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Porophyllum ruderale

Porophyllum ruderale - 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 UUID643fc7c797339463124011
Scientific name Porophyllum ruderale
Authority (Jacq.) Cass.
First published in Dict. Sci. Nat., ed. 2. [F. Cuvier] 43: 56. 1826 [Sep 1826]

Description Top

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Synonyms Top

Scientific name Authority First published in
Cacalia porophyllum L. Sp. Pl. : 834 (1753)
Cacalia ruderalis Sw. Prodr. Veg. Ind. Occ. : 110 (1788)
Porophyllum ruderale var. angustifolia Hassl. Trab. Mus. Farmacol. 21: 131 (1909)
Porophyllum ruderale var. ellipticum (Cass.) A.Gray ex B.L.Rob. Proc. Amer. Acad. Arts 49: 509 (1913)
Porophyllum ruderale var. glandulosum Chodat Bull. Herb. Boissier ser. 2, 3: 729. 1903
Kleinia porophyllum Willd. Sp. Pl., ed. 4 , 3: 1738 (1803)
Porophyllum ellipticum Cass. Dict. Sci. Nat. 43: 56 (1826)
Porophyllum ellipticum var. intermedium DC. Prodr. 5: 648 (1836)
Kleinia ruderalis Jacq. Enum. Syst. Pl. : 8 & 28 (1760)
Porophyllum macrolepidium Malme Kongl. Svenska Vetensk. Acad. Handl. , n.s., 32(5): 69 (1899)
Tagetes integrifolia Muschl. Beibl. Bot. Jahrb. Syst. 111: 77 (1913)
Porophyllum ruderale var. glandulosum (Salisb.) Chodat 573+, ser. 2,+ 3(8): 729 1903
Porophyllum macrocephalum var. macrocephalum DC. 1836
Porophyllum ruderale var. macrolepidium Chodat Bull. Herb. Boissier 3: 729 (1903)
Porophyllum ruderale subsp. ruderale (Jacq.) Cass.
Porophyllum ruderale f. suffruticosa Chodat Bull. Herb. Boissier 3: 729 (1903)

Common names Top

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Language Common/alternative name
English bolivian coriander
English yerba porosa
Spanish porophyllum ruderale subsp macrocephalum
Spanish quirquiña (cilandro boliviano)
Spanish quirquina (cilandro boliviano)
Spanish quirquina
Spanish quilquiña
Spanish quilquina
Spanish porophyllum ruderale subsp. macrocephalum
Spanish porophyllum porophyllum
Spanish kleinia ruderalis
Spanish cilandro boliviano
Spanish porophyllum ellipticum
Spanish cacalia porophyllum
Spanish cacalia ruderalis
Spanish kleinia porophyllum
Spanish tagetes integrifolia
Spanish porophyllum macrocephalum
Spanish quirquiña
Spanish pápalo
Spanish papalo
Spanish porophyllum latifolium
German bolivianischer koriander
French coriandre bolivienne
Indonesian ketumbar bolivia
pam bolivian coriander
Portuguese porophyllum
Quechua kirkiña
Quechua killkiña
Russian Порофиллум мусорный
Russian Боливийский кориандр
Swedish boliviansk koriander
Chinese 葩葩洛
Chinese 香蝶菊
Chinese 点叶菊

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Porophyllum ruderale var. macrocephalum (DC.) Cronquist Madroño 20: 255 (1970)

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-0000017330
UNII Y23O9UP02L
USDA Plants PORU6
Tropicos 2701154
INPN 630472
KEW urn:lsid:ipni.org:names:208446-2
The Plant List gcc-116772
Open Tree Of Life 621466
Observations.org 198838
NCBI Taxonomy 169599
Nature Serve 2.140217
IPNI 239369-1
iNaturalist 78701
iNaturalist 315923
GBIF 3103948
Freebase /m/049h2f
EOL 509389
Elurikkus 730360
Calflora (Californian flora) 8495
USDA GRIN 29440
Wikipedia Porophyllum_ruderale
CMAUP NPO8286

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
Potential Interest of Oxalis pes-caprae L., a Wild Edible Plant, for the Food and Pharmaceutical Industries Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA Foods 12-Mar-2024
PMCID:PMC10969124
doi:10.3390/foods13060858
PMID:38540848
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
Oxalate in Foods: Extraction Conditions, Analytical Methods, Occurrence, and Health Implications Salgado N, Silva MA, Figueira ME, Costa HS, Albuquerque TG Foods 25-Aug-2023
PMCID:PMC10486698
doi:10.3390/foods12173201
PMID:37685134
Comparison of Phytochemical Composition and Untargeted Metabolomic Analysis of an Extract from Cnidoscolus aconitifolius (Mill.) I. I. Johnst and Porophyllum ruderale (Jacq.) Cass. and Biological Cytotoxic and Antiproliferative Activity In Vitro Vargas-Madriz ÁF, Luzardo-Ocampo I, Moreno-Celis U, Roldán-Padrón O, Chávez-Servín JL, Vergara-Castañeda HA, Martínez-Pacheco M, Mejía C, García-Gasca T, Kuri-García A Plants (Basel) 15-May-2023
PMCID:PMC10222540
doi:10.3390/plants12101987
PMID:37653904
Traditional Mexican Food: Phenolic Content and Public Health Relationship Alatorre-Cruz JM, Carreño-López R, Alatorre-Cruz GC, Paredes-Esquivel LJ, Santiago-Saenz YO, Nieva-Vázquez A Foods 14-Mar-2023
PMCID:PMC10048498
doi:10.3390/foods12061233
PMID:36981159
Nephroprotective Activity of Papaloquelite (Porophyllum ruderale) in Thioacetamide-Induced Injury Model Vázquez-Atanacio MJ, Bautista M, González-Cortazar M, Romero-Estrada A, De la O-Arciniega M, Castañeda-Ovando A, Sosa-Gutiérrez CG, Ojeda-Ramírez D Plants (Basel) 10-Dec-2022
PMCID:PMC9784717
doi:10.3390/plants11243460
PMID:36559573
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
The Main Protease of SARS-CoV-2 as a Target for Phytochemicals against Coronavirus Issa SS, Sokornova SV, Zhidkin RR, Matveeva TV Plants (Basel) 17-Jul-2022
PMCID:PMC9319234
doi:10.3390/plants11141862
PMID:35890496
Assessment of the Volatile Profiles and Identification of Differentiating Aromas of Wild Undervalued Plants Fukalova Fukalova T, Moreno-Peris E, García-Martínez MD, Raigón Jiménez MD Front Nutr 08-Jul-2022
PMCID:PMC9305174
doi:10.3389/fnut.2022.912680
PMID:35873421
Natural compounds based chemotherapeutic against Chagas disease and leishmaniasis: mitochondrion as a strategic target Lazarin-Bidóia D, Garcia FP, Ueda-Nakamura T, Silva SD, Nakamura CV Mem Inst Oswaldo Cruz 30-Mar-2022
PMCID:PMC8970591
doi:10.1590/0074-02760220396
PMID:35352776
Nutritional Composition, Bioactive Compounds, and Volatiles Profile Characterization of Two Edible Undervalued Plants: Portulaca oleracea L. and Porophyllum ruderale (Jacq.) Cass Fukalova Fukalova T, García-Martínez MD, Raigón MD Plants (Basel) 29-Jan-2022
PMCID:PMC8839399
doi:10.3390/plants11030377
PMID:35161358
Interstitial Arabidopsis-Type Telomeric Repeats in Asteraceae Maravilla AJ, Rosato M, Álvarez I, Nieto Feliner G, Rosselló JA Plants (Basel) 17-Dec-2021
PMCID:PMC8705333
doi:10.3390/plants10122794
PMID:34961265
A Comprehensive Review of the Coffee Leaf Miner Leucoptera coffeella (Lepidoptera: Lyonetiidae)—A Major Pest for the Coffee Crop in Brazil and Others Neotropical Countries Dantas J, Motta IO, Vidal LA, Nascimento EF, Bilio J, Pupe JM, Veiga A, Carvalho C, Lopes RB, Rocha TL, Silva LP, Pujol-Luz JR, Albuquerque ÉV Insects 17-Dec-2021
PMCID:PMC8707027
doi:10.3390/insects12121130
PMID:34940218
Boiling Technique-Based Food Processing Effects on the Bioactive and Antimicrobial Properties of Basil and Rosemary Salamatullah AM, Hayat K, Arzoo S, Alzahrani A, Ahmed MA, Yehia HM, Alsulami T, Al-Badr N, Al-Zaied BA, Althbiti MM Molecules 04-Dec-2021
PMCID:PMC8658947
doi:10.3390/molecules26237373
PMID:34885955
Sepal Identity of the Pappus and Floral Organ Development in the Common Dandelion (Taraxacum officinale; Asteraceae) Vijverberg K, Welten M, Kraaij M, van Heuven BJ, Smets E, Gravendeel B Plants (Basel) 16-Aug-2021
PMCID:PMC8398263
doi:10.3390/plants10081682
PMID:34451727

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 / Phenol ethers / Anisoles
Anethole 637563 Click to see CC=CC1=CC=C(C=C1)OC 148.20 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
> Benzenoids / Phenols / Cresols / Meta cresols
m-Cresol 342 Click to see CC1=CC(=CC=C1)O 108.14 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Triacontene 87639 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC=C 420.80 unknown via CMAUP database
1-Undecene 13190 Click to see CCCCCCCCCC=C 154.29 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Decanol 8174 Click to see CCCCCCCCCCO 158.28 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Heptadecanal 71552 Click to see CCCCCCCCCCCCCCCCC=O 254.50 unknown https://doi.org/10.1016/S0031-9422(98)00189-7
Pentadecanal 17697 Click to see CCCCCCCCCCCCCCC=O 226.40 unknown https://doi.org/10.1016/S0031-9422(98)00189-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(5S,6S)-6-ethenyl-3,6-dimethyl-5-prop-1-en-2-yl-5,7-dihydro-1-benzofuran-4-one 10376566 Click to see CC1=COC2=C1C(=O)C(C(C2)(C)C=C)C(=C)C 230.30 unknown via CMAUP database
2-Isopropyl-5-methylanisole 14104 Click to see CC1=CC(=C(C=C1)C(C)C)OC 164.24 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
Cuminaldehyde 326 Click to see CC(C)C1=CC=C(C=C1)C=O 148.20 unknown via CMAUP database
Furanoelemene 12305300 Click to see CC1=COC2=C1CC(C(C2)(C)C=C)C(=C)C 216.32 unknown via CMAUP database
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
https://doi.org/10.1016/S0031-9422(98)00189-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(98)00189-7
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(98)00189-7
https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,5R,6R)-5-[(2R)-2-hydroxybutan-2-yl]-2-methyl-6-(2-methylprop-1-enyl)cyclohex-2-en-1-ol 11843778 Click to see CCC(C)(C1CC=C(C(C1C=C(C)C)O)C)O 238.37 unknown via CMAUP database
(8S)-1,5,8-Trimethyl-8,9-dihydronaphtho[2,1-b]furan-6(7H)-one 71349601 Click to see CC1CC2=C(C(=CC3=C2C(=CO3)C)C)C(=O)C1 228.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Furanoeudesma 1,3-diene 643237 Click to see CC1=CC=CC2(C1CC3=C(C2)OC=C3C)C 214.30 unknown via CMAUP database
Lindestrene 12311270 Click to see CC1=COC2=C1CC3C(=C)CC=CC3(C2)C 214.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(5E,9E)-3,6,10-trimethyl-8,11-dihydro-7H-cyclodeca[b]furan-4-one 6506548 Click to see CC1=CC(=O)C2=C(CC(=CCC1)C)OC=C2C 230.30 unknown via CMAUP database
(5R,6S,8S,9Z)-3,6,10-Trimethyl-4-oxo-8-methoxy-4,5,6,7,8,11-hexahydrocyclodeca[b]furan-5-ol acetate 101149318 Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1OC(=O)C)C)OC 320.40 unknown via CMAUP database
(6S,7R,8E)-7-methoxy-3,6-dimethyl-10-methylidene-5,6,7,11-tetrahydrocyclodeca[b]furan-4-one 10923274 Click to see CC1CC(=O)C2=C(CC(=C)C=CC1OC)OC=C2C 260.33 unknown via CMAUP database
(R,5E,9E)-8-Methoxy-3,6,10-trimethyl-4,7,8,11-tetrahydrocyclodeca[b]furan 91711711 Click to see CC1=CCC2=C(CC(=CC(C1)OC)C)OC=C2C 246.34 unknown via CMAUP database
[(1(10)E,2R,4R)]-2-Methoxy-8,12-epoxygemacra-1(10),7,11-trien-6-one 11747425 Click to see CC1CC(C=C(CC2=C(C(=CO2)C)C(=O)C1)C)OC 262.34 unknown via CMAUP database
Furanodiene 636458 Click to see CC1=CCC2=C(CC(=CCC1)C)OC=C2C 216.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1R,3aR,4R,8aS)-1-methoxy-1,4-dimethyl-7-propan-2-yl-2,3,3a,5,6,8a-hexahydroazulen-4-ol 15896127 Click to see CC(C)C1=CC2C(CCC2(C)OC)C(CC1)(C)O 252.39 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Hydroxyisogermafurenolide 14038425 Click to see CC1=C2CC(C(CC2(OC1=O)O)(C)C=C)C(=C)C 248.32 unknown via CMAUP database
Myrrhanolide C 42636912 Click to see CC1CC2=C(C(CC3(C2=C(C(=O)O3)C)O)C)C(=O)C1 262.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
9a-Hydroxy-3,8a-dimethyl-5-methylene-4,4a,5,6,9,9a-hexahydronaphtho[2,3-b]furan-2(8aH)-one 101938021 Click to see CC1=C2CC3C(=C)CC=CC3(CC2(OC1=O)O)C 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3S,5S,8R,9S,10R,13S,17S)-4,4,8,10,13-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,9,11,12,16,17-decahydro-1H-cyclopenta[a]phenanthrene-1,3-diol 42632429 Click to see CC(CCC=C(C)C)C1CC=C2C1(CCC3C2(CCC4C3(C(CC(C4(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinyl Estradiol 5991 Click to see CC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)O 296.40 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
cis-4-Decenal 5362620 Click to see CCCCCC=CCCC=O 154.25 unknown https://doi.org/10.1016/S0031-9422(98)00189-7
Decanal 8175 Click to see CCCCCCCCCC=O 156.26 unknown https://doi.org/10.1002/(SICI)1099-1026(199911/12)14:6<393::AID-FFJ849>3.0.CO;2-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
1,2-Epoxy-10(14)-furanogermacren-6-one 10444597 Click to see CC1CC2C(O2)C(=C)CC3=C(C(=CO3)C)C(=O)C1 246.30 unknown via CMAUP database
> Organoheterocyclic compounds / Bi- and oligothiophenes
2,2':5',2''-Terthiophene, 5-methyl- 176446 Click to see CC1=CC=C(S1)C2=CC=C(S2)C3=CC=CS3 262.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263252/
4-[5-[5-(Acetyloxymethyl)thiophen-2-yl]thiophen-2-yl]but-3-ynyl acetate 162923044 Click to see CC(=O)OCCC#CC1=CC=C(S1)C2=CC=C(S2)COC(=O)C 348.40 unknown https://doi.org/10.1016/S0031-9422(00)83961-8
5'-Methyl-[5-(4-acetoxy-1-butynyl)]-2,2'-bithiophene 71696677 Click to see CC1=CC=C(S1)C2=CC=C(S2)C#CCCOC(=O)C 290.40 unknown https://doi.org/10.1016/S0031-9422(00)83961-8
6-[5-(5-Methylthiophen-2-yl)thiophen-2-yl]hex-5-yn-2-one 162869323 Click to see CC1=CC=C(S1)C2=CC=C(S2)C#CCCC(=O)C 274.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263252/
> Organoheterocyclic compounds / Naphthofurans
Myrrhanolide A 42632428 Click to see CC1=C2CC3=C(C(=O)OC3(CC2=C(C=C1)C)O)C 244.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown via CMAUP database

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