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Cestrum parqui

Cestrum parqui - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Cestrum parqui - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440410eeff3f392070328
Scientific name Cestrum parqui
Authority L'Hér.
First published in Stirp. Nov. 4: 73, pl. 36. 1788.

Description Top

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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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Language Common/alternative name
English chilean jessamine
Spanish palqui
Spanish cestrum virgatum
Spanish cestrum campestre
Spanish cestrum foetidissimum
Spanish cestrum glaucescens
Spanish cestrum jamaicense var. parqui
Spanish cestrum poeppigii
Spanish cestrum salicifolium
Spanish cestrum salicifolium var. angustifolium
Spanish cestrum spurium
German c. parqui
German chilenischer hammerstrauch
German palqui
Persian گل محبوبه شب
Quechua andres waylla
Quechua anrreswaylla
Swedish cestrum campestre
Swedish grön nattjasmin
Chinese 大夜香樹
Chinese 大夜香树
Chinese 大夜丁香

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
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
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
Pest categorisation of Colletotrichum fructicola Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Campese C, Maiorano A, Streissl F, Reignault PL EFSA J 18-Aug-2021
PMCID:PMC8372655
doi:10.2903/j.efsa.2021.6803
PMID:34434287
The “Bipartite” Structure of the First Genome of Ampelomyces quisqualis, a Common Hyperparasite and Biocontrol Agent of Powdery Mildews, May Point to Its Evolutionary Origin from Plant Pathogenic Fungi Huth L, Ash GJ, Idnurm A, Kiss L, Vaghefi N Genome Biol Evol 07-Aug-2021
PMCID:PMC8382677
doi:10.1093/gbe/evab182
PMID:34363471

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> 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
(3S,5R,6S,7E)-5,6-Epoxy-3-hydroxy-7-megastigmen-9-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
(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://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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