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Sarcopyramis bodinieri

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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 UUID64404939cb5c0980790444
Scientific name Sarcopyramis bodinieri
Authority H.Lév.
First published in Mém. Soc. Sci. Nat. Math. Cherbourg 35: 397 (1906)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sarcopyramis bodinieri var. delicata (C.B.Rob.) C.Chen Bull. Bot. Res., Harbin 4(3): 63 (1984)
Sarcopyramis napalensis var. bodinieri (H.Lév. & Vaniot) H.Lév. Fl. Kouy-Tchéou 278 1914
Sarcopyramis delicata C.B.Rob. Bull. Torrey Bot. Club 1908, xxxv. 72.
Sarcopyramis crenata H.L.Li J. Arnold Arbor. xxv. 26 (1944).
Sarcopyramis parvifolia Merr. ex H.L.Li J. Arnold Arbor. xxv. 26 (1944)
Sarcopyramis napalensis var. delicata (C.B.Rob.) S.F.Huang & T.C.Huang Taiwania 36(2): 134 (1991): (1991)

Common names Top

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Language Common/alternative name
Chinese 肉穗草
Chinese 肉穗野牡丹
Chinese 东方肉穗草
Chinese 小肉穗草

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001083364
Tropicos 20305308
KEW urn:lsid:ipni.org:names:575629-1
The Plant List tro-20305308
Open Tree Of Life 7057904
NCBI Taxonomy 2293687
IPNI 575629-1
iNaturalist 737197
GBIF 3859693
EOL 2890354

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
Sephadex® LH-20, Isolation, and Purification of Flavonoids from Plant Species: A Comprehensive Review Mottaghipisheh J, Iriti M Molecules 10-Sep-2020
PMCID:PMC7570886
doi:10.3390/molecules25184146
PMID:32927822
Two new flavonol glycosides from Sarcopyramis bodinieri var. delicate. Wang XM, Wan CP, Zhou SR, Qiu Y Molecules 19-Jun-2008
PMCID:PMC6245408
doi:10.3390/MOLECULES13061399
PMID:18596665
Two New Flavonol Glycosides from Sarcopyramis bodinieri var. delicate Wang XM, Wan CP, Zhou SR, Qiu Y Molecules 19-Jun-2008
PMCID:PMC6245408
doi:10.3390/molecules13061399
PMID:18596665

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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162990408 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O 654.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 72992711 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O 610.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
[6-[5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162990405 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O 654.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
[6-[5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 74977622 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O 624.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
Helichrysoside 5317991 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O 610.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
isorhamnetin 3-O-(6"-O-feruloyl)-glucoside 90657785 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O 654.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
isorhamnetin 3-O-(6"-O-p-coumaroyl)-glucoside 44429737 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O 624.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[6-[5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 74977619 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O 520.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
4',5,7-Trihydroxy-3'-methoxy-3-(6-O-acetyl-beta-D-glucopyranosyloxy)flavone 44429735 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O 520.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
Quercetin 3-O-(6''-acetyl-glucoside) 10006384 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 506.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/
Quercetin-3-O-glucosyl-6''-acetate 15596585 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 506.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245408/

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