Scientific name	Authority	First published in
Ilex bonplandiana	Münter	Mitth. Naturwiss. Vereine Neu-Vorpommern 14: 183 (1883)
Ilex congonhas	Liais	Clim. Géol. Brésil : 563 (1872)
Ilex curitibensis	Miers	Ann. Mag. Nat. Hist. , ser. 3, 8: 393 (1861)
Ilex domestica	Reissek	Fl. Bras. 11(1): 67 (1861)
Ilex domestica var. glabra	Reissek	Fl. Bras. 11(1): 67 (1861)
Ilex mate	A.St.-Hil.	Hist. Pl. Remarq. Brésil : xli (1824)
Ilex paraguariensis var. acutifolia	Mart.	Syst. Mat. Med. Bras. : 61 (1843)
Ilex paraguariensis var. angustifolia	Reissek	Fl. Bras. 11(1): 63 (1861)
Ilex paraguariensis f. confusa	Loes.	Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 308 (1901)
Ilex paraguariensis f. dasyprionata	Loes.	Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 308. 1901 [1 Mar 1901]
Ilex paraguariensis f. domestica	Loes.	Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 306 (1901)
Ilex paraguariensis var. euneura	Loes.	Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 309 (1901)
Ilex paraguariensis var. guaranina	Loes.	Notizbl. Königl. Bot. Gart. Berlin 1: 315 (1897)
Ilex paraguariensis var. latifolia	Reissek	Fl. Bras. 11(1): 62 (1861)
Ilex paraguariensis f. latifolia	Chodat	Bull. Herb. Boissier , sér. 2, 2: 741 (1902)
Ilex paraguariensis f. microphylla	Reissek	Fl. Bras. 11(1): t. 13, f. 18 (1861)
Ilex paraguariensis f. parvifolia	Chodat	Bull. Herb. Boissier , sér. 2, 2: 741 (1902)
Ilex paraguariensis f. sorbilis	Loes.	Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 307. 1901 [1 Mar 1901]
Ilex paraguariensis var. ulei	Loes.	Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 309 (1901)
Ilex paraguayensis	Hook.	Bot. Mag. 69: t. 3992 (1843)
Ilex sorbitis	Reissek	Fl. Bras. 11(1): 66 (1861)
Ilex theaezans	Bonpl. ex Miers	Ann. Mag. Nat. Hist. , ser. 3, 8: 389 (1861)

Common names Top

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Filter by language:

Language	Common/alternative name
English	mate
English	yerba maté
English	yerba mate
English	holly
English	paraguay tea
Spanish	yerba
Spanish	yerba mate
Spanish	kaa
Spanish	kaá
Spanish	yerba de los jesuitas
Spanish	yerba del paraguay
Arabic	البهشية الباراجوانية
Arabic	بهشية براغوانية
Azerbaijani	paraqvay pirkalı
Azerbaijani	yerba mate
Bulgarian	йерба мате
br	yerba mate
Catalan	herba mate
Catalan	mate
ceb	hierba mate
ceb	hierba maté
ceb	yerba maté
ceb	yerba mate
Czech	cesmína paraguayská
Czech	cesmína paraquayská
Welsh	yerba mate
Danish	paraguaykristtorn
German	mate-baum
German	mate-strauch
German	matetee
German	chimarrao
German	chimarrão
German	mate
German	maté
German	yerba
German	yerba mate
German	mate-tee
Esperanto	paragvaja ilekso
Esperanto	matea herbo
Basque	mate
Persian	ماته
Finnish	matee
French	thé des jésuites
French	thé du brésil
French	thé du paraguay
French	yerba maté
French	yerba mate
frr	mate
Irish	yerba mate
Galician	herba mate
gn	ka'a
gn	ka`a
Hebrew	צינית מאטה
Croatian	mate čaj
Croatian	maté-čaj
Croatian	mate
Hungarian	maté
Indonesian	yerba mate
Italian	yerba mate
Japanese	マテチャノキ
Japanese	イェルバ・マテ
Kazakh	Мате
Korean	마테나무
Lithuanian	matės žolė
Lithuanian	paragvajinis bugienis
Latvian	paragvajas ilekss
Malay	yerba mate
mt	yerba mate
Norwegian Bokmål	erva mate
Norwegian Bokmål	erva-mate
Norwegian Bokmål	yerba mate
Norwegian Bokmål	yerbamaté
Dutch	matéplant
Dutch	mate
Dutch	mateplant
Dutch	yerba mate
Polish	ostrokrzew paragwajski
Polish	yerba mate
Portuguese	congonha
Portuguese	erva-mate
Portuguese	mate
Portuguese	chá mate
Portuguese	erva mate
Quechua	hierba mate
Quechua	yerba mate
Quechua	mati wayusa
Russian	Падуб парагвайский
Slovak	cezmína paraguajská
Slovenian	mate
Serbian	Мате
Swedish	mate
Swedish	yerba mate
Swedish	yerba maté
Thai	ชาบราซิล
Thai	มาเต
Turkish	yerba mate
Ukrainian	Гостролист парагвайський
Ukrainian	Йерба-мате
Ukrainian	Падуб парагвайський
Ukrainian	Парагвайський падуб
Chinese	巴拉圭冬青
Chinese	巴拉圭茶
Chinese	瑪黛茶
Chinese	马黛
Chinese	马黛茶

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Ilex paraguariensis var. sincorensis	Loes.	Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 89: 285 (1908)
Ilex paraguariensis var. vestita	Loes.	Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 309 (1901)

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

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Brazil
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Southern South America
  - Argentina Northeast
  - Paraguay
  - Uruguay

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000729719
UNII	QJB02841ZY
USDA Plants	ILPA3
Tropicos	2000339
KEW	urn:lsid:ipni.org:names:315555-2
The Plant List	kew-2861242
Open Tree Of Life	589430
Observations.org	412721
NCBI Taxonomy	185542
IUCN Red List	32982
IPNI	315555-2
iNaturalist	193722
GBIF	5414252
Freebase	/m/01614n
EPPO	ILEPA
EOL	484975
Elurikkus	534806
US Library of Congress	sh85082047
USDA GRIN	19756
Wikipedia	Yerba_mate

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_963454935.2	ILEXP v3	Scaffold	UNIVERSIDAD DE BUENOS AIRES	2024-03-04	10.0x	0.99 Gb

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 revisited history of cacao domestication in pre-Columbian times revealed by archaeogenomic approaches

Lanaud C, Vignes H, Utge J, Valette G, Rhoné B, Garcia Caputi M, Angarita Nieto NS, Fouet O, Gaikwad N, Zarrillo S, Powis TG, Cyphers A, Valdez F, Olivera Nunez SQ, Speller C, Blake M, Valdez FJ, Raymond S, Rowe SM, Duke GS, Romano FE, Loor Solórzano RG, Argout X

Sci Rep

07-Mar-2024

PMCID:	PMC10920634
doi:	10.1038/s41598-024-53010-6
PMID:	38453955

The Effects of Chia Defatted Flour as a Nutritional Supplement in C57BL/6 Mice Fed a Low-Quality Diet

Lucini Mas A, Canalis AM, Pasqualini ME, Wunderlin DA, Baroni MV

Foods

23-Feb-2024

PMCID:	PMC10930959
doi:	10.3390/foods13050678
PMID:	38472791

Leaves, Infusion, and Grounds—A Three–Stage Assessment of Element Content in Yerba Mate (Ilex paraguariensis) Based on the Dynamic Extraction and Mineralization of Residues

Różewska A, Proch J, Niedzielski P

Foods

06-Feb-2024

PMCID:	PMC10887975
doi:	10.3390/foods13040509
PMID:	38397486

Pseudolycoriella hygida (Sauaia and Alves)—An Overview of a Model Organism in Genetics, with New Aspects in Morphology and Systematics

Menzel F, Kramp K, Amorim DD, Gorab E, Uliana JV, Sauaia H, Monesi N

Insects

06-Feb-2024

PMCID:	PMC10889529
doi:	10.3390/insects15020118
PMID:	38392537

Volatilome, Microbial, and Sensory Profiles of Coffee Leaf and Coffee Leaf-Toasted Maté Kombuchas

Sales AL, Cunha SC, Ferreira IM, Morgado J, Melo L, DePaula J, Miguel MA, Farah A

Foods

02-Feb-2024

PMCID:	PMC10855110
doi:	10.3390/foods13030484
PMID:	38338619

Ilex paraguariensis A.St.-Hil. improves lipid metabolism in high-fat diet-fed obese rats and suppresses intracellular lipid accumulation in 3T3-L1 adipocytes via the AMPK-dependent and insulin signaling pathways

Kudo M, Gao M, Hayashi M, Kobayashi Y, Yang J, Liu T

Food Nutr Res

22-Jan-2024

PMCID:	PMC10845893
doi:	10.29219/fnr.v68.10307
PMID:	38327997

The metabolic effect of Momordica charantia cannot be determined based on the available clinical evidence: a systematic review and meta-analysis of randomized clinical trials

Laczkó-Zöld E, Csupor-Löffler B, Kolcsár EB, Ferenci T, Nan M, Tóth B, Csupor D

Front Nutr

11-Jan-2024

PMCID:	PMC10808600
doi:	10.3389/fnut.2023.1200801
PMID:	38274207

Enhancing satiety and aerobic performance with beer microparticles-based non-alcoholic drinks: exploring dose and duration effects

Cahuê FL, Maia PD, de Brito LR, da Silva VP, Gomes DV, Pierucci AP

Front Nutr

03-Jan-2024

PMCID:	PMC10791988
doi:	10.3389/fnut.2023.1225189
PMID:	38235440

Inhibition of Glycation End Products Formation and Antioxidant Activities of Ilex paraguariensis: comparative study of fruit and leaves extracts

Cogoi L, Marrassini C, Martin EM, Alonso MR, Filip R, Anesini C

J Pharmacopuncture

31-Dec-2023

PMCID:	PMC10739477
doi:	10.3831/KPI.2023.26.4.338
PMID:	38162469

Green Synthesis of Metal and Metal Oxide Nanoparticles: A Review of the Principles and Biomedical Applications

Radulescu DM, Surdu VA, Ficai A, Ficai D, Grumezescu AM, Andronescu E

Int J Mol Sci

20-Oct-2023

PMCID:	PMC10607471
doi:	10.3390/ijms242015397
PMID:	37895077

Interaction of Garcinia cambogia (Gaertn.) Desr. and Drugs as a Possible Mechanism of Liver Injury: The Case of Montelukast

Di Giacomo S, Di Sotto A, Percaccio E, Scuotto E, Battistelli C, Mazzanti G, Menniti-Ippolito F, Ippoliti I

Antioxidants (Basel)

16-Sep-2023

PMCID:	PMC10525400
doi:	10.3390/antiox12091771
PMID:	37760074

Phytochemical and functional characterization of fermented Yerba mate using Rhizopus oligosporus

Kwak SH, Kim H, Jeon JH, Pal K, Kang DH, Kim D

AMB Express

09-Sep-2023

PMCID:	PMC10492770
doi:	10.1186/s13568-023-01600-4
PMID:	37689820

Perspectives on Saponins: Food Functionality and Applications

Timilsena YP, Phosanam A, Stockmann R

Int J Mol Sci

31-Aug-2023

PMCID:	PMC10487995
doi:	10.3390/ijms241713538
PMID:	37686341

Use of Bio-Waste of Ilex paraguariensis A. St. Hil. (Yerba mate) to Obtain an Extract Rich in Phenolic Compounds with Preservative Potential

Menezes B, Caleja C, Calhelha RC, Pinela J, Dias MI, Stojković D, Soković M, Gonçalves OH, Leimann FV, Pereira E, Barros L

Foods

28-Aug-2023

PMCID:	PMC10486667
doi:	10.3390/foods12173241
PMID:	37685174

Harnessing Natural Antioxidants for Enhancing Food Shelf Life: Exploring Sources and Applications in the Food Industry

Petcu CD, Tăpăloagă D, Mihai OD, Gheorghe-Irimia RA, Negoiță C, Georgescu IM, Tăpăloagă PR, Borda C, Ghimpețeanu OM

Foods

23-Aug-2023

PMCID:	PMC10486681
doi:	10.3390/foods12173176
PMID:	37685108

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 / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1021/JF00025A023
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Octanoic acid	379	Click to see CCCCCCCC(=O)O	144.21	unknown	https://doi.org/10.1021/JF00025A023
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(R)-Linalyl beta-vicianoside	23815399	Click to see CC(=CCCC(C)(C=C)OC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O)C	448.50	unknown	https://doi.org/10.1248/CPB.57.257
L-Linalool 3-[xylosyl-(1->6)-glucoside]	73410547	Click to see CC(=CCCC(C)(C=C)OC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O)C	448.50	unknown	https://doi.org/10.1248/CPB.57.257
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol	957	Click to see CCCCCCCCO	130.23	unknown	https://doi.org/10.1021/JF00025A023
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1021/JF00025A023
Geranylacetone	1549778	Click to see CC(=CCCC(=CCCC(=O)C)C)C	194.31	unknown	https://doi.org/10.1021/JF00025A023
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1021/JF00025A023
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1021/JF00025A023
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,6E)-nerolidol	11241545	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1021/JF00025A023
alpha-IONONE	5282108	Click to see CC1=CCCC(C1C=CC(=O)C)(C)C	192.30	unknown	https://doi.org/10.1021/JF00025A023
beta-Ionone	638014	Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C	192.30	unknown	https://doi.org/10.1021/JF00025A023
Nerolidol	8888	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1021/JF00025A023
> 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] (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-acetyloxy-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	162954377	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC(=O)C)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	955.10	unknown	https://doi.org/10.1248/CPB.57.257
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	163014295	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	897.10	unknown	https://doi.org/10.1248/CPB.57.257
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	101920696	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O	1059.20	unknown	https://doi.org/10.1021/NP50117A015 https://doi.org/10.1248/CPB.57.257
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-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-carboxylate	102037109	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	929.10	unknown	https://doi.org/10.1248/CPB.57.257
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	25231432	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	767.00	unknown	https://doi.org/10.1248/CPB.57.257
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,10S,12aR,14bR)-10-[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-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	196359	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C	913.10	unknown	https://doi.org/10.1002/1099-1565(200101/02)12:1<48::AID-PCA560>3.0.CO;2-#
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-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	155559142	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)O)O)O)O	897.10	unknown	https://doi.org/10.1248/CPB.57.257
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	162993017	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O	1059.20	unknown	https://doi.org/10.1248/CPB.57.257
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3S,4R,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	101920697	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O	1075.20	unknown	https://doi.org/10.1021/NP50117A015 https://doi.org/10.1248/CPB.57.257
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-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	25231433	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O	1221.40	unknown	https://doi.org/10.1248/CPB.57.257
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3-acetyloxy-5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	162954376	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC(=O)C)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	955.10	unknown	https://doi.org/10.1248/CPB.57.257
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	15625530	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	913.10	unknown	https://doi.org/10.1248/CPB.57.257
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-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-carboxylate	162896601	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	929.10	unknown	https://doi.org/10.1248/CPB.57.257
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	163014294	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	897.10	unknown	https://doi.org/10.1248/CPB.57.257
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-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	73157174	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)O)O)O)O	897.10	unknown	https://doi.org/10.1248/CPB.57.257
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-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	73157175	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O	1059.20	unknown	https://doi.org/10.1248/CPB.57.257
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	74409910	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	767.00	unknown	https://doi.org/10.1248/CPB.57.257
[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 10-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	162993016	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O	1059.20	unknown	https://doi.org/10.1248/CPB.57.257
[3,4,5-Trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-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	74409911	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O	1221.40	unknown	https://doi.org/10.1248/CPB.57.257
Araliasaponin X	73157196	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O	1075.20	unknown	https://doi.org/10.1248/CPB.57.257
ilexoside II	44201980	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1(C)O)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	929.10	unknown	https://doi.org/10.1590/S0103-50532004000200008
Matesaponin 1	44575759	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O	913.10	unknown	https://doi.org/10.1248/CPB.57.257
Matesaponin 2	73157195	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O	1059.20	unknown	https://doi.org/10.1248/CPB.57.257
Matesaponin 3	44575760	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O	1075.20	unknown	https://doi.org/10.1248/CPB.57.257
Matesaponin 4	44575761	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1C)C)C(=O)OC9C(C(C(C(O9)COC1C(C(C(C(O1)CO)O)O)O)O)O)O	1221.40	unknown	https://doi.org/10.1021/NP50117A015 https://doi.org/10.1248/CPB.57.257
Matesaponin 5	131753118	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1C)C)C(=O)OC9C(C(C(C(O9)COC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O	1383.50	unknown	https://doi.org/10.1016/0031-9422(96)00036-2 https://doi.org/10.1248/CPB.57.257
Nudicaucin C	21635821	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O	1059.20	unknown	https://doi.org/10.1248/CPB.57.257
Urs-12-en-28-oic acid, 3-[(O-6-deoxy-alpha-L-mannopyranosyl-(1-->2)-O-[beta-D-glucopyranosyl-(1-->3)]-alpha-L-arabinopyranosyl)oxy]-, 6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl ester, (3beta)-	73157197	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1C)C)C(=O)OC9C(C(C(C(O9)COC1C(C(C(C(O1)CO)O)O)O)O)O)O	1221.40	unknown	https://doi.org/10.1248/CPB.57.257
Ziyuglycoside I	71609288	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1(C)O)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O	767.00	unknown	https://doi.org/10.1590/S0103-50532004000200008
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aR,10E,12aR,14bS)-10-hydroxyimino-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,5,6,6a,7,8,8a,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	11328874	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=NO)C5(C)C)C)C)C2C1C)C)C(=O)O	469.70	unknown	https://doi.org/10.1016/J.EJMECH.2007.11.021
(4aS,6aR,6aS,6bR,12aR,14bS)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	137705463	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1590/S0103-50532004000200008
10-hydroxy-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	14136880	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	https://doi.org/10.1248/CPB.57.257
2-Cyano-2,3-seco-4-yliden-olean-12-enoic acid	44562528	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CCC#N)C(=C)C)C)C2C1C)C)C(=O)O	451.70	unknown	https://doi.org/10.1016/J.EJMECH.2007.11.021
23-Hydroxyursolic Acid	14136881	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	https://doi.org/10.1248/CPB.57.257 https://doi.org/10.1590/S0103-50532004000200008
3-Hydroxy-11-ursen-28,13-olide	21606663	Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C	454.70	unknown	https://doi.org/10.1248/CPB.57.257
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1248/CPB.57.257
beta-Ursolic acid	220774	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/10.1021/JO01209A003 https://doi.org/10.1248/CPB.57.257 https://doi.org/10.1016/J.EJMECH.2007.11.021
CID 4450096	4450096	Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C	454.70	unknown	https://doi.org/10.1248/CPB.57.257
N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-3-O-acetylursolamide	25111796	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)NCCCN6CCN(CC6)CCCN	681.00	unknown	https://doi.org/10.1016/J.EJMECH.2007.11.021
N-{3-[4-(3-aminopropyl)piperazinyl]propyl}-ursolamide	25111799	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)NCCCN6CCN(CC6)CCCN	639.00	unknown	https://doi.org/10.1016/J.EJMECH.2007.11.021
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1248/CPB.57.257
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/10.1248/CPB.57.257 https://doi.org/10.1016/J.EJMECH.2007.11.021 https://doi.org/10.1021/JO01209A003 https://doi.org/10.1590/S0103-50532004000200008
Ursolic acid acetate	6475119	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1016/J.EJMECH.2007.11.021
Ursonic acid	9890209	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O	454.70	unknown	https://doi.org/10.1016/J.EJMECH.2007.11.021
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-carbamoyl-alpha amino acids and derivatives / N-carbamoyl-alpha amino acids
Allantoic acid	203	Click to see C(C(=O)O)(NC(=O)N)NC(=O)N	176.13	unknown	https://doi.org/10.1016/0031-9422(93)85103-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid	311	Click to see C(C(=O)O)C(CC(=O)O)(C(=O)O)O	192.12	unknown	https://doi.org/10.1002/ARDP.18932310709
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,3,4,5-Tetrahydroxycyclohexanecarboxylic acid	1064	Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O	192.17	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149459/
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1248/CPB.57.257 https://doi.org/10.1016/S0367-326X(01)00331-8
3,5-Dicaffeoyl-epi-quinic acid	60150332	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O	516.40	unknown	https://doi.org/10.1016/S0367-326X(01)00331-8
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1002/PCA.647 https://doi.org/10.1016/S0308-8146(96)00311-1
Isochlorogenic acid A	6474310	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O	516.40	unknown	https://doi.org/10.1016/0308-8146(90)90126-O
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1016/0308-8146(90)90126-O https://doi.org/10.1248/CPB.57.257
Quinic acid	6508	Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O	192.17	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149459/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	https://doi.org/10.1007/978-3-540-71095-0_5152
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	https://doi.org/10.1007/978-3-540-71095-0_5152
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Raffinose	439242	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O	504.40	unknown	https://doi.org/10.1007/978-3-540-71095-0_5152
> Organoheterocyclic compounds / Azepines
4-aza-A-homo-3-oxo-ursolic acid	44562549	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)NC5(C)C)C)C)C2C1C)C)C(=O)O	469.70	unknown	https://doi.org/10.1016/J.EJMECH.2007.11.021
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin	204	Click to see C1(C(=O)NC(=O)N1)NC(=O)N	158.12	unknown	https://doi.org/10.1016/0031-9422(93)85103-X
> Organoheterocyclic compounds / Benzodioxoles
Safrole	5144	Click to see C=CCC1=CC2=C(C=C1)OCO2	162.18	unknown	https://doi.org/10.1021/JF00025A023
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine	2519	Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C	194.19	unknown	https://doi.org/10.1016/0308-8146(90)90126-O https://doi.org/10.1021/JF020128V https://doi.org/10.1016/0378-8741(86)90005-X https://doi.org/10.1021/JF902255H https://doi.org/10.1002/PCA.647 https://doi.org/10.1016/0031-9422(91)83637-Z https://doi.org/10.1016/S0031-9422(00)00324-1 https://doi.org/10.1248/CPB.57.257 https://doi.org/10.1016/S0308-8146(96)00311-1 https://doi.org/10.1590/S0103-50531999000600004 https://doi.org/10.1016/0031-9422(93)85103-X https://doi.org/10.1021/JF981369Z
Theobromine	5429	Click to see CN1C=NC2=C1C(=O)NC(=O)N2C	180.16	unknown	https://doi.org/10.1016/0378-8741(86)90005-X https://doi.org/10.1016/0031-9422(93)85103-X https://doi.org/10.1016/0308-8146(90)90126-O https://doi.org/10.1248/CPB.57.257 https://doi.org/10.1002/PCA.647 https://doi.org/10.1590/S0103-50531999000600004 https://doi.org/10.1016/S0031-9422(00)00324-1 https://doi.org/10.1021/JF981369Z
Theophylline	2153	Click to see CN1C2=C(C(=O)N(C1=O)C)NC=N2	180.16	unknown	https://doi.org/10.1016/0378-8741(86)90005-X https://doi.org/10.1002/PCA.647 https://doi.org/10.1002/(SICI)1099-1573(199803)12:2<129::AID-PTR191>3.0.CO;2-1 https://doi.org/10.1021/JF981369Z
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole	798	Click to see C1=CC=C2C(=C1)C=CN2	117.15	unknown	https://doi.org/10.1021/JF00025A023
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149459/
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1016/S0308-8146(96)00311-1 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149459/
> 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/10.1016/S0367-326X(01)00331-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12313332	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	594.50	unknown	https://doi.org/10.1248/CPB.57.257
Kaempferol-3-O-rutinoside	5318767	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	594.50	unknown	https://doi.org/10.1248/CPB.57.257
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.57.257 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149459/
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.57.257 https://doi.org/10.1016/S0367-326X(01)00331-8 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149459/

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Ilex paraguariensis

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