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Rhododendron aureum

Rhododendron aureum - 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 UUID6440768f0cb97130218586
Scientific name Rhododendron aureum
Authority Georgi
First published in Bemerk. Reise Russ. Reich 1: 214 (1775)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Azalea chrysantha (Pall.) Kuntze Revis. Gen. Pl. 2: 387 (1891)
Rhododendron chrysanthum Pall. Reise Russ. Reich. 3: 729 (1776)

Common names Top

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Language Common/alternative name
Azerbaijani qızılı rododendron
Bulgarian златист рододендрон
Japanese キバナシャクナゲ
Korean 만병초
Korean 노랑만병초
Russian Золотистый рододендрон
Russian Рододендрон золотистый
Chinese 牛皮杜鹃
Chinese 牛皮茶
Chinese 牛皮杜鵑

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Rhododendron aureum var. aureum
Rhododendron aureum var. hypopitys (Pojark.) D.F.Chamb. Notes Roy. Bot. Gard. Edinburgh 37(2): 335. 1979

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Kamchatka
      • Khabarovsk
      • Kuril Islands
      • Magadan
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001046884
UNII MM2Y21LFIT
Tropicos 12300086
KEW urn:lsid:ipni.org:names:331982-1
The Plant List tro-12300086
Open Tree Of Life 695232
Observations.org 121253
NCBI Taxonomy 184574
IPNI 331982-1
iNaturalist 732942
GBIF 7328058
Freebase /m/0j9pwsh
EPPO RHOAQ
Elurikkus 6809
USDA GRIN 105057
Wikipedia Rhododendron_aureum
CMAUP NPO21437

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
Nose of dog, eye of elk, and wolf’s liver: exploring the interconnectedness of Indigenous health and foraging among the Dukha reindeer herders of Mongolia Hatcherson J Int J Circumpolar Health 18-Apr-2024
PMCID:PMC11028006
doi:10.1080/22423982.2024.2343454
PMID:38634711
Abscisic Acid Affects Phenolic Acid Content to Increase Tolerance to UV-B Stress in Rhododendron chrysanthum Pall. Zhou X, Gong F, Dong J, Lin X, Cao K, Xu H, Zhou X Int J Mol Sci 19-Jan-2024
PMCID:PMC10816200
doi:10.3390/ijms25021234
PMID:38279235
Rhododendron chrysanthum’s Primary Metabolites Are Converted to Phenolics More Quickly When Exposed to UV-B Radiation Gong F, Yu W, Zeng Q, Dong J, Cao K, Xu H, Zhou X Biomolecules 24-Nov-2023
PMCID:PMC10742171
doi:10.3390/biom13121700
PMID:38136571
Integration of Phosphoproteomics and Transcriptome Studies Reveals ABA Signaling Pathways Regulate UV-B Tolerance in Rhododendron chrysanthum Leaves Sun Q, Zhou X, Yang L, Xu H, Zhou X Genes (Basel) 25-May-2023
PMCID:PMC10297884
doi:10.3390/genes14061153
PMID:37372333
Patterns and drivers of soil surface‐dwelling Oribatida diversity along an altitudinal gradient on the Changbai Mountain, China Lin Y, Wu H, Liu D, Li Y, Kang Y, Zhang Z, Wang W Ecol Evol 19-May-2023
PMCID:PMC10196937
doi:10.1002/ece3.10105
PMID:37214606
Transcriptome and proteome depth analysis indicate ABA, MAPK cascade and Ca2+ signaling co-regulate cold tolerance in Rhododendron chrysanthum Pall. Zhang Q, Li Y, Cao K, Xu H, Zhou X Front Plant Sci 21-Feb-2023
PMCID:PMC9989302
doi:10.3389/fpls.2023.1146663
PMID:36895874
Acetylated Proteomics of UV-B Stress-Responsive in Photosystem II of Rhododendron chrysanthum Liu M, Sun Q, Cao K, Xu H, Zhou X Cells 01-Feb-2023
PMCID:PMC9913721
doi:10.3390/cells12030478
PMID:36766818
Ecological and Geographical Structure of the Plant Cover of the East Asian Boreal–Nemoral Ecotone (the Lower Amur Region, Far East Russia) Kryukova MV Plants (Basel) 30-Jan-2023
PMCID:PMC9919551
doi:10.3390/plants12030615
PMID:36771699
Contrasting responses of soil microbial biomass and extracellular enzyme activity along an elevation gradient on the eastern Qinghai-Tibetan Plateau Liu S, Xu G, Chen H, Zhang M, Cao X, Chen M, Chen J, Feng Q, Shi Z Front Microbiol 18-Jan-2023
PMCID:PMC9889656
doi:10.3389/fmicb.2023.974316
PMID:36744094
Changes in root chemical diversity along an elevation gradient of Changbai Mountain, China Wu S, Wang R, Zhu H, Wang Y, Du Y, Zhu S, Zhao N Front Plant Sci 07-Nov-2022
PMCID:PMC9676470
doi:10.3389/fpls.2022.897838
PMID:36420024
Carbohydrates and secondary compounds of alpine tundra shrubs in relation to experimental warming Zhou Y, Yang M, Tai Z, Jia J, Luan D, Ma X BMC Plant Biol 10-Oct-2022
PMCID:PMC9549620
doi:10.1186/s12870-022-03851-y
PMID:36210454
Metabolic Analyses and Evaluation of Antioxidant Activity in Purple Kohlrabi Sprouts after Exposed to UVB Radiation Yeo HJ, Lim SY, Park CH, Kim CY, Sathasivam R, Kim JK, Park SU Antioxidants (Basel) 25-Jul-2022
PMCID:PMC9332045
doi:10.3390/antiox11081443
PMID:35892645
Metabolism of Enantiomers of Rhododendrol in Human Skin Homogenate Gu L, Maeda K Metabolites 03-May-2022
PMCID:PMC9143848
doi:10.3390/metabo12050412
PMID:35629916
Inhibition of the main protease of SARS-CoV-2 (Mpro) by repurposing/designing drug-like substances and utilizing nature’s toolbox of bioactive compounds Antonopoulou I, Sapountzaki E, Rova U, Christakopoulos P Comput Struct Biotechnol J 14-Mar-2022
PMCID:PMC8920478
doi:10.1016/j.csbj.2022.03.009
PMID:35308802
Evaluation of environmental factors affecting the genetic diversity, genetic structure, and the potential distribution of Rhododendron aureum Georgi under changing climate Zhao W, Wang X, Li L, Li J, Yin H, Zhao Y, Chen X Ecol Evol 25-Aug-2021
PMCID:PMC8462154
doi:10.1002/ece3.7803
PMID:34594500

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 / Diphenylethers
2-Hydroxy-6-[2-hydroxy-6-(hydroxymethyl)-4-methyl-phenoxy]-3-(3-methylbut-2-enyl)benzoic acid 23843930 Click to see CC1=CC(=C(C(=C1)O)OC2=C(C(=C(C=C2)CC=C(C)C)O)C(=O)O)CO 358.40 unknown via CMAUP database
6-[2-hydroxy-6-(hydroxymethyl)-4-methylphenoxy]-2-methoxy-3-[(1S)-1-methoxy-3-methylbutyl]benzoic acid 38351229 Click to see CC1=CC(=C(C(=C1)O)OC2=C(C(=C(C=C2)C(CC(C)C)OC)OC)C(=O)O)CO 404.50 unknown via CMAUP database
6-[2-hydroxy-6-(hydroxymethyl)-4-methylphenoxy]-3-[(1S)-1-hydroxy-3-methylbutyl]-2-methoxybenzoic acid 71608329 Click to see CC1=CC(=C(C(=C1)O)OC2=C(C(=C(C=C2)C(CC(C)C)O)OC)C(=O)O)CO 390.40 unknown via CMAUP database
7-O-Acetylsecopenicillide C 71460590 Click to see CC1=CC(=C(C(=C1)O)OC2=C(C(=C(C=C2)CC=C(C)C)O)C(=O)O)COC(=O)C 400.40 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Rhododendrol 919205 Click to see CC(CCC1=CC=C(C=C1)O)O 166.22 unknown via CMAUP database
> Benzenoids / Tetralins
(1R,3R)-spiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354124 Click to see C1C(C2=C(C=CC=C2O)C3(C1O)OC4=CC=CC5=C4C(=CC=C5)O3)O 336.30 unknown via CMAUP database
(1S,2R,3S)-2-chlorospiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354126 Click to see C1=CC2=C3C(=C1)OC4(C(C(C(C5=C4C=CC=C5O)O)Cl)O)OC3=CC=C2 370.80 unknown via CMAUP database
(1S,3R)-spiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354123 Click to see C1C(C2=C(C=CC=C2O)C3(C1O)OC4=CC=CC5=C4C(=CC=C5)O3)O 336.30 unknown via CMAUP database
(2S)-1,1-[Naphthalene-1,8-diylbis(oxy)]-3beta-chlorotetralin-2alpha,4alpha,5-triol 51354127 Click to see C1=CC2=C3C(=C1)OC4(C(C(C(C5=C4C=CC=C5O)O)Cl)O)OC3=CC=C2 370.80 unknown via CMAUP database
Palmarumycin BG-1 51354122 Click to see C1C(C2(C3=C(C1=O)C(=CC=C3)O)OC4=CC=CC5=C4C(=CC=C5)O2)O 334.30 unknown via CMAUP database
Sulfuric acid (2R)-1,1-[naphthalene-1,8-diylbis(oxy)]-2alpha,4beta-dihydroxytetralin-5-yl ester 51354125 Click to see C1C(C2=C(C=CC=C2OS(=O)(=O)O)C3(C1O)OC4=CC=CC5=C4C(=CC=C5)O3)O 416.40 unknown via CMAUP database
Sulfuric acid (2S)-1,1-[naphthalene-1,8-diylbis(oxy)]-2alpha,4beta-dihydroxy-3alpha-chlorotetralin-5-yl ester 51354407 Click to see C1=CC2=C3C(=C1)OC4(C(C(C(C5=C4C=CC=C5OS(=O)(=O)O)O)Cl)O)OC3=CC=C2 450.80 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 450.90 unknown via CMAUP database
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown via CMAUP database
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown via CMAUP database
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown via CMAUP database
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown via CMAUP database
Pentatriacontane 12413 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 492.90 unknown via CMAUP database
Triacontane 12535 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 422.80 unknown via CMAUP database
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ustusolate A 23843911 Click to see CC=CC=CC=CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(CO)O)CO 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
3-Hexadecenoic acid 5312418 Click to see CCCCCCCCCCCCC=CCC(=O)O 254.41 unknown via CMAUP database
7-Hexadecenoic acid 543268 Click to see CCCCCCCCC=CCCCCCC(=O)O 254.41 unknown via CMAUP database
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
c9-Heptadecenoic acid acid 3014063 Click to see CCCCCCCC=CCCCCCCCC(=O)O 268.40 unknown via CMAUP database
Heptadecanoic acid 10465 Click to see CCCCCCCCCCCCCCCCC(=O)O 270.50 unknown via CMAUP database
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Nonadecanoic acid 12591 Click to see CCCCCCCCCCCCCCCCCCC(=O)O 298.50 unknown via CMAUP database
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Palmitolinoleic acid 4668 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Pentadecanoic acid 13849 Click to see CCCCCCCCCCCCCCC(=O)O 242.40 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
Vaccenic acid 122325 Click to see CCCCCCC=CCCCCCCCCCC(=O)O 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see CCCCCCCCCCCC(=O)O 200.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(2S)-4-(4-hydroxyphenyl)butan-2-yl]oxyoxane-3,4,5-triol 9883892 Click to see CC(CCC1=CC=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O 328.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S)-1-[(2S,4aR,4bR,5R,8aR)-5-hydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]ethane-1,2-diol 11602232 Click to see CC1(CCC(C2(C1CCC3=CC(CCC32)(C)C(CO)O)C)O)C 322.50 unknown via CMAUP database
(1S)-1-[(2S,4aR,4bR,8aR)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]ethane-1,2-diol 11551288 Click to see CC1(CCCC2(C1CCC3=CC(CCC32)(C)C(CO)O)C)C 306.50 unknown via CMAUP database
(4aR,4bR,7S,10aR)-7-[(1S)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-2,3,4b,5,6,9,10,10a-octahydrophenanthren-4-one 11702511 Click to see CC1(CCC(=O)C2(C1CCC3=CC(CCC32)(C)C(CO)O)C)C 320.50 unknown via CMAUP database
(5S,8R,9R,10S,13S)-17-Hydroxy-16-oxobeyerane-18-al 11392987 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C(=O)C4)CO)C)C=O 318.40 unknown via CMAUP database
Ceriopsin C 101202346 Click to see CC1(CCC(C2(C1CC=C3C2CCC(C3)(C)C(CO)O)C)O)C 322.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
13-Hydroxykaur-16-en-18-al 100967712 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C(=C)C4)O)C)C=O 302.50 unknown via CMAUP database
13,16alpha,17-Trihydroxy-ent-9(11)-kauren-19-oic acid 11428064 Click to see CC12CCCC(C1CCC34C2=CCC(C3)(C(C4)(CO)O)O)(C)C(=O)O 350.40 unknown via CMAUP database
16,17-Dihydroxykaura-18-one 44575992 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C=O 320.50 unknown via CMAUP database
16alpha,17-Dihydroxy-ent-9(11)-kauren-19-al 11324617 Click to see CC1(CCCC2(C1CCC34C2=CCC(C3)C(C4)(CO)O)C)C=O 318.40 unknown via CMAUP database
16alphaH-17,19-ent-kauranediol 102594837 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO 306.50 unknown via CMAUP database
17-Chloro-13,16beta-dihydroxy-ent-kauran-19-al 21589750 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C(C4)(CCl)O)O)C)C=O 354.90 unknown via CMAUP database
17-Hydroxykaura-18-oic acid 46210307 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)CO)(C)C(=O)O 320.50 unknown via CMAUP database
ent-16beta,17-Dihydroxy-9(11)-kauren-19-oic acid 23249404 Click to see CC12CCCC(C1CCC34C2=CCC(C3)C(C4)(CO)O)(C)C(=O)O 334.40 unknown via CMAUP database
ent-Kaur-16-en-19-ol 443465 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C)C4)C)CO 288.50 unknown via CMAUP database
Kaur-16-ene-13,18-diol 100967711 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C(=C)C4)O)C)CO 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 392170 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1007/BF00564187
https://doi.org/10.1007/BF01032020
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1007/BF01032020
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 https://doi.org/10.1007/BF00564187
https://doi.org/10.1007/BF01032020
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3beta,16alpha)-13,28-Epoxyoleanane-3,16-diol 12114129 Click to see CC1(CCC23COC4(C2C1)CCC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)C)O)C)C 458.70 unknown via CMAUP database
11alpha-Hydroxypurimlagenin A 101426135 Click to see CC1(CCC2(C(C1)C3=CC(C4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)O)CO)C 474.70 unknown via CMAUP database
3beta-Acetoxy-13beta,16alpha-dihydroxyoleanane-28-oic acid gamma-lactone 101426129 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC45C3(CC(C6(C4CC(CC6)(C)C)C(=O)O5)O)C)C)C 514.70 unknown via CMAUP database
3beta-Acetoxy-13beta,28-epoxyoleanane-16-one 101426127 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC45C3(CC(=O)C6(C4CC(CC6)(C)C)CO5)C)C)C 498.70 unknown via CMAUP database
3beta-Acetoxy-13beta,28-epoxyoleanane-16alpha-ol 101426128 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC45C3(CC(C6(C4CC(CC6)(C)C)CO5)O)C)C)C 500.80 unknown via CMAUP database
3beta-Acetyl-11alpha,28-dihydroxyschimperone 101426134 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C(C=C4C3(CC(=O)C5(C4CC(CC5)(C)C)CO)C)O)C)C 514.70 unknown via CMAUP database
3beta-Acetylschimperinone 101426133 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CC(=O)C5(C4CC(CC5)(C)C)CO)C)C)C 498.70 unknown via CMAUP database
3beta,16alpha-Diacetoxy-13beta,28-epoxyoleanane 101426131 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CCC45C3(CC(C6(C4CC(CC6)(C)C)CO5)OC(=O)C)C)C)C 542.80 unknown via CMAUP database
3beta,28-Diacetylpurimlagenin A 15382797 Click to see CC(=O)OCC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC(=O)C)C)(C)C 542.80 unknown via CMAUP database
Aegicerin 15558423 Click to see CC1(CCC23COC4(C2C1)CCC5C6(CCC(C(C6CCC5(C4(CC3=O)C)C)(C)C)O)C)C 456.70 unknown via CMAUP database
bruguierins A 11513260 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CC(C2(C3CCC4C(CCC4(C3(CCC2C1(C)C)C)C)C(C)(CCC=C(C)C)O)C)O 727.20 unknown via CMAUP database
bruguierins B 11657758 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C(CC4C3(CCC4C(C)(CCC=C(C)C)O)C)O)C)C 727.20 unknown via CMAUP database
bruguierins C 11629176 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CC(C2(C3CCC4C(CCC4(C3(CCC2C1(C)C)C)C)C(C)(CC=CC(C)(C)OO)O)C)O 759.20 unknown via CMAUP database
Embelinone 12114128 Click to see CC1(CCC23COC4(C2C1)CCC5C6(CCC(=O)C(C6CCC5(C4(CC3=O)C)C)(C)C)C)C 454.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1007/BF01032020
Primulagenin A 10004345 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO)C 458.70 unknown via CMAUP database
Scimperinone 21578112 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2=O)C)C)(C)C)O)C)CO)C 456.70 unknown via CMAUP database
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
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
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Ustusol C 44557563 Click to see CC1(CCCC2(C1C(C=C(C2(CO)O)CO)OC)C)C 284.39 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Ustusol A 44480213 Click to see CC1=CC(=O)C2C(C(CCC2(C1(CO)O)C)O)(C)C 268.35 unknown via CMAUP database
Ustusol B 44557562 Click to see CC1=CC(=O)C2C(CC(CC2(C1(CO)O)C)O)(C)C 268.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
3-[(R)-1-Hydroxy-3-methylbutyl]-4-methoxy-9-methyl-11-hydroxy-5H,7H-dibenzo[b,g][1,5]dioxocin-5-one 25273618 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C(CC(C)C)O)OC)C(=O)OC2 372.40 unknown via CMAUP database
3'-O-Methyldehydroisopenicillide 9864866 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C=CC(C)(C)OC)OC)C(=O)OC2 384.40 unknown via CMAUP database
NCGC00386098-01_C21H22O6_11-Hydroxy-3-[(1E)-3-hydroxy-3-methyl-1-buten-1-yl]-4-methoxy-9-methyl-5H,7H-dibenzo[b,g][1,5]dioxocin-5-one 9896819 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C=CC(C)(C)O)OC)C(=O)OC2 370.40 unknown via CMAUP database
Neosarphenol B 71451577 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C=CC(=C)C)OC)C(=O)OC2 352.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(+)-Bruguierol C 17752611 Click to see CC12CCC(O1)CC3=C2C(=CC(=C3)O)O 206.24 unknown via CMAUP database
(1S,9R)-1-methyl-12-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-5-ol 11148193 Click to see CC12CCC(O1)CC3=C2C=CC(=C3)O 190.24 unknown via CMAUP database
(2S,7R,9S)-9-methoxy-7-methyl-2-propan-2-yl-7,9-dihydro-6H-furo[3,2-h]isochromen-3-one 73356791 Click to see CC1CC2=C(C(O1)OC)C3=C(C=C2)C(=O)C(O3)C(C)C 276.33 unknown via CMAUP database
7H-Furo(3,2-h)(2)benzopyran-3(2H)-one, 6,9-dihydro-7-hydroxy-7-methyl-2-(1-methylethylidene)-, (7R)- 156523 Click to see CC(=C1C(=O)C2=C(O1)C3=C(CC(OC3)(C)O)C=C2)C 260.28 unknown via CMAUP database
9beta-Methyl-6alpha,9alpha-epoxy-6,7,8,9-tetrahydro-5H-benzocycloheptene-2,3-diol 11367742 Click to see CC12CCC(O1)CC3=CC(=C(C=C23)O)O 206.24 unknown via CMAUP database
Aspergillumarin A 38346998 Click to see CC(=O)CCCC1CC2=C(C(=CC=C2)O)C(=O)O1 248.27 unknown via CMAUP database
Aspergillumarin B 38347996 Click to see CC(CCCC1CC2=C(C(=CC=C2)O)C(=O)O1)O 250.29 unknown via CMAUP database
Ustusorane B 44557645 Click to see CC1=CC2=C(CO1)C3=C(C=C2)C(=O)C(=C(C)C)O3 242.27 unknown via CMAUP database
Ustusorane C 44557646 Click to see CC1CC2=C(C(O1)OC)C3=C(C=C2)C(=O)C(=C(C)C)O3 274.31 unknown via CMAUP database
> Organoheterocyclic compounds / Dithiolanes / 1,2-dithiolanes
Bruguiesulfurol 11513780 Click to see C1C(CS(=O)(=O)S1)O 154.21 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
4,25-Dehydro-22-deoxyminiolutelide B 71608261 Click to see CC1C2(C3(C4C(O1)OC(=O)C4(CC5C3(C(O2)C=C6C(=CC(=O)OC6(C)C)C5=C)C)C)C(=O)OC)O 486.50 unknown via CMAUP database
4,25-Dehydrominiolutelide B 71608260 Click to see CC1C2(C3(C4(C(CC5(C3(C(O1)OC5=O)O)C)C(=C)C6=CC(=O)OC(C6=CC4O2)(C)C)C)C(=O)OC)O 502.50 unknown via CMAUP database
berkeleyacetal A 24179625 Click to see CC1C(=O)C2(C3C(O1)OC(=O)C3(CC4C2(CC=C5C(=C4C)CC(=O)OC5(C)C)C)C)C(=O)OC 472.50 unknown via CMAUP database
berkeleyacetal B 24179626 Click to see CC1C(=O)C2(C3C(O1)OC(=O)C3(CC4C2(CC=C5C(=CC(=O)OC5(C)C)C46CO6)C)C)C(=O)OC 486.50 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(2E,4E)-2,4,6-Octatrienoic acid [(5R)-1,3,5,5aalpha,6,7,8,9,9a,9balpha-decahydro-9balpha-hydroxy-6,6,9abeta-trimethyl-1-oxonaphtho[1,2-c]furan]-5beta-yl ester 10407821 Click to see CC=CC=CC=CC(=O)OC1C=C2COC(=O)C2(C3(C1C(CCC3)(C)C)C)O 386.50 unknown via CMAUP database
[(5R,5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-3,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-5-yl] (2E,4E,7S)-7-hydroxyocta-2,4-dienoate 51693297 Click to see CC(CC=CC=CC(=O)OC1C=C2COC(=O)C2(C3(C1C(CCC3)(C)C)C)O)O 404.50 unknown via CMAUP database
Ustusolate D 44557643 Click to see CC1(CCCC2(C1C(C=C3C2(C(=O)OC3)O)OC(=O)C=CC=CC(OC)OC)C)C 420.50 unknown via CMAUP database
Ustusolate E 44480472 Click to see CC1(CCCC2(C1C(C=C3C2(C(=O)OC3)O)OC(=O)C=CC=CC=O)C)C 374.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
octadecyl (2R,3S)-2-(3-hydroxy-5-methoxyphenyl)-7-methoxy-5-[(E)-3-octadecoxy-3-oxoprop-1-enyl]-2,3-dihydro-1-benzofuran-3-carboxylate 25105546 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC2=C(C(=C1)OC)OC(C2C(=O)OCCCCCCCCCCCCCCCCCC)C3=CC(=CC(=C3)OC)O 891.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolactams
(1S,4R,5E,7S,10Z,20S,21S)-4-ethyl-17-hydroxy-7-[(1S)-1-hydroxy-3-methylbut-2-enyl]-10,21-dimethyl-8,24,26-trioxa-14-azatetracyclo[13.8.2.11,20.019,25]hexacosa-5,10,15,17,19(25)-pentaene-9,13,22-trione 53235715 Click to see CCC1CCC23CC(=O)C(C(O2)C4=C(O3)C(=CC(=C4)O)NC(=O)CC=C(C(=O)OC(C=C1)C(C=C(C)C)O)C)C 553.60 unknown via CMAUP database
(9R,10E,12S,15Z,17S,24R)-9-ethyl-4,24-dihydroxy-12-[(1S)-1-hydroxy-3-methylbut-2-enyl]-3,15-dimethyl-13-oxa-19-azatetracyclo[15.6.1.05,23.020,24]tetracosa-1(23),2,4,10,15,20-hexaene-6,14,18,22-tetrone 72715428 Click to see CCC1CCC(=O)C2=C(C(=CC3=C2C(=O)C=C4C3(C(C=C(C(=O)OC(C=C1)C(C=C(C)C)O)C)C(=O)N4)O)C)O 549.60 unknown via CMAUP database
Divergolide B 53235716 Click to see CCC1CCC(=O)C=C2C(=CC3=C(O2)C(=CC(=C3)O)NC(=O)CC=C(C(=O)OC(C(C=C1)O)C=C(C)C)C)C 535.60 unknown via CMAUP database

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