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Lethedon tannensis

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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 UUID6440584a369b7264498893
Scientific name Lethedon tannensis
Authority Biehler
First published in Pl. Nov. Herb. Spreng. : 40 (1807)

Description Top

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Synonyms Top

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Common names Top

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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-0001268523
Tropicos 50232932
KEW urn:lsid:ipni.org:names:465242-1
The Plant List tro-50232932
Open Tree Of Life 6119544
IPNI 465242-1
GBIF 3569368

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)!
Title Authors Publication Released IDs
Redox regulation of tumor cell toxicity by flavones from Lethedon tannaensis. Bensasson RV, Jossang A, Zahir A, Bodo B, Land EJ Free Radic Biol Med 01-Jul-1999
doi:10.1016/S0891-5849(99)00039-8
PMID:10443925
Five new flavone 5-O-glycosides from Lethedon tannaensis: lethedosides and lethediosides. Zahir A, Jossang A, Bodo B, Provost J, Cosson JP, Sévenet T J Nat Prod 01-Feb-1999
doi:10.1021/NP980284P
PMID:10075750
DNA topoisomerase I inhibitors: cytotoxic flavones from Lethedon tannaensis. Zahir A, Jossang A, Bodo B, Provost J, Cosson JP, Sévenet T J Nat Prod 01-Jul-1996
doi:10.1021/NP960336F
PMID:8759170

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-(3-hydroxy-4,5-dimethoxyphenyl)-7-methoxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 10391471 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC(=C(C(=C4)OC)OC)O 506.50 unknown https://doi.org/10.1021/NP980284P
2-(3-hydroxy-4,5-dimethoxyphenyl)-7-methoxy-5-[(2S,3R,4S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163194678 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC(=C(C(=C4)OC)OC)O 506.50 unknown https://doi.org/10.1021/NP980284P
2-(3,4-dimethoxyphenyl)-7-methoxy-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162975590 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC)OC 622.60 unknown https://doi.org/10.1021/NP980284P
2-(3,4-dimethoxyphenyl)-7-methoxy-5-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163033217 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)OC)OC 490.50 unknown https://doi.org/10.1021/NP980284P
7-methoxy-5-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-2-(3,4,5-trimethoxyphenyl)chromen-4-one 162907500 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C=C(O2)C5=CC(=C(C(=C5)OC)OC)OC 652.60 unknown https://doi.org/10.1021/NP980284P
Lethedioside A 10394124 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC)OC 622.60 unknown https://doi.org/10.1021/NP980284P
Lethedioside B 44258397 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C=C(O2)C5=CC(=C(C(=C5)OC)OC)OC 652.60 unknown https://doi.org/10.1021/NP980284P
Lethedoside A 10390853 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)OC)OC 490.50 unknown https://doi.org/10.1021/NP980284P
Lethedoside B 11756418 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC(=C(C(=C4)OC)OC)OC 520.50 unknown https://doi.org/10.1021/NP980284P
Lethedoside C 44258394 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC(=C(C(=C4)OC)OC)O 506.50 unknown https://doi.org/10.1021/NP980284P
https://doi.org/10.1016/S0891-5849(99)00039-8
Tricetin 7,3',4',5'-trimethyl eter 5-glucoside 44258395 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C=C(O2)C4=CC(=C(C(=C4)OC)OC)OC 520.50 unknown https://doi.org/10.1021/NP980284P
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3',4',7-trimethoxyflavone 5272653 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown https://doi.org/10.1021/NP960336F
5,4'-Dihydroxy-7,3',5'-trimethoxyflavone 15222911 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3)OC)O)OC)O 344.30 unknown https://doi.org/10.1021/NP960336F
Corymbosin 10970376 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3)OC)OC)OC)O 358.30 unknown https://doi.org/10.1016/S0891-5849(99)00039-8
https://doi.org/10.1021/NP960336F
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1016/S0891-5849(99)00039-8
https://doi.org/10.1021/NP960336F
Lethedocin 5496476 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3)OC)OC)O)O 344.30 unknown https://doi.org/10.1016/S0891-5849(99)00039-8
https://doi.org/10.1021/NP960336F
Velutin 5464381 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1016/S0891-5849(99)00039-8
https://doi.org/10.1021/NP960336F

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