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Aster spathulifolius

Aster spathulifolius - 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 UUID643fcf8886684399414124
Scientific name Aster spathulifolius
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg xvi. (1871) 216.

Description Top

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Synonyms Top

Scientific name Authority First published in
Erigeron spathulifolius (Maxim.) H.S.Pak Fl. Coreana 7: 297 (1999) (1999)
Heteropappus krylovianus Kom. Bot. Mater. Gerb. Glavn. Bot. Sada S.S.S.R. vi. 14 (1926).
Aster feddei H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 8: 168 (1910)
Heteropappus oharae (Nakai) Kitam. Acta Phytotax. Geobot. 2: 44 (1933)
Erigeron oharae (Nakai) Botsch. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 16: 389 (1954)
Aster chusanensis Y.S.Lim, Hyun, Y.D.Kim & H.C.Shin J. Pl. Biol. 48(4): 479 (-482; fig. 1) (2005)
Aster spathulifolius var. oharae (Nakai) Y.N.Lee Fl. Korea : 1162 (1996)
Aster spathulifolius f. albiflorus H.Nakan. J. Phytogeogr. Taxon. 30(2): 112 (1982) (1982)
Aster oharai Nakai Bot. Mag. (Tokyo) 32: 110 (1918)
Erigeron feddei (H.Lév. & Vaniot) Botsch. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 16: 389 (1954)
Erigeron spathulifolius var. oharae (Nakai) H.S.Pak Fl. Coreana 7: 298 (1999)

Common names Top

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Language Common/alternative name
Korean 해국
Chinese 海菊

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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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
  • Asia-temperate
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000091190
Tropicos 2701878
KEW urn:lsid:ipni.org:names:182343-1
The Plant List gcc-47459
Open Tree Of Life 1009964
Observations.org 145306
NCBI Taxonomy 947974
IPNI 182343-1
iNaturalist 452200
GBIF 5387539
EPPO ASTSF
USDA GRIN 5659
Wikipedia Aster_spathulifolius
CMAUP NPO16949

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
Characterization and phylogenetic analysis of the complete chloroplast genome of Asterothamnus centraliasiaticus Novopokr. (Asteraceae: Asterothamnus) Li Z, Liu Y, Ma Y Mitochondrial DNA B Resour 24-Jan-2024
PMCID:PMC10810623
doi:10.1080/23802359.2024.2306207
PMID:38274851
A review of recently introduced Aspergillus, Penicillium, Talaromyces and other Eurotiales species Visagie CM, Yilmaz N, Kocsubé S, Frisvad JC, Hubka V, Samson RA, Houbraken J Stud Mycol 10-Jan-2024
PMCID:PMC11003441
doi:10.3114/sim.2024.107.01
PMID:38600958
Population Structure and Genetic Diversity Analyses Provide New Insight into the Endemic Species Aster spathulifolius Maxim. and Its Evolutionary History Raman G, Choi KS, Park S Plants (Basel) 27-Dec-2023
PMCID:PMC10780962
doi:10.3390/plants13010088
PMID:38202396
Metabolomic and transcriptomic analyses provide insights into variations in flavonoids contents between two Artemisia cultivars Qiao Y, Wu L, Yang S, Wang Q, Gu H, Wei L, Liu G, Zhou S, Wang P, Song M BMC Plant Biol 30-May-2023
PMCID:PMC10228080
doi:10.1186/s12870-023-04295-8
PMID:37254042
Analysis of Floral Scent and Volatile Profiles of Different Aster Species by E-nose and HS-SPME-GC-MS Song SY, Ahn MS, Mekapogu M, Jung JA, Song HY, Lim SH, Jin JS, Kwon OK Metabolites 31-Mar-2023
PMCID:PMC10141722
doi:10.3390/metabo13040503
PMID:37110161
Effects of caffeoylquinic acid analogs derived from aerial parts of Artemisia iwayomogi on adipogenesis Han SY, Kim J, Kim BK, Whang WK, Min H Food Sci Biotechnol 06-Feb-2023
PMCID:PMC10289966
doi:10.1007/s10068-023-01262-9
PMID:37362808
Comparative and phylogenetic analysis based on chloroplast genome of Heteroplexis (Compositae), a protected rare genus Duan N, Deng L, Zhang Y, Shi Y, Liu B BMC Plant Biol 22-Dec-2022
PMCID:PMC9773445
doi:10.1186/s12870-022-04000-1
PMID:36550394
The Modulation of Melanogenesis in B16 Cells Upon Treatment with Plant Extracts and Isolated Plant Compounds Merecz-Sadowska A, Sitarek P, Kowalczyk T, Zajdel K, Kucharska E, Zajdel R Molecules 07-Jul-2022
PMCID:PMC9324663
doi:10.3390/molecules27144360
PMID:35889231
Sequence Characteristics and Phylogenetic Analysis of the Artemisia argyi Chloroplast Genome Chen C, Miao Y, Luo D, Li J, Wang Z, Luo M, Zhao T, Liu D Front Plant Sci 20-Jun-2022
PMCID:PMC9252292
doi:10.3389/fpls.2022.906725
PMID:35795352
Edible Mushrooms as Novel Myco-Therapeutics: Effects on Lipid Level, Obesity, and BMI Mustafa F, Chopra H, Baig AA, Avula SK, Kumari S, Mohanta TK, Saravanan M, Mishra AK, Sharma N, Mohanta YK J Fungi (Basel) 21-Feb-2022
PMCID:PMC8880354
doi:10.3390/jof8020211
PMID:35205965
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Approaches to Decrease Hyperglycemia by Targeting Impaired Hepatic Glucose Homeostasis Using Medicinal Plants Mata-Torres G, Andrade-Cetto A, Espinoza-Hernández F Front Pharmacol 23-Dec-2021
PMCID:PMC8733686
doi:10.3389/fphar.2021.809994
PMID:35002743
The Challenging Melanoma Landscape: From Early Drug Discovery to Clinical Approval Matias M, Pinho JO, Penetra MJ, Campos G, Reis CP, Gaspar MM Cells 09-Nov-2021
PMCID:PMC8621991
doi:10.3390/cells10113088
PMID:34831311
Fungal Community Analyses of Endophytic Fungi from Two Oak Species, Quercus mongolica and Quercus serrata, in Korea Nguyen MH, Shin KC, Lee JK Mycobiology 09-Aug-2021
PMCID:PMC8409933
doi:10.1080/12298093.2021.1948175
PMID:34512082
Herbal Medicines Targeting the Improved β-Cell Functions and β-Cell Regeneration for the Management of Diabetes Mellitus Wickramasinghe AS, Kalansuriya P, Attanayake AP Evid Based Complement Alternat Med 14-Jul-2021
PMCID:PMC8298154
doi:10.1155/2021/2920530
PMID:34335803

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
(1R,2R,4aR,8aS)-1-[(3R)-3-hydroxy-3-methyl-pent-4-enyl]-2,5,5,8a-tetramethyl-decalin-2-ol 11869525 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1016/0040-4039(80)80175-4
https://doi.org/10.1021/NP058044E
(2R,4R,4aS,8aR)-4-[(3R)-3-hydroxy-3-methylpent-4-enyl]-4a,8,8-trimethyl-3-methylidene-2,4,5,6,7,8a-hexahydro-1H-naphthalen-2-ol 163044734 Click to see CC1(CCCC2(C1CC(C(=C)C2CCC(C)(C=C)O)O)C)C 306.50 unknown https://doi.org/10.1021/NP058044E
(2S,3R,4R,5R,6S)-2-[(3R)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-6-methyloxane-3,4,5-triol 101320314 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)O)O 436.60 unknown https://doi.org/10.1021/NP020119G
(2S,3R,4S,5R,6R)-2-[(3R)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-6-methyloxane-3,4,5-triol 11619408 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C3(CCCC(C3CCC2(C)O)(C)C)C)C=C)O)O)O 454.60 unknown https://doi.org/10.1021/NP058044E
(2S,3R,4S,5R,6R)-2-[(3R)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-6-methyloxane-3,4,5-triol 44584270 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)O)O 436.60 unknown https://doi.org/10.1021/NP058044E
(2S,3R,4S,5S,6S)-2-[(3R)-5-[(1R,2R,4aS,8aS)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-6-methyloxane-3,4,5-triol 162996199 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C3(CCCC(C3CCC2(C)O)(C)C)C)C=C)O)O)O 454.60 unknown https://doi.org/10.1021/NP058044E
https://doi.org/10.1016/0040-4039(80)80175-4
(2S,3R,4S,5S,6S)-2-[(3R)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-6-methyloxane-3,4,5-triol 44584268 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)O)O 436.60 unknown https://doi.org/10.1021/NP058044E
https://doi.org/10.1016/0040-4039(80)80175-4
https://doi.org/10.1021/NP020119G
(2S,4aS,8S,8aS)-8-[(3R)-3-hydroxy-3-methylpent-4-enyl]-4,4,8a-trimethyl-7-methylidene-2,3,4a,5,6,8-hexahydro-1H-naphthalen-2-ol 163092936 Click to see CC1(CC(CC2(C1CCC(=C)C2CCC(C)(C=C)O)C)O)C 306.50 unknown https://doi.org/10.1021/NP058044E
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-ol 162988904 Click to see CC1=CCC2C(CCCC2(C1CCC(C)(C=C)O)C)(C)C 290.50 unknown https://doi.org/10.1021/NP058044E
[(13R)-7alpha-Hydroperoxylabda-8,14-diene-13-yl]4-O-acetyl-6-deoxy-alpha-L-idopyranoside 11049491 Click to see CC1C(C(C(C(O1)OC(C)(CCC2=C(C(CC3C2(CCCC3(C)C)C)OO)C)C=C)O)O)OC(=O)C 510.70 unknown https://doi.org/10.1021/NP020119G
[(13R)-Labda-7,14-diene-13-yl]2-O-acetyl-alpha-L-rhamnopyranoside 44576001 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)OC(=O)C)O)O 478.70 unknown https://doi.org/10.1021/NP020119G
[(13R)-Labda-7,14-diene-13-yl]3-O-acetyl-alpha-L-rhamnopyranoside 44576000 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)OC(=O)C)O 478.70 unknown https://doi.org/10.1021/NP020119G
[(2R,3R,4R,5R,6S)-6-[(3R)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 11719917 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)O)OC(=O)C 478.70 unknown https://doi.org/10.1021/NP058044E
[(2S,3R,4S,5R,6S)-6-[(3R)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 44575999 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)O)OC(=O)C 478.70 unknown https://doi.org/10.1021/NP020119G
[(2S,3R,4S,5S,6R)-2-[(3R)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] acetate 11712695 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)OC(=O)C)O 478.70 unknown https://doi.org/10.1021/NP058044E
[(2S,3S,4R,5R,6S)-6-[(3R)-5-[(1R,3R,4aS,8aS)-3-hydroperoxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 10481452 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=C)C(CC3C2(CCCC3(C)C)C)OO)C=C)O)O)OC(=O)C 510.70 unknown https://doi.org/10.1021/NP020119G
[(2S,3S,4R,5R,6S)-6-[(3R)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 44584267 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)O)OC(=O)C 478.70 unknown https://doi.org/10.1021/NP020119G
https://doi.org/10.1016/0040-4039(80)80175-4
https://doi.org/10.1021/NP058044E
[(2S,3S,4R,5R,6S)-6-[(3R)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 44575995 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=C)CCC3C2(CCCC3(C)C)C)C=C)O)O)OC(=O)C 478.70 unknown https://doi.org/10.1021/NP020119G
[1R-[1alpha(R*),2beta,4abeta,8aalpha]]-2-hydroxy-alpha,2,5,5,8a-pentamethyl-alpha-vinyldecahydronaphthalene-1-propan-1-ol 7093249 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1021/NP058044E
[2-[5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-1-en-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] acetate 73070258 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)OC(=O)C)O 478.70 unknown https://doi.org/10.1021/NP058044E
https://doi.org/10.1021/NP020119G
[2-[5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] acetate 75049129 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)OC(=O)C)O)O 478.70 unknown https://doi.org/10.1021/NP020119G
[6-[5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 73072576 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)O)OC(=O)C 478.70 unknown https://doi.org/10.1021/NP020119G
https://doi.org/10.1016/0040-4039(80)80175-4
https://doi.org/10.1021/NP058044E
[6-[5-(3-Hydroperoxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 73880600 Click to see CC1C(C(C(C(O1)OC(C)(CCC2=C(C(CC3C2(CCCC3(C)C)C)OO)C)C=C)O)O)OC(=O)C 510.70 unknown https://doi.org/10.1021/NP020119G
[6-[5-(3-hydroperoxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-1-en-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 85154840 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=C)C(CC3C2(CCCC3(C)C)C)OO)C=C)O)O)OC(=O)C 510.70 unknown https://doi.org/10.1021/NP020119G
1-Naphthalenepropanol, alpha-ethenyldecahydro-2-hydroxy-alpha,2,5,5,8a-pentamethyl-, [1R-[1alpha(R*),2beta,4abeta,8aalpha]]- 521332 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1021/NP020119G
https://doi.org/10.1016/0040-4039(80)80175-4
https://doi.org/10.1021/NP058044E
2-[5-(2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-methylpent-1-en-3-yl]oxy-6-methyloxane-3,4,5-triol 73031646 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C3(CCCC(C3CCC2(C)O)(C)C)C)C=C)O)O)O 454.60 unknown https://doi.org/10.1016/0040-4039(80)80175-4
https://doi.org/10.1021/NP058044E
5-(2,5,5,8a-Tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-1-en-3-ol 15923775 Click to see CC1=CCC2C(CCCC2(C1CCC(C)(C=C)O)C)(C)C 290.50 unknown https://doi.org/10.1016/0040-4039(80)80175-4
https://doi.org/10.1021/NP058044E
8-(3-hydroxy-3-methylpent-4-enyl)-4,4,8a-trimethyl-7-methylidene-2,3,4a,5,6,8-hexahydro-1H-naphthalen-2-ol 163092935 Click to see CC1(CC(CC2(C1CCC(=C)C2CCC(C)(C=C)O)C)O)C 306.50 unknown https://doi.org/10.1021/NP058044E
Isomanool 15923774 Click to see CC1=CCC2C(CCCC2(C1CCC(C)(C=C)O)C)(C)C 290.50 unknown https://doi.org/10.1016/0040-4039(80)80175-4
https://doi.org/10.1021/NP058044E
Labdane diterpene, alpha-L-deoxyidopyranose 340124 Click to see CC1C(C(C(C(O1)OC(C)(CCC2C(=CCC3C2(CCCC3(C)C)C)C)C=C)O)O)O 436.60 unknown https://doi.org/10.1021/NP020119G
https://doi.org/10.1016/0040-4039(80)80175-4
https://doi.org/10.1021/NP058044E
Sclareol 163263 Click to see CC1(CCCC2(C1CCC(C2CCC(C)(C=C)O)(C)O)C)C 308.50 unknown https://doi.org/10.1021/NP020119G
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2S,3R,4R,5R,6S)-2-[(3R)-5-[(1S,4aS,8aS)-2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-1-en-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44576002 Click to see CC1=CCC2C(CCCC2(C1CCC(C)(C=C)OC3C(C(C(C(O3)CO)O)O)O)C)(C)C 452.60 unknown https://doi.org/10.1021/NP020119G
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,7R,10aS,10bR)-3-ethenyl-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid 162970570 Click to see CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C(=O)O)C)C=C 320.50 unknown https://doi.org/10.1021/NP020119G
(3R,4aS,6aS,7S,10aR,10bS)-3-ethenyl-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid 162970569 Click to see CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C(=O)O)C)C=C 320.50 unknown https://doi.org/10.1021/NP020119G
(3S,4aS,6aS,7R,10aR,10bS)-3-ethenyl-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid 162970567 Click to see CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C(=O)O)C)C=C 320.50 unknown https://doi.org/10.1021/NP058044E
(3S,4aS,6aS,7S,10aR,10bS)-3-ethenyl-3,4a,7,10a-tetramethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene-7-carboxylic acid 163189156 Click to see CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C(=O)O)C)C=C 320.50 unknown https://doi.org/10.1021/NP020119G
8alpha,13R-Epoxy-14-labden-19-oic acid 14589048 Click to see CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C(=O)O)C)C=C 320.50 unknown https://doi.org/10.1021/NP058044E
https://doi.org/10.1021/NP020119G
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1007/BF02976874
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(5S,9S,10S,13R,14R)-17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 137706369 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/BF02976874
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/BF02976874
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S)-3,4-bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 129316855 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1007/BF02976874
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Melilotoside 5280759 Click to see C1=CC=C(C(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
2-Hydroxycinnamic acid, (2E)- 637540 Click to see C1=CC=C(C(=C1)C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Morin 5281670 Click to see C1=CC(=C(C=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 302.23 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 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
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 3,7-diglucoside 6325460 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown via CMAUP database
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database

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