Melampodium divaricatum - Unknown
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Details Top

Internal ID UUID643fc98d77ba9448686349
Scientific name Melampodium divaricatum
Authority DC.
First published in Prodr. 5: 520 (1836)

Description Top

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Melampodium divaricatum, also known as gold medallion, is a type of flowering plant belonging to the Melampodium genus. It was first identified in 1836 and is commonly found in gardens and landscapes. This species is known for its vibrant yellow flowers, which resemble a medallion, hence its common name. It is a popular choice for its attractive appearance and easy maintenance.

Synonyms Top

Scientific name Authority First published in
Dysodium divaricatum Pers. 1807
Eleutheranthera divaricata Millsp. Publ. Field Columb. Mus., Bot. Ser. 1: 53 (1895)
Melampodium paludosum Kunth Nov. Gen. Sp. 4(17): 215 (ed. fol.) (1818)
Melampodium divaricatum var. macranthum Schlecht.
Melampodium tenellum var. flaccidum Benth. Bot. Voy. Sulphur : 115 (1845)
Zarabellia rhomboidea Cass. Dict. Sci. Nat., ed. 2. 59: 240 (1829)
Melampodium flaccidum (Benth.) Benth. Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1852(5-7): 86. 1853 [1852 publ. 1853]
Melampodium flaccidum Benth. ex Oerst. Vidensk. Meddel. Dansk Naturhist. Foren. Kjobenhavn (1852) 86.
Melampodium ovatifolium Rchb. Iconogr. Bot. Exot. 1: t. 42 (1824)
Melampodium berteroanum Spreng. Syst. Veg. 3: 619 (1826)
Alcina minor Cass. Dict. Sci. Nat., ed. 2. 59: 243 (1829)
Wedelia ovatifolia Willd. Enum. Pl. Suppl. [Willdenow] 61. 1814 [Jul-Dec 1814]
Dysodium divaricatum Rich. Syn. Pl. ii. 489 (1807)
Melampodium copiosum Klatt Bot. Jahrb. Syst. 8(1): 41 (1886)
Alcina ovatifolia J.Jacq. Ecl. Pl. Rar. : 78
Alcina ovatifolia Lag. Gen. Sp. Pl. 32. 1816.
Melampodium pumilum Benth. Pl. Hartw. : 64 (1840)
Dysodium radiatum Desf. Tabl. École Bot. : 182 (1829)
Wedelia minor Hornem. Hort. Bot. Hafn. : 855 (1815)
Melampodium panamense Klatt Bot. Jahrb. Syst. 8(1): 42 (1886)
Alcina ovalifolia Lag. Gen. Sp. Pl. 32 1816

Common names Top

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Language Common/alternative name
English boton de oro
Thai กระดุมทอง
Chinese 黃帝菊
Chinese 黄帝菊
Chinese 帝王菊
Chinese 美兰菊
Chinese 黄油菊

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Sri Lanka
    • Indo-China
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Philippines
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
    • Caribbean
      • Cuba
      • Dominican Republic
      • Leeward Islands
      • Puerto Rico
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000031493
UNII 09251ZM83D
Florida Plant Atlas 103
Flora of Alabama 874
USDA Plants MEDI4
Tropicos 2702893
INPN 915026
KEW urn:lsid:ipni.org:names:156179-2
The Plant List gcc-130451
Missouri Botanical Garden 277348
Open Tree Of Life 481300
Observations.org 198328
NCBI Taxonomy 176609
IPNI 156179-2
iNaturalist 288660
GBIF 3138949
EPPO MEMDI
EOL 400360
Elurikkus 730351
USDA GRIN 315867
Wikipedia Melampodium_divaricatum

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 Effects of Essential Oil from Plinia cauliflora (Mart.) Kausel on Leishmania: In Vivo, In Vitro, and In Silico Approaches Holanda VN, Brito TG, de Oliveira JR, da Cunha RX, da Silva AP, da Silva WV, Araújo TF, Tavares JF, dos Santos SG, Figueiredo RC, Lima VL Microorganisms 19-Jan-2024
PMCID:PMC10819817
doi:10.3390/microorganisms12010207
PMID:38276192
Machine Learning Analysis of Essential Oils from Cuban Plants: Potential Activity against Protozoa Parasites Barros de Menezes RP, Scotti L, Scotti MT, García J, González R, Monzote L, Setzer WN Molecules 17-Feb-2022
PMCID:PMC8878085
doi:10.3390/molecules27041366
PMID:35209156
The Compositional Aspects of Edible Flowers as an Emerging Horticultural Product Pires ED Jr, Di Gioia F, Rouphael Y, Ferreira IC, Caleja C, Barros L, Petropoulos SA Molecules 17-Nov-2021
PMCID:PMC8619536
doi:10.3390/molecules26226940
PMID:34834031
Green Approach: ‘‘A Forwarding Step for Curing Leishmaniasis—A Neglected Tropical Disease’’ Sharma L, Dhiman M, Singh A, Sharma MM Front Mol Biosci 28-May-2021
PMCID:PMC8193676
doi:10.3389/fmolb.2021.655584
PMID:34124148
7-Isopentenyloxycoumarin: What Is New across the Last Decade Preziuso F, Genovese S, Marchetti L, Sharifi-Rad M, Palumbo L, Epifano F, Fiorito S Molecules 14-Dec-2020
PMCID:PMC7765079
doi:10.3390/molecules25245923
PMID:33327602
Insecticidal and Cholinesterase Activity of Dichloromethane Extracts of Tithonia diversifolia on Atta cephalotes Worker Ants (Formicidae: Myrmicinae) Pantoja-Pulido KD, Rodríguez J, Isaza-Martínez JH, Gutiérrez-Cabrera M, Colmenares-Dulcey AJ, Montoya-Lerma J Insects 11-Mar-2020
PMCID:PMC7142932
doi:10.3390/insects11030180
PMID:32168911
Antileishmanial activity of Melampodium divaricatum and Casearia sylvestris essential oils on Leishmania amazonensis Moreira RR, dos Santos AG, Carvalho FA, Perego CH, Crevelin EJ, Crotti AE, Cogo J, Cardoso ML, Nakamura CV Rev Inst Med Trop Sao Paulo 01-Jul-2019
PMCID:PMC6609133
doi:10.1590/S1678-9946201961033
PMID:31269109
Ixcatec ethnoecology: plant management and biocultural heritage in Oaxaca, Mexico Rangel-Landa S, Casas A, Rivera-Lozoya E, Torres-García I, Vallejo-Ramos M J Ethnobiol Ethnomed 20-Jul-2016
PMCID:PMC4955254
doi:10.1186/s13002-016-0101-3
PMID:27439512
Use of herbarium data to evaluate weediness in five congeners Hanan-A. AM, Vibrans H, Cacho NI, Villaseñor JL, Ortiz E, Gómez-G. VA AoB Plants 15-Dec-2015
PMCID:PMC4740360
doi:10.1093/aobpla/plv144
PMID:26672076
Spatiotemporal variation of mosquito diversity (Diptera: Culicidae) at places with different land-use types within a neotropical montane cloud forest matrix Abella-Medrano CA, Ibáñez-Bernal S, MacGregor-Fors I, Santiago-Alarcon D Parasit Vectors 24-Sep-2015
PMCID:PMC4581103
doi:10.1186/s13071-015-1086-9
PMID:26399854
Effect of drought on safflower natural dyes and their biological activities Salem N, Msaada K, Dhifi W, Sriti J, Mejri H, Limam F, Marzouk B EXCLI J 28-Jan-2014
PMCID:PMC4464500
PMID:26417239
The Effect of the Landscape Matrix on the Distribution of Dung and Carrion Beetles in a Fragmented Tropical Rain Forest Díaz A, Galante E, Favila ME J Insect Sci 29-Jun-2010
PMCID:PMC3383436
doi:10.1673/031.010.8101
PMID:20673066
Plants used traditionally to treat malaria in Brazil: the archives of Flora Medicinal Botsaris AS J Ethnobiol Ethnomed 01-May-2007
PMCID:PMC1891273
doi:10.1186/1746-4269-3-18
PMID:17472740
Isolation and synthesis of two coumarins from melampodium divaricatum Juan Borges-Del-Castillo, Ana I. Martinez-Martir, Francisco Rodriguez-Luis, Juan C. Rodriguez-Ubis, Purificacion Vazquez-Bueno Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85043-8
Terpen-glycoside aus Melampodium divaricatum Ferdinand Bohlmann, Ngo Le Van Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(71)85085-9

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
5-(1,2,4a,5-Tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-ol 73808214 Click to see CC1CCC2(C(C1(C)CCC(=CCO)C)CCC=C2C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
Kolavenol 6442554 Click to see CC1CCC2(C(C1(C)CCC(=CCO)C)CCC=C2C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
1,1,7-Trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 522266 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
1-Methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydroazulen-1-ol 73102746 Click to see CC(C)C1=CC2C(CCC2(C)O)C(=C)CC1 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
Alismol 15934381 Click to see CC(C)C1=CC2C(CCC2(C)O)C(=C)CC1 220.35 unknown https://doi.org/10.1016/S0031-9422(00)81099-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(2R,3R,4R,5R,6S)-4-[(2S,3R,4R,5R,6R)-3,4-dihydroxy-6-methyl-5-(3-methylbutanoyloxy)oxan-2-yl]oxy-5-hydroxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyloxan-3-yl] (Z)-2-methylbut-2-enoate 100938432 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)OC(=O)CC(C)C)O)O)O)OC3=C(C=CC(=C3O)C)C(C)C)C 624.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-[(2S,3R,4R,5R,6R)-3-hydroxy-2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-5-[(Z)-2-methylbut-2-enoyl]oxyoxan-4-yl]oxy-2-methyloxan-3-yl] (2R)-2-methylbutanoate 163186414 Click to see CCC(C)C(=O)OC1C(OC(C(C1O)O)OC2C(C(OC(C2OC(=O)C(=CC)C)C)OC3=C(C=CC(=C3O)C)C(C)C)O)C 624.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-[(2S,3R,4S,5S,6R)-2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-3-(3-methylbutanoyloxy)-5-[(Z)-2-methylbut-2-enoyl]oxyoxan-4-yl]oxy-2-methyloxan-3-yl] (Z)-2-methylbut-2-enoate 100938430 Click to see CC=C(C)C(=O)OC1C(OC(C(C1O)O)OC2C(C(OC(C2OC(=O)CC(C)C)OC3=C(C=CC(=C3O)C)C(C)C)C)OC(=O)C(=CC)C)C 706.80 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-[(2S,3R,4S,5S,6R)-2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-3,5-bis[[(Z)-2-methylbut-2-enoyl]oxy]oxan-4-yl]oxy-2-methyloxan-3-yl] (Z)-2-methylbut-2-enoate 100938426 Click to see CC=C(C)C(=O)OC1C(OC(C(C1O)O)OC2C(C(OC(C2OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C)OC(=O)C(=CC)C)C 704.80 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3R,4R,5R,6S)-6-[(2S,3R,4S,5S,6R)-5-acetyloxy-2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-3-[(Z)-2-methylbut-2-enoyl]oxyoxan-4-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] (Z)-2-methylbut-2-enoate 100938428 Click to see CC=C(C)C(=O)OC1C(OC(C(C1O)O)OC2C(C(OC(C2OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C)OC(=O)C)C 664.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3R,4S,5R,6S)-4-[(2S,3R,4R,5R,6R)-5-acetyloxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-5-[(Z)-2-methylbut-2-enoyl]oxyoxan-3-yl] (Z)-2-methylbut-2-enoate 100938434 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)OC(=O)C)O)O)OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C 664.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3R,4S,5R,6S)-4-[(2S,3R,4S,5S,6R)-3,5-dihydroxy-6-methyl-4-[(Z)-2-methylbut-2-enoyl]oxyoxan-2-yl]oxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-5-[(Z)-2-methylbut-2-enoyl]oxyoxan-3-yl] (Z)-2-methylbut-2-enoate 100938433 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)O)OC(=O)C(=CC)C)O)OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C 704.80 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3R,4S,5R,6S)-4-[(2S,3R,4S,5S,6R)-4-acetyloxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-5-[(Z)-2-methylbut-2-enoyl]oxyoxan-3-yl] (Z)-2-methylbut-2-enoate 100938435 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)O)OC(=O)C)O)OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C 664.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3S,4R,5R,6S)-4-[(2S,3R,4S,5S,6R)-3,5-dihydroxy-6-methyl-4-[(Z)-2-methylbut-2-enoyl]oxyoxan-2-yl]oxy-5-hydroxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyloxan-3-yl] (Z)-2-methylbut-2-enoate 100938429 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)O)OC(=O)C(=CC)C)O)O)OC3=C(C=CC(=C3O)C)C(C)C)C 622.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3S,4S,5R,6S)-4-[(2S,3R,4S,5S,6R)-3,5-dihydroxy-6-methyl-4-[(Z)-2-methylbut-2-enoyl]oxyoxan-2-yl]oxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-5-(3-methylbutanoyloxy)oxan-3-yl] (Z)-2-methylbut-2-enoate 100938425 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)O)OC(=O)C(=CC)C)O)OC(=O)CC(C)C)OC3=C(C=CC(=C3O)C)C(C)C)C 706.80 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2R,3S,4S,5R,6S)-4-[(2S,3R,4S,5S,6R)-3,5-dihydroxy-6-methyl-4-[(Z)-2-methylbut-2-enoyl]oxyoxan-2-yl]oxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-5-[(Z)-2-methylbut-2-enoyl]oxyoxan-3-yl] (Z)-2-methylbut-2-enoate 100938427 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)O)OC(=O)C(=CC)C)O)OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C 704.80 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2S,3R,4S,5S,6R)-2-[(2S,3R,4R,5S,6R)-5-acetyloxy-3-hydroxy-2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyloxan-4-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] (Z)-2-methylbut-2-enoate 100938431 Click to see CC=C(C)C(=O)OC1C(C(OC(C1O)OC2C(C(OC(C2OC(=O)C)C)OC3=C(C=CC(=C3O)C)C(C)C)O)C)O 582.60 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[(2S,3R,4S,5S,6S)-5-acetyloxy-6-(2-acetyloxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-4-(3-methylbutanoyloxy)oxan-3-yl] (Z)-2-methylbut-2-enoate 163192875 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC(=O)CC(C)C)OC(=O)C)OC2=C(C=CC(=C2OC(=O)C)C)C(C)C)C 562.60 unknown https://doi.org/10.1016/0031-9422(71)85085-9
[(2S,3S,4S,5R,6S)-5-acetyloxy-2-(2-acetyloxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-4-(3-methylbutanoyloxy)oxan-3-yl] (Z)-2-methylbut-2-enoate 163189398 Click to see CC=C(C)C(=O)OC1C(C(C(OC1OC2=C(C=CC(=C2OC(=O)C)C)C(C)C)C)OC(=O)C)OC(=O)CC(C)C 562.60 unknown https://doi.org/10.1016/0031-9422(71)85085-9
[2-[5-Acetyloxy-3-hydroxy-2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyloxan-4-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] 2-methylbut-2-enoate 163017686 Click to see CC=C(C)C(=O)OC1C(C(OC(C1O)OC2C(C(OC(C2OC(=O)C)C)OC3=C(C=CC(=C3O)C)C(C)C)O)C)O 582.60 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[4-(4-Acetyloxy-3,5-dihydroxy-6-methyloxan-2-yl)oxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-5-(2-methylbut-2-enoyloxy)oxan-3-yl] 2-methylbut-2-enoate 162959395 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)O)OC(=O)C)O)OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C 664.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[4-(5-Acetyloxy-3,4-dihydroxy-6-methyloxan-2-yl)oxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-5-(2-methylbut-2-enoyloxy)oxan-3-yl] 2-methylbut-2-enoate 163054754 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)OC(=O)C)O)O)OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C 664.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[4-[3,4-Dihydroxy-6-methyl-5-(3-methylbutanoyloxy)oxan-2-yl]oxy-5-hydroxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyloxan-3-yl] 2-methylbut-2-enoate 163037375 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)OC(=O)CC(C)C)O)O)O)OC3=C(C=CC(=C3O)C)C(C)C)C 624.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[4-[3,5-Dihydroxy-6-methyl-4-(2-methylbut-2-enoyloxy)oxan-2-yl]oxy-5-hydroxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyloxan-3-yl] 2-methylbut-2-enoate 162965628 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)O)OC(=O)C(=CC)C)O)O)OC3=C(C=CC(=C3O)C)C(C)C)C 622.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[4-[3,5-Dihydroxy-6-methyl-4-(2-methylbut-2-enoyloxy)oxan-2-yl]oxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-5-(2-methylbut-2-enoyloxy)oxan-3-yl] 2-methylbut-2-enoate 163076783 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)O)OC(=O)C(=CC)C)O)OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C 704.80 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[4-[3,5-Dihydroxy-6-methyl-4-(2-methylbut-2-enoyloxy)oxan-2-yl]oxy-6-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-5-(3-methylbutanoyloxy)oxan-3-yl] 2-methylbut-2-enoate 163014022 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC2C(C(C(C(O2)C)O)OC(=O)C(=CC)C)O)OC(=O)CC(C)C)OC3=C(C=CC(=C3O)C)C(C)C)C 706.80 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[4,5-Dihydroxy-6-[2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-3-(3-methylbutanoyloxy)-5-(2-methylbut-2-enoyloxy)oxan-4-yl]oxy-2-methyloxan-3-yl] 2-methylbut-2-enoate 162929800 Click to see CC=C(C)C(=O)OC1C(OC(C(C1O)O)OC2C(C(OC(C2OC(=O)CC(C)C)OC3=C(C=CC(=C3O)C)C(C)C)C)OC(=O)C(=CC)C)C 706.80 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[4,5-Dihydroxy-6-[2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-3,5-bis(2-methylbut-2-enoyloxy)oxan-4-yl]oxy-2-methyloxan-3-yl] 2-methylbut-2-enoate 162904977 Click to see CC=C(C)C(=O)OC1C(OC(C(C1O)O)OC2C(C(OC(C2OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C)OC(=O)C(=CC)C)C 704.80 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[4,5-Dihydroxy-6-[3-hydroxy-2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-5-(2-methylbut-2-enoyloxy)oxan-4-yl]oxy-2-methyloxan-3-yl] 2-methylbutanoate 163026032 Click to see CCC(C)C(=O)OC1C(OC(C(C1O)O)OC2C(C(OC(C2OC(=O)C(=CC)C)C)OC3=C(C=CC(=C3O)C)C(C)C)O)C 624.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
[5-Acetyloxy-2-(2-acetyloxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-4-(3-methylbutanoyloxy)oxan-3-yl] 2-methylbut-2-enoate 162990637 Click to see CC=C(C)C(=O)OC1C(C(C(OC1OC2=C(C=CC(=C2OC(=O)C)C)C(C)C)C)OC(=O)C)OC(=O)CC(C)C 562.60 unknown https://doi.org/10.1016/0031-9422(71)85085-9
[5-Acetyloxy-6-(2-acetyloxy-3-methyl-6-propan-2-ylphenoxy)-2-methyl-4-(3-methylbutanoyloxy)oxan-3-yl] 2-methylbut-2-enoate 162857601 Click to see CC=C(C)C(=O)OC1C(OC(C(C1OC(=O)CC(C)C)OC(=O)C)OC2=C(C=CC(=C2OC(=O)C)C)C(C)C)C 562.60 unknown https://doi.org/10.1016/0031-9422(71)85085-9
[6-[5-Acetyloxy-2-(2-hydroxy-3-methyl-6-propan-2-ylphenoxy)-6-methyl-3-(2-methylbut-2-enoyloxy)oxan-4-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] 2-methylbut-2-enoate 162982766 Click to see CC=C(C)C(=O)OC1C(OC(C(C1O)O)OC2C(C(OC(C2OC(=O)C(=CC)C)OC3=C(C=CC(=C3O)C)C(C)C)C)OC(=O)C)C 664.70 unknown https://doi.org/10.1016/S0031-9422(98)00700-6
> Organoheterocyclic compounds / Pyrrolidines
2-Pyrrolidineacetic acid 123784 Click to see C1CC(NC1)CC(=O)O 129.16 unknown https://doi.org/10.1016/S0305-1978(99)00102-7
> Organoheterocyclic compounds / Pyrrolizidines
Isotussilagine 149801 Click to see CC1(CN2CCCC2C1C(=O)OC)O 199.25 unknown https://doi.org/10.1016/S0305-1978(99)00102-7
Neotussilagine 4484216 Click to see CC1(CN2CCCC2C1C(=O)OC)O 199.25 unknown https://doi.org/10.1016/S0305-1978(99)00102-7
Tussilagine 185071 Click to see CC1(CN2CCCC2C1C(=O)OC)O 199.25 unknown https://doi.org/10.1016/S0305-1978(99)00102-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
8-Hydroxy-7-((3-methyl-2-butenyl)oxy)-2H-1-benzopyran-2-one 44439634 Click to see CC(=CCOC1=C(C2=C(C=C1)C=CC(=O)O2)O)C 246.26 unknown https://doi.org/10.1016/S0031-9422(00)85043-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-8-((3-methyl-2-butenyl)oxy)-2H-1-benzopyran-2-one 86254474 Click to see CC(=CCOC1=C(C=CC2=C1OC(=O)C=C2)O)C 246.26 unknown https://doi.org/10.1016/S0031-9422(00)85043-8

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