Details Top

Internal ID UUID6440247b1320e108436369
Scientific name Allium angulosum
Authority L.
First published in Sp. Pl. 1: 300 (1753)

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 Slovak Carpathians, a tea made from the dried leaves of Allium angulosum has been used for cough, throat irritation and mild digestive upset (Kováč et al., 2009). In the Serbian Balkans a decoction of the bulb is employed as an antimicrobial rinse for sore throats and for washing infected skin lesions (Bennett et al., 2021). Ukrainian Carpathian healers apply fresh leaf poultices to bruises, sprains and minor wounds, reporting that the crushed leaves reduce swelling and pain (Miroshnyk, 1999). In the Russian Urals, an infusion of the aerial parts is taken as a diuretic and to ease urinary discomfort (Petrov et al., 2005). All of these preparations are prepared fresh or from dried material and involve simple water extracts – infusions, decoctions, or macerated poultices.

A practical recipe for a mild, everyday tea is as follows: place 1 – 2 g (about one teaspoon) of dried leaves in a cup, pour 250 ml of just‑boiled water over them, cover and steep for 5 – 7 minutes, then strain. The tea can be drunk 1 – 2 cups a day, preferably after meals. Safety notes: the plant contains garlic‑like sulfur compounds and may cause gastrointestinal irritation if taken in large quantities; it is not recommended for pregnant or nursing women and should be avoided by anyone allergic to Allium species. If a stronger preparation is desired, a 1:5 (w/v) ethanol tincture can be made by macerating 100 g of freshly crushed leaves in 500 ml of 45 % ethanol for 14 days, shaking daily, then filtering; a typical adult dose is 1–2 ml diluted in water, taken up to three times daily.

Phytochemical studies of Allium angulosum consistently report high levels of the sulfur‑containing amino acid alliin, which is enzymatically converted to allicin when the tissue is crushed (Kostic et al., 2015). The species also contains flavonoids such as quercetin‑3‑O‑glucoside and kaempferol derivatives, phenolic acids including caffeic and chlorogenic acids, and a suite of saponins that contribute to its bitter taste (Kostić et al., 2015). These compounds are well‑established for the genus and plausibly underlie the observed antimicrobial, expectorant and anti‑inflammatory actions recorded in folk practice.

Modern relevance is evident in continued pharmacological research on the plant’s antimicrobial and antioxidant activities, with recent in‑vitro studies confirming growth inhibition of Staphylococcus aureus and Escherichia coli (Kostic et al., 2015). Allium angulosum extracts are marketed in several Central and Eastern European herbal‑supplement shops as “wild‑garlic tea” or “carpathian garlic tincture,” and many local communities still harvest the plant in spring for home remedies, linking centuries‑old practice with contemporary interest in natural health products.

General Uses Top

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Common products:
Angular onion (Allium angulosum) is cultivated as an ornamental for rock gardens and border plantings, valued for its compact habit and late-summer blooming.

Industrial and craft applications:
No commercial, industrial, or craft applications have been documented for this species.

Food and beverages (non-medicinal):
No non-medicinal food or beverage uses are documented for this species.

Colorants and tanning:
No colorant or tanning uses are documented for this species.

Wood and fiber:
No wood or fiber uses are documented for this species.

Fragrance and cosmetics:
No fragrance or cosmetic uses are documented for this species.

Properties relevant to use:
No physical or chemical properties relevant to commercial use are documented for this species.

Standards and regulation:
No relevant standards or regulatory frameworks are documented for this species.

Sustainability and sourcing:
Sourcing information is limited to horticulture; no sustainability or production data have been documented.

Synonyms Top

Scientific name Authority First published in
Cepa angulosa (L.) Bernh. Syst. Verz. Erf. : 202 (1800)
Maliga fastigiata Raf. Fl. Tellur. 2: 19. 1837 [1836 publ. Jan-Mar 1837]
Xylorhiza angulosa (L.) Salisb. Gen. Pl. [Salisbury] 89. 1866 [Apr-May 1866]
Allium acutangulum Schrad. Index Seminum (GOET, Gottingensis) 1808: s.p. (1808)
Allium angulare Pall. Reise Russ. Reich. 3: 299 (1776)
Allium angulatum Pall. Reise Russ. Reich. 3: 408 (1776)
Allium calcareum Wallr. Erst. Beitr. Fl. Hercyn. 2: 196 (1840)
Allium danubiale Spreng. Mant. Prim. Fl. Hal. : 38 (1807)
Allium laxum G.Don Mem. Wern. Nat. Hist. Soc. 6: 63 (1827)
Allium microcephalum Willd. ex Kunth Enum. Pl. 4: 425 (1843)
Allium triquetrum Schrad. ex Schult. & Schult.f. Syst. Veg., ed. 15 bis 7: 1078 (1830)
Allium acutangulum var. senescens Nyman Consp. Fl. Eur. 739. 1882
Allium flavescens var. stramineum Nyman Consp. Fl. Eur. 739. 1882
Allium angulosum var. latifolium Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 3(2): 145. 1875
Allium angulosum subsp. latifolium (Regel) K.Richt. Pl. Eur. 1: 204. 1890 (1890)
Allium angulosum var. danubiale (Spreng.) Trevir. Index Seminum (WROCL) 1818: 1 1918
Allium angulosum Krock. Fl. Siles. 1: 524 (1787)
Allium inodorum Willd. Sp. Pl., ed. 4 , 2: 76 (1799)
Allium odorum Kar. & Kir. Bull. Soc. Imp. Naturalistes Moscou 14: 854 (1841)
Allium reticulatum Wallr. Sched. Crit. : 135 (1822)
Allium stramineum Schur Enum. Pl. Transsilv. : 674 (1866)
Allium uliginosum Kanitz Linnaea 32: 339 (1863)

Common names Top

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Language Common/alternative name
English wild chives
English chives
English mouse garlic
Belarusian цыбуля вуглаватая
Belarusian часнык палявы
Belarusian часнок дзікі
Belarusian цыбуля палявая
Belarusian цыбуля лугавая
Belarusian цыбулька
Bulgarian миши чесън
Bulgarian ръбестостъблен лук
Czech česnek hranatý
German kanten-lauch
German kantenlauch
German kantiger lauch
Estonian kantlauk
Finnish särmälaukka
French ail anguleux
Upper Sorbian hraničkaty kobołk
Hungarian gyíkhagyma
Icelandic vætulaukur
Lithuanian kampuotasis česnakas
Latvian Šķautņainais sīpols
Norwegian Nynorsk prydlauk
Polish czosnek kątowy
Polish czosnek kątowaty
Russian Лук угловатый
Slovak cesnak hranatý
Swedish rysslök
Tamil எலிப் பூண்டு
Ukrainian Часник заячий
Ukrainian Цибуля гранчаста
Chinese 鼠蒜
Chinese 起阳草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow at 4°C for 3 weeks, then increase to 20°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Kazakhstan
    • Siberia
      • Altay
      • Krasnoyarsk
      • West Siberia
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
      • Switzerland
    • Southeastern Europe
      • Bulgaria
      • Italy
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000755648
UNII 5U7R1V14XV
Tropicos 18403348
INPN 81316
Flora of Italy 6880
KEW urn:lsid:ipni.org:names:527602-1
The Plant List kew-295009
PFAF Allium angulosum
Open Tree Of Life 346324
Observations.org 114219
NCBI Taxonomy 105301
IPNI 527602-1
iNaturalist 55506
GBIF 2855717
Freebase /m/0105jzm4
EPPO ALLAN
EOL 1084242
Elurikkus 2645
USDA GRIN 2219
Wikipedia Allium_angulosum
CMAUP NPO25389

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
Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L Plants (Basel) 24-Feb-2024
PMCID:PMC10934440
doi:10.3390/plants13050621
PMID:38475472
Annual (2023) taxonomic update of RNA-directed RNA polymerase-encoding negative-sense RNA viruses (realm Riboviria: kingdom Orthornavirae: phylum Negarnaviricota) Kuhn JH, Abe J, Adkins S, Alkhovsky SV, Avšič-Županc T, Ayllón MA, Bahl J, Balkema-Buschmann A, Ballinger MJ, Kumar Baranwal V, Beer M, Bejerman N, Bergeron É, Biedenkopf N, Blair CD, Blasdell KR, Blouin AG, Bradfute SB, Briese T, Brown PA, Buchholz UJ, Buchmeier MJ, Bukreyev A, Burt F, Büttner C, Calisher CH, Cao M, Casas I, Chandran K, Charrel RN, Kumar Chaturvedi K, Chooi KM, Crane A, Dal Bó E, Carlos de la Torre J, de Souza WM, de Swart RL, Debat H, Dheilly NM, Di Paola N, Di Serio F, Dietzgen RG, Digiaro M, Drexler JF, Duprex WP, Dürrwald R, Easton AJ, Elbeaino T, Ergünay K, Feng G, Firth AE, Fooks AR, Formenty PB, Freitas-Astúa J, Gago-Zachert S, Laura García M, García-Sastre A, Garrison AR, Gaskin TR, Gong W, Gonzalez JP, de Bellocq J, Griffiths A, Groschup MH, Günther I, Günther S, Hammond J, Hasegawa Y, Hayashi K, Hepojoki J, Higgins CM, Hongō S, Horie M, Hughes HR, Hume AJ, Hyndman TH, Ikeda K, Jiāng D, Jonson GB, Junglen S, Klempa B, Klingström J, Kondō H, Koonin EV, Krupovic M, Kubota K, Kurath G, Laenen L, Lambert AJ, Lǐ J, Li JM, Liu R, Lukashevich IS, MacDiarmid RM, Maes P, Marklewitz M, Marshall SH, Marzano SY, McCauley JW, Mirazimi A, Mühlberger E, Nabeshima T, Naidu R, Natsuaki T, Navarro B, Navarro JA, Neriya Y, Netesov SV, Neumann G, Nowotny N, Nunes MR, Ochoa-Corona FM, Okada T, Palacios G, Pallás V, Papa A, Paraskevopoulou S, Parrish CR, Pauvolid-Corrêa A, Pawęska JT, Pérez DR, Pfaff F, Plemper RK, Postler TS, Rabbidge LO, Radoshitzky SR, Ramos-González PL, Rehanek M, Resende RO, Reyes CA, Rodrigues TC, Romanowski V, Rubbenstroth D, Rubino L, Runstadler JA, Sabanadzovic S, Sadiq S, Salvato MS, Sasaya T, Schwemmle M, Sharpe SR, Shi M, Shimomoto Y, Kavi Sidharthan V, Sironi M, Smither S, Song JW, Spann KM, Spengler JR, Stenglein MD, Takada A, Takeyama S, Tatara A, Tesh RB, Thornburg NJ, Tian X, Tischler ND, Tomitaka Y, Tomonaga K, Tordo N, Tu C, Turina M, Tzanetakis IE, Maria Vaira A, van den Hoogen B, Vanmechelen B, Vasilakis N, Verbeek M, von Bargen S, Wada J, Wahl V, Walker PJ, Waltzek TB, Whitfield AE, Wolf YI, Xia H, Xylogianni E, Yanagisawa H, Yano K, Ye G, Yuan Z, Zerbini FM, Zhang G, Zhang S, Zhang YZ, Zhao L, Økland AL J Gen Virol 25-Aug-2023
PMCID:PMC10721048
doi:10.1099/jgv.0.001864
PMID:37622664
Examination of the Effects of Domestic Water Buffalo (Bubalus bubalis) Grazing on Wetland and Dry Grassland Habitats Fűrész A, Penksza K, Sipos L, Turcsányi-Járdi I, Szentes S, Fintha G, Penksza P, Viszló L, Szalai F, Wagenhoffer Z Plants (Basel) 31-May-2023
PMCID:PMC10255522
doi:10.3390/plants12112184
PMID:37299162
In situ occurrence and protection of crop wild relatives in Italian sites of natura 2000 network: Insights from a data-driven approach Raggi L, Zucchini C, Gigante D, Negri V Front Plant Sci 22-Dec-2022
PMCID:PMC9814127
doi:10.3389/fpls.2022.1080615
PMID:36618609
Responses of Diversity and Productivity to Organo-Mineral Fertilizer Inputs in a High-Natural-Value Grassland, Transylvanian Plain, Romania Gaga I, Pacurar F, Vaida I, Plesa A, Rotar I Plants (Basel) 29-Jul-2022
PMCID:PMC9370819
doi:10.3390/plants11151975
PMID:35956453
Illuminating the Plant Rhabdovirus Landscape through Metatranscriptomics Data Bejerman N, Dietzgen RG, Debat H Viruses 05-Jul-2021
PMCID:PMC8310260
doi:10.3390/v13071304
PMID:34372509
Seed mass, hardness, and phylogeny explain the potential for endozoochory by granivorous waterbirds Lovas‐Kiss Á, Vincze O, Kleyheeg E, Sramkó G, Laczkó L, Fekete R, Molnár V. A, Green AJ Ecol Evol 15-Jan-2020
PMCID:PMC7029096
doi:10.1002/ece3.5997
PMID:32076524
The effect of gut passage by waterbirds on the seed coat and pericarp of diaspores lacking “external flesh”: Evidence for widespread adaptation to endozoochory in angiosperms Costea M, El Miari H, Laczkó L, Fekete R, Molnár AV, Lovas-Kiss Á, Green AJ PLoS One 19-Dec-2019
PMCID:PMC6922415
doi:10.1371/journal.pone.0226551
PMID:31856213
Crop wild relatives of Kazakhstani Tien Shan: Flora, vegetation, resources Sitpayeva GT, Kudabayevа GM, Dimeyeva LA, Gemejiyeva NG, Vesselova PV Plant Divers 31-Oct-2019
PMCID:PMC7046504
doi:10.1016/j.pld.2019.10.003
PMID:32140634
Ethanol extracts of Allium sp. regulate cyclooxygenase-2 and E-cadherin expression in gastric cancer MKN74 cell line and enhance doxorubicin toxicity Korga A, Ostrowska M, Iwan M, Skierucha M, Józefczyk A, Pawłowski P, Dudka J, Maciejewski R, Sitarz R Food Nutr Res 25-Jun-2019
PMCID:PMC6604903
doi:10.29219/fnr.v63.3449
PMID:31297043
Predicting the establishment success of introduced target species in grassland restoration by functional traits Engst K, Baasch A, Bruelheide H Ecol Evol 11-Aug-2017
PMCID:PMC5606862
doi:10.1002/ece3.3268
PMID:28944029
Arbuscular mycorrhizal fungi associations of vascular plants confined to river valleys: towards understanding the river corridor plant distribution Nobis A, Błaszkowski J, Zubek S J Plant Res 25-Nov-2014
PMCID:PMC4302419
doi:10.1007/s10265-014-0680-9
PMID:25421921
Synergids and filiform apparatus in the sexual and apomictic dandelions from section Palustria (Taraxacum, Asteraceae) Płachno BJ, Musiał K, Świątek P, Tuleja M, Marciniuk J, Grabowska-Joachimiak A Protoplasma 24-Aug-2013
PMCID:PMC3893458
doi:10.1007/s00709-013-0539-2
PMID:23974526
Diosgenin from Allium angulosum A. F. Azarkova, G. S. Glyzina, T. M. Mel'nikova, N. I. Maisuradze, Lenoid M. Kogan Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563918

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
> Alkaloids and derivatives / Cytochalasans
[(1S,2R,3E,5R,7S,9E,11S,14S,15R,16S)-16-benzyl-5-hydroxy-13-(hydroxymethyl)-5,7,14-trimethyl-6,18-dioxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9,12-trien-2-yl] acetate 102258993 Click to see 507.60 unknown via CMAUP database
Cytochalasin D 5458428 Click to see 507.60 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
7-Chloromellein-5-ol 102258989 Click to see CC1CC2=C(C(=C(C=C2O)Cl)O)C(=O)O1 228.63 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carboxylic acid 25769005 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
(3S)-8-Hydroxy-3-methyl-1-oxoisochromane-5-carboxylic acid 486250 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
> Benzenoids / Naphthalenes
2-[(8S)-1,8-dimethyl-7,8-dihydronaphthalen-2-yl]propane-1,2,3-triol 44555346 Click to see CC1CC=CC2=C1C(=C(C=C2)C(CO)(CO)O)C 248.32 unknown via CMAUP database
> Benzenoids / Tetralins
(1S,2S,4S)-6-(3-hydroxyprop-1-en-2-yl)-4,5-dimethyl-1,2,3,4-tetrahydronaphthalene-1,2-diol 44255026 Click to see 248.32 unknown via CMAUP database
7-Chloroscytalone 102258990 Click to see C1C(CC(=O)C2=C(C(=C(C=C21)O)Cl)O)O 228.63 unknown via CMAUP database
Isosclerone 13369486 Click to see C1CC(=O)C2=C(C1O)C=CC=C2O 178.18 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
9,9'-O-Isopropyllidene-isolariciresinol 91885030 Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)OC)O)OC)C 400.50 unknown via CMAUP database
Isotaxiresinol 9,9'-acetonide 102004573 Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)O)O)OC)C 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 101568249 Click to see 344.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
4-[(2R,3S,4S,5R)-4-(ethoxymethyl)-5-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenol 101936591 Click to see 404.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(7R)-7-Hydroxylariciresinol 10022393 Click to see 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4R)-3-hydroxy-4-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 101369318 Click to see COC1=C(C=CC(=C1)CC2(C(COC2=O)C(C3=CC(=C(C=C3)O)OC)O)O)O 390.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(1S,3R,11S)-8,9-dimethoxy-15,15-dimethyl-4,14-dioxo-7-propan-2-yl-2-oxatetracyclo[9.4.0.01,3.05,10]pentadeca-5,7,9,12-tetraene-11-carbaldehyde 100952777 Click to see 384.40 unknown via CMAUP database
(2S,4aS,10aR)-2,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 101529198 Click to see 316.40 unknown via CMAUP database
13alpha-Ethenyl-13-methyl-19-hydroxy-podocarpa-8(14)-ene-7-one 100952776 Click to see CC1(CCC2C(=C1)C(=O)CC3C2(CCCC3(C)CO)C)C=C 302.50 unknown via CMAUP database
Hinokiol 12310492 Click to see 302.50 unknown via CMAUP database
Sugiol 94162 Click to see 300.40 unknown via CMAUP database
Taxamairin A 130631 Click to see CC(C)C1=C(C(=C2C=C3C=CC(=O)C(C3=CC(=O)C2=C1)(C)C)O)OC 338.40 unknown via CMAUP database
Taxamairin B 130632 Click to see 352.40 unknown via CMAUP database
Taxamairin H 100952784 Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3=C(C2=O)C=CC(=O)C3(C)C)O)OC 338.40 unknown via CMAUP database
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 via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(1'R,2S,2'R,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',7',9',10',13'-pentaacetyloxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] (3R)-3-(dimethylamino)-3-phenylpropanoate 5319245 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)CO4)OC(=O)CC(C5=CC=CC=C5)N(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C 769.90 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'R,9'R,10'R,13'S)-2',5',10',13'-tetraacetyloxy-1',9'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 21159040 Click to see 610.60 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',13'-diacetyloxy-1',7',9',10'-tetrahydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 102066555 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)O 526.60 unknown via CMAUP database
[(1'S,2S,2'R,3'R,5'S,8'R,9'R,10'R,14'S)-9'-acetyloxy-2',5',14'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-10'-yl] acetate 11247972 Click to see CC1=C2C(C(C3(CCC(C4(C3C(C(C2(C)C)C(C1)O)O)CO4)O)C)OC(=O)C)OC(=O)C 452.50 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',10',13'-triacetyloxy-1',7',9'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 5321726 Click to see 568.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetraacetyloxy-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321730 Click to see 610.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',13'-tetraacetyloxy-1',10'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321728 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',9',10',13'-tetraacetyloxy-1',7'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 5316776 Click to see 610.60 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-12-acetyloxy-3,9,14-trihydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 24862000 Click to see 450.50 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-3,12,14-triacetyloxy-9-hydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 101006401 Click to see 534.60 unknown via CMAUP database
[(1R,2S,3S,5S,8R,9R,10R,11S,13R,16S)-5,16-diacetyloxy-10-(acetyloxymethyl)-8,9,11-trihydroxy-3-(2-hydroxypropan-2-yl)-6-methyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-2-yl] benzoate 10886794 Click to see 646.70 unknown via CMAUP database
[(2R,3Z,5S,7S,8E,10S,11R,13S)-2,3,10-triacetyloxy-5,7-dihydroxy-8-(hydroxymethyl)-4,14,15,15-tetramethyl-13-bicyclo[9.3.1]pentadeca-1(14),3,8-trienyl] acetate 6325023 Click to see 552.60 unknown via CMAUP database
[(2S,4R,5R,5aS,6S,8S,9R,9aR,10S,10aS)-2,5,6,8,10-pentaacetyloxy-4-hydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-1,2,4,5,6,7,8,9,9a,10-decahydrobenzo[f]azulen-9-yl]methyl acetate 5321724 Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O 654.70 unknown via CMAUP database
[(2S,4R,5R,5aS,6S,8S,9R,9aR,10S,10aS)-5,6,8,10-tetraacetyloxy-2,4-dihydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-1,2,4,5,6,7,8,9,9a,10-decahydrobenzo[f]azulen-9-yl]methyl acetate 5321723 Click to see 612.70 unknown via CMAUP database
1-Acetoxy-5-deacetylbaccatin I 102004901 Click to see 652.70 unknown via CMAUP database
13-Deacetylcanadensene_758363543 6325022 Click to see CC1=C2C(C(=C(C(CC(C(=CC(C(C2(C)C)CC1O)OC(=O)C)CO)O)OC(=O)C)C)OC(=O)C)OC(=O)C 552.60 unknown via CMAUP database
13-O-Deacetyltaxumairol Z 10864961 Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)COC(=O)C)O)O 604.60 unknown via CMAUP database
1beta-Acetoxy-baccatin I 5319668 Click to see 652.70 unknown via CMAUP database
1beta-Hydroxy-7-deacetylbaccatin I 21159039 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
CID 5318150 5318150 Click to see 652.70 unknown via CMAUP database
Taxin B 5321699 Click to see 534.60 unknown via CMAUP database
Taxumairol B 10053709 Click to see 568.60 unknown via CMAUP database
Taxumairol D 102065502 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
taxumairol F 10651372 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1O)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
Taxumairol K 10769688 Click to see 588.60 unknown via CMAUP database
Taxumairol U 11124920 Click to see 612.70 unknown via CMAUP database
Taxumairol V 10875480 Click to see 570.60 unknown via CMAUP database
Taxumairol W 10918805 Click to see 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8-triacetyloxy-12,13-dihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10918656 Click to see 550.60 unknown via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8-diacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10907330 Click to see 508.60 unknown via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-8-acetyloxy-4,7,12,13-tetrahydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 11733602 Click to see 484.50 unknown via CMAUP database
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8,10-triacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11814223 Click to see 630.70 unknown via CMAUP database
Sporogen-AO 1 177175 Click to see CC1C(CCC2=CC(=O)C3(C(C12C)O3)C(=C)C)O 248.32 unknown via CMAUP database
Taxumairol Y 11005902 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC4)O)O)OC(=O)C)C)OC(=O)C)O 526.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Taxusabietane D 100952779 Click to see CC(C)C1=C(C(=C2C(=C1)C(CC3C2(CCC(=O)C3(C)C)COC(=O)C)OC(=O)C)O)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 762.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,9S,10S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-8,12,15-trione 100952778 Click to see 384.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,4S,5'R,6R,7S,8R,9S,12R,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-ol 124485504 Click to see 414.60 unknown https://doi.org/10.1007/BF00563918
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1007/BF00563918
Spirost-5-en-3-ol 234096 Click to see 414.60 unknown https://doi.org/10.1007/BF00563918
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8,10,13-pentaacetyloxy-12-hydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11072583 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)OC(=O)C5=CC=CC=C5)OC4)OC(=O)C)O)OC(=O)C)C)OC(=O)C)OC(=O)C 714.80 unknown via CMAUP database
Taxacin 15226199 Click to see 816.80 unknown via CMAUP database
Taxumairol R 21593833 Click to see 728.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1E,3S,4R,6S,9R,11S)-3,9-diacetyloxy-7,11,16,16-tetramethyl-10,14-dioxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7,12-trienyl] acetate 10027779 Click to see 472.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carbaldehyde 44577733 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O 206.19 unknown via CMAUP database
Cis-7-chloro-4-hydroxymellein 102258988 Click to see 228.63 unknown via CMAUP database
trans-4-Hydroxymellein 10262028 Click to see 194.18 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5R)-5-hydroxy-4-methoxy-5-prop-1-en-2-ylfuran-2-one 40468114 Click to see 170.16 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-1,7-dioxaspiro[4.4]non-2-ene-4,8-dione 639435 Click to see 154.12 unknown via CMAUP database
Sphaeropsidin A 51361447 Click to see 346.40 unknown via CMAUP database
Sphaeropsidin B 57396736 Click to see CC1(CCCC23C1C(C(C4=CC(CCC42O)(C)C=C)O)(OC3=O)O)C 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxocins
(2S,3S,4Z,6S,8S)-3,6,8-trihydroxy-2-nonyl-2,3,6,7,8,9-hexahydrooxecin-10-one 44632077 Click to see CCCCCCCCCC1C(C=CC(CC(CC(=O)O1)O)O)O 328.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Xylaric acid 3084064 Click to see 154.12 unknown via CMAUP database

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