Adonis amurensis

Details

Ethnobotanical Use

General Uses

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Gallery

Contributors

Collections

Details Top

Internal ID	UUID64400783009f8499103126
Scientific name	Adonis amurensis
Authority	Regel & Radde
First published in	Bull. Soc. Imp. Naturalistes Moscou 34(II): 35 (1862)

Ethnobotanical Use Top

Write a new one!

No ethnobotanical data added yet. Help us by writing one.

General Uses Top

Suggest a correction!

Common products:
- Whole plants sold as ornamental herbaceous perennials for spring garden displays.
- Cut‑flower stems with showy yellow‑orange blossoms marketed for floristry.

Properties relevant to use:
- Early spring flowering (generally March–April), providing early‑season garden color.
- Large, brightly colored corollas (yellow to orange) that are attractive in ornamental horticulture.
- Herbaceous perennial growth habit, allowing multi‑year garden use and ease of propagation.

Synonyms Top

Scientific name	Authority	First published in
Adonanthe amurensis	(Regel & Radde) Chrtek & Slavíková	Preslia 50: 24 (1978)
Adonis amurensis var. angustiloba	A.I.Baranov & Skvortsov	Zap. Kharbin. Obshch. Estestvoisp. Etnogr. 12: 35. 1954
Adonis amurensis var. parviflora	Nakai
Adonis amurensis var. puberula	Honda	Bot. Mag. (Tokyo) 52: 49 1939
Adonis amurensis var. uniflora	Makino	Bot. Mag. (Tokyo) 8: 97 1894
Adonis barthei	Franch.	Bull. Annuel Soc. Philom. Paris , sér. 8, 6: 89 (1894)
Adonis vernalis var. amurensis	(Regel & Radde) Regel & Radde	Bull. Soc. Bot. France 51: 132 1904
Chrysocyathus amurensis	(Regel & Radde) Holub	Preslia 70: 102 (1998)
Adonis amurensis var. yezoensis	Kudô	Hokk.-Yak.-Shokub.-Zui 44 1922

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Arabic	أدونيس آموري
Azerbaijani	amur xoruzgülü
Tibetan	མེ་ཏོག་གར་ཚུགས་ཆུང་བ་
Czech	hlaváček amurský
German	amur-adonisröschen
Persian	آدونیس آمورنسیس
Finnish	amurinruusuleinikki
French	adonide de l'amour
Upper Sorbian	amurowa horiwka
Japanese	キタミフクジュソウ
Japanese	北見福寿草
Korean	복수초
mnc	ᠠᠰᡳᡥᠠᠨ ᠠᡳᠰᡳᠨ ᡥᡡᠨᡨᠠᡥᠠᠨ ᡳᠯᠠᡥ
Polish	miłek amurski
Russian	Адонис амурский
Slovak	hlaváčik amurský
Chinese	福壽草
Chinese	顶冰花
Chinese	福寿草
Chinese	冰凉花
Chinese	側金盞花
Chinese	侧金盏花(冰凉花）
Chinese	侧金盏花

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!

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

Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

much chaff and nonviable seed is typical; short viability; very poor germination; does not need chilling if seed is fresh. Seedlings will probably die if transplanted, so wait till they have got some size and transplant while dormant.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
- Russian Far East
  - Amur
  - Khabarovsk
  - Kuril Islands
  - Primorye
  - Sakhalin

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000521126
UNII	F2563E84RC
Tropicos	27100020
KEW	urn:lsid:ipni.org:names:708061-1
The Plant List	kew-2623058
Open Tree Of Life	243850
Observations.org	113960
NCBI Taxonomy	196574
IPNI	708061-1
iNaturalist	437861
GBIF	7277921
Freebase	/m/0nbgs85
EPPO	ADOAM
EOL	2873427
Elurikkus	581865
USDA GRIN	1503
Wikipedia	Adonis_amurensis
PFAF	Adonis amurensis

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

Dynamic transcriptome analysis provides molecular insights into underground floral differentiation in Adonis Amurensis Regel & Radde

Xin H, Zhang L, Wang H, Zhu X

BMC Genom Data

21-Mar-2024

PMCID:	PMC10956236
doi:	10.1186/s12863-024-01220-2
PMID:	38515034

Karyotypes and Physical Mapping of Ribosomal DNA with Oligo-Probes in Eranthis sect. Eranthis (Ranunculaceae)

Mitrenina EY, Alekseeva SS, Badaeva ED, Peruzzi L, Artemov GN, Krivenko DA, Pinzani L, Aytaç Z, Çeçen Ö, Baasanmunkh S, Choi HJ, Mesterházy A, Tashev AN, Bancheva S, Lian L, Xiang K, Wang W, Erst AS

Plants (Basel)

22-Dec-2023

PMCID:	PMC10780877
doi:	10.3390/plants13010047
PMID:	38202355

Comparative plastome genomics and phylogenetic relationships of the genus Trollius

Li J, Du Y, Xie L, Jin X, Zhang Z, Yang M

Front Plant Sci

17-Nov-2023

PMCID:	PMC10690957
doi:	10.3389/fpls.2023.1293091
PMID:	38046610

Astaxanthin: Past, Present, and Future

Nishida Y, Berg PC, Shakersain B, Hecht K, Takikawa A, Tao R, Kakuta Y, Uragami C, Hashimoto H, Misawa N, Maoka T

Mar Drugs

28-Sep-2023

PMCID:	PMC10608541
doi:	10.3390/md21100514
PMID:	37888449

Beyond NPK: Mineral Nutrient-Mediated Modulation in Orchestrating Flowering Time

Jun SE, Shim JS, Park HJ

Plants (Basel)

18-Sep-2023

PMCID:	PMC10535918
doi:	10.3390/plants12183299
PMID:	37765463

Complete chloroplast genome of Adonis pseudoamurensis W.T.Wang (Ranunculaceae)

Zhang XY, Zhang ZL, Zhang LQ, Zhang LF, Zhu JY, Xue CS

Mitochondrial DNA B Resour

15-Sep-2023

PMCID:	PMC10506428
doi:	10.1080/23802359.2023.2256493
PMID:	37727834

How to deal with frenemy NRF2: Targeting NRF2 for chemoprevention and cancer therapy

Tang YC, Chuang YJ, Chang HH, Juang SH, Yen GC, Chang JY, Kuo CC

J Food Drug Anal

31-Aug-2023

PMCID:	PMC10629913
doi:	10.38212/2224-6614.3463
PMID:	39666284

Genome-Wide Identification and Expression Analysis of C3H Zinc Finger Family in Potato (Solanum tuberosum L.)

Deng Z, Yang Z, Liu X, Dai X, Zhang J, Deng K

Int J Mol Sci

17-Aug-2023

PMCID:	PMC10454627
doi:	10.3390/ijms241612888
PMID:	37629069

Expanding the Repertoire of the Plant-Infecting Ophioviruses through Metatranscriptomics Data

Debat H, Garcia ML, Bejerman N

Viruses

25-Mar-2023

PMCID:	PMC10144540
doi:	10.3390/v15040840
PMID:	37112821

Phytochemicals and Regulation of NF-kB in Inflammatory Bowel Diseases: An Overview of In Vitro and In Vivo Effects

Laurindo LF, dos Santos AR, de Carvalho AC, Bechara MD, Guiguer EL, Goulart RD, Vargas Sinatora R, Araújo AC, Barbalho SM

Metabolites

07-Jan-2023

PMCID:	PMC9862976
doi:	10.3390/metabo13010096
PMID:	36677021

Comparative Transcriptome Analysis of CCCH Family in Roles of Flower Opening and Abiotic Stress in Osmanthus fragrans

Ye Y, Cao S, Shen L, Wang Y, Zhong S, Yang L, Xiao Z, Fang Q, Zhao H, Dong B

Int J Mol Sci

06-Dec-2022

PMCID:	PMC9735588
doi:	10.3390/ijms232315363
PMID:	36499688

Astaxanthin Protection against Neuronal Excitotoxicity via Glutamate Receptor Inhibition and Improvement of Mitochondrial Function

Kandy SK, Nimonkar MM, Dash SS, Mehta B, Markandeya YS

Mar Drugs

18-Oct-2022

PMCID:	PMC9605357
doi:	10.3390/md20100645
PMID:	36286468

Analysis of Floral Organ Development and Sex Determination in Schisandra chinensis by Scanning Electron Microscopy and RNA-Sequencing

Liu X, Zhang L, Yang S

Life (Basel)

18-Aug-2022

PMCID:	PMC9410518
doi:	10.3390/life12081260
PMID:	36013439

AaZFP3, a Novel CCCH-Type Zinc Finger Protein from Adonis amurensis, Promotes Early Flowering in Arabidopsis by Regulating the Expression of Flowering-Related Genes

Wang M, Zhang H, Dai S, Feng S, Gong S, Wang J, Zhou A

Int J Mol Sci

25-Jul-2022

PMCID:	PMC9332444
doi:	10.3390/ijms23158166
PMID:	35897742

Characterization of Phytohormones and Transcriptomic Profiling of the Female and Male Inflorescence Development in Manchurian Walnut (Juglans mandshurica Maxim.)

Li X, Han R, Cai K, Guo R, Pei X, Zhao X

Int J Mol Sci

13-May-2022

PMCID:	PMC9143237
doi:	10.3390/ijms23105433
PMID:	35628244

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
(3S,8R,9R,10R,17S)-17-acetyl-3-hydroxy-10-methyl-2,3,4,7,8,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-one	162883828	Click to see CC(=O)C1CCC2=C1C(=O)CC3C2CC=C4C3(CCC(C4)O)C	314.40	unknown	https://doi.org/10.1007/BF01900226
17-acetyl-3-hydroxy-10-methyl-2,3,4,7,8,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-one	78384929	Click to see	314.40	unknown	https://doi.org/10.1007/BF01900226
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
3-[(3S,5S,8R,9S,10R,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4S,5S,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-10-(hydroxymethyl)-13-methyl-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2H-furan-5-one	129628835	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)CO)OC)O	550.70	unknown	https://doi.org/10.1002/PTR.1184
CID 6708764	6708764	Click to see	548.70	unknown	https://doi.org/10.1002/PTR.1184
Cymarine	441853	Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)OC)O	548.70	unknown	https://doi.org/10.1002/PTR.1184
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4S,5S,6R)-2-[(2R,3S,4R,6S)-6-[(2R,3R,4S,6S)-6-[(2R,3R,4S,6S)-6-[(2R,3R,4R,6S)-6-[(2R,3R,4R,6R)-6-[[(3S,8R,9S,10R,12S,13S,14S,17R)-12,14-dihydroxy-17-[(1S)-1-hydroxyethyl]-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162881866	Click to see	1233.50	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
(3S,8R,9S,10R,17S)-17-acetyl-17-hydroxy-3-[(2R,4R,5R,6R)-4-methoxy-5-[(2S,4R,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-methyl-1,2,3,4,7,8,9,11-octahydrocyclopenta[a]phenanthren-12-one	162912770	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(=O)C5=C(C4CC=C3C2)C=CC5(C(=O)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC	1211.40	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
(3S,8R,9S,10R,17S)-17-acetyl-3-[(2R,4R,5R,6R)-4-methoxy-5-[(2S,4R,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-methyl-2,3,4,7,8,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-one	44818335	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(=O)C5=C(C4CC=C3C2)CCC5C(=O)C)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC	1197.40	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
[(3S,8S,9R,10R,12R,13S,14R,17R)-17-acetyl-8,14-dihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] benzoate	44817974	Click to see	1063.20	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
[(3S,8S,9R,10R,12R,13S,14R,17S)-17-acetyl-8,14-dihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] benzoate	44817802	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)OC(=O)C6=CC=CC=C6)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC	1063.20	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
[(3S,8S,9R,10R,12R,13S,14R,17S)-17-acetyl-8,14-dihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] pyridine-3-carboxylate	44817975	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)OC(=O)C6=CN=CC=C6)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC	1064.20	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
[17-acetyl-8,14-dihydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] benzoate	75076495	Click to see	1063.20	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
[17-acetyl-8,14-dihydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-yl] pyridine-3-carboxylate	75076568	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)OC(=O)C6=CN=CC=C6)C)OC)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC)OC	1064.20	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
1-[(3S,8S,9R,10R,12R,13S,14R,17S)-8,12,14-trihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone	44818334	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC	959.10	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
1-[(3S,8S,9S,10R,11R,13R,14R,17S)-8,11,14-trihydroxy-3-[(2R,4S,5R,6R)-4-methoxy-5-[(2S,4S,5R,6R)-4-methoxy-5-[(2S,4R,5S,6R)-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone	44818153	Click to see CC1C(C(CC(O1)OC2CCC3(C4C(CC5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC	959.10	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
1-[8,11,14-trihydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone	75076640	Click to see	959.10	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
1-[8,12,14-trihydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone	75076713	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4(CC=C3C2)O)O)C(=O)C)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)OC)OC	959.10	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
17-Acetyl-17-hydroxy-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-methyl-1,2,3,4,7,8,9,11-octahydrocyclopenta[a]phenanthren-12-one	75076837	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(=O)C5=C(C4CC=C3C2)C=CC5(C(=O)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC	1211.40	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
17-acetyl-3-[4-methoxy-5-[4-methoxy-5-[4-methoxy-5-[4-methoxy-5-[4-methoxy-6-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-10-methyl-2,3,4,7,8,9,11,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-12-one	75076714	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(=O)C5=C(C4CC=C3C2)CCC5C(=O)C)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC	1197.40	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
2-[6-[6-[6-[6-[6-[[12,14-Dihydroxy-17-(1-hydroxyethyl)-10,13-dimethyl-1,2,3,4,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-4-methoxy-2-methyloxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	75076780	Click to see CC1C(C(CC(O1)OC2CCC3(C4CC(C5(C(CCC5(C4CC=C3C2)O)C(C)O)C)O)C)OC)OC6CC(C(C(O6)C)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9CC(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)OC)OC)OC)OC	1233.50	unknown	https://doi.org/10.1016/J.STEROIDS.2009.10.008
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.1007/BF00568428

Gallery Top

We don't have an image yet. Upload an image!

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.

Adonis amurensis

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top