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Habropetalum dawei

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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 UUID64405404716fe043922108
Scientific name Habropetalum dawei
Authority (Huchinson & Dalziel) Airy Shaw
First published in Kew Bull. 6: 336 (1951 publ. 1952)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Japanese ハブロペタルム・ダウェイ
Chinese 道氏盾籽藤
Chinese 盾籽藤属
Chinese 盾籽藤屬

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001224122
Tropicos 50040753
KEW urn:lsid:ipni.org:names:317594-1
The Plant List tro-50040753
Open Tree Of Life 596668
NCBI Taxonomy 122300
IPNI 317594-1
iNaturalist 317894
GBIF 4161359
EOL 6875221
CMAUP NPO15515

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
The potential of anti-malarial compounds derived from African medicinal plants, part I: a pharmacological evaluation of alkaloids and terpenoids Amoa Onguéné P, Ntie-Kang F, Lifongo LL, Ndom JC, Sippl W, Mbaze LM Malar J 13-Dec-2013
PMCID:PMC3878730
doi:10.1186/1475-2875-12-449
PMID:24330395
HPLC−CD On-Line Coupling in Combination with HPLC−NMR and HPLC−MS/MS for the Determination of the Full Absolute Stereostructure of New Metabolites in Plant Extracts Gerhard Bringmann, Kim Messer, Michael Wohlfarth, Jürgen Kraus, Karifala Dumbuya, Markus Rückert American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/AC990001D
(+)-Isoshinanolone and 2-methylbenzofuran-4-carbaldehyde from the fish-stunning plant Habropetalum dawei Steven W. Hanson, Malcolm Crawford, Devavaram P.J. Thanasingh Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)83057-9

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 / Tetralins
(3S,4S)-4,8-dihydroxy-3-methyl-tetralin-1-one 46888858 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1016/0031-9422(81)83057-9
4,8-dihydroxy-3-methyl-3,4-dihydro-2H-naphthalen-1-one 71329296 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1016/0031-9422(81)83057-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1S,2S,6R,7S,8R,12R,14S,15S,19S,20R)-7,10-dihydroxy-17-methoxy-7,15,19,20-tetramethyl-3,5,11-trioxapentacyclo[10.7.1.02,6.08,20.014,19]icos-16-en-18-one 101921953 Click to see CC1C=C(C(=O)C2(C1CC3C4(C2C5C(C(C4CC(O3)O)(C)O)OCO5)C)C)OC 408.50 unknown https://doi.org/10.1021/AC990001D
> Organoheterocyclic compounds / Benzofurans
2-Methylbenzofuran-4-carbaldehyde 13170313 Click to see CC1=CC2=C(C=CC=C2O1)C=O 160.17 unknown https://doi.org/10.1016/0031-9422(81)83057-9
> Organoheterocyclic compounds / Isoquinolines and derivatives / Naphthylisoquinolines
(1R,3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,2,3-trimethyl-3,4-dihydro-1H-isoquinolin-8-ol 14844756 Click to see CC1CC2=C(C(N1C)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 391.50 unknown https://doi.org/10.1021/AC990001D
(3R)-7-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 375943 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1021/AC990001D
(3R)-7-[5-hydroxy-2-(hydroxymethyl)-4-methoxynaphthalen-1-yl]-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-8-ol 375947 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)O)O 379.40 unknown https://doi.org/10.1021/AC990001D
Dioncopeltine A 185971 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3CO)OC)O)O 379.40 unknown https://doi.org/10.1021/AC990001D
Dioncophylline A 443773 Click to see CC1CC2=C(C(N1)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 377.50 unknown https://doi.org/10.1021/AC990001D
N-Methyldioncophyllin a 633164 Click to see CC1CC2=C(C(N1C)C)C(=C(C=C2)C3=C4C=CC=C(C4=C(C=C3C)OC)OC)O 391.50 unknown https://doi.org/10.1021/AC990001D
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)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)O)O 610.50 unknown via CMAUP database
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database

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