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Aframomum aulacocarpos

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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 UUID643ff1748e059447270962
Scientific name Aframomum aulacocarpos
Authority Pellegr. ex Koechlin
First published in Fl. Gabon 44

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-0000338043
Tropicos 100447872
KEW urn:lsid:ipni.org:names:871833-1
The Plant List kew-218353
Open Tree Of Life 3946683
Observations.org 373347
IUCN Red List 117205974
IPNI 871833-1
GBIF 2758872
EOL 1127039
Elurikkus 297556
Wikipedia Aframomum_aulacocarpos

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
Aframodial and other bioactive diterpenoids from Aframomum species J. F. Ayafor, M. H. K. Tchuendem, B. Nyasse, F. Tillequin, H. Anke Walter de Gruyter GmbH 23-Oct-2007
doi:10.1351/PAC199466102327
Trypanocidal labdane diterpenoids from the seeds of Aframomum aulacocarpos (Zingiberaceae) Sylvain Valère T. Sob, Pierre Tane, Bonaventure T. Ngadjui, Joseph D. Connolly, Dawei Ma Elsevier BV 07-Jun-2007
doi:10.1016/J.TET.2007.05.120
Five labdane diterpenoids from the seeds of Aframomum zambesiacum. Kenmogne M, Prost E, Harakat D, Jacquier MJ, Frédérich M, Sondengam LB, Zèches M, Waffo-Téguo P Phytochemistry 01-Mar-2006
doi:10.1016/J.PHYTOCHEM.2005.10.015
PMID:16321410
Novel bioactive diterpenoids from Aframomum aulacocarpos. Ayafor JF, Tchuendem MH, Nyasse B, Tillequin F, Anke H J Nat Prod 01-Jul-1994
doi:10.1021/NP50109A007
PMID:7964787

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,3Z)-3-[2-[(1R,2S,4aS,8aS)-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]ethylidene]butane-1,2,4-triol 162951053 Click to see CC1(CCCC2(C1CCC3(C2CC=C(CO)C(CO)O)CO3)C)C 338.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
(E)-4-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-2-[(2R)-oxiran-2-yl]but-2-enal 163007135 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(C=O)C3CO3)C)C 302.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
3-[2-(5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl)ethylidene]butane-1,2,4-triol 73033373 Click to see CC1(CCCC2(C1CCC3(C2CC=C(CO)C(CO)O)CO3)C)C 338.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
4-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-2-(oxiran-2-yl)but-2-enal 78201248 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(C=O)C3CO3)C)C 302.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
8b,17-Epoxy-12E-labdene-15,16-dial 131752056 Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC=O)C=O)CO3)C)C 318.40 unknown https://doi.org/10.1021/NP50109A007
Aulacocarpin B 44559688 Click to see CC1(C(CCC2(C1C(CC3(C2CC=C(C4CO4)C(=O)OC)CO3)O)C)O)C 380.50 unknown https://doi.org/10.1351/PAC199466102327
https://doi.org/10.1021/NP50109A007
Aulacocarpine A 44559687 Click to see CC1(C2CCC3(CO3)C(C2(CCC1O)C)CC=C(C4CO4)C(=O)OC)C 364.50 unknown https://doi.org/10.1021/NP50109A007
https://doi.org/10.1351/PAC199466102327
methyl (E)-4-[(1R,2S,4aR,6S,8aR)-6-hydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]-2-[(2R)-oxiran-2-yl]but-2-enoate 163001087 Click to see CC1(C2CCC3(CO3)C(C2(CCC1O)C)CC=C(C4CO4)C(=O)OC)C 364.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
methyl (E)-4-[(1R,2S,4S,4aS,6S,8aS)-4,6-dihydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]-2-[(2R)-oxiran-2-yl]but-2-enoate 163009579 Click to see CC1(C(CCC2(C1C(CC3(C2CC=C(C4CO4)C(=O)OC)CO3)O)C)O)C 380.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.10.015
methyl (E)-4-[(1S,2S,4R,4aR,6S,8aR)-4,6-dihydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]-2-[(2R)-oxiran-2-yl]but-2-enoate 163009584 Click to see CC1(C(CCC2(C1C(CC3(C2CC=C(C4CO4)C(=O)OC)CO3)O)C)O)C 380.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
methyl 4-(4,6-dihydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl)-2-(oxiran-2-yl)but-2-enoate 75069550 Click to see CC1(C(CCC2(C1C(CC3(C2CC=C(C4CO4)C(=O)OC)CO3)O)C)O)C 380.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
15,16-Epoxy-12R-hydroxylabda-8(17),13(16),14-triene 10518493 Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=COC=C3)O)C)C 302.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-1-(furan-3-yl)ethanol 85169048 Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=COC=C3)O)C)C 302.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
3-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethenyl]furan 85079076 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=COC=C3)C)C 284.40 unknown https://doi.org/10.1016/J.TET.2007.05.120
Coronarin E 9971144 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=COC=C3)C)C 284.40 unknown https://doi.org/10.1016/J.TET.2007.05.120
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Aulacocarpinolide 44559677 Click to see CC1(C2CCC3=C(C2(CCC1O)C)CC(OC3)C4=CCOC4=O)C 332.40 unknown https://doi.org/10.1351/PAC199466102327
https://doi.org/10.1021/NP50109A007
> Organoheterocyclic compounds / Azaphilones
Fusaraisochromenone 132566876 Click to see CC1CC2=C(CO1)C(=O)C(C(C2)O)(C)O 212.24 unknown https://doi.org/10.1016/J.TET.2007.05.120
> Organoheterocyclic compounds / Tetrahydrofurans
(2S,3E,4R)-3-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-2,4-dimethoxyoxolane 162961762 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C3C(COC3OC)OC)C)C 348.50 unknown https://doi.org/10.1016/J.TET.2007.05.120
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(Z)-1-[(8S,9R,10R)-3,9-dihydroxy-4,5,19-trimethoxy-10-methyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl]-2-methylbut-2-en-1-one 46883432 Click to see CC=C(C)C(=O)C1C(C(CC2=CC3=C(C(=C2C4=C(C(=C(C=C14)OC)OC)O)OC)OCO3)C)O 470.50 unknown https://doi.org/10.1016/J.TET.2007.05.120

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