Scientific name	Authority	First published in
Tamarix cretica	Bunge	Tent. Gen. Tamar. : 33 (1852)
Tamarix laxa var. subspicata	Ehrenb.	Linnaea 2: 254 1827
Tamarix rubella	Batt.	Bull. Soc. Bot. France 54: 256 (1907)
Tamarix lucronensis	Sennen & Elias	Bol. Soc. Ibér. Ci. Nat. 27: 67 (1928)

Common names Top

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Filter by language:

Language	Common/alternative name
English	smallflower tamarisk
Czech	tamaryšek malokvětý
German	kleinblütige tamariske
Esperanto	malgrandflora tamariko
Persian	گز گلریز
Upper Sorbian	nalětnja tamariska
Hungarian	kisvirágú tamariska
Portuguese	cedro-do-sal
Portuguese	tamargueira
Slovenian	drobnocvetna tamariša
Swedish	junitamarisk
Chinese	小花柽柳

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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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

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Algeria
  - Libya
- Southern Africa
  - Cape Provinces

Asia-temperate click to expand
- Western Asia
  - East Aegean Islands
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan
  - West Himalaya

Europe click to expand
- Middle Europe
  - Austria
- Southeastern Europe
  - Albania
  - Greece
  - Italy
  - Kriti
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - Spain

Northern America click to expand
- Mexico
  - Mexico Northwest
- North-central U.S.A.
  - Illinois
  - Kansas
  - Oklahoma
- Northeastern U.S.A.
  - New York
- Northwestern U.S.A.
  - Colorado
  - Oregon
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Kentucky
  - Maryland
  - Mississippi
  - North Carolina
- Southwestern U.S.A.
  - Arizona
  - California
  - Nevada

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000458666
Canadensys	9399
USDA Plants	TAPA4
UConn	493
Tropicos	31100007
INPN	125437
Flora of Italy	3292
KEW	urn:lsid:ipni.org:names:828188-1
The Plant List	kew-2520133
PFAF	Tamarix parviflora
Open Tree Of Life	674341
Observations.org	137731
NCBI Taxonomy	189801
NBN Atlas	NBNSYS0200003282
Nature Serve	2.155916
IUCN Red List	19179463
IPNI	828188-1
iNaturalist	56011
GBIF	2874706
Freebase	/m/0dgnyng
EPPO	TAAPA
EOL	585678
Elurikkus	323004
Calflora (Californian flora)	7916
USDA GRIN	103148
Wikipedia	Tamarix_parviflora

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

A Circular Economy Approach to Restoring Soil Substrate Ameliorated by Sewage Sludge with Amendments

Halecki W, López-Hernández NA, Koźmińska A, Ciarkowska K, Klatka S

Int J Environ Res Public Health

27-Apr-2022

PMCID:	PMC9103250
doi:	10.3390/ijerph19095296
PMID:	35564693

Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections

Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM

Plants (Basel)

04-Jul-2021

PMCID:	PMC8309379
doi:	10.3390/plants10071367
PMID:	34371570

Storage Period and Different Abiotic Factors Regulate Seed Germination of Two Apocynum Species — Cash Crops in Arid Saline Regions in the Northwestern China

Jiang L, She C, Tian C, Tanveer M, Wang L

Front Plant Sci

17-Jun-2021

PMCID:	PMC8248540
doi:	10.3389/fpls.2021.671157
PMID:	34220893

Aplication of Soil Productivity Index after Eight Years of Soil Reclamation with Sewage Sludge Amendments

Halecki W, Klatka S

Environ Manage

18-Jan-2021

PMCID:	PMC8032590
doi:	10.1007/s00267-020-01422-1
PMID:	33462681

A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens

Frey D, Moretti M

Data Brief

23-May-2019

PMCID:	PMC6545399
doi:	10.1016/j.dib.2019.103982
PMID:	31194048

The Development of a Plant Risk Evaluation (PRE) Tool for Assessing the Invasive Potential of Ornamental Plants

Conser C, Seebacher L, Fujino DW, Reichard S, DiTomaso JM

PLoS One

24-Mar-2015

PMCID:	PMC4372384
doi:	10.1371/journal.pone.0121053
PMID:	25803830

Persistent hamathecial threads in the Nectriaceae, Hypocreales: Thyronectria revisited and re-instated

Jaklitsch WM, Voglmayr H

Persoonia

09-Oct-2014

PMCID:	PMC4312933
doi:	10.3767/003158514X685211
PMID:	25737600

Plants as Useful Vectors to Reduce Environmental Toxic Arsenic Content

Mirza N, Mahmood Q, Maroof Shah M, Pervez A, Sultan S

ScientificWorldJournal

09-Jan-2014

PMCID:	PMC3913097
doi:	10.1155/2014/921581
PMID:	24526924

Hydrolyzable tannins of tamaricaceous plants. IV: Micropropagation and ellagitannin production in shoot cultures of Tamarix tetrandra.

Orabi MA, Taniguchi S, Terabayashi S, Hatano T

Phytochemistry

01-Nov-2011

doi:	10.1016/J.PHYTOCHEM.2011.07.011
PMID:	21831401

Occurrence and stress response of N-methylproline compounds in Tamarix species.

Jones GP, Naidu BP, Waisel Y, Solomon A, Paleg LG

Phytochemistry

01-Jan-2006

doi:	10.1016/J.PHYTOCHEM.2005.10.027
PMID:	16359712

Hybrid Tamarix widespread in U.S. invasion and undetected in native Asian range

Gaskin JF, Schaal BA

Proc Natl Acad Sci U S A

12-Aug-2002

PMCID:	PMC123243
doi:	10.1073/pnas.132403299
PMID:	12177412

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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
1-Methylpyrrolidine-2-carboxylic acid	557	Click to see CN1CCCC1C(=O)O	129.16	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.027
N-Methyl-L-proline	643474	Click to see CN1CCCC1C(=O)O	129.16	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.027
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[4-[[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl]oxycarbonyl]-2,6-dihydroxyphenoxy]-3,4,5-trihydroxybenzoate	155559851	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)OC4=C(C(=C(C=C4C(=O)OC5C(C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC5OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1875.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
[(11R,12S,13R,31R,33S,50R,51S,52R,70R,72S)-4,5,6,18,19,20,23,24,25,38,39,43,44,45,57,58,59,62,63,64,77,78-docosahydroxy-9,15,28,35,48,54,67,74-octaoxo-51-(3,4,5-trihydroxybenzoyl)oxy-2,10,14,29,32,34,41,49,53,68,71,73-dodecaoxatridecacyclo[73.3.1.136,40.03,8.011,33.013,31.016,21.022,27.042,47.050,72.052,70.055,60.061,66]octaconta-1(79),3,5,7,16,18,20,22,24,26,36,38,40(80),42,44,46,55,57,59,61,63,65,75,77-tetracosaen-12-yl] 3,4,5-trihydroxybenzoate	16143906	Click to see C1C2C(C(C3C(O2)OC(=O)C4=CC(=C(C(=C4)OC5=C(C(=C(C=C5C(=O)OC6C(C7C(COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC6OC(=O)C2=CC(=C(C(=C2)OC2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate	5153915	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[[4,5,18,19,20,23,24,25,38,39-decahydroxy-9,15,28,35-tetraoxo-12-(3,4,5-trihydroxybenzoyl)oxy-2,10,14,29,32,34-hexaoxaheptacyclo[34.3.1.03,8.011,33.013,31.016,21.022,27]tetraconta-1(40),3,5,7,16,18,20,22,24,26,36,38-dodecaen-6-yl]oxy]-3,4,5-trihydroxybenzoate	139600674	Click to see C1C2C(C(C3C(O2)OC(=O)C4=CC(=C(C(=C4)OC5=C(C(=C(C=C5C(=O)O3)OC6=C(C(=C(C=C6C(=O)OC7C(C8C(COC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O8)O)O)O)O)O)O)OC7OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[4-[[3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl]oxycarbonyl]-2,6-dihydroxyphenoxy]-3,4,5-trihydroxybenzoate	162991523	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)OC4=C(C(=C(C=C4C(=O)OC5C(C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC5OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1875.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[5-[[3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxybenzoate	163007941	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)OC4=C(C(=C(C=C4C(=O)OC5C(C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC5OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1875.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
[4,5,6,18,19,20,23,24,25,38,39,43,44,45,57,58,59,62,63,64,77,78-Docosahydroxy-9,15,28,35,48,54,67,74-octaoxo-12-(3,4,5-trihydroxybenzoyl)oxy-2,10,14,29,32,34,41,49,53,68,71,73-dodecaoxatridecacyclo[73.2.2.136,40.03,8.011,33.013,31.016,21.022,27.042,47.050,72.052,70.055,60.061,66]octaconta-1(77),3,5,7,16,18,20,22,24,26,36,38,40(80),42,44,46,55,57,59,61,63,65,75,78-tetracosaen-51-yl] 3,4,5-trihydroxybenzoate	162887665	Click to see C1C2C(C(C3C(O2)OC(=O)C4=CC(=C(C(=C4)O)OC5=C(C(=C(C=C5C(=O)OC6C(C7C(COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC6OC(=O)C2=CC(=C(C(=C2)OC2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
[4,5,6,18,19,20,23,24,25,38,42,43,44,56,57,58,61,62,63,76,77,79-Docosahydroxy-9,15,28,35,47,53,66,73-octaoxo-50-(3,4,5-trihydroxybenzoyl)oxy-2,10,14,29,32,34,40,48,52,67,70,72-dodecaoxatridecacyclo[72.2.2.236,39.03,8.011,33.013,31.016,21.022,27.041,46.049,71.051,69.054,59.060,65]octaconta-1(76),3,5,7,16,18,20,22,24,26,36,38,41,43,45,54,56,58,60,62,64,74,77,79-tetracosaen-12-yl] 3,4,5-trihydroxybenzoate	163052251	Click to see C1C2C(C(C3C(O2)OC(=O)C4=CC(=C(C(=C4)O)OC5=C(C(=C(C=C5C(=O)OC6C(C7C(COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC6OC(=O)C2=CC(=C(C(=C2)O)OC2=C(C(=C(C=C2C(=O)O3)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
1-Desgalloyleugeniin	9918701	Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
3-[6-[[(10R,11S,12R,13R,15R)-3,4,5,21,22,23-hexahydroxy-13-methoxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl]oxycarbonyl]-2,3,4-trihydroxyphenoxy]-4,5-dihydroxybenzoic acid	102163696	Click to see COC1C(C(C2C(O1)COC(=O)C3=CC(=C(C(=C3C4=C(C(=C(C=C4C(=O)O2)O)O)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6OC7=CC(=CC(=C7O)O)C(=O)O)O)O)O	968.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
3-[6-[[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl]oxycarbonyl]-2,3,4-trihydroxyphenoxy]-4,5-dihydroxybenzoic acid	46894058	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4OC5=CC(=CC(=C5O)O)C(=O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	1106.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
3-[6-[[3,4,5,21,22,23-Hexahydroxy-13-methoxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl]oxycarbonyl]-2,3,4-trihydroxyphenoxy]-4,5-dihydroxybenzoic acid	162896358	Click to see COC1C(C(C2C(O1)COC(=O)C3=CC(=C(C(=C3C4=C(C(=C(C=C4C(=O)O2)O)O)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6OC7=CC(=CC(=C7O)O)C(=O)O)O)O)O	968.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
Eugeniin	442679	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	938.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
Hirtellin A	16130371	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)OC4=C(C(=C(C=C4C(=O)OC5C(C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC5OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1875.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
Hirtellin B	16133926	Click to see C1C2C(C(C3C(O2)OC(=O)C4=CC(=C(C(=C4)OC5=C(C(=C(C=C5C(=O)O3)OC6=C(C(=C(C=C6C(=O)OC7C(C8C(COC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O8)O)O)O)O)O)O)OC7OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
Hirtellin C	16130408	Click to see C1C2C(C(C3C(O2)OC(=O)C4=CC(=C(C(=C4)O)OC5=C(C(=C(C=C5C(=O)OC6C(C7C(COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC6OC(=O)C2=CC(=C(C(=C2)OC2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
Isohirtellin C	16130420	Click to see C1C2C(C(C3C(O2)OC(=O)C4=CC(=C(C(=C4)OC5=C(C(=C(C=C5C(=O)OC6C(C7C(COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC6OC(=O)C2=CC(=C(C(=C2)OC2=C(C(=C(C=C2C(=O)O3)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
Remurin A	16130314	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4OC5=CC(=CC(=C5O)O)C(=O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	1106.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
Tamarixinin B	16131652	Click to see C1C2C(C(C3C(O2)OC(=O)C4=CC(=C(C(=C4)O)OC5=C(C(=C(C=C5C(=O)OC6C(C7C(COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC6OC(=O)C2=CC(=C(C(=C2)O)OC2=C(C(=C(C=C2C(=O)O3)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1873.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011
Tellimagrandin II	151590	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	938.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2011.07.011

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Tamarix parviflora

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