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Internal ID UUID643feeeca5772903816861
Scientific name Teucrium gracile
Authority Barbey & Major
First published in Karpathos : 127 (1895)

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Synonyms Top

Scientific name Authority First published in
Teucrium alpestre subsp. gracile (Barbey & Major) D.Wood Bot. J. Linn. Soc. 65: 261 (1972)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000322165
Tropicos 100266017
KEW urn:lsid:ipni.org:names:460435-1
The Plant List kew-202957
Open Tree Of Life 6086512
IPNI 460435-1
iNaturalist 993951
GBIF 3896571

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)!
Title Authors Publication Released IDs
Neo-clerodane diterpenoids fromTeucrium gracile Maurizio Bruno, Gema Domi´nguez, Ana Lourenço, Franco Piozzi, Benjami´n Rodri´guez, Giuseppe Savona, Mari´a C. De la Torre, Nelly A. Arnold Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)80092-F
Neo- and seco-neo-clerodane diterpenoids from Teucrium gracile and T. Fruticans Maurizio Bruno, Roberto Alcázar, María C. de la Torre, Franco Piozzi, Benjamín Rodríguez, Giuseppe Savona, Aurea Perales, Nelly A. Arnold Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83722-B
Neo-clerodane diterpenoids from Teucrium pernyi Xie Ning, Min Zhi-da, Zhao Shou-xun, Wu Bing, Zheng Qi-tai, Zhang Pei Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)85048-5

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1S,7S,12S,13S,14S)-14-acetyloxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadeca-3,8,16-trien-12-yl] benzoate 162877670 Click to see CC1=CC2C(=C(C(=O)O2)C)CC3C(=CCC(C3(C(CC1)OC(=O)C4=CC=CC=C4)C)OC(=O)C)C 478.60 unknown https://doi.org/10.1016/0031-9422(91)80092-F
CID 23757056 23757056 Click to see CC1CC(=O)C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C 418.40 unknown https://doi.org/10.1016/0031-9422(92)83722-B
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(3S,4R,4aR,5S,7R,8S,8aR)-8-[(2S)-2-acetyloxy-2-(furan-3-yl)ethyl]-3,5-dihydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 23254270 Click to see CC1CC(C2(C(C1(C)CC(C3=COC=C3)OC(=O)C)CCC(C24CO4)O)COC(=O)C)O 450.50 unknown https://doi.org/10.1016/0031-9422(91)80092-F
[(3S,4R,4aR,5S,7R,8S,8aR)-8-[2-acetyloxy-2-(furan-3-yl)ethyl]-3,5-dihydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 15109174 Click to see CC1CC(C2(C(C1(C)CC(C3=COC=C3)OC(=O)C)CCC(C24CO4)O)COC(=O)C)O 450.50 unknown https://doi.org/10.1016/0031-9422(91)85048-5
[8-[2-acetyloxy-2-(furan-3-yl)ethyl]-3,5-dihydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 74034899 Click to see CC1CC(C2(C(C1(C)CC(C3=COC=C3)OC(=O)C)CCC(C24CO4)O)COC(=O)C)O 450.50 unknown https://doi.org/10.1016/0031-9422(91)80092-F
CID 101634638 101634638 Click to see CC1CC(C2(C(C13CC(OC3OC(=O)C)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)O 464.50 unknown https://doi.org/10.1016/0031-9422(92)83722-B
CID 162919008 162919008 Click to see CC1CC(C2(C(C13CC(OC3OC(=O)C)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)O 464.50 unknown https://doi.org/10.1016/0031-9422(92)83722-B
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1R,2R,4S,4aR,5R,6S,8aR)-4,6-diacetyloxy-1-[2-acetyloxy-2-(furan-3-yl)ethyl]-4a-(acetyloxymethyl)-2-methylspiro[3,4,6,7,8,8a-hexahydro-2H-naphthalene-5,2'-oxirane]-1-yl]methyl acetate 101634639 Click to see CC1CC(C2(C(C1(CC(C3=COC=C3)OC(=O)C)COC(=O)C)CCC(C24CO4)OC(=O)C)COC(=O)C)OC(=O)C 592.60 unknown https://doi.org/10.1016/0031-9422(92)83722-B
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
CID 101617532 101617532 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)OC(=O)C)COC(=O)C)O 462.50 unknown https://doi.org/10.1016/0031-9422(91)85048-5
CID 101617535 101617535 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)OC(=O)C)COC(=O)C)O 462.50 unknown https://doi.org/10.1016/0031-9422(91)85048-5
CID 163078839 163078839 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)OC(=O)C)COC(=O)C)O 462.50 unknown https://doi.org/10.1016/0031-9422(91)80092-F
CID 163078840 163078840 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)OC(=O)C)COC(=O)C)O 462.50 unknown https://doi.org/10.1016/0031-9422(91)80092-F
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 101617533 101617533 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)O 420.50 unknown https://doi.org/10.1016/0031-9422(91)85048-5
https://doi.org/10.1016/0031-9422(92)83722-B
CID 101617534 101617534 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)O 404.50 unknown https://doi.org/10.1016/0031-9422(92)83722-B
https://doi.org/10.1016/0031-9422(91)85048-5
CID 101679037 101679037 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)O 420.50 unknown https://doi.org/10.1016/0031-9422(91)80092-F
CID 162873277 162873277 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCC(C25CO5)O)COC(=O)C)O 420.50 unknown https://doi.org/10.1016/0031-9422(91)80092-F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162847768 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 656.50 unknown https://doi.org/10.1016/0031-9422(91)80092-F

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