Conchocarpus heterophyllus

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Internal ID UUID64401314ae0c4973144855
Scientific name Conchocarpus heterophyllus
Authority (A.St.-Hil.) Kallunki & Pirani
First published in Kew Bull. 53: 300 (1998)

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Synonyms Top

Scientific name Authority First published in
Rossenia pentaphylla Vell. Fl. Flumin. : 31 (1829)
Angostura heterophylla (A.St.-Hil.) Albuq. Acta Amazonica 11(4): 850 (1981):.
Bonplandia heterophylla (A.St.-Hil.) Spreng. Syst. Veg., ed. 16 [Sprengel] 1: 780. 1824 [dated 1825; publ. in late 1824]
Bonplandia lasiostemon Spreng. Syst. Veg., ed. 16 [Sprengel] 1: 780. 1824 [dated 1825; publ. in late 1824]
Cusparia heterophylla (A.St.-Hil.) Engl. Fl. Bras. 12(2): 114 (1874)
Cusparia undulata Hemsl. Gard. Chron. ser. 3, 12: 396. 1892
Galipea heterophylla A.St.-Hil. Bull. Sci. Soc. Philom. Paris 10: 131 (1823)
Angostura undulata (Hemsl.) Albuq. Acta Amazonica 11(4): 852 (1981):.

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil Southeast
    • Northern South America
      • Suriname
      • Venezuela

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000617722
Tropicos 100289291
KEW urn:lsid:ipni.org:names:13724-2
The Plant List kew-2639461
Open Tree Of Life 6125797
IPNI 908317-1
GBIF 3836200
Tropicos 50125319
KEW urn:lsid:ipni.org:names:1001940-1
The Plant List kew-2733922
Open Tree Of Life 5747632
NCBI Taxonomy 1654686
IUCN Red List 180076759
IPNI 1001940-1
GBIF 3835541
EOL 5623572

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
New Polymethoxyflavones from Hottonia palustris Evoke DNA Biosynthesis-Inhibitory Activity in An Oral Squamous Carcinoma (SCC-25) Cell Line Strawa JW, Jakimiuk K, Szoka Ł, Brzezinski K, Drozdzal P, Pałka JA, Tomczyk M Molecules 10-Jul-2022
PMCID:PMC9325269
doi:10.3390/molecules27144415
PMID:35889288
Trypanocidal Activity of Flavanone Derivatives Maciel Diogo G, Andrade JS, Sales Junior PA, Maria Fonseca Murta S, Dos Santos VM, Taylor JG Molecules 17-Jan-2020
PMCID:PMC7024391
doi:10.3390/molecules25020397
PMID:31963596
Almeidea A. St.-Hil. Belongs to Conchocarpus J.C. Mikan (Galipeinae, Rutaceae): Evidence from Morphological and Molecular Data, with a First Analysis of Subtribe Galipeinae Poleselli Bruniera C, Kallunki JA, Groppo M PLoS One 07-May-2015
PMCID:PMC4423776
doi:10.1371/journal.pone.0125650
PMID:25951371
Fusion within and between whorls of floral organs in Galipeinae (Rutaceae): structural features and evolutionary implications El Ottra JH, Pirani JR, Endress PK Ann Bot 04-Mar-2013
PMCID:PMC3631327
doi:10.1093/aob/mct039
PMID:23463590
Trypanocidal activity of flavonoids and limonoids isolated from Myrsinaceae and Meliaceae active plant extracts Ana C. Leite, Artur Placeres Neto, Alessandra R. P. Ambrozin, João B. Fernandes, Paulo C. Vieira, Maria F. das G. F. da Silva, Sérgio de Albuquerque Springer Science and Business Media LLC 29-Apr-2010
doi:10.1590/S0102-695X2010000100002
Piranoflavonas inéditas e atividades tripanocidas das substâncias isoladas de conchocarpus heterophyllus Alessandra Regina Pepe Ambrozin, Paulo Cezar Vieira, João Batista Fernandes, Maria Fátima das Graças Fernandes d Silva, Sérgio de Albuquerque FapUNIFESP (SciELO) 19-Jun-2008
doi:10.1590/S0100-40422008000400005

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Tropanserin 68600 Click to see CC1=CC(=CC(=C1)C(=O)OC2CC3CCC(C2)N3C)C 273.37 unknown https://doi.org/10.1590/S0100-40422008000400005
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
[(3aS,6S,6aR,9S,9aS,9bR)-9-acetyloxy-6a-hydroxy-6-methyl-3-methylidene-2-oxo-3a,4,5,6,7,8,9,9b-octahydroazuleno[4,5-b]furan-9a-yl]methyl acetate 101306774 Click to see 366.40 unknown https://doi.org/10.1590/S0100-40422008000400005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3beta)-Stigmast-5-en-3-yl benzoate 102181 Click to see 518.80 unknown https://doi.org/10.1590/S0100-40422008000400005
17-(4-Ethyl-1,5-dimethylhexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[A]phenanthren-3-YL benzoate 3107312 Click to see 518.80 unknown https://doi.org/10.1590/S0100-40422008000400005
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
1,4-Dimethoxy-2-quinolone 21770010 Click to see COC1=CC(=O)N(C2=CC=CC=C21)OC 205.21 unknown https://doi.org/10.1590/S0100-40422008000400005
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5-Hydroxyflavone 68112 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=CC=C3O2)O 238.24 unknown https://doi.org/10.1590/S0100-40422008000400005
Flavone 10680 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=CC=CC=C3O2 222.24 unknown https://doi.org/10.1590/S0102-695X2010000100002
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
7-Methoxyflavone 466268 Click to see 252.26 unknown https://doi.org/10.1590/S0102-695X2010000100002
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
6-decyl-6H-chromeno[4,3-b]chromen-7-one 162820272 Click to see 390.50 unknown https://doi.org/10.1590/S0100-40422008000400005
6-dodecyl-6H-chromeno[4,3-b]chromen-7-one 162820236 Click to see 418.60 unknown https://doi.org/10.1590/S0100-40422008000400005
6-heptadecyl-6H-chromeno[4,3-b]chromen-7-one 163099104 Click to see 488.70 unknown https://doi.org/10.1590/S0100-40422008000400005
6-octadec-16-enyl-6H-chromeno[4,3-b]chromen-7-one 163016877 Click to see CC=CCCCCCCCCCCCCCCCC1C2=C(C3=CC=CC=C3O1)OC4=CC=CC=C4C2=O 500.70 unknown https://doi.org/10.1590/S0100-40422008000400005
6-octadecyl-6H-chromeno[4,3-b]chromen-7-one 162820157 Click to see 502.70 unknown https://doi.org/10.1590/S0100-40422008000400005

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