Acanthospermum australe

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643fd15c3a4ee407131100
Scientific name	Acanthospermum australe
Authority	(Loefl.) Kuntze
First published in	Revis. Gen. Pl. 1: 303. 1891 [5 Nov 1891]

Description Top

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Acanthospermum australe, also known as Paraguayan starburr, is a herbaceous plant species that was first described in 1758. It is native to South America, including countries such as Brazil, Argentina, and Paraguay, as well as some Caribbean islands. However, it has also been introduced in other parts of the world, such as China, and has become an invasive species in the United States, Canada, and South Africa. This plant is known for its antiviral properties, with extracts showing activity against herpesvirus and poliovirus in laboratory studies. However, its effects on humans have not been studied. Acanthospermum australe is commonly found in tropical and sub-tropical regions, where it is considered a pioneer species.

Synonyms Top

Scientific name	Authority	First published in
Acanthospermum xanthioides	DC.	Prodr. 5: 521 (1836)
Centrospermum xanthioides	Kunth	Nov. Gen. Sp. 4: 213 (1818)
Orcya adhaerescens	Vell.	Fl. Flumin. : 345 (1825)
Echinodium prostratum	Poit.
Acanthospermum brasilum	Schrank	Pl. Rar. Hort. Monac. 2(6): 53 (1820)
Melampodium australe	Loefl.	Iter Hispan. : 268 (1758)
Acanthospermum hirsutum	DC.	Prodr.
Orcya adhaerens	Vell.	Fl. Flumin. : 345 (1825)

Common names Top

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Filter by language:

Language	Common/alternative name
English	paraguayan starbur
English	paraguay bur
English	paraguay burr
English	paraguayan starburr
English	sheepbur
English	spiny-bur
English	spiny-burr
Spanish	tapekue
gn	tapekue
Chinese	刺苞果
Chinese	南方刺苞果

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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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
- South Tropical Africa
  - Angola
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Cape Provinces
  - Kwazulu-Natal
  - Northern Provinces
  - Swaziland
- West-central Tropical Africa
  - Cameroon
  - Zaïre

Asia-tropical click to expand
- Malesia
  - Malaya

Australasia click to expand
- Australia
  - New South Wales
  - Queensland

Northern America click to expand
- Northeastern U.S.A.
  - Massachusetts
  - New York
  - Pennsylvania
- Northwestern U.S.A.
  - Oregon
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Florida
  - Georgia
  - Louisiana
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Venezuelan Antilles
  - Windward Islands
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia
  - Colombia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000114552
UNII	DQ0373SW6A
Florida Plant Atlas	1712
Flora of Alabama	494
USDA Plants	ACAU2
Tropicos	2717091
INPN	629007
KEW	urn:lsid:ipni.org:names:1692-2
The Plant List	gcc-76043
Open Tree Of Life	633173
NCBI Taxonomy	185140
NBN Atlas	NBNSYS0200001642
Nature Serve	2.150257
IPNI	1692-2
iNaturalist	147343
GBIF	3100364
Freebase	/m/02qch_4
EPPO	ACNAU
EOL	468842
USDA GRIN	316532
Wikipedia	Acanthospermum_australe

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 antioxidant potential of endophytic fungi: a review on methods for extraction and quantification of total antioxidant capacity (TAC)

Asomadu RO, Ezeorba TP, Ezike TC, Uzoechina JO

3 Biotech

05-Apr-2024

PMCID:	PMC10997672
doi:	10.1007/s13205-024-03970-3
PMID:	38585410

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Meloidogyne enterolobii risk to agriculture, its present status and future prospective for management

Sikandar A, Jia L, Wu H, Yang S

Front Plant Sci

24-Jan-2023

PMCID:	PMC9902769
doi:	10.3389/fpls.2022.1093657
PMID:	36762171

Biogenic silver nanoparticles as antifungal agents

Mussin J, Giusiano G

Front Chem

06-Oct-2022

PMCID:	PMC9583421
doi:	10.3389/fchem.2022.1023542
PMID:	36277355

Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review

Salazar-Gómez A, Alonso-Castro AJ

Pharmaceuticals (Basel)

31-Aug-2022

PMCID:	PMC9505834
doi:	10.3390/ph15091095
PMID:	36145316

Correction: Loredo Varela, R.C.; Fail, J. Host Plant Association and Distribution of the Onion Thrips, Thrips tabaci Cryptic Species Complex. Insects 2022, 13, 298

Loredo Varela RC, Fail J

Insects

07-May-2022

PMCID:	PMC9143062
doi:	10.3390/insects13050442
PMID:	35621825

Host Plant Association and Distribution of the Onion Thrips, Thrips tabaci Cryptic Species Complex

Loredo Varela RC, Fail J

Insects

17-Mar-2022

PMCID:	PMC8952806
doi:	10.3390/insects13030298
PMID:	35323598

Screening of Natural Products Inhibitors of SARS-CoV-2 Entry

González-Maldonado P, Alvarenga N, Burgos-Edwards A, Flores-Giubi ME, Barúa JE, Romero-Rodríguez MC, Soto-Rifo R, Valiente-Echeverría F, Langjahr P, Cantero-González G, Sotelo PH

Molecules

07-Mar-2022

PMCID:	PMC8911944
doi:	10.3390/molecules27051743
PMID:	35268843

Endophytic Fungi: An Effective Alternative Source of Plant-Derived Bioactive Compounds for Pharmacological Studies

Wen J, Okyere SK, Wang S, Wang J, Xie L, Ran Y, Hu Y

J Fungi (Basel)

20-Feb-2022

PMCID:	PMC8877053
doi:	10.3390/jof8020205
PMID:	35205959

The Emerging Role of Ionic Liquid-Based Approaches for Enhanced Skin Permeation of Bioactive Molecules: A Snapshot of the Past Couple of Years

Gomes A, Aguiar L, Ferraz R, Teixeira C, Gomes P

Int J Mol Sci

05-Nov-2021

PMCID:	PMC8584570
doi:	10.3390/ijms222111991
PMID:	34769430

Dataset, including a photo-guide, of alien plants sold in traditional medicine markets and healthcare outlets in three South African cities, specifically by traders of Indian, West African, East African, and Chinese origin

Williams VL, Burness A, Wojtasik EM, Byrne MJ

Data Brief

21-Sep-2021

PMCID:	PMC8479245
doi:	10.1016/j.dib.2021.107395
PMID:	34621926

Antimicrobial and cytotoxic activity of green synthesis silver nanoparticles targeting skin and soft tissue infectious agents

Mussin J, Robles-Botero V, Casañas-Pimentel R, Rojas F, Angiolella L, San Martín-Martínez E, Giusiano G

Sci Rep

15-Jul-2021

PMCID:	PMC8282796
doi:	10.1038/s41598-021-94012-y
PMID:	34267298

Natural product diversity from the endophytic fungi of the genus Aspergillus

El-hawary SS, Moawad AS, Bahr HS, Abdelmohsen UR, Mohammed R

RSC Adv

09-Jun-2020

PMCID:	PMC9054607
doi:	10.1039/d0ra04290k
PMID:	35516645

Yerba Mate (Ilex paraguariensis) Beverage: Nutraceutical Ingredient or Conveyor for the Intake of Medicinal Plants? Evidence from Paraguayan Folk Medicine

Kujawska M

Evid Based Complement Alternat Med

14-Mar-2018

PMCID:	PMC5872613
doi:	10.1155/2018/6849317
PMID:	29725356

Data on introduced plants in Zimbabwe: Floristic changes and patterns of collection based on historical herbarium records

Maroyi A

Data Brief

22-Sep-2017

PMCID:	PMC5712053
doi:	10.1016/j.dib.2017.09.046
PMID:	29214198

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 alcohol esters
[(E,6R)-6-hydroxy-3-methyl-6-[(2S)-2-methyl-6-(4-methylpent-3-enyl)-7-oxo-3,4-dihydrooxepin-2-yl]hex-2-enyl] acetate	162995282	Click to see CC(=CCCC1=CCCC(OC1=O)(C)C(CCC(=CCOC(=O)C)C)O)C	378.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
[6-Hydroxy-3-methyl-6-[2-methyl-6-(4-methylpent-3-enyl)-7-oxo-3,4-dihydrooxepin-2-yl]hex-2-enyl] acetate	162995281	Click to see CC(=CCCC1=CCCC(OC1=O)(C)C(CCC(=CCOC(=O)C)C)O)C	378.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2R)-2-[(E,1R)-1,6-dihydroxy-4-methylhex-4-enyl]-2-methyl-6-(4-methylpent-3-enyl)-3,4-dihydrooxepin-7-one	162874021	Click to see CC(=CCCC1=CCCC(OC1=O)(C)C(CCC(=CCO)C)O)C	336.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
(2S)-2-[(Z,1R)-1,6-dihydroxy-4-methylhex-4-enyl]-2-methyl-6-(4-methylpent-3-enyl)-3,4-dihydrooxepin-7-one	162874020	Click to see CC(=CCCC1=CCCC(OC1=O)(C)C(CCC(=CCO)C)O)C	336.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
2-(1,6-Dihydroxy-4-methylhex-4-enyl)-2-methyl-6-(4-methylpent-3-enyl)-3,4-dihydrooxepin-7-one	162874019	Click to see CC(=CCCC1=CCCC(OC1=O)(C)C(CCC(=CCO)C)O)C	336.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
> 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/10.1021/NP50050A054
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1021/NP50050A054
> 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 CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1021/NP50050A054
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	44583886	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	https://doi.org/10.1021/NP50050A054
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(-)-Germacrene A	9548706	Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C	204.35	unknown	https://doi.org/10.1021/NP50050A054
germacrene C	25244915	Click to see CC1=CCCC(=CC=C(CC1)C(C)C)C	204.35	unknown	https://doi.org/10.1021/NP50050A054
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,4S,5S,6E,10Z,11aR)-10-methyl-4,5-bis[[(Z)-2-methylbut-2-enoyl]oxy]-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylic acid	162887835	Click to see CC=C(C)C(=O)OC1C2C(C=C(CCC=C(C1OC(=O)C(=CC)C)C(=O)O)C)OC(=O)C2=C	458.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
(6-Formyl-10-methyl-3-methylidene-2-oxo-3a,4,9,11a-tetrahydrocyclodeca[b]furan-4-yl) 2-methylpropanoate	73190636	Click to see CC1=CC2C(C(C=C(C=CC1)C=O)OC(=O)C(C)C)C(=C)C(=O)O2	330.40	unknown	https://doi.org/10.1016/0040-4039(96)82932-7
[(3aR,4R,5E,7Z,10Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,9,11a-tetrahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate	10336745	Click to see CC1=CC2C(C(C=C(C=CC1)C=O)OC(=O)C(C)C)C(=C)C(=O)O2	330.40	unknown	https://doi.org/10.1016/0040-4039(96)82932-7
[(3aR,4S,5S,6E,10E,11aS)-6-formyl-10-methyl-3-methylidene-4-(2-methylpropanoyloxy)-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] 2-hydroxy-2-methylpropanoate	162878379	Click to see CC1=CC2C(C(C(C(=CCC1)C=O)OC(=O)C(C)(C)O)OC(=O)C(C)C)C(=C)C(=O)O2	434.50	unknown	https://doi.org/10.1021/JO00912A004
[(3aR,5E,7Z,10Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,9,11a-tetrahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate	101693153	Click to see CC1=CC2C(C(C=C(C=CC1)C=O)OC(=O)C(C)C)C(=C)C(=O)O2	330.40	unknown	https://doi.org/10.1016/0040-4039(96)82932-7
[(3aS,4R,5E,7Z,10Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,9,11a-tetrahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate	643651	Click to see CC1=CC2C(C(C=C(C=CC1)C=O)OC(=O)C(C)C)C(=C)C(=O)O2	330.40	unknown	https://doi.org/10.1016/0040-4039(96)82932-7
[(3aS,4S,5S,6E,10E,11aR)-6-formyl-10-(hydroxymethyl)-5-[(Z)-2-methylbut-2-enoyl]oxy-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate	162874253	Click to see CC=C(C)C(=O)OC1C2C(C=C(CCC=C(C1OC(=O)C(=CC)C)C=O)CO)OC(=O)C2=C	458.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
[(3aS,4S,5S,6E,10E,11aR)-6-formyl-10-methyl-3-methylidene-4-(2-methylpropanoyloxy)-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] 2-hydroxy-2-methylpropanoate	21593572	Click to see CC1=CC2C(C(C(C(=CCC1)C=O)OC(=O)C(C)(C)O)OC(=O)C(C)C)C(=C)C(=O)O2	434.50	unknown	https://doi.org/10.1021/JO00912A004
[(3aS,4S,5S,6E,10Z,11aR)-6-formyl-10-methyl-3-methylidene-4-(2-methylpropanoyloxy)-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] 2-hydroxy-2-methylpropanoate	131701322	Click to see CC1=CC2C(C(C(C(=CCC1)C=O)OC(=O)C(C)(C)O)OC(=O)C(C)C)C(=C)C(=O)O2	434.50	unknown	https://doi.org/10.1021/NP50050A054
[(3aS,4S,5S,6E,10Z,11aR)-6-formyl-5-methoxy-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate	93959096	Click to see CC1=CC2C(C(C(C(=CCC1)C=O)OC)OC(=O)C(C)C)C(=C)C(=O)O2	362.40	unknown	https://doi.org/10.1021/NP50050A054
[6-Formyl-10-(hydroxymethyl)-5-(2-methylbut-2-enoyloxy)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylbut-2-enoate	162874252	Click to see CC=C(C)C(=O)OC1C2C(C=C(CCC=C(C1OC(=O)C(=CC)C)C=O)CO)OC(=O)C2=C	458.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
[6-Formyl-10-methyl-3-methylidene-4-(2-methylpropanoyloxy)-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] 2-hydroxy-2-methylpropanoate	321966	Click to see CC1=CC2C(C(C(C(=CCC1)C=O)OC(=O)C(C)(C)O)OC(=O)C(C)C)C(=C)C(=O)O2	434.50	unknown	https://doi.org/10.1021/JO00912A004
10-Methyl-4,5-bis(2-methylbut-2-enoyloxy)-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carboxylic acid	162887834	Click to see CC=C(C)C(=O)OC1C2C(C=C(CCC=C(C1OC(=O)C(=CC)C)C(=O)O)C)OC(=O)C2=C	458.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
9-Hydroxyglabratolide	5991494	Click to see CC1=CC2C(C(C(C(=CCC1)C=O)O)OC(=O)C(C)C)C(=C)C(=O)O2	348.40	unknown	https://doi.org/10.1021/NP50050A054
Acanthamolide	118855998	Click to see CC1=CC2C(C(C(C(=CCC1)C=O)NC(=O)C(C)C)O)C(=C)C(=O)O2	347.40	unknown	https://doi.org/10.1021/NP50050A054
Dihydroacanthospermal A	5358826	Click to see CC1=CC2C(C(C(C(=CCC1)CO)OC(=O)C(C)(C)O)OC(=O)C(C)C)C(=C)C(=O)O2	436.50	unknown	https://doi.org/10.1021/JO00912A004
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(E)-5-[(2S,3R)-3-hydroxy-3-methyl-6-(4-methylpent-3-enyl)-7-oxo-2,4-dihydrooxepin-2-yl]-3-methylpent-2-enyl] acetate	163035402	Click to see CC(=CCCC1=CCC(C(OC1=O)CCC(=CCOC(=O)C)C)(C)O)C	364.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
[5-[3-Hydroxy-3-methyl-6-(4-methylpent-3-enyl)-7-oxo-2,4-dihydrooxepin-2-yl]-3-methylpent-2-enyl] acetate	163035401	Click to see CC(=CCCC1=CCC(C(OC1=O)CCC(=CCOC(=O)C)C)(C)O)C	364.50	unknown	https://doi.org/10.1016/0031-9422(81)83031-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3,4-Dihydroxy cinnamic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1248/CPB.35.1234
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1248/CPB.35.1234
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1248/CPB.35.1234
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1248/CPB.35.1234
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1248/CPB.35.1234
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1248/CPB.35.1234
Trifolin	5282149	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1248/CPB.35.1234
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1248/CPB.35.1234
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone	5352032	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O	330.29	unknown	https://doi.org/10.1248/CPB.35.1234
Axillarin	5281603	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O	346.30	unknown	https://doi.org/10.1021/NP50050A054
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
chrysoplenol D	5280699	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC	360.30	unknown	https://doi.org/10.1021/NP50050A054
Penduletin	5320462	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC	344.30	unknown	https://doi.org/10.1021/NP50050A054

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Acanthospermum australe

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