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Croton hemiargyreus

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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 UUID644036bd1fce5299386245
Scientific name Croton hemiargyreus
Authority Müll.Arg.
First published in Linnaea 34: 81 (1865)

Description Top

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Synonyms Top

Scientific name Authority First published in
Oxydectes hemiargyrea Kuntze Revis. Gen. Pl. 2: 612 (1891)
Croton hemiargyreus var. gymnodiscus Müll.Arg. Fl. Bras. 11(2): 88 (1873)
Croton hemiargyreus var. genuinus Müll.Arg. Fl. Bras. 11(2): 88 (1873)

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

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Database ID/link to page
World Flora Online wfo-0000931216
Tropicos 12800951
KEW urn:lsid:ipni.org:names:342653-1
The Plant List kew-50101
Open Tree Of Life 740784
NCBI Taxonomy 765397
IUCN Red List 177817681
IPNI 342653-1
GBIF 3060012
EOL 1147119

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
Anticholinesterase Activity of Endemic Plant Extracts from Soqotra Bakthira H, Awadh Ali NA, Arnold N, Teichert A, Wessjohann L Afr J Tradit Complement Altern Med 02-Apr-2011
PMCID:PMC3252222
doi:10.4314/ajtcam.v8i3.65292
PMID:22468008
Identification of Isoquinoline alkaloids in crude extracts by high temperature gas chromatography-mass spectrometry Alberto S. Pereira, Ana Claudia F. Amaral, Roderick A. Barnes, Jari N. Cardoso, Francisco R. Aquino Neto Wiley 02-Dec-2005
doi:10.1002/(SICI)1099-1565(199909/10)10:5<254::AID-PCA462>3.0.CO;2-Q
A tetrahydroprotoberberine alkaloid from Croton hemiargyreus Ana Claudia F. Amaral, Roderick A. Barnes Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(97)00764-4
Rapid screening of natural products by high-resolution high-temperature gas chromatography. Carbonell SA, de Aquino Neto FR, Cardoso JN, dos Santos Pereira A, Amaral AC, Barnes RA J Chromatogr Sci 01-Jun-2000
doi:10.1093/CHROMSCI/38.6.234
PMID:10890746

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
> Alkaloids and derivatives / Aporphines
4,5,15,16-Tetramethoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),10,13,15-octaen-12-one 163026311 Click to see COC1=CC2=CC3=C4C(=CC(=C(C4=C2C=C1OC)OC)OC)C(=O)C=N3 351.40 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
Corydine 10153 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199909/10)10:5<254::AID-PCA462>3.0.CO;2-Q
Glaucine 16754 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
https://doi.org/10.1002/(SICI)1099-1565(199909/10)10:5<254::AID-PCA462>3.0.CO;2-Q
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199909/10)10:5<254::AID-PCA462>3.0.CO;2-Q
Oxoglaucine 97662 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC(=C(C=C42)OC)OC)OC 351.40 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(8S,13aR)-3,10-dimethoxy-8-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,11-diol 15380319 Click to see CC1C2=CC(=C(C=C2CC3N1CCC4=CC(=C(C=C34)O)OC)O)OC 341.40 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
3,10-dimethoxy-8-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,11-diol 163067845 Click to see CC1C2=CC(=C(C=C2CC3N1CCC4=CC(=C(C=C34)O)OC)O)OC 341.40 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
https://doi.org/10.1002/(SICI)1099-1565(199909/10)10:5<254::AID-PCA462>3.0.CO;2-Q
> 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 COC1=C(C2=C(CC3C4=CC(=O)C(=CC42CCN3)OC)C=C1)O 313.30 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
N-Norsinoactine 12313591 Click to see COC1=C(C2=C(CC3C4=CC(=O)C(=CC42CCN3)OC)C=C1)O 313.30 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
Salutaridine 5408233 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC 327.40 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
Sinoacutine 625160 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC 327.40 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Excisanin H 10066342 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C 348.40 unknown https://doi.org/10.1016/S0031-9422(97)00764-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1093/CHROMSCI/38.6.234
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1093/CHROMSCI/38.6.234
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1093/CHROMSCI/38.6.234
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aristolane sesquiterpenoids
Calarene 28481 Click to see CC1CCC=C2C1(C3C(C3(C)C)CC2)C 204.35 unknown https://doi.org/10.1093/CHROMSCI/38.6.234
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1093/CHROMSCI/38.6.234
> Organoheterocyclic compounds / Epoxides
Humulene epoxyde 5463721 Click to see CC1=CCC(C=CCC2(C(O2)CC1)C)(C)C 220.35 unknown https://doi.org/10.1093/CHROMSCI/38.6.234
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Reticulin 10233 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199909/10)10:5<254::AID-PCA462>3.0.CO;2-Q
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1002/(SICI)1099-1565(199909/10)10:5<254::AID-PCA462>3.0.CO;2-Q

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