Siphoneugena densiflora is a plant species belonging to the Myrtaceae family and is native to Brazil. It can grow as a shrub up to 3 meters in height or as a tree reaching 12-13 meters tall. The plant bears small, edible fruit with a purplish-black color and a diameter of less than 10mm.

Synonyms Top

Scientific name	Authority	First published in
Paramitranthes densiflora	(O.Berg) Burret	Notizbl. Bot. Gart. Berlin-Dahlem 15: 541. 1941
Calycorectes densiflorus	Nied.	Nat. Pflanzenfam. 3(7): 82 (1893)

Common names Top

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Language	Common/alternative name
English	hoja menuda

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Siphoneugena densiflora var. densiflora		Unknown

Subvarieties (abbr. subvar.) Top

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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

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil Southeast
  - Brazil West-central

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000311347
USDA Plants	SIDE6
Tropicos	22101798
INPN	630678
KEW	urn:lsid:ipni.org:names:601229-1
The Plant List	kew-192507
Open Tree Of Life	61053
NCBI Taxonomy	420630
IPNI	601229-1
iNaturalist	963588
GBIF	3181153
Freebase	/m/02y_k3m
Wikipedia	Siphoneugena_densiflora

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

Humid and cold forest connections in South America between the eastern Andes and the southern Atlantic coast during the LGM

Pinaya JL, Pitman NC, Cruz FW, Akabane TK, Lopez MD, Pereira-Filho AJ, Grohman CH, Reis LS, Rodrigues ES, Ceccantini GC, De Oliveira PE

Sci Rep

24-Jan-2024

PMCID:	PMC10808232
doi:	10.1038/s41598-024-51763-8
PMID:	38267489

Opportunities and Scope for Botanical Extracts and Products for the Management of Fall Armyworm (Spodoptera frugiperda) for Smallholders in Africa

Rioba NB, Stevenson PC

Plants (Basel)

06-Feb-2020

PMCID:	PMC7076698
doi:	10.3390/plants9020207
PMID:	32041322

Flavonoids from Brazilian Cerrado: Biosynthesis, Chemical and Biological Profile

Peixoto JD, Neves BJ, Vasconcelos FG, Napolitano HB, Barbalho MG, Silva SD, Rosseto LP

Molecules

09-Aug-2019

PMCID:	PMC6720525
doi:	10.3390/molecules24162891
PMID:	31395797

Extract of Nicotiana tabacum as a potential control agent of Grapholita molesta (Lepidoptera: Tortricidae)

Sarker S, Lim UT

PLoS One

23-Aug-2018

PMCID:	PMC6107112
doi:	10.1371/journal.pone.0198302
PMID:	30138428

The evolutionary history of Eugenia sect. Phyllocalyx (Myrtaceae) corroborates historically stable areas in the southern Atlantic forests

de Oliveira Bünger M, Fernanda Mazine F, Forest F, Leandro Bueno M, Renato Stehmann J, Lucas EJ

Ann Bot

09-Dec-2016

PMCID:	PMC5155605
doi:	10.1093/aob/mcw209
PMID:	27974324

Chemical Characterization and in Vitro Antibacterial Activity of Myrcianthes hallii (O. Berg) McVaugh (Myrtaceae), a Traditional Plant Growing in Ecuador

Chavez Carvajal P, Coppo E, Di Lorenzo A, Gozzini D, Bracco F, Zanoni G, Nabavi SM, Marchese A, Arciola CR, Daglia M

Materials (Basel)

07-Jun-2016

PMCID:	PMC5456788
doi:	10.3390/ma9060454
PMID:	28773577

Phylogenetic analysis in Myrcia section Aulomyrcia and inferences on plant diversity in the Atlantic rainforest

Staggemeier VG, Diniz-Filho JA, Forest F, Lucas E

Ann Bot

09-Mar-2015

PMCID:	PMC4373287
doi:	10.1093/aob/mcv005
PMID:	25757471

Isolation of arginase inhibitors from the bioactivity-guided fractionation of Byrsonima coccolobifolia leaves and stems.

de Sousa LR, Ramalho SD, Burger MC, Nebo L, Fernandes JB, da Silva MF, Iemma MR, Corrêa CJ, de Souza DH, Lima MI, Vieira PC

J Nat Prod

28-Feb-2014

doi:	10.1021/NP400717M
PMID:	24521209

Constituintes químicos e atividade antimicrobiana dos extratos de Dilodendron bipinnatum (sapindaceae)

Josiane Cristina dos Santos, Carlos Alberto Nastally de Oliveira, Larissa Varella, Andréia Pereira Matos, Ana Paula Terezan, Ana Cristina Leite, João Batista Fernandes, Paulo Cezar Vieira, Maria Fátima das Graças Fernandes d Silva, José Rubens Pirani

FapUNIFESP (SciELO)

20-Dec-2010

doi:	10.1590/S0100-40422010001000014

Trypanocidal activity of flavonoids and limonoids isolated from Myrsinaceae and Meliaceae active plant extracts

Ana C. Leite, Artur Placeres Neto, Alessandra R. P. Ambrozin, João B. Fernandes, Paulo C. Vieira, Maria F. das G. F. da Silva, Sérgio de Albuquerque

Springer Science and Business Media LLC

29-Apr-2010

doi:	10.1590/S0102-695X2010000100002

Structural Features and Biological Properties of Ellagitannins in Some Plant Families of the Order Myrtales

Yoshida T, Amakura Y, Yoshimura M

Int J Mol Sci

06-Jan-2010

PMCID:	PMC2820991
doi:	10.3390/ijms11010079
PMID:	20162003

Bioactive Pentacyclic Triterpenes from the Stems of Combretum laxum

Bisoli E, Garcez WS, Hamerski L, Tieppo C, Garcez FR

Molecules

01-Nov-2008

PMCID:	PMC6245402
doi:	10.3390/molecules13112717
PMID:	18978701

Enzymatic inhibitory activity and trypanocidal effects of extracts and compounds from Siphoneugena densiflora O. Berg and Vitex polygama Cham.

Gallo MB, Marques AS, Vieira PC, da Silva MF, Fernandes JB, Silva M, Guido RV, Oliva G, Thiemann OH, Albuquerque S, Fairlamb AH

Z Naturforsch C J Biosci

01-May-2008

PMCID:	PMC3428908
doi:	10.1515/ZNC-2008-5-611
PMID:	18669023

Enzymatic Inhibitory Activity and Trypanocidal Effects of Extracts and Compounds from Siphoneugena densiflora O. Berg and Vitex polygama Cham

Gallo MB, Marques AS, Vieira PC, da Silva MF, Fernandes JB, Silva M, Guido RV, Oliva G, Thiemann OH, Albuquerque S, Fairlamb AH

Z Naturforsch C

01-May-2008

PMCID:	PMC3428908
doi:	10.1515/znc-2008-5-611
PMID:	18669023

New natural products from Siphoneugena densiflora Berg (Myrtaceae) and their chemotaxonomic significance

Margareth B. C. Gallo, Fernando C. da Silva, Paulo C. Vieira, João B. Fernandes, Maria Fátima das G. F. da Silva

FapUNIFESP (SciELO)

08-Nov-2006

doi:	10.1590/S0103-50532006000200010

Phytochemical Profile Top

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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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/ https://doi.org/10.1590/S0103-50532006000200010
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1590/S0103-50532006000200010
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1002/PS.1278 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2,4,6-Trimethoxybenzaldehyde	70019	Click to see COC1=CC(=C(C(=C1)OC)C=O)OC	196.20	unknown	https://doi.org/10.1002/PS.1278
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,10R,11R,12aR,14bS)-8,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162913249	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)C)O)O)C)O)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	650.80	unknown	https://doi.org/10.1590/S0103-50532006000200010
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,9S,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	102005082	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	666.80	unknown	https://doi.org/10.1590/S0103-50532006000200010
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 8,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162913248	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)C)O)O)C)O)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	650.80	unknown	https://doi.org/10.1590/S0103-50532006000200010
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	74191789	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	666.80	unknown	https://doi.org/10.1590/S0103-50532006000200010
Chebuloside II, >=95% (LC/MS-ELSD)	44567150	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	666.80	unknown	https://doi.org/10.1002/PS.1278
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	12073157	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	https://doi.org/10.1002/PS.1278
(2alpha,3beta,4alpha,6beta)-2,3,6,23-Tetrahydroxy-urs-12-en-28-oic acid	137705969	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)O	504.70	unknown	https://doi.org/10.1590/S0103-50532006000200010
(3,4,5,6-Tetrahydroxyoxan-2-yl)methyl 10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboperoxoate	162820414	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OOCC6C(C(C(C(O6)O)O)O)O)C	650.80	unknown	https://doi.org/10.1002/PS.1278
(4aS,6aS,6bR,8R,9R,10R,11R,12aR)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	12073159	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)O)C	504.70	unknown	https://doi.org/10.1002/PS.1278
(4aS,6aS,6bR,9S,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162418178	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
[(2R,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl (4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboperoxoate	162820415	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)OOCC6C(C(C(C(O6)O)O)O)O)C	650.80	unknown	https://doi.org/10.1002/PS.1278
10,11-Dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	5320146	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	https://doi.org/10.1002/PS.1278
2,3,24-Trihydroxy-12-ursen-28-oic acid	296191	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	https://doi.org/10.1590/S0103-50532006000200010
2,3,6,23-Tetrahydroxyurs-12-en-28-oic acid	258809	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)O	504.70	unknown	https://doi.org/10.1590/S0103-50532006000200010
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1002/PS.1278
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1002/PS.1278 https://doi.org/10.1590/S0103-50532006000200010
Arjunolic acid	73641	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	https://doi.org/10.1002/PS.1278 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
Asiatic Acid	119034	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	https://doi.org/10.1590/S0103-50532006000200010 https://doi.org/10.1002/PS.1278
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1590/S0103-50532006000200010
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1590/S0103-50532006000200010
Madecassic Acid	73412	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)O	504.70	unknown	https://doi.org/10.1590/S0103-50532006000200010 https://doi.org/10.1002/PS.1278
Madecassicside,(S)	12073158	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)O	504.70	unknown	https://doi.org/10.1002/PS.1278
Terminolic acid	12314613	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)O)C	504.70	unknown	https://doi.org/10.1590/S0103-50532006000200010
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(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	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1590/S0103-50532006000200010
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1590/S0103-50532006000200010
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1590/S0103-50532006000200010
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1590/S0103-50532006000200010 https://doi.org/10.1590/S0100-40422010001000014
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal	19233	Click to see CC(C(C(C(C=O)O)O)O)O	164.16	unknown	https://doi.org/10.1590/S0103-50532006000200010
6-Deoxy-L-altrose	5319755	Click to see CC(C(C(C(C=O)O)O)O)O	164.16	unknown	https://doi.org/10.1590/S0103-50532006000200010
6-Deoxyglucose	93579	Click to see CC(C(C(C(C=O)O)O)O)O	164.16	unknown	https://doi.org/10.1590/S0103-50532006000200010
L-(-)-Fucose	220001	Click to see CC(C(C(C(C=O)O)O)O)O	164.16	unknown	https://doi.org/10.1590/S0103-50532006000200010
L-Rhamnose	25310	Click to see CC1C(C(C(C(O1)O)O)O)O	164.16	unknown	https://doi.org/10.1590/S0103-50532006000200010
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural	237332	Click to see C1=C(OC(=C1)C=O)CO	126.11	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
> Organoheterocyclic compounds / Benzodioxins / Benzo-p-dioxins / Dibenzo-p-dioxins
4-hydroxy-6,8-dimethoxy-7-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]dibenzo-p-dioxin-2-carboxylic acid	162820319	Click to see COC1=C(C(=C2C(=C1)OC3=CC(=CC(=C3O2)O)C(=O)O)OC)OCC4C(C(C(C(O4)CO)O)O)O	496.40	unknown	https://doi.org/10.1002/PS.1278
4-Hydroxy-6,8-dimethoxy-7-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]methoxy]dibenzo-p-dioxin-2-carboxylic acid	162820318	Click to see COC1=C(C(=C2C(=C1)OC3=CC(=CC(=C3O2)O)C(=O)O)OC)OCC4C(C(C(C(O4)CO)O)O)O	496.40	unknown	https://doi.org/10.1590/S0103-50532006000200010
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(2,4,6-Trimethoxyphenyl)prop-2-enal	10536994	Click to see COC1=CC(=C(C(=C1)OC)C=CC=O)OC	222.24	unknown	https://doi.org/10.1002/PS.1278
CID 79331614	79331614	Click to see COC1=CC(=C(C(=C1)OC)C=CC=O)OC	222.24	unknown	https://doi.org/10.1002/PS.1278
> 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/10.1590/S0102-695X2010000100002 https://doi.org/10.1590/S0103-50532006000200010
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one	44259215	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1590/S0103-50532006000200010
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-{[(2S,3R,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}chromen-4-one	121540514	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1590/S0103-50532006000200010
Guaijaverin	5481224	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1590/S0103-50532006000200010
Quercetin-3-D-xyloside	5320863	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1590/S0103-50532006000200010
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1590/S0103-50532006000200010 https://doi.org/10.1021/NP400717M
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1R,2S,20S,42S,46S)-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37,46-hexadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone	162934488	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
[(10R,11R)-10-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate	101601178	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1590/S0103-50532006000200010
[(2R,3R,4S,5R,6S)-4-acetyloxy-3,5-dihydroxy-6-[(14-hydroxy-7,13-dimethoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]oxan-2-yl]methyl acetate	162820251	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)OC)C(=O)O3)OC)O)OC(=O)C)O	576.50	unknown	https://doi.org/10.1002/PS.1278
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(14-hydroxy-7,13-dimethoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]oxan-2-yl]methyl acetate	162877399	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)OC)C(=O)O3)OC)O)O)O	534.40	unknown	https://doi.org/10.1002/PS.1278
[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]oxan-3-yl] acetate	162902753	Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)OC(=O)C)O)O	490.40	unknown	https://doi.org/10.1002/PS.1278
[(2S,3R,4S,5R,6S)-4,5-dihydroxy-2-methyl-6-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]oxan-3-yl] acetate	10951064	Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)O)O)OC(=O)C	490.40	unknown	https://doi.org/10.1590/S0103-50532006000200010
[(2S,3S,4R,5R,6S)-3,5-dihydroxy-2-methyl-6-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]oxan-4-yl] acetate	163060608	Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)O)OC(=O)C)O	490.40	unknown	https://doi.org/10.1002/PS.1278
[10-[(19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate	3009654	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/
7,8,9,12,13,14,20,28,29,30,33,34,35-Tridecahydroxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaene-4,17,25,38-tetrone	492391	Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	784.50	unknown	https://doi.org/10.1002/PS.1278
Casuarinin	442673	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/ https://doi.org/10.1590/S0103-50532006000200010
CID 12302513	12302513	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1590/S0103-50532006000200010
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/ https://doi.org/10.1590/S0103-50532006000200010
Eschweilenol C	10026656	Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)O)O)O	448.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/ https://doi.org/10.1590/S0103-50532006000200010
Pedunculagin	442688	Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	784.50	unknown	https://doi.org/10.1002/PS.1278
Stachyurin	157395	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	https://doi.org/10.1590/S0103-50532006000200010
Vescalagin	168165	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	https://doi.org/10.1590/S0103-50532006000200010 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428908/

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Siphoneugena densiflora

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