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Lettowianthus stellatus

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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 UUID644046b95dfae401301078
Scientific name Lettowianthus stellatus
Authority Diels
First published in Notizbl. Bot. Gart. Berlin-Dahlem 13: 266 (1936)

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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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-0001066193
Tropicos 1601760
KEW urn:lsid:ipni.org:names:73779-1
The Plant List tro-1601760
Open Tree Of Life 6290
NCBI Taxonomy 489335
IUCN Red List 32853
IPNI 73779-1
iNaturalist 143769
GBIF 3158226
EOL 305114
Wikipedia Lettowianthus_stellatus

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
A mega-phylogeny of the Annonaceae: taxonomic placement of five enigmatic genera and support for a new tribe, Phoenicantheae Guo X, Tang CC, Thomas DC, Couvreur TL, Saunders RM Sci Rep 04-Aug-2017
PMCID:PMC5544705
doi:10.1038/s41598-017-07252-2
PMID:28779135
Geranylbenzoquinonoids from Lettowianthus stellatus fruits. Makangara JJ, Nkunya MH, Jonker SS Nat Prod Res 01-May-2010
doi:10.1080/14786410802573693
PMID:20432152
Total Syntheses of Telisatin A, Telisatin B and Lettowianthine Nimgirawath S, Udomputtimekakul P Molecules 26-Feb-2009
PMCID:PMC6253876
doi:10.3390/molecules14030917
PMID:19255550
Aporphinoid alkaloids and other constituents from Lettowianthus stellatus. Nkunya MH, Jonker SA, Makangara JJ, Waibel R, Achenbach H Phytochemistry 01-Apr-2000
doi:10.1016/S0031-9422(00)00012-1
PMID:10820832

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
19-Methoxy-3,5-dioxa-11-azahexacyclo[9.9.2.02,6.08,21.014,22.015,20]docosa-1(21),2(6),7,14(22),15(20),16,18-heptaene-12,13-dione 162940780 Click to see COC1=CC=CC2=C1C3=C4C(=CC5=C3OCO5)CCN6C4=C2C(=O)C6=O 347.30 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
19-Methoxy-3,5-dioxa-11-azahexacyclo[9.9.2.02,6.08,21.014,22.015,20]docosa-1(21),2(6),7,9,14(22),15(20),16,18-octaene-12,13-dione 102369815 Click to see COC1=CC=CC2=C1C3=C4C(=CC5=C3OCO5)C=CN6C4=C2C(=O)C6=O 345.30 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
Lettowianthine 21593830 Click to see C1CN2C3=C(C4=CC=CC=C4C5=C3C1=CC6=C5OCO6)C(=O)C2=O 317.30 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
> Benzenoids / Phenols / Methoxyphenols
3,4,5-Trimethoxyphenol 69505 Click to see COC1=CC(=CC(=C1OC)OC)O 184.19 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z)-7-octedecan-9-ynoic acid 14309405 Click to see CCCCCCCCC#CC=CCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
https://doi.org/10.1080/14786410802573693
13,17-Octadecadiene-9,11-diynoic acid 10355900 Click to see C=CCCC=CC#CC#CCCCCCCCC(=O)O 272.40 unknown https://doi.org/10.1080/14786410802573693
Octadec-7-en-9-ynoic acid 56628602 Click to see CCCCCCCCC#CC=CCCCCCC(=O)O 278.40 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
https://doi.org/10.1080/14786410802573693
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
methyl 2-[(4R,4aS,8aS)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-methyl-4-(3-methylbut-2-enyl)-5,8-dioxo-4,8a-dihydro-1H-naphthalen-4a-yl]acetate 162888201 Click to see CC1=CCC2C(=O)C(=CC(=O)C2(C1CC=C(C)C)CC(=O)OC)CC=C(C)CCC=C(C)C 452.60 unknown https://doi.org/10.1080/14786410802573693
methyl 2-[7-(3,7-dimethylocta-2,6-dienyl)-3-methyl-4-(3-methylbut-2-enyl)-5,8-dioxo-4,8a-dihydro-1H-naphthalen-4a-yl]acetate 162888200 Click to see CC1=CCC2C(=O)C(=CC(=O)C2(C1CC=C(C)C)CC(=O)OC)CC=C(C)CCC=C(C)C 452.60 unknown https://doi.org/10.1080/14786410802573693
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
JH III 5281523 Click to see CC(=CCCC(=CC(=O)OC)C)CCC1C(O1)(C)C 266.38 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
https://doi.org/10.1080/14786410802573693
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones
2-(3,7-Dimethylocta-2,6-dienyl)-6-[7-(3,7-dimethylocta-2,6-dienyl)-5-hydroxy-1-benzofuran-2-yl]cyclohexa-2,5-diene-1,4-dione 162938077 Click to see CC(=CCCC(=CCC1=CC(=O)C=C(C1=O)C2=CC3=CC(=CC(=C3O2)CC=C(C)CCC=C(C)C)O)C)C 512.70 unknown https://doi.org/10.1080/14786410802573693
dimethyl (2S,3R)-2,3-bis[5-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,6-dioxocyclohexa-1,4-dien-1-yl]butanedioate 162914073 Click to see CC(=CCCC(=CCC1=CC(=O)C=C(C1=O)C(C(C2=CC(=O)C=C(C2=O)CC=C(C)CCC=C(C)C)C(=O)OC)C(=O)OC)C)C 630.80 unknown https://doi.org/10.1080/14786410802573693
Dimethyl 2,3-bis[5-(3,7-dimethylocta-2,6-dienyl)-3,6-dioxocyclohexa-1,4-dien-1-yl]butanedioate 162914072 Click to see CC(=CCCC(=CCC1=CC(=O)C=C(C1=O)C(C(C2=CC(=O)C=C(C2=O)CC=C(C)CCC=C(C)C)C(=O)OC)C(=O)OC)C)C 630.80 unknown https://doi.org/10.1080/14786410802573693
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
methyl (2E,6E,10R)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate 71509917 Click to see CC(=CCCC(=CC(=O)OC)C)CCC(C(C)(C)O)O 284.39 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
Methyl 10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoate 390644 Click to see CC(=CCCC(=CC(=O)OC)C)CCC(C(C)(C)O)O 284.39 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
2-(3,8-Dimethyl-1,2,6,7,8,8a-hexahydroazulen-5-yl)propan-2-ol 73094701 Click to see CC1CCC(=CC2=C(CCC12)C)C(C)(C)O 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
2-[(8R,8aS)-3,8-dimethyl-1,2,6,7,8,8a-hexahydroazulen-5-yl]propan-2-ol 51041637 Click to see CC1CCC(=CC2=C(CCC12)C)C(C)(C)O 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
2-[(8S,8aS)-3,8-dimethyl-1,2,6,7,8,8a-hexahydroazulen-5-yl]propan-2-ol 11770005 Click to see CC1CCC(=CC2=C(CCC12)C)C(C)(C)O 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00012-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
7-(3,7-dimethylocta-2,6-dienyl)-5-hydroxy-3H-1-benzofuran-2-one 91411536 Click to see CC(=CCCC(=CCC1=CC(=CC2=C1OC(=O)C2)O)C)C 286.40 unknown https://doi.org/10.1080/14786410802573693
Lettowienolide 102025309 Click to see CC(=CCCC(=CCC1=CC(=CC2=C1OC(=O)C2)O)C)C 286.40 unknown https://doi.org/10.1080/14786410802573693
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
methyl 2-[(2R)-6-hydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]acetate 162940293 Click to see CC(=CCCC1(C=CC2=C(O1)C(=CC(=C2)O)CC(=O)OC)C)C 316.40 unknown https://doi.org/10.1080/14786410802573693
Methyl 2-[6-hydroxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]acetate 90735326 Click to see CC(=CCCC1(C=CC2=C(O1)C(=CC(=C2)O)CC(=O)OC)C)C 316.40 unknown https://doi.org/10.1080/14786410802573693
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 5-O-methylated isoflavonoids
(3S)-7-hydroxy-3-(4-hydroxy-2-methoxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one 162925665 Click to see COC1=CC(=CC2=C1C(=O)C(CO2)C3=C(C=C(C=C3)O)OC)O 316.30 unknown https://doi.org/10.1080/14786410802573693
https://doi.org/10.1016/S0031-9422(00)00012-1

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