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Marrubium globosum

Marrubium globosum - 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 UUID643fe2a54f21c750599737
Scientific name Marrubium globosum
Authority Montbret & Aucher ex Benth.
First published in Ann. Sci. Nat., Bot. , sér. 2, 6: 53 (1836)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English horehound

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Marrubium globosum subsp. globosum Unknown
Marrubium globosum subsp. libanoticum (Boiss.) P.H.Davis Kew Bull. 6: 71 (1951)
Marrubium globosum subsp. micranthum (Boiss. & Heldr.) P.H.Davis Kew Bull. 6: 71 (1951)

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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No germination or propagation data was added yet.

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-0000236602
Tropicos 100220110
KEW urn:lsid:ipni.org:names:449889-1
The Plant List kew-120853
Open Tree Of Life 6081188
NCBI Taxonomy 1907156
IPNI 449889-1
iNaturalist 908637
GBIF 3881740
CMAUP NPO16763

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
Exploring the Role of Apigenin in Neuroinflammation: Insights and Implications Charrière K, Schneider V, Perrignon-Sommet M, Lizard G, Benani A, Jacquin-Piques A, Vejux A Int J Mol Sci 06-May-2024
PMCID:PMC11084463
doi:10.3390/ijms25095041
PMID:38732259
Analysis of Marrubiin in Marrubium alysson L. Extract Using Advanced HPTLC: Chemical Profiling, Acetylcholinesterase Inhibitory Activity, and Molecular Docking Eltahawy NA, Ali AI, Ibrahim SA, Nafie MS, Sindi AM, Alkharobi H, Almalki AJ, Badr JM, Elhady SS, Abdelhameed RF Metabolites 30-Dec-2023
PMCID:PMC10821196
doi:10.3390/metabo14010027
PMID:38248830
Pharmacological and Molecular Insight on the Cardioprotective Role of Apigenin Thomas SD, Jha NK, Jha SK, Sadek B, Ojha S Nutrients 12-Jan-2023
PMCID:PMC9866972
doi:10.3390/nu15020385
PMID:36678254
Multidrug-Resistant Bacteria: Their Mechanism of Action and Prophylaxis Bharadwaj A, Rastogi A, Pandey S, Gupta S, Sohal JS Biomed Res Int 05-Sep-2022
PMCID:PMC9467707
doi:10.1155/2022/5419874
PMID:36105930
Application of Pauson–Khand reaction in the total synthesis of terpenes Heravi MM, Mohammadi L RSC Adv 29-Nov-2021
PMCID:PMC9044263
doi:10.1039/d1ra05673e
PMID:35493249
Antimicrobial Potential of Naturally Occurring Bioactive Secondary Metabolites Allemailem KS J Pharm Bioallied Sci 26-May-2021
PMCID:PMC8291113
doi:10.4103/jpbs.JPBS_753_20
PMID:34349474
Cornus officinalis Ethanolic Extract with Potential Anti-Allergic, Anti-Inflammatory, and Antioxidant Activities Quah Y, Lee SJ, Lee EB, Birhanu BT, Ali MS, Abbas MA, Boby N, Im ZE, Park SC Nutrients 29-Oct-2020
PMCID:PMC7692184
doi:10.3390/nu12113317
PMID:33138027
Plant-Derived Nutraceuticals and Immune System Modulation: An Evidence-Based Overview Di Sotto A, Vitalone A, Di Giacomo S Vaccines (Basel) 22-Aug-2020
PMCID:PMC7563161
doi:10.3390/vaccines8030468
PMID:32842641
Essential Oils and Mono/bi/tri-Metallic Nanocomposites as Alternative Sources of Antimicrobial Agents to Combat Multidrug-Resistant Pathogenic Microorganisms: An Overview Basavegowda N, Patra JK, Baek KH Molecules 27-Feb-2020
PMCID:PMC7179174
doi:10.3390/molecules25051058
PMID:32120930
A Review on Flavonoid Apigenin: Dietary Intake, ADME, Antimicrobial Effects, and Interactions with Human Gut Microbiota Wang M, Firrman J, Liu L, Yam K Biomed Res Int 16-Oct-2019
PMCID:PMC6817918
doi:10.1155/2019/7010467
PMID:31737673
Natural Antispasmodics: Source, Stereochemical Configuration, and Biological Activity Martínez-Pérez EF, Juárez ZN, Hernández LR, Bach H Biomed Res Int 08-Oct-2018
PMCID:PMC6196993
doi:10.1155/2018/3819714
PMID:30402474
Apigenin Impacts the Growth of the Gut Microbiota and Alters the Gene Expression of Enterococcus Wang M, Firrman J, Zhang L, Arango-Argoty G, Tomasula P, Liu L, Xiao W, Yam K Molecules 03-Aug-2017
PMCID:PMC6152273
doi:10.3390/molecules22081292
PMID:28771188
Anti-oxidant activity and major chemical component analyses of twenty-six commercially available essential oils Wang HF, Yih KH, Yang CH, Huang KF J Food Drug Anal 15-Jun-2017
PMCID:PMC9328889
doi:10.1016/j.jfda.2017.05.007
PMID:28987365
Ethnobotanical survey of plants used in Afyonkarahisar-Turkey Arı S, Temel M, Kargıoğlu M, Konuk M J Ethnobiol Ethnomed 23-Dec-2015
PMCID:PMC4690277
doi:10.1186/s13002-015-0067-6
PMID:26701098
In-vitro assessment of antioxidant and antimicrobial activities of methanol extracts and essential oil of Thymus hirtus sp. algeriensis Fatma G, Mouna BF, Mondher M, Ahmed L Lipids Health Dis 14-Jul-2014
PMCID:PMC4115217
doi:10.1186/1476-511X-13-114
PMID:25022197

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 / Fatty Acyls / Fatty acids and conjugates / Heterocyclic fatty acids
4-(9-Hydroxy-4,8,10-trimethyl-3-oxo-2-oxatricyclo[6.3.1.04,12]dodecan-9-yl)butanoic acid 73047812 Click to see CC1CC2C3C(CCCC3(C1(CCCC(=O)O)O)C)(C(=O)O2)C 324.40 unknown https://doi.org/10.1021/NP0505420
4-[(1R,4S,8S,9R,10R,12R)-9-hydroxy-4,8,10-trimethyl-3-oxo-2-oxatricyclo[6.3.1.04,12]dodecan-9-yl]butanoic acid 46883326 Click to see CC1CC2C3C(CCCC3(C1(CCCC(=O)O)O)C)(C(=O)O2)C 324.40 unknown https://doi.org/10.1021/NP0505420
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(8S,11bS)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1,2,8,9-tetrahydronaphtho[2,1-f][1]benzofuran-6-one 11174780 Click to see CC1COC2=C(C3=C(C(=O)C=C4C3(CCC(=C4C)C)C)C(=C12)O)O 326.40 unknown via CMAUP database
CID 10807787 10807787 Click to see CC1CC(C2C(CCCC2(C13CC(=O)C4(O3)COC=C4)C)(C)CO)O 350.40 unknown https://doi.org/10.1248/CPB.48.1234
CID 85274642 85274642 Click to see CC1CC(C2C(CCCC2(C13CC(=O)C4(O3)COC=C4)C)(C)CO)O 350.40 unknown https://doi.org/10.1248/CPB.48.1234
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
9-hydroxy-4,8,10-trimethyl-9-[2-(5-oxo-2H-furan-3-yl)ethyl]-2-oxatricyclo[6.3.1.04,12]dodecan-3-one 73153367 Click to see CC1CC2C3C(CCCC3(C1(CCC4=CC(=O)OC4)O)C)(C(=O)O2)C 348.40 unknown https://doi.org/10.1055/S-2006-931557
https://doi.org/10.1021/NP0505420
Marrulibanoside 46883184 Click to see CC1CC2C3C(CCCC3(C1(CCC4=CC(=O)OC4)O)C)(C(=O)O2)C 348.40 unknown https://doi.org/10.1055/S-2006-931557
https://doi.org/10.1021/NP0505420
https://doi.org/10.1021/NP9002756
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
3-[2-(1,4-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-2H-naphthalen-1-yl)ethyl]-2H-furan-5-one 46705500 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)O 336.50 unknown https://doi.org/10.1021/NP0505420
3-[2-[(1R,2R,4R,4aS,8aS)-1,4-dihydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-2H-naphthalen-1-yl]ethyl]-2H-furan-5-one 46883141 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)O 336.50 unknown https://doi.org/10.1021/NP0505420
https://doi.org/10.1021/NP9002756
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-O-Acetyloleanolic acid 151202 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown via CMAUP database
O-Acetyloleanolic aldehyde 14829106 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
22-Dehydroclerosterol 15608667 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
4-Hydroxy-4-(2-hydroxyethyl)cyclohexan-1-one 184824 Click to see C1CC(CCC1=O)(CCO)O 158.19 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1R,3'aS,4S,8S,9R,10R,12R)-2'-ethoxy-3',3'a-dihydroxy-4,8,10-trimethylspiro[2-oxatricyclo[6.3.1.04,12]dodecane-9,6'-3,4,5,7a-tetrahydro-2H-furo[2,3-b]pyran]-3-one 102597519 Click to see CCOC1C(C2(CCC3(C(CC4C5C3(CCCC5(C(=O)O4)C)C)C)OC2O1)O)O 410.50 unknown https://doi.org/10.1021/NP9002756
> Organoheterocyclic compounds / Benzofurans
(3aR,6R,7aS)-3,4,5,6,7,7a-hexahydro-2H-1-benzofuran-3a,6-diol 11744892 Click to see C1CC2(CCOC2CC1O)O 158.19 unknown via CMAUP database
(3aS,4R,7aS)-3a,4-dihydroxy-2,3,4,5,7,7a-hexahydro-1-benzofuran-6-one 10749706 Click to see C1COC2C1(C(CC(=O)C2)O)O 172.18 unknown via CMAUP database
Cleroindicin C 10975728 Click to see C1CC2(CCOC2CC1=O)O 156.18 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Marrulactone 44254165 Click to see CC1CC2C3C(CCCC3(C14CCCC(=O)O4)C)(C(=O)O2)C 306.40 unknown https://doi.org/10.1021/NP9002756
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
13-epicyllenin A 44254085 Click to see CC1CC2C3C(CCCC3(C14CCC5(O4)CC(OC5)O)C)(C(=O)O2)C 350.40 unknown https://doi.org/10.1021/NP9002756
CID 101682668 101682668 Click to see CC1CC2C3C(CCCC3(C14CC(=O)C5(O4)COC=C5)C)(C(=O)O2)C 346.40 unknown https://doi.org/10.1248/CPB.48.1234
CID 10472811 10472811 Click to see CC1CC2C3C(CCCC3(C14CC(=O)C5(O4)COC=C5)C)(C(=O)O2)C 346.40 unknown https://doi.org/10.1248/CPB.48.1234
CID 46883138 46883138 Click to see CC1CC2C3C(CCCC3(C14CCC5(O4)CC(OC5)O)C)(C(=O)O2)C 350.40 unknown https://doi.org/10.1021/NP9002756
CID 46883139 46883139 Click to see CC1CC2C3C(CCCC3(C14CCC5(O4)CC(OC5)O)C)(C(=O)O2)C 350.40 unknown https://doi.org/10.1021/NP9002756
CID 73321375 73321375 Click to see CC1CC2C3C(CCCC3(C14CC(=O)C5(O4)COC=C5)C)(C(=O)O2)C 346.40 unknown https://doi.org/10.1248/CPB.48.1234
Marrubiin 73401 Click to see CC1CC2C3C(CCCC3(C1(CCC4=COC=C4)O)C)(C(=O)O2)C 332.40 unknown https://doi.org/10.1248/CPB.48.1234
Marrubin 235392 Click to see CC1CC2C3C(CCCC3(C1(CCC4=COC=C4)O)C)(C(=O)O2)C 332.40 unknown https://doi.org/10.1248/CPB.48.1234
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Scutellarein 5281697 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 5318059 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 476.40 unknown via CMAUP database
beta-D-Glucopyranosiduronic acid, 2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-1-benzopyran-7-yl 158227 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 492.40 unknown via CMAUP database
Scutellarin 185617 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database

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