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Internal ID UUID644036c69ef5c881343137
Scientific name Croton laevigatus
Authority Vahl
First published in Symb. Bot. 2: 97 (1791)

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Synonyms Top

Scientific name Authority First published in
Oxydectes laevigata Kuntze Revis. Gen. Pl. 2: 612 (1891)

Common names Top

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Language Common/alternative name
Arabic كروتون ناعم
French oxydectes oblongifolia
Chinese 光叶巴豆树
Chinese 光叶巴豆

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000931418
Tropicos 12804842
KEW urn:lsid:ipni.org:names:342808-1
The Plant List kew-50290
Open Tree Of Life 3913350
NCBI Taxonomy 1336182
IUCN Red List 152844445
IPNI 342808-1
iNaturalist 363034
GBIF 3059370
Freebase /m/03h4j5r
EOL 1147020
USDA GRIN 423370
Wikipedia Croton_laevigatus

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_949640765.1 SAMN08770956-DRAFT-NextGenCassava-1.0 Contig Cornell University 2023-04-09 142 586.19 Mb

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
The complete chloroplast genome of Euphorbia prostrata (Euphorbiaceae) Oh A, Kang ES, Son DC, Lee SR Mitochondrial DNA B Resour 08-Feb-2024
PMCID:PMC10860408
doi:10.1080/23802359.2024.2313039
PMID:38348094
Soil microbes support Janzen’s mountain passes hypothesis: The role of local-scale climate variability along a tropical montane gradient Feng Y, Wang J, Zhang J, Qi X, Long W, Ding Y, Liu L Front Microbiol 13-Mar-2023
PMCID:PMC10040759
doi:10.3389/fmicb.2023.1135116
PMID:36992924
Complete plastome sequence of Balakata baccata (Roxb.) Esser (Euphorbiaceae) Guo LY, Zhang XF, Zhu ZX, Wang HF Mitochondrial DNA B Resour 24-Apr-2021
PMCID:PMC8078922
doi:10.1080/23802359.2021.1910083
PMID:33969187
Complete plastome sequence of Croton laevigatus Vahl (Euphorbiaceae): an endemic species in Hainan, China Liao X, Wang HX, Zhu ZX, Wang HF Mitochondrial DNA B Resour 09-Jan-2020
PMCID:PMC7748857
doi:10.1080/23802359.2019.1704659
PMID:33366600
Tropical forest soils serve as substantial and persistent methane sinks Zhao JF, Peng SS, Chen MP, Wang GZ, Cui YB, Liao LG, Feng JG, Zhu B, Liu WJ, Yang LY, Tan ZH Sci Rep 14-Nov-2019
PMCID:PMC6856371
doi:10.1038/s41598-019-51515-z
PMID:31728015
Semisynthetic and SAR Studies of Amide Derivatives of Neocrotocembraneic Acid as Potential Antitumor Agents Shang H, Li LY, Cheng WH, Luo J, Zhang HW, Zou ZM Molecules 19-Nov-2016
PMCID:PMC6273784
doi:10.3390/molecules21111581
PMID:27869782
Chemical composition of Croton laevigatus G. A. Zou, H. A. Aisa, H. W. Zhang, J. S. Yang, Z. M. Zou Springer Science and Business Media LLC 06-Jan-2012
doi:10.1007/S10600-012-0126-3
Labdane diterpenoids from Croton oblongifolius S Roengsumran, A Petsom, D Sommit, T Vilaivan Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00604-9
Cytotoxic labdane diterpenoids from Croton oblongifolius. Roengsumran S, Petsom A, Kuptiyanuwat N, Vilaivan T, Ngamrojnavanich N, Chaichantipyuth C, Phuthong S Phytochemistry 01-Jan-2001
doi:10.1016/S0031-9422(00)00358-7
PMID:11198816

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
3-(4-hydroxy-3,5-dimethoxy-phenyl)propyl Benzoate 11623835 Click to see 316.30 unknown https://doi.org/10.1007/S10600-012-0126-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(1R,4aS,8aS)-5,5,8a-trimethyl-1-[(2E)-3-methylpenta-2,4-dienyl]-1,4,4a,6,7,8-hexahydronaphthalen-2-yl]methanol 100958596 Click to see CC(=CCC1C(=CCC2C1(CCCC2(C)C)C)CO)C=C 288.50 unknown https://doi.org/10.1016/S0031-9422(98)00604-9
[(2R,3R,4aR,5S,8aS)-3-hydroxy-1,1,4a-trimethyl-6-methylidene-5-[(2E)-3-methylpenta-2,4-dienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-yl] acetate 162965331 Click to see CC(=CCC1C(=C)CCC2C1(CC(C(C2(C)C)OC(=O)C)O)C)C=C 346.50 unknown https://doi.org/10.1016/S0031-9422(00)00358-7
[(2R,3R,4aS,8S,8aR)-3-hydroxy-4,4,8a-trimethyl-7-methylidene-8-[(2E)-3-methylpenta-2,4-dienyl]-2,3,4a,5,6,8-hexahydro-1H-naphthalen-2-yl] acetate 162874726 Click to see 346.50 unknown https://doi.org/10.1016/S0031-9422(00)00358-7
[3-hydroxy-4,4,8a-trimethyl-7-methylidene-8-(3-methylpenta-2,4-dienyl)-2,3,4a,5,6,8-hexahydro-1H-naphthalen-2-yl] acetate 78200769 Click to see CC(=CCC1C(=C)CCC2C1(CC(C(C2(C)C)O)OC(=O)C)C)C=C 346.50 unknown https://doi.org/10.1016/S0031-9422(00)00358-7
[5,5,8a-Trimethyl-1-(3-methylpenta-2,4-dienyl)-1,4,4a,6,7,8-hexahydronaphthalen-2-yl]methanol 78385187 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(98)00604-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[(1S,4S,5R)-4-[(3R)-3-hydroxybutyl]-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21630884 Click to see CC1CC(CC(C1CCC(C)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O 376.50 unknown https://doi.org/10.1007/S10600-012-0126-3
2-[4-(3-Hydroxybutyl)-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 73815020 Click to see 376.50 unknown https://doi.org/10.1007/S10600-012-0126-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1007/S10600-012-0126-3
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/10.1007/S10600-012-0126-3
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/10.1007/S10600-012-0126-3
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/10.1007/S10600-012-0126-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides
Piperacillin 43672 Click to see CCN1CCN(C(=O)C1=O)C(=O)NC(C2=CC=CC=C2)C(=O)NC3C4N(C3=O)C(C(S4)(C)C)C(=O)O 517.60 unknown https://doi.org/10.1016/S0031-9422(98)00604-9

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