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Croton celtidifolius

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644036715ec79508420680
Scientific name Croton celtidifolius
Authority Baill.
First published in Adansonia 4: 331 (1864)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Oxydectes celtidifolia (Baill.) Kuntze Revis. Gen. Pl. 2: 611 (1891)
Croton cynanchicus Baill. Adansonia 4: 329 (1864)
Croton oreophilus Müll.Arg. Linnaea 34: 84 (1865)
Croton sanguis-draconis Mart. ex Baill. Adansonia 4: 327 (1864)

Common names Top

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Language Common/alternative name
French oxydectes celtidifolia
French croton cynanchicus
French croton oreophilus
French croton sanguis-draconis

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
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000927616
Tropicos 12800847
KEW urn:lsid:ipni.org:names:70018-2
The Plant List kew-49582
Open Tree Of Life 271746
NCBI Taxonomy 518845
IUCN Red List 189601462
IPNI 70018-2
GBIF 3059987
EOL 1147373
CMAUP NPO15573

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
Catechins and Proanthocyanidins Involvement in Metabolic Syndrome Patanè GT, Putaggio S, Tellone E, Barreca D, Ficarra S, Maffei C, Calderaro A, Laganà G Int J Mol Sci 25-May-2023
PMCID:PMC10252413
doi:10.3390/ijms24119228
PMID:37298181
Essential Oils of Aromatic Plant Species from the Atlantic Rainforest Exhibit Extensive Chemical Diversity and Antimicrobial Activity Perigo CV, Haber LL, Facanali R, Vieira MA, Torres RB, Bernacci LC, Guimarães EF, Baitello JB, Sobral ME, Quecini V, Marques MO Antibiotics (Basel) 19-Dec-2022
PMCID:PMC9774909
doi:10.3390/antibiotics11121844
PMID:36551501
Tap the sap – investigation of latex-bearing plants in the search of potential anticancer biopharmaceuticals Mazur O, Bałdysz S, Warowicka A, Nawrot R Front Plant Sci 01-Nov-2022
PMCID:PMC9664067
doi:10.3389/fpls.2022.979678
PMID:36388598
Climate change threatens native potential agroforestry plant species in Brazil Lima VP, de Lima RA, Joner F, Siddique I, Raes N, ter Steege H Sci Rep 10-Feb-2022
PMCID:PMC8831634
doi:10.1038/s41598-022-06234-3
PMID:35145191
Tannins as Hemostasis Modulators Marcińczyk N, Gromotowicz-Popławska A, Tomczyk M, Chabielska E Front Pharmacol 13-Jan-2022
PMCID:PMC8793672
doi:10.3389/fphar.2021.806891
PMID:35095516
Myorelaxation, respiratory depression and electrocardiographic changes caused by the administration of extract of açai (Euterpe oleracea Mart.) stone in rats Muto NA, Hamoy M, Rodrigues Lucas DC, Teixeira BB, Santos Almeida AF, de Castro Navegantes T, de Sousa Ferreira de Sá VS, de Moraes BP, do Vale Medeiros JP, dos Santos YA, da Rocha CQ, de Mello VJ, Rogez H Toxicol Rep 31-Mar-2021
PMCID:PMC8044785
doi:10.1016/j.toxrep.2021.03.024
PMID:33868963
Automatic Identification of Players in the Flavonoid Biosynthesis with Application on the Biomedicinal Plant Croton tiglium Pucker B, Reiher F, Schilbert HM Plants (Basel) 27-Aug-2020
PMCID:PMC7570183
doi:10.3390/plants9091103
PMID:32867203
Screening of plants from the Brazilian Atlantic Forest led to the identification of Athenaea velutina (Solanaceae) as a novel source of antimetastatic agents Almeida AA, Lima GD, Simão MV, Moreira GA, Siqueira RP, Zanatta AC, Vilegas W, Machado‐Neves M, Bressan GC, Leite JP Int J Exp Pathol 26-May-2020
PMCID:PMC7370850
doi:10.1111/iep.12351
PMID:32452573
Antidiabetic Potential of Medicinal Plants and Their Active Components Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J Biomolecules 30-Sep-2019
PMCID:PMC6843349
doi:10.3390/biom9100551
PMID:31575072
Polyphenols in Parkinson’s Disease: A Systematic Review of In Vivo Studies Kujawska M, Jodynis-Liebert J Nutrients 19-May-2018
PMCID:PMC5986521
doi:10.3390/nu10050642
PMID:29783725
Brazilian medicinal plants with corroborated anti-inflammatory activities: a review Ribeiro VP, Arruda C, Abd El-Salam M, Bastos JK Pharm Biol 12-Apr-2018
PMCID:PMC6130656
doi:10.1080/13880209.2018.1454480
PMID:29648503
Antinociceptive effects of hydroalcoholic extract from Euterpe oleracea Mart. (Açaí) in a rodent model of acute and neuropathic pain Sudo RT, Neto ML, Monteiro CE, Amaral RV, Resende ÂC, Souza PJ, Zapata-Sudo G, Moura RS BMC Complement Altern Med 02-Jul-2015
PMCID:PMC4489033
doi:10.1186/s12906-015-0724-2
PMID:26134625
Neuroprotective effects of anthocyanin- and proanthocyanidin-rich extracts in cellular models of Parkinson’s disease Strathearn KE, Yousef GG, Grace MH, Roy SL, Tambe MA, Ferruzzi MG, Wu QL, Simon JE, Lila MA, Rochet JC Brain Res 03-Feb-2014
PMCID:PMC4024464
doi:10.1016/j.brainres.2014.01.047
PMID:24502982
Recent Updates in Redox Regulation and Free Radical Scavenging Effects by Herbal Products in Experimental Models of Parkinson’s Disease Koppula S, Kumar H, More SV, Lim HW, Hong SM, Choi DK Molecules 26-Sep-2012
PMCID:PMC6268813
doi:10.3390/molecules171011391
PMID:23014498
Database Survey of Anti-Inflammatory Plants in South America: A Review de Morais Lima GR, de Albuquerque Montenegro C, de Almeida CL, de Athayde-Filho PF, Barbosa-Filho JM, Batista LM Int J Mol Sci 21-Apr-2011
PMCID:PMC3127143
doi:10.3390/ijms12042692
PMID:21731467

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
> Alkaloids and derivatives / Aporphines
Isoboldine 133323 Click to see 327.40 unknown https://doi.org/10.1055/S-2006-957745
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
(9R)-4,16-dimethoxy-12-methyl-12-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,13,15-hexaene-5,15-diol 163195216 Click to see 327.40 unknown https://doi.org/10.1055/S-2006-957745
4,16-Dimethoxy-12-methyl-12-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,13,15-hexaene-5,15-diol 162894725 Click to see 327.40 unknown https://doi.org/10.1055/S-2006-957745
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(6aR,9R,9aS,9bS)-9-prop-1-en-2-yl-5,6,6a,7,8,9,9a,9b-octahydro-1H-azuleno[4,5-c]furan-3-one 162872212 Click to see 232.32 unknown https://doi.org/10.1016/S0031-9422(00)84129-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84129-1
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/S0031-9422(00)84129-1
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84129-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)84129-1
An inositol 892 Click to see 180.16 unknown https://doi.org/10.1016/S0031-9422(00)84129-1
Npc174356 440079 Click to see 194.18 unknown https://doi.org/10.1016/S0031-9422(00)84129-1
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
4-Isopropyl-2-cyclohexen-1-one, (S)-(+)- 11542798 Click to see CC(C)C1CCC(=O)C=C1 138.21 unknown https://doi.org/10.1016/S0031-9422(00)84129-1
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(-)-Reticuline 440586 Click to see 329.40 unknown https://doi.org/10.1055/S-2006-957745
(S)-Laudanine 821396 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC)OC 343.40 unknown https://doi.org/10.1055/S-2006-957745
1-((3-Hydroxy-4-methoxyphenyl)methyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-7-ol 10233 Click to see 329.40 unknown https://doi.org/10.1055/S-2006-957745
Laudanidine 442304 Click to see 343.40 unknown https://doi.org/10.1055/S-2006-957745
Laudanine 92732 Click to see 343.40 unknown https://doi.org/10.1055/S-2006-957745
Reticuline 439653 Click to see 329.40 unknown https://doi.org/10.1055/S-2006-957745
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Quercetin 3-alloside 12304327 Click to see 464.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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