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Croton crassifolius

Croton crassifolius - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64403678323dc275713649
Scientific name Croton crassifolius
Authority Geiseler
First published in Croton. Monogr. : 19 (1807)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tridesmis tomentosa Lour. Fl. Cochinch. : 576 (1790)
Oxydectes tomentosa Kuntze Revis. Gen. Pl. 2: 613 (1891)
Tridesmis hispida Lour. Fl. Cochinch. : 576 (1790)
Croton chinensis Benth. Fl. Hongk. : 309 (1861)
Croton crozophoroides Kurz J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 42: 243 (1873)
Croton kroneanus Miq. J. Bot. Néerl. 1: 97 (1861)
Croton tomentosus (Lour.) Müll.Arg. Linnaea 34: 107 (1865)

Common names Top

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Language Common/alternative name
French croton chinensis
French croton crozophoroides
French croton kroneanus
French oxydectes tomentosa
French tridesmis hispida
French tridesmis tomentosa
Chinese 鸡骨香
Chinese 雞骨香
Chinese 黃牛香

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

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Database ID/link to page
World Flora Online wfo-0000927753
Tropicos 50064912
KEW urn:lsid:ipni.org:names:342364-1
The Plant List kew-49708
Open Tree Of Life 850988
NCBI Taxonomy 323043
IPNI 342364-1
iNaturalist 707916
GBIF 3058629
EOL 1147298

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
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B Molecules 21-Dec-2023
PMCID:PMC10780140
doi:10.3390/molecules29010060
PMID:38202643
Halimanes and cancer: ent-halimic acid as a starting material for the synthesis of antitumor drugs Roncero AM, Tobal IE, Moro RF, Diez D, Marcos IS Front Chem 22-Aug-2023
PMCID:PMC10477373
doi:10.3389/fchem.2023.1225355
PMID:37674527
Study on the Comprehensive Phytochemicals and the Anti-Ulcerative Colitis Effect of Saussurea pulchella Liu Y, Wang C, Wu J, Tan L, Gao P, Wu S, Tang D, Wang Q, Wang C, Li P, Liu J Molecules 04-Feb-2023
PMCID:PMC9964537
doi:10.3390/molecules28041526
PMID:36838515
Mallotucin D, a Clerodane Diterpenoid from Croton crassifolius, Suppresses HepG2 Cell Growth via Inducing Autophagic Cell Death and Pyroptosis Dai X, Sun F, Deng K, Lin G, Yin W, Chen H, Yang D, Liu K, Zhang Y, Huang L Int J Mol Sci 17-Nov-2022
PMCID:PMC9698996
doi:10.3390/ijms232214217
PMID:36430694
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
Advances on Natural Abietane, Labdane and Clerodane Diterpenes as Anti-Cancer Agents: Sources and Mechanisms of Action Acquaviva R, Malfa GA, Loizzo MR, Xiao J, Bianchi S, Tundis R Molecules 26-Jul-2022
PMCID:PMC9330018
doi:10.3390/molecules27154791
PMID:35897965
Neuroprotective Effects of Oligosaccharides in Rehmanniae Radix on Transgenic Caenorhabditis elegans Models for Alzheimer’s Disease Kang N, Luan Y, Jiang Y, Cheng W, Liu Y, Su Z, Liu Y, Tan P Front Pharmacol 17-Jun-2022
PMCID:PMC9247152
doi:10.3389/fphar.2022.878631
PMID:35784741
Therapeutic Potential of Natural Products in the Treatment of Renal Cell Carcinoma: A Review Feng C, Lyu Y, Gong L, Wang J Nutrients 28-May-2022
PMCID:PMC9182762
doi:10.3390/nu14112274
PMID:35684073
Anticancer Effect of Tanshinones on Female Breast Cancer and Gynecological Cancer Jin Z, Chenghao Y, Cheng P Front Pharmacol 25-Jan-2022
PMCID:PMC8822147
doi:10.3389/fphar.2021.824531
PMID:35145409
Crassifolins Q−W: Clerodane Diterpenoids From Croton crassifolius With Anti-Inflammatory and Anti-Angiogenesis Activities Li C, Sun X, Yin W, Zhan Z, Tang Q, Wang W, Zhuo X, Wu Z, Zhang H, Li Y, Zhang Y, Wang G Front Chem 20-Sep-2021
PMCID:PMC8488372
doi:10.3389/fchem.2021.733350
PMID:34616713
Antiviral medicinal plants found in Lanna traditional medicine Julsrigival J, Sirisa-ard P, Julsrigival S, Akarchariya N Chin Herb Med 20-Sep-2021
PMCID:PMC8451407
doi:10.1016/j.chmed.2021.09.006
PMID:34567096
Potential of Bioactive Food Components against Gastric Cancer: Insights into Molecular Mechanism and Therapeutic Targets Kang SY, Hwang D, Shin S, Park J, Kim M, Rahman MH, Rahman MA, Ko SG, Kim B Cancers (Basel) 07-Sep-2021
PMCID:PMC8469857
doi:10.3390/cancers13184502
PMID:34572730
Osteoimmunology: The Regulatory Roles of T Lymphocytes in Osteoporosis Zhang W, Dang K, Huai Y, Qian A Front Endocrinol (Lausanne) 11-Aug-2020
PMCID:PMC7431602
doi:10.3389/fendo.2020.00465
PMID:32849268
Assessing the Identity of Commercial Herbs From a Cambodian Market Using DNA Barcoding Cui X, Li W, Wei J, Qi Y, Li R, Yang Y, Shi Y, Meng X, Mi Y, Huot T, Sun W, Zheng X Front Pharmacol 24-Mar-2020
PMCID:PMC7105672
doi:10.3389/fphar.2020.00244
PMID:32265692

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
methyl (1S,5S,6R,8aR)-5-[2-(furan-3-yl)-2-oxoethyl]-8a-hydroxy-1,5,6-trimethyl-3-oxo-2,6,7,8-tetrahydronaphthalene-1-carboxylate 102022433 Click to see CC1CCC2(C(=CC(=O)CC2(C)C(=O)OC)C1(C)CC(=O)C3=COC=C3)O 374.40 unknown https://doi.org/10.5246/JCPS.2016.11.092
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.5246/JCPS.2016.11.092

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