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Teucrium scorodonia

Teucrium scorodonia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Teucrium scorodonia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643feefe3d2dc310896621
Scientific name Teucrium scorodonia
Authority L.
First published in Sp. Pl. : 564 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Monochilon cordifolius Dulac Fl. Hautes-Pyrénées : 406 (1867)
Scorodonia heteromalla Moench Methodus : 384 (1794)
Scorodonia scorodonia H.Karst. Deut. Fl. (Karsten) 1016. 1883 [Mar 1883]
Scorodonia solitaria Stokes Bot. Mat. Med. 3: 374 (1812)
Scorodonia sylvestris Link Handbuch 1: 458 (1829)
Scorodonia trivialis Raf. Fl. Tellur. 3: 85 (1837)
Teucrium salviifolium Salisb. Prodr. Stirp. Chap. Allerton : 76 (1796)
Teucrium sylvestre Lam. Fl. Franç. 2: 412 (1779)
Scorodonia vulgaris Raf. Specchio Sci. 2: 171. 1814 (1814)

Common names Top

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Language Common/alternative name
English woodland germander
Spanish germandrina de bosque
Spanish escordio
Arabic المريمية الخشبية
Czech ožanka lesní
Welsh chwerwlys yr eithin
German salbei-gamander
French germandrée scorodine
French germandree scorodoine
French sauge des bois
French germandrée scorodoine
Irish iúr sléibhe
Galician teudo
Galician seixebra
Galician xinxebra
Galician teúdo
Galician sarxa brava
Galician ourego bravo
Galician gingebra
Galician sinxebra
Upper Sorbian lěsna dubčica
Hungarian fenyérgamandor
Norwegian Bokmål firtann
Dutch valse salie
nrm ambrais
Polish ożanka nierównoząbkowa
Swedish lundgamander
Walloon såvaedje saedje
Walloon saedje des bwès

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 seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Australasia
    • Australia
      • Tasmania
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Italy
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
      • Québec
    • Northeastern U.S.A.
      • Massachusetts
    • Southeastern U.S.A.
      • Tennessee

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000322618
UNII 2MJ724W91Q
Canadensys 6478
USDA Plants TESC
Tropicos 17600407
INPN 126035
Flora of Italy 4425
KEW urn:lsid:ipni.org:names:460717-1
The Plant List kew-203387
Open Tree Of Life 382149
Observations.org 7546
NCBI Taxonomy 53178
NBN Atlas NBNSYS0000004267
Nature Serve 2.143854
IPNI 460717-1
iNaturalist 57439
GBIF 2926901
Freebase /m/0h1s7j
EPPO TEUSC
EOL 579684
Elurikkus 335737
USDA GRIN 316850
Wikipedia Teucrium_scorodonia
CMAUP NPO9947

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Discrepancies between the drivers of alpha and beta plant diversity in arable field margins Boinot S, Alignier A Proc Biol Sci 01-Feb-2023
PMCID:PMC9890110
doi:10.1098/rspb.2022.2179
PMID:36722079
Correction: Loredo Varela, R.C.; Fail, J. Host Plant Association and Distribution of the Onion Thrips, Thrips tabaci Cryptic Species Complex. Insects 2022, 13, 298 Loredo Varela RC, Fail J Insects 07-May-2022
PMCID:PMC9143062
doi:10.3390/insects13050442
PMID:35621825
Differentiation of natural scrub communities of the Cotoneastro-Amelanchieretum group in Central Europe Świerkosz K, Reczyńska K PLoS One 12-Apr-2022
PMCID:PMC9004749
doi:10.1371/journal.pone.0266868
PMID:35413069
Host Plant Association and Distribution of the Onion Thrips, Thrips tabaci Cryptic Species Complex Loredo Varela RC, Fail J Insects 17-Mar-2022
PMCID:PMC8952806
doi:10.3390/insects13030298
PMID:35323598
Genetic diversity and volatile oil components variation in Achillea fragrantissima wild accessions and their regenerated genotypes Badr A, El-Shazly HH, Sakr M, Farid MM, Hamouda M, Elkhateeb E, Ahmad HS J Genet Eng Biotechnol 25-Oct-2021
PMCID:PMC8546000
doi:10.1186/s43141-021-00267-3
PMID:34694505
A Novel and Efficient In Vitro Organogenesis Approach for Ajuga lupulina Maxim Wu Q, Yang H, Yang Y, He J, Aer E, Ma Y, Zou L Plants (Basel) 15-Sep-2021
PMCID:PMC8472894
doi:10.3390/plants10091918
PMID:34579450
The importance of small natural features in forests—How the overgrowth of forest gaps affects indigenous flower supply and flower‐visiting insects and seed sets of six Campanula species Braun‐Reichert R, Rubanschi S, Poschlod P Ecol Evol 01-Aug-2021
PMCID:PMC8427581
doi:10.1002/ece3.7965
PMID:34522355
Characterization of Essential Oils from Different Taxa Belonging to the Genus Teucrium in Sardinia Island, Italy Maccioni A, Falconieri D, Sanna C, Porcedda S, Piras A, Maxia A Plants (Basel) 02-Jul-2021
PMCID:PMC8309330
doi:10.3390/plants10071359
PMID:34371562
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Applying pollen DNA metabarcoding to the study of plant–pollinator interactions Bell KL, Fowler J, Burgess KS, Dobbs EK, Gruenewald D, Lawley B, Morozumi C, Brosi BJ Appl Plant Sci 12-Jun-2017
PMCID:PMC5499302
doi:10.3732/apps.1600124
PMID:28690929
The Search for Herbal Antibiotics: An In-Silico Investigation of Antibacterial Phytochemicals Snow Setzer M, Sharifi-Rad J, Setzer WN Antibiotics (Basel) 12-Sep-2016
PMCID:PMC5039526
doi:10.3390/antibiotics5030030
PMID:27626453
Detecting Fragmentation Extinction Thresholds for Forest Understory Plant Species in Peninsular Spain Rueda M, Moreno Saiz JC, Morales-Castilla I, Albuquerque FS, Ferrero M, Rodríguez MÁ PLoS One 15-May-2015
PMCID:PMC4433258
doi:10.1371/journal.pone.0126424
PMID:25978329
Ethnoveterinary practices of Covasna County, Transylvania, Romania Bartha SG, Quave CL, Balogh L, Papp N J Ethnobiol Ethnomed 06-May-2015
PMCID:PMC4449595
doi:10.1186/s13002-015-0020-8
PMID:25943542
Endophytic fungi: a reservoir of antibacterials Deshmukh SK, Verekar SA, Bhave SV Front Microbiol 08-Jan-2015
PMCID:PMC4288058
doi:10.3389/fmicb.2014.00715
PMID:25620957

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
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(+)-Nortrachelogenin 479756 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
3-Hydroxy-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 321311 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
Nortrachelogenin 394846 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,5,6,9,10,10a-octahydrophenanthrene-1-carboxylic acid 92166187 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Dextropimarinal 12304198 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C=O)C)C=C 286.50 unknown via CMAUP database
Isopimara-7,15-dienal 12311183 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C=O)C)C1)C=C 286.50 unknown via CMAUP database
Isopimaric acid 442048 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown via CMAUP database
Palustric acid 443613 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown via CMAUP database
Pimaric acid 220338 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Retene 10222 Click to see CC1=C2C=CC3=C(C2=CC=C1)C=CC(=C3)C(C)C 234.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1016/0031-9422(90)85421-B
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-(5-Methyl-2-propan-2-ylphenyl)acetic acid 67235673 Click to see CC1=CC(=C(C=C1)C(C)C)CC(=O)O 192.25 unknown https://doi.org/10.1016/0031-9422(90)85421-B
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1016/0031-9422(90)85421-B
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Fenchol 439711 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown via CMAUP database
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1016/0031-9422(90)85421-B
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/0031-9422(90)85421-B
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1016/0031-9422(90)85421-B
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1016/0031-9422(90)85421-B
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/0031-9422(90)85421-B
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene 101708 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85421-B
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1016/0031-9422(90)85421-B
3-Cyclohexen-1-ol, 1-(1,5-dimethyl-4-hexenyl)-4-methyl- 27208 Click to see CC1=CCC(CC1)(C(C)CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/0031-9422(90)85421-B
alpha-Cubebene 442359 Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85421-B
Farnesylacetic acid 152470 Click to see CC(=CCCC(=CCCC(=CCCC(=O)O)C)C)C 264.40 unknown https://doi.org/10.1016/0031-9422(90)85421-B
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85421-B
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
(1S,2R,5S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene 442348 Click to see CC1CCC2C13CC=C(C(C3)C2(C)C)C 204.35 unknown https://doi.org/10.1016/0031-9422(90)85421-B
Cedrol 65575 Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O 222.37 unknown https://doi.org/10.1016/0031-9422(90)85421-B
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Nookatone 20797 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C 218.33 unknown https://doi.org/10.1016/0031-9422(90)85421-B
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(3R,3aR,5'S,6aS,7R,8R,10aR)-5'-(furan-3-yl)-3-hydroxy-8-methylspiro[3,3a,4,5,6,6a,8,9-octahydro-1H-benzo[d][2]benzofuran-7,3'-oxolane]-2',10-dione 163194754 Click to see CC1CC(=O)C23COC(C2CCCC3C14CC(OC4=O)C5=COC=C5)O 360.40 unknown https://doi.org/10.1016/S0031-9422(00)86971-X
https://doi.org/10.1016/S0031-9422(00)80676-7
(3R,3aR,5'S,6aS,7R,8R,10aS)-5'-(furan-3-yl)-3-hydroxy-8-methylspiro[3,3a,4,5,6,6a,8,9-octahydro-1H-benzo[d][2]benzofuran-7,3'-oxolane]-2',10-dione 163013783 Click to see CC1CC(=O)C23COC(C2CCCC3C14CC(OC4=O)C5=COC=C5)O 360.40 unknown https://doi.org/10.1016/S0031-9422(00)98084-1
[(4aR,5R,5'S,7R,8R,8aS)-4-formyl-5'-(furan-3-yl)-5-hydroxy-7-methyl-2'-oxospiro[1,2,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-4a-yl]methyl acetate 162964848 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC=C2C=O)COC(=O)C)O 402.40 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
https://doi.org/10.1016/0031-9422(82)85258-8
[4-Formyl-5'-(furan-3-yl)-5-hydroxy-7-methyl-2'-oxospiro[1,2,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-4a-yl]methyl acetate 15627945 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC=C2C=O)COC(=O)C)O 402.40 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
https://doi.org/10.1016/0031-9422(82)85258-8
[5'-(Furan-3-yl)-5-hydroxy-4-(hydroxymethyl)-7-methyl-2'-oxospiro[1,2,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-4a-yl]methyl acetate 162899554 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC=C2CO)COC(=O)C)O 404.50 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
5'-(furan-3-yl)-3-hydroxy-8-methylspiro[3,3a,4,5,6,6a,8,9-octahydro-1H-benzo[d][2]benzofuran-7,3'-oxolane]-2',10-dione 163013782 Click to see CC1CC(=O)C23COC(C2CCCC3C14CC(OC4=O)C5=COC=C5)O 360.40 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
https://doi.org/10.1016/S0031-9422(00)86971-X
Teuscorodol 146116211 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC=C2CO)COC(=O)C)O 404.50 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Pentacyclo[4.2.0.02,5.03,8.04,7]oct-2-en-1-ol 53436347 Click to see C12C3C4C1C5(C2C3=C45)O 118.13 unknown https://doi.org/10.1016/0031-9422(90)85421-B
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,5'S,6R,8S,9R,10R,12R)-5'-(furan-3-yl)-6-hydroxy-12-(hydroxymethyl)-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-4-ene-9,3'-oxolane]-2',3-dione 162989561 Click to see CC1CC2C3(C(C14CC(OC4=O)C5=COC=C5)CC(C=C3C(=O)O2)O)CO 374.40 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
(1R,5'S,8S,9R,10R,12R)-5'-(furan-3-yl)-12-(hydroxymethyl)-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-4-ene-9,3'-oxolane]-2',3-dione 45033629 Click to see CC1CC2C3(C(C14CC(OC4=O)C5=COC=C5)CCC=C3C(=O)O2)CO 358.40 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
https://doi.org/10.1016/S0031-9422(00)86971-X
(5'S,6R,8S,9R,10R)-5'-(furan-3-yl)-6-hydroxy-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodeca-1(11),4(12)-diene-9,3'-oxolane]-2',3-dione 162972277 Click to see CC1C=C2C3=C(CC(CC3C14CC(OC4=O)C5=COC=C5)O)C(=O)O2 342.30 unknown https://doi.org/10.1016/S0031-9422(00)86971-X
(5'S,8S,9S,10R)-5'-(furan-3-yl)-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodeca-1(11),4(12)-diene-9,3'-oxolane]-2',3-dione 100988745 Click to see CC1C=C2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 326.30 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
https://doi.org/10.1016/S0031-9422(00)86971-X
5'-(Furan-3-yl)-6-hydroxy-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodeca-1(11),4(12)-diene-9,3'-oxolane]-2',3-dione 162972276 Click to see CC1C=C2C3=C(CC(CC3C14CC(OC4=O)C5=COC=C5)O)C(=O)O2 342.30 unknown https://doi.org/10.1016/S0031-9422(00)86971-X
5'-(Furan-3-yl)-6-hydroxy-12-(hydroxymethyl)-10-methylspiro[2-oxatricyclo[6.3.1.04,12]dodec-4-ene-9,3'-oxolane]-2',3-dione 162989560 Click to see CC1CC2C3(C(C14CC(OC4=O)C5=COC=C5)CC(C=C3C(=O)O2)O)CO 374.40 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
CID 13855360 13855360 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O 404.50 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
Eugarzasidine I 316446 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
Teuflin 13071598 Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2 328.40 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
Teupolin I 156030 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O 404.50 unknown https://doi.org/10.1016/S0031-9422(00)80676-7
Teuscordonin 159081 Click to see CC1CC2C3(C(C14CC(OC4=O)C5=COC=C5)CCC=C3C(=O)O2)CO 358.40 unknown https://doi.org/10.1016/S0031-9422(00)86971-X
https://doi.org/10.1016/S0031-9422(00)80676-7
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,4beta)-3,3',4,4'-Tetrahydro-2alpha,2'alpha-bis(3,4-dihydroxyphenyl)-4'beta-(benzylthio)-4,8'-bi(2H-1-benzopyran)-3alpha,3'alpha,5,5',7,7'-hexol 10372558 Click to see C1=CC=C(C=C1)CSC2C(C(OC3=C(C(=CC(=C23)O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)C7=CC(=C(C=C7)O)O)O 700.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(4S)-Epicatechin benzylthioether 10645351 Click to see C1=CC=C(C=C1)CSC2C(C(OC3=CC(=CC(=C23)O)O)C4=CC(=C(C=C4)O)O)O 412.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin 73202 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-7-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162899355 Click to see CC1C(C(C(C(O1)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)83747-4
> Phenylpropanoids and polyketides / Macrolides and analogues
(4Z)-4-Ethylidene-7,12-dihydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadecane-3,8-dione 12315046 Click to see CC=C1CC(C(C(=O)OCC2C(CN3C2C(CC3)OC1=O)O)(C)O)C 353.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene 5316874 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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