Iochroma fuchsioides - Unknown
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Internal ID UUID644041243a181376666679
Scientific name Iochroma fuchsioides
Authority (Bonpl.) Miers
First published in London J. Bot. 7: 345. 1848

Description Top

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Synonyms Top

Scientific name Authority First published in
Chaenesthes fuchsioides (Bonpl.) Miers London J. Bot. 4: 337. 1845
Dunalia aurantiaca Dunal Prodr. [A. P. de Candolle] 13(1): 527. 1852 [10 May 1852]
Iochroma edule S.Leiva Arnaldoa 3: 41, fig. 1995
Iochroma longipes Miers London J. Bot. 7: 344. 1848
Iochroma puniceum Werderm. Notizbl. Bot. Gart. Berlin-Dahlem 12: 371. 1935
Iochroma sodiroi Dammer Bot. Jahrb. Syst. 36: 385. 1905
Lycium fuchsioides Bonpl. Pl. Aequinoct. 1(6): 147. 1807 [Nov 1807]
Valteta fuchsioides (Bonpl.) Raf. Sylva Tellur. 53 (1838).

Common names Top

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Language Common/alternative name
German roter veilchenstrauch
Swedish röd violbuske
Chinese 金钟悬铃果

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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-0001021907
USDA Plants IOFU
Tropicos 29605037
KEW urn:lsid:ipni.org:names:815977-1
The Plant List tro-29605037
Open Tree Of Life 315013
Observations.org 370822
NCBI Taxonomy 304105
IPNI 815977-1
iNaturalist 550255
GBIF 3802334
Freebase /m/0zdk1s8
Elurikkus 416995
Wikipedia Iochroma_fuchsioides

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
A Systematic Review on the Therapeutic Effects of Ayahuasca Gonçalves J, Luís Â, Gallardo E, Duarte AP Plants (Basel) 07-Jul-2023
PMCID:PMC10346174
doi:10.3390/plants12132573
PMID:37447135
Psychoactive Substances of Natural Origin: Toxicological Aspects, Therapeutic Properties and Analysis in Biological Samples Gonçalves J, Luís Â, Gallardo E, Duarte AP Molecules 05-Mar-2021
PMCID:PMC7961374
doi:10.3390/molecules26051397
PMID:33807728
Toxicological Aspects and Determination of the Main Components of Ayahuasca: A Critical Review Simão AY, Gonçalves J, Duarte AP, Barroso M, Cristóvão AC, Gallardo E Medicines (Basel) 18-Oct-2019
PMCID:PMC6963515
doi:10.3390/medicines6040106
PMID:31635364
Sequencing the Vine of the Soul: Full Chloroplast Genome Sequence of Banisteriopsis caapi Ramachandran P, Zhang N, McLaughlin WB, Luo Y, Handy S, Duke JA, Vasquez R, Ottesen A Genome Announc 21-Jun-2018
PMCID:PMC6013603
doi:10.1128/genomeA.00203-18
PMID:29930028
The ethnobotany of psychoactive plant use: a phylogenetic perspective Alrashedy NA, Molina J PeerJ 05-Oct-2016
PMCID:PMC5068365
doi:10.7717/peerj.2546
PMID:27761334
How to make a red flower: the combinatorial effect of pigments Ng J, Smith SD AoB Plants 01-Mar-2016
PMCID:PMC4804202
doi:10.1093/aobpla/plw013
PMID:26933150
Discovery of novel plastid phenylalanine (trnF) pseudogenes defines a distinctive clade in Solanaceae Poczai P, Hyvönen J Springerplus 12-Sep-2013
PMCID:PMC3786074
doi:10.1186/2193-1801-2-459
PMID:24083106
The Withanolides of Iochroma fuchsioides Robert F. Raffauf, Melvin J. Shemluck, Philip W. Le Quesne American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50078A017

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 / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
18-acetoxywithanolide D 15519705 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)COC(=O)C)O)C 528.60 unknown https://doi.org/10.1021/NP50078A017
Withanolide D 161671 Click to see CC1=C(C(=O)OC(C1)C(C)(C2CCC3C2(CCC4C3CC5C6(C4(C(=O)C=CC6O)C)O5)C)O)C 470.60 unknown https://doi.org/10.1021/NP50078A017
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
Alanine 5950 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1021/NP50078A017
D-alanine 71080 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1021/NP50078A017
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Threonine 6288 Click to see CC(C(C(=O)O)N)O 119.12 unknown https://doi.org/10.1021/NP50078A017
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
l-Isoleucine 6306 Click to see CCC(C)C(C(=O)O)N 131.17 unknown https://doi.org/10.1021/NP50078A017
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine 6106 Click to see CC(C)CC(C(=O)O)N 131.17 unknown https://doi.org/10.1021/NP50078A017
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1021/NP50078A017
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
Serine 5951 Click to see C(C(C(=O)O)N)O 105.09 unknown https://doi.org/10.1021/NP50078A017
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Tyrosine 6057 Click to see C1=CC(=CC=C1CC(C(=O)O)N)O 181.19 unknown https://doi.org/10.1021/NP50078A017
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.1021/NP50078A017

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