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Aframomum sceptrum

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Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
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Details Top

Internal ID UUID643ff178812bf418057141
Scientific name Aframomum sceptrum
Authority (Oliv. & D.Hanb.) K.Schum.
First published in Pflanzenr. IV (Heft 20):214

Description Top

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Synonyms Top

Scientific name Authority First published in
Aframomum masuianum (De Wild. & T.Durand) K.Schum. Pflanzenr. IV (Heft 20):212
Amomum masuianum De Wild. & T.Durand Bull. Soc. Roy. Bot. Belgique 38:138. (1899)
Amomum sceptrum Oliv. & D.Hanb. J. Proc. Linn. Soc., Bot. 7:109. (1864)
Cardamomum sceptrum (Oliv. & D.Hanb.) Kuntze Revis. gen. pl. 687

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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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000338106
Tropicos 34500356
KEW urn:lsid:ipni.org:names:871892-1
Open Tree Of Life 6326
NCBI Taxonomy 199617
IUCN Red List 126039924
IPNI 871892-1
GBIF 2758946
USDA GRIN 101021
EPPO AFRSC

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
Essential Oils and Terpenic Compounds as Potential Hits for Drugs against Amitochondriate Protists Menezes SA, Tasca T Trop Med Infect Dis 05-Jan-2023
PMCID:PMC9865018
doi:10.3390/tropicalmed8010037
PMID:36668944
Anthelmintic Agents from African Medicinal Plants: Review and Prospects Jato J, Orman E, Duah Boakye Y, Oppong Bekoe E, Oppong Bekoe S, Asare-Nkansah S, Spiegler V, Hensel A, Liebau E, Agyare C Evid Based Complement Alternat Med 31-Dec-2022
PMCID:PMC9825222
doi:10.1155/2022/8023866
PMID:36624864
Identification of the Constituents in Cnidii Fructus Active Against Trichomonas vaginalis Parasites Yu CC, Chiang YT, Cham TM Dose Response 10-Nov-2022
PMCID:PMC9661559
doi:10.1177/15593258221131646
PMID:36387775
A review of Cameroonian medicinal plants with potentials for the management of the COVID-19 pandemic Fongnzossie Fedoung E, Biwole AB, Nyangono Biyegue CF, Ngansop Tounkam M, Akono Ntonga P, Nguiamba VP, Essono DM, Forbi Funwi P, Tonga C, Nguenang GM, Kemeuze V, Sonwa DJ, Tsabang N, Bouelet IS, Tize Z, Boum AT, Momo Solefack MC, Betti JL, Nouga Bissoue A, Lehman LG, Mapongmetsem PM, Nneme Nneme L, Ngono Ngane RA, Ngogang Yonkeu J 26-Mar-2021
PMCID:PMC7994110
doi:10.1007/s13596-021-00567-6
The importance of choosing appropriate methods for assessing wild food plant knowledge and use: A case study among the Baka in Cameroon Gallois S, Heger T, Henry AG, van Andel T PLoS One 18-Feb-2021
PMCID:PMC7891729
doi:10.1371/journal.pone.0247108
PMID:33600479
Trypanocidal Essential Oils: A Review de Morais MC, de Souza JV, da Silva Maia Bezerra Filho C, Dolabella SS, de Sousa DP Molecules 06-Oct-2020
PMCID:PMC7583723
doi:10.3390/molecules25194568
PMID:33036315
Anti-trichomonad activities of different compounds from foods, marine products, and medicinal plants: a review Friedman M, Tam CC, Cheng LW, Land KM BMC Complement Med Ther 09-Sep-2020
PMCID:PMC7479404
doi:10.1186/s12906-020-03061-9
PMID:32907567
Methanol extracts of Fagara zanthoxyloides leaves possess antimalarial effects and normalizes haematological and biochemical status of Plasmodium berghei-passaged mice Enechi OC, Amah CC, Okagu IU, Ononiwu CP, Azidiegwu VC, Ugwuoke EO, Onoh AP, Ndukwe EE Pharm Biol 09-Sep-2019
PMCID:PMC6746293
doi:10.1080/13880209.2019.1656753
PMID:31500475
HPLC-DAD Phenolic Profiling and In Vitro Antioxidant Activities of Three Prominent Nigerian Spices Omoba OS, Olagunju AI, Salawu SO, Boligon AA Prev Nutr Food Sci 30-Jun-2019
PMCID:PMC6615355
doi:10.3746/pnf.2019.24.2.179
PMID:31328123
Active Essential Oils and Their Components in Use against Neglected Diseases and Arboviruses Luna EC, Luna IS, Scotti L, Monteiro AF, Scotti MT, de Moura RO, de Araújo RS, Monteiro KL, de Aquino TM, Ribeiro FF, Mendonça FJ Junior Oxid Med Cell Longev 07-Feb-2019
PMCID:PMC6387720
doi:10.1155/2019/6587150
PMID:30881596
Induction of programmed cell death in Trypanosoma cruzi by Lippia alba essential oils and their major and synergistic terpenes (citral, limonene and caryophyllene oxide) Moreno ÉM, Leal SM, Stashenko EE, García LT BMC Complement Altern Med 27-Jul-2018
PMCID:PMC6062979
doi:10.1186/s12906-018-2293-7
PMID:30053848
Role of bitter leaf (Vernonia amygdalina) extract in prevention of renal toxicity induced by crude petroleum contaminated diets in rats Achuba FI Int J Vet Sci Med 12-Jul-2018
PMCID:PMC6286397
doi:10.1016/j.ijvsm.2018.07.002
PMID:30564592
Compounds from African Medicinal Plants with Activities Against Selected Parasitic Diseases: Schistosomiasis, Trypanosomiasis and Leishmaniasis Simoben CV, Ntie-Kang F, Akone SH, Sippl W Nat Prod Bioprospect 09-May-2018
PMCID:PMC5971035
doi:10.1007/s13659-018-0165-y
PMID:29744736
Potential antimalarials from African natural products: A reviw Lawal B, Shittu OK, Kabiru AY, Jigam AA, Umar MB, Berinyuy EB, Alozieuwa BU J Intercult Ethnopharmacol 29-Oct-2015
PMCID:PMC4665028
doi:10.5455/jice.20150928102856
PMID:26649238
Dental calculus evidence of Taï Forest Chimpanzee plant consumption and life history transitions Power RC, Salazar-García DC, Wittig RM, Freiberg M, Henry AG Sci Rep 19-Oct-2015
PMCID:PMC4611876
doi:10.1038/srep15161
PMID:26481858

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R,5R,7R)-3-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-7-hydroxydioxepane-5-carbaldehyde 163034905 Click to see CC1(CCCC2(C1CCC(=C)C2C3CC(CC(OO3)O)C=O)C)C 336.50 unknown https://doi.org/10.1055/S-2002-32888
(E)-4-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-2-(2,2-diethoxyethyl)but-2-enal 162941900 Click to see CCOC(CC(=CCC1C(=C)CCC2C1(CCCC2(C)C)C)C=O)OCC 376.60 unknown https://doi.org/10.1055/S-2002-32888
2-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethylidene]butanedial 75094027 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown https://doi.org/10.1055/S-2002-32888
3-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-7-hydroxydioxepane-5-carbaldehyde 163034904 Click to see CC1(CCCC2(C1CCC(=C)C2C3CC(CC(OO3)O)C=O)C)C 336.50 unknown https://doi.org/10.1055/S-2002-32888
4-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-2-(2,2-diethoxyethyl)but-2-enal 162941898 Click to see CCOC(CC(=CCC1C(=C)CCC2C1(CCCC2(C)C)C)C=O)OCC 376.60 unknown https://doi.org/10.1055/S-2002-32888
7-[(1R,4aR,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-hydroxy-4,7-dihydro-3H-dioxepine-5-carbaldehyde 129316571 Click to see CC1(CCCC2(C1CCC(=C)C2C3C=C(CC(OO3)O)C=O)C)C 334.40 unknown https://doi.org/10.1055/S-2002-32888
Labda-8(17),12-diene-15,16-dial 11077520 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown https://doi.org/10.1055/S-2002-32888
methyl (E)-4-[(1R,2S,3S,4aR,6S,8aR)-3,6-dihydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]-2-(2-hydroxyethyl)but-2-enoate 162907185 Click to see CC1(C(CCC2(C1CC(C3(C2CC=C(CCO)C(=O)OC)CO3)O)C)O)C 382.50 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
methyl (E)-4-[(1R,2S,3S,4aR,6S,8aS)-3,6-dihydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]-2-(2-hydroxyethyl)but-2-enoate 102271959 Click to see CC1(C(CCC2(C1CC(C3(C2CC=C(CCO)C(=O)OC)CO3)O)C)O)C 382.50 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
methyl 4-(3,6-dihydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl)-2-(2-hydroxyethyl)but-2-enoate 162907184 Click to see CC1(C(CCC2(C1CC(C3(C2CC=C(CCO)C(=O)OC)CO3)O)C)O)C 382.50 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
(S)-(+)-Nerolidol 70702 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1055/S-2002-32888
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2R)-4-[(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2-methoxy-2H-furan-5-one 124635187 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CC(OC3=O)OC)C)C 330.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
(2R)-4-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2-methoxy-2H-furan-5-one 162867082 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CC(OC3=O)OC)C)C 330.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
(2S)-4-[(1S)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-hydroxyethyl]-2-methoxy-2H-furan-5-one 162872176 Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CC(OC3=O)OC)O)C)C 348.50 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
(3R)-3-[(1S)-2-[(1R,2S,3S,4aR,6S,8aS)-2,3,6-trihydroxy-2-(hydroxymethyl)-5,5,8a-trimethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-1-hydroxyethyl]oxolan-2-one 162865903 Click to see CC1(C(CCC2(C1CC(C(C2CC(C3CCOC3=O)O)(CO)O)O)C)O)C 386.50 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
3-[1-hydroxy-2-[2,3,6-trihydroxy-2-(hydroxymethyl)-5,5,8a-trimethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethyl]oxolan-2-one 162865901 Click to see CC1(C(CCC2(C1CC(C(C2CC(C3CCOC3=O)O)(CO)O)O)C)O)C 386.50 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
Cholesterol-3-13C 304 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(6beta,24R)-6-Hydroxystigmast-4-en-3-one 14769504 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C 428.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
Stigmast-4-en-3a-ol 56612475 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(CCC34C)O)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOL.2011.04.006
> Organic oxygen compounds / Organic oxides / Organic peroxides / Dialkyl peroxides
7-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)-3-hydroxy-4,7-dihydro-3H-dioxepine-4-carbaldehyde 5316081 Click to see CC1(CCCC2(C1CCC(=C)C2C3C=CC(C(OO3)O)C=O)C)C 334.40 unknown https://doi.org/10.1055/S-2002-32888
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E)-3-[2-[(1R,2S,3S,4aR,6S,8aR)-3,6-dihydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]ethylidene]oxolan-2-one 163046217 Click to see CC1(C(CCC2(C1CC(C3(C2CC=C4CCOC4=O)CO3)O)C)O)C 350.40 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
(3E)-3-[2-[(1R,2S,3S,4aR,6S,8aS)-3,6-dihydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl]ethylidene]oxolan-2-one 102271960 Click to see CC1(C(CCC2(C1CC(C3(C2CC=C4CCOC4=O)CO3)O)C)O)C 350.40 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
3-[2-(3,6-dihydroxy-5,5,8a-trimethylspiro[3,4,4a,6,7,8-hexahydro-1H-naphthalene-2,2'-oxirane]-1-yl)ethylidene]oxolan-2-one 85409968 Click to see CC1(C(CCC2(C1CC(C3(C2CC=C4CCOC4=O)CO3)O)C)O)C 350.40 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl] acetate 54434051 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 330.29 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
3-Acetoxy-5,7,4'-trihydroxyflavanone 14861264 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 330.29 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(02)00075-4
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(02)00075-4

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