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Helianthus maximiliani

Helianthus maximiliani - 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 UUID643fcdb803832176643374
Scientific name Helianthus maximiliani
Authority Schrad.
First published in Index Seminum (GOET, Gottingensis) [unpaged] (1835)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Helianthus dalyi Britton J. New York Bot. Gard. 2: 89 (1901)

Common names Top

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Language Common/alternative name
English maximilian sunflower
Hebrew חמנית מקסמיליאן
Chinese 糙叶向日葵

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • Ontario
      • Québec
    • Mexico
      • Mexico Northeast
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • Oklahoma
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Washington
      • Wyoming
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Kentucky
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • California
      • Utah
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000074910
Flora of Alabama 800
Canadensys 3196
USDA Plants HEMA2
Tropicos 2702641
INPN 611201
KEW urn:lsid:ipni.org:names:329260-2
The Plant List gcc-31619
Missouri Botanical Garden 261947
Open Tree Of Life 718839
NCBI Taxonomy 73297
Nature Serve 2.135891
IUCN Red List 20694305
IPNI 329260-2
iNaturalist 130192
GBIF 3119206
Freebase /m/03ylkb2
WisFlora 3817
FEIS plants/forb/helmax
EPPO HELMA
EOL 468062
USDA GRIN 27931
Wikipedia Helianthus_maximiliani
CMAUP NPO16913

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
Adaptation of perennial flowering phenology across the European range of Arabis alpina Wunder J, Fulgione A, Toräng P, Wötzel S, Herzog M, Obeso JR, Kourmpetis Y, van Ham R, Odong T, Bink M, Kemi U, Ågren J, Coupland G Proc Biol Sci 22-Nov-2023
PMCID:PMC10688268
doi:10.1098/rspb.2023.1401
PMID:37989245
Economically viable flower drying techniques to sustain flower industry amid COVID-19 pandemic Kumar M, Chaudhary V, Sirohi U, Srivastav AL Environ Dev Sustain 29-May-2023
PMCID:PMC10225293
doi:10.1007/s10668-023-03376-w
PMID:37363010
Sunflower plantings reduce a common gut pathogen and increase queen production in common eastern bumblebee colonies Malfi RL, McFrederick QS, Lozano G, Irwin RE, Adler LS Proc Biol Sci 05-Apr-2023
PMCID:PMC10072944
doi:10.1098/rspb.2023.0055
PMID:37015273
A review on Q ST – F ST comparisons of seed plants: Insights for conservation Chung MY, Merilä J, Kim Y, Mao K, López‐Pujol J, Chung MG Ecol Evol 28-Mar-2023
PMCID:PMC10049885
doi:10.1002/ece3.9926
PMID:37006890
Re-evaluating Homoploid Reticulate Evolution in Helianthus Sunflowers Owens GL, Huang K, Todesco M, Rieseberg LH Mol Biol Evol 17-Jan-2023
PMCID:PMC9907532
doi:10.1093/molbev/msad013
PMID:36648104
Genome Survey and SSR Analysis of Camellia nitidissima Chi (Theaceae) Bai Y, Ye L, Yang K, Wang H Genet Res (Camb) 02-Nov-2022
PMCID:PMC9646326
doi:10.1155/2022/5417970
PMID:36407084
A Mixed Model for Assessing the Effect of Numerous Plant Species Interactions on Grassland Biodiversity and Ecosystem Function Relationships McDonnell J, McKenna T, Yurkonis KA, Hennessy D, de Andrade Moral R, Brophy C J Agric Biol Environ Stat 01-Sep-2022
PMCID:PMC9908731
doi:10.1007/s13253-022-00505-2
PMID:36779040
A Quantitative Genetic Study of Sclerotinia Head Rot Resistance Introgressed from the Wild Perennial Helianthus maximiliani into Cultivated Sunflower (Helianthus annuus L.) Talukder ZI, Underwood W, Misar CG, Seiler GJ, Cai X, Li X, Qi L Int J Mol Sci 13-Jul-2022
PMCID:PMC9321925
doi:10.3390/ijms23147727
PMID:35887074
Reinventory of the vascular plants of Mormon Island Crane Meadows after forty years of restoration, invasion, and climate change Caven AJ, Wiese JD Heliyon 03-Jun-2022
PMCID:PMC9192816
doi:10.1016/j.heliyon.2022.e09640
PMID:35711997
The Microbial Nitrogen Cycling, Bacterial Community Composition, and Functional Potential in a Natural Grassland Are Stable from Breaking Dormancy to Being Dormant Again Das BK, Ishii S, Antony L, Smart AJ, Scaria J, Brözel VS Microorganisms 28-Apr-2022
PMCID:PMC9148154
doi:10.3390/microorganisms10050923
PMID:35630367
Population genomics of free‐ranging Great Plains white‐tailed and mule deer reflects a long history of interspecific hybridization Combe FJ, Jaster L, Ricketts A, Haukos D, Hope AG Evol Appl 14-Dec-2021
PMCID:PMC8792484
doi:10.1111/eva.13330
PMID:35126651
Patch utilization and flower visitations by wild bees in a honey bee‐dominated, grassland landscape Otto CR, Bailey LL, Smart AH Ecol Evol 10-Oct-2021
PMCID:PMC8571640
doi:10.1002/ece3.8174
PMID:34765148
Testing for evolutionary change in restoration: A genomic comparison between ex situ, native, and commercial seed sources of Helianthus maximiliani Braasch JE, Di Santo LN, Tarble ZJ, Prasifka JR, Hamilton JA Evol Appl 19-Jul-2021
PMCID:PMC8477598
doi:10.1111/eva.13275
PMID:34603493
Examining the utility of DNA barcodes for the identification of tallgrass prairie flora Herzog SA, Latvis M Appl Plant Sci 24-Jan-2021
PMCID:PMC7845766
doi:10.1002/aps3.11405
PMID:33552747
Genome Survey Sequencing of In Vivo Mother Plant and In Vitro Plantlets of Mikania cordata Hong Y, Huang X, Li C, Ruan X, Wang Z, Su Y, Wang T Plants (Basel) 27-Nov-2020
PMCID:PMC7759884
doi:10.3390/plants9121665
PMID:33261119

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,4aS,5R,8aS)-1,4a-dimethyl-6-methylidene-5-[(2Z)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 162987477 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
[1-(Hydroxymethyl)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,7,9,10,10a-decahydrophenanthren-9-yl] acetate 162974782 Click to see CC(C)C1CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)OC(=O)C 348.50 unknown https://doi.org/10.1016/S0031-9422(00)83135-0
1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 72957164 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1-Hydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl) 2-methylbut-2-enoate 72816393 Click to see CC=C(C)C(=O)OC1CC2(CCC(O2)(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
(12-Hydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl) 2-methylbut-2-enoate 433434 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
(8-Acetyloxy-4-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-6,12-dioxatricyclo[9.3.0.05,7]tetradec-9-en-2-yl) 2-methylbut-2-enoate 433433 Click to see CC=C(C)C(=O)OC1CC(C2C(O2)C(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)(C)O 420.50 unknown https://doi.org/10.1016/0031-9422(81)85224-7
[(1R,2Z,4S,8R,9R,11S)-1-hydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 162982463 Click to see CC=C(C)C(=O)OC1CC2(CCC(O2)(C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
[(1S,2R,4R,5R,7R,8R,9Z,11S)-8-acetyloxy-4-hydroxy-4,9-dimethyl-14-methylidene-13-oxo-6,12-dioxatricyclo[9.3.0.05,7]tetradec-9-en-2-yl] (Z)-2-methylbut-2-enoate 162888854 Click to see CC=C(C)C(=O)OC1CC(C2C(O2)C(C(=CC3C1C(=C)C(=O)O3)C)OC(=O)C)(C)O 420.50 unknown https://doi.org/10.1016/0031-9422(81)85224-7
[(1S,2Z,4R,8R,9R,11S,12R)-1,12-dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 10667367 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)C)O)O)C 378.40 unknown via CMAUP database
[(1S,2Z,4S,8R,9R,11R,12S)-1,12-dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 163099939 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)C)O)O)C 378.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
[(1S,2Z,4S,8R,9R,11R,12S)-12-hydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-2-en-9-yl] (Z)-2-methylbut-2-enoate 162943534 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)C(=CC3C1C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
Annuithrin 3487849 Click to see CC=C(C)C(=O)OC1CC2(C(CC(O2)(C(=CC3C1C(=C)C(=O)O3)C)O)O)C 378.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3R,3aS,4R,5aR,9bR)-4-hydroxy-3,5a,9-trimethyl-3a,4,5,9b-tetrahydro-3H-benzo[g][1]benzofuran-2,8-dione 162944449 Click to see CC1C2C(CC3(C=CC(=O)C(=C3C2OC1=O)C)C)O 262.30 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(6,7,9-trihydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-4-yl) 2-methylbut-2-enoate 433437 Click to see CC=C(C)C(=O)OC1CC(C(CC(C(=CC2C1C(=C)C(=O)O2)C)O)O)(C)O 380.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
(6,9-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-4-yl) 2-methylbut-2-enoate 433436 Click to see CC=C(C)C(=O)OC1CC(CCC(C(=CC2C1C(=C)C(=O)O2)C)O)(C)O 364.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
(6,9-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,9,11a-tetrahydro-3aH-cyclodeca[b]furan-4-yl) 2-methylbut-2-enoate 433435 Click to see CC=C(C)C(=O)OC1CC(C=CC(C(=CC2C1C(=C)C(=O)O2)C)O)(C)O 362.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
(8-Hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2-(hydroxymethyl)but-2-enoate 74036903 Click to see CC=C(CO)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
(8-Hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2,3-dimethyloxirane-2-carboxylate 433036 Click to see CC1C(O1)(C)C(=O)OC2CC(=CC(CC(=CC3C2C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
https://doi.org/10.1016/S0031-9422(00)80710-4
(9-acetyloxy-6-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,9,11a-tetrahydro-3aH-cyclodeca[b]furan-4-yl) 2-methylbut-2-enoate 433432 Click to see CC=C(C)C(=O)OC1CC(C=CC(C(=CC2C1C(=C)C(=O)O2)C)OC(=O)C)(C)O 404.50 unknown https://doi.org/10.1016/0031-9422(81)85224-7
(9-Hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 2-(hydroxymethyl)but-2-enoate 3467449 Click to see CC=C(CO)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
[(3aR,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2S,3S)-2,3-dimethyloxirane-2-carboxylate 163193205 Click to see CC1C(O1)(C)C(=O)OC2CC(=CC(CC(=CC3C2C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
[(3aR,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (3S)-3-hydroxy-2-methylidenebutanoate 162974203 Click to see CC1=CC2C(C(CC(=CC(C1)O)C)OC(=O)C(=C)C(C)O)C(=C)C(=O)O2 362.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
[(3aR,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-(hydroxymethyl)but-2-enoate 163085030 Click to see CC=C(CO)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
[(3aR,4R,6S,9S,10Z,11aS)-6,9-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 162873156 Click to see CC=C(C)C(=O)OC1CC(CCC(C(=CC2C1C(=C)C(=O)O2)C)O)(C)O 364.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
[(3aS,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2R,3R)-2,3-dimethyloxirane-2-carboxylate 162987704 Click to see CC1C(O1)(C)C(=O)OC2CC(=CC(CC(=CC3C2C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
[(3aS,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2S,3S)-2,3-dimethyloxirane-2-carboxylate 162987702 Click to see CC1C(O1)(C)C(=O)OC2CC(=CC(CC(=CC3C2C(=C)C(=O)O3)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
[(3aS,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-2-methylbut-2-enoate 162980139 Click to see CC=C(C)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 346.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
[(3aS,4R,6E,8R,10E,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 163194898 Click to see CC=C(C)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 346.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
[(3aS,4R,6R,7E,9S,10Z,11aS)-6,9-dihydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,9,11a-tetrahydro-3aH-cyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 162989635 Click to see CC=C(C)C(=O)OC1CC(C=CC(C(=CC2C1C(=C)C(=O)O2)C)O)(C)O 362.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
[(3aS,4R,6R,7E,9S,10Z,11aS)-9-acetyloxy-6-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,9,11a-tetrahydro-3aH-cyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 162912639 Click to see CC=C(C)C(=O)OC1CC(C=CC(C(=CC2C1C(=C)C(=O)O2)C)OC(=O)C)(C)O 404.50 unknown https://doi.org/10.1016/0031-9422(81)85224-7
[(3aS,4R,6R,7S,9S,10Z,11aS)-6,7,9-trihydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 162977610 Click to see CC=C(C)C(=O)OC1CC(C(CC(C(=CC2C1C(=C)C(=O)O2)C)O)O)(C)O 380.40 unknown https://doi.org/10.1016/0031-9422(81)85224-7
[(3aS,4R,8R,11aR)-8-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-methylbut-2-enoate 162980142 Click to see CC=C(C)C(=O)OC1CC(=CC(CC(=CC2C1C(=C)C(=O)O2)C)O)C 346.40 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
4-Hydroxy-10-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-6-carbaldehyde 73207605 Click to see CC1=CC2C(C(CC(=CCC1)C=O)O)C(=C)C(=O)O2 262.30 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
Allo-schkuhriolide 10015562 Click to see CC1=CC2C(C(CC(=CCC1)C=O)O)C(=C)C(=O)O2 262.30 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
Desacetyleupaserrin 5281439 Click to see CC=C(CO)C(=O)OC1CC(=CCC(C(=CC2C1C(=C)C(=O)O2)C)O)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) 2-(hydroxymethyl)but-2-enoate 433925 Click to see CC=C(CO)C(=O)OC1CC(C2CC=C(C2C3C1C(=C)C(=O)O3)C)(C)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
(6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) 2-methylbut-2-enoate 5255772 Click to see CC=C(C)C(=O)OC1CC(C2CC=C(C2C3C1C(=C)C(=O)O3)C)(C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
(6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) 2,3-dimethyloxirane-2-carboxylate 162858709 Click to see CC1C(O1)(C)C(=O)OC2CC(C3CC=C(C3C4C2C(=C)C(=O)O4)C)(C)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
(6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) 3-hydroxy-2-methylidenebutanoate 163013465 Click to see CC1=CCC2C1C3C(C(CC2(C)O)OC(=O)C(=C)C(C)O)C(=C)C(=O)O3 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
[(3aR,4R,6R,6aR,9aR,9bR)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (3R)-3-hydroxy-2-methylidenebutanoate 163013466 Click to see CC1=CCC2C1C3C(C(CC2(C)O)OC(=O)C(=C)C(C)O)C(=C)C(=O)O3 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
[(3aR,4R,6R,6aR,9aR,9bR)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (Z)-2-(hydroxymethyl)but-2-enoate 162879764 Click to see CC=C(CO)C(=O)OC1CC(C2CC=C(C2C3C1C(=C)C(=O)O3)C)(C)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
[(3aS,4S,6S,6aS,9aS,9bS)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (2S,3S)-2,3-dimethyloxirane-2-carboxylate 162858710 Click to see CC1C(O1)(C)C(=O)OC2CC(C3CC=C(C3C4C2C(=C)C(=O)O4)C)(C)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
8beta-Angeloyloxycumambranolide 44583813 Click to see CC=C(C)C(=O)OC1CC(C2CC=C(C2C3C1C(=C)C(=O)O3)C)(C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)84950-X
> Lipids and lipid-like molecules / Saccharolipids
[(1S,3S,4R,5S,6S,8S,10S,16S,23S,24R,25R,26R)-16-acetyloxy-4,5,26-trihydroxy-6-methyl-17,20-dioxo-24-[(E)-3-phenylprop-2-enoyl]oxy-10-propyl-2,7,9,21,27-pentaoxatricyclo[21.3.1.03,8]heptacosan-25-yl] (Z)-2-methylbut-2-enoate 102397824 Click to see CCCC1CCCCCC(C(=O)CCC(=O)OCC2C(C(C(C(O2)OC3C(C(C(OC3O1)C)O)O)O)OC(=O)C(=CC)C)OC(=O)C=CC4=CC=CC=C4)OC(=O)C 818.90 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Atranone M 139590222 Click to see CC1CCC2(C(CC=C(C3C(C1=O)C(C(=O)O3)(C)C(=O)OC)C)C(=C(C(=O)O2)OC)C(C)C)C 476.60 unknown https://doi.org/10.1016/S0031-9422(00)80710-4
> Organoheterocyclic compounds / Azoles / Thiazoles / 2,4-disubstituted thiazoles
Melithiazol L 10813610 Click to see CC(COC)C1=NC(CS1)C2=NC(=CS2)C=CC(C(C)C(=CC(=O)OC)OC)OC 454.60 unknown https://doi.org/10.1016/S0031-9422(00)83135-0
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
8-Methyl-3-methylidene-5,14-dioxatricyclo[10.2.1.02,6]pentadeca-7,11-diene-4,13-dione 162927348 Click to see CC1=CC2C(C3CC(=CCC1)C(=O)O3)C(=C)C(=O)O2 260.28 unknown https://doi.org/10.1016/S0031-9422(00)83135-0
https://doi.org/10.1016/S0031-9422(00)80710-4
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(+)-Gallocatechin-(4alpha->6)-(+)-catechin 72193636 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 594.50 unknown via CMAUP database
(+)-Gallocatechin-(4alpha->8)-(+)-catechin 13831063 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 594.50 unknown via CMAUP database
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Prodelphinidin B3 13831068 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown via CMAUP database
Prodelphinidin C2 71623698 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C(=C7)O)O)O)O)C8=CC(=C(C(=C8)O)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 898.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(+)-Catechin gallate 5276454 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside 5491814 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 616.50 unknown via CMAUP database
Quercetin 3-O-beta-D-arabinofuranoside 5320668 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Naringin 442428 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database

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