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Dehaasia hainanensis

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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 UUID644015f8ca119112649055
Scientific name Dehaasia hainanensis
Authority Kosterm.
First published in Bot. Jahrb. Syst. 93: 439 (1973)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Chinese 莲桂

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-0000639224
Tropicos 17805723
KEW urn:lsid:ipni.org:names:464296-1
The Plant List kew-2758915
Open Tree Of Life 374588
NCBI Taxonomy 610223
IPNI 464296-1
GBIF 4179578
EOL 5400575

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 Litsea genome and the evolution of the laurel family Chen YC, Li Z, Zhao YX, Gao M, Wang JY, Liu KW, Wang X, Wu LW, Jiao YL, Xu ZL, He WG, Zhang QY, Liang CK, Hsiao YY, Zhang DY, Lan SR, Huang L, Xu W, Tsai WC, Liu ZJ, Van de Peer Y, Wang YD Nat Commun 03-Apr-2020
PMCID:PMC7125107
doi:10.1038/s41467-020-15493-5
PMID:32245969
Isoquinoline Alkaloids from the Leaves of <i>Dehaasia Hainanensis</i> Chien-Kuang Chen, Su-Chang Chen, Chung-Hsiung Chen, Shoei-Sheng Lee SAGE Publications 25-Mar-2019
doi:10.1177/1934578X0700200115
Alseodaphnopsis: A new genus of Lauraceae based on molecular and morphological evidence Mo YQ, Li L, Li JW, Rohwer JG, Li HW, Li J PLoS One 18-Oct-2017
PMCID:PMC5646853
doi:10.1371/journal.pone.0186545
PMID:29045488

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
(6aS)-1,10-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,11-diol 101289740 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)O)OC)C=C1)O 313.30 unknown https://doi.org/10.1177/1934578X0700200115
1,2,10-Trimethoxy-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolin-9-ol 267400 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown https://doi.org/10.1177/1934578X0700200115
Corydine 10153 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown https://doi.org/10.1177/1934578X0700200115
Laurolitsine 22179 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1177/1934578X0700200115
Nantenine 197001 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)OC 339.40 unknown https://doi.org/10.1177/1934578X0700200115
> Benzenoids / Phenanthrenes and derivatives
Pallidine 12313923 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)O)OC 327.40 unknown https://doi.org/10.1177/1934578X0700200115
Salutaridine 5408233 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC 327.40 unknown https://doi.org/10.1177/1934578X0700200115
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
7-methoxy-1-[(4-methoxyphenyl)methyl]-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 13258331 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)O 313.40 unknown https://doi.org/10.1177/1934578X0700200115
Guattegaumerine 159911 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)O)OC 596.70 unknown https://doi.org/10.1177/1934578X0700200115
O-Methylarmepavine, (R)- 821338 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)OC 327.40 unknown https://doi.org/10.1177/1934578X0700200115
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1177/1934578X0700200115
Reticuline N-oxide 139292178 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC)[O-] 345.40 unknown https://doi.org/10.1177/1934578X0700200115

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Collections Top

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