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Amsinckia menziesii

Amsinckia menziesii - Unknown
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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 UUID644008ecd3b47011532976
Scientific name Amsinckia menziesii
Authority (Lehm.) A.Nelson & J.F.Macbr.
First published in Bot. Gaz. 61: 36 (1916)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Amsinckia copelandii Suksd. Werdenda 1: 62 (1931)
Amsinckia douglasiana var. interior J.F.Macbr. Contr. Gray Herb. 49: 13 (1917)
Amsinckia eatonii Suksd. Werdenda 1: 64 (1931)
Amsinckia helleri Brand Repert. Spec. Nov. Regni Veg. 25: 212 (1928)
Amsinckia hirticaulis Suksd. Werdenda 1: 55 (1931)
Amsinckia hispidissima Suksd. Deutsche Bot. Monatsschr. 18: 133 (1900)
Amsinckia menziesii f. angustisepala Faegri Bergens Mus. Årbog (Årbok) 15. 1929
Amsinckia menziesii f. latisepala Faegri Bergens Mus. Årbog (Årbok) 15. 1929
Amsinckia menziesii var. microcarya Brand Pflanzenr. , IV, 252(97): 211 (1931)
Amsinckia menziesii var. retrorsa (Suksd.) Reveal & Schuyler Proc. Acad. Nat. Sci. Philadelphia 149: 8 (1999)
Amsinckia micrantha Suksd. Deutsche Bot. Monatsschr. 18: 134 (1900)
Amsinckia parviflora A.Heller Muhlenbergia 2: 313. 1907
Amsinckia retrorsa Suksd. Deutsche Bot. Monatsschr. 18: 134 (1900)
Amsinckia sparsiflora Suksd. Werdenda 1: 77 (1931)
Benthamia menziesii (Lehm.) Druce Bot. Exch. Club Brit. Isles Rep. 5: 570. 1920 [Oct 1920]
Benthamia parviflora Druce Rep. Bot. Soc. Exch. Club Brit. Isles 7(5): 777. 1926 [Jun 1926]
Echium menziesii Lehm. Nov. Stirp. Pug. 2: 29 (1830)
Benthamia micrantha (Suksd.) Druce Bot. Exch. Club Brit. Isles Rep. 4: 299. 1916
Benthamia retrorsa (Suksd.) Druce Bot. Exch. Club Brit. Isles Rep. 4: 299. 1916

Common names Top

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Language Common/alternative name
English menzies' fiddleneck
Welsh amsincia
Finnish lännenkeltalemmikki
Swedish ogräsgullört

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Amsinckia menziesii var. intermedia Ganders Jepson Man. 368. 1993 [pro 1993]

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • North European Russia
    • Middle Europe
      • Belgium
      • Germany
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Greece
  • Northern America
    • Mexico
      • Mexican Pacific Islands
      • Mexico Northeast
      • Mexico Northwest
    • North-central U.S.A.
      • Illinois
      • Missouri
      • Nebraska
      • North Dakota
    • Northeastern U.S.A.
      • Connecticut
      • Maine
      • Massachusetts
      • New Hampshire
      • New York
      • Pennsylvania
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
      • Oregon
      • Washington
      • Wyoming
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • North Carolina
      • South Carolina
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
      • Utah
    • Subarctic America
      • Alaska
      • Aleutian Islands
      • Yukon
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000532148
Canadensys 3739
USDA Plants AMME
Tropicos 4000778
Flora of Italy 12851
KEW urn:lsid:ipni.org:names:11839-2
The Plant List kew-2635052
Open Tree Of Life 416440
NCBI Taxonomy 1213287
Nature Serve 2.149774
IPNI 11839-2
iNaturalist 55436
GBIF 2925870
Freebase /m/03ykj_2
EPPO AMSME
EOL 580757
Calflora (Californian flora) 326
USDA GRIN 453243
Wikipedia Amsinckia_menziesii
CMAUP NPO12225

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Development of an IPM Strategy for Thrips and Tomato spotted wilt virus in Processing Tomatoes in the Central Valley of California Batuman O, Turini TA, LeStrange M, Stoddard S, Miyao G, Aegerter BJ, Chen LF, McRoberts N, Ullman DE, Gilbertson RL Pathogens 05-Aug-2020
PMCID:PMC7459483
doi:10.3390/pathogens9080636
PMID:32764311
Decades of native bee biodiversity surveys at Pinnacles National Park highlight the importance of monitoring natural areas over time Meiners JM, Griswold TL, Carril OM PLoS One 17-Jan-2019
PMCID:PMC6336250
doi:10.1371/journal.pone.0207566
PMID:30653514
Weed responses to fallow management in Pacific Northwest dryland cropping systems San Martín C, Long DS, Gourlie JA, Barroso J PLoS One 20-Sep-2018
PMCID:PMC6147650
doi:10.1371/journal.pone.0204200
PMID:30235310
Data on introduced plants in Zimbabwe: Floristic changes and patterns of collection based on historical herbarium records Maroyi A Data Brief 22-Sep-2017
PMCID:PMC5712053
doi:10.1016/j.dib.2017.09.046
PMID:29214198
Post-Fire Recovery in Coastal Sage Scrub: Seed Rain and Community Trajectory Conlisk E, Swab R, Martínez-Berdeja A, Daugherty MP PLoS One 20-Sep-2016
PMCID:PMC5029939
doi:10.1371/journal.pone.0162777
PMID:27649564
Resource colimitation governs plant community responses to altered precipitation Eskelinen A, Harrison SP Proc Natl Acad Sci U S A 05-Oct-2015
PMCID:PMC4620885
doi:10.1073/pnas.1508170112
PMID:26438856
Plant functional traits and the multidimensional nature of species coexistence Kraft NJ, Godoy O, Levine JM Proc Natl Acad Sci U S A 05-Jan-2015
PMCID:PMC4311865
doi:10.1073/pnas.1413650112
PMID:25561561
Activated carbon decreases invasive plant growth by mediating plant–microbe interactions Nolan NE, Kulmatiski A, Beard KH, Norton JM AoB Plants 10-Nov-2014
PMCID:PMC4303759
doi:10.1093/aobpla/plu072
PMID:25387751
Profiling of Dehydropyrrolizidine Alkaloids and their N-Oxides in Herbarium-Preserved Specimens of Amsinckia Species Using HPLC-esi(+)MS Colegate SM, Welsh SL, Gardner DR, Betz JM, Panter KE J Agric Food Chem 23-Mar-2014
PMCID:PMC4117384
doi:10.1021/jf500425v
PMID:24655304
The alkaloids of Amsinckia species: A. intermedia Fisch. & Mey., A. hispida (Ruiz. & Pav.) Johnst. and A. lycopsoides Lehm CCJ Culvenor, LW Smith CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9661955
The pyrrolizidine alkaloids of Amsinckia menziesii JN Roitman CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9830769
California annual grass invaders: the drivers or passengers of change? HilleRisLambers J, Yelenik SG, Colman BP, Levine JM J Ecol 01-Sep-2010
PMCID:PMC2936119
doi:10.1111/j.1365-2745.2010.01706.x
PMID:20852668
Pyrrolizidine alkaloids from Amsinckia Ronald B. Kelley, James N. Seiber Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83312-M
Pyrrolizidine alkaloid chemosystematics in Amsinckia Ronald B. Kelley, James N. Seiber Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83282-4

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
> Alkaloids and derivatives
(7-acetyloxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-(1-acetyloxyethyl)-2-hydroxy-3-methylbutanoate 162893716 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C)O 383.40 unknown https://doi.org/10.1071/CH9830769
https://doi.org/10.1016/0031-9422(92)83312-M
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-(1-acetyloxyethyl)-2-hydroxy-3-methylbutanoate 78384682 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)O)O 341.40 unknown https://doi.org/10.1071/CH9830769
[(7R,8R)-7-acetyloxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-[(1S)-1-acetyloxyethyl]-2-hydroxy-3-methylbutanoate 163194082 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C)O 383.40 unknown https://doi.org/10.1071/CH9830769
https://doi.org/10.1016/0031-9422(92)83312-M
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-[(1S)-1-acetyloxyethyl]-2-hydroxy-3-methylbutanoate 162973293 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)O)O 341.40 unknown https://doi.org/10.1071/CH9830769
3'-Acetyllycopsamine 586647 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C)O 341.40 unknown https://doi.org/10.1071/CH9830769
3'-Acetylmyoscorpine 91751311 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)C)(C(C)OC(=O)C)O 423.50 unknown https://doi.org/10.1016/0031-9422(92)83282-4
7-Acetyllycopsamine 156006 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C)O 341.40 unknown https://doi.org/10.1071/CH9830769
Amabiline 442706 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1CCC2)O 283.36 unknown https://doi.org/10.1016/0031-9422(92)83282-4
Echinatine 22384 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1071/CH9830769
Intermedine, (+)- 114843 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1016/0031-9422(92)83282-4
https://doi.org/10.1071/CH9661955
https://doi.org/10.1071/CH9830769
Lycopsamine 107938 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1071/CH9830769
https://doi.org/10.1016/0031-9422(92)83282-4
Myoscorpine 6440700 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)C)(C(C)O)O 381.50 unknown https://doi.org/10.1016/0031-9422(92)83282-4
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
2-Hydroxy-3-methoxybenzoic acid 70140 Click to see COC1=CC=CC(=C1O)C(=O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic acid 19 Click to see C1=CC(=C(C(=C1)O)O)C(=O)O 154.12 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron;phenoxide 20488062 Click to see [H+].C1=CC=C(C=C1)[O-] 94.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown via CMAUP database
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
8,11,13-Abietatriene-3beta-ol 13996029 Click to see CC(C)C1=CC2=C(C=C1)C3(CCC(C(C3CC2)(C)C)O)C 286.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Dihydrosolidagenone 101717490 Click to see CC1CC(=O)C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C 318.40 unknown via CMAUP database
Rotundifuran 9841926 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown via CMAUP database
Vitetrifolin B 15543011 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown via CMAUP database
Vitetrifolin C 15543012 Click to see CC1C(C=C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 360.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate 93317 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
gamma-Tocopherol 92729 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1R,4aS,5R,7aR)-5-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate 51346123 Click to see C1=COC(C2C1C(C=C2COC(=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 466.40 unknown via CMAUP database
6'-O-p-Hydroxybenzoylmussaenosidic acid 23955877 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)COC(=O)C4=CC=C(C=C4)O)O)O)O)O 496.50 unknown via CMAUP database
Mussaenosidic acid 21633105 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown via CMAUP database
Negundoside 9935561 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O 496.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(5S,6R,8R,9R,10S)-6-Acetoxy-9,15-dihydroxylabda-13-ene-16-oic acid 16,15-lactone 10022565 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
(8alpha)-9,16-Dihydroxylabda-13-ene-15-oic acid gamma-lactone 102105798 Click to see CC1CCC2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C 320.50 unknown via CMAUP database
Previtexilactone 21636179 Click to see CC1CC(C2C(CCCC2(C13CCC4(O3)CC(=O)OC4)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
Vitexilactone 21636178 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Epiursolic acid 7163177 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
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 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 / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(1R,2R,4aalpha,5'E)-2alpha,5,5,8abeta-Tetramethyl-4beta-acetoxy-4',5'-dihydrospiro[decalin-1,2'(3'H)-furan]-5'-ylidene]acetic acid 101357917 Click to see CC1CC(C2C(CCCC2(C13CCC(=CC(=O)O)O3)C)(C)C)OC(=O)C 364.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Isoambreinolide 15559824 Click to see CC1CCC2C(CCCC2(C13CCC(=O)O3)C)(C)C 264.40 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Vitex norditerpenoid 1 11208535 Click to see CC1CCC2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C 290.40 unknown via CMAUP database
Vitex norditerpenoid 2 11462191 Click to see CC1CC(C2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C)OC(=O)C 348.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-3,6,3',4'-tetramethoxyflavone 5379563 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)OC 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
chrysoplenol D 5280699 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC 360.30 unknown via CMAUP database

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