Details Top

Internal ID UUID64400210a8662815500937
Scientific name Paeonia obovata
Authority Maxim.
First published in Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 39 (1859)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Paeonia obovata is cultivated as an ornamental perennial and sold by horticultural nurseries. Plants are marketed as potted perennials or bareroot clumps for garden planting. Propagation material includes seed and division of mature clumps.
- Some commercial growers also offer the species as a source of seed for breeding and conservation programmes.

Properties relevant to use:
- The species is a spring‑blooming herbaceous peony with large (up to 15 cm) white‑to‑pink flowers, a mild fragrance, and attractive foliage that persists through summer. It tolerates partial shade, prefers well‑drained loamy soils, and is hardy to USDA Zone 5, making it suitable for a range of temperate garden settings.
- Its early flowering period (April–May) provides a seasonal accent, while its moderate growth habit (height 60–90 cm) suits mixed perennial borders and woodland edges.

Standards and regulation:
- Cultivar naming follows the International Code of Nomenclature for Cultivated Plants (ICNCP); no cultivar names for Paeonia obovata have been formally registered in the International Register of Ornamental Peony Cultivars.
- Trade of ornamental plants is subject to national phytosanitary regulations (e.g., U.S. Department of Agriculture, European Union Plant Passport). The species is not listed under CITES or any other international trade‑restriction list, and only standard plant health certificates are required for import/export.

Sustainability and sourcing:
- The species is propagated almost exclusively by nursery division and seed; wild‑collected material is not part of the commercial supply chain. This practice reduces pressure on natural populations and aligns with sustainable horticultural production guidelines.
- Paeonia obovata is not currently listed as threatened, and commercial production relies on cultivated material, limiting impact on wild populations.

Synonyms Top

Scientific name Authority First published in
Paeonia obovata var. japonica Makino Bot. Mag. (Tokyo) 12: 302 1898
Paeonia japonica var. pilosa Nakai J. Jap. Bot. 13: 395 1937
Paeonia obovata f. oreogeton (S.Moore) Kitag. Lin. Fl. Manshur. 221 1939
Paeonia obovata var. amurensis Schipcz. Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 2: 44. 1921
Paeonia obovata var. australis Schipcz. Bot. Mater. Gerb. Glavn. Bot. Sada R.S.F.S.R. 2: 44. 1921
Paeonia obovata var. glabra Makino J. Jap. Bot. 5(9): 33. 1928
Paeonia obovata var. alba Saunders Natl. Hort. Mag. 13: 277. 1934

Common names Top

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Language Common/alternative name
Finnish amurinpioni
Japanese ベニバナヤマシャクヤク
Japanese ベニバナヤマシャクヤク(紅花山芍薬)
Japanese ヤマシャクヤク
Korean 산작약
Russian Пион обратнояйцевидный
Russian Пион обратно-овальный
Slovenian japonska potonika
Swedish lackpion
Swedish japansk pion
Vietnamese thảo thược dược
Chinese 赤芍
Chinese 草芍藥
Chinese 野芍药
Chinese 山芍药
Chinese 草芍药

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Paeonia obovata subsp. japonica (Makino) Halda Acta Mus. Richnov., Sect. Nat. 4: 30 (1997)
Paeonia obovata subsp. obovata
Paeonia obovata subsp. willmottiae (Stapf) D.Y.Hong & K.Y.Pan Higher Pl. China 4: 560 (2000)

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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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
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000480650
UNII 6N822K36FD
Tropicos 27100119
KEW urn:lsid:ipni.org:names:711834-1
The Plant List kew-2561046
Missouri Botanical Garden 286084
PFAF Paeonia obovata
Open Tree Of Life 163406
Observations.org 136132
NCBI Taxonomy 40716
IPNI 711834-1
iNaturalist 508429
GBIF 7316524
Freebase /m/03gql6v
EPPO PAOJA
EOL 2873858
USDA GRIN 26328
Wikipedia Paeonia_obovata

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
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
A meta-analysis of the efficacy and safety of the traditional Chinese medicine formula Kaixinsan decoction for depression Li JL, Lin L, Wu MM, Zhang JY, Zhang YX, Cao MR, Wang L Medicine (Baltimore) 05-Jan-2024
PMCID:PMC10766321
doi:10.1097/MD.0000000000036719
PMID:38181245
Network medicine framework reveals generic herb-symptom effectiveness of traditional Chinese medicine Gan X, Shu Z, Wang X, Yan D, Li J, Ofaim S, Albert R, Li X, Liu B, Zhou X, Barabási AL Sci Adv 27-Oct-2023
PMCID:PMC10610911
doi:10.1126/sciadv.adh0215
PMID:37889962
Paeoniflorin in Paeoniaceae: Distribution, influencing factors, and biosynthesis Zhang XX, Zuo JQ, Wang YT, Duan HY, Yuan JH, Hu YH Front Plant Sci 02-Sep-2022
PMCID:PMC9478390
doi:10.3389/fpls.2022.980854
PMID:36119574
Meta-Analysis of Naoxintong Capsule for Patients with Vascular Dementia Li L, Zheng Y, Bao J, Zhao Y, Zhang Q, Li W, Wu M Evid Based Complement Alternat Med 06-Jul-2022
PMCID:PMC9279031
doi:10.1155/2022/5000948
PMID:35845570
Acidic and Alkaline Conditions Affect the Growth of Tree Peony Plants via Altering Photosynthetic Characteristics, Limiting Nutrient Assimilation, and Impairing ROS Balance Aung TT, Shi F, Zhai Y, Xue J, Wang S, Ren X, Zhang X Int J Mol Sci 03-May-2022
PMCID:PMC9099645
doi:10.3390/ijms23095094
PMID:35563483
Operational definition of complementary, alternative, and integrative medicine derived from a systematic search Ng JY, Dhawan T, Dogadova E, Taghi-Zada Z, Vacca A, Wieland LS, Moher D BMC Complement Med Ther 12-Apr-2022
PMCID:PMC9006507
doi:10.1186/s12906-022-03556-7
PMID:35413882
Elucidating the Synergistic Effect of Multiple Chinese Herbal Prescriptions in the Treatment of Post-stroke Neurological Damage Xu A, Wen ZH, Su SX, Chen YP, Liu WC, Guo SQ, Li XF, Zhang X, Li R, Xu NB, Wang KX, Li WX, Guan DG, Duan CZ Front Pharmacol 09-Mar-2022
PMCID:PMC8959705
doi:10.3389/fphar.2022.784242
PMID:35355727
Pharmacodynamic Evaluation of the Gexia Zhuyu Decoction in the Treatment of NAFLD and the Molecular Mechanism Underlying the TRPM4 Pathway Regulation Zhao YW, Yang J, Niu J, Wang T, Liang XD, Ren Y, Wang R Evid Based Complement Alternat Med 30-Nov-2021
PMCID:PMC8651363
doi:10.1155/2021/3364579
PMID:34887931
Molecular Basis of Prostate Cancer and Natural Products as Potential Chemotherapeutic and Chemopreventive Agents Bai B, Chen Q, Jing R, He X, Wang H, Ban Y, Ye Q, Xu W, Zheng C Front Pharmacol 23-Sep-2021
PMCID:PMC8495205
doi:10.3389/fphar.2021.738235
PMID:34630112
Simiao Qingwen Baidu decoction inhibits Epstein–Barr virus-induced B lymphoproliferative disease and lytic viral replication Yang X, Liu L, Zhang H, Sun X, Yan Y, Ran R Pharm Biol 22-Jun-2021
PMCID:PMC8221142
doi:10.1080/13880209.2021.1934038
PMID:34155950
Comparative analysis of plastomes in Oxalidaceae: Phylogenetic relationships and potential molecular markers Li X, Zhao Y, Tu X, Li C, Zhu Y, Zhong H, Liu ZJ, Wu S, Zhai J Plant Divers 04-May-2021
PMCID:PMC8390927
doi:10.1016/j.pld.2021.04.004
PMID:34485770
Tongqiaohuoxue Hinders Development and Progression of Atherosclerosis: A Possible Role in Alzheimer’s Disease Ha E, Kim M, Chun J, Seo CS, Ahn Y, Jung J Biology (Basel) 27-Oct-2020
PMCID:PMC7692730
doi:10.3390/biology9110363
PMID:33121058
Potential Benefits of Acupuncture and Herbs for Obesity-Related Chronic Inflammation by Adipokines Kim JY, Baek SE, Ginting RP, Lee MW, Yoo JE Evid Based Complement Alternat Med 09-Oct-2020
PMCID:PMC7568779
doi:10.1155/2020/3285363
PMID:33133214
Plant Extracts as Possible Agents for Sequela of Cancer Therapies and Cachexia Lee J, Jeong MI, Kim HR, Park H, Moon WK, Kim B Antioxidants (Basel) 07-Sep-2020
PMCID:PMC7555300
doi:10.3390/antiox9090836
PMID:32906727

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 / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown https://doi.org/10.1248/CPB.48.201
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1248/CPB.48.201
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1248/CPB.48.201
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1248/CPB.48.201
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
1'-O-Galloylsucrose 14055559 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 494.40 unknown https://doi.org/10.1248/CPB.48.201
CID 14055547 14055547 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(O2)(CO)OC3C(C(C(C(O3)CO)O)O)O)O)O 494.40 unknown https://doi.org/10.1248/CPB.48.201
galloyl(-6)Hex(?1-2?)Hex2ulof 14055557 Click to see 494.40 unknown https://doi.org/10.1248/CPB.48.201
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1248/CPB.48.201
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Galloyloxypaeoniflorin 3036133 Click to see 648.60 unknown https://doi.org/10.1248/CPB.48.201
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1S,2S,3R,5S,6R,8S)-6-hydroxy-8-methyl-3-[(2R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-2-yl]methyl 4-hydroxybenzoate 137704782 Click to see 496.50 unknown https://doi.org/10.1248/CPB.48.201
[6-[[(1R,2S,3R,5S,6R,8S)-2-(benzoyloxymethyl)-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 138113865 Click to see 632.60 unknown https://doi.org/10.1248/CPB.48.201
[6-[[(1S,2S,3R,5R,6R,8S)-2-(benzoyloxymethyl)-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.02,5.03,8]decan-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl benzoate 137704709 Click to see 584.60 unknown https://doi.org/10.1248/CPB.48.201
CID 429559 429559 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC=C(C=C5)O)OC6C(C(C(C(O6)CO)O)O)O)O 496.50 unknown https://doi.org/10.1016/J.JPBA.2014.06.027
Moudanpioside F 21631108 Click to see 344.36 unknown https://doi.org/10.1248/CPB.48.201
Paeoniflorin 442534 Click to see 480.50 unknown https://doi.org/10.1248/CPB.48.201
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown https://doi.org/10.1248/CPB.48.201
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 1'-benzoate 10225582 Click to see C1=CC=C(C=C1)C(=O)OCC2(C(C(C(O2)CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 446.40 unknown https://doi.org/10.1248/CPB.48.201
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Proanthocyanidin 108065 Click to see 592.50 unknown https://doi.org/10.1248/CPB.48.201
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1248/CPB.48.201
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1248/CPB.48.201
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1248/CPB.48.201
(+)-Catechin 3-Gallate 5276454 Click to see 442.40 unknown https://doi.org/10.1248/CPB.48.201
Catechin 7-O-gallate 471393 Click to see 442.40 unknown https://doi.org/10.1248/CPB.48.201
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Catechin 5-O-beta-D-glucopyranoside 44257081 Click to see 452.40 unknown https://doi.org/10.1248/CPB.48.201
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Catechin-7-O-glucoside 44257085 Click to see C1C(C(OC2=CC(=CC(=C21)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown https://doi.org/10.1248/CPB.48.201
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,13R,14R,15S)-3,4,5,11,20,21,22-heptahydroxy-13-(hydroxymethyl)-8,17-dioxo-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-14-yl] 3,4,5-trihydroxybenzoate 14057219 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C3C2OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)O)CO 634.50 unknown https://doi.org/10.1248/CPB.48.201
Casuariin 14035442 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1248/CPB.48.201
Eugeniin 442679 Click to see 938.70 unknown https://doi.org/10.1248/CPB.48.201
Mudanpioside E 86278277 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC(=C(C=C5)O)OC)OC6C(C(C(C(O6)CO)O)O)O)O 526.50 unknown https://doi.org/10.1248/CPB.48.201
Pedunculagin 442688 Click to see 784.50 unknown https://doi.org/10.1248/CPB.48.201

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