Pyrola renifolia - Unknown
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Internal ID UUID64404d16b4738175602048
Scientific name Pyrola renifolia
Authority Maxim.
First published in Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 190 (1859)

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Synonyms Top

Scientific name Authority First published in
Pyrola soldanellifolia Andres Deutsche Bot. Monatsschr. 22: 18 (1910)

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Language Common/alternative name
Japanese ジンヨウイチヤクソウ
Russian Грушанка почковидная
Chinese 肾叶鹿蹄草

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • 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-0001128992
Tropicos 26800193
KEW urn:lsid:ipni.org:names:331840-1
The Plant List tro-26800193
Open Tree Of Life 755291
Observations.org 141099
NCBI Taxonomy 642537
IPNI 331840-1
GBIF 4170383
EPPO PYWRE
EOL 2891107
Elurikkus 479253
USDA GRIN 30424

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Structure of renifolin and reconfirmation of the structure of pirolatin Hiroyuki Inouye, Kenichiro Inoue Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82573-X
[ON THE CONSTITUENTS OF PYROLACEAE. XI. THE CONSTITUENTS OF PYROLA REINFOLIA MAXIM.(1)]. INOUYE H, ARAI T Chem Pharm Bull (Tokyo) 01-Jan-1970
doi:10.1248/CPB.12.533
PMID:14192413

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 / Naphthalenes / Naphthoquinones
Chimaphilin 101211 Click to see CC1=CC2=C(C=C1)C(=O)C=C(C2=O)C 186.21 unknown https://doi.org/10.1248/CPB.12.533
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,7S,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid 154497023 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1248/CPB.12.533
Monotropein 73466 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1248/CPB.12.533
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3R,4S,5S,6R)-2-[(4-hydroxy-2,7-dimethyl-5,8-dihydronaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162955592 Click to see CC1=CCC2=C(C=C(C(=C2C1)OC3C(C(C(C(O3)CO)O)O)O)C)O 352.40 unknown https://doi.org/10.1248/CPB.12.533
(2R,3R,4S,5S,6R)-2-[(4-hydroxy-3,6-dimethyl-5,8-dihydronaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162871425 Click to see CC1=CCC2=C(C=C(C(=C2C1)O)C)OC3C(C(C(C(O3)CO)O)O)O 352.40 unknown https://doi.org/10.1248/CPB.12.533
(2S,3R,4S,5S,6R)-2-[(4-hydroxy-2,7-dimethyl-5,8-dihydronaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 90471769 Click to see CC1=CCC2=C(C=C(C(=C2C1)OC3C(C(C(C(O3)CO)O)O)O)C)O 352.40 unknown https://doi.org/10.1016/S0031-9422(00)82573-X
(2S,3R,4S,5S,6R)-2-[(4-hydroxy-3,6-dimethyl-5,8-dihydronaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5320926 Click to see CC1=CCC2=C(C=C(C(=C2C1)O)C)OC3C(C(C(C(O3)CO)O)O)O 352.40 unknown https://doi.org/10.1016/S0031-9422(00)82573-X
2-[(4-Hydroxy-3,6-dimethyl-5,8-dihydronaphthalen-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73981720 Click to see CC1=CCC2=C(C=C(C(=C2C1)O)C)OC3C(C(C(C(O3)CO)O)O)O 352.40 unknown https://doi.org/10.1248/CPB.12.533
b-D-Glucopyranoside,5,8-dihydro-4-hydroxy-2,7-dimethyl-1-naphthalenyl 162955591 Click to see CC1=CCC2=C(C=C(C(=C2C1)OC3C(C(C(C(O3)CO)O)O)O)C)O 352.40 unknown https://doi.org/10.1248/CPB.12.533

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