Miyamayomena koraiensis, also known as Korean starwort, is a perennial plant found in temperate regions, mainly in Korea. It belongs to the Asteraceae family and was first named in 1909. Its leaves are used in food preparation in Korea. The plant has green, lanceolate leaves and pale violet flowers that bloom from June to September. It is found throughout the Korean peninsula and is known for its ability to easily grow in various environments, making it useful for erosion control. The name "Aster koraiensis" comes from the Greek word for "star" and "from Korea," while its Korean name, "Beolgaemichui," means "bee flower." In the language of flowers, it symbolizes memories and nostalgia.

Synonyms Top

Scientific name	Authority	First published in
Gymnaster koraiensis	(Nakai) Kitam.	Mem. Coll. Sci. Kyoto Imp. Univ., Ser. B, Biol. xiii. (Compos. Jap. 1.) 303 (
Kitamuraster koraiensis	(Nakai) Soják	Sborn. Nár. Muz. Praze 1982(1–2): 108 (1982), genus illegit.:.
Miyamayomena koraiensis	(Nakai) Kitam.	Acta Phytotax. Geobot. 33: 409 (1982)
Kitamuraea koraiensis	(Nakai) Rauschert	Taxon 31: 557 (1982), genus illeg (1982)
Asteromoea koraiensis	(Nakai) Kitam.	Acta Phytotax. Geobot. 2: 37 (1933)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Korean	벌개미취

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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 click to expand
- Eastern Asia
  - Korea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000071769
Tropicos	2738406
KEW	urn:lsid:ipni.org:names:181529-1
Open Tree Of Life	1009959
NCBI Taxonomy	947972
IPNI	181529-1
iNaturalist	933829
GBIF	5387457
Freebase	/m/0bs7d8r
USDA GRIN	433771
Wikipedia	Miyamayomena_koraiensis
CMAUP	NPO23708
PFAF	Aster koraiensis

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

Triterpenoidal Saponins from the Leaves of Aster koraiensis Offer Inhibitory Activities against SARS-CoV-2

Kim JY, Kim TY, Son SR, Kim SY, Kwon J, Kwon HC, Lee CJ, Jang DS

Plants (Basel)

19-Jan-2024

PMCID:	PMC10819127
doi:	10.3390/plants13020303
PMID:	38276760

Antioxidant potential of chlorogenic acid in Age‐Related eye diseases

Tang Y, Fang C, Shi J, Chen H, Chen X, Yao X

Pharmacol Res Perspect

08-Jan-2024

PMCID:	PMC10772849
doi:	10.1002/prp2.1162
PMID:	38189160

Lid scrubbing with a gel combining natural extracts for dry eye treatment

Diaz-Vega B, Rodriguez-Fabuel C, Vitores-Mate S, Carpena-Torres C

Int J Ophthalmol

18-Jul-2023

PMCID:	PMC10333254
doi:	10.18240/ijo.2023.07.08
PMID:	37465519

NLRP3 Inflammasome as a Potential Therapeutic Target in Dry Eye Disease

Zhuang D, Misra SL, Mugisho OO, Rupenthal ID, Craig JP

Int J Mol Sci

29-Jun-2023

PMCID:	PMC10341612
doi:	10.3390/ijms241310866
PMID:	37446038

Nutrients, herbal bioactive derivatives and commensal microbiota as tools to lower the risk of SARS-CoV-2 infection

Romani A, Sergi D, Zauli E, Voltan R, Lodi G, Vaccarezza M, Caruso L, Previati M, Zauli G

Front Nutr

01-Jun-2023

PMCID:	PMC10267353
doi:	10.3389/fnut.2023.1152254
PMID:	37324739

New Sesquiterpene Glycosides from the Flowers of Aster koraiensis and Their Inhibition Activities on EGF- and TPA-Induced Cell Transformation

Seo YH, Kim JY, Ryu SM, Hwang SY, Lee MH, Kim N, Son H, Lee AY, Kim HS, Moon BC, Jang DS, Lee J

Plants (Basel)

20-Apr-2023

PMCID:	PMC10146194
doi:	10.3390/plants12081726
PMID:	37111949

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

Extract of Aster koraiensis Nakai Leaf Ameliorates Memory Dysfunction via Anti-inflammatory Action

Lee SE, Park S, Jang GY, Lee J, Moon M, Ji YJ, Jung JW, Nam Y, Shin SJ, Lee Y, Choi J, Kim DH

Int J Mol Sci

17-Mar-2023

PMCID:	PMC10052554
doi:	10.3390/ijms24065765
PMID:	36982837

Plants as Biofactories for Therapeutic Proteins and Antiviral Compounds to Combat COVID-19

England C, TrejoMartinez J, PerezSanchez P, Karki U, Xu J

Life (Basel)

23-Feb-2023

PMCID:	PMC10054913
doi:	10.3390/life13030617
PMID:	36983772

Astersaponin I from Aster koraiensis is a natural viral fusion blocker that inhibits the infection of SARS-CoV-2 variants and syncytium formation

Kim TY, Kim JY, Kwon HC, Jeon S, Lee SJ, Jung H, Kim S, Jang DS, Lee CJ

Antiviral Res

15-Oct-2022

PMCID:	PMC9568284
doi:	10.1016/j.antiviral.2022.105428
PMID:	36252824

Efficacy of a Horticultural Therapy Program Designed for Emotional Stability and Career Exploration among Adolescents in Juvenile Detention Centers

Park KH, Kim SY, Park SA

Int J Environ Res Public Health

20-Jul-2022

PMCID:	PMC9319874
doi:	10.3390/ijerph19148812
PMID:	35886667

Neuroprotective Effect of Astersaponin I against Parkinson’s Disease through Autophagy Induction

Zhang L, Park JY, Zhao D, Kwon HC, Yang HO

Biomol Ther (Seoul)

02-Jul-2021

PMCID:	PMC8551730
doi:	10.4062/biomolther.2021.004
PMID:	34210894

Alternative Therapies for Dry Eye Disease

Mittal R, Patel S, Galor A

Curr Opin Ophthalmol

01-Jul-2021

PMCID:	PMC8169641
doi:	10.1097/ICU.0000000000000768
PMID:	34010229

Potential Effects of Nutraceuticals in Retinopathy of Prematurity

Tsang JK, Wolf SA, Pompoes IM, Joussen AM, Lam WC, Yang D, Lo AC

Life (Basel)

22-Jan-2021

PMCID:	PMC7912639
doi:	10.3390/life11020079
PMID:	33499180

New Eudesmane-Type Sesquiterpene Glycosides from the Leaves of Aster koraiensis

Kim JY, Seo YH, Lee IH, Choi HY, Kwon HC, Choi JH, Lee J, Jang DS

Plants (Basel)

21-Dec-2020

PMCID:	PMC7766762
doi:	10.3390/plants9121811
PMID:	33371294

Phytochemical Profile Top

Add a new one!

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
> Benzenoids / Benzene and substituted derivatives / Acetophenones
Viscidone	44584263	Click to see CC(=O)C1=C(C=C2CC(OC2=C1)C(=C)CO)O	234.25	unknown	https://doi.org/10.1007/BF02975112
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(E)-8-Decene-4,6-diynyl 6-O-D-apio-beta-D-furanosyl beta-D-glucopyranoside	46830373	Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O	442.50	unknown	https://doi.org/10.3987/COM-09-11773
[(3S,8E)-3-Hydroxy-8-decene-4,6-diynyl]beta-D-glucopyranoside	10268235	Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O	326.34	unknown	https://doi.org/10.3987/COM-09-11773
2-(3-Hydroxydec-8-en-4,6-diynoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	85059308	Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O	326.34	unknown	https://doi.org/10.3987/COM-09-11773 https://doi.org/10.1248/CPB.50.685
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(3-hydroxydec-8-en-4,6-diynoxy)oxane-3,4,5-triol	85395715	Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O)O	458.50	unknown	https://doi.org/10.1248/CPB.50.685
2-Dec-8-en-4,6-diynoxy-6-(hydroxymethyl)oxane-3,4,5-triol	73802885	Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)CO)O)O)O	310.34	unknown	https://doi.org/10.1021/NP200646E https://doi.org/10.3987/COM-09-11773
2-Dec-8-en-4,6-diynoxy-6-[[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]oxane-3,4,5-triol	75214695	Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O	442.50	unknown	https://doi.org/10.3987/COM-09-11773
Bidenoside C	70695725	Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)CO)O)O)O	310.34	unknown	https://doi.org/10.1021/NP200646E https://doi.org/10.3987/COM-09-11773
Bidensyneoside A1	10903496	Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O	326.34	unknown	https://doi.org/10.1248/CPB.50.685
Gymnasterkoreaside B	11091753	Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O)O	458.50	unknown	https://doi.org/10.1248/CPB.50.685
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Gymnasterkoreayne C	11779567	Click to see CC(=O)OC(C=C)C#CC#CC(C=CCCCCCC=C)O	300.40	unknown	https://doi.org/10.1021/NP0104018
Gymnasterkoreayne D	9972025	Click to see CC(=O)OCC=CC#CC#CC(C=CCCCCCC=C)O	300.40	unknown	https://doi.org/10.1021/NP0104018
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2E,8S,9Z)-2,9,16-Heptadecatriene-4,6-diyne-8-ol	101745966	Click to see CC=CC#CC#CC(C=CCCCCCC=C)O	242.36	unknown	https://doi.org/10.1248/CPB.53.1194
(5S,6Z)-1-[(2R,3R)-3-methyloxiran-2-yl]tetradeca-6,13-dien-1,3-diyn-5-ol	163094272	Click to see CC1C(O1)C#CC#CC(C=CCCCCCC=C)O	258.35	unknown	https://doi.org/10.1021/NP0104018
(5S,6Z)-1-[(2R,3S)-3-methyloxiran-2-yl]tetradeca-6,13-dien-1,3-diyn-5-ol	163094271	Click to see CC1C(O1)C#CC#CC(C=CCCCCCC=C)O	258.35	unknown	https://doi.org/10.1248/CPB.53.1194 https://doi.org/10.5012/BKCS.2010.31.01.227
1-(3-Methyloxiran-2-yl)tetradeca-6,13-dien-1,3-diyn-5-ol	73805560	Click to see CC1C(O1)C#CC#CC(C=CCCCCCC=C)O	258.35	unknown	https://doi.org/10.1248/CPB.53.1194 https://doi.org/10.5012/BKCS.2010.31.01.227
Gymnasterkoreayne A	636738	Click to see CC=CC#CC#CC(CCO)O	164.20	unknown	https://doi.org/10.1021/NP200646E https://doi.org/10.1021/NP0104018
Gymnasterkoreayne B	10264498	Click to see CC1C(O1)C#CC#CC(C=CCCCCCC=C)O	258.35	unknown	https://doi.org/10.1248/CPB.53.1194 https://doi.org/10.1021/NP0104018
Heptadeca-2,9,16-trien-4,6-diyn-8-ol	75072244	Click to see CC=CC#CC#CC(C=CCCCCCC=C)O	242.36	unknown	https://doi.org/10.1248/CPB.53.1194
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(2R,3S,8S,9Z)-heptadeca-9,16-dien-4,6-diyne-2,3,8-triol	101745967	Click to see CC(C(C#CC#CC(C=CCCCCCC=C)O)O)O	276.40	unknown	https://doi.org/10.1248/CPB.53.1194
(8Z,10S,15R,16S)-1,8-Heptadecadiene-11,13-diyne-10,15,16-triol	11514622	Click to see CC(C(C#CC#CC(C=CCCCCCC=C)O)O)O	276.40	unknown	https://doi.org/10.1248/CPB.53.1194 https://doi.org/10.5012/BKCS.2010.31.01.227
1,9,16-Heptadecatriene-4,6-diyne-3,8-diol	5469786	Click to see C=CCCCCCC=CC(C#CC#CC(C=C)O)O	258.35	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
Gymnasterkoreayne E	44566958	Click to see CC(C(C#CC#CC(C=CCCCCCC=C)O)O)O	276.40	unknown	https://doi.org/10.1021/NP200646E https://doi.org/10.1248/CPB.53.1194 https://doi.org/10.1021/NP0104018
Gymnasterkoreayne F	10355169	Click to see C=CCCCCCC=CC(C#CC#CC=CCO)O	258.35	unknown	https://doi.org/10.1248/CPB.53.1194 https://doi.org/10.5012/BKCS.2010.31.01.227 https://doi.org/10.1021/NP0104018
Heptadeca-1,9,16-trien-4,6-diyne-3,8-diol	1446	Click to see C=CCCCCCC=CC(C#CC#CC(C=C)O)O	258.35	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
Heptadeca-2,9,16-trien-4,6-diyne-1,8-diol	73805562	Click to see C=CCCCCCC=CC(C#CC#CC=CCO)O	258.35	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
Heptadeca-9,16-dien-4,6-diyne-2,3,8-triol	72990989	Click to see CC(C(C#CC#CC(C=CCCCCCC=C)O)O)O	276.40	unknown	https://doi.org/10.1248/CPB.53.1194 https://doi.org/10.5012/BKCS.2010.31.01.227
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-[(1S,3aR,4R,7S,7aS)-4-methyl-7-propan-2-yl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone	162954699	Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)OC3C(C(C(C(O3)CO)O)O)O	400.50	unknown	https://doi.org/10.3987/COM-09-11773
1-[4-Methyl-7-propan-2-yl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,3a,5,6,7,7a-octahydroinden-1-yl]ethanone	162954697	Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)OC3C(C(C(C(O3)CO)O)O)O	400.50	unknown	https://doi.org/10.3987/COM-09-11773
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[[(1R,2R,4R,4aR,5R,8aS)-4,5-dihydroxy-4a,8-dimethyl-2-propan-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163020854	Click to see CC1=CCC(C2(C1C(C(CC2O)C(C)C)OC3C(C(C(C(O3)CO)O)O)O)C)O	416.50	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
(2R,3R,4S,5S,6R)-2-[[(1S,2S,4R,4aR,5R,8aS)-4,5-dihydroxy-2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163014392	Click to see CC1=CCC(C2(C1C(C(CC2O)C(C)(C)O)OC3C(C(C(C(O3)CO)O)O)O)C)O	432.50	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
(E)-1-[(1S,3R,4R,4aS,8S,8aS)-8-hydroxy-3-(2-hydroxypropan-2-yl)-5,8a-dimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,4a,7,8-hexahydro-1H-naphthalen-1-yl]-4-(4-hydroxyphenyl)but-3-en-2-one	70681005	Click to see CC1=CCC(C2(C1C(C(CC2CC(=O)C=CC3=CC=C(C=C3)O)C(C)(C)O)OC4C(C(C(C(O4)CO)O)O)O)C)O	576.70	unknown	https://doi.org/10.1021/NP200646E
[(1R)-4alpha-Hydroxy-4,8aalpha-dimethyl-6-isopropyl-1,2,3,4,4abeta,5,8,8a-octahydronaphthalene-1alpha-yl]beta-D-glucopyranoside	102523032	Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)OC3C(C(C(C(O3)CO)O)O)O)C	400.50	unknown	https://doi.org/10.3987/COM-09-11773
[(1R)-4alpha-Hydroxy-4,8aalpha-dimethyl-6-isopropyl-1,2,3,4,4abeta,7,8,8a-octahydronaphthalene-1alpha-yl]beta-D-glucopyranoside	102523031	Click to see CC(C)C1=CC2C(CC1)(C(CCC2(C)O)OC3C(C(C(C(O3)CO)O)O)O)C	400.50	unknown	https://doi.org/10.3987/COM-09-11773
[(1S,3S,4R,4aS,8R,8aR)-8-hydroxy-5,8a-dimethyl-3-propan-2-yl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,4a,7,8-hexahydro-1H-naphthalen-1-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	57333878	Click to see CC1=CCC(C2(C1C(C(CC2OC(=O)C=CC3=CC=C(C=C3)O)C(C)C)OC4C(C(C(C(O4)CO)O)O)O)C)O	562.60	unknown	https://doi.org/10.1021/NP200646E
2-[(4-Hydroxy-4,8a-dimethyl-6-propan-2-yl-1,2,3,4a,5,8-hexahydronaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163091852	Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)OC3C(C(C(C(O3)CO)O)O)O)C	400.50	unknown	https://doi.org/10.3987/COM-09-11773
2-[(4-Hydroxy-4,8a-dimethyl-6-propan-2-yl-1,2,3,4a,7,8-hexahydronaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	162990708	Click to see CC(C)C1=CC2C(CC1)(C(CCC2(C)O)OC3C(C(C(C(O3)CO)O)O)O)C	400.50	unknown	https://doi.org/10.3987/COM-09-11773
2-[(4,5-dihydroxy-4a,8-dimethyl-2-propan-2-yl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163020853	Click to see CC1=CCC(C2(C1C(C(CC2O)C(C)C)OC3C(C(C(C(O3)CO)O)O)O)C)O	416.50	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
2-[[4,5-dihydroxy-2-(2-hydroxypropan-2-yl)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163014391	Click to see CC1=CCC(C2(C1C(C(CC2O)C(C)(C)O)OC3C(C(C(C(O3)CO)O)O)O)C)O	432.50	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.1248/CPB.53.1194
Friedelan-3-one	244297	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1248/CPB.53.1194
Friedelanol	101341	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/10.1248/CPB.53.1194
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1248/CPB.53.1194
Friedelinol	348029	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/10.1248/CPB.53.1194
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	https://doi.org/10.1248/CPB.53.1194
Super Squalene; trans-Squalene;AddaVax	1105	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	https://doi.org/10.1248/CPB.53.1194
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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	521229	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1021/NP200646E
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/10.1021/NP200646E
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1021/NP200646E
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	https://doi.org/10.1021/NP200646E
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	348159	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1021/NP200646E
3,4-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid	3802778	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/10.1021/NP200646E
3,4-Dicaffeoylquinic acid	6474309	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/10.1021/NP200646E
3,5-Dicaffeoyl-epi-quinic acid	60150332	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O	516.40	unknown	https://doi.org/10.1021/NP200646E
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1021/NP200646E
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	https://doi.org/10.1021/NP200646E
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Polyols / 1,2-diols
meso-2,3-Butanediol	220010	Click to see CC(C(C)O)O	90.12	unknown	https://doi.org/10.1248/CPB.53.1194
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
1-[(2R,3S)-5-hydroxy-3-methoxy-2-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-1-en-2-yl]-2,3-dihydro-1-benzofuran-6-yl]ethanone	57331845	Click to see CC(=O)C1=C(C=C2C(C(OC2=C1)C(=C)COC3C(C(C(C(O3)CO)O)O)O)OC)O	426.40	unknown	https://doi.org/10.1021/NP200646E
1-[(2R,3S)-5-hydroxy-3-methoxy-2-[3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-1-en-2-yl]-2,3-dihydro-1-benzofuran-6-yl]ethanone	162866810	Click to see CC(=O)C1=C(C=C2C(C(OC2=C1)C(=C)COC3C(C(C(C(O3)CO)O)O)O)OC)O	426.40	unknown	https://doi.org/10.1021/NP200646E
2-phenylethyl beta-D-glucopyranoside	468284	Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O	284.30	unknown	https://doi.org/10.3987/COM-09-11773
Phenylethyl beta-D-glucopyranoside	11289099	Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O	284.30	unknown	https://doi.org/10.3987/COM-09-11773
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Citrusin C	9945189	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O	326.34	unknown	https://doi.org/10.1021/NP200646E https://doi.org/10.3987/COM-09-11773
Eugenyl glucoside	3084296	Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O	326.34	unknown	https://doi.org/10.1021/NP200646E https://doi.org/10.3987/COM-09-11773
> Organoheterocyclic compounds / Benzofurans
1-[5-Hydroxy-2-(1,2,3-trihydroxypropan-2-yl)-1-benzofuran-6-yl]ethanone	163192551	Click to see CC(=O)C1=C(C=C2C=C(OC2=C1)C(CO)(CO)O)O	266.25	unknown	https://doi.org/10.1007/BF02975112
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione	78108622	Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl	351.80	unknown	https://doi.org/10.1021/NP200646E
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin	182232	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 / Flavanones
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one	932	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
Naringenin	439246	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	272.25	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	5387370	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
Apigenin 7-glucuronide	5319484	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-5-methoxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	74978324	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)OC)O)O)O)O)O	478.40	unknown	https://doi.org/10.1021/NP200646E
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one	5317847	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1021/NP200646E
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5378597	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	https://doi.org/10.5012/BKCS.2010.31.01.227 https://doi.org/10.1021/NP200646E
3'-O-methyltricetin 3-O-alpha-L-rhamnopyranoside	72551450	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)OC)O)O)O)O)O	478.40	unknown	https://doi.org/10.1021/NP200646E
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one	5320020	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1021/NP200646E
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	12313332	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP200646E
Guaijaverin	5481224	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1021/NP200646E
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	https://doi.org/10.5012/BKCS.2010.31.01.227 https://doi.org/10.1021/NP200646E
Isorhamnetin 3-galactoside	13245586	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1021/NP200646E https://doi.org/10.5012/BKCS.2010.31.01.227
isorhamnetin 3-O-glucoside	5318645	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1021/NP200646E https://doi.org/10.5012/BKCS.2010.31.01.227
Isorhamnetin 3-robinobioside	6223069	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1021/NP200646E
Kaempferol-3-O-rutinoside	5318767	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP200646E
Narcissin	5481663	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1021/NP200646E
Reynoutrin	5878729	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	434.30	unknown	https://doi.org/10.1021/NP200646E
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside	5385553	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.5012/BKCS.2010.31.01.227

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Aster koraiensis

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top