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Clematis parviloba

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644011d982164436573748
Scientific name Clematis parviloba
Authority Gardner & Champ.
First published in Hooker's J. Bot. Kew Gard. Misc. 1: 241 (1849)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Japanese クレマティス・パルヴィローバ
Chinese 川木通
Chinese 裂叶铁线莲

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Clematis parviloba var. bartlettii (Yamam.) W.T.Wang Acta Phytotax. Sin. 38: 405 (2000)
Clematis parviloba var. longianthera W.T.Wang Acta Phytotax. Sin. 36: 156 (1998)
Clematis parviloba var. rhombicoelliptica W.T.Wang Acta Phytotax. Sin. 38: 405 (2000)
Clematis parviloba var. suboblonga W.T.Wang Acta Phytotax. Sin. 38: 405 (2000)

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
    • Eastern Asia
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000610455
Tropicos 27104529
KEW urn:lsid:ipni.org:names:709960-1
The Plant List kew-2726518
Open Tree Of Life 5737758
NCBI Taxonomy 1857144
IPNI 709960-1
GBIF 7277979
EOL 2873604
USDA GRIN 407391

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
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Advances in Chemistry and Bioactivity of Magnoflorine and Magnoflorine-Containing Extracts Okon E, Kukula-Koch W, Jarzab A, Halasa M, Stepulak A, Wawruszak A Int J Mol Sci 16-Feb-2020
PMCID:PMC7072879
doi:10.3390/ijms21041330
PMID:32079131
Aporphine alkaloids from Clematis parviloba and their antifungal activity. Chen JH, Du ZZ, Shen YM, Yang YP Arch Pharm Res 01-Jan-2009
doi:10.1007/S12272-009-1111-7
PMID:19183870

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
> Alkaloids and derivatives / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1007/S12272-009-1111-7
Corytuberine 160500 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC 327.40 unknown https://doi.org/10.1007/S12272-009-1111-7
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://doi.org/10.1007/S12272-009-1111-7
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
4-Hydroxyphenylacetaldehyde 440113 Click to see 136.15 unknown https://doi.org/10.1007/S12272-009-1111-7
> Benzenoids / Benzene and substituted derivatives / Phenylpyruvic acid derivatives
4-Hydroxyphenylpyruvic acid 979 Click to see C1=CC(=CC=C1CC(=O)C(=O)O)O 180.16 unknown https://doi.org/10.1007/S12272-009-1111-7
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
Dopamine 681 Click to see 153.18 unknown https://doi.org/10.1007/S12272-009-1111-7
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(-)-Higenamine 440927 Click to see 271.31 unknown https://doi.org/10.1007/S12272-009-1111-7
(S)-3'-Hydroxy-N-methylcoclaurine 440591 Click to see 315.40 unknown https://doi.org/10.1007/S12272-009-1111-7
(S)-N-Methylcoclaurine 440584 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1007/S12272-009-1111-7
Coclaurine 160487 Click to see 285.34 unknown https://doi.org/10.1007/S12272-009-1111-7
Reticuline 439653 Click to see 329.40 unknown https://doi.org/10.1007/S12272-009-1111-7

Gallery Top

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Contributors Top

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Collections Top

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