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Potentilla longifolia

Potentilla longifolia - 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 UUID644040532835e353709253
Scientific name Potentilla longifolia
Authority D.F.K.Schltdl.
First published in Mag. Neuesten Entdeck. Gesammten Naturk. Ges. Naturf. Freunde Berlin 7: 287 (1816)

Description Top

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Synonyms Top

Scientific name Authority First published in
Potentilla viscosa Donn ex Lehm. Monographia generis Potentillarum ; 1820 57 1820
Potentilla viscosa var. macrophylla Kom. ; 1904 501 1904
Drymocallis viscosa Rydb. N. Amer. Fl. 22: 372 (1908)
Potentilla hispida Nestl. Monogr. Potentilla : 36 (1816)
Potentilla tanacetifolia var. longifolia (Willd. ex Schltdl.) Vorosch. Florist. Issl. Razn. Raionakh SSSR : 177 (1985)

Common names Top

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Language Common/alternative name
Chinese 浮尸草
Chinese 粘委陵菜
Chinese 腺毛委陵菜
Chinese 粘萎陵菜

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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No forms added yet.

Germination/Propagation Top

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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
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
    • Eastern Asia
      • Korea
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
  • Europe
    • Eastern Europe
      • Belarus
      • East European Russia
      • North European Russia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001016002
Tropicos 27804575
KEW urn:lsid:ipni.org:names:728426-1
The Plant List rjp-6600
Open Tree Of Life 809911
Observations.org 132421
NCBI Taxonomy 667264
IPNI 728426-1
iNaturalist 787928
GBIF 5365820
Freebase /m/0wxnt28
EPPO PTLLO
EOL 229513
Elurikkus 653727
USDA GRIN 317731
Wikipedia Potentilla_longifolia

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
Effects of Spring Drought and Nitrogen Addition on Productivity and Community Composition of Degraded Grasslands Li S, Lu S, Li X, Hou X, Zhao X, Xu X, Zhao N Plants (Basel) 31-Jul-2023
PMCID:PMC10421370
doi:10.3390/plants12152836
PMID:37570989
Fecal Microbiota and Diet Composition of Buryatian Horses Grazing Warm- and Cold-Season Grass Pastures Zaitseva S, Dagurova O, Radnagurueva A, Kozlova A, Izotova A, Krylova A, Noskov S, Begmatov S, Patutina E, Barkhutova DD Microorganisms 30-Jul-2023
PMCID:PMC10459317
doi:10.3390/microorganisms11081947
PMID:37630507
A review of the bioactive properties of Mongolian plants, with a focus on their potential as natural food preservatives Burenjargal M, Narangerel T, Batmunkh T, Dong A, Idesh S Food Sci Nutr 05-Jul-2023
PMCID:PMC10563759
doi:10.1002/fsn3.3529
PMID:37823130
Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K In Silico Pharmacol 28-Apr-2023
PMCID:PMC10141836
doi:10.1007/s40203-023-00143-7
PMID:37131867
Impact of Phytochemicals on PPAR Receptors: Implications for Disease Treatments Enayati A, Ghojoghnejad M, Roufogalis BD, Maollem SA, Sahebkar A PPAR Res 31-Aug-2022
PMCID:PMC9453090
doi:10.1155/2022/4714914
PMID:36092543
Enhancing Testing Laboratory Engagement in Plant DNA Barcoding through a Routine Workflow—A Case Study on Chinese Materia Medica (CMM) Ha WY, Wong KL, Ma WY, Lau YY, Chan WH Plants (Basel) 16-May-2022
PMCID:PMC9146924
doi:10.3390/plants11101317
PMID:35631742
Effects of large herbivore grazing on relics of the presumed mammoth steppe in the extreme climate of NE-Siberia Reinecke J, Ashastina K, Kienast F, Troeva E, Wesche K Sci Rep 21-Jun-2021
PMCID:PMC8217226
doi:10.1038/s41598-021-92079-1
PMID:34155242
Inhibitory Effects of Twenty-Nine Compounds From Potentilla longifolia on Lipid Accumulation and Their Mechanisms in 3T3-L1 Cells Ma Q, Ye L, Li W, Lin S, Zhao X, Jin C, Liu G, Liu H, Sun Y, Yuan H, Piao G Front Pharmacol 09-Nov-2020
PMCID:PMC7680851
doi:10.3389/fphar.2020.555715
PMID:33240084
Wild edible plants collected and consumed by the locals in Daqinggou, Inner Mongolia, China Sachula, Geilebagan, Zhang YY, Zhao H, Khasbagan J Ethnobiol Ethnomed 09-Oct-2020
PMCID:PMC7547461
doi:10.1186/s13002-020-00411-2
PMID:33036666
Phenolome of Asian Agrimony Tea (Agrimonia asiatica Juz., Rosaceae): LC-MS Profile, α-Glucosidase Inhibitory Potential and Stability I. Kashchenko N, Olennikov DN Foods 23-Sep-2020
PMCID:PMC7598702
doi:10.3390/foods9101348
PMID:32977706
Inhibitory effects of compounds from the roots of Potentilla longifolia on lipid accumulation Lin S, Zhao X, Sun Y, Liu H, Shang M, Gong J, Ma Q, Piao G, Yuan H PLoS One 09-Sep-2020
PMCID:PMC7480838
doi:10.1371/journal.pone.0238917
PMID:32903285
Medicinal wild plants used by the Mongol herdsmen in Bairin Area of Inner Mongolia and its comparative study between TMM and TCM Wurchaih, Huar, Menggenqiqig, Khasbagan J Ethnobiol Ethnomed 03-Jul-2019
PMCID:PMC6609360
doi:10.1186/s13002-019-0300-9
PMID:31269968
Response of aboveground biomass and diversity to nitrogen addition along a degradation gradient in the Inner Mongolian steppe, China Xu X, Liu H, Song Z, Wang W, Hu G, Qi Z Sci Rep 21-Jul-2015
PMCID:PMC4508527
doi:10.1038/srep10284
PMID:26194184
Potentillanin, a biflavanoid and a procyanidin glycoside from Potentilla viscosa Ben Zhang, Gen-ichiro Nonaka, Itsuo Nishioka Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80042-6

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
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162999814 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)OC7C(C(C(C(O7)CO)O)O)O 740.70 unknown https://doi.org/10.1016/0031-9422(88)80042-6
(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 101683293 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 562.50 unknown https://doi.org/10.1016/0031-9422(88)80042-6
2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 14104296 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)OC7C(C(C(C(O7)CO)O)O)O 740.70 unknown https://doi.org/10.1016/0031-9422(88)80042-6
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 130556 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(88)80042-6
2-(3,4-dihydroxyphenyl)-8-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 5089688 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 562.50 unknown https://doi.org/10.1016/0031-9422(88)80042-6
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(88)80042-6
Procyanidin C2 11182062 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/0031-9422(88)80042-6
Procyanidin trimer T2 13751990 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/0031-9422(88)80042-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(88)80042-6
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/0031-9422(88)80042-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(+)-Catechin-3'-O-beta-D-glucoside 21626705 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 452.40 unknown https://doi.org/10.1016/0031-9422(88)80042-6
Catechin 3'-glucoside 73813317 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 452.40 unknown https://doi.org/10.1016/0031-9422(88)80042-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R,4S,5S,6R)-2-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[2-[(2R,3S)-5,7-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-2-yl]-4,5-dihydroxyphenyl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14104295 Click to see C1C(C(OC2=C1C(=CC(=C2C3=CC(=C(C=C3C4C(CC5=C(C=C(C=C5O4)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC8C(C(C(C(O8)CO)O)O)O 902.80 unknown https://doi.org/10.1016/0031-9422(88)80042-6
2-[[2-(3,4-dihydroxyphenyl)-8-[2-[5,7-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromen-2-yl]-4,5-dihydroxyphenyl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14104294 Click to see C1C(C(OC2=C1C(=CC(=C2C3=CC(=C(C=C3C4C(CC5=C(C=C(C=C5O4)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC8C(C(C(C(O8)CO)O)O)O 902.80 unknown https://doi.org/10.1016/0031-9422(88)80042-6

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