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Croton salutaris

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 UUID644036e9cb5f2512833323
Scientific name Croton salutaris
Authority Casar.
First published in Nov. Stirp. Bras. 10: 89 (1845)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Oxydectes salutaris Kuntze Revis. Gen. Pl. 2: 612 (1891)
Croton angularis Klotzsch ex Baill. Adansonia 4: 299 (1864)
Croton urceolatus Baill. Adansonia 4: 299 (1864)

Common names Top

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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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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-0000932255
Tropicos 50169632
KEW urn:lsid:ipni.org:names:343416-1
The Plant List kew-51078
Open Tree Of Life 464300
NCBI Taxonomy 765406
IUCN Red List 189625565
IPNI 343416-1
GBIF 3058577
EOL 1146627
Wikipedia Croton_salutaris

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
Botanical Drugs in Traditional Chinese Medicine With Wound Healing Properties Ning S, Zang J, Zhang B, Feng X, Qiu F Front Pharmacol 12-May-2022
PMCID:PMC9133888
doi:10.3389/fphar.2022.885484
PMID:35645789
Dracorhodin perchlorate enhances wound healing via β-catenin, ERK/p38, and AKT signaling in human HaCaT keratinocytes Lu CC, Yang JS, Chiu YJ, Tsai FJ, Hsu YM, Yin MC, Juan YN, Ho TJ, Chen HP Exp Ther Med 02-Jun-2021
PMCID:PMC8193218
doi:10.3892/etm.2021.10254
PMID:34131445
In vivo pro-angiogenic effects of dracorhodin perchlorate in zebrafish embryos: A novel bioactivity evaluation platform for commercial dragon blood samples Krishnaraj P, Chang Y, Ho TJ, Lu NC, Lin MD, Chen HP J Food Drug Anal 28-Sep-2018
PMCID:PMC9298644
doi:10.1016/j.jfda.2018.08.005
PMID:30648579
Enantiomeric Natural Products: Occurrence and Biogenesis Finefield JM, Sherman DH, Kreitman M, Williams RM Angew Chem Int Ed Engl 03-May-2012
PMCID:PMC3498912
doi:10.1002/anie.201107204
PMID:22555867
Diterpenes from Croton salutaris Hideji Itokawa, Yoshitatsu Ichihara, Koichi Takeya, Hiroshi Morita, Mario Motidome Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83469-2
The alkaloids of Croton salutaris Roderick A. Barnes, Orlando M. Soeiro Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84192-8

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 / Phenanthrenes and derivatives
3-Hydroxy-4,13-dimethoxy-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5,10,13-pentaen-12-one 12313590 Click to see 313.30 unknown https://doi.org/10.1016/S0031-9422(00)84192-8
3-Hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo(7.5.3.01,10.02,7)heptadeca-2(7),3,5,10,13-pentaen-12-one 625160 Click to see 327.40 unknown https://doi.org/10.1016/S0031-9422(00)84192-8
N-Norsinoactine 12313591 Click to see 313.30 unknown https://doi.org/10.1016/S0031-9422(00)84192-8
Salutaridine, (-)- 821366 Click to see 327.40 unknown https://doi.org/10.1016/S0031-9422(00)84192-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aR,10aS)-6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 15127170 Click to see 272.40 unknown https://doi.org/10.1016/0031-9422(91)83469-2
6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 73033076 Click to see 272.40 unknown https://doi.org/10.1016/0031-9422(91)83469-2
8-ethenyl-6-hydroxy-1,1,4a,7-tetramethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one 162954057 Click to see 298.40 unknown https://doi.org/10.1016/0031-9422(91)83469-2
Sonderianol 15127169 Click to see CC1=C(C=C2C(=C1C=C)CCC3C2(CCC(=O)C3(C)C)C)O 298.40 unknown https://doi.org/10.1016/0031-9422(91)83469-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(5R,6E,10E,14S)-5,14-dihydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraene-4,12-dione 162957362 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(91)83469-2
(5R,6E,10Z,14S)-5,14-dihydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraene-4,12-dione 162957361 Click to see CC(=CC(=O)C(C(=CCCC(=CC(=O)CC(C)(C=C)O)C)C)O)C 334.40 unknown https://doi.org/10.1016/0031-9422(91)83469-2
5,14-Dihydroxy-2,6,10,14-tetramethylhexadeca-2,6,10,15-tetraene-4,12-dione 162957360 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(91)83469-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5S,6E,10R,14S)-5,14-dihydroxy-2,6,10,14-tetramethylhexadeca-2,6,15-triene-4,12-dione 162881288 Click to see 336.50 unknown https://doi.org/10.1016/0031-9422(91)83469-2
5,14-Dihydroxy-2,6,10,14-tetramethylhexadeca-2,6,15-triene-4,12-dione 162881287 Click to see 336.50 unknown https://doi.org/10.1016/0031-9422(91)83469-2

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