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Croton jacobinensis

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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
Contributors
Collections

Details Top

Internal ID UUID644036c2c5ae4397128328
Scientific name Croton jacobinensis
Authority Baill.
First published in Adansonia 4: 302 (1864)

Description Top

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Synonyms Top

Scientific name Authority First published in
Oxydectes jacobinensis Kuntze Revis. Gen. Pl. 2: 612 (1891)
Croton auriculatus Müll.Arg. Linnaea 34: 98 (1865)

Common names Top

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Language Common/alternative name
French croton auriculatus
French oxydectes jacobinensis

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000931336
Tropicos 12800967
KEW urn:lsid:ipni.org:names:342744-1
The Plant List kew-50212
Open Tree Of Life 740794
NCBI Taxonomy 765399
IPNI 342744-1
GBIF 3057489
EOL 1147058

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
Chemistry and Bioactivity of Croton Essential Oils: Literature Survey and Croton hirtus from Vietnam Luu-dam NA, Le CV, Satyal P, Le TM, Bui VH, Vo VH, Ngo GH, Bui TC, Nguyen HH, Setzer WN Molecules 03-Mar-2023
PMCID:PMC10005233
doi:10.3390/molecules28052361
PMID:36903605
Chemical Composition and In Vitro and In Silico Antileishmanial Evaluation of the Essential Oil from Croton linearis Jacq. Stems García-Díaz J, Escalona-Arranz JC, Ochoa-Pacheco A, Santos SG, González-Fernández R, Rojas-Vargas JA, Monzote L, Setzer WN Antibiotics (Basel) 28-Nov-2022
PMCID:PMC9774621
doi:10.3390/antibiotics11121712
PMID:36551370
Local Knowledge and Use of Medicinal Plants in a Rural Community in the Agreste of Paraíba, Northeast Brazil da Costa Ferreira E, Anselmo MD, Guerra NM, Marques de Lucena C, Felix CD, Bussmann RW, Paniagua-Zambrana NY, Paiva de Lucena RF Evid Based Complement Alternat Med 29-Dec-2021
PMCID:PMC8731275
doi:10.1155/2021/9944357
PMID:35003314
Aqueous and Ethanolic Plant Extracts as Bio-Insecticides—Establishing a Bridge between Raw Scientific Data and Practical Reality Tavares WR, Barreto MD, Seca AM Plants (Basel) 04-May-2021
PMCID:PMC8147817
doi:10.3390/plants10050920
PMID:34064367
Cabbage Production in West Africa and IPM with a Focus on Plant-Based Extracts and a Complementary Worldwide Vision Mondédji AD, Silvie P, Nyamador WS, Martin P, Agboyi LK, Amévoin K, Ketoh GK, Glitho IA Plants (Basel) 11-Mar-2021
PMCID:PMC7998567
doi:10.3390/plants10030529
PMID:33799877
Volatile Constituents of Brazilian Euphorbiaceae. Genus Croton A. A. Craveiro, A. S. Rodrigues, C. H. S. Andrade, F. J. A. Matos, J. W. Alencar, M. I. L. Machado American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50017A019
The use of carbon-carbon connectivity in the structure determination of marmelerin, a novel benzofuran sesquiterpene from Croton sonderianus James D. McChesney, Edilberto R. Silveira, Afranio A. Craveiro, James N. Shoolery American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00200A028

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1021/NP50017A019
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1021/NP50017A019
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1021/NP50017A019
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,6,10-Trimethyl-2,6,9,11-dodecatetraene 442368 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1021/NP50017A019
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1021/NP50017A019
beta Farnesene 15228937 Click to see CCC(=C)CCC=C(C)CCC=C(C)C 206.37 unknown https://doi.org/10.1021/NP50017A019
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1021/JO00200A028
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C 204.35 unknown https://doi.org/10.1021/NP50017A019
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1021/NP50017A019

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Contributors Top

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Collections Top

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