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Swertia calycina

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 UUID644046565ec12010511917
Scientific name Swertia calycina
Authority Franch.
First published in Bull. Soc. Bot. France 46: 311 1899

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 叶萼獐牙菜
Chinese 草黄莲

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001063813
Tropicos 13802814
KEW urn:lsid:ipni.org:names:370825-1
The Plant List tro-13802814
Open Tree Of Life 776379
NCBI Taxonomy 166613
IPNI 370825-1
GBIF 5596333
EOL 2892709
CMAUP NPO22457

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
Identification and Mode of Action of a Plant Natural Product Targeting Human Fungal Pathogens Dorsaz S, Snäkä T, Favre-Godal Q, Maudens P, Boulens N, Furrer P, Ebrahimi SN, Hamburger M, Allémann E, Gindro K, Queiroz EF, Riezman H, Wolfender JL, Sanglard D Antimicrob Agents Chemother 24-Aug-2017
PMCID:PMC5571344
doi:10.1128/AAC.00829-17
PMID:28674054
Two New Xanthone Glucosides from Swertia mussotii Franch Ganpeng Li, Lu Gao, Yongfu Zhou, Haiying Yan, Feiyan Huang, Rongrong Wen The Japan Institute of Heterocyclic Chemistry 13-Jun-2011
doi:10.3987/COM-11-12257
In Vitro Activity of 2-methoxy-1,4-naphthoquinone and Stigmasta-7,22-diene-3β-ol from Impatiens balsamina L. against Multiple Antibiotic-Resistant Helicobacter pylori Wang YC, Li WY, Wu DC, Wang JJ, Wu CH, Liao JJ, Lin CK Evid Based Complement Alternat Med 14-Feb-2011
PMCID:PMC3137247
doi:10.1093/ecam/nep147
PMID:19773391
Swertia (Gentianaceae): chemical and pharmacological aspects. Brahmachari G, Mondal S, Gangopadhyay A, Gorai D, Mukhopadhyay B, Saha S, Brahmachari AK Chem Biodivers 01-Nov-2004
doi:10.1002/CBDV.200490123
PMID:17191805
The potential of LC-NMR in phytochemical analysis. Wolfender JL, Ndjoko K, Hostettmann K Phytochem Anal 01-Jan-2001
doi:10.1002/1099-1565(200101/02)12:1<2::AID-PCA552>3.0.CO;2-K
PMID:11704957
An antifungal naphthoquinone, xanthones and secoiridoids from Swertia calycina. Rodriguez S, Wolfender JL, Hakizamungu E, Hostettmann K Planta Med 01-Aug-1995
doi:10.1055/S-2006-958102
PMID:7480185

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 / Naphthalenes / Naphthoquinones
2-Methoxy-1,4-naphthoquinone 16871 Click to see COC1=CC(=O)C2=CC=CC=C2C1=O 188.18 unknown https://doi.org/10.1055/S-2006-958102
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
trans-Norbixin 25245949 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC(=O)[O-])C=CC=C(C)C=CC(=O)[O-] 378.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
(2S)-2-ammonio-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoate 25201348 Click to see 776.87 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(2R,3R,4S,5R,6S)-6-hydroxy-3,4,5-tris(3-nitropropanoyloxy)oxan-2-yl]methyl 3-nitropropanoate 14261126 Click to see 584.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(-)-Sweroside 161036 Click to see 358.34 unknown https://doi.org/10.1055/S-2006-958102
https://doi.org/10.1002/1099-1565(200101/02)12:1<2::AID-PCA552>3.0.CO;2-K
(3R,4S,4aR)-4-ethenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 9906781 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown via CMAUP database
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 354447 Click to see 358.34 unknown https://doi.org/10.1002/1099-1565(200101/02)12:1<2::AID-PCA552>3.0.CO;2-K
https://doi.org/10.1055/S-2006-958102
Gentiopicroside 88708 Click to see 356.32 unknown https://doi.org/10.1055/S-2006-958102
Indoxyl-beta-D-glucoside 441564 Click to see 295.29 unknown via CMAUP database
Iridiod monoterpenoid 12443156 Click to see 374.34 unknown via CMAUP database
Swertiapunimarin 192515 Click to see 520.50 unknown via CMAUP database
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins / Allantoins
(S)-(+)-allantoin 439714 Click to see 158.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxy-3,5-dimethoxy-xanthen-9-one 5479773 Click to see COC1=CC=CC2=C1OC3=CC(=CC(=C3C2=O)O)OC 272.25 unknown https://doi.org/10.1055/S-2006-958102
1,5-dihydroxy-3-methoxy-8-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 44144324 Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)O)O 436.40 unknown https://doi.org/10.3987/COM-11-12257
2,6,8-trihydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 5321889 Click to see 422.30 unknown via CMAUP database
3-O-Demethylswertipunicoside 10372399 Click to see 680.50 unknown https://doi.org/10.3987/COM-11-12257
Decussatin 5378284 Click to see 302.28 unknown https://doi.org/10.1002/CBDV.200490123
https://doi.org/10.1055/S-2006-958102
Demethylbellidifolin 5281626 Click to see 260.20 unknown via CMAUP database
Isogentiakochianoside 15714468 Click to see 568.50 unknown https://doi.org/10.1055/S-2006-958102
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-2006-958102
Swerchirin 5281660 Click to see 288.25 unknown via CMAUP database
Swertianin 5281661 Click to see 274.22 unknown https://doi.org/10.1055/S-2006-958102
Swertianolin 5281662 Click to see 436.40 unknown via CMAUP database
Swertipunicoside 5321573 Click to see COC1=CC(=C2C(=C1)OC3=C(C=C(C(=C3C2=O)O)C4=C5C(=C(C(=C4O)C6C(C(C(C(O6)CO)O)O)O)O)C(=O)C7=CC(=C(C=C7O5)O)O)O)O 694.50 unknown https://doi.org/10.3987/COM-11-12257
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
2-(3-oxo-1H-indol-2-ylidene)-1H-indol-3-one 5464295 Click to see C1=CC=C2C(=C1)C(=O)C(=C3C(=O)C4=CC=CC=C4N3)N2 262.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(2E)-1-(2,4-Dihydroxy-6-methoxyphenyl)-3-(2,6-dihydroxyphenyl)-2-propen-1-one 5321869 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=C(C=CC=C2O)O)O)O 302.28 unknown via CMAUP database

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