Cestrum parqui, also known as palqui, green cestrum or willow-leaved jessamine, is a flowering plant native to Chile. In Australia, it is considered a noxious invasive weed and a danger to livestock. However, in the United Kingdom, it has received the Royal Horticultural Society's Award of Garden Merit. This fast-growing shrub produces small, pungent-scented yellow-green flowers and black berries, all of which are highly toxic. The plant is dispersed by birds and water, making it easy to spread and a common garden escape. It has been used in folk medicine for its medicinal properties, but also as a tobacco substitute and in ritualistic ceremonies.

Synonyms Top

Scientific name	Authority	First published in
Cestrum adelbertii	Bakh.f.	Blumea 12: 65. 1963
Cestrum bonariense	Dunal	Prodr. [A. P. de Candolle] 13(1): 666. 1852 [10 May 1852]
Cestrum brasiliense	Larrañaga	Escritos Damaso Antonio Larranaga 1: 412. 1922
Cestrum campestre	Griseb.	Abh. Königl. Ges. Wiss. Göttingen 24: 244. 1879
Cestrum foetidissimum	Jacq.	Pl. Rar. Hort. Schoenbr. 3: 43, t. 329. 1798
Cestrum glaucescens	Sendtn.	Fl. Bras. (Martius) 10: 222. 1846 [1 Jul 1846]
Cestrum mandoni	Rusby	Bull. New York Bot. Gard. 4: 425. 1907
Cestrum heterophyllum	Kuntze	Kuntze et al., Revis. Gen. Pl. 3[3]: 219. 1898 [28 Sep 1898], 1898.
Cestrum parqui var. glabriusculum	Kuntze	Revis. Gen. Pl. 3[3]: 219. 1898 [28 Sep 1898]
Cestrum parqui var. longiflorum	Francey	Candollea 7 (preprint): 45. 1936
Cestrum parqui var. macrocalyx	Francey	Candollea 7 (preprint): 45. 1936
Cestrum parqui var. oranense	Scolnik	Revista Argent. Agron. 21: 30. 1954
Cestrum parqui var. poeppigii	Dunal	Prodr. [A. P. de Candolle] 13(1): 617. 1852 [10 May 1852]
Cestrum parqui var. tomentistipes	Kuntze	Revis. Gen. Pl. 3[3]: 219. 1898 [28 Sep 1898]
Cestrum plicatum	Francey	Candollea 7 (preprint): 52. 1936
Cestrum psittacinum	Stapf	Bot. Mag. 152: t. 9158. 1928
Cestrum salicifolium	Hort. Monsp. ex Dunal	Prodr. [A. P. de Candolle] 13(1): 616. 1852 [10 May 1852]
Cestrum spurium	Hort. Geneve ex Dunal	Prodr. [A. P. de Candolle] 13(1): 617. 1852 [10 May 1852]
Cestrum cyanodontum	Rusby
Cestrum jamaicense var. parqui	Lam.
Cestrum parqui f. heterophyllum	Kuntze

Common names Top

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Filter by language:

Language	Common/alternative name
English	chilean jessamine
Spanish	palqui
Spanish	duraznillo negro
German	c. parqui
German	chilenischer hammerstrauch
German	palqui
Persian	گل محبوبه شب
Quechua	andres waylla
Quechua	anrreswaylla
Swedish	grön nattjasmin
Chinese	大夜丁香
Chinese	大夜香树
Chinese	大夜香樹

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001020770
Florida Plant Atlas	4271
USDA Plants	CEPA9
Tropicos	29602399
INPN	90286
Flora of Italy	4732
KEW	urn:lsid:ipni.org:names:30046363-2
The Plant List	kew-2713698
Open Tree Of Life	868259
Observations.org	137689
NCBI Taxonomy	142762
Nature Serve	2.132388
IUCN Red List	82861249
IPNI	815209-1
iNaturalist	76226
GBIF	2928792
Freebase	/m/043rwtz
EPPO	CEMPA
EOL	581102
Calflora (Californian flora)	8746
USDA GRIN	9998
Wikipedia	Cestrum_parqui

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

Assessing Alien Plant Invasions in Urban Environments: A Case Study of Tshwane University of Technology and Implications for Biodiversity Conservation

Nelufule T, Shivambu TC, Shivambu N, Moshobane MC, Seoraj-Pillai N, Nangammbi T

Plants (Basel)

18-Mar-2024

PMCID:	PMC10975853
doi:	10.3390/plants13060872
PMID:	38592858

Camptothecin bioprocessing from Aspergillus terreus, an endophyte of Catharanthus roseus: antiproliferative activity, topoisomerase inhibition and cell cycle analysis

El-Sayed AS, ElSayed AI, Wadan KM, El-Saadany SS, Abd El-Hady NA

Microb Cell Fact

05-Jan-2024

PMCID:	PMC10768243
doi:	10.1186/s12934-023-02270-4
PMID:	38183118

Tetraenone A: A New β-Ionone Derivative from Tetraena aegyptia

Ashour A, Sherif AE, El-Sayed SM, Kim JY, Jang DS, Anvari A, Farahat AA, Ibrahim SR, Mohamed GA, Ainousah BE, Aljohani RF, Al-Hejaili RR, Khoja RH, Hassan AH, Zaki AA

Metabolites

18-Dec-2023

PMCID:	PMC10744760
doi:	10.3390/metabo13121202
PMID:	38132884

Proteomics and metabolomics analyses of camptothecin-producing Aspergillus terreus reveal the integration of PH domain-containing proteins and peptidylprolyl cis/trans isomerase in restoring the camptothecin biosynthesis

Rady AM, El-Sayed AS, El-Baz AF, Abdel-Fattah GG, Magdeldin S, Ahmed E, Osama A, Hassanein SE, Saed H, Yassin M

Microbiol Spectr

19-Oct-2023

PMCID:	PMC10714794
doi:	10.1128/spectrum.02281-23
PMID:	37855596

Production, bioprocessing and antiproliferative activity of camptothecin from Aspergillus terreus, endophyte of Cinnamomum camphora: restoring their biosynthesis by indigenous microbiome of C. camphora

Eldeghidy A, Abdel-Fattah G, El-Sayed AS, Abdel-Fattah GG

Microb Cell Fact

03-Aug-2023

PMCID:	PMC10399021
doi:	10.1186/s12934-023-02158-3
PMID:	37533061

Harnessing a decade of research at the Research Institute for Bioscience and Biotechnology in Kathmandu, Nepal: Proceedings of the Fourth International Conference ICBB-2022

N/A

BMC Proc

02-Jun-2023

PMCID:	PMC10236390
doi:	10.1186/s12919-023-00252-3
PMID:	37268936

Nuclear phylogeny and insights into whole-genome duplications and reproductive development of Solanaceae plants

Huang J, Xu W, Zhai J, Hu Y, Guo J, Zhang C, Zhao Y, Zhang L, Martine C, Ma H, Huang CH

Plant Commun

25-Mar-2023

PMCID:	PMC10363554
doi:	10.1016/j.xplc.2023.100595
PMID:	36966360

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

Production and bioprocessing of camptothecin from Aspergillus terreus, an endophyte of Cestrum parqui, restoring their biosynthetic potency by Citrus limonum peel extracts

El-Sayed AS, George NM, Abou-Elnour A, El-Mekkawy RM, El-Demerdash MM

Microb Cell Fact

06-Jan-2023

PMCID:	PMC9824926
doi:	10.1186/s12934-022-02012-y
PMID:	36609265

The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature

Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR

Vet Med Sci

29-Aug-2022

PMCID:	PMC9677405
doi:	10.1002/vms3.912
PMID:	36037401

The Allelopathic Activity of Extracts and Isolated from Spirulina platensis

Charoenying P, Laosinwattana C, Chotsaeng N

Molecules

15-Jun-2022

PMCID:	PMC9227131
doi:	10.3390/molecules27123852
PMID:	35744974

Novel land uses shape meta-community structures in neighbouring native forests: Dataset across Uruguay

Säumel I, Ramírez LR

Data Brief

16-May-2022

PMCID:	PMC9130530
doi:	10.1016/j.dib.2022.108267
PMID:	35647241

Insularity and Aridity as Drivers of Mandibular Disparity in Thylamys elegans (Waterhouse, 1839) from Populations of the Atacama Desert, Chile

Arriagada JI, Benítez HA, Toro F, Suazo MJ, Abarca P, Canto J, Vilina YA, Cruz-Jofré F

Animals (Basel)

04-May-2022

PMCID:	PMC9100870
doi:	10.3390/ani12091179
PMID:	35565606

Oligo-FISH Can Identify Chromosomes and Distinguish Hippophaë rhamnoides L. Taxa

Luo X, Liu J, He Z

Genes (Basel)

22-Jan-2022

PMCID:	PMC8872433
doi:	10.3390/genes13020195
PMID:	35205242

Interstitial Telomeric-like Repeats (ITR) in Seed Plants as Assessed by Molecular Cytogenetic Techniques: A Review

Maravilla AJ, Rosato M, Rosselló JA

Plants (Basel)

22-Nov-2021

PMCID:	PMC8621592
doi:	10.3390/plants10112541
PMID:	34834904

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 / Anilides / Aromatic anilides / Benzanilides
Methyl 4-[(4-hydroxybenzoyl)amino]benzoate	43422486	Click to see COC(=O)C1=CC=C(C=C1)NC(=O)C2=CC=C(C=C2)O	271.27	unknown	https://doi.org/10.1021/JF049847V
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1021/JF049847V
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 4-hydroxy-3,5-dimethoxybenzoate	70164	Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC	212.20	unknown	https://doi.org/10.1021/JF049847V
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	https://doi.org/10.1021/JF049847V
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate	19844	Click to see COC1=C(C=CC(=C1)C(=O)OC)O	182.17	unknown	https://doi.org/10.1021/JF049847V
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1021/JF049847V
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben	7456	Click to see COC(=O)C1=CC=C(C=C1)O	152.15	unknown	https://doi.org/10.1021/JF049847V
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3,5-Dimethoxybenzaldehyde	81747	Click to see COC1=CC(=CC(=C1)C=O)OC	166.17	unknown	https://doi.org/10.1021/JF049847V
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol	10393	Click to see C1=CC(=CC=C1CCO)O	138.16	unknown	https://doi.org/10.1021/JF049847V
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 3-(4-hydroxyphenyl)propionate	79706	Click to see COC(=O)CCC1=CC=C(C=C1)O	180.20	unknown	https://doi.org/10.1021/JF049847V
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Blumenol C glucoside	14135394	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	372.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
Byzantionoside B	14135395	Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C	372.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,5S)-2-[(E,3R)-3-hydroxybut-1-enyl]-1,3,3-trimethyl-5-propan-2-yloxycyclohexane-1,2-diol	21574479	Click to see CC(C)OC1CC(C(C(C1)(C)O)(C=CC(C)O)O)(C)C	286.41	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
(1R,4R)-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-ol	14159755	Click to see CC1=CC(CC(C1C=CC(C)O)(C)C)O	210.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
(1R)-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-3-en-1-ol	23251168	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(C)O	210.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
(3R,6R)-hydroxy-alpha-ionone	10889124	Click to see CC1=CC(CC(C1C=CC(=O)C)(C)C)O	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
(4R)-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one	13857510	Click to see CC1=CC(=O)CC(C1C=CC(C)O)(C)C	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
(4S,6R)-6-hydroxy-4-[(3R)-3-hydroxybutyl]-3,5,5-trimethylcyclohex-2-en-1-one	11218401	Click to see CC1=CC(=O)C(C(C1CCC(C)O)(C)C)O	226.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
(6S,9S)-vomifoliol	10537120	Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C	224.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
(6Z,9S)-9-Hydroxy-4,6-megastigmadien-3-one	101338768	Click to see CC1=CC(=O)CC(C1=CCC(C)O)(C)C	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
1-(3-Hydroxybut-1-en-1-yl)-2,6,6-trimethylcyclohexane-1,2,4-triol	72751004	Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)O	244.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
2-(3-Hydroxybut-1-enyl)-1,3,3-trimethyl-5-propan-2-yloxycyclohexane-1,2-diol	73797118	Click to see CC(C)OC1CC(C(C(C1)(C)O)(C=CC(C)O)O)(C)C	286.41	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
2-Cyclohexen-1-one, 4-(3-hydroxybutylidene)-3,5,5-trimethyl-	527057	Click to see CC1=CC(=O)CC(C1=CCC(C)O)(C)C	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
3-(3-Hydroxybut-1-en-1-yl)-2,4,4-trimethylcyclohex-2-en-1-one	54056905	Click to see CC1=C(C(CCC1=O)(C)C)C=CC(C)O	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
3-[(E,3R)-3-hydroxybut-1-enyl]-2,4,4-trimethylcyclohex-2-en-1-one	162880335	Click to see CC1=C(C(CCC1=O)(C)C)C=CC(C)O	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
3-Cyclohexen-1-ol, 4-(3-hydroxy-1-butenyl)-3,5,5-trimethyl-	528969	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(C)O	210.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
4-(3-Hydroxybut-1-en-1-yl)-3,5,5-trimethylcyclohex-2-en-1-ol	71384106	Click to see CC1=CC(CC(C1C=CC(C)O)(C)C)O	210.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
4-(3-Hydroxybutyl)-3,5,5-trimethylcyclohex-2-en-1-one	118284	Click to see CC1=CC(=O)CC(C1CCC(C)O)(C)C	210.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
4-(4-Hydroxy-2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one	25202738	Click to see CC1=CC(CC(C1C=CC(=O)C)(C)C)O	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
4-[(S)-3-Hydroxybutylidene]-3,5,5-trimethyl-2-cyclohexen-1-one	73354989	Click to see CC1=CC(=O)CC(C1=CCC(C)O)(C)C	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohex-2-en-1-one	440244	Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C	224.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
6-Hydroxy-4-(3-hydroxybutyl)-3,5,5-trimethylcyclohex-2-en-1-one	72755850	Click to see CC1=CC(=O)C(C(C1CCC(C)O)(C)C)O	226.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
CID 520684	520684	Click to see CC1=CC(=O)CC(C1C=CC(C)O)(C)C	208.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
Megastigm-7-ene-3,5,6,9-tetraol	23251170	Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)O	244.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
Ueejdiuocucvhn-pwsuyjocsa-	14135400	Click to see CC1=CC(=O)CC(C1CCC(C)O)(C)C	210.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(4aS,7R)-7-(3-hydroxyprop-1-en-2-yl)-1,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one	10966448	Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)CO	234.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
7-(3-Hydroxyprop-1-en-2-yl)-1,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one	14021353	Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)CO	234.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(1R,4S,7S,9S,10S,13R,15R)-7-[(2R,3R,4R,5R,6R)-4-carboxy-4-hydroxy-5-[(2S,3S)-3-hydroxy-3-(hydroxymethyl)-4,5-dioxooxolan-2-yl]oxy-6-(hydroxymethyl)-3-(3-methylbutanoyloxy)oxan-2-yl]oxy-15-hydroxy-9-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5,5-dicarboxylic acid	101619594	Click to see CC(C)CC(=O)OC1C(OC(C(C1(C(=O)O)O)OC2C(C(=O)C(=O)O2)(CO)O)CO)OC3CC4(C5CCC6CC5(CCC4C(C3)(C(=O)O)C(=O)O)C(C6=C)O)C	798.80	unknown	https://doi.org/10.1039/P19920000593
(2R,3R,4R,5R,6R)-2-[[(1R,4R,5R,7R,9R,10S,13R,15R)-5-carboxy-15-hydroxy-9-methyl-14-methylidene-7-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]oxy]-4-hydroxy-5-[(2S,3S)-3-hydroxy-3-(hydroxymethyl)-4,5-dioxooxolan-2-yl]oxy-6-(hydroxymethyl)-3-(3-methylbutanoyloxy)oxane-4-carboxylic acid	101619595	Click to see CC(C)CC(=O)OC1C(OC(C(C1(C(=O)O)O)OC2C(C(=O)C(=O)O2)(CO)O)CO)OC3CC(C4CCC56CC(CCC5C4(C3)C)C(=C)C6O)C(=O)O	754.80	unknown	https://doi.org/10.1039/P19920000593
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,3R,4R,5'R,6R,7S,8R,9R,10R,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-3,10,16-triol	162978351	Click to see CC1CCC2(C(C3C(O2)C(C4C3(C(CC5C4CCC6C5(CCC(C6)O)C)O)C)O)C)OC1	448.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
(1R,2S,3R,4R,5'R,6R,7S,8R,9S,10R,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-3,10,16-triol	11525201	Click to see CC1CCC2(C(C3C(O2)C(C4C3(C(CC5C4CCC6C5(CCC(C6)O)C)O)C)O)C)OC1	448.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
(1R,2S,3S,4R,5'R,6R,7S,8R,9S,12R,13S,15R,16R,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-3,15,16-triol	162961998	Click to see CC1CCC2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)O)C)OC1	448.60	unknown	https://doi.org/10.1002/JPS.2600510323
5',7,9,13-Tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-3,10,16-triol	72994550	Click to see CC1CCC2(C(C3C(O2)C(C4C3(C(CC5C4CCC6C5(CCC(C6)O)C)O)C)O)C)OC1	448.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
5',7,9,13-Tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-3,15,16-triol	4483041	Click to see CC1CCC2(C(C3C(O2)C(C4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)O)C)OC1	448.60	unknown	https://doi.org/10.1002/JPS.2600510323
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,4'S,5'S,6R,7S,8R,9S,12S,13R,16S)-4'-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101157247	Click to see CC1COC2(CC1O)C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C	1047.20	unknown	https://doi.org/10.1002/1522-2675(20011114)84:11<3350::AID-HLCA3350>3.0.CO;2-U
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-6-[(2R,3R,4S,5S,6R)-5-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,4'S,5'S,6R,7S,8R,9S,12S,13R,16S)-4'-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101157248	Click to see CC1COC2(CC1O)C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(C(O1)C)O)O)O)O)O)C)C)C	1193.30	unknown	https://doi.org/10.1002/1522-2675(20011114)84:11<3350::AID-HLCA3350>3.0.CO;2-U
[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-(hydroxymethyl)-6-[(2R)-4-[(1R,2S,4S,8S,9S,12S,13S,16S,18S)-16-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-6-yl]-2-methylbutoxy]oxan-4-yl] 3-methylbutanoate	163047761	Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CCC5C4(CCC(C5)O)C)C)CCC(C)COC6C(C(C(C(O6)CO)O)OC(=O)CC(C)C)O	662.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
[3,5-Dihydroxy-2-(hydroxymethyl)-6-[4-(16-hydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-6-yl)-2-methylbutoxy]oxan-4-yl] 3-methylbutanoate	73797120	Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CCC5C4(CCC(C5)O)C)C)CCC(C)COC6C(C(C(C(O6)CO)O)OC(=O)CC(C)C)O	662.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
2-[5-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-(4'-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162943444	Click to see CC1COC2(CC1O)C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C	1047.20	unknown	https://doi.org/10.1002/1522-2675(20011114)84:11<3350::AID-HLCA3350>3.0.CO;2-U
2-[6-[5-[3,4-Dihydroxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-(4'-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163046095	Click to see CC1COC2(CC1O)C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(C(O1)C)O)O)O)O)O)C)C)C	1193.30	unknown	https://doi.org/10.1002/1522-2675(20011114)84:11<3350::AID-HLCA3350>3.0.CO;2-U
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	https://doi.org/10.1021/JF049847V
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(3aS,7R,8S,8aR,8bS)-7-hydroxy-3a,7,8-trimethyl-2,3,6,8,8a,8b-hexahydro-1H-acenaphthylen-4-one	21574480	Click to see CC1C2CCC3(C2C(=CC(=O)C3)CC1(C)O)C	234.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
7-hydroxy-3a,7,8-trimethyl-2,3,6,8,8a,8b-hexahydro-1H-acenaphthylen-4-one	73797119	Click to see CC1C2CCC3(C2C(=CC(=O)C3)CC1(C)O)C	234.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Danielone	146167	Click to see COC1=CC(=CC(=C1O)OC)C(=O)CO	212.20	unknown	https://doi.org/10.1021/JF049847V
> Organoheterocyclic compounds / Oxepanes
(1R,3S,6S)-6-[(E,3R)-3-hydroxybut-1-enyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol	23251169	Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)O	226.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
(1S,5R,8R)-8-[(3R)-3-hydroxybutyl]-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-3-one	163009756	Click to see CC(CCC1C2(CC(=O)CC1(OC2)C)C)O	226.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
(E)-4-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-one	14605580	Click to see CC(=O)C=CC12C(CC(CC1(O2)C)O)(C)C	224.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
4-(4-Hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]hept-1-yl)-3-buten-2-one	181574	Click to see CC(=O)C=CC12C(CC(CC1(O2)C)O)(C)C	224.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
6-(3-Hydroxybut-1-enyl)-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol	539381	Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)O	226.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2003.11.018
8-(3-Hydroxybutyl)-1,5-dimethyl-6-oxabicyclo[3.2.1]octan-3-one	163009755	Click to see CC(CCC1C2(CC(=O)CC1(OC2)C)C)O	226.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.09.011
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Caffeic acid methyl ester	689075	Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O	194.18	unknown	https://doi.org/10.1021/JF049847V
Methyl 3,4-dihydroxycinnamate	92202	Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O	194.18	unknown	https://doi.org/10.1021/JF049847V
Methyl 4-hydroxy-3-methoxy-cinnamate	16830	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O	208.21	unknown	https://doi.org/10.1021/JF049847V
Methyl ferulate	5357283	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O	208.21	unknown	https://doi.org/10.1021/JF049847V
> 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/10.1021/JF049847V
4-Hydroxycinnamic acid	322	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1021/JF049847V
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1021/JF049847V
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1021/JF049847V
> 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/10.1021/JF049847V
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retrochalcones
4-Methoxy-4'-hydroxychalcone	97793	Click to see COC1=CC=C(C=C1)C=CC(=O)C2=CC=C(C=C2)O	254.28	unknown	https://doi.org/10.1021/JF049847V
4'-Hydroxy-4-methoxychalcone	5355594	Click to see COC1=CC=C(C=C1)C=CC(=O)C2=CC=C(C=C2)O	254.28	unknown	https://doi.org/10.1021/JF049847V
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid	10394	Click to see C1=CC(=CC=C1CCC(=O)O)O	166.17	unknown	https://doi.org/10.1021/JF049847V

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Cestrum parqui

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