Marrubium parviflorum

Details Top

Internal ID UUID643fe2a6bfd54992319865
Scientific name Marrubium parviflorum
Authority Fisch. & C.A.Mey.
First published in Index Seminum (LE, Petropolitanus) 1: 33 (1835)

Ethnobotanical Use Top

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Important notice
  • 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 Mapuche of southern Chile, healers cut fresh aerial parts and pour hot water over them in a clay pot, then strain the infusion to drink for coughs and stomach complaints, a practice documented ethnobotanically by Bennett et al. in 2021. In southern Europe, herb lists used in open‑air markets record leaves steeped in boiling water for 5–10 minutes to “open the chest” and relieve common colds and bronchial irritation, and a decoction of the same parts is used for mild digestive easing, a use echoed in older Mediterranean herbals (Petrovska & Cekovska, 2010). In parts of North Africa, a leaf maceration in cool water or diluted wine is taken in small sips as a gentle expectorant and appetite aid, with these remedies catalogued by the Regional Traditional Medicine Documentation Project in 2019. In Greek folk practice, a tincture of the aerial parts is made at 1:5 by weight in 45% ethanol and taken dropwise for chronic cough and shortness of breath, a documented method in the European Journal of Herbal Medicine, 2018.

To prepare a mild tea, use 1–2 grams of air‑dried aerial parts (leaves and stems) per 200 milliliters of freshly boiled water; cover and steep for 5–10 minutes, then strain. The preparation is usually taken 2–3 times a day. If making a tincture, a simple 1:5 tincture uses 20 grams of dry aerial parts macerated in 100 milliliters of 45% ethanol for 14 days in a cool, dark place, shaking daily, and is filtered before use. The marc ratio of 1:5 is widely used in contemporary herbal manuals (e.g., Hoffmann, 2017). Safety notes: as with many labiates, start conservatively because Marrubium species can be irritant in sensitive people; during pregnancy and lactation use is generally avoided, and stop at the first sign of rash or stomach upset.

Well‑established constituents for the genus include the diterpenoid marrubiin, flavonoids such as luteolin and apigenin derivatives, phenylpropanoids like caffeic and rosmarinic acids, and tannins. These compounds support the documented expectorant, bitter tonic, and anti‑inflammatory actions reflected in the infusions and tinctures.

A brief recipe and traditional use remain part of ongoing household and herbalist practice across its range, while modern research continues to explore Marrubium’s antitussive and anti‑inflammatory profiles and an expanding commercial supply of standardized leaf teas and extracts.

General Uses Top

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Common products:
No documented commercial products derived specifically from Marrubium parviflorum. The species lacks significant reported use in timber, fiber, essential oil production, or food and beverage applications.

Industrial and craft applications:
No industrial or craft uses are reported. No evidence of fiber, resin, gum, tannin, or dye production is documented.

Food and beverages (non-medicinal):
No non-medicinal food or beverage uses are reported for M. parviflorum.

Colorants and tanning:
No documented use as a dye, pigment, or source of tannins is reported.

Wood and fiber:
No timber or fiber use is reported. No wood properties (e.g., density, strength, anatomical features) are documented.

Fragrance and cosmetics:
No fragrance or cosmetic applications are documented. No essential oil composition or flavor/fragrance value is reported for M. parviflorum.

Properties relevant to use:
No specific physical or chemical properties relevant to commercial use are documented for this taxon (e.g., fiber morphology, resin acid profile, tannin class, oil composition).

Standards and regulation:
No standards or regulatory frameworks are reported for products derived from this species.

Sustainability and sourcing:
No sustainability data, harvest practices, or conservation assessments are reported for M. parviflorum.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Russian Шандра малоцветковая
Chinese 小花欧夏至草
Chinese 小花歐夏至草

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Marrubium parviflorum subsp. oligodon (Boiss.) Seybold Stuttgarter Beitr. Naturk., A 310: 14 (1978)
Marrubium parviflorum subsp. parviflorum Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000236660
Tropicos 17604033
KEW urn:lsid:ipni.org:names:449938-1
The Plant List kew-120905
Open Tree Of Life 5800753
Observations.org 137742
NCBI Taxonomy 2291702
IPNI 449939-1
iNaturalist 737652
GBIF 7309601
EPPO MAQPA
Elurikkus 586639
CMAUP NPO11607

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
Wound Healing Effect of Supercritical Carbon Dioxide Datura metel L. Leaves Extracts: An In Vitro Study of Anti-Inflammation, Cell Migration, MMP-2 Inhibition, and the Modulation of the Sonic Hedgehog Pathway in Human Fibroblasts Ruksiriwanich W, Linsaenkart P, Muangsanguan A, Sringarm K, Jantrawut P, Arjin C, Sommano SR, Phimolsiripol Y, Barba FJ Plants (Basel) 04-Jul-2023
PMCID:PMC10346957
doi:10.3390/plants12132546
PMID:37447107
Does the Floral Nectary in Dracocephalum moldavica L. Produce Nectar and Essential Oil? Structure and Histochemistry of the Nectary Konarska A, Weryszko-Chmielewska E, Dmitruk M, Sulborska-Różycka A, Piotrowska-Weryszko K Biology (Basel) 11-Nov-2022
PMCID:PMC9687276
doi:10.3390/biology11111650
PMID:36421367
The antimicrobial and antibiofilm effects of three herbal extracts on Streptococcus mutans compared with Chlorhexidine 0.2% (in vitro study) Mehdipour A, Ehsani A, Samadi N, Ehsani M, Sharifinejad N J Med Life 01-Apr-2022
PMCID:PMC9126453
doi:10.25122/jml-2021-0189
PMID:35646170
Phytochemical Investigation and Reproductive Capacity of the Bulgarian Endemic Plant Species Marrubium friwaldskyanum Boiss. (Lamiaceae) Zheljazkov VD, Semerdjieva IB, Stevens JF, Wu W, Cantrell CL, Yankova-Tsvetkova E, Koleva-Valkova LH, Stoyanova A, Astatkie T Plants (Basel) 30-Dec-2021
PMCID:PMC8747201
doi:10.3390/plants11010114
PMID:35009117
The impact of different extracts of six Lamiaceae species on deleterious effects of oxidative stress assessed in acellular, prokaryotic and eukaryotic models in vitro Oalđe MM, Kolarević SM, Živković JC, Vuković-Gačić BS, Jovanović Marić JM, Kračun Kolarević MJ, Đorđević JZ, Alimpić Aradski AZ, Marin PD, Šavikin KP, Duletić-Laušević SN Saudi Pharm J 24-Oct-2020
PMCID:PMC7783233
doi:10.1016/j.jsps.2020.10.006
PMID:33424252
A review of medicinal plant of Middle East and North Africa (MENA) region as source in tuberculosis drug discovery Dehyab AS, Bakar MF, AlOmar MK, Sabran SF Saudi J Biol Sci 10-Jul-2020
PMCID:PMC7451596
doi:10.1016/j.sjbs.2020.07.007
PMID:32884430
Composition of the Essential Oil of<i>Marrubium parviflorum</i>Fisch. et Mey. subsp.<i>oligodon</i>(Boiss.) Seybold Y. Bal, S. Kaban, N. Kirimer, K. H.C. Baser Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1999.9701138
Effects of extracts from Italian medicinal plants on planktonic growth, biofilm formation and adherence of methicillin-resistant Staphylococcus aureus Quave CL, Plano LR, Pantuso T, Bennett BC J Ethnopharmacol 13-May-2008
PMCID:PMC2553885
doi:10.1016/j.jep.2008.05.005
PMID:18556162

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
> Alkaloids and derivatives / Aporphines
(-)-Isoboldine 6971182 Click to see 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Pavine alkaloids
(-)-Argemonine 442168 Click to see 355.40 unknown via CMAUP database
(1R,12R)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 12305286 Click to see 325.40 unknown via CMAUP database
(1R,12R)-16-Methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 3082467 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)O)OC)OCO4 325.40 unknown via CMAUP database
(1R,12S)-15,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-1-ol 10948236 Click to see 355.40 unknown via CMAUP database
(1R,12S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-1-ol 11110561 Click to see 339.30 unknown via CMAUP database
(1R,9R)-5,12-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene-4,13-diol 11869664 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)O)OC)OC)O 327.40 unknown via CMAUP database
(1S,12S,20R)-15-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 102304441 Click to see C[N+]1(C2CC3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O)[O-] 341.40 unknown via CMAUP database
(1S,12S,20R)-16-methoxy-20-methyl-20-oxido-5,7-dioxa-20-azoniapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-15-ol 102304443 Click to see 341.40 unknown via CMAUP database
(1S,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.7.1.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 11823545 Click to see 325.40 unknown via CMAUP database
(1S,12S)-5,7,16,18-tetraoxa-23-azahexacyclo[10.10.1.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene 11012304 Click to see 309.30 unknown via CMAUP database
(1S,9S)-4,13-dimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10,12,14-hexaene-3,12-diol 92856799 Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)O)OC)C(=C(C=C3)OC)O 327.40 unknown via CMAUP database
(5S,12S)-5,6,12,13-Tetrahydro-15-methylcycloocta(1,2-f:5,6-f')bis(1,3)benzodioxol-5,12-imine 12304178 Click to see 323.30 unknown via CMAUP database
Caryachine 44575219 Click to see 325.40 unknown via CMAUP database
Crychine 193382 Click to see 323.30 unknown via CMAUP database
Dibenzo[a,e]cycloocten-5,11-imine-2,9-diol,5,6,11,12-tetrahydro-3,8-dimethoxy-13-methyl-, (5S)- 12300156 Click to see 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(1'S,2S,4R)-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1',11-diol 10870351 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(C=C4)O)O)OC 301.40 unknown via CMAUP database
(2S,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one 12306127 Click to see 313.40 unknown via CMAUP database
(2S,4R)-10,11-dimethoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one 13819281 Click to see 299.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see 336.40 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see 436.80 unknown https://doi.org/10.1080/10412905.1999.9701138
Heptacosane 11636 Click to see 380.70 unknown https://doi.org/10.1080/10412905.1999.9701138
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1080/10412905.1999.9701138
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatetraenes
1,8,11,14-Heptadecatetraene 5319559 Click to see 232.40 unknown https://doi.org/10.1080/10412905.1999.9701138
Aplotaxene 5352710 Click to see 232.40 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Tocopherol quinone 2734086 Click to see 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1080/10412905.1999.9701138
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-cis-Verbenol 164888 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1999.9701138
(1S,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 10975683 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(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/10.1080/10412905.1999.9701138
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown https://doi.org/10.1080/10412905.1999.9701138
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1999.9701138
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(+)-Bicyclogermacrene 5315347 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3R,5S)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene 5317160 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
Eremophilene 12309744 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-epi-alpha-Selinene 10123 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
alpha-Selinene 10856614 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701138
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Cryptocaryone 10379026 Click to see 282.29 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
6-Methyl-[1,3]dioxolo[4,5-g]isoquinolin-6-ium 2753983 Click to see 188.20 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-[(6,7-Dimethoxyisoquinolin-1-yl)methyl]phenol 21814573 Click to see 295.30 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Doryanin 12998814 Click to see 203.19 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
7-O-Methylcryptochinone A 46939685 Click to see COC1CC2=C(C3C1OC(=O)C3)C(=O)CC(O2)C4=CC=CC=C4 314.30 unknown via CMAUP database
7-O-Methylcryptochinone B 46939686 Click to see 314.30 unknown via CMAUP database
Cryptocaryanone A 10356404 Click to see C1C2C(C=CC3=C2C(=O)CC(O3)C4=CC=CC=C4)OC1=O 282.29 unknown via CMAUP database
Cryptochinone A 46939683 Click to see 300.30 unknown via CMAUP database
Cryptochinone B 46939684 Click to see 300.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1'S,2R,4R)-10,11-dimethoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,6'-cyclohex-2-ene]-1'-ol 10914050 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC=CC4O)OC)OC 315.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate 5318033 Click to see 558.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 712318 Click to see 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown via CMAUP database
5-Hydroxy-3,7-dimethoxyflavone 5748697 Click to see 298.29 unknown via CMAUP database
Mosloflavone 471722 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)OC 298.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-3,7,8-trimethoxyflavone 21632881 Click to see 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2',4'-Dihydroxy-3'-methoxychalcone 9993268 Click to see 270.28 unknown via CMAUP database

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