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Paeonia tenuifolia

Paeonia tenuifolia - 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 UUID6440020f292b4228014918
Scientific name Paeonia tenuifolia
Authority L.
First published in Syst. Nat. ed. 10 , 2: 1079 (1759)

Description Top

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Synonyms Top

Scientific name Authority First published in
Paeonia hybrida Pall. Fl. Ross. 1(2): 94 (1789)
Paeonia laciniata Pall. Fl. Ross. 1(2): 93 (1788)
Paeonia lithophila Kotov Bot. Zurn. (Kiev) 13(3): 49 (1956)
Paeonia biebersteiniana Rupr. Fl. Caucasi : 47 (1869)
Paeonia carthalinica Ketzch. Zametki Sist. Geogr. Rast. 21: 18 (1959)
Paeonia tenuifolia subsp. biebersteiniana (Rupr.) Halda Acta Mus. Richnov., Sect. Nat. 4(2): 29 (1997):.
Paeonia multifida Gueldenst. Reis. Russland 2: 19 (1791)
Paeonia tenuifolia var. biebersteiniana (Rupr.) N.Busch Mat. Fl. Kavk. 3(3): 9, 224 1901
Paeonia tenuifolia var. laciniata Salm-Dyck Hort. Dyck. 371. 1834
Paeonia tenuifolia var. latisecta Neilr. Aufz. Ungarn Slavon. Gefässpfl. Nachtr.: 70. 1870
Paeonia tenuifolia f. latisecta (Neilr.) Borza Consp. Fl. Roman. 1: 94 1947
Paeonia tenuifolia var. parviflora Huth Bot. Jahrb. Syst. 14: 271. 1891
Paeonia tenuifolia f. parviflora (Huth) Borza Consp. Fl. Roman. 1: 94 1947
Paeonia tenuifolia var. hybrida (Pall.) Lipsky Trudy Tiflissk. Bot. Sada 4: 235. 1899
Paeonia tenuifolia f. brevifolia (Prodán & Borza) Borza Consp. Fl. Roman. 1: 94 1947
Paeonia tenuifolia f. latifolia (Prodán & Borza) Borza Consp. Fl. Roman. 1: 94 1947
Paeonia tenuifolia var. brevifolia Prodán & Borza Bul. Acad. Stud. Agron. Cluj ser. 5, 1: 278. 1935
Paeonia tenuifolia var. latifolia Prodán & Borza Bul. Acad. Stud. Agron. Cluj ser. 5, 1: 278. 1935

Common names Top

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Language Common/alternative name
Azerbaijani nazikyarpaq pion
Bulgarian теснолистен божур
Bulgarian теснолист божур
Persian گل صدتومانی رومانیایی
Finnish tillipioni
Hungarian keleti bazsarózsa
Armenian Քաջվարդ նեղատերև
Norwegian Bokmål trådpeon
Romanian bujor de stepă
Russian Пион тонколистный
Russian Пион узколистный
Russian Воронец
Serbian Степски божур
Swedish dillpion
Ukrainian Півонія вузьколиста
Ukrainian Півонія тонколиста
Chinese 细叶芍药

Subspecies (abbr. subsp./ssp.) Top

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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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Start at 4°C for 3 months, then warm to 20°C for another 3 months.
unlike other peonies, doesn't need a warm period first; radicle appears after cold/moist stratification.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Siberia
      • Altay
  • Europe
    • Eastern Europe
      • East European Russia
      • Krym
      • South European Russia
    • Southeastern Europe
      • Bulgaria
      • Romania
      • Yugoslavia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000480574
Tropicos 27100124
KEW urn:lsid:ipni.org:names:711880-1
The Plant List kew-2560967
Plantarium 26671
Missouri Botanical Garden 286087
Open Tree Of Life 747773
Observations.org 147378
NCBI Taxonomy 13626
NBN Atlas NBNSYS0000163773
IPNI 711880-1
iNaturalist 520910
GBIF 7316533
Freebase /m/0b74sn4
EPPO PAOTE
EOL 2879979
Elurikkus 216069
USDA GRIN 26333
Wikipedia Paeonia_tenuifolia

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
Phytochemical, In Vitro, In Vivo, and In Silico Research on the Extract of Ajuga chamaepitys (L.) Schreb. Ionus E, Schröder V, Chiţescu CL, Bucur LA, Lupu CE, Dumitrescu DE, Popescu L, Mihai DP, Olaru OT, Nițulescu GM, Boscencu R, Gîrd CE Plants (Basel) 25-Apr-2024
PMCID:PMC11085171
doi:10.3390/plants13091192
PMID:38732407
Phytochemical Analysis, Biological Activities, and Molecular Docking Studies of Root Extracts from Paeonia Species in Serbia Batinić P, Jovanović A, Stojković D, Zengin G, Cvijetić I, Gašić U, Čutović N, Pešić MB, Milinčić DD, Carević T, Marinković A, Bugarski B, Marković T Pharmaceuticals (Basel) 17-Apr-2024
PMCID:PMC11054981
doi:10.3390/ph17040518
PMID:38675478
Metal Nanoparticles: Advanced and Promising Technology in Diabetic Wound Therapy Zheng Q, Chen C, Liu Y, Gao J, Li L, Yin C, Yuan X Int J Nanomedicine 26-Jan-2024
PMCID:PMC10826594
doi:10.2147/IJN.S434693
PMID:38293611
Liposomal and Liposomes-Film Systems as Carriers for Bioactives from Paeonia tenuifolia L. Petals: Physicochemical Characterization and Biological Potential Čutović N, Marković T, Carević T, Stojković D, Bugarski B, Jovanović AA Pharmaceutics 07-Dec-2023
PMCID:PMC10747293
doi:10.3390/pharmaceutics15122742
PMID:38140083
Paeonia peregrina Mill Petals as a New Source of Biologically Active Compounds: Chemical Characterization and Skin Regeneration Effects of the Extracts Marković T, Čutović N, Carević T, Gašić U, Stojković D, Xue J, Jovanović A Int J Mol Sci 21-Jul-2023
PMCID:PMC10380736
doi:10.3390/ijms241411764
PMID:37511520
Chemical Profile and Skin-Beneficial Activities of the Petal Extracts of Paeonia tenuifolia L. from Serbia Čutović N, Marković T, Kostić M, Gašić U, Prijić Ž, Ren X, Lukić M, Bugarski B Pharmaceuticals (Basel) 11-Dec-2022
PMCID:PMC9787298
doi:10.3390/ph15121537
PMID:36558988
Phytochemistry, Pharmacology and Molecular Mechanisms of Herbal Bioactive Compounds for Sickness Behaviour Alotaibi GH, Shivanandappa TB, Chinnadhurai M, Reddy Dachani S, Dabeer Ahmad M, Abdullah Aldaajanii K Metabolites 02-Dec-2022
PMCID:PMC9782141
doi:10.3390/metabo12121215
PMID:36557252
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
Phytochemical studies on traditional herbal medicines based on the ethnopharmacological information obtained by field studies Tanaka N, Kashiwada Y J Nat Med 13-Jul-2021
PMCID:PMC8397699
doi:10.1007/s11418-021-01545-7
PMID:34255289
Nanoparticles in the Food Industry and Their Impact on Human Gut Microbiome and Diseases Ghebretatios M, Schaly S, Prakash S Int J Mol Sci 16-Feb-2021
PMCID:PMC7920074
doi:10.3390/ijms22041942
PMID:33669290
Anthocyanins, Vibrant Color Pigments, and Their Role in Skin Cancer Prevention Diaconeasa Z, Știrbu I, Xiao J, Leopold N, Ayvaz Z, Danciu C, Ayvaz H, Stǎnilǎ A, Nistor M, Socaciu C Biomedicines 09-Sep-2020
PMCID:PMC7555344
doi:10.3390/biomedicines8090336
PMID:32916849
Distribution of plastids and mitochondria during male gametophyte formation in Tinantia erecta (Jacq.) Fenzl Marciniec R, Zięba E, Winiarczyk K Protoplasma 09-Mar-2019
PMCID:PMC6579867
doi:10.1007/s00709-019-01363-5
PMID:30852672
Expression of Hepatic Cytochrome P450s in Rats Administered with Guibi-tang, a Traditional Herbal Formula Jin SE, Ha H, Seo CS, Shin HK, Jeong SJ Pharmacogn Mag 31-Jan-2018
PMCID:PMC5822506
doi:10.4103/pm.pm_107_17
PMID:29491639
Chondriokinesis during microsporogenesis in plants Tchórzewska D Planta 08-May-2017
PMCID:PMC5486550
doi:10.1007/s00425-017-2706-8
PMID:28484865
Studies on metabolism of total glucosides of paeony from Paeoniae Radix Alba in rats by UPLC-Q-TOF-MS/MS. Cao W, Wang X, Li H, Shi X, Fan W, Zhao S, Liu M, Niu L Biomed Chromatogr 01-Nov-2015
doi:10.1002/BMC.3493
PMID:26058364

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 acid esters
[(1S,3S,6R,8R)-8-hydroxy-3-methyl-5-oxo-2,9-dioxatricyclo[4.3.1.03,8]decan-10-yl]methyl benzoate 6325770 Click to see CC12CC(=O)C3CC1(OC(C3COC(=O)C4=CC=CC=C4)O2)O 318.32 unknown https://doi.org/10.1515/ZNC-2002-3-406
https://doi.org/10.1080/14756360802667977
[(1S,3S,6R,8S,10R)-8-hydroxy-3-methyl-5-oxo-2,9-dioxatricyclo[4.3.1.03,8]decan-10-yl]methyl benzoate 157288674 Click to see CC12CC(=O)C3CC1(OC(C3COC(=O)C4=CC=CC=C4)O2)O 318.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.016
> 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/10.1016/J.PHYTOCHEM.2008.02.016
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.016
> 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/10.1016/J.PHYTOCHEM.2008.02.016
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1R,3R,4R,6S)-4-hydroxy-4,6-dimethyl-8-oxo-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxatricyclo[4.3.0.03,9]nonan-9-yl]methyl benzoate 11968455 Click to see CC1(CC2(C3(CC1C3(C(=O)O2)COC(=O)C4=CC=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)C)O 494.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.016
[(1S,3S,4R,6R,9R)-4-hydroxy-6-methyl-8-oxo-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxatricyclo[4.3.0.03,9]nonan-9-yl]methyl benzoate 162968326 Click to see CC12CC(C3CC1(C3(C(=O)O2)COC(=O)C4=CC=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O 480.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.016
[(2R,3S,4S,5R,6S)-6-[[(1R,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 3,4,5-trihydroxybenzoate 101604718 Click to see CC12CC3(C4CC1(C4(C(O2)O3)COC(=O)C5=CC=CC=C5)OC6C(C(C(C(O6)COC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)O)O 632.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.016
[4-Hydroxy-6-methyl-8-oxo-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxatricyclo[4.3.0.03,9]nonan-9-yl]methyl benzoate 15558589 Click to see CC12CC(C3CC1(C3(C(=O)O2)COC(=O)C4=CC=CC=C4)OC5C(C(C(C(O5)CO)O)O)O)O 480.50 unknown https://doi.org/10.1002/BMC.3493
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/10.1016/J.PHYTOCHEM.2008.02.016
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(1R,3R,4S,5S,6S,8S,10R,12R,15S,16R)-4,5-dihydroxy-6-(hydroxymethyl)-10-methyl-14-oxo-2,7,9,13-tetraoxapentacyclo[8.7.0.01,15.03,8.012,16]heptadecan-15-yl]methyl benzoate 154496862 Click to see CC12CC3C4CC1(C4(C(=O)O3)COC(=O)C5=CC=CC=C5)OC6C(C(C(OC6O2)CO)O)O 462.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.02.016
[(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/J.PHYTOCHEM.2008.02.016
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
methyl 2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxybenzoate 162987339 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/10.1016/J.PHYTOCHEM.2008.02.016
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxychromen-4-one 162911857 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 670.60 unknown https://doi.org/10.1002/HLCA.19880710207
3-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-methoxychromen-4-one 162996583 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O 640.50 unknown https://doi.org/10.1002/HLCA.19880710207
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-methoxychromen-4-one 14017571 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 670.60 unknown https://doi.org/10.1002/HLCA.19880710207
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-methoxychromen-4-one 14017569 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O 640.50 unknown https://doi.org/10.1002/HLCA.19880710207

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