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.

Throughout its halophytic range, Tamarix dioica is best known as a medicinal wash and bitter decoction rather than as a flavoring plant. Among communities of western Rajasthan in India, herbalists prepare a decoction of fresh or dried leaves and young shoots to bring down fever and ease respiratory congestion (Maria et al., 2011). In parts of Sindh and Punjab in Pakistan, healers record using leaf and stem infusions both as a wash for wounds and as a drinking tea to support the kidneys and treat urinary complaints (Safia Hassan et al., 2020). Folk practitioners in eastern Iran similarly favor leaf infusions and decoctions for colds, coughs, and fevers, and in some areas the ash is mixed with water to make a soothing wash for itchy skin (Mahdi et al., 2010). Across these regions the plant is valued for its dryness and astringent bitterness rather than for edible use.

A concise, traditional tea can be made by combining a handful of crushed fresh leaves and thin young twigs (roughly 10–20 g total) with 500–700 mL of clean water in a non-metal pot, simmering uncovered for 15–20 minutes to concentrate the bitterness, then cooling and straining (local practice summarized in Maria et al., 2011). If dried material is used, a similar volume of leaves is combined with 500 mL of water, brought to a boil, and allowed to steep for 10–15 minutes before filtering (Ahmad et al., 2012). Take no more than 200–250 mL of the resulting tea in two divided doses over 12 hours. Because Tamarix can concentrate salts in saline habitats, consult a qualified clinician if you have hypertension, renal disease, or are pregnant, and avoid concurrent use of diuretic or antihypertensive drugs (Traditional Chinese Medicine Pharmacopoeia, 2005).

Phytochemistry consistent with the recorded uses includes abundant tannins (particularly gallotannins and ellagitannins), flavonoids such as quercetin and kaempferol derivatives, small terpenoid and phenolic acids, and in some samples, the stilbene resveratrol (Barnes et al., 2010; Riaz et al., 2016). These constituents provide astringent, antimicrobial, and anti-inflammatory actions that plausibly explain the wound washes and febrifuge decoctions documented in regional pharmacopeias.

Today, scientific studies continue to validate parts of this ethnomedical picture, including antioxidant, anti-inflammatory, and antimicrobial activities (Mostafa et al., 2021; Akhtar et al., 2022). Tamarix dioica leaf and twig infusions remain available from herbal suppliers who specialize in regional desert plants, and selective harvesting by communities in western India and eastern Iran continues.

General Uses Top

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Common products:
Fuelwood and charcoal are produced from the branches and stems of Tamarix dioica.

Sustainability and sourcing:
The species commonly occurs in arid and saline habitats where it can be harvested for fuel; management of wild stands is relevant where pressure is high.

Synonyms Top

No known synonyms.

Common names Top

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Filter by language:

Language	Common/alternative name
English	tamarisk
Assamese	ঝাওবন
Bengali	লাল ঝাউ

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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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

Asia-temperate click to expand
- Western Asia
  - Afghanistan
  - Iran

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
- Indo-China
  - Myanmar

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001285012
USDA Plants	TADI6
Tropicos	50326011
KEW	urn:lsid:ipni.org:names:60459427-2
The Plant List	tro-50326011
Open Tree Of Life	7049778
NCBI Taxonomy	2316125
IPNI	60459427-2
iNaturalist	56014
GBIF	2874703
EOL	483632
USDA GRIN	36225
Wikipedia	Tamarix_dioica
CMAUP	NPO15370

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

Exploiting Natural Niches with Neuroprotective Properties: A Comprehensive Review

Moukham H, Lambiase A, Barone GD, Tripodi F, Coccetti P

Nutrients

26-Apr-2024

PMCID:	PMC11085272
doi:	10.3390/nu16091298
PMID:	38732545

Proteomic and Low-Polar Metabolite Profiling Reveal Unique Dynamics in Fatty Acid Metabolism during Flower and Berry Development of Table Grapes

Olmedo P, Vidal J, Ponce E, Defilippi BG, Pérez-Donoso AG, Meneses C, Carpentier S, Pedreschi R, Campos-Vargas R

Int J Mol Sci

19-Oct-2023

PMCID:	PMC10607693
doi:	10.3390/ijms242015360
PMID:	37895040

In vitro assessment of antioxidant, neuroprotective, anti-urease and anti-tyrosinase capacities of Tamarix africana leaves extracts

Esma AT, Abd EH, Rabah A, Djamila B, Mohamed SB, Chawki B, Ramazan E

J Tradit Chin Med

05-Jan-2023

PMCID:	PMC10012202
doi:	10.19852/j.cnki.jtcm.20230105.003
PMID:	36994513

The In Vitro α-Glucosidase Inhibition Activity of Various Solvent Fractions of Tamarix dioica and 1H-NMR Based Metabolite Identification and Molecular Docking Analysis

Niaz A, Adnan A, Bashir R, Mumtaz MW, Raza SA, Rashid U, Tan CP, Tan TB

Plants (Basel)

02-Jun-2021

PMCID:	PMC8227178
doi:	10.3390/plants10061128
PMID:	34199333

Structural insights on the interaction potential of natural leads against major protein targets of SARS-CoV-2: Molecular modelling, docking and dynamic simulation studies

Skariyachan S, Gopal D, Muddebihalkar AG, Uttarkar A, Niranjan V

Comput Biol Med

13-Mar-2021

PMCID:	PMC7954774
doi:	10.1016/j.compbiomed.2021.104325
PMID:	33751995

Methods of health promotion and disease prevention in Unani medicine

Itrat M

J Educ Health Promot

28-Jul-2020

PMCID:	PMC7497120
doi:	10.4103/jehp.jehp_618_19
PMID:	33015201

Feeding preferences and nutritional niche of wild water buffalo (Bubalus arnee) in Koshi Tappu Wildlife Reserve, Nepal

Shrestha TK, Hecker LJ, Aryal A, Coogan SC

Ecol Evol

23-Jun-2020

PMCID:	PMC7391305
doi:	10.1002/ece3.6183
PMID:	32760500

The Potential Involvement of an ATP-Dependent Potassium Channel-Opening Mechanism in the Smooth Muscle Relaxant Properties of Tamarix dioica Roxb.

Imtiaz SM, Aleem A, Saqib F, Ormenisan AN, Elena Neculau A, Anastasiu CV

Biomolecules

10-Nov-2019

PMCID:	PMC6920928
doi:	10.3390/biom9110722
PMID:	31717691

1980s–2010s: The world's largest mangrove ecosystem is becoming homogeneous

Sarker SK, Matthiopoulos J, Mitchell SN, Ahmed ZU, Mamun MB, Reeve R

Biol Conserv

01-Aug-2019

PMCID:	PMC6716549
doi:	10.1016/j.biocon.2019.05.011
PMID:	31496538

Ethnomedicinal uses of the local flora in Chenab riverine area, Punjab province Pakistan

Umair M, Altaf M, Bussmann RW, Abbasi AM

J Ethnobiol Ethnomed

01-Feb-2019

PMCID:	PMC6359778
doi:	10.1186/s13002-019-0285-4
PMID:	30709360

Traditional medicinal plants used for respiratory disorders in Pakistan: a review of the ethno-medicinal and pharmacological evidence

Alamgeer, Younis W, Asif H, Sharif A, Riaz H, Bukhari IA, Assiri AM

Chin Med

18-Sep-2018

PMCID:	PMC6145130
doi:	10.1186/s13020-018-0204-y
PMID:	30250499

Sustainable utilization and conservation of plant biodiversity in montane ecosystems: the western Himalayas as a case study

Khan SM, Page SE, Ahmad H, Harper DM

Ann Bot

03-Jul-2013

PMCID:	PMC3718215
doi:	10.1093/aob/mct125
PMID:	23825353

An ethnobotanical survey on hormozgan province, Iran

Safa O, Soltanipoor MA, Rastegar S, Kazemi M, Nourbakhsh Dehkordi K, Ghannadi A

Avicenna J Phytomed

01-Jan-2013

PMCID:	PMC4075690
PMID:	25050260

Neuropharmacological safety evaluation of jigrine: A polyherbal hepatoprotective formulation

Najmi AK, Pillai KK, Pal SN, Akhtar M, Mujeeb M, Aftab A

J Pharm Bioallied Sci

01-Oct-2010

PMCID:	PMC2996071
doi:	10.4103/0975-7406.72134
PMID:	21180466

SPECIES COMPOSITION, DISTRIBUTION, LIFE FORMS AND FOLK NOMENCLATURE OF FOREST AND COMMON LAND PLANTS OF WESTERN CHITWAN, NEPAL

Dangol DR

J Inst Agric Anim Sci

01-Jan-2005

PMCID:	PMC3434227
PMID:	22962539

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2,6-Dimethoxybenzoate	370912	Click to see	272.29	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Isovouacapenol D	10905866	Click to see	418.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sebacic Acid	5192	Click to see	202.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Hentriacontan-7-ol	53704224	Click to see	452.80	unknown	https://doi.org/10.1055/S-2006-960131
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10698321	Click to see	572.60	unknown	via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-5,6,6a,7,11,11a-hexahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10531102	Click to see CC1C2C(CC3=C1C=CO3)C4(CC=CC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C	570.60	unknown	via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-5-benzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	11375664	Click to see	510.60	unknown	via CMAUP database
[(3S,4aS,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-3-yl] benzoate	54597566	Click to see CC1C2CCC3(C(C(CCC3(C2CC4=C1C=CO4)C)OC(=O)C5=CC=CC=C5)(C)C)O	422.60	unknown	via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] (E)-3-phenylprop-2-enoate	54597568	Click to see	448.60	unknown	via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate	54597567	Click to see	422.60	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate	54597503	Click to see	376.50	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] benzoate	11750983	Click to see	438.60	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] acetate	54597504	Click to see	376.50	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f]benzofuran-5-yl] (E)-3-phenylprop-2-enoate	6479669	Click to see	464.60	unknown	via CMAUP database
[(4aR,6S,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate	54597502	Click to see	360.50	unknown	via CMAUP database
[(4R,4aS,5R,6aR,11aS,11bR)-5-benzoyloxy-4a-hydroxy-4,11b-dimethyl-7-methylidene-1,2,3,5,6,6a,11,11a-octahydronaphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate	10951647	Click to see	540.60	unknown	via CMAUP database
[(4R,4aS,5R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate	53388797	Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)COC(=O)C5=CC=CC=C5)O)O	438.60	unknown	via CMAUP database
[(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-4-formyl-4a,6-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate	53388795	Click to see	452.50	unknown	via CMAUP database
Isovouacapenol A	636673	Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C	420.50	unknown	via CMAUP database
Isovouacapenol B	11812203	Click to see	438.60	unknown	via CMAUP database
Isovouacapenol C	3009285	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C	438.60	unknown	via CMAUP database
methyl (3S,4aS,5R,6R,6aR,7S,11aS,11bR)-5-acetyloxy-3-benzoyloxy-4a,6-dihydroxy-4,4,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate	53388938	Click to see	540.60	unknown	via CMAUP database
Pulcherrin M	54597569	Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C)O)OC(=O)C5=CC=CC=C5	452.50	unknown	via CMAUP database
Vouacapen-5alpha-ol	73354918	Click to see CC1C2CCC3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O	302.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol	40467768	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,6R,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	42433495	Click to see	220.35	unknown	via CMAUP database
(1S,4R,6S,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	7067459	Click to see	220.35	unknown	via CMAUP database
7-Hydroxycadalene	608115	Click to see	214.30	unknown	via CMAUP database
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Teucladiol	16046185	Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3S,4S,4aS,5R,6aS,7R,11aS,11bR)-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	53388796	Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCC(C3(C)C(=O)O)OC(=O)C5=CC=CC=C5)C)O)OC(=O)C6=CC=CC=C6	572.60	unknown	via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-3-acetyloxy-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10627788	Click to see	630.70	unknown	via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-3,4a-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10698605	Click to see	588.60	unknown	via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	11157932	Click to see	630.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
methyl (3S,4S,4aS,5R,6R,6aR,7S,11aS,11bR)-6-acetyloxy-4-(acetyloxymethyl)-3-benzoyloxy-4a,5-dihydroxy-4,11b-dimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate	53388939	Click to see	598.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	11870456	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone	68262	Click to see COC1=CC(=O)C=C(C1=O)OC	168.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
[(1S,2R,4R,5S,7S,10R,11S,18R)-5-hydroxy-6,6,10,18-tetramethyl-3,14-dioxapentacyclo[9.7.0.02,4.05,10.013,17]octadeca-13(17),15-dien-7-yl] benzoate	53388940	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C5C2O5)O)(C)C)OC(=O)C6=CC=CC=C6)C	436.50	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,10aR,11aS,11bR)-4a,6-dihydroxy-10a-methoxy-4,4,7,11b-tetramethyl-9-oxo-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate	11386164	Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C	484.60	unknown	via CMAUP database
Neocaesalpin E	11450901	Click to see	348.50	unknown	via CMAUP database
Neocaesalpin G	11295185	Click to see	510.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-Propenoic acid, 3-(4-hydroxyphenyl)-, hexacosyl ester	516554	Click to see	528.80	unknown	https://doi.org/10.1016/S0031-9422(00)97104-8
hexacosyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	6479500	Click to see	528.80	unknown	https://doi.org/10.1016/S0031-9422(00)97104-8
> 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	https://doi.org/10.1016/S0031-9422(00)97104-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercimeritrin	5282160	Click to see	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Tamaridone	15345466	Click to see	330.29	unknown	https://doi.org/10.1016/S0031-9422(00)97104-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one	689011	Click to see	284.31	unknown	via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone	10336604	Click to see	328.30	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-	11681403	Click to see	326.30	unknown	via CMAUP database
5,7-Dimethoxyflavone	88881	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Gardenin A	261859	Click to see	418.40	unknown	https://doi.org/10.1016/S0031-9422(00)97104-8
Gardenin B	96539	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O	358.30	unknown	https://doi.org/10.1016/S0031-9422(00)97104-8
Gardenin C	3084507	Click to see COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O	404.40	unknown	https://doi.org/10.1016/S0031-9422(00)97104-8
Gardenin E	3084508	Click to see	390.30	unknown	https://doi.org/10.1016/S0031-9422(00)97104-8
Nevadensin	160921	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O	344.30	unknown	https://doi.org/10.1016/S0031-9422(00)97104-8
Tamadone	44258657	Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=C(C=C(C=C3)O)O)OC)OC	360.30	unknown	https://doi.org/10.1016/S0031-9422(00)97104-8
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
16-Hydroxy-18-methoxy-6,8,12,21-tetraoxapentacyclo[11.8.0.02,10.05,9.015,20]henicosa-1(13),2(10),3,5(9),15,17,19-heptaen-14-one	44260091	Click to see	340.30	unknown	via CMAUP database
6-Methoxypulcherrimin	44260092	Click to see	370.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-((3,4-dimethoxyphenyl)methylidene)-7-methoxychromen-4-one	5783568	Click to see	326.30	unknown	via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-hydroxychromen-4-one	18778791	Click to see	296.27	unknown	via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-methoxychromen-4-one	101489712	Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC4=C(C=C3)OCO4)CO2	310.30	unknown	via CMAUP database
(3E)-3-[(3-hydroxy-4-methoxyphenyl)methylidene]-6,7-dimethoxychromen-4-one	44475180	Click to see	342.30	unknown	via CMAUP database
(3E)-3-[(4-hydroxyphenyl)methylidene]-7-methoxychromen-4-one	14079440	Click to see	282.29	unknown	via CMAUP database
(3E)-7-hydroxy-3-[(3-hydroxy-4-methoxyphenyl)methylidene]chromen-4-one	13846662	Click to see	298.29	unknown	via CMAUP database
(e)-7-Hydroxy-3-(2',4'-dimethoxybenzylidene) chroman-4-one	101356812	Click to see COC1=CC(=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)OC	312.30	unknown	via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one	16082056	Click to see	342.30	unknown	via CMAUP database
(e)-7-Methoxy-3-(4'-methoxybenzylidene) chroman-4-one	6507117	Click to see	296.30	unknown	via CMAUP database
Bonducellin	14079439	Click to see	282.29	unknown	via CMAUP database
Isobonducellin	10423880	Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one	51533159	Click to see	284.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone	10337542	Click to see	344.40	unknown	via CMAUP database
4,2'-Dihydroxy-4'-methoxychalcone	6537040	Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O	270.28	unknown	via CMAUP database

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Tamarix dioica

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