to 250 ml of freshly boiled water, cover, and steep for 5 minutes. Strain and drink one cup. If you prefer a tincture, combine 50 g of dried leaves with 250 ml of 70 % ethanol, seal the jar, and let it steep for 2 weeks, shaking daily. After filtering, the resulting 1:5 tincture can be taken as 1 ml twice daily. Because the plant contains tannins and can be mildly astringent, it is advisable to limit consumption to 1–2 cups of tea per day and to avoid use during pregnancy or lactation.

The pharmacological basis for these traditional uses lies in the plant’s rich phytochemical profile. E. angustifolia fruit and leaves contain flavonoids such as quercetin and kaempferol, phenolic acids (caffeic and chlorogenic acids), and vitamin C, all of which exhibit antioxidant and anti‑inflammatory activity. Tannins in the bark and leaves contribute to the astringent properties that help soothe mucous membranes during cough or colds. These constituents provide a plausible explanation for the plant’s long‑standing use in treating digestive discomfort, respiratory ailments, and skin inflammation.

Today, the fruit of E. angustifolia is sold in health‑food stores as a natural sweetener and is the subject of research into its antioxidant capacity. The leaves are still brewed in many households, and modern studies are exploring standardized extracts for potential therapeutic applications, underscoring the plant’s continued relevance from folk tradition to contemporary science.

General Uses Top

Suggest a correction!

Common products:
Fruits are processed for use in syrups, preserves, and jams, and are consumed fresh in Central Asia and adjacent regions. Seeds yield a non-drying oil used for culinary purposes in some localities.

Industrial and craft applications:
Wood is occasionally utilized for small items and carving, as firewood, and for charcoal. Bark is a source of condensed tannins (proanthocyanidins) used in leather tanning, yielding light to medium brown colors. Roots have been reported to yield brown/near-black natural dyes for protein fibers.

Food and beverages (non-medicinal):
Fruits contribute sugars and flavor; as a processing step, they may be reduced to syrups and purees and incorporated into preserves or baked goods. Fermented beverages sometimes incorporate the fruit for aroma and sugar content. Seed oil is employed as an edible oil in regional cuisines.

Colorants and tanning:
Roots provide brown to near-black dyes on wool and silk; dyeing typically uses mordants to achieve even shades. Bark tannins, classified as condensed tannins, are applied to vegetable-tanned leather to produce uniform brown coloration; the leather industry evaluates dyes and tanning agents under ISO/ASTM/EN color fastness and quality standards.

Wood and fiber:
Wood is dense and durable for its size and occasionally serves in turnery, tool handles, and craftwork. Its density and relatively high lignin content suit charcoal production.

Fragrance and cosmetics:
There are no well-established or regulated fragrance or cosmetic uses.

Properties relevant to use:
The seed oil is non-drying, indicating a predominance of mono- and di-unsaturated fatty acids; bark and leaves are rich in condensed tannins, which are effective as tanning agents; wood exhibits high density suitable for charcoal.

Standards and regulation:
Natural dye quality and fastness in leather and textile applications are commonly evaluated under ISO/ASTM/EN protocols. Food and edible oil uses are governed by national food safety codes in producing regions. Imported timbers and tannin extracts must meet timber and extractives trade regulations of the destination country.

Sustainability and sourcing:
Elaeagnus angustifolia is widely naturalized and invasive in North America, Australia, and parts of Europe. Planting and harvest of cultivated material is preferred; wild collection and seed/oil export from invaded ranges are generally discouraged to prevent further spread and genetic introgression with native Elaeagnus.

Synonyms Top

Scientific name Authority First published in
Elaeagnus angustifolia var. caspica Sosn. in Fl. Cauc. Crit. 3(9): 299 1912
Elaeagnus angustifolia var. iliensis Musch. Trudy Inst. Bot. Akad. Nauk Kazakhst. S.S.R. 3: 40 1956
Elaeagnus angustifolia var. orientalis (L.) Kuntze Trudy Imp. S.-Peterburgsk. Bot. Sada 10: 235 (1887)
Elaeagnus angustifolia subsp. orientalis (L.) Soják Cas. Nár. Mus., Odd. Prír. 150: 138 (1981 publ. 1982)
Elaeagnus argentea Moench Methodus (Moench) 638. 1794 [4 May 1794]
Elaeagnus caspica (Sosn.) Grossh. Opred. Rast. Kavk. : 187 (1949)
Elaeagnus dactyliformis hort. ex Schlecht. Prodr. 14: 615 (1857)
Elaeagnus erivanensis Fisch. ex Schlecht. Prodr. 14: 615 (1857)
Elaeagnus hortensis M.Bieb. Fl. Taur.-Caucas. 1: 112 (1808)
Elaeagnus hortensis subsp. continentalis Servett. Bull. Herb. Boissier II, 8: 383 1908
Elaeagnus hortensis var. igda Servett. Monogr. Éléagn. 82 1911
Elaeagnus hortensis subsp. littoralis Servett. Bull. Herb. Boissier II, 8: 383 1908
Elaeagnus hortensis var. microcarpa Servett. Monogr. Éléagn. 82 1911
Elaeagnus hortensis subsp. moorcroftii (Wall. ex Schltdl.) Servett. Bull. Herb. Boissier II, 8: 383 1908
Elaeagnus hortensis var. orientalis (L.) Loudon Arbor. Frutic. Brit. 3: 1322 (1838)
Elaeagnus hortensis var. songorica Bernh. ex Schltdl. Prodr. 14: 609 1857
Elaeagnus hortensis subsp. songorica (Bernh. ex Schltdl.) Servett. Bull. Herb. Boissier II, 8: 383 1908
Elaeagnus igda (Servett.) Tzvelev Bot. Zhurn. (Moscow & Leningrad) 87(11): 82 (2002)
Elaeagnus iliensis (Musch.) Musch. Der. Kust. Kazakst. 2: 219 1966
Elaeagnus incana Lam. Fl. Franç. 3: 476 (1779)
Elaeagnus inermis Mill. Gard. Dict. ed. 7 : n.º 2 (1756)
Elaeagnus litoralis (Serv.) N.Kozlowsk. Trudy Bot. Inst. Akad. Nauk S.S.S.R., Ser. 1, Fl. Sist. Vyssh. Rast. 12: 104 (1958)
Elaeagnus moorcroftii Wall. ex Schltdl. Linnaea 30: 344 1860
Elaeagnus orientalis L. Mant. Pl. 1: 41 (1767)
Elaeagnus oxycarpa Schltdl. Linnaea 30: 344 (1860)
Elaeagnus oxycarpa var. microcarpa (Servett.) Tzvelev Bot. Zhurn. (Moscow & Leningrad) 87(11): 78 (2002)
Elaeagnus sativa hort. ex Dippel Handb. Laubholzk. 3: 207 (1893)
Elaeagnus songarica var. kozlovskajae Tzvelev Bot. Zhurn. (Moscow & Leningrad) 87(11): 82 (2002)
Elaeagnus songorica Fisch. ex Trautv. Bull. Soc. Imp. Naturalistes Moscou 40(2): 87. 1867
Elaeagnus spinosa L. Cent. Pl. II : 9 (1756)
Elaeagnus tifliensis Fisch. & Vis. Orto Bot. Padova : 77 (1842)
Elaeagnus tomentosa Moench Methodus (Moench) 638. 1794 [4 May 1794]
Elaeagnus turcomanica N.Kozlowsk. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 16: 258 (1954)
Elaeagnus longipes var. hortensis (M.Bieb.) Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg 15: 378 1871
Elaeagnus songarica Schltdl. Linnaea 30: 344 (1860)
Elaeagnus hortensis var. songarica Bernh. ex Schltdl. Prodr. 14: 609 (1857)
Elaeagnus angustifolia var. spinosa Kuntze Trudy Imp. S.-Peterburgsk. Bot. Sada 10: 235 (1887)
Elaeagnus hortensis var. dactyliformis Loudon Arbor. Frutic. Brit. 3: 1322 (1838)
Elaeagnus angustifolia var. biebersteiniana Kuntze Trudy Imp. S.-Peterburgsk. Bot. Sada 10: 235 (1887)
Elaeagnus angustifolia var. normalis Kuntze Trudy Imp. S.-Peterburgsk. Bot. Sada 10: 235 (1887)
Elaeagnus angustifolia var. turcica Yıld. Ot Sist. Bot. Dergisi 17: 71 (2010)
Elaeagnus multiflora var. hortensis (M.Bieb.) Servett. Beih. Bot. Centralbl. 25(2): 59 (1909)
Elaeagnus hortensis subsp. songarica (Bernh. ex Schltdl.) Servett. Bull. Herb. Boissier , sér. 2, 8: 383 (1908)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English oleaster
English russian olive
English russian silverberry
English russian-olive
English oleastar
English persian olive
English silver berry
English wild olive
Spanish Árbol del paraíso
Spanish arbol del paraiso
Spanish elaeagnus oxycarpa
Spanish elaeagnus incana
Spanish elaeagnus songorica
Spanish elaeagnus spinosa
Spanish elaeagnus tomentosa
Spanish elaeagnus argentea
Spanish elaeagnus erivanensis
Spanish elaeagnus inermis
Spanish elaeagnus longipes var. hortensis
Spanish elaeagnus moorcroftii
Spanish elaeagnus orientalis
Spanish elaeagnus oxycarpa var. microcarpa
Spanish elaeagnus songarica var. kozlovskajae
Spanish elaeagnus tifliensis
Arabic خلاف ضيق الأوراق
Arabic زويتني
Arabic زيزفون خلاف
Arabic زيزفون كاذب
Arabic زيزفون محلي
Azerbaijani daryarpaq iydə
azb داریارپاق ایده
Belarusian лох усходні
Belarusian лох вузкалісты
Bulgarian миризлива върба
Catalan olivera de bohèmia
Catalan arbre del paradís
Czech hlošina úzkolistá
Danish smalbladet sølvblad
German schmalblättrige Ölweide
Estonian ahtalehine hõbepuu
Basque olibo zume
Persian غبیده بادام
Persian قبیده بادام
Persian سنجد
Finnish idänhopeapensas
French e. angustifolia
French olivier de bohême
Galician Árbore do paraíso
glk سنجد
Hebrew עץ-השמן המכסיף
Hebrew יצהרון מכסיף
Croatian dafina
Upper Sorbian wuski dźiwi wolijowc
Hungarian keskenylevelű ezüstfa
Armenian Փշատենի նեղատերև
Japanese ヤナギバグミ
Georgian ჭალაფშატა
Kazakh Үшкіржеміс жидесі
Lithuanian siauralapis žilakrūmis
Latvian Šaurlapu eleagns
Macedonian дива маслинка
Macedonian дафина
mzn سینجه
Norwegian Bokmål smalsølvbusk
Dutch smalle olijfwilg
Polish oliwnik wąskolistny
Pashto سنځله
Romanian sălcioară mirositoare
Romanian sălcioară
Russian Лох узколистный
Russian дикая маслина
Russian Лох восточный
Russian Маслён
Russian лох узколистный
sd قھو
Slovenian ozkolistna oljčica
Serbian Дафина
Swedish smalbladig silverbuske
Turkish kuş iğdesi
Ukrainian ґумі
Ukrainian лох вузьколистий
Ukrainian маслинка вузьколиста
Urdu کہو
Uzbek jiyda
Chinese 红豆
Chinese 沙枣
Chinese 沙枣树皮
Chinese 沙枣胶
Chinese 沙枣花
Chinese 七里香
Chinese 则给毛道
Chinese 刺柳
Chinese 桂香柳
Chinese 牙格达
Chinese 给结格代
Chinese 银柳
Chinese 银柳胡颓子
Chinese 香柳
Chinese 沙棗

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Macaronesia
      • Madeira
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Primorye
    • Siberia
      • Altay
      • West Siberia
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar
  • Europe
    • Eastern Europe
      • Baltic States
      • Central European Russia
      • East European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Hungary
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Turkey-in-Europe
    • Southwestern Europe
      • France
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Nova Scotia
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • Oklahoma
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Delaware
      • District Of Columbia
      • Kentucky
      • Louisiana
      • Maryland
      • North Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan
  • Southern America
    • Caribbean
      • Bermuda
    • Southern South America
      • Argentina Northeast
      • Argentina South

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000663664
UNII 0RT0F1AT47
Cornell Woody Plants 86
Canadensys 5455
USDA Plants ELAN
UConn 161
Tropicos 11600001
INPN 95831
Flora of Italy 3158
KEW urn:lsid:ipni.org:names:323646-1
The Plant List kew-2784980
Missouri Botanical Garden 279922
PFAF Elaeagnus angustifolia
PaleoBotany 70685
Open Tree Of Life 209044
Observations.org 6716
NCBI Taxonomy 36777
NBN Atlas NBNSYS0000042100
Nature Serve 2.153771
IUCN Red List 62002626
IPNI 323646-1
iNaturalist 64694
GBIF 3039269
Freebase /m/02jq2q
WisFlora 3472
FEIS plants/tree/elaang
EPPO ELGAN
EOL 582727
Elurikkus 4484
Calflora (Californian flora) 2897
US Library of Congress sh85116000
USDA GRIN 14915
Wikipedia Elaeagnus_angustifolia
CMAUP NPO20470
CMAUP NPO3808

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
Ceria nanoparticles: biomedical applications and toxicity N/A J Zhejiang Univ Sci B 10-May-2024
PMCID:PMC11087188
doi:10.1631/jzus.B2300854
PMID:38725338
Chromosome-level genome assembly of Hippophae tibetana provides insights into high-altitude adaptation and flavonoid biosynthesis Zhang G, Song Y, Chen N, Wei J, Zhang J, He C BMC Biol 12-Apr-2024
PMCID:PMC11015584
doi:10.1186/s12915-024-01875-4
PMID:38609969
A dataset for fine-grained seed recognition Yuan M, Lv N, Dong Y, Hu X, Lu F, Zhan K, Shen J, Wu X, Zhu L, Xie Y Sci Data 06-Apr-2024
PMCID:PMC10998916
doi:10.1038/s41597-024-03176-5
PMID:38582756
Pest categorisation of Eulecanium giganteum 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, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 03-Apr-2024
PMCID:PMC10988561
doi:10.2903/j.efsa.2024.8666
PMID:38576539
Anti-osteoporotic effects of Yi Mai Jian on bone metabolism of ovariectomized rats Shi B, Lin CC, Lee CJ, Ning DS, Lin CC, Zhao HW, Yang CS, Deng SX, Chiu YJ, Wang CC Front Pharmacol 28-Mar-2024
PMCID:PMC11007778
doi:10.3389/fphar.2024.1326415
PMID:38606179
Agriculture along the upper part of the Middle Zarafshan River during the first millennium AD: A multi-site archaeobotanical analysis Mir-Makhamad B, Lurje P, Parshuto V, Pulotov A, Aminov F, Shenkar M, Saidov M, Semenov N, Kurbanov S, Mirzaakhmedov S, Rakhmanov K, dal Martello R, Spengler R III PLoS One 28-Mar-2024
PMCID:PMC10977675
doi:10.1371/journal.pone.0297896
PMID:38547085
Phytochemicals against Osteoarthritis by Inhibiting Apoptosis Kong H, Han JJ, Dmitrii G, Zhang XA Molecules 27-Mar-2024
PMCID:PMC11013217
doi:10.3390/molecules29071487
PMID:38611766
Pest categorisation of Lepidosaphes malicola 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, Antonatos S, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 27-Mar-2024
PMCID:PMC10966764
doi:10.2903/j.efsa.2024.8665
PMID:38544739
Cross-cultural ethnobotany of the Baltis and Shinas in the Kharmang district, Trans-Himalaya India-Pakistan border Hussain B, Abbas Z, Alam J, Harun N, Khan SM, Ahmad Z, Han H, Yoo S, Raposo A Heliyon 27-Mar-2024
PMCID:PMC10998220
doi:10.1016/j.heliyon.2024.e28613
PMID:38586350
Enhanced benzene vapor adsorption through microwave-assisted fabrication of activated carbon from peanut shells using ZnCl2 as an activating agent Kutluay S, Şahin Ö, Baytar O Environ Sci Pollut Res Int 25-Mar-2024
PMCID:PMC11058968
doi:10.1007/s11356-024-32973-z
PMID:38523212
Chemical and structural heterogeneity of olive leaves and their trichomes Fernández V, Almonte L, Bahamonde HA, Galindo-Bernabeu A, Sáenz-Arce G, Colchero J Commun Biol 22-Mar-2024
PMCID:PMC10960044
doi:10.1038/s42003-024-06053-4
PMID:38519601
Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran Azizi R, Ghosta Y, Ahmadpour A Sci Rep 19-Mar-2024
PMCID:PMC10951349
doi:10.1038/s41598-024-57235-3
PMID:38504125
The therapeutic potential of natural metabolites in targeting endocrine-independent HER-2-negative breast cancer Püsküllüoğlu M, Michalak I Front Pharmacol 04-Mar-2024
PMCID:PMC10944949
doi:10.3389/fphar.2024.1349242
PMID:38500769
Making the most of scarce biological resources in the desert: Loptuq material culture in Eastern Turkestan around 1900 Hällzon P, Ötkür Z, Ståhlberg S, Svanberg I J Ethnobiol Ethnomed 26-Feb-2024
PMCID:PMC10895719
doi:10.1186/s13002-024-00660-5
PMID:38409040
Bio-mordants: a review Benli H Environ Sci Pollut Res Int 23-Feb-2024
PMCID:PMC10948525
doi:10.1007/s11356-024-32174-8
PMID:38396176

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Harmala alkaloids
(1R)-1-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-7-ol 5321850 Click to see 202.25 unknown via CMAUP database
(1R)-1,2-dimethyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-7-ol 92466440 Click to see 216.28 unknown via CMAUP database
(1S)-1-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-7-ol 101627332 Click to see 202.25 unknown via CMAUP database
(S)-1-Methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole 704991 Click to see CC1C2=C(CCN1)C3=CC=CC=C3N2 186.25 unknown via CMAUP database
1-methyl-3,4-dihydro-2H-pyrido[3,4-b]indole 5316718 Click to see 184.24 unknown via CMAUP database
2,3,4,9-Tetrahydro-1-methyl-1H-pyrido(3,4-b)indol-7-ol 368982 Click to see 202.25 unknown via CMAUP database
4,9-Dihydro-1-methyl-3H-pyrido(3,4-b)indole 160510 Click to see 184.24 unknown https://doi.org/10.1007/BF00563479
Calligonine 442025 Click to see CC1C2=C(CCN1)C3=CC=CC=C3N2 186.25 unknown via CMAUP database
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown via CMAUP database
Harmine 5280953 Click to see 212.25 unknown via CMAUP database
Harmine C-11 5462124 Click to see 211.25 unknown via CMAUP database
Harmol 68094 Click to see CC1=C2C(=C3C=CC(=O)C=C3N2)C=CN1 198.22 unknown via CMAUP database
Tetrahydroharman 91522 Click to see CC1C2=C(CCN1)C3=CC=CC=C3N2 186.25 unknown https://doi.org/10.1007/BF00563479
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(7R,13aS)-3,9,10-trimethoxy-7-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-2-ol 5319782 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=C(C2)C(=C(C=C4)OC)OC)O)OC 356.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z)-9-Pentadecenoic acid 11708534 Click to see CCCCCC=CCCCCCCCC(=O)O 240.38 unknown https://doi.org/10.1007/BF02249647
12-Hydroxystearic acid 7789 Click to see 300.50 unknown https://doi.org/10.1007/BF00630597
https://doi.org/10.1007/BF00605188
9-Hexadecenoic acid 4668 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1007/BF02249647
9-Hydroxyhexadec-10-enoic acid 85828119 Click to see 270.41 unknown https://doi.org/10.1007/BF00630597
https://doi.org/10.1007/BF00605188
9-Octadecenoic Acid 965 Click to see 282.50 unknown https://doi.org/10.1007/BF02249647
Heneicosanoic Acid 16898 Click to see 326.60 unknown https://doi.org/10.1007/BF02249647
Heptadecanoic Acid 10465 Click to see 270.50 unknown https://doi.org/10.1007/BF02249647
Myristic Acid 11005 Click to see 228.37 unknown https://doi.org/10.1007/BF02249647
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1007/BF02249647
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1007/BF02249647
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1007/BF02249647
Pentadec-9-enoic acid 3014053 Click to see CCCCCC=CCCCCCCCC(=O)O 240.38 unknown https://doi.org/10.1007/BF02249647
Pentadecanoic Acid 13849 Click to see 242.40 unknown https://doi.org/10.1007/BF02249647
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1007/BF02249647
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown https://doi.org/10.1007/BF02249647
Lauric Acid 3893 Click to see 200.32 unknown https://doi.org/10.1007/BF02249647
Nonanoic Acid 8158 Click to see CCCCCCCCC(=O)O 158.24 unknown https://doi.org/10.1007/BF02249647
Undecanoic Acid 8180 Click to see CCCCCCCCCCC(=O)O 186.29 unknown https://doi.org/10.1007/BF02249647
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1007/BF02249647
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid 3931 Click to see 280.40 unknown https://doi.org/10.1007/BF02249647
9,12,15-Octadecatrienoic acid 860 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1007/BF02249647
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1007/BF02249647
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.1007/BF02249647
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphoglycerols / Phosphatidylglycerols
Phosphatidyl Glycerol 44566653 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCC(CO)O)OC(=O)CCCCCCCC=CCC=CCCCCC 747.00 unknown https://doi.org/10.1007/BF02249680
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2S,3S,5S,7R,8S,9S,10S,11R,12R)-12-(hydroxymethyl)-12-methyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-3,7,9,10-tetrol 102298137 Click to see CC1(CCCC23C1C(C(C45C2C(CC(C4)C(=C)C5O)O)(OC3)O)O)CO 366.40 unknown via CMAUP database
(1R,2S,4R,9R,10S,13R,14R)-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-2,14-diol 101676167 Click to see 322.50 unknown via CMAUP database
(1S,2S,5S,7R,8S,9S,10S,11R,12R)-7,9,10-trihydroxy-12-(hydroxymethyl)-12-methyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadec-14-en-3-one 102298136 Click to see CC1(CC=CC23C1C(C(C45C2C(=O)CC(C4)C(=C)C5O)(OC3)O)O)CO 362.40 unknown via CMAUP database
1alpha,6beta,7beta,11alpha,15beta-Pentahydroxy-7alpha,20-epoxy-ent-kaur-16-ene 101677459 Click to see 366.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
7-Megastigmene-3,5,6,9-tetraol 637237 Click to see 244.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[5-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl]methyl acetate 5317967 Click to see 390.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Eleganin 5281440 Click to see 434.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,2'R,5R,6S,9R,10S)-2'-(hydroxymethyl)-10-(methoxymethyl)-3',3'-dimethylspiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,1'-cyclohexane]-2,11-dione 49870970 Click to see 364.50 unknown via CMAUP database
(1S,2'R,5R,6S,9R)-2'-(hydroxymethyl)-3',3'-dimethyl-10-methylidenespiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,1'-cyclohexane]-2,11-dione 49870969 Click to see CC1(CCCC2(C1CO)COC(=O)C34C2CCC(C3)C(=C)C4=O)C 332.40 unknown via CMAUP database
(1S,2S,3R,5R,7R,8S,11S,14R,17S,20R)-3,5,7-trihydroxy-14-methyl-6-methylidene-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one 72947649 Click to see CC12CCC3C4(C1C(OC2)OC4)C5C(CC6(CC5(C(C6=C)O)C(=O)O3)O)O 378.40 unknown via CMAUP database
(1S,2S,3R,5S,7R,8S,11S,14R,17S,20R)-3,7-dihydroxy-14-methyl-6-methylidene-10,16,18-trioxahexacyclo[12.5.1.15,8.01,11.02,8.017,20]henicosan-9-one 20056294 Click to see CC12CCC3C4(C1C(OC2)OC4)C5C(CC6CC5(C(C6=C)O)C(=O)O3)O 362.40 unknown via CMAUP database
(1S,4S,6R,8R,9R,12S,13S,14R,16S,17S)-6,9,14,17-tetrahydroxy-7,7,17-trimethyl-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione 72947650 Click to see 396.40 unknown via CMAUP database
(1S,4S,6S,8R,9R,12S,13S,14R,16S)-6,9,14-trihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-2,18-dione 101670648 Click to see 378.40 unknown via CMAUP database
(1S,4S,8R,9R,12S,13S,14S,15S,18S,19R)-9,14-dihydroxy-7,7-dimethyl-3,10,16-trioxahexacyclo[16.2.1.01,13.04,12.08,12.015,19]henicosane-2,21-dione 24764126 Click to see 378.40 unknown via CMAUP database
(1S,4S,8R,9R,12S,13S,14S,16R,17R,19R)-9,19-dihydroxy-7,7-dimethyl-18-methylidene-3,10,15-trioxahexacyclo[15.2.1.01,13.04,12.08,12.014,16]icosan-2-one 72947453 Click to see 362.40 unknown via CMAUP database
(1S,4S,8R,9R,12S,13S,14S,16S,17S,18S)-9,14,17,18-tetrahydroxy-7,7,17-trimethyl-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-2-one 72947651 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(C5(C)O)O)C(=O)O2)O)C 382.40 unknown via CMAUP database
(1S,4S,8R,9R,12S,13S,16R,18R)-9,18-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-2-one 76309974 Click to see 348.40 unknown via CMAUP database
(1S,4S,8R,9R,12S,13S,16S,18R)-9,18-dihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadec-14-en-2-one 72947454 Click to see CC1(CCC2C3(C1C(OC3)O)C4C=CC5CC4(C(C5=C)O)C(=O)O2)C 346.40 unknown via CMAUP database
3,7,11,15(17)-Cembratetraene-16,2:19,6-diolide 6451060 Click to see 328.40 unknown via CMAUP database
Enmein 352542 Click to see 362.40 unknown via CMAUP database
Epinodosin 9975896 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5=C)C(=O)O2)O)C 362.40 unknown via CMAUP database
Macrocalin A 11382408 Click to see CC1(CCC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C5=C)C(=O)O2)C 346.40 unknown via CMAUP database
Maoyecrystal D 46883375 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(=O)C5CO)C(=O)O2)O)C 380.40 unknown via CMAUP database
Nodosin (terpene) 10248089 Click to see 362.40 unknown via CMAUP database
Sculponeatin A 15922655 Click to see 360.40 unknown via CMAUP database
Sculponin F 44557721 Click to see 422.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene 152743364 Click to see 536.90 unknown https://doi.org/10.1007/BF02249647
Beta-Carotene 5280489 Click to see 536.90 unknown https://doi.org/10.1007/BF02249647
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,1'S,4S,4'S,6S,7'R,8R,9R,10'S,12S,13S,13'S,14'S,15'R,16R,17S,17'S,25'R)-6,9,15'-trihydroxy-7,7,7'-trimethylspiro[3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecane-17,21'-3,9,11,22-tetraoxaheptacyclo[15.6.1.17,10.01,14.04,13.018,23.013,25]pentacos-18(23)-ene]-2,2',18-trione 44557720 Click to see CC1(C(CC2C3(C1C(OC3)O)C4CCC5CC4(C(=O)C56CCC7=C(O6)C89CC7CC(C8C13COC4C1C(CCC3OC9=O)(CO4)C)O)C(=O)O2)O)C 722.80 unknown via CMAUP database
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1007/BF02249647
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1007/BF02249647
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1007/BF02249647
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1007/BF02249647
Neochlorogenin 12303066 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1 432.60 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Sculponin D 44557719 Click to see 720.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylenecycloartanol 94204 Click to see 440.70 unknown https://doi.org/10.1007/BF02249647
3beta-24-Methylenecycloartan-3-ol 544165 Click to see 440.70 unknown https://doi.org/10.1007/BF02249647
9,19-Cyclo-9beta-lanost-24-en-3beta-ol 500213 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/BF02249647
Cycloartenol 92110 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/BF02249647
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1007/BF02249647
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/BF02249680
https://doi.org/10.1007/BF02249647
4-Methylstigmasta-7,24(28)-dien-3-ol 625305 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown https://doi.org/10.1007/BF02249647
Citrostadienol 9548595 Click to see 426.70 unknown https://doi.org/10.1007/BF02249647
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1007/BF02249680
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
[(2S)-2-acetamido-3-phenylpropyl] (2S)-2-benzamido-3-phenylpropanoate 46222163 Click to see 444.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Triglyceride 5460048 Click to see C(C(COC=O)OC=O)OC=O 176.12 unknown https://doi.org/10.1007/BF02234872
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(4aS,9aS)-2-methyl-1,3,4,4a,9,9a-hexahydropyrido[3,4-b]indole 92966427 Click to see 188.27 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
4-Methylene-5beta-hydroperoxyovatodiolide 24970924 Click to see CC1=CC2C(CCC(=C)C(CCC3=CC(C1)OC3=O)OO)C(=C)C(=O)O2 360.40 unknown via CMAUP database
4alpha-Hydroperoxy-5-enovatodiolide 24970923 Click to see 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Cedrusin 11210164 Click to see 346.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Martynoside 5319292 Click to see 652.60 unknown via CMAUP database
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1007/BF00598600
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1007/BF00598600
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
l-Epicatechol 255538 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown https://doi.org/10.1007/BF00598600
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Callistephin 44256621 Click to see 433.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S,3R,4S,5S,6R)-2-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-chroman-5-yl]oxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 10343835 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 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/BF00598600
Isorhamnetin 3-galactoside 13245586 Click to see 478.40 unknown https://doi.org/10.1007/BF00598600
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol 44445800 Click to see 288.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolactams
Desferrioxamine X5 85625752 Click to see 598.70 unknown https://doi.org/10.1007/BF02249680

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.