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Raphanus raphanistrum

Raphanus raphanistrum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Raphanus raphanistrum - 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 UUID643ff8a0e4c0f194694108
Scientific name Raphanus raphanistrum
Authority L.
First published in Sp. Pl. : 669 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Raphanus raphanellus Schr. ex Colla Herb. Pedem. 1: 128 (1833)
Raphanus microcarpus Lange Prodr. Fl. Hispan. 3: 750 (1880)
Raphanus sylvestris Lam. Fl. Franç. (Lamarck) 2: 495. 1779 [1778 publ. after 21 Mar 1779]
Raphanus syylosus Dulac Fl. Hautes-Pyrénées : 194 (1867)
Raphanus articulatus Stokes Bot. Mat. Med. 3: 482 (1812)
Raphanistrum segetale Henckel Enum. Pl. Regiomont. : 172 (1817)
Raphanistrum segetum Baumg. Enum. Stirp. Transsilv. 2: 280 (1816)
Raphanistrum silvestre Asch. Fl. Brandenburg 1: 65 (1860)
Raphanistrum vulgare Gray Nat. Arr. Brit. Pl. 2: 687 (1821 publ. 1822)
Raphanus infestus Salisb. Prodr. Stirp. Chap. Allerton : 273 (1796)
Raphanus landroides Rouy & Foucaud Fl. France 1: 68 (1895)
Raphanus longistylus St.-Lag. Ann. Soc. Bot. Lyon 7: 65 (1880)
Raphanus fugax C.Presl Fl. Sicul. : 109 (1826)
Rapistrum arvense All. Fl. Pedem. 1: 258 (1785)
Raphanistrum lampsana Gaertn. Fruct. Sem. Pl. 2: 300 (1791)
Raphanistrum fugax Nyman Consp. Fl. Eur. : 29 (1878)
Raphanistrum microcarpum Nyman Consp. Fl. Eur. , Suppl. 2: 18 (1889)
Raphanistrum innocuum Moench Methodus : 217 (1794)
Raphanistrum raphanistrum H.Karst. Ill. Repert. Pharm.-Med. Bot. : 673 (1886)
Brassica heleniana Burch. ex Loudon Hort. Brit. [Loudon] 264. 1830
Crucifera raphanistrum E.H.L.Krause Deutschl. Fl. Abbild. , ed. 2, 6: 124 (1902)
Durandea unilocularis Delarbre Fl. Auvergne (Delarbre) ed. 2, 365. 1800
Raphanus raphanistrum var. microcarpus Lange Vidensk. Meddel. Dansk Naturhist. Foren. Kjøbenhavn 7: 82 1865
Raphanus raphanistrum subsp. microcarpus (Lange) Thell. Ill. Fl. Mitt.-Eur. 4: 275 1918
Raphanistrum arvense Wallr. Sched. Crit. 336. 1822
Raphanus segetum Clavaud Actes Soc. Linn. Bordeaux 35: 288 (1881)
Raphanistrum innocuum subsp. fugax Nyman Consp. Fl. Eur. 29. 1878
Raphanus raphanistrum subsp. segetum Clavaud 64. 64. 1882
Raphanus raphanistrum var. purpurascens Dumort.
Raphanus raphanistrum f. carneus Thell.
Rapistrum raphanistrum Crantz Cl. Crucif. Emend. : 107 (1769)
Sinapis raphanistrum Gueldenst. ex Ledeb. Fl. Ross. 1: 225 (1841)

Common names Top

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Language Common/alternative name
English wild rape
English wild radish
Spanish rabizon
Spanish rabizón
Arabic فجل الخيل
Arabic عيش وجبن
Arabic فجل بري
Bulgarian дива ряпа
Catalan rave bord
co armuraccia
Czech ředkev ohnice
Czech ohnice polní
Czech ohnice obecná
cv Тискер йӳç кăшман
Welsh rhuddygl
German ackerrettich
German acker-rettich
Estonian põldrõigas
Persian ترب وحشی
Finnish peltoretikka
French ravenelle
frr krook
Galician saramago
Hebrew צנון מצוי
Croatian divlja rotkva
Armenian Բողկ վայրի
Italian ravanello selvatico
Japanese セイヨウノダイコン
Japanese 西洋野大根
Japanese ラファヌス・ラファニストゥルム
Georgian ბოლოკურა
Kazakh Жабайы шомыр
Lithuanian dirvinis ridikas
Lithuanian svėrė
Latvian tīruma pērkone
Macedonian дива ротква
Dutch knopherik
Polish rzodkiew świrzepa
Russian Редька полевая
Russian Редька дикая
Samogitian svierie
Slovak reďkev ohnicová
Serbian дивља ротква
Swedish Åkerrättika
Ukrainian Редька дика
Ukrainian Дика редька
Chinese 野芥菜
Chinese 野蘿蔔
Chinese 野萝卜

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Raphanus raphanistrum subsp. landra (Moretti ex DC.) Bonnier & Layens Tabl. Syn. Pl. Vasc. France : 21 (1894)
Raphanus raphanistrum subsp. rostratus (DC.) Thell. Ill. Fl. Mitt.-Eur. 4(1): 279. 1918 (1918)
Raphanus raphanistrum subsp. sativus (L.) Domin Beih. Bot. Centralbl. 26(2): 255 (1910)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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

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-0000402425
Florida Plant Atlas 1275
Flora of Alabama 1278
Canadensys 4100
USDA Plants RARA2
Tropicos 4100237
INPN 117353
Flora of Italy 1687
KEW urn:lsid:ipni.org:names:217826-2
The Plant List kew-2422367
PFAF Raphanus raphanistrum
Open Tree Of Life 376999
Observations.org 7302
NCBI Taxonomy 109996
NBN Atlas NBNSYS0000002815
Nature Serve 2.140911
IPNI 288483-1
iNaturalist 55411
GBIF 3040983
Freebase /m/07kytl
WisFlora 4771
EPPO RAPRA
EOL 584018
Elurikkus 6764
Calflora (Californian flora) 7063
USDA GRIN 30856
Wikipedia Raphanus_raphanistrum
CMAUP NPO22272

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
Name Level Submitter Released Coverage Size
GCA_019706035.1 IVFCAAS_Rs09_1.0 Chromosome Institiute of Vegetables and Flowers, Chinese Acadmy of Agricultural Science 2021-08-25 173.0x 402.02 Mb

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
Insect floral visitors of thermo-Mediterranean shrubland maquis (Ajaccio, Corsica, France) Maestracci PY, Plume L, Gibernau M Biodivers Data J 25-Apr-2024
PMCID:PMC11079593
doi:10.3897/BDJ.12.e118614
PMID:38726024
Distribution and Mechanism of Japanese Brome (Bromus japonicus) Resistance to ALS-Inhibiting Herbicides in China Bai L, Li X, Guo X, Chen J, Yu H, Cui H Plants (Basel) 19-Apr-2024
PMCID:PMC11054565
doi:10.3390/plants13081139
PMID:38674548
Fuel Characteristics and Phytotoxicity Assay of Biochar Derived from Rose Pruning Waste Stefanów J, Sobieraj K, Hejna M, Pawęska K, Świechowski K Materials (Basel) 19-Apr-2024
PMCID:PMC11051787
doi:10.3390/ma17081895
PMID:38673252
RafanoSet: Dataset of raw, manually, and automatically annotated Raphanus Raphanistrum weed images for object detection and segmentation. Rana S, Gerbino S, Barretta D, Carillo P, Crimaldi M, Cirillo V, Maggio A, Sarghini F Data Brief 16-Apr-2024
PMCID:PMC11063987
doi:10.1016/j.dib.2024.110430
PMID:38698801
Root-Applied Cerium Oxide Nanoparticles and Their Specific Effects on Plants: A Review Pietrzak M, Skiba E, Wolf WM Int J Mol Sci 04-Apr-2024
PMCID:PMC11012102
doi:10.3390/ijms25074018
PMID:38612829
New Light on Plants and Their Chemical Compounds Used in Polish Folk Medicine to Treat Urinary Diseases Olas B, Różański W, Urbańska K, Sławińska N, Bryś M Pharmaceuticals (Basel) 28-Mar-2024
PMCID:PMC11054606
doi:10.3390/ph17040435
PMID:38675397
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Nutrient Uptake Potential of Nonleguminous Species and Its Interaction with Soil Characteristics and Enzyme Activities in the Agro-ecosystem Solangi F, Zhu X, Cao W, Dai X, Solangi KA, Zhou G, Alwasel YA ACS Omega 17-Mar-2024
PMCID:PMC10975627
doi:10.1021/acsomega.3c08794
PMID:38559976
Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy) Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F J Ethnobiol Ethnomed 12-Mar-2024
PMCID:PMC10936038
doi:10.1186/s13002-024-00664-1
PMID:38475780
Antioxidant Responses and Phytochemical Accumulation in Raphanus Species Sprouts through Elicitors and Predictive Models under High Temperature Stress Toro MT, Fustos-Toribio R, Ortiz J, Becerra J, Zapata N, López-Belchí MD Antioxidants (Basel) 08-Mar-2024
PMCID:PMC10967877
doi:10.3390/antiox13030333
PMID:38539866
Non-destructive real-time monitoring of underground root development with distributed fiber optic sensing Tei M, Soma F, Barbieri E, Uga Y, Kawahito Y Plant Methods 29-Feb-2024
PMCID:PMC10905790
doi:10.1186/s13007-024-01160-z
PMID:38424594
Comprehensive Evaluation of Multispectral Image Registration Strategies in Heterogenous Agriculture Environment Rana S, Gerbino S, Crimaldi M, Cirillo V, Carillo P, Sarghini F, Maggio A J Imaging 29-Feb-2024
PMCID:PMC10970895
doi:10.3390/jimaging10030061
PMID:38535141
Hybridization and introgression events in cooccurring populations of closely related grasses (Poaceae: Stipa) in high mountain steppes of Central Asia Sinaga P, Klichowska E, Nowak A, Nobis M PLoS One 27-Feb-2024
PMCID:PMC10898772
doi:10.1371/journal.pone.0298760
PMID:38412151
Efficacy of Herbivore-Induced Plant Volatile Methyl Salicylate in Evaluating the Seasonal Abundance of Herbivorous Thrips (Thysanoptera: Thripidae) in Sweet Pepper Abana UC, Amarasekare KG Insects 25-Feb-2024
PMCID:PMC10971140
doi:10.3390/insects15030156
PMID:38535352

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 / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol 10439806 Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O 714.80 unknown via CMAUP database
Di-(Z)-feruloylsecoisolariciresinol 24898244 Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O 714.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
triptogelin C-1 10459206 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C 516.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,4S,5R,8R,9R,13R,14R,17S,18R,19S,20R)-9-(hydroxymethyl)-4,5,9,13,19,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-10,16-dione 101485480 Click to see CC1CCC23CCC4(C5(CCC6C(C5CC(=O)C4(C2C1C)OC3)(CCC(=O)C6(C)CO)C)C)C 470.70 unknown via CMAUP database
(1S,4S,5R,8R,9S,10S,13R,14R,17S,18R,19S,20R)-10-hydroxy-4,5,9,13,19,20-hexamethyl-16-oxo-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosane-9-carbaldehyde 101485479 Click to see CC1CCC23CCC4(C5(CCC6C(C5CC(=O)C4(C2C1C)OC3)(CCC(C6(C)C=O)O)C)C)C 470.70 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(2S,3S,4aS,6aS,8R,10aR,10bS)-3-ethenyl-3,4a,7,7,10a-pentamethyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101506969 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(C(O3)(C)C=C)OC5C(C(C(C(O5)CO)O)O)O)C)C 646.80 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(3R,4aS,6aS,8R,10aR,10bS)-3-[(1S)-1,2-dihydroxyethyl]-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101506966 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(CO)O)C)C 502.60 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(3R,4aS,6aS,8R,10aR,10bS)-3-[(1S)-2-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromen-8-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101506967 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(CO)OC5C(C(C(C(O5)CO)O)O)O)C)C 664.80 unknown via CMAUP database
(3S,4aR,6aR,6bS,8S,8aS,11R,12S,12aS,14R,14aR,14bS)-14-methoxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-3,8-diol 44235666 Click to see CC1CCC2(C(CC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)OC)C2C1C)C)O)C 472.70 unknown via CMAUP database
(3S,4S,4aR,6aR,6bS,8aR,11R,12S,12aR,14S,14aR,14bS)-3,13-dihydroxy-14-methoxy-4,6a,6b,8a,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4-carbaldehyde 44235896 Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CCC5C4(CCC(C5(C)C=O)O)C)C)OC)O)C2C1C)C)C 486.70 unknown via CMAUP database
(4R,4aR,6aR,6bS,8aR,11R,12S,12aR,14S,14aR,14bS)-13-hydroxy-4-(hydroxymethyl)-14-methoxy-4,6a,6b,8a,11,12,14b-heptamethyl-1,2,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydropicen-3-one 44235900 Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)OC)O)C2C1C)C)C 486.70 unknown via CMAUP database
6beta,12-Dihydroxy-11alpha-methoxy-24-norurs-12-ene-3-one 44235898 Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CC(C5C4(CCC(=O)C5C)C)O)C)OC)O)C2C1C)C)C 472.70 unknown via CMAUP database
Microtropioside D 101506968 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(COC5C(C(C(C(O5)CO)O)O)O)O)C)C 664.80 unknown via CMAUP database
Microtropioside F 101506970 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(C(O3)(C)C=C)OC5C(C(C(C(O5)CO)O)O)O)C)C 646.80 unknown via CMAUP database
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 via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
[(2R,3S,4S,5R,6R)-6-[(2R,3R)-3-cyanobutan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (2S,3R)-2-ethyl-2,3-dihydroxybutanoate 102448005 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O 391.40 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-6-[(2S,3S)-3-cyanobutan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (2S,3R)-2-ethyl-2,3-dihydroxybutanoate 102448006 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O 391.40 unknown via CMAUP database
[(2R,3S,4S,5R,6R)-6-[(E)-3-cyano-4-hydroxybut-2-enoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (2S,3R)-2-ethyl-2,3-dihydroxybutanoate 102448007 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OCC=C(CO)C#N)O)O)O)O 405.40 unknown via CMAUP database
Microtropin A 102448004 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O 391.40 unknown via CMAUP database
Microtropin E 102448008 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C)O)O)O)O 352.38 unknown via CMAUP database
Microtropin F 102448009 Click to see CCC(COC1C(C(C(C(O1)COC(=O)C(CC)(C(C)O)O)O)O)O)O 382.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
2-[(1R,2R,4aR,4bS,6aS,10aS,12aR)-6a-(hydroxymethyl)-2-(1-methoxy-2-methyl-1-oxopropan-2-yl)-1,4a,4b,9,9-pentamethyl-3,4,5,6,7,8,10,10a,12,12a-decahydro-2H-chrysen-1-yl]acetic acid 44235899 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)O)C(C)(C)C(=O)OC)C)C2C1)C)CO)C 502.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
8-Benzoyloxymutangin 24898243 Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)COC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C 756.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,2R,4S,5R,6R,7S,9R,12R)-4,5-diacetyloxy-7,12-dibenzoyloxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-6-yl]methyl benzoate 16109789 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C5=CC=CC=C5)COC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C 698.80 unknown via CMAUP database
[(1S,2R,4S,5R,6R,7S,9R,12R)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14414924 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 574.60 unknown via CMAUP database
15-Acetoxyorbiculin G 24898039 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C5=CC=CC=C5)COC(=O)C)OC(=O)C)OC(=O)C6=CC=CC=C6 698.80 unknown via CMAUP database
Mutangin 44419602 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C 636.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Ethyl Vanillin 8467 Click to see CCOC1=C(C=CC(=C1)C=O)O 166.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see COC1=C(C=CC(=C1)C(=O)CCO)O 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1S,4S,6R,9R,10S,13R,14S)-14-hydroxy-5,5,9,13-tetramethyl-16,18-dioxatetracyclo[11.4.1.01,10.04,9]octadecan-6-yl]oxy]oxane-3,4,5-triol 101506965 Click to see CC1(C2CCC34COCC(C(O3)(CCC4C2(CCC1OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C 500.60 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / N-alkylpyrrolidines
1-Methyl-2-pyrrolidinone 13387 Click to see CN1CCCC1=O 99.13 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(-)-Evofolin B 46229015 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown via CMAUP database

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