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Campylospermum flavum

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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
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Details Top

Internal ID UUID64400f1c479db729776816
Scientific name Campylospermum flavum
Authority (Schumach.) Farron
First published in Bull. Jard. Bot. État Bruxelles 35: 397 (1965)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ouratea ashantiensis De Wild. Pl. Bequaert. 4: 441 (1928)
Ouratea flava Hutch. & Dalziel ex Stapf Bot. Mag. 149: t. 9023 (1924)
Ouratea talbotii De Wild. Pl. Bequaert. 4: 514 (1929)
Ouratea schlechteri Gilg Bot. Jahrb. Syst. 33: 269 (1903)
Ouratea spinuloso-serrata Gilg Bot. Jahrb. Syst. 33: 265 (1903)
Ouratea laurentii De Wild. Rev. Zool. Bot. Africaines 7(Suppl. Bot.): 57 (1920)
Ouratea pynaertii De Wild. Rev. Zool. Bot. Africaines 7(Suppl. Bot.): 62 (1920)
Ouratea newiensis De Wild. Pl. Bequaert. 4: 501 (1929)
Ouratea monticola Gilg Bot. Jahrb. Syst. 33: 272 (1903)
Monelasmum fuscum Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 16: 330 (1902)
Monelasmum nanense Tiegh. Ann. Sci. Nat., Bot. , sér. 9, 5: 171 (1907)
Monelasmum monticola Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 18: 36 (1903)
Monelasmum krebedjense Tiegh. Ann. Sci. Nat., Bot. , sér. 9, 5: 171 (1907)
Monelasmum chevalieri Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 16: 333 (1902)
Monelasmum acutum Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 16: 331 (1902)
Monelasmum bolamense Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 16: 334 (1902)
Monelasmum souzae Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 16: 334 (1902)
Monelasmum thoirei Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 16: 332 (1902)
Monelasmum schlechteri Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 18: 36 (1903)
Monelasmum pungens Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 16: 333 (1902)
Monelasmum spinuloso-serratum Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 18: 36 (1903)
Monelasmum viride Tiegh. Ann. Sci. Nat., Bot. , sér. 8, 16: 332 (1902)
Campylospermum monticola (Gilg) Cheek Pl. Mt. Cameroon : 92 (1998 publ. 1999)
Gomphia flava Schumach. & Thonn. Beskr. Guin. Pl. : 216 (1827)

Common names Top

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Language Common/alternative name
Vietnamese gomphia flava

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
  • Africa
    • Northeast Tropical Africa
      • Chad
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000583248
Tropicos 22800436
KEW urn:lsid:ipni.org:names:605885-1
The Plant List kew-2695516
Open Tree Of Life 4730007
NCBI Taxonomy 1321791
IUCN Red List 116868721
IPNI 605885-1
GBIF 5552819
EPPO CAMFL

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
Diversity, above-ground biomass, and vegetation patterns in a tropical dry forest in Kimbi-Fungom National Park, Cameroon Sainge MN, Nchu F, Townsend Peterson A Heliyon 31-Jan-2020
PMCID:PMC7002822
doi:10.1016/j.heliyon.2020.e03290
PMID:32042986
Phenolic dimers and an indole alkaloid from Campylospermum flavum (Ochnaceae). Ndongo JT, Shaaban M, Mbing JN, Bikobo DN, Atchadé Ade T, Pegnyemb DE, Laatsch H Phytochemistry 01-Nov-2010
doi:10.1016/J.PHYTOCHEM.2010.08.006
PMID:20822781
Two biflavonoids from Ouratea flava stem bark. Mbing JN, Pegnyemb DE, Tih RG, Sondengam BL, Blond A, Bodo B Phytochemistry 01-Jun-2003
doi:10.1016/S0031-9422(03)00161-4
PMID:12770592
Constituents of Ouratea flava J.N Mbing, M.Y Bassomo, D.E Pegnyemb, R.G Tih, B.L Sondemgam, A Blond, B Bodo Elsevier BV 17-Jan-2003
doi:10.1016/S0305-1978(02)00083-2

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
(2,4-dihydroxyphenyl)-[(2S,3S,4R,5S)-5-(2,4-dihydroxyphenyl)-4-[(R)-hydroxy-(4-hydroxyphenyl)methyl]-2-(4-hydroxyphenyl)oxolan-3-yl]methanone 102053244 Click to see C1=CC(=CC=C1C2C(C(C(O2)C3=C(C=C(C=C3)O)O)C(C4=CC=C(C=C4)O)O)C(=O)C5=C(C=C(C=C5)O)O)O 530.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
(2,4-Dihydroxyphenyl)-[5-(2,4-dihydroxyphenyl)-4-[hydroxy-(4-hydroxyphenyl)methyl]-2-(4-hydroxyphenyl)oxolan-3-yl]methanone 75287600 Click to see C1=CC(=CC=C1C2C(C(C(O2)C3=C(C=C(C=C3)O)O)C(C4=CC=C(C=C4)O)O)C(=O)C5=C(C=C(C=C5)O)O)O 530.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
[(2S,3S,4S,5S)-4-(2,4-dihydroxybenzoyl)-2,5-bis(4-hydroxyphenyl)oxolan-3-yl]-(2,4-dihydroxyphenyl)methanone 102056153 Click to see C1=CC(=CC=C1C2C(C(C(O2)C3=CC=C(C=C3)O)C(=O)C4=C(C=C(C=C4)O)O)C(=O)C5=C(C=C(C=C5)O)O)O 528.50 unknown https://doi.org/10.1016/S0305-1978(02)00083-2
> Lignans, neolignans and related compounds / Lignan glycosides
2-[4-[2-[4-[3,4-Dimethyl-5-(3,4,5-trimethoxyphenyl)oxolan-2-yl]-2,6-dimethoxyphenoxy]-1-hydroxypropyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162881044 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC(C)C(C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC)O)OC)C 790.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/S0305-1978(02)00083-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2R)-Taxiphyllin 4475719 Click to see C1=CC(=CC=C1C(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 311.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
(2S)-2-[(4S)-4-hydroxycyclohexa-1,5-dien-1-yl]-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyacetonitrile 162988367 Click to see C1C=C(C=CC1O)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 313.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
Dhurrin 161355 Click to see C1=CC(=CC=C1C(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 311.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
6-Hydroxyindolin-2-one 2784139 Click to see C1C2=C(C=C(C=C2)O)NC1=O 149.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(3R,4S)-3-(4-hydroxy-3-methoxyphenyl)-2-oxa-6,11-diazatetracyclo[7.5.2.04,15.012,16]hexadeca-1(15),9,12(16),13-tetraene-5,8-dione 163185223 Click to see COC1=C(C=CC(=C1)C2C3C4=C(O2)C=CC5=C4C(=CN5)C(=O)CNC3=O)O 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
(7R)-3-(2,4-dihydroxybenzoyl)-4-hydroxy-2,7-bis(4-hydroxyphenyl)-7,8-dihydrofuro[2,3-f]chromen-9-one 162852486 Click to see C1C(OC2=C(C1=O)C3=C(C(=C2)O)C(=C(O3)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5)O)O)C6=CC=C(C=C6)O 524.50 unknown https://doi.org/10.1016/S0031-9422(03)00161-4
(E)-1-[3-(2,4-dihydroxybenzoyl)-4,5,6-trihydroxy-2-(4-hydroxyphenyl)-1-benzofuran-7-yl]-3-(4-hydroxyphenyl)prop-2-en-1-one 12096478 Click to see C1=CC(=CC=C1C=CC(=O)C2=C3C(=C(C(=C2O)O)O)C(=C(O3)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5)O)O)O 540.50 unknown https://doi.org/10.1016/S0031-9422(03)00161-4
3-(2,4-Dihydroxybenzoyl)-2,7-bis(4-hydroxyphenyl)-7,8-dihydrofuro[2,3-f]chromen-9-one 101251736 Click to see C1C(OC2=C(C1=O)C3=C(C=C2)C(=C(O3)C4=CC=C(C=C4)O)C(=O)C5=C(C=C(C=C5)O)O)C6=CC=C(C=C6)O 508.50 unknown https://doi.org/10.1016/S0031-9422(03)00161-4
3-(4-Hydroxy-3-methoxyphenyl)-2-oxa-6,11-diazatetracyclo[7.5.2.04,15.012,16]hexadeca-1(15),9,12(16),13-tetraen-5-one 73074609 Click to see COC1=C(C=CC(=C1)C2C3C4=C(O2)C=CC5=C4C(=CN5)CCNC3=O)O 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
3-(4-Hydroxy-3-methoxyphenyl)-2-oxa-6,11-diazatetracyclo[7.5.2.04,15.012,16]hexadeca-1(15),9,12(16),13-tetraene-5,8-dione 75287601 Click to see COC1=C(C=CC(=C1)C2C3C4=C(O2)C=CC5=C4C(=CN5)C(=O)CNC3=O)O 364.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
Moschamindole 25233004 Click to see COC1=C(C=CC(=C1)C2C3C4=C(O2)C=CC5=C4C(=CN5)CCNC3=O)O 350.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S)-8-[(2R,3S,4S)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 15297951 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC=C(C=C5)O)O)O)O)C6=CC=C(C=C6)O)O 530.50 unknown https://doi.org/10.1016/S0031-9422(03)00161-4
8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-6-yl]-5,7-dihydroxy-2-(4-methoxyphenyl)chromen-4-one 49817769 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C5=C(C=C4O)OC(=CC5=O)C6=CC=C(C=C6)O)O 552.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
Agathisflavone 5281599 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O)O 538.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-8-yl]-6-(hydroxymethyl)oxan-3-yl] acetate 162960267 Click to see CC(=O)OC1C(C(C(OC1C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)O)O)OC)CO)O)O 488.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
[4,5-Dihydroxy-2-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-8-yl]-6-(hydroxymethyl)oxan-3-yl] acetate 74977776 Click to see CC(=O)OC1C(C(C(OC1C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)O)O)OC)CO)O)O 488.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
4'-O-Methylvitexin 21161135 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
Trematin 5378503 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.08.006
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Lophirone A 5488805 Click to see C1=CC(=CC=C1C(C2=CC=C(C=C2)O)C(C3=COC4=C(C3=O)C=CC(=C4)O)C(=O)C5=C(C=C(C=C5)O)O)O 510.50 unknown https://doi.org/10.1016/S0031-9422(03)00161-4
https://doi.org/10.1016/S0305-1978(02)00083-2

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