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Swertia ciliata

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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 UUID6440465c82202918838581
Scientific name Swertia ciliata
Authority (G.Don) B.L.Burtt
First published in Notes Roy. Bot. Gard. Edinburgh 25: 272 (1965)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ophelia purpurascens D.Don London Edinburgh Philos. Mag. & J. Sci. 8: 77 (1836)
Ophelia ciliata D.Don ex G.Don Gen. Hist. 4: 178 (1837)
Swertia purpurascens Wall. ex Boiss. Fl. Orient. [Boissier] Suppl. 347. 1888 [Oct 1888]
Ophelia purpurascens var. ciliata (D.Don ex G.Don) D.Don Trans. Linn. Soc. London 17(4): 526. 1837 [18 Jul-8 Aug 1837]
Ophelia dalhousiana Griseb. Gen. Sp. Gent. 313–314 1839

Common names Top

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Language Common/alternative name
Chinese 大苦草
Chinese 普兰獐牙菜

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

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Database ID/link to page
World Flora Online wfo-0001063916
Tropicos 13802934
KEW urn:lsid:ipni.org:names:370838-1
The Plant List tro-13802934
Open Tree Of Life 776370
NCBI Taxonomy 166614
IPNI 370838-1
GBIF 5596312
EOL 2892710

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
In Vitro and In Silico Studies for the Identification of Potent Metabolites of Some High-Altitude Medicinal Plants from Nepal Inhibiting SARS-CoV-2 Spike Protein Basnet S, Marahatha R, Shrestha A, Bhattarai S, Katuwal S, Sharma KR, Marasini BP, Dahal SR, Basnyat RC, Patching SG, Parajuli N Molecules 15-Dec-2022
PMCID:PMC9786757
doi:10.3390/molecules27248957
PMID:36558090
Climate change‐induced distributional change of medicinal and aromatic plants in the Nepal Himalaya Shrestha UB, Lamsal P, Ghimire SK, Shrestha BB, Dhakal S, Shrestha S, Atreya K Ecol Evol 15-Aug-2022
PMCID:PMC9379350
doi:10.1002/ece3.9204
PMID:35991283
Traditional Herbal Knowledge among the Inhabitants: A Case Study in Urgam Valley of Chamoli Garhwal, Uttarakhand, India Singh A, Hart R, Chandra S, Nautiyal MC, Sayok AK Evid Based Complement Alternat Med 03-Jun-2019
PMCID:PMC6582913
doi:10.1155/2019/5656925
PMID:31275412
A Xanthone Dixylopyranoside from Swertia thomsonii Viqar Uddin Ahmad, Inayat-ur- Rahman, Murad Ali Khana, Muhammad Arfan, Mohammad Tariq Siddiqui Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNB-2002-0115
Phytochemical investigation of crude methanol extracts of different species of Swertia from Nepal Khanal S, Shakya N, Thapa K, Pant DR BMC Res Notes 26-Dec-2015
PMCID:PMC4691535
doi:10.1186/s13104-015-1753-0
PMID:26708007
Sustainable utilization and conservation of plant biodiversity in montane ecosystems: the western Himalayas as a case study Khan SM, Page SE, Ahmad H, Harper DM Ann Bot 03-Jul-2013
PMCID:PMC3718215
doi:10.1093/aob/mct125
PMID:23825353
Medicinal flora and ethnoecological knowledge in the Naran Valley, Western Himalaya, Pakistan Khan SM, Page S, Ahmad H, Shaheen H, Ullah Z, Ahmad M, Harper DM J Ethnobiol Ethnomed 10-Jan-2013
PMCID:PMC3570439
doi:10.1186/1746-4269-9-4
PMID:23302393
Ecological status and traditional knowledge of medicinal plants in Kedarnath Wildlife Sanctuary of Garhwal Himalaya, India Bhat JA, Kumar M, Bussmann RW J Ethnobiol Ethnomed 02-Jan-2013
PMCID:PMC3560114
doi:10.1186/1746-4269-9-1
PMID:23281594
Antiviral Activity of Some Plants Used in Nepalese Traditional Medicine Rajbhandari M, Mentel R, Jha PK, Chaudhary RP, Bhattarai S, Gewali MB, Karmacharya N, Hipper M, Lindequist U Evid Based Complement Alternat Med 25-Oct-2007
PMCID:PMC2781767
doi:10.1093/ecam/nem156
PMID:18955262
Flafvonoids of Swertia purpurascens G.A. Miana Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84477-5
Chemical constituents of gentianaceae. X. Xanthone-O-glucosides of Swertia purpurascens Wall. Ghosal S, Sharma PV, Chaudhuri RK J Pharm Sci 01-Aug-1974
doi:10.1002/JPS.2600630827
PMID:4527698

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 / Prenol lipids / Triterpenoids
(4aS,6aR,6aR,6bS,8aS,10R,12aS,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162942879 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)84477-5
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(00)84477-5
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1515/ZNB-2002-0115
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17S)-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 162965363 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84477-5
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1515/ZNB-2002-0115
https://doi.org/10.1016/S0031-9422(00)84477-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,5-dihydroxy-3-methoxy-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 5321571 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/10.1002/JPS.2600630827
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/10.1515/ZNB-2002-0115
1,5-Dihydroxy-3-methoxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 5858086 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/10.1002/JPS.2600630827
5,8-dihydroxy-3-methoxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 162943176 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C=CC(=C4O2)O)O 436.40 unknown https://doi.org/10.1002/JPS.2600630827
5,8-Dihydroxy-3-methoxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-xanthen-9-one 5479784 Click to see COC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C=CC(=C4O2)O)O 436.40 unknown https://doi.org/10.1002/JPS.2600630827
Bellidifolin 5281623 Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)O)O)O 274.22 unknown https://doi.org/10.1515/ZNB-2002-0115
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/10.1515/ZNB-2002-0115
Swertianolin 5281662 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/10.1002/JPS.2600630827
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(3E)-3-(aminomethylidene)oxane-2,4-dione 5281569 Click to see C1COC(=O)C(=CN)C1=O 141.12 unknown https://doi.org/10.1016/S0031-9422(00)84477-5
Enicoflavine 5281564 Click to see C=CC(C=O)C1(CCOC(=O)C1=CN)O 211.21 unknown https://doi.org/10.1016/S0031-9422(00)84477-5
> Organoheterocyclic compounds / Pyranopyridines
Gentianine 354616 Click to see C=CC1=CN=CC2=C1CCOC2=O 175.18 unknown https://doi.org/10.1016/S0031-9422(00)84477-5

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