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Teucrium sandrasicum

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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 UUID643feefd34c6a304030023
Scientific name Teucrium sandrasicum
Authority O.Schwarz
First published in J. Roy. Hort. Soc. 74: 115 (1949)

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000322602
Tropicos 100266332
KEW urn:lsid:ipni.org:names:460703-1
The Plant List kew-203372
Open Tree Of Life 6086626
NCBI Taxonomy 1854046
IPNI 460703-1
GBIF 3893397

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
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
A Review of Cytotoxic Plants of the Indian Subcontinent and a Broad-Spectrum Analysis of Their Bioactive Compounds Mazumder K, Biswas B, Raja IM, Fukase K Molecules 20-Apr-2020
PMCID:PMC7221707
doi:10.3390/molecules25081904
PMID:32326113
Medicinal Plants from Near East for Cancer Therapy Abu-Darwish MS, Efferth T Front Pharmacol 31-Jan-2018
PMCID:PMC5797783
doi:10.3389/fphar.2018.00056
PMID:29445343
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
Composition of the Essential Oils of Three<i>Teucrium</i>Species from Turkey K. H.C. Baser, B. Demirçakmak, H. Duman Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1997.9700774
C-10 oxygenated neo-clerodane diterpenes from Teucrium sandrasicum G. Topcu, C. Eriş, C-T. Che, A. Ulubelen Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(96)00002-7
Neo-clerodane diterpenoids from Teucrium sandrasicum María C. De la Torre, Benjamín Rodríguez, Maurizio Bruno, Caterina Fazio, K.Husnu Can Baser, Hayri Duman Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00258-6

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
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700774
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700774
(1R,4S,6R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]decan-4-ol 11543111 Click to see CC1CCC(C2C13C2C(CC3)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1997.9700774
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700774
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700774
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1997.9700774
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700774
Cubebol 11276107 Click to see CC1CCC(C2C13C2C(CC3)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1997.9700774
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1997.9700774
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,2R,3R,5'S,6R,7S)-5'-(furan-3-yl)-6,7-bis(hydroxymethyl)-3-methylspiro[11-oxatricyclo[5.3.1.01,6]undecane-2,3'-oxolane]-2',5-dione 101714004 Click to see CC1CC(=O)C2(C3(CCCC2(C14CC(OC4=O)C5=COC=C5)O3)CO)CO 376.40 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
(1R,2R,3R,5S,5'S,6R,7S)-5'-(furan-3-yl)-5-hydroxy-6,7-bis(hydroxymethyl)-3-methylspiro[11-oxatricyclo[5.3.1.01,6]undecane-2,3'-oxolane]-2'-one 101714005 Click to see CC1CC(C2(C3(CCCC2(C14CC(OC4=O)C5=COC=C5)O3)CO)CO)O 378.40 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
(2aR,5'S,5aR,6R,7R,9S,9aR)-5'-(furan-3-yl)-5a,9-dihydroxy-2a-(hydroxymethyl)-7-methylspiro[3,4,5,7,8,9-hexahydro-1H-naphtho[1,8a-b]oxete-6,3'-oxolane]-2'-one 101714003 Click to see CC1CC(C23COC2(CCCC3(C14CC(OC4=O)C5=COC=C5)O)CO)O 378.40 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
(2aR,5'S,5aR,6R,7S,9S,9aR)-5'-(furan-3-yl)-5a,7,9-trihydroxy-2a-(hydroxymethyl)-7-methylspiro[1,3,4,5,8,9-hexahydronaphtho[1,8a-b]oxete-6,3'-oxolane]-2'-one 101714002 Click to see CC1(CC(C23COC2(CCCC3(C14CC(OC4=O)C5=COC=C5)O)CO)O)O 394.40 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
(3R,4R,4aS,5'R,8R,8aR)-5'-(furan-3-yl)-4a,8-dihydroxy-8,8a-bis(hydroxymethyl)-3-methylspiro[3,5,6,7-tetrahydro-2H-naphthalene-4,3'-oxolane]-1,2'-dione 10572688 Click to see CC1CC(=O)C2(C(CCCC2(C13CC(OC3=O)C4=COC=C4)O)(CO)O)CO 394.40 unknown https://doi.org/10.1016/0031-9422(96)00002-7
5'-(furan-3-yl)-4a,8-dihydroxy-8,8a-bis(hydroxymethyl)-3-methylspiro[3,5,6,7-tetrahydro-2H-naphthalene-4,3'-oxolane]-1,2'-dione 85190108 Click to see CC1CC(=O)C2(C(CCCC2(C13CC(OC3=O)C4=COC=C4)O)(CO)O)CO 394.40 unknown https://doi.org/10.1016/0031-9422(96)00002-7
5'-(Furan-3-yl)-5-hydroxy-6,7-bis(hydroxymethyl)-3-methylspiro[11-oxatricyclo[5.3.1.01,6]undecane-2,3'-oxolane]-2'-one 163045226 Click to see CC1CC(C2(C3(CCCC2(C14CC(OC4=O)C5=COC=C5)O3)CO)CO)O 378.40 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
5'-(Furan-3-yl)-5a,7,9-trihydroxy-2a-(hydroxymethyl)-7-methylspiro[1,3,4,5,8,9-hexahydronaphtho[1,8a-b]oxete-6,3'-oxolane]-2'-one 162902628 Click to see CC1(CC(C23COC2(CCCC3(C14CC(OC4=O)C5=COC=C5)O)CO)O)O 394.40 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
5'-(furan-3-yl)-5a,9-dihydroxy-2a-(hydroxymethyl)-7-methylspiro[3,4,5,7,8,9-hexahydro-1H-naphtho[1,8a-b]oxete-6,3'-oxolane]-2'-one 163084529 Click to see CC1CC(C23COC2(CCCC3(C14CC(OC4=O)C5=COC=C5)O)CO)O 378.40 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
5'-(Furan-3-yl)-6,7-bis(hydroxymethyl)-3-methylspiro[11-oxatricyclo[5.3.1.01,6]undecane-2,3'-oxolane]-2',5-dione 162875155 Click to see CC1CC(=O)C2(C3(CCCC2(C14CC(OC4=O)C5=COC=C5)O3)CO)CO 376.40 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
CID 101714000 101714000 Click to see CC(=O)OCC12C(CC(C3(C1(CCCC24CO4)O)CC(OC3=O)C5=COC=C5)(C)O)OC(=O)C 478.50 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
CID 101995265 101995265 Click to see CC(=O)OCC12C(CC(C3(C1(CCCC24CO4)O)CC(OC3=O)C5=COC=C5)(C)O)OC(=O)C 478.50 unknown https://doi.org/10.1016/0031-9422(96)00002-7
CID 10552642 10552642 Click to see CC(=O)OCC12C(CC(C3(C1(CCCC24CO4)O)CC(OC3=O)C5=COC=C5)(C)O)OC(=O)C 478.50 unknown https://doi.org/10.1016/0031-9422(96)00002-7
CID 3036767 3036767 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)OC(=O)C 446.50 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
CID 4623644 4623644 Click to see CC1CC(C2(C(C13CC(OC3=O)C4=COC=C4)CCCC25CO5)COC(=O)C)OC(=O)C 446.50 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
CID 85182436 85182436 Click to see CC(=O)OCC12C(CC(C3(C1(CCCC24CO4)O)CC(OC3=O)C5=COC=C5)(C)O)OC(=O)C 478.50 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
https://doi.org/10.1016/0031-9422(96)00002-7
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 101714001 101714001 Click to see CC(=O)OCC12C(CC(C3(C1(CCCC24CO4)O)CC(OC3=O)C5=COC=C5)(C)O)O 436.50 unknown https://doi.org/10.1016/S0031-9422(97)00258-6
CID 10765376 10765376 Click to see CC(=O)OCC12C(CC(C3(C1(CCCC24CO4)O)CC(OC3=O)C5=COC=C5)(C)O)O 436.50 unknown https://doi.org/10.1016/0031-9422(96)00002-7
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(97)00258-6
CID 85260191 85260191 Click to see CC(=O)OCC12C(CC(C3(C1(CCCC24CO4)O)CC(OC3=O)C5=COC=C5)(C)O)O 436.50 unknown https://doi.org/10.1016/0031-9422(96)00002-7
https://doi.org/10.1016/S0031-9422(97)00258-6
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(97)00258-6

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