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Gentianella nitida

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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 UUID64401dcd2db83579039612
Scientific name Gentianella nitida
Authority (Griseb.) Fabris
First published in Bol. Soc. Argent. Bot. 7: 91 (1958)

Description Top

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Synonyms Top

Scientific name Authority First published in
Gentiana nitida Griseb. Gen. Sp. Gent. : 216 (1838)
Gentiana trichostemma Wedd. Chlor. Andina 2: 56 (1859)

Common names Top

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Language Common/alternative name
Dutch hercampuri

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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No forms added yet.

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000699352
KEW urn:lsid:ipni.org:names:108709-2
The Plant List kew-2822194
Open Tree Of Life 6069101
NCBI Taxonomy 2576744
IUCN Red List 133312230
IPNI 108709-2
GBIF 3841226
Freebase /m/0_x9m87
Wikipedia Gentianella_nitida

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
Population-Related Variability in Qualitative and Quantitative Secondary Metabolite Profile of Gentianella austriaca (A. & J. Kern.) Holub Popović Z, Vidaković V, Mijalković T, Krstić-Milošević D Plants (Basel) 23-Jun-2023
PMCID:PMC10346188
doi:10.3390/plants12132434
PMID:37446995
Total Synthesis of Terpenes and Their Biological Significance: A Critical Review Kanwal A, Bilal M, Rasool N, Zubair M, Shah SA, Zakaria ZA Pharmaceuticals (Basel) 11-Nov-2022
PMCID:PMC9699253
doi:10.3390/ph15111392
PMID:36422521
Peril in the market-classification and dosage of species used as anti-diabetics in Lima, Peru Bussmann RW, Paniagua-Zambrana N, Chamorro MR, Moreira NM, del Rosario Cuadros Negri ML, Olivera J J Ethnobiol Ethnomed 30-May-2013
PMCID:PMC3738155
doi:10.1186/1746-4269-9-37
PMID:23718140
Nitidasin, a Novel Sesterterpenoid, from the Peruvian Folk Medicine "Hercampuri" (Gentianella nitida). Nobuo KAWAHARA, Masato NOZAWA, Diana FLORES, Pablo BONILLA, Setsuko SEKITA, Motoyoshi SATAKE, Ken-ichi KAWAI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.45.1717
A new secoiridoid glucoside, amaronitidin, from the Peruvian folk medicine "Hercampuri" (Gentianella nitida). Kawahara N, Masuda K, Sekita S, Satake M Chem Pharm Bull (Tokyo) 01-Jun-2001
doi:10.1248/CPB.49.771
PMID:11411536
A novel sesterterpenoid, nitiol, as a potent enhancer of IL-2 gene expression in a human T cell line, from the Peruvian folk medicine "Hercumpuri" (Gentianella nitida). Kawahara N, Nozawa M, Kurata A, Hakamatsuka T, Sekita S, Satake M Chem Pharm Bull (Tokyo) 01-Sep-1999
doi:10.1248/CPB.47.1344
PMID:10517015
Secoiridoids and xanthones from Gentianella nitida. Lacaille-Dubois MA, Galle K, Wagner H Planta Med 01-Aug-1996
doi:10.1055/S-2006-957908
PMID:17252473

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
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[2-[(4-Ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 2,4-dihydroxy-6-(3-hydroxyphenyl)benzoate 12305846 Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O 602.50 unknown https://doi.org/10.1248/CPB.49.771
https://doi.org/10.1055/S-2006-957908
[2-[[(4aR)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 2,4-dihydroxy-6-(3-hydroxyphenyl)benzoate 137795174 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O 586.50 unknown https://doi.org/10.1248/CPB.49.771
https://doi.org/10.1055/S-2006-957908
Amarogentin 115149 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O 586.50 unknown https://doi.org/10.1248/CPB.49.771
https://doi.org/10.1055/S-2006-957908
Amaronitidin 101720810 Click to see C=CC1C(OC=C2C1=CCOC2=O)OC3C(C(C(C(O3)CO)O)O)OC4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O 556.50 unknown https://doi.org/10.1248/CPB.49.771
Amaroswerin 45359883 Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O 602.50 unknown https://doi.org/10.1055/S-2006-957908
https://doi.org/10.1248/CPB.49.771
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
[(2E,5S,6R,9R,11Z,15S,16S)-9,12,16-trimethyl-6-propan-2-yl-2-tricyclo[13.3.0.05,9]octadeca-1(18),2,11-trienyl]methanol 100983736 Click to see CC1CC=C2C1CCC(=CCC3(CCC(C3CC=C2CO)C(C)C)C)C 356.60 unknown https://doi.org/10.1248/CPB.47.1344
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(1R,2R,4S,7S,8S,11R,12R,14S,17R,18S)-1-hydroxy-2,7,11,14-tetramethyl-17-propan-2-yl-3-oxapentacyclo[10.7.0.02,4.04,8.014,18]nonadecan-16-one 10548340 Click to see CC1CCC2C(CCC23C(O3)(C4(C1CC5(CC(=O)C(C5C4)C(C)C)C)O)C)C 388.60 unknown https://doi.org/10.1248/CPB.45.1717
1-Hydroxy-2,7,11,14-tetramethyl-17-propan-2-yl-3-oxapentacyclo[10.7.0.02,4.04,8.014,18]nonadecan-16-one 53463029 Click to see CC1CCC2C(CCC23C(O3)(C4(C1CC5(CC(=O)C(C5C4)C(C)C)C)O)C)C 388.60 unknown https://doi.org/10.1248/CPB.45.1717
Nitidasin 177415 Click to see CC1CCC2C(CCC23C(O3)(C4(C1CC5(CC(=O)C(C5C4)C(C)C)C)O)C)C 388.60 unknown https://doi.org/10.1248/CPB.45.1717
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (2S,3R,4S)-3-ethenyl-4-(2-oxoethyl)-2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 162903410 Click to see COC(=O)C1=COC(C(C1CC=O)C=C)OC2C(C(C(C(O2)CO)O)O)O 388.40 unknown https://doi.org/10.1055/S-2006-957908
Methyl 2-(hexopyranosyloxy)-4-(2-oxoethyl)-3-vinyl-3,4-dihydro-2H-pyran-5-carboxylate 369002 Click to see COC(=O)C1=COC(C(C1CC=O)C=C)OC2C(C(C(C(O2)CO)O)O)O 388.40 unknown https://doi.org/10.1055/S-2006-957908
Secologanoside 14136854 Click to see C=CC1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC(=O)O 390.34 unknown https://doi.org/10.1055/S-2006-957908
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[2-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl] 3-hydroxybenzoate 75596313 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=CC=C4)O)O 478.40 unknown https://doi.org/10.1248/CPB.49.771
Decentapicrin A 157079 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=CC=C4)O)O 478.40 unknown https://doi.org/10.1248/CPB.49.771
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,2-Dihydroxy-6-methoxy-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyxanthen-9-one 85446566 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C5=C(O2)C=CC(=C5O)O 568.50 unknown https://doi.org/10.1055/S-2006-957908
1,2,6-Trihydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 78385589 Click to see C1=CC2=C(C(=C1O)O)C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1055/S-2006-957908
1,3,5-Trihydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 5857493 Click to see C1=CC(=C2C(=C1O)OC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 422.30 unknown https://doi.org/10.1055/S-2006-957908
1,3,5,8-Tetrahydroxyxanthone 5281626 Click to see C1=CC(=C2C(=C1O)C(=O)C3=C(C=C(C=C3O2)O)O)O 260.20 unknown https://doi.org/10.1055/S-2006-957908
1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one 5358385 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1055/S-2006-957908
2,8-Dihydroxy-6-methoxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 162915580 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 436.40 unknown https://doi.org/10.1055/S-2006-957908
Isogentiakochianoside 15714468 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)C(=O)C5=C(O2)C=CC(=C5O)O 568.50 unknown https://doi.org/10.1055/S-2006-957908
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1055/S-2006-957908
Norswertianin 5281658 Click to see C1=CC2=C(C(=C1O)O)C(=O)C3=C(C=C(C=C3O2)O)O 260.20 unknown https://doi.org/10.1055/S-2006-957908
Norswertianin 1-glucoside 5321888 Click to see C1=CC2=C(C(=C1O)O)C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown https://doi.org/10.1055/S-2006-957908
Norswertianolin 5281659 Click to see C1=CC(=C2C(=C1O)OC3=CC(=CC(=C3C2=O)O)O)OC4C(C(C(C(O4)CO)O)O)O 422.30 unknown https://doi.org/10.1055/S-2006-957908
Swertianin 5281661 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=C(C=C3)O)O)O 274.22 unknown https://doi.org/10.1055/S-2006-957908
Swertianin 8-glucoside 102506431 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 436.40 unknown https://doi.org/10.1055/S-2006-957908
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 6426860 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-957908
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-957908

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