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Marrubium thessalum

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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 UUID643fe2a807387050351966
Scientific name Marrubium thessalum
Authority Boiss. & Heldr.
First published in Diagn. Pl. Orient. , ser. 2, 4: 50 (1859)

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-0000236696
Tropicos 17600530
KEW urn:lsid:ipni.org:names:449978-1
The Plant List kew-120939
Open Tree Of Life 1057997
Observations.org 147628
NCBI Taxonomy 694371
IPNI 449978-1
iNaturalist 512066
GBIF 3905732
EPPO MAQTH
Elurikkus 437635

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
Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S Biomolecules 02-Dec-2022
PMCID:PMC9775335
doi:10.3390/biom12121807
PMID:36551235
A neoclerodane orthoester and other new neoclerodane diterpenoids from Teucrium yemense chemistry and effect on secretion of insulin Nur-e-Alam M, Parveen I, Wilkinson B, Ahmed S, Hafizur RM, Bari A, Woodman TJ, Threadgill MD, Al-Rehaily AJ Sci Rep 13-Apr-2021
PMCID:PMC8044157
doi:10.1038/s41598-021-87513-3
PMID:33850244
Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL Chem Rev 09-Nov-2020
PMCID:PMC8183567
doi:10.1021/acs.chemrev.0c00922
PMID:33164487
Anticancer Activity of Essential Oils and Other Extracts from Aromatic Plants Grown in Greece Fitsiou E, Pappa A Antioxidants (Basel) 07-Aug-2019
PMCID:PMC6720353
doi:10.3390/antiox8080290
PMID:31394842
Phenylethanoid Glycosides: Research Advances in Their Phytochemistry, Pharmacological Activity and Pharmacokinetics Xue Z, Yang B Molecules 29-Jul-2016
PMCID:PMC6273160
doi:10.3390/molecules21080991
PMID:27483229
Marrubiin Popoola OK, Elbagory AM, Ameer F, Hussein AA Molecules 29-Jul-2013
PMCID:PMC6269822
doi:10.3390/molecules18089049
PMID:23899837
Labdane diterpenes from Marrubium thessalum. Argyropoulou C, Karioti A, Skaltsa H Phytochemistry 01-Mar-2009
doi:10.1016/J.PHYTOCHEM.2009.03.011
PMID:19361824

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 / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(2R)-2-[(2R,8R,8aR)-8,8a-dimethyl-2,3,5,6,7,8-hexahydro-1H-naphthalen-2-yl]propane-1,2-diol 162922156 Click to see CC1CCCC2=CCC(CC12C)C(C)(CO)O 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,4R,5R,8S,9R,10R,12R)-9-[2-(furan-3-yl)ethyl]-5,9-dihydroxy-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 162989334 Click to see CC1CC2C3C(C1(CCC4=COC=C4)O)(CCC(C3(C(=O)O2)C)O)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
(1R,4R,8S,9R,10R,12R)-9-hydroxy-9-[2-(2-methoxy-5-oxo-2H-furan-4-yl)ethyl]-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecane-3,5-dione 101470899 Click to see CC1CC2C3C(C1(CCC4=CC(OC4=O)OC)O)(CCC(=O)C3(C(=O)O2)C)C 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
(1R,4R,8S,9R,10R,12R)-9-hydroxy-9-[2-[(2R)-2-methoxy-5-oxo-2H-furan-4-yl]ethyl]-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecane-3,5-dione 163026250 Click to see CC1CC2C3C(C1(CCC4=CC(OC4=O)OC)O)(CCC(=O)C3(C(=O)O2)C)C 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
(1R,4R,8S,9R,10R,12R)-9-hydroxy-9-[2-[(2S)-2-methoxy-5-oxo-2H-furan-4-yl]ethyl]-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecane-3,5-dione 163026251 Click to see CC1CC2C3C(C1(CCC4=CC(OC4=O)OC)O)(CCC(=O)C3(C(=O)O2)C)C 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
3-Oxomarrubiin 7091745 Click to see CC1CC2C3C(C1(CCC4=COC=C4)O)(CCC(=O)C3(C(=O)O2)C)C 346.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
9-[2-(Furan-3-yl)ethyl]-5,9-dihydroxy-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 45359568 Click to see CC1CC2C3C(C1(CCC4=COC=C4)O)(CCC(C3(C(=O)O2)C)O)C 348.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
9-hydroxy-9-[2-(2-methoxy-5-oxo-2H-furan-4-yl)ethyl]-4,8,10-trimethyl-2-oxatricyclo[6.3.1.04,12]dodecane-3,5-dione 163026249 Click to see CC1CC2C3C(C1(CCC4=CC(OC4=O)OC)O)(CCC(=O)C3(C(=O)O2)C)C 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
CID 101695765 101695765 Click to see CC1CC2C3C(C14CCC5(O4)CC(OC5)O)(CCC(=O)C3(C(=O)O2)C)C 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
CID 162885070 162885070 Click to see CC1CC2C3C(C14CCC5(O4)CC(OC5)OC)(CCC(=O)C3(C(=O)O2)C)C 378.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
CID 162885071 162885071 Click to see CC1CC2C3C(C14CCC5(O4)CC(OC5)OC)(CCC(=O)C3(C(=O)O2)C)C 378.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
CID 163002553 163002553 Click to see CC1CC2C3C(C14CCC5(O4)CC(OC5)O)(CCC(=O)C3(C(=O)O2)C)C 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
CID 163097015 163097015 Click to see CC1CC2C3C(C14CCC5(O4)COC=C5)(CCC(=O)C3(C(=O)O2)C)C 346.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
CID 163097016 163097016 Click to see CC1CC2C3C(C14CCC5(O4)COC=C5)(CCC(=O)C3(C(=O)O2)C)C 346.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
CID 163097017 163097017 Click to see CC1CC2C3C(C14CCC5(O4)COC=C5)(CCC(=O)C3(C(=O)O2)C)C 346.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ladanein 3084066 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O 314.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.03.011

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