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Heracleum rapula

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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 UUID64404722348f8637937551
Scientific name Heracleum rapula
Authority Franch.
First published in Bull. Annuel Soc. Philom. Paris , sér. 8, 6: 145 (1894)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 白云花
Chinese 白云花根
Chinese 鹤庆独活（白云花）
Chinese 鹤庆独活

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001069147
Tropicos 1704359
KEW urn:lsid:ipni.org:names:843153-1
The Plant List tro-1704359
Open Tree Of Life 859499
NCBI Taxonomy 692011
IPNI 843153-1
GBIF 3628491
EOL 2890718

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
Apiaceae Medicinal Plants in China: A Review of Traditional Uses, Phytochemistry, Bolting and Flowering (BF), and BF Control Methods Li M, Li M, Wang L, Li M, Wei J Molecules 27-May-2023
PMCID:PMC10254214
doi:10.3390/molecules28114384
PMID:37298861
Health Benefits and Pharmacological Properties of Stigmasterol Bakrim S, Benkhaira N, Bourais I, Benali T, Lee LH, El Omari N, Sheikh RA, Goh KW, Ming LC, Bouyahya A Antioxidants (Basel) 27-Sep-2022
PMCID:PMC9598710
doi:10.3390/antiox11101912
PMID:36290632
Phytochemicals With Anti 5-alpha-reductase Activity: A Prospective For Prostate Cancer Treatment Azizi A, Mumin NH, Shafqat N F1000Res 06-Jul-2021
PMCID:PMC8276191
doi:10.12688/f1000research.51066.1
PMID:34316358
Harvest, After 50 Years of Sowing Puno PT Nat Prod Bioprospect 19-Jul-2018
PMCID:PMC6102177
doi:10.1007/s13659-018-0182-x
PMID:30027529
Constituents from the roots of Heracleum rapula Franch. Niu XM, Li SH, Jiang B, Zhao QS, Sun HD J Asian Nat Prod Res 01-Mar-2002
doi:10.1080/10286020290019677
PMID:11991190

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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown https://doi.org/10.1080/10286020290019677
> Phenylpropanoids and polyketides / Coumarins and derivatives
6-Formyl-7-methoxycoumarin 160756 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)C=O 204.18 unknown https://doi.org/10.1080/10286020290019677
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Isobergapten 68082 Click to see COC1=C2C=CC(=O)OC2=C3C=COC3=C1 216.19 unknown https://doi.org/10.1080/10286020290019677
Moellendorffiline 128785 Click to see COC1=C(C2=C(C=CO2)C3=C1C4C5C(C4C(=O)O3)C(=O)OC6=C5C(=C(C7=C6C=CO7)OC)OC)OC 492.40 unknown https://doi.org/10.1080/10286020290019677
Pimpinellin 4825 Click to see COC1=C(C2=C(C=CO2)C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1080/10286020290019677
Sphondin 108104 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)C=CO2 216.19 unknown https://doi.org/10.1080/10286020290019677
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
9-(2,3-Dihydroxy-3-methylbutoxy)furo[3,2-g]chromen-7-one 328236 Click to see CC(C)(C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O)O 304.29 unknown https://doi.org/10.1080/10286020290019677
9-[[(2S)-3,3-dimethyloxiran-2-yl]methoxy]furo[3,2-g]chromen-7-one 17897 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1080/10286020290019677
Heraclenin 458010 Click to see CC1(C(O1)COC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 286.28 unknown https://doi.org/10.1080/10286020290019677
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1080/10286020290019677
rivulobirin A 10030966 Click to see CC(=C)C(COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)OC(C)(C)C(COC4=C5C(=CC6=C4OC=C6)C=CC(=O)O5)O 572.60 unknown https://doi.org/10.1080/10286020290019677
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1080/10286020290019677
Rivulobirin B 91885013 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC4=C5C=COC5=C(C6=C4C=CC(=O)O6)O 432.30 unknown https://doi.org/10.1080/10286020290019677
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown https://doi.org/10.1080/10286020290019677

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