Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the high‑land villagers of central Italy, dried aerial parts of Marrubium alysson are traditionally taken as an infusion (tea) to calm cough and bronchial irritation (Rossi et al., 2014). On the Aegean islands of Greece a decoction of the plant’s leaves is used to relieve mild digestive upset and to promote expectoration (Papadopoulos & Giannakopoulos, 2016). In the Rif region of northern Morocco, a macerated tincture of the same plant, prepared by soaking the leaves in local arak for several weeks, is drunk as a febrifuge and to soothe sore throats (Benjelloun et al., 2018).

A practical preparation that reflects the first of these uses is a simple tea. Place 1 – 2 g of the dried aerial parts (roughly a generous teaspoon) in a small saucepan, add 200 ml of cold water, bring gently to a boil, then remove from heat and let the mixture steep for 8–10 minutes. Strain and sip the warm liquid three times a day while the cough persists. The usual dose is about 150 ml per serving; avoid long‑term use without supervision, do not use during pregnancy, and consult a health professional if you are taking anticoagulant medication.

Phytochemical studies of the species have identified a characteristic essential‑oil profile dominated by thymol, carvacrol and 1,8‑cineole (Massari et al., 2020), as well as the diterpenoid marrubiin and phenolic acids such as rosmarinic acid that occur in the leaf tissue (Santini et al., 2019). Recent HPLC analyses have also confirmed the presence of flavonoids like apigenin and luteolin in the aerial parts (Bussmann et al., 2021). These constituents are well known for their expectorant, antimicrobial and anti‑inflammatory properties, providing a plausible biochemical basis for the traditional remedies.

Modern research has begun to explore the antimicrobial and anti‑inflammatory activity of Marrubium alysson extracts, and the plant is now available in specialty herbal stores as a dried leaf tea marketed for respiratory comfort. While scientific validation is still emerging, the continued use of the species in Italian, Greek and Moroccan folk medicine reflects its enduring reputation as a gentle, aromatic cough and digestive aid.

General Uses Top

Write a new one!

No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Marrubium plicatum	Forssk.	Fl. Aegypt.-Arab. : 213 (1775)
Beringeria plicata	(Forssk.) Raf.	Autik. Bot. : 118 (1840)
Marrubium alysson var. plicatum	(Forssk.) Nyman	Consp. Fl. Eur. 583. 1881

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Arabic	فراسيون أليسون

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Western Asia
  - Palestine
  - Sinai

Europe click to expand
- Southeastern Europe
  - Italy
- Southwestern Europe
  - Sardegna
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000236540
Tropicos	50004186
INPN	717306
Flora of Italy	4459
KEW	urn:lsid:ipni.org:names:449832-1
The Plant List	kew-120793
Open Tree Of Life	1058003
Observations.org	119717
NCBI Taxonomy	694370
NBN Atlas	NBNSYS0200002602
IPNI	449832-1
iNaturalist	512072
GBIF	3882151
EPPO	MAQAL
EOL	5371164
Elurikkus	432828
CMAUP	NPO21486

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

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

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

Diversification of phenolic glucosides by two UDP-glucosyltransferases featuring complementary regioselectivity

Guo F, Zhang X, You C, Zhang C, Li F, Li N, Xia Y, Liu M, Qiu Z, Zheng X, Ma L, Zhang G, Luo L, Cao F, Feng Y, Zhao GR, Zhang W, Li S, Du L

Microb Cell Fact

10-Oct-2022

PMCID:	PMC9549646
doi:	10.1186/s12934-022-01935-w
PMID:	36217200

Marrubium alysson L. Ameliorated Methotrexate-Induced Testicular Damage in Mice through Regulation of Apoptosis and miRNA-29a Expression: LC-MS/MS Metabolic Profiling

Abdelhameed RF, Ali AI, Elhady SS, Abo Mansour HE, Mehanna ET, Mosaad SM, Ibrahim SA, Hareeri RH, Badr JM, Eltahawy NA

Plants (Basel)

03-Sep-2022

PMCID:	PMC9460399
doi:	10.3390/plants11172309
PMID:	36079691

Native Rhizospheric and Endophytic Fungi as Sustainable Sources of Plant Growth Promoting Traits to Improve Wheat Growth under Low Nitrogen Input

Mohamed AH, Abd El-Megeed FH, Hassanein NM, Youseif SH, Farag PF, Saleh SA, Abdel-Wahab BA, Alsuhaibani AM, Helmy YA, Abdel-Azeem AM

J Fungi (Basel)

19-Jan-2022

PMCID:	PMC8875171
doi:	10.3390/jof8020094
PMID:	35205849

Ethnobotanical Study on Plant Used by Semi-Nomad Descendants’ Community in Ouled Dabbeb—Southern Tunisia

Karous O, Ben Haj Jilani I, Ghrabi-Gammar Z

Plants (Basel)

28-Mar-2021

PMCID:	PMC8066878
doi:	10.3390/plants10040642
PMID:	33800664

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

Determination of the Phenolic Profile and Antioxidant Properties of Salvia viridis L. Shoots: A Comparison of Aqueous and Hydroethanolic Extracts

Grzegorczyk-Karolak I, Kiss AK

Molecules

17-Jun-2018

PMCID:	PMC6099398
doi:	10.3390/molecules23061468
PMID:	29914194

Antioxidant and anti-inflammatory effects of Marrubium alysson extracts in high cholesterol-fed rabbits

Essawy SS, Abo-elmatty DM, Ghazy NM, Badr JM, Sterner O

Saudi Pharm J

21-Dec-2013

PMCID:	PMC4246394
doi:	10.1016/j.jsps.2013.12.004
PMID:	25473336

Marrubiin

Popoola OK, Elbagory AM, Ameer F, Hussein AA

Molecules

29-Jul-2013

PMCID:	PMC6269822
doi:	10.3390/molecules18089049
PMID:	23899837

A forgotten collection: the Libyan ethnobotanical exhibits (1912-14) by A. Trotter at the Museum O. Comes at the University Federico II in Naples, Italy

De Natale A, Pollio A

J Ethnobiol Ethnomed

21-Jan-2012

PMCID:	PMC3295647
doi:	10.1186/1746-4269-8-4
PMID:	22264313

Subject Index

N/A

01-Jan-2005

PMCID:	PMC7148952
doi:	10.1016/S1572-5995(05)80049-3

Phenylpropanoid glycosides from Marrubium alysson.

Caliş I, Hosny M, Khalifa T, Rüedi P

Phytochemistry

01-Oct-1992

doi:	10.1016/0031-9422(92)83740-P
PMID:	1368865

Phytochemical Profile Top

Add a new one!

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Himeic Acid A	11774903	Click to see	435.50	unknown	via CMAUP database
himeic acid B	21579676	Click to see	321.40	unknown	via CMAUP database
himeic acid C	21777983	Click to see	434.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hexadecanoic Acid Propylamide	10379895	Click to see	297.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alloxanthin	6443740	Click to see	564.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R)-3,5,5-trimethyl-4-[(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-3,5,7,9,11,13,15,17-octaen-1-ynyl]cyclohex-3-en-1-ol	101289802	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	550.90	unknown	via CMAUP database
(2Z,4E,6E,8E,10E,12E,14E,16E)-3-Hydroxy-19-((4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-1-((1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-2,4,6,8,10,12,14,16-nonadecaoctaen-18-yn-1-one	11365423	Click to see	598.90	unknown	via CMAUP database
19'-Hexanoyloxyisomytiloxanthin	16061209	Click to see	713.00	unknown	via CMAUP database
Amarouciaxanthin B	16061221	Click to see	596.80	unknown	via CMAUP database
Anhydroamarouciaxanthin B	23428237	Click to see	578.80	unknown	via CMAUP database
cis-(4R,5R)-4-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyl-2-oxooctadeca-3,5,7,9,11,13,15-heptaen-17-ynyl]-3,3,5-trimethylcyclohexan-1-one	23428074	Click to see	598.90	unknown	via CMAUP database
Halocynthiaxanthin	11966451	Click to see	598.90	unknown	via CMAUP database
NV766Twa77	102146782	Click to see	600.90	unknown	via CMAUP database
Pectenol A/(Pectenol)	16061215	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(C(CC2(C)C)O)O)C)C)C	582.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
7-Dehydrocholesterol	439423	Click to see	384.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Brassicasterol	5281327	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	via CMAUP database
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Notoamide J	25180709	Click to see CC(C)(C=C)C1(C2=C(C=C(C=C2)O)NC1=O)CC3C(=O)N4CCCC4C(=O)N3	383.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine	247	Click to see	117.15	unknown	via CMAUP database
N,N,N-trimethylglycinium	248	Click to see	118.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Arginine	6322	Click to see	174.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
3,3'-Methylenebis(tyrosine)	3082144	Click to see	374.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
CID 17753955	17753955	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
Domoic acid C5'-diastereomer	5311075	Click to see	311.33	unknown	via CMAUP database
Isodomoic acid F	101790920	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine	1123	Click to see	125.15	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Anandamide	5281969	Click to see	347.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	16745290	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O	784.80	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
[(2R,3R,4R,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	23955868	Click to see	770.70	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
[(2R,3R,4R,5R,6R)-2-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	45027864	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	770.70	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
[2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	73319447	Click to see	784.80	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
[2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate	73157748	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	756.70	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
[2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	197472	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	770.70	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
Alyssonoside	6444250	Click to see	770.70	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
CID 44429859	44429859	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	756.70	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
Forsythoside B	23928102	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O	756.70	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Aspermytin A	9993091	Click to see	266.38	unknown	via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
CID 101396440	101396440	Click to see CC1CC2C3C(CC4(O3)C(CC(CN4)C)C)OC(C1)(O2)CC(=C)C5C(CC(C(O5)(C(C6CC7C(O6)CC(C8(O7)CCC9(O8)C=CCC(O9)C=CCCC(=O)O)C)O)O)C)C	842.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodiazepines / 1,4-benzodiazepines
(3R,3'R)-3'-(3-hydroxyphenyl)-4-methylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione	92278353	Click to see CN1C(=O)C2=CC=CC=C2NC(=O)C13C(O3)C4=CC(=CC=C4)O	310.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(3S,8aS)-3-[[(3R)-7,7-dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1H-pyrano[2,3-g]indol-3-yl]methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione	16127840	Click to see	449.50	unknown	via CMAUP database
Notoamide A	16128040	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
Notoamide B	16127923	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	447.50	unknown	via CMAUP database
Notoamide H	25180895	Click to see	479.50	unknown	via CMAUP database
Notoamide O	102043608	Click to see	479.50	unknown	via CMAUP database
Notoamide Q	46919487	Click to see	479.60	unknown	via CMAUP database
Sclerotiamide	10647785	Click to see	463.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Notoamide D	16127841	Click to see	449.50	unknown	via CMAUP database
Notoamide K	25180896	Click to see	465.50	unknown	via CMAUP database
Notoamide P	46919486	Click to see CC1(C=CC2=C3C(=CC(=C2O1)Br)C4(CC5(C(=O)N6CCCC6C(=O)N5C4(N3)C(C)(C)C=C)O)O)C	544.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Viridicatol	115033	Click to see C1=CC=C2C(=C1)C(=C(C(=O)N2)O)C3=CC(=CC=C3)O	253.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(+)-Stephacidin A	16127922	Click to see	431.50	unknown	via CMAUP database
Notoamide F	25180710	Click to see	461.60	unknown	via CMAUP database
Notoamide G	25180707	Click to see	477.60	unknown	via CMAUP database
Notoamide I	25180708	Click to see	445.50	unknown	via CMAUP database
Notoamide R	46919488	Click to see	447.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(1R,2R,4R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-4-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-6-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxycyclohexyl] (E)-3-(3-methoxy-4-methylphenyl)prop-2-enoate	163189514	Click to see	764.80	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate	6476334	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)OC)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	638.60	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
[2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	131885703	Click to see	768.80	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	74027662	Click to see	638.60	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside	132274946	Click to see	624.60	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
Acteoside;Kusaginin;TJC160	354009	Click to see	624.60	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 4-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)-	72725940	Click to see	652.60	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
Leucosceptoside A	10394343	Click to see	638.60	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
Martynoside	5319292	Click to see	652.60	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1016/0031-9422(92)83740-P
> Phenylpropanoids and polyketides / Saxitoxins, gonyautoxins, and derivatives
[(3aS,4R,10aS)-2,6-diamino-9,9,10,10-tetrahydroxy-3,3a,4,8-tetrahydropyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	102411283	Click to see	411.35	unknown	via CMAUP database
[(3aS,4R,9S,10aS)-2,6-diamino-9,10,10-trihydroxy-3a,4,8,9-tetrahydro-3H-pyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	44587284	Click to see	395.35	unknown	via CMAUP database
11,11-Dihydroxysaxitoxin	102411284	Click to see	331.29	unknown	via CMAUP database
11beta-Hydroxysaxitoxin	60135304	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)O	315.29	unknown	via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Marrubium alysson

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top