Trichoscypha acuminata, also known as amvout, is a plant species belonging to the Anacardiaceae family. It is primarily found in several African countries, including Nigeria, Cameroon, and Angola. This tree can grow up to 20m tall and has leaves that can reach up to 1.5m in length. Its natural habitat is in the rainforest. The plant produces dark red fruits that are edible.

Synonyms Top

Scientific name	Authority	First published in
Trichoscypha flamignii	De Wild.	Repert. Spec. Nov. Regni Veg. 13: 375 (1914)
Trichoscypha laurentii	De Wild.	Miss. Ém. Laurent : 144 (1905)
Trichoscypha ferruginea	Engl.	Bot. Jahrb. Syst. 15: 112 (1892)
Trichoscypha redingi	De Wild.	Bull. Jard. Bot. État Bruxelles 4: 369 (1914)
Emiliomarcelia braunii	T.Durand & H.Durand	Syll. Fl. Congol. : 115 (1909)
Emiliomarcelia congoensis	T.Durand & H.Durand	Syll. Fl. Congol. : 115 (1909)
Emiliomarcelia laurentii	T.Durand & H.Durand	Syll. Fl. Congol. : 115 (1909)
Sorindeia mannii	Oliv.	Fl. Trop. Afr. 1: 441 (1868)
Trichoscypha braunii	Engl.	Bot. Jahrb. Syst. 15: 111 (1892)
Trichoscypha buettneri	Engl.	Bot. Jahrb. Syst. 15(1): 113, nomen, in obs. 1892 [26 Jan 1892]
Trichoscypha congoensis	Engl.	Bot. Jahrb. Syst. 36: 222 (1905)

Common names Top

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Language	Common/alternative name
Chinese	米娜塔果

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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

Africa click to expand
- West Tropical Africa
  - Nigeria
- West-central Tropical Africa
  - Cabinda
  - Cameroon
  - Central African Republic
  - Congo
  - Equatorial Guinea
  - Gabon
  - Zaïre

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000409281
Tropicos	1300681
KEW	urn:lsid:ipni.org:names:71836-1
The Plant List	kew-2435121
Open Tree Of Life	982263
NCBI Taxonomy	289776
IUCN Red List	143712891
IPNI	71836-1
iNaturalist	1139412
GBIF	5544166
Wikipedia	Trichoscypha_acuminata
CMAUP	NPO13028

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

Ethnobotanical study and vulnerability of medicinal plants used against the symptoms of COVID-19 in the Lomié subdivision, East Region of Cameroon

Ngamsou Abdel K, Mala WA, Chimi PM, Funwi FP, Engoulou C, Messi Effa JA, Kouoguem Kamdem ME, Nzoyeuem Djonko F, Landry Fokoua U, Brice Adounga S, Marguerite Mbolo M

Heliyon

21-Mar-2024

PMCID:	PMC10999872
doi:	10.1016/j.heliyon.2024.e28247
PMID:	38590891

Assessing plant diversity change in logged and unlogged dense semi-deciduous production forest of eastern Cameroon

Hubert Kpoumie Mounmemi, Mensah Ekué MR, Funwi Preasious Forbi, Roger Kabelong Banoho LP, Tiokeng B, Maffo Maffo NL, Lagarde Jean Betti, Carole Mireil Votio Tchoupou, Amandine Flore Yonkeu Ntonmen, Taedoumg HE, Zapfack L

Heliyon

12-May-2023

PMCID:	PMC10199262
doi:	10.1016/j.heliyon.2023.e16199
PMID:	37215910

Ethnobotanical survey of wild edible plants used by Baka people in southeastern Cameroon

Billong Fils PE, Afiong Nana N, Betti JL, Farick Njimbam O, Tientcheu Womeni S, Ávila Martin E, Ros Brull G, Okale R, Fa JE, Funk SM

J Ethnobiol Ethnomed

22-Oct-2020

PMCID:	PMC7579891
doi:	10.1186/s13002-020-00413-0
PMID:	33092623

To move or to evolve: contrasting patterns of intercontinental connectivity and climatic niche evolution in “Terebinthaceae” (Anacardiaceae and Burseraceae)

Weeks A, Zapata F, Pell SK, Daly DC, Mitchell JD, Fine PV

Front Genet

28-Nov-2014

PMCID:	PMC4247111
doi:	10.3389/fgene.2014.00409
PMID:	25506354

Mixed-Forest Species Establishment in a Monodominant Forest in Central Africa: Implications for Tropical Forest Invasibility

Peh KS, Sonké B, Séné O, Djuikouo MN, Nguembou CK, Taedoumg H, Begne SK, Lewis SL

PLoS One

20-May-2014

PMCID:	PMC4028239
doi:	10.1371/journal.pone.0097585
PMID:	24844914

Comparative Phylogeography in Rainforest Trees from Lower Guinea, Africa

Heuertz M, Duminil J, Dauby G, Savolainen V, Hardy OJ

PLoS One

08-Jan-2014

PMCID:	PMC3885573
doi:	10.1371/journal.pone.0084307
PMID:	24416215

Carbon pools of an intact forest in Gabon

Gautam S, Pietsch SA

Afr J Ecol

02-May-2012

PMCID:	PMC3636713
doi:	10.1111/j.1365-2028.2012.01337.x
PMID:	23641117

Acuminatanol, the first 2′,2‴-bis-dihydrobiflavonol from the aqueous extract of Trichoscypha acuminata

Jin-Feng Hu, Eliane Garo, Grayson W. Hough, Matt G. Goering, Mark O’Neil-Johnson, Gary R. Eldridge

Elsevier BV

26-Jun-2007

doi:	10.1016/J.TETLET.2007.06.094

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
4-[(2-amino-4-oxo-1H-pteridin-6-yl)methyl-formylamino]benzoic acid	97575	Click to see C1=CC(=CC=C1C(=O)O)N(CC2=CN=C3C(=N2)C(=O)N=C(N3)N)C=O	340.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic acid	5280896	Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C	264.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	92835934	Click to see CC12CCCCC1C(CC3C2C(CC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
(3beta,5alpha,7alpha)-3,7-Dihydroxyandrostan-17-one	9815044	Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3R,5R,7S,8R,9S,10S,13S,14S)-3,7-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	57386710	Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3R,5R,8R,9S,10S,13S,14S,17S)-3,17-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one	69924431	Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3R,5R,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-7,17-dione	57386713	Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
(3R,5S,6S,8R,9S,10R,13S,14S)-3,6-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	69766330	Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3S,5R,7R,8S,9S,10S,13R,14S,16S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7,16-triol	99574281	Click to see CC12CCC3C(C1CC(C2)O)C(CC4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
(3S,5R,7S,8S,9S,10S,13S,14S,16S)-3,7,16-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one	99572894	Click to see CC12CCC(CC1CC(C3C2C(=O)CC4(C3CC(C4)O)C)O)O	322.40	unknown	via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one	99573267	Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one	99573266	Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5S,6S,8R,9S,10R,13S,14S)-3,6-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	15917986	Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3S,5S,6S,8S,9S,10R,13R,14S,16R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,6,16-triol	99574278	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one	99571962	Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one	99571961	Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5S,8S,9S,10S,11R,13S,14S,16S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,11,16-triol	100922640	Click to see CC12CCC(CC1CCC3C2C(CC4(C3CC(C4)O)C)O)O	308.50	unknown	via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one	99601533	Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CC(C4)O)C)O	306.40	unknown	via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one	99575783	Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CC(C4)O)C)O	306.40	unknown	via CMAUP database
(5R,8S,9S,10R,13S,14S,17S)-5,17-dihydroxy-10,13-dimethyl-2,4,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one	10979706	Click to see CC12CCC3C(C1CCC2O)CCC4(C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5R,8S,9S,10S,13R,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-dione	99571971	Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(=O)C4)C	304.40	unknown	via CMAUP database
(5S,6R,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99573707	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16R)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99573706	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99573705	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99574441	Click to see CC12CCCC1C3CC(C4CC(=O)CCC4(C3C(C2)O)C)O	306.40	unknown	via CMAUP database
(5S,8S,9R,10S,13S,14S,16R)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione	99571360	Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O	320.40	unknown	via CMAUP database
(5S,8S,9R,10S,13S,14S,16S)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione	99571358	Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O	320.40	unknown	via CMAUP database
(5S,8S,9S,10S,13S,14S,16R)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione	99574177	Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C	304.40	unknown	via CMAUP database
(5S,8S,9S,10S,13S,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione	99574175	Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C	304.40	unknown	via CMAUP database
11-Hydroxyandrosterone	21139727	Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
11alpha-Hydroxy-5alpha-androstane-3,17-dione	101709630	Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
11alpha,16alpha-Dihydroxy-5alpha-androstan-3-one	100922644	Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CC(C4)O)C)O	306.40	unknown	via CMAUP database
3beta-Hydroxy-5alpha-androstane-7,17-dione	11954160	Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
5alpha-Androstan-11-one, 3alpha,17beta-dihydroxy-	10125601	Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CCC4O)C)O	306.40	unknown	via CMAUP database
5alpha-Androstan-3-one, 11alpha,17beta-dihydroxy-	22796602	Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4O)C)O	306.40	unknown	via CMAUP database
5alpha-Androstan-3beta,17beta-diol-7-one	11868973	Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
5alpha-Androstan-6-one, 3beta,17beta-dihydroxy-	11551286	Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
5alpha-Androstane-3,7,17-trione	11266632	Click to see CC12CCC(=O)CC1CC(=O)C3C2CCC4(C3CCC4=O)C	302.40	unknown	via CMAUP database
7-beta-Hydroxyepiandrosterone	9836181	Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
Androstan-3-one, 6,17-dihydroxy-, (5alpha,6alpha,17beta)-	15838416	Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
Androstan-6-one, 3,17-dihydroxy-, (3alpha,5alpha,17beta)-	15929496	Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
Androstane-3,11,17-triol	57396177	Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4O)C)O)O	308.50	unknown	via CMAUP database
Androstane-3,17-dione, 6-hydroxy-, (5alpha,6alpha)-	22296022	Click to see CC12CCC(=O)CC1C(CC3C2CCC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
Androstane-3,6,17-triol	170796	Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
Jgd4N79M5A	68995028	Click to see CC12CCC3C(C1CCC2O)C(CC4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
10-Hydroxy-3-oxoestr-4-en-17-yl acetate	91691749	Click to see CC(=O)OC1CCC2C1(CCC3C2CCC4=CC(=O)CCC34O)C	332.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron	21883788	Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-]	116.07	unknown	via CMAUP database
Butanedioate;hydron	21952380	Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-]	118.09	unknown	via CMAUP database
Glutaric acid	743	Click to see C(CC(=O)O)CC(=O)O	132.11	unknown	via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
2-Oxonioacetate	3698251	Click to see C(C(=O)[O-])[OH2+]	76.05	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxylic acids
Quininic acid	345824	Click to see COC1=CC2=C(C=CN=C2C=C1)C(=O)O	203.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(2S,3S)-3,5,7-trihydroxy-2-[3,4,5-trihydroxy-2-[2,3,4-trihydroxy-6-[(2S,3S)-3,5,7-trihydroxy-4-oxo-2,3-dihydrochromen-2-yl]phenyl]phenyl]-2,3-dihydrochromen-4-one	162848280	Click to see C1=C(C=C2C(=C1O)C(=O)C(C(O2)C3=CC(=C(C(=C3C4=C(C(=C(C=C4C5C(C(=O)C6=C(C=C(C=C6O5)O)O)O)O)O)O)O)O)O)O)O	638.50	unknown	https://doi.org/10.1016/J.TETLET.2007.06.094
3,5,7-Trihydroxy-2-[3,4,5-trihydroxy-2-[2,3,4-trihydroxy-6-(3,5,7-trihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenyl]phenyl]-2,3-dihydrochromen-4-one	73407795	Click to see C1=C(C=C2C(=C1O)C(=O)C(C(O2)C3=CC(=C(C(=C3C4=C(C(=C(C=C4C5C(C(=O)C6=C(C=C(C=C6O5)O)O)O)O)O)O)O)O)O)O)O	638.50	unknown	https://doi.org/10.1016/J.TETLET.2007.06.094

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Trichoscypha acuminata

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

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