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Details Top

Internal ID UUID643feef6763b6823475097
Scientific name Teucrium oliverianum
Authority Ging. ex Benth.
First published in Labiat. Gen. Spec. : 668 (1835)

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Synonyms Top

No known synonyms.

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Language Common/alternative name
Arabic عيهلان

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Kuwait
      • Oman
      • Saudi Arabia
    • Western Asia
      • Iran
      • Iraq

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000322386
Tropicos 100266162
KEW urn:lsid:ipni.org:names:460595-1
The Plant List kew-203169
Open Tree Of Life 5232629
NCBI Taxonomy 1209878
IPNI 460595-1
iNaturalist 1171335
GBIF 3894837
Wikipedia Teucrium_oliverianum

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
Special Issue—“Bioactive Compounds from Natural Sources II” Sytar O, Smetanska I Molecules 31-May-2023
PMCID:PMC10254469
doi:10.3390/molecules28114450
PMID:37298926
Bio-Active Compounds from Teucrium Plants Used in the Traditional Medicine of Kurdistan Region, Iraq Abdullah FO, Hussain FH, Sardar AS, Gilardoni G, Thu ZM, Vidari G Molecules 12-May-2022
PMCID:PMC9145536
doi:10.3390/molecules27103116
PMID:35630593
Bioactive Constituents and Toxicological Evaluation of Selected Antidiabetic Medicinal Plants of Saudi Arabia Alqahtani AS, Ullah R, Shahat AA Evid Based Complement Alternat Med 17-Jan-2022
PMCID:PMC8786507
doi:10.1155/2022/7123521
PMID:35082904
Antidiabetic Potential of Medicinal Plants and Their Active Components Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J Biomolecules 30-Sep-2019
PMCID:PMC6843349
doi:10.3390/biom9100551
PMID:31575072
Ecological significance of floristic composition and life forms of Riyadh region, Central Saudi Arabia Al Shaye NA, Masrahi YS, Thomas J Saudi J Biol Sci 17-Apr-2019
PMCID:PMC6933222
doi:10.1016/j.sjbs.2019.04.009
PMID:31889814
Pollen morphology of certain species of the family Lamiaceae in Saudi Arabia Doaigey AR, El-Zaidy M, Alfarhan A, Milagy AE, Jacob T Saudi J Biol Sci 08-Mar-2017
PMCID:PMC5815984
doi:10.1016/j.sjbs.2017.03.001
PMID:29472790
ANTIMICROBIAL ACTIVITIES OF SOME SAUDI ARABIAN HERBAL PLANTS Shahat AA, Mahmoud EA, Al-Mishari AA, Alsaid MS Afr J Tradit Complement Altern Med 13-Jan-2017
PMCID:PMC5446440
doi:10.21010/ajtcam.v14i2.17
PMID:28573232
Clerodane diterpenes: sources, structures, and biological activities Li R, Morris-Natschke SL, Lee KH Nat Prod Rep 18-Jul-2016
PMCID:PMC5154363
doi:10.1039/c5np00137d
PMID:27433555
Floristic diversity and vegetation analysis of Wadi Arar: A typical desert Wadi of the Northern Border region of Saudi Arabia Osman AK, Al-Ghamdi F, Bawadekji A Saudi J Biol Sci 18-Feb-2014
PMCID:PMC4250517
doi:10.1016/j.sjbs.2014.02.001
PMID:25473364
Cytotoxicity, mode of action and antibacterial activities of selected Saudi Arabian medicinal plants Kuete V, Wiench B, Alsaid MS, Alyahya MA, Fankam AG, Shahat AA, Efferth T BMC Complement Altern Med 12-Dec-2013
PMCID:PMC4029389
doi:10.1186/1472-6882-13-354
PMID:24330397
Neocleordane Diterpenoids and Their Artifacts from Teucrium olivarianum Mohammed A. Al-Yahya, Ilias Muhammad, Humayun H. Mirza, Farouk S. El-Feraly, Andrew T. McPhail American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50096A005
Neo-clerodane diterpenoids from Teucrium oliverianum Maurizio Bruno, Abdallah A. Omar, Aurea Perales, Franco Piozzi, Benjamín Rodríguez, Giuseppe Savona, Maria C.De la Torre Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)84137-H
Teucrolivins D–F, neo-clerodane derivatives from Teucrium oliverianum María C. De La Torre, Maurizio Bruno, Franco Piozzi, Giuseppe Savona, Benjamín Rodríguez, Abdallah A. Omar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)84216-F
Two neo-clerodane diterpenoids containing an unusual 2,6-dioxabicyclo[2.2.1]heptane structural moiety María C. de la Torre, Maurizio Bruno, Franco Piozzi, Giuseppe Savon, Abdallah A. Omar, Aurea Perales, Benjamin Rodríguez Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)86408-5
neo-Clerodane diterpenoids from Teucrium oliverianum and structure revision of teucrolin E. Al-Yahya MA, El-Feraly FS, Dunbar DC, Muhammad I Phytochemistry 01-Feb-2002
doi:10.1016/S0031-9422(01)00396-X
PMID:11830158

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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
[(2S,4aR,6R,7R)-6-acetyloxy-7-(3-methoxy-3-oxoprop-1-en-2-yl)-1,4a-dimethyl-3,4,5,6,7,8-hexahydro-2H-naphthalen-2-yl] 2-methylpropanoate 13895624 Click to see CC1=C2CC(C(CC2(CCC1OC(=O)C(C)C)C)OC(=O)C)C(=C)C(=O)OC 392.50 unknown https://doi.org/10.1016/0031-9422(91)84137-H
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(4aS,7S,7aR)-4a,5-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] acetate 137703299 Click to see CC(=O)OC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)C 406.40 unknown https://doi.org/10.1021/NP50096A005
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(15alpha)-15-Hydroxysoyasapogenol 101952807 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(C(CC2(C(C1)O)C)O)C)C)(C)CO)O)C)C 474.70 unknown https://doi.org/10.1016/0031-9422(91)84137-H
https://doi.org/10.1016/S0031-9422(01)00396-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(3S,4R,4aR,5R,6R,7S,8R,8aR)-5-acetyloxy-8-[2-(furan-3-yl)ethyl]-3,6-dihydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 636533 Click to see CC1C(C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)O)COC(=O)C)OC(=O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[(3S,4R,4aR,5R,6R,7S,8S,8aR)-5-acetyloxy-8-[2-(furan-3-yl)ethyl]-3,6-dihydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 162905063 Click to see CC1C(C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)O)COC(=O)C)OC(=O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[(3S,4R,4aR,5R,7S,8R,8aR)-3-acetyloxy-8-[2-(furan-3-yl)ethyl]-5-hydroxy-7,8-dimethyl-6-oxospiro[1,2,3,5,7,8a-hexahydronaphthalene-4,2'-oxirane]-4a-yl]methyl acetate 14845536 Click to see CC1C(=O)C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)OC(=O)C)COC(=O)C)O 448.50 unknown https://doi.org/10.1016/0031-9422(91)84216-F
[(3S,4R,4aR,5R,7S,8S,8aR)-3-acetyloxy-8-[2-(furan-3-yl)ethyl]-5-hydroxy-7,8-dimethyl-6-oxospiro[1,2,3,5,7,8a-hexahydronaphthalene-4,2'-oxirane]-4a-yl]methyl acetate 101602315 Click to see CC1C(=O)C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)OC(=O)C)COC(=O)C)O 448.50 unknown https://doi.org/10.1016/0031-9422(91)84216-F
[(3S,4R,4aS,5R,6R,7S,8S,8aR)-5-acetyloxy-8-[2-(furan-3-yl)ethyl]-3,6-dihydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 102372183 Click to see CC1C(C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)O)COC(=O)C)OC(=O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[(3S,4R,4aS,5R,7S,8S,8aR)-3-acetyloxy-8-[(2S)-2-(furan-3-yl)-2-hydroxyethyl]-5-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 163105712 Click to see CC1CC(C2(C(C1(C)CC(C3=COC=C3)O)CCC(C24CO4)OC(=O)C)COC(=O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[(4R,4aR,5R,6R,7S,8R,8aR)-5-acetyloxy-8-[(2S)-2-(furan-3-yl)-2-hydroxyethyl]-6-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 162972795 Click to see CC1C(C(C2(C(C1(C)CC(C3=COC=C3)O)CCCC24CO4)COC(=O)C)OC(=O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[(4R,4aR,5R,6R,7S,8S,8aR)-5-acetyloxy-8-[(2S)-2-(furan-3-yl)-2-hydroxyethyl]-6-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 162972796 Click to see CC1C(C(C2(C(C1(C)CC(C3=COC=C3)O)CCCC24CO4)COC(=O)C)OC(=O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[3-acetyloxy-8-[2-(furan-3-yl)-2-hydroxyethyl]-5-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 163105711 Click to see CC1CC(C2(C(C1(C)CC(C3=COC=C3)O)CCC(C24CO4)OC(=O)C)COC(=O)C)O 450.50 unknown https://doi.org/10.1021/NP50096A005
[3-Acetyloxy-8-[2-(furan-3-yl)ethyl]-5-hydroxy-7,8-dimethyl-6-oxospiro[1,2,3,5,7,8a-hexahydronaphthalene-4,2'-oxirane]-4a-yl]methyl acetate 14845535 Click to see CC1C(=O)C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)OC(=O)C)COC(=O)C)O 448.50 unknown https://doi.org/10.1016/0031-9422(91)84216-F
[5-acetyloxy-8-[2-(furan-3-yl)-2-hydroxyethyl]-6-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 162972793 Click to see CC1C(C(C2(C(C1(C)CC(C3=COC=C3)O)CCCC24CO4)COC(=O)C)OC(=O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[5-acetyloxy-8-[2-(furan-3-yl)ethyl]-3,6-dihydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 78200672 Click to see CC1C(C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)O)COC(=O)C)OC(=O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
Teucrolin G 102372184 Click to see CC1C(C(C2(C(C1(C)CC(C3=COC=C3)O)CCCC24CO4)COC(=O)C)OC(=O)C)O 450.50 unknown https://doi.org/10.1016/S0040-4020(01)86408-5
https://doi.org/10.1016/S0031-9422(01)00396-X
Teucrolivin B 14805995 Click to see CC1C(=O)C(C2(C(C1(C)CCC3=COC=C3)(CCC(C24CO4)OC(=O)C)O)COC(=O)C)O 464.50 unknown https://doi.org/10.1021/NP50096A005
https://doi.org/10.1016/0031-9422(91)84137-H
https://doi.org/10.1016/S0031-9422(01)00396-X
https://doi.org/10.1016/0031-9422(91)84216-F
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(3R,4R,4aR,5S,7R,8S,8aR)-3,5-diacetyloxy-8-[2-(furan-3-yl)-2-oxoethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 163103753 Click to see CC1CC(C2(C(C1(C)CC(=O)C3=COC=C3)CCC(C24CO4)OC(=O)C)COC(=O)C)OC(=O)C 490.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[(3S,4R,4aR,5R,6R,7S,8R,8aR)-3,6-diacetyloxy-8-[2-(furan-3-yl)ethyl]-5-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 162847501 Click to see CC1C(C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)OC(=O)C)COC(=O)C)O)OC(=O)C 492.60 unknown https://doi.org/10.1016/0031-9422(91)84216-F
[(3S,4R,4aR,5R,6R,7S,8S,8aR)-3,6-diacetyloxy-8-[2-(furan-3-yl)ethyl]-5-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 101602314 Click to see CC1C(C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)OC(=O)C)COC(=O)C)O)OC(=O)C 492.60 unknown https://doi.org/10.1016/0031-9422(91)84216-F
[3,5-diacetyloxy-8-[2-(furan-3-yl)-2-oxoethyl]-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 163103752 Click to see CC1CC(C2(C(C1(C)CC(=O)C3=COC=C3)CCC(C24CO4)OC(=O)C)COC(=O)C)OC(=O)C 490.50 unknown https://doi.org/10.1021/NP50096A005
[3,6-diacetyloxy-8-[2-(furan-3-yl)ethyl]-5-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 14845533 Click to see CC1C(C(C2(C(C1(C)CCC3=COC=C3)CCC(C24CO4)OC(=O)C)COC(=O)C)O)OC(=O)C 492.60 unknown https://doi.org/10.1016/0031-9422(91)84216-F
> Organoheterocyclic compounds / Heteroaromatic compounds
(1R,3S,4S,4aS,7S,8R,8aR)-4-[2-(furan-3-yl)ethyl]-1,4a,7-trihydroxy-8a-(hydroxymethyl)-3,4-dimethylspiro[3,5,6,7-tetrahydro-1H-naphthalene-8,2'-oxirane]-2-one 101594600 Click to see CC1C(=O)C(C2(C(C1(C)CCC3=COC=C3)(CCC(C24CO4)O)O)CO)O 380.40 unknown https://doi.org/10.1021/NP50096A005
https://doi.org/10.1016/0031-9422(91)84137-H
https://doi.org/10.1016/S0031-9422(01)00396-X
[(3S,4R,4aR,5R,7S,8S,8aS)-8-[2-(furan-3-yl)ethyl]-3,5,8a-trihydroxy-7,8-dimethyl-6-oxospiro[2,3,5,7-tetrahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 163086778 Click to see CC1C(=O)C(C2(C(C1(C)CCC3=COC=C3)(CCC(C24CO4)O)O)COC(=O)C)O 422.50 unknown https://doi.org/10.1016/0031-9422(91)84137-H
> Organoheterocyclic compounds / Naphthofurans
(6-Acetyloxy-3a,4-dimethyl-2,8-dioxospiro[3,4,5,6,9,10-hexahydrobenzo[h][1]benzofuran-7,2'-oxirane]-6a-yl)methyl acetate 14845537 Click to see CC1CC(C2(C3(C1(CC(=O)O3)C)CCC(=O)C24CO4)COC(=O)C)OC(=O)C 394.40 unknown https://doi.org/10.1016/0031-9422(91)84216-F
(6,8-diacetyloxy-3a,4-dimethyl-2-oxospiro[4,5,6,8,9,10-hexahydro-3H-benzo[h][1]benzofuran-7,2'-oxirane]-6a-yl)methyl acetate 162987544 Click to see CC1CC(C2(C3(C1(CC(=O)O3)C)CCC(C24CO4)OC(=O)C)COC(=O)C)OC(=O)C 438.50 unknown https://doi.org/10.1021/NP50096A005
[(1S,5R,6R,7S,9R,11S,13S)-7-acetyloxy-11-(furan-3-yl)-9,13-dimethyl-4-oxospiro[10,14-dioxatetracyclo[9.2.1.01,6.09,13]tetradecane-5,2'-oxirane]-6-yl]methyl acetate 101357807 Click to see CC(=O)OCC12C(CC3(C4(C1(CCC(=O)C25CO5)OC(C4)(O3)C6=COC=C6)C)C)OC(=O)C 460.50 unknown https://doi.org/10.1016/S0040-4020(01)86408-5
[(2S,3aS,4S,6R,6aS,7S,8R,10aR)-6,8-diacetyloxy-2-(furan-3-yl)-2-hydroxy-3a,4-dimethylspiro[4,5,6,8,9,10-hexahydro-3H-benzo[h][1]benzofuran-7,2'-oxirane]-6a-yl]methyl acetate 162851075 Click to see CC1CC(C2(C3(C1(CC(O3)(C4=COC=C4)O)C)CCC(C25CO5)OC(=O)C)COC(=O)C)OC(=O)C 506.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[(3aR,4S,6S,6aS,7R,8S,10aS)-6,8-diacetyloxy-3a,4-dimethyl-2-oxospiro[4,5,6,8,9,10-hexahydro-3H-benzo[h][1]benzofuran-7,2'-oxirane]-6a-yl]methyl acetate 162987546 Click to see CC1CC(C2(C3(C1(CC(=O)O3)C)CCC(C24CO4)OC(=O)C)COC(=O)C)OC(=O)C 438.50 unknown https://doi.org/10.1016/S0031-9422(01)00396-X
[(3aS,4R,6S,6aR,7R,10aS)-6-acetyloxy-3a,4-dimethyl-2,8-dioxospiro[3,4,5,6,9,10-hexahydrobenzo[h][1]benzofuran-7,2'-oxirane]-6a-yl]methyl acetate 101602679 Click to see CC1CC(C2(C3(C1(CC(=O)O3)C)CCC(=O)C24CO4)COC(=O)C)OC(=O)C 394.40 unknown https://doi.org/10.1016/0031-9422(91)84216-F
[6-Acetyloxy-2-(furan-3-yl)-2-hydroxy-3a,4-dimethyl-8-oxospiro[3,4,5,6,9,10-hexahydrobenzo[h][1]benzofuran-7,2'-oxirane]-6a-yl]methyl acetate 14805993 Click to see CC1CC(C2(C3(C1(CC(O3)(C4=COC=C4)O)C)CCC(=O)C25CO5)COC(=O)C)OC(=O)C 462.50 unknown https://doi.org/10.1016/0031-9422(91)84137-H
[6,8-diacetyloxy-2-(furan-3-yl)-2-hydroxy-3a,4-dimethylspiro[4,5,6,8,9,10-hexahydro-3H-benzo[h][1]benzofuran-7,2'-oxirane]-6a-yl]methyl acetate 162851074 Click to see CC1CC(C2(C3(C1(CC(O3)(C4=COC=C4)O)C)CCC(C25CO5)OC(=O)C)COC(=O)C)OC(=O)C 506.50 unknown https://doi.org/10.1021/NP50096A005
[7-Acetyloxy-11-(furan-3-yl)-9,13-dimethyl-4-oxospiro[10,14-dioxatetracyclo[9.2.1.01,6.09,13]tetradecane-5,2'-oxirane]-6-yl]methyl acetate 73657370 Click to see CC(=O)OCC12C(CC3(C4(C1(CCC(=O)C25CO5)OC(C4)(O3)C6=COC=C6)C)C)OC(=O)C 460.50 unknown https://doi.org/10.1016/S0040-4020(01)86408-5
Teucrolivin A 14805994 Click to see CC1CC(C2(C3(C1(CC(O3)(C4=COC=C4)O)C)CCC(=O)C25CO5)COC(=O)C)OC(=O)C 462.50 unknown https://doi.org/10.1021/NP50096A005
https://doi.org/10.1016/0031-9422(91)84137-H
https://doi.org/10.1016/0031-9422(91)84216-F
> Organoheterocyclic compounds / Oxepanes
[(1S,2S,3S,5R,6S,7R,8S)-2-[2-(furan-3-yl)ethyl]-5,7,8-trihydroxy-2,3-dimethyl-4-oxo-11-oxatricyclo[5.3.2.01,6]dodecan-6-yl]methyl acetate 102372182 Click to see CC1C(=O)C(C2(C3(C1(C)CCC4=COC=C4)CCC(C2(CO3)O)O)COC(=O)C)O 422.50 unknown https://doi.org/10.1021/NP50096A005
https://doi.org/10.1016/S0031-9422(01)00396-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1021/NP50096A005
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1021/NP50096A005

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