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Heliotropium taltalense

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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 UUID64402014bf07e165283475
Scientific name Heliotropium taltalense
Authority I.M.Johnst.
First published in Contr. Gray Herb. 81: 27 (1928)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cochranea taltalensis Phil. Anales Univ. Chile 90: 349 (1895)
Cochranea rugosa Phil. Anales Univ. Chile 90: 351 (1895)

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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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-0000718974
Tropicos 4000532
KEW urn:lsid:ipni.org:names:119895-2
The Plant List kew-2844532
Open Tree Of Life 357663
NCBI Taxonomy 248303
IPNI 119895-2
GBIF 4061361

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
Antiviral Properties of Polyphenols from Plants Chojnacka K, Skrzypczak D, Izydorczyk G, Mikula K, Szopa D, Witek-Krowiak A Foods 26-Sep-2021
PMCID:PMC8534698
doi:10.3390/foods10102277
PMID:34681326
The Effects of Flavonoids in Cardiovascular Diseases Ciumărnean L, Milaciu MV, Runcan O, Vesa ȘC, Răchișan AL, Negrean V, Perné MG, Donca VI, Alexescu TG, Para I, Dogaru G Molecules 21-Sep-2020
PMCID:PMC7571023
doi:10.3390/molecules25184320
PMID:32967119
Chemical Fingerprinting, Isolation and Characterization of Polyphenol Compounds from Heliotropium taltalense (Phil.) I.M. Johnst and Its Endothelium-Dependent Vascular Relaxation Effect in Rat Aorta Barrientos RE, Simirgiotis MJ, Palacios J, Paredes A, Bórquez J, Bravo A, Cifuentes F Molecules 08-Jul-2020
PMCID:PMC7397318
doi:10.3390/molecules25143105
PMID:32650373
Phytochemical Analysis, Antioxidant Activity, Fatty Acids Composition, and Functional Group Analysis of Heliotropium bacciferum Ahmad S, Ahmad S, Bibi A, Ishaq MS, Afridi MS, Kanwal F, Zakir M, Fatima F ScientificWorldJournal 12-Nov-2014
PMCID:PMC4247971
doi:10.1155/2014/829076
PMID:25489605
4′,5-Dihy­droxy-7-meth­oxy­flavanone dihydrate Brito I, Bórquez J, Simirgiotis M, Cárdenas A, López-Rodríguez M Acta Crystallogr Sect E Struct Rep Online 07-Dec-2011
PMCID:PMC3254395
doi:10.1107/S1600536811051221
PMID:22259537
Chemical analysis of the resinous exudate isolated from Heliotropium taltalense and evaluation of the antioxidant activity of the phenolics components and the resin in homogeneous and heterogeneous systems. Modak B, Rojas M, Torres R Molecules 02-Jun-2009
PMCID:PMC6254288
doi:10.3390/MOLECULES14061980
PMID:19512999
Chemical Analysis of the Resinous Exudate Isolated from Heliotropium taltalense and Evaluation of the Antioxidant Activity of the Phenolics Components and the Resin in Homogeneous and Heterogeneous Systems Modak B, Rojas M, Torres R Molecules 02-Jun-2009
PMCID:PMC6254288
doi:10.3390/molecules14061980
PMID:19512999

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Organoheterocyclic compounds / Benzofurans
(5-acetyl-2',2',4'-trimethylspiro[3H-1-benzofuran-2,3'-cyclohexane]-1'-yl) 3-methylbut-2-enoate 162856078 Click to see CC1CCC(C(C12CC3=C(O2)C=CC(=C3)C(=O)C)(C)C)OC(=O)C=C(C)C 370.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254288/
[(1'R,2R,4'S)-5-acetyl-2',2',4'-trimethylspiro[3H-1-benzofuran-2,3'-cyclohexane]-1'-yl] 3-methylbut-2-enoate 162856079 Click to see CC1CCC(C(C12CC3=C(O2)C=CC(=C3)C(=O)C)(C)C)OC(=O)C=C(C)C 370.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254288/
1-(3'-hydroxy-2',2',6'-trimethylspiro[3H-1-benzofuran-2,1'-cyclohexane]-5-yl)ethanone 162962344 Click to see CC1CCC(C(C12CC3=C(O2)C=CC(=C3)C(=O)C)(C)C)O 288.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254288/
1-[(2R,3'R,6'S)-3'-hydroxy-2',2',6'-trimethylspiro[3H-1-benzofuran-2,1'-cyclohexane]-5-yl]ethanone 162962345 Click to see CC1CCC(C(C12CC3=C(O2)C=CC(=C3)C(=O)C)(C)C)O 288.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254288/
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254288/
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254288/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Galangin 3-methyl ether 5281946 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 284.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254288/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
7-O-Methyleriodictyol 1268276 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)O 302.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254288/
Sternbin 4872981 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)O 302.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254288/

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