Paeonia anomala - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Paeonia anomala - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID6440020de7256611539752
Scientific name Paeonia anomala
Authority L.
First published in Mant. Pl. 2: 247 (1771)

Description Top

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Paeonia anomala is a species of herbaceous perennial peony that is native to a region between northern European Russia and northern Mongolia, and south to the Tien Shan Mountains. It grows up to 1m tall and has deeply incised leaves with fine segments. The plant produces magenta-red flowers in early summer, typically with only one fully developed flower per stem. In garden cultivation, it prefers full sun or partial shade and well-drained soil. This species is closely related to Paeonia veitchii and is often mistaken for it, but can be distinguished by its single flower per stem. P. anomala has been used in traditional medicine for treating various ailments and has also been consumed as food in some regions. It is now becoming more widely available as an ornamental plant for gardens.

Synonyms Top

Scientific name Authority First published in
Paeonia anomala var. insignis Lynch J. Roy. Hort. Soc. 12: 435. 1890
Paeonia anomala var. nudicarpa Huth Bot. Jahrb. Syst. 14: 269. 1891

Common names Top

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Language Common/alternative name
ba Дөр-дөр сәскә
Catalan peònia asiàtica
Estonian anomaalne pojeng
Finnish kuolanpioni
Kazakh Таушымылдық
kv Маръямоль
Lithuanian sibirinis bijūnas
mn Ягаан цээнэ
Russian пион необычайный
Russian пион уклоняющийся
Russian шегня
Russian пион неправильный
Russian пион Марьин корень
Russian Марьина трава
Russian Марьин корень
Swedish sibirisk pion
tyv Шеңне
Vietnamese thược dược lá hẹp
Chinese 新疆苟药(阿尔泰赤苟、奇特赤苟)
Chinese 川赤苟
Chinese 花蚁虫
Chinese 窄叶芍药
Chinese 赤芍

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Paeonia anomala subsp. anomala
Paeonia anomala subsp. veitchii (Lynch) D.Y.Hong & K.Y.Pan Novon 11: 317 (2001)

Varieties (abbr. var.) Top

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No variety added yet.

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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20°C x 3 months or longer until a 4 cm radicle appears, then 4°C x 3 months, leaf appears while chilled or in next 20°C cycle

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Buryatiya
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
  • Europe
    • Eastern Europe
      • East European Russia
      • North European Russia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000480534
UNII 6I6XN4YFKF
KEW urn:lsid:ipni.org:names:711738-1
The Plant List kew-2560924
Plantarium 26648
PFAF Paeonia anomala
Open Tree Of Life 985348
Observations.org 120336
NCBI Taxonomy 40698
IPNI 711738-1
iNaturalist 414267
iNaturalist 410856
iNaturalist 414268
GBIF 7316516
Freebase /m/0b74wh0
EOL 2873853
Elurikkus 6071
USDA GRIN 26307
Wikipedia Paeonia_anomala

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
Three-tiered authentication of herbal traditional Chinese medicine ingredients used in women’s health provides progressive qualitative and quantitative insight Mück F, Scotti F, Mauvisseau Q, Thorbek BL, Wangensteen H, de Boer HJ Front Pharmacol 05-Feb-2024
PMCID:PMC10875096
doi:10.3389/fphar.2024.1353434
PMID:38375033
Antiviral, antioxidant, and anti-inflammatory activities of rhein against white spot syndrome virus infection in red swamp crayfish (Procambarus clarkii) Chen C, Liang CS, Wang T, Shen JL, Ling F, Jiang HF, Li PF, Wang GX Microbiol Spectr 19-Oct-2023
PMCID:PMC10714825
doi:10.1128/spectrum.01047-23
PMID:37855526
Efficacy and Key Materials of East Asian Herbal Medicine Combined with Conventional Medicine on Inflammatory Skin Lesion in Patients with Psoriasis Vulgaris: A Meta-Analysis, Integrated Data Mining, and Network Pharmacology Jo HG, Kim H, Baek E, Lee D, Hwang JH Pharmaceuticals (Basel) 15-Aug-2023
PMCID:PMC10459676
doi:10.3390/ph16081160
PMID:37631075
Effects of genus Epimedium in the treatment of osteoarthritis and relevant signaling pathways Tong X, Wang Y, Dong B, Li Y, Lang S, Ma J, Ma X Chin Med 31-Jul-2023
PMCID:PMC10388486
doi:10.1186/s13020-023-00788-8
PMID:37525296
Combination of BFHY with Cisplatin Relieved Chemotherapy Toxicity and Altered Gut Microbiota in Mice Feng Y, Jiang Y, Zhou Y, Li ZH, Yang QQ, Mo JF, Wen YY, Shen LP Int J Genomics 19-May-2023
PMCID:PMC10219777
doi:10.1155/2023/3568416
PMID:37252635
Traditional Chinese medicine for heart failure with preserved ejection fraction: clinical evidence and potential mechanisms Fan Y, Yang Z, Wang L, Liu Y, Song Y, Liu Y, Wang X, Zhao Z, Mao J Front Pharmacol 10-May-2023
PMCID:PMC10206212
doi:10.3389/fphar.2023.1154167
PMID:37234711
DUS evaluation of nine intersubgeneric hybrids of Paeonia lactiflora and fingerprint analysis of the chemical components in the roots Xu S, Liu W, Liu X, Qin C, He L, Wang P, Kong L, Chen X, Liu Z, Ma W Front Chem 10-Mar-2023
PMCID:PMC10038168
doi:10.3389/fchem.2023.1158727
PMID:36970400
Electrochemical Characterization of the Antioxidant Properties of Medicinal Plants and Products: A Review Ziyatdinova G, Kalmykova A Molecules 02-Mar-2023
PMCID:PMC10004803
doi:10.3390/molecules28052308
PMID:36903553
Bu-Fei-Huo-Xue capsule alleviates bleomycin-induced pulmonary fibrosis in mice through modulating gut microbiota Hu H, Wang F, Han P, Li P, Wang K, Song H, Zhao G, Li Y, Lu X, Tao W, Cui H Front Pharmacol 08-Feb-2023
PMCID:PMC9944029
doi:10.3389/fphar.2023.1084617
PMID:36843927
Responses of photosystem to long-term light stress in a typically shade-tolerant species Panax notoginseng Cun Z, Xu XZ, Zhang JY, Shuang SP, Wu HM, An TX, Chen JW Front Plant Sci 12-Jan-2023
PMCID:PMC9878349
doi:10.3389/fpls.2022.1095726
PMID:36714733
Clinical efficacy of Bupleurum inula flower soup for immune damage intervention in Hashimoto’s thyroiditis: A placebo-controlled randomized trial Meng X, Liu S, Deng X, Li X, Lei J, Jiang H, Liu M, Zhang N, Liu S Front Pharmacol 24-Nov-2022
PMCID:PMC9730284
doi:10.3389/fphar.2022.1049618
PMID:36506504
Application of herbal traditional Chinese medicine in the treatment of lupus nephritis Liu L, Zhang L, Li M Front Pharmacol 24-Nov-2022
PMCID:PMC9729561
doi:10.3389/fphar.2022.981063
PMID:36506523
Rapid Identification of Paeoniae Radix and Moutan Radicis Cortex Using a SCAR Marker-Based Conventional PCR Assay Kim WJ, Noh S, Choi G, Moon BC Plants (Basel) 27-Oct-2022
PMCID:PMC9653921
doi:10.3390/plants11212870
PMID:36365322
Systematic review and meta-analysis of Coptis chinensis Franch.-containing traditional Chinese medicine as an adjunct therapy to metformin in the treatment of type 2 diabetes mellitus Pan L, Zhai X, Duan Z, Xu K, Liu G Front Pharmacol 08-Sep-2022
PMCID:PMC9492976
doi:10.3389/fphar.2022.956313
PMID:36160405

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
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1007/BF00629664
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Methyl benzoate 7150 Click to see COC(=O)C1=CC=CC=C1 136.15 unknown https://doi.org/10.1007/BF00629664
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate 4133 Click to see COC(=O)C1=CC=CC=C1O 152.15 unknown https://doi.org/10.1007/BF00629664
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown https://doi.org/10.1007/BF00629791
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1007/BF00629791
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown https://doi.org/10.1007/BF00629791
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1007/BF00629664
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
phenyl 2-[6,7-dihydroxy-5-(hydroxymethyl)-6'-methyl-4'-oxospiro[5,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-b]pyran-2,9'-7-oxatricyclo[4.2.1.03,8]nonane]-1'-yl]acetate 162912413 Click to see CC12CC(=O)C3CC(C3O1)(C24OC5C(C(C(OC5O4)CO)O)O)CC(=O)OC6=CC=CC=C6 462.40 unknown https://doi.org/10.1016/0031-9422(90)85347-I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1007/BF00629664
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1S,2R,3S,5S,6S,8R)-6-hydroxy-8-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-2-yl]methyl benzoate 12313907 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC=CC=C5)OC6C(C(C(C(O6)CO)O)O)O)O 480.50 unknown https://doi.org/10.1007/BF00629791
Paeoniflorin 425990 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC=CC=C5)OC6C(C(C(C(O6)CO)O)O)O)O 480.50 unknown https://doi.org/10.1007/BF00629791
Peoniflorin 442534 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC=CC=C5)OC6C(C(C(C(O6)CO)O)O)O)O 480.50 unknown https://doi.org/10.1007/BF00629791
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-12-methyl-14-oxo-2,7,9,13-tetraoxapentacyclo[8.7.0.01,15.03,8.012,16]heptadecan-15-yl]methyl benzoate 5318917 Click to see CC12CC3C4(CC1C4(C(=O)O2)COC(=O)C5=CC=CC=C5)OC6C(C(C(OC6O3)CO)O)O 462.40 unknown https://doi.org/10.1016/0031-9422(90)85347-I
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00629791
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00629791
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00629791
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-[6-O-(alpha-L-Arabinopyranosyl)-beta-D-glucopyranosyloxy]benzoic acid methyl ester 21770576 Click to see COC(=O)C1=CC=CC=C1OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1007/BF00629791
Methyl 2-[(6-o-pentopyranosylhexopyranosyl)oxy]benzoate 10278 Click to see COC(=O)C1=CC=CC=C1OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1007/BF00629791
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1007/BF00629664

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