Scientific name	Authority	First published in
Eupatorium montevidense	Spreng.	Syst. Veg. 3: 417 (1826)
Baccharis montevidensis	Sch.Bip. ex Baker	Fl. Bras. 6(3): 57 (1882)
Lanugothamnus montevidensis	(Spreng.) Deble	Balduinia 37: 15 (2012)

Common names Top

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Filter by language:

Language	Common/alternative name
Quechua	miyu-miyu

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

Southern America click to expand
- Brazil
  - Brazil South
  - Brazil Southeast
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000005974
Tropicos	2700004
KEW	urn:lsid:ipni.org:names:183215-1
The Plant List	gcc-10575
Open Tree Of Life	7599897
NCBI Taxonomy	2707402
IPNI	183215-1
iNaturalist	563932
GBIF	3129366
EPPO	BACCO
USDA GRIN	6228

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

Antimicrobial activity in Asterceae: The selected genera characterization and against multidrug resistance bacteria

Gou J, Lu Y, Xie M, Tang X, Chen L, Zhao J, Li G, Wang H

Heliyon

31-Mar-2023

PMCID:	PMC10161380
doi:	10.1016/j.heliyon.2023.e14985
PMID:	37151707

Natural Compounds with Antimicrobial Properties in Cosmetics

Rybczyńska-Tkaczyk K, Grenda A, Jakubczyk A, Kiersnowska K, Bik-Małodzińska M

Pathogens

15-Feb-2023

PMCID:	PMC9959536
doi:	10.3390/pathogens12020320
PMID:	36839592

Plants causing poisoning outbreaks of livestock in South America: A review

Riet-Correa F, Machado M, Micheloud JF

Toxicon X

21-Jan-2023

PMCID:	PMC9898795
doi:	10.1016/j.toxcx.2023.100150
PMID:	36747993

The Symbiotic Fungus Leucoagaricus gongylophorus (Möller) Singer (Agaricales, Agaricaceae) as a Target Organism to Control Leaf-Cutting Ants

Araújo S, Seibert J, Ruani A, Alcántara-de la Cruz R, Cruz A, Pereira A, Zandonai D, Forim M, Silva MF, Bueno O, Fernandes J

Insects

06-Apr-2022

PMCID:	PMC9029082
doi:	10.3390/insects13040359
PMID:	35447801

A Phytosociological Study on Andean Rainforests of Peru, and a Comparison with the Surrounding Countries

Galán-de-Mera A, Campos-de-la-Cruz J, Linares-Perea E, Montoya-Quino J, Torres-Marquina I, Vicente-Orellana JA

Plants (Basel)

26-Nov-2020

PMCID:	PMC7761437
doi:	10.3390/plants9121654
PMID:	33256180

Chemopreventive Potential of Caryophyllane Sesquiterpenes: An Overview of Preliminary Evidence

Di Sotto A, Mancinelli R, Gullì M, Eufemi M, Mammola CL, Mazzanti G, Di Giacomo S

Cancers (Basel)

18-Oct-2020

PMCID:	PMC7603190
doi:	10.3390/cancers12103034
PMID:	33081075

Acute lead arsenate poisoning in beef cattle in Uruguay

Schild CO, Giannitti F, Medeiros RM, da Silva Silveira C, Caffarena RD, Poppenga RH, Riet-Correa F

J Vet Diagn Invest

08-Feb-2019

PMCID:	PMC6838832
doi:	10.1177/1040638719831413
PMID:	30734668

Cytotoxic Activity of Extracts from Plants of Central Argentina on Sensitive and Multidrug-Resistant Leukemia Cells: Isolation of an Active Principle from Gaillardia megapotamica

González ML, Joray MB, Laiolo J, Crespo MI, Palacios SM, Ruiz GM, Carpinella MC

Evid Based Complement Alternat Med

10-May-2018

PMCID:	PMC5971282
doi:	10.1155/2018/9185935
PMID:	29861776

Local ecological knowledge and its relationship with biodiversity conservation among two Quilombola groups living in the Atlantic Rainforest, Brazil

Conde BE, Ticktin T, Fonseca AS, Macedo AL, Orsi TO, Chedier LM, Rodrigues E, Pimenta DS

PLoS One

28-Nov-2017

PMCID:	PMC5705149
doi:	10.1371/journal.pone.0187599
PMID:	29182637

Flavonone treatment reverses airway inflammation and remodelling in an asthma murine model

Toledo A, Sakoda C, Perini A, Pinheiro N, Magalhães R, Grecco S, Tibério I, Câmara N, Martins M, Lago J, Prado C

Br J Pharmacol

12-Mar-2013

PMCID:	PMC3605879
doi:	10.1111/bph.12062
PMID:	23170811

Masked mycotoxins: A review

Berthiller F, Crews C, Dall'Asta C, Saeger SD, Haesaert G, Karlovsky P, Oswald IP, Seefelder W, Speijers G, Stroka J

Mol Nutr Food Res

10-Oct-2012

PMCID:	PMC3561696
doi:	10.1002/mnfr.201100764
PMID:	23047235

Essential Oil of Female Plants ofBaccharis coridifoliaDe Candole

Pedro N. Bailac, Alejandro D. Dellacasa, Hugo O. Bernasconi, Marta I. Ponzi, Norberto H. Firpo

Informa UK Limited

24-Apr-2012

doi:	10.1080/10412905.2001.9699593

Medicinal plants used for traditional veterinary in the Sierras de Córdoba (Argentina): An ethnobotanical comparison with human medicinal uses

Martínez GJ, Luján MC

J Ethnobiol Ethnomed

04-Aug-2011

PMCID:	PMC3163512
doi:	10.1186/1746-4269-7-23
PMID:	21816043

Macrocyclic Trichothecene Production by the Fungus Epibiont of Baccharis Coridifolia

M. Rosso, M. Maier, M. Bertoni

MDPI AG

27-Nov-2008

doi:	10.3390/50300345

Macrocyclische Trichothecene aus Baccharis coridifolia, II Miotoxin D und Isomiotoxin D, zwei neue macrocyclische Trichothecene aus Baccharis coridifolia DC

Gerhard G. Habermehl, Ludwig Busam, Manfred Spraul

Wiley

19-Jul-2007

doi:	10.1002/JLAC.198519850325

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 / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.2001.9699593
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.2001.9699593
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.2001.9699593
Isocaryophyllene	5281522	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.2001.9699593
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-Selinene	442393	Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C	204.35	unknown	https://doi.org/10.1080/10412905.2001.9699593
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Trichothecenes
(19Z,21Z)-18-(1-hydroxyethyl)-5,14,26-trimethylspiro[2,10,13,17,24-pentaoxapentacyclo[23.2.1.03,8.08,26.012,14]octacosa-4,19,21-triene-27,2'-oxirane]-11,23-dione	5883014	Click to see CC1=CC2C3(CC1)COC(=O)C4C(O4)(CCOC(C=CC=CC(=O)OC5C3(C6(CO6)C(C5)O2)C)C(C)O)C	530.60	unknown	https://doi.org/10.1016/S0041-0101(96)00149-3 https://doi.org/10.1021/NP50058A012
(1R,3R,8R,12E,15R,17S,18S,19E,21Z,25R,26S,27S)-5,13,17,26-tetramethylspiro[2,10,16,24,29-pentaoxapentacyclo[23.2.1.115,18.03,8.08,26]nonacosa-4,12,19,21-tetraene-27,2'-oxirane]-11,23-dione	139072267	Click to see CC1C2C=CC=CC(=O)OC3CC4C5(C3(C6(CCC(=CC6O4)C)COC(=O)C=C(CC(O1)O2)C)C)CO5	512.60	unknown	https://doi.org/10.1016/S0041-0101(96)00149-3
(1R,3R,8R,12R,13S,17R,18E,20Z,24R,25S,26S)-12-hydroxy-17-[(1S)-1-hydroxyethyl]-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,18,20-triene-26,2'-oxirane]-11,22-dione	162991007	Click to see CC1CCOC(C=CC=CC(=O)OC2CC3C4(C2(C5(CCC(=CC5O3)C)COC(=O)C1O)C)CO4)C(C)O	532.60	unknown	https://doi.org/10.3390/50300345
(1R,3R,8R,12S,13R,17R,18Z,20Z,24R,25S)-12-hydroxy-17-[(1R)-1-hydroxyethyl]-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,18,20-triene-26,2'-oxirane]-11,22-dione	139596298	Click to see CC1CCOC(C=CC=CC(=O)OC2CC3C4(C2(C5(CCC(=CC5O3)C)COC(=O)C1O)C)CO4)C(C)O	532.60	unknown	https://doi.org/10.1021/NP50058A012 https://doi.org/10.1016/0031-9422(91)85253-V https://doi.org/10.1016/0041-0101(85)90003-0 https://doi.org/10.1007/BF00396694
(1R,3R,8R,12Z,17R,18Z,20Z,24R,25S)-17-[(1R)-1-hydroxyethyl]-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,12,18,20-tetraene-26,2'-oxirane]-11,22-dione	139595713	Click to see CC1=CC2C3(CC1)COC(=O)C=C(CCOC(C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C(C)O)C	514.60	unknown	https://doi.org/10.1016/0031-9422(91)85253-V https://doi.org/10.1021/NP50058A012 https://doi.org/10.1007/BF00396694 https://doi.org/10.1016/0041-0101(85)90003-0
(1R,3R,8R,12Z,18Z,20Z,24R,25S,26S)-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,12,18,20-tetraene-26,2'-oxirane]-11,17,22-trione	23305159	Click to see CC1=CC2C3(CC1)COC(=O)C=C(CCOC(=O)C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C	484.50	unknown	https://doi.org/10.1021/NP50058A012 https://doi.org/10.1016/0031-9422(91)85253-V
(1R,3R,8R,12Z,18Z,20Z,24R,25S)-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,12,18,20-tetraene-26,2'-oxirane]-11,17,22-trione	139595166	Click to see CC1=CC2C3(CC1)COC(=O)C=C(CCOC(=O)C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C	484.50	unknown	https://doi.org/10.1021/NP50058A012 https://doi.org/10.1016/0031-9422(91)85253-V
(1R,3R,8R,13R,14S,17R,18E,20Z,24R,25S,26S)-14-hydroxy-17-[(1S)-1-hydroxyethyl]-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,18,20-triene-26,2'-oxirane]-11,22-dione	163080458	Click to see CC1CC(=O)OCC23CCC(=CC2OC4CC(C3(C45CO5)C)OC(=O)C=CC=CC(OCC1O)C(C)O)C	532.60	unknown	https://doi.org/10.1002/JLAC.198519850325
12-Hydroxy-5,13,25-trimethylspiro[2,10,16,23-tetraoxatetracyclo[22.2.1.03,8.08,25]heptacosa-4,18,20-triene-26,2'-oxirane]-11,17,22-trione	104830	Click to see CC1CCOC(=O)C=CC=CC(=O)OC2CC3C4(C2(C5(CCC(=CC5O3)C)COC(=O)C1O)C)CO4	502.60	unknown	https://doi.org/10.3390/50300345
CID 22524147	22524147	Click to see CC1CCOC(C=CC=CC(=O)OC2CC3C4(C2(C5(CCC(=CC5O3)C)COC(=O)C1O)C)CO4)C(C)O	532.60	unknown	https://doi.org/10.1016/0031-9422(91)85253-V https://doi.org/10.1016/0041-0101(85)90003-0 https://doi.org/10.1021/NP50058A012 https://doi.org/10.1016/S0041-0101(96)00149-3
CID 22524715	22524715	Click to see CC1C2C=CC=CC(=O)OC3CC4C5(C3(C6(CCC(=CC6O4)C)COC(=O)C=C(CC(O1)O2)C)C)CO5	512.60	unknown	https://doi.org/10.1016/S0041-0101(96)00149-3
Epiroridin E	11799977	Click to see CC1=CC2C3(CC1)COC(=O)C=C(CCOC(C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C(C)O)C	514.60	unknown	https://doi.org/10.3390/50300345
Miotoxin B	122201365	Click to see CC1CC(=O)OCC23CCC(=CC2OC4CC(C3(C45CO5)C)OC(=O)C=CC=CC(OCC1=O)C(C)O)C	530.60	unknown	https://doi.org/10.1016/0041-0101(85)90003-0
Miotoxin C	131634203	Click to see CC1=CC2C3(CC1)COC(=O)CC(C(COC(C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C(C)OC(=O)C)O)(C)O	590.70	unknown	https://doi.org/10.1016/0031-9422(91)85253-V https://doi.org/10.1016/0041-0101(85)90003-0
Muconomycin A	23304727	Click to see CC1CCOC(=O)C=CC=CC(=O)OC2CC3C4(C2(C5(CCC(=CC5O3)C)COC(=O)C1O)C)CO4	502.60	unknown	https://doi.org/10.1021/NP50058A012 https://doi.org/10.1016/0031-9422(91)85253-V https://doi.org/10.1016/S0041-0101(96)00149-3
Myotoxin A	56843811	Click to see CC1=CC2C3(CC1)COC(=O)C=C(C(COC(C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C(C)O)O)C	530.60	unknown	https://doi.org/10.1016/0041-0101(85)90003-0
Roridin D	5477986	Click to see CC1=CC2C3(CC1)COC(=O)C4C(O4)(CCOC(C=CC=CC(=O)OC5C3(C6(CO6)C(C5)O2)C)C(C)O)C	530.60	unknown	https://doi.org/10.1021/NP50058A012
Verrucarin A	6326658	Click to see CC1CCOC(=O)C=CC=CC(=O)OC2CC3C4(C2(C5(CCC(=CC5O3)C)COC(=O)C1O)C)CO4	502.60	unknown	https://doi.org/10.3390/50300345 https://doi.org/10.1016/0031-9422(91)85253-V https://doi.org/10.1021/NP50058A012
Verrucarin J	12444784	Click to see CC1=CC2C3(CC1)COC(=O)C=C(CCOC(=O)C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C	484.50	unknown	https://doi.org/10.3390/50300345
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides / Steviol glycosides
6beta-Hydroxypaniculoside III	98049792	Click to see CC12CCCC(C1C(CC34C2C(CC(C3)C(=C)C4=O)O)O)(C)C(=O)OC5C(C(C(C(O5)CO)O)O)O	510.60	unknown	https://doi.org/10.1002/JLAC.198419841015
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	293273	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	https://doi.org/10.1055/S-2007-969601
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1055/S-2007-969601
Uvaol	92802	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	https://doi.org/10.1055/S-2007-969601
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids
(E)-2-hydroxy-N-[(4E,8E)-3-hydroxy-9-methyl-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]hexadec-3-enamide	100925207	Click to see CCCCCCCCCCCCC=CC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=C(C)CCCCCCCCC)O)O	726.00	unknown	https://doi.org/10.1016/0041-0101(85)90003-0 https://doi.org/10.1016/0031-9422(91)85253-V
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[[(1S,2R,5S,7S,10R,11S,14R,15S,16R,17S,20S,23R)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosan-7-yl]peroxy]oxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	163023037	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CCC6C5(CCC(C6)OOC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C	1064.20	unknown	https://doi.org/10.1021/NP50058A012 https://doi.org/10.1016/0031-9422(91)85253-V https://doi.org/10.1016/0041-0101(85)90003-0 https://doi.org/10.1016/S0041-0101(96)00149-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
2-(Hydroxymethyl)-6-[[8-(6-hydroxy-6-methylhept-4-en-2-yl)-19-methoxy-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-yl]oxy]oxane-3,4,5-triol	78157516	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2C=CC5(C3CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)OC4OC)C)C	648.90	unknown	https://doi.org/10.3390/50300345
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[6-[3,5-Dihydroxy-2-(4-hydroxybenzoyl)phenoxy]-3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	75169192	Click to see C1=CC(=CC=C1C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O	712.60	unknown	https://doi.org/10.1016/0041-0101(85)90003-0
7-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxy-5-hydroxy-6,8-dimethylchromen-4-one	162964804	Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)CO)OC)O)O)C)OC=CC2=O)O	382.40	unknown	https://doi.org/10.1002/JLAC.198419841015
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(3,4,5-Trihydroxy-6-methyloxan-2-yl) 2,4-dimethylfuran-3-carboxylate	85159317	Click to see CC1C(C(C(C(O1)OC(=O)C2=C(OC=C2C)C)O)O)O	286.28	unknown	https://doi.org/10.3390/50300345
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
1-[(2S,5R)-1,10-dioxaspiro[4.5]dec-3-en-2-yl]hexa-2,4-diyn-1-one	101631675	Click to see CC#CC#CC(=O)C1C=CC2(O1)CCCCO2	230.26	unknown	https://doi.org/10.1002/JLAC.198519850325
> Organoheterocyclic compounds / Oxepanes
Miophytocen A	122201252	Click to see CC1=CC(=O)OCC23CC=C(C4C2OC5CC(C3(C5(C4)O)C)OC(=O)C=CC=CC(OCC1)C(C)O)C	514.60	unknown	https://doi.org/10.1016/0041-0101(85)90003-0
Miophytocen B	14353782	Click to see CC1=CC(=O)OCC23CCC(=C)C4C2OC5CC(C3(C5(C4)O)C)OC(=O)C=CC=CC(OCC1)C(C)O	514.60	unknown	https://doi.org/10.1016/0041-0101(85)90003-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-[3,4-dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one	74978105	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)CO)O)O)O)O)O)O	742.60	unknown	https://doi.org/10.3390/50300345
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,3R,6Z,8E,10R,14R,19R,23R,24R,25S,26R)-10-[(1S)-1-hydroxyethyl]-14,21,25-trimethylspiro[4,11,17,27-tetraoxatetracyclo[21.3.1.03,25.019,24]heptacosa-6,8,21-triene-26,2'-oxirane]-5,13,16-trione	162843356	Click to see CC1CC(=O)OCC2CC(=CC3C2C4(C(CC(C45CO5)O3)OC(=O)C=CC=CC(OCC1=O)C(C)O)C)C	530.60	unknown	https://doi.org/10.1002/JLAC.198419841015
[(1R,3R,6Z,8E,10S,13S,14R,19R,23R,24S,25S,26R)-13-hydroxy-10-[(1S)-1-hydroxyethyl]-14,21,25-trimethyl-5,16-dioxospiro[4,11,17,27-tetraoxatetracyclo[21.3.1.03,25.019,24]heptacosa-6,8,21-triene-26,2'-oxirane]-14-yl] acetate	162971242	Click to see CC1=CC2C3C(C1)COC(=O)CC(C(COC(C=CC=CC(=O)OC4C3(C5(CO5)C(C4)O2)C)C(C)O)O)(C)OC(=O)C	590.70	unknown	https://doi.org/10.1002/JLAC.198419841015

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Baccharis coridifolia

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