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Croton sublyratus

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 UUID644036f3ea55d886706758
Scientific name Croton sublyratus
Authority Kurz
First published in J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 42: 243 (1873)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Oxydectes sublyrata Kuntze Revis. Gen. Pl. 2: 614 (1891)

Common names Top

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Language Common/alternative name
Chinese 矮巴豆

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-0000932489
Tropicos 50179976
KEW urn:lsid:ipni.org:names:343576-1
The Plant List kew-51298
Open Tree Of Life 542043
NCBI Taxonomy 107238
IPNI 343576-1
GBIF 3059809
EOL 1146516
USDA GRIN 465123

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
The Capsicum terpenoid biosynthetic module is affected by spider-mite herbivory Zhang Y, Kashkooli AB, Blom S, Zhao T, Bouwmeester HJ, Kappers IF Plant Mol Biol 23-Nov-2023
PMCID:PMC10721696
doi:10.1007/s11103-023-01390-0
PMID:37995005
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
Health Benefits and Pharmacological Properties of Stigmasterol Bakrim S, Benkhaira N, Bourais I, Benali T, Lee LH, El Omari N, Sheikh RA, Goh KW, Ming LC, Bouyahya A Antioxidants (Basel) 27-Sep-2022
PMCID:PMC9598710
doi:10.3390/antiox11101912
PMID:36290632
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
The Modulation of Melanogenesis in B16 Cells Upon Treatment with Plant Extracts and Isolated Plant Compounds Merecz-Sadowska A, Sitarek P, Kowalczyk T, Zajdel K, Kucharska E, Zajdel R Molecules 07-Jul-2022
PMCID:PMC9324663
doi:10.3390/molecules27144360
PMID:35889231
Phytochemicals With Anti 5-alpha-reductase Activity: A Prospective For Prostate Cancer Treatment Azizi A, Mumin NH, Shafqat N F1000Res 06-Jul-2021
PMCID:PMC8276191
doi:10.12688/f1000research.51066.1
PMID:34316358
Chemical Structure and Biological Activities of Secondary Metabolites from Salicornia europaea L. Kim S, Lee EY, Hillman PF, Ko J, Yang I, Nam SJ Molecules 13-Apr-2021
PMCID:PMC8069253
doi:10.3390/molecules26082252
PMID:33924656
Plants against Helicobacter pylori to combat resistance: An ethnopharmacological review Baker DA Biotechnol Rep (Amst) 21-May-2020
PMCID:PMC7248673
doi:10.1016/j.btre.2020.e00470
PMID:32477900
Anti-melanogenic effects of extracellular vesicles derived from plant leaves and stems in mouse melanoma cells and human healthy skin Lee R, Ko HJ, Kim K, Sohn Y, Min SY, Kim JA, Na D, Yeon JH J Extracell Vesicles 18-Dec-2019
PMCID:PMC6968621
doi:10.1080/20013078.2019.1703480
PMID:32002169
Screening for Plant Volatile Emissions with Allelopathic Activity and the Identification of L-Fenchone and 1,8-Cineole from Star Anise (Illicium verum) Leaves Kang G, Mishyna M, Appiah KS, Yamada M, Takano A, Prokhorov V, Fujii Y Plants (Basel) 28-Oct-2019
PMCID:PMC6918414
doi:10.3390/plants8110457
PMID:31661792
Tracing the biosynthetic origin of limonoids and their functional groups through stable isotope labeling and inhibition in neem tree (Azadirachta indica) cell suspension Aarthy T, Mulani FA, Pandreka A, Kumar A, Nandikol SS, Haldar S, Thulasiram HV BMC Plant Biol 11-Oct-2018
PMCID:PMC6186041
doi:10.1186/s12870-018-1447-6
PMID:30314459
Chemopreventive and anti-breast cancer activity of compounds isolated from leaves of Abrus precatorius L. Sofi MS, Sateesh MK, Bashir M, Ganie MA, Nabi S 3 Biotech 11-Aug-2018
PMCID:PMC6087508
doi:10.1007/s13205-018-1395-8
PMID:30105196
Biotechnology, In Vitro Production of Natural Bioactive Compounds, Herbal Preparation, and Disease Management (Treatment and Prevention) Alamgir AN Therapeutic Use of Medicinal Plants and their Extracts: Volume 2 24-Jun-2018
PMCID:PMC7123938
doi:10.1007/978-3-319-92387-1_7
Anti melanogenic effect of Croton roxburghii and Croton sublyratus leaves in α-MSH stimulated B16F10 cells Chatatikun M, Yamauchi T, Yamasaki K, Aiba S, Chiabchalard A J Tradit Complement Med 30-Apr-2018
PMCID:PMC6335448
doi:10.1016/j.jtcme.2017.12.002
PMID:30671368
Thai plants with high antioxidant levels, free radical scavenging activity, anti-tyrosinase and anti-collagenase activity Chatatikun M, Chiabchalard A BMC Complement Altern Med 09-Nov-2017
PMCID:PMC5679376
doi:10.1186/s12906-017-1994-7
PMID:29121910

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
(2S,4aS,5R,8aS)-5-[(3R)-3-hydroxy-3-methylpent-4-enyl]-1,1,4a-trimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol 162880531 Click to see 306.50 unknown https://doi.org/10.1016/0031-9422(81)85108-4
5-(3-hydroxy-3-methylpent-4-enyl)-1,1,4a-trimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol 13918625 Click to see 306.50 unknown https://doi.org/10.1016/0031-9422(81)85108-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Plaunotol 5282197 Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)CO)C)C 306.50 unknown https://doi.org/10.1007/S002990050195
https://doi.org/10.1055/S-2006-957428
https://doi.org/10.1016/S0031-9422(97)00743-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Kauran-16,17-diol 13816761 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C 306.50 unknown https://doi.org/10.1016/0031-9422(81)85108-4
Kaurane-16,17-diol 13816758 Click to see 306.50 unknown https://doi.org/10.1016/0031-9422(81)85108-4
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
5(S),9(S),10(S)-15,16-Epoxycleroda-3,8,13(16),14-tetraene-19,18:20,12(S)-diolactone (swassin) 91741938 Click to see 340.40 unknown https://doi.org/10.1016/S0031-9422(00)80114-4
https://doi.org/10.1107/S010827018300431X
Plaunolide 155330 Click to see C=C1CCC23COC(=O)C2=CCCC3C14CC(OC4=O)C5=COC=C5 340.40 unknown https://doi.org/10.1016/S0031-9422(00)80114-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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(02)00555-1
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(02)00555-1
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(02)00555-1
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,5'S,6S,8S,9S,12R)-5'-(furan-3-yl)-6-hydroxy-12-(hydroxymethyl)-10-methylidenespiro[2-oxatricyclo[6.3.1.04,12]dodec-4-ene-9,3'-oxolane]-2',3-dione 5320635 Click to see 372.40 unknown https://doi.org/10.1248/CPB.28.227
5'-(Furan-3-yl)-12-(hydroxymethyl)-10-methylidenespiro[2-oxatricyclo[6.3.1.04,12]dodec-4-ene-9,3'-oxolane]-2',3-dione 433180 Click to see 356.40 unknown https://doi.org/10.1248/CPB.28.227
5'-(Furan-3-yl)-6-hydroxy-12-(hydroxymethyl)-10-methylidenespiro[2-oxatricyclo[6.3.1.04,12]dodec-4-ene-9,3'-oxolane]-2',3-dione 78385415 Click to see 372.40 unknown https://doi.org/10.1248/CPB.28.227
Plaunol B 442074 Click to see C=C1CC2C3(C(C14CC(OC4=O)C5=COC=C5)CCC=C3C(=O)O2)CO 356.40 unknown https://doi.org/10.1248/CPB.28.227
> Organoheterocyclic compounds / Oxanes
(1S,2S,4S,9R,12S,13R)-12-[(2S)-2-(furan-3-yl)-2-hydroxyethyl]-4,13-dihydroxy-11-methylidene-8,14-dioxatetracyclo[7.6.0.01,6.02,12]pentadec-5-en-7-one 163185627 Click to see 374.40 unknown https://doi.org/10.1248/CPB.28.227
[(1S)-2-[(1R,2S,4S,9R,12S,13R)-4,13-dihydroxy-11-methylidene-7-oxo-8,14-dioxatetracyclo[7.6.0.01,6.02,12]pentadec-5-en-12-yl]-1-(furan-3-yl)ethyl] acetate 5320637 Click to see 416.40 unknown https://doi.org/10.1248/CPB.28.227
[2-(4,13-Dihydroxy-11-methylidene-7-oxo-8,14-dioxatetracyclo[7.6.0.01,6.02,12]pentadec-5-en-12-yl)-1-(furan-3-yl)ethyl] acetate 78385416 Click to see 416.40 unknown https://doi.org/10.1248/CPB.28.227
12-[2-(Furan-3-yl)-2-hydroxyethyl]-4,13-dihydroxy-11-methylidene-8,14-dioxatetracyclo[7.6.0.01,6.02,12]pentadec-5-en-7-one 5088770 Click to see C=C1CC2C34COC(C1(C3CC(C=C4C(=O)O2)O)CC(C5=COC=C5)O)O 374.40 unknown https://doi.org/10.1248/CPB.28.227

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