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Swertia mussotii

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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 UUID6440465b1f346997964838
Scientific name Swertia mussotii
Authority Franch.
First published in Bull. Soc. Bot. France 46: 316 (1899)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 藏茵陈
Chinese 桑斗
Chinese 川西獐牙菜
Chinese 藏菌陈

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Swertia mussotii var. flavescens T.N.Ho & S.W.Liu Acta Biol. Plateau Sin. 1: 47 (1982)

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

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-0001063891
Tropicos 13802901
KEW urn:lsid:ipni.org:names:370996-1
The Plant List tro-13802901
Open Tree Of Life 1000746
NCBI Taxonomy 137888
GBIF 7270272
EOL 2892742
CMAUP NPO927
IPNI 370996-1

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
Molecular Characterization and Phylogenetic Analysis of Centipedegrass [Eremochloa ophiuroides (Munro) Hack.] Based on the Complete Chloroplast Genome Sequence Wang H, Zhang Y, Zhang L, Wang J, Guo H, Zong J, Chen J, Li D, Li L, Liu J, Li J Curr Issues Mol Biol 19-Feb-2024
PMCID:PMC10888139
doi:10.3390/cimb46020106
PMID:38392224
Mechanisms and Therapeutic Strategies for MAFLD Targeting TLR4 Signaling Pathways Ren G, Bai C, Yi S, Cong Q, Zhu Y J Innate Immun 21-Dec-2023
PMCID:PMC10783892
doi:10.1159/000535524
PMID:38128497
Chia (Salvia hispanica L.), a Pre-Hispanic Food in the Treatment of Diabetes Mellitus: Hypoglycemic, Antioxidant, Anti-Inflammatory, and Inhibitory Properties of α-Glucosidase and α-Amylase, and in the Prevention of Cardiovascular Disease Tavera-Hernández R, Jiménez-Estrada M, Alvarado-Sansininea JJ, Huerta-Reyes M Molecules 13-Dec-2023
PMCID:PMC10745661
doi:10.3390/molecules28248069
PMID:38138560
Recent advances towards natural plants as potential inhibitors of SARS-Cov-2 targets He Z, Yuan J, Zhang Y, Li R, Mo M, Wang Y, Ti H Pharm Biol 22-Aug-2023
PMCID:PMC10446791
doi:10.1080/13880209.2023.2241518
PMID:37605622
Comparative transcriptome analysis to identify putative genes involved in carvacrol biosynthesis pathway in two species of Satureja, endemic medicinal herbs of Iran Shams S, Ismaili A, Firouzabadi FN, Mumivand H, Sorkheh K PLoS One 07-Jul-2023
PMCID:PMC10328369
doi:10.1371/journal.pone.0281351
PMID:37418504
Geographical equations of Swertia mussotii bioactivities: evidence from the western Sichuan region of China Wang X, Shen C, Chen T, Zhou X, Li Y Front Plant Sci 28-Jun-2023
PMCID:PMC10338117
doi:10.3389/fpls.2023.1112164
PMID:37448873
Comparative chloroplast genomics of 34 species in subtribe Swertiinae (Gentianaceae) with implications for its phylogeny Yang L, Deng S, Zhu Y, Da Q BMC Plant Biol 28-Mar-2023
PMCID:PMC10044379
doi:10.1186/s12870-023-04183-1
PMID:36977991
Transcriptome analysis and exploration of genes involved in the biosynthesis of secoiridoids in Gentiana rhodantha Zhang T, Wang M, Li Z, Wu X, Liu X PeerJ 08-Mar-2023
PMCID:PMC10007974
doi:10.7717/peerj.14968
PMID:36915654
Application of third-generation sequencing to herbal genomics Gao L, Xu W, Xin T, Song J Front Plant Sci 07-Mar-2023
PMCID:PMC10027759
doi:10.3389/fpls.2023.1124536
PMID:36959935
Antimicrobial and antibiofilm activity of isoorientin against carbapenem non-sensitive Escherichia coli from raw milk of goats Zuo J, Liu L, Hou S, Liu X, Teng J, Li P, Liu X J Anim Sci 10-Feb-2023
PMCID:PMC9985329
doi:10.1093/jas/skad047
PMID:36762933
Carbohydrates and secondary compounds of alpine tundra shrubs in relation to experimental warming Zhou Y, Yang M, Tai Z, Jia J, Luan D, Ma X BMC Plant Biol 10-Oct-2022
PMCID:PMC9549620
doi:10.1186/s12870-022-03851-y
PMID:36210454
A highly contiguous, scaffold-level nuclear genome assembly for the fever tree (Cinchona pubescens Vahl) as a novel resource for Rubiaceae research Canales NA, Pérez-Escobar OA, Powell RF, Töpel M, Kidner C, Nesbitt M, Maldonado C, Barnes CJ, Rønsted N, Przelomska NA, Leitch IJ, Antonelli A GigaByte 06-Oct-2022
PMCID:PMC10027117
doi:10.46471/gigabyte.71
PMID:36950143
An overview of remote monitoring methods in biodiversity conservation Kerry RG, Montalbo FJ, Das R, Patra S, Mahapatra GP, Maurya GK, Nayak V, Jena AB, Ukhurebor KE, Jena RC, Gouda S, Majhi S, Rout JR Environ Sci Pollut Res Int 05-Oct-2022
PMCID:PMC9534007
doi:10.1007/s11356-022-23242-y
PMID:36197618
RNA-dependent RNA polymerase (RdRp) natural antiviral inhibitors: a review Leite DR, Mantovani KM, Cordeiro SP, Maia FB, Betim FC, de Bona Sartor E, Montrucchio DP, de Fátima Gaspari Dias J, Miguel OG, Miguel MD Med Chem Res 29-Sep-2022
PMCID:PMC9520115
doi:10.1007/s00044-022-02963-2
PMID:36193545
Comparative chloroplast genome analyses of 23 species in Swertia L. (Gentianaceae) with implications for its phylogeny Yang L, Li J, Zhou G Front Genet 31-Aug-2022
PMCID:PMC9470856
doi:10.3389/fgene.2022.895146
PMID:36118878

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
> Alkaloids and derivatives / Protopine alkaloids
5,7,8,15-Tetrahydro-4-hydroxy-3-methoxy-6-methyl[1,3]benzodioxolo[5,6-e][2]benzazecin-14(6H)-one 1275589 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)O)OCO3 355.40 unknown via CMAUP database
7-Hydroxy-8-methoxy-11-methyl-17,19-dioxa-11-azatetracyclo[12.7.0.0(4,9).0(16,20)]henicosa-1(21),4(9),5,7,14,16(20)-hexaen-2-one 5321910 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)O)OC)OCO3 355.40 unknown via CMAUP database
Allocryptopine 98570 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3 369.40 unknown via CMAUP database
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[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/10.3987/COM-11-12257
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-O-Acetyl shanzhiside methyl ester 162823 Click to see CC(=O)OC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)C 448.40 unknown via CMAUP database
Mussaenoside 182423 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aS,6bR,10S,12aR)-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-carboxylate 10416408 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 618.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Lupeol palmitate 161739 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 665.10 unknown via CMAUP database
Oleanolic Acid (Caryophyllin) 49867939 Click to see CC1(CC2C(CCC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(C1)C(=O)O)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(Z)-6-[(3R,6S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enoic acid 5319260 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
beta-D-glucose 64689 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,8-Dihydroxy-2,6-dimethoxy-9H-xanthen-9-one 5281653 Click to see COC1=C(C2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)OC)O 288.25 unknown via CMAUP database
3,5,6-trimethoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one 54672679 Click to see COC1=C(C2=C(C=C1)C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)OC)OC 464.40 unknown https://doi.org/10.3987/COM-11-12257
Decussatin 5378284 Click to see COC1=C(C2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)OC)OC 302.28 unknown via CMAUP database
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/10.3987/COM-11-12257
Norathyriol 5281656 Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)O 260.20 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-Reticuline 440586 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown via CMAUP database
Norsanguinarine 97679 Click to see C1OC2=C(O1)C3=CN=C4C(=C3C=C2)C=CC5=CC6=C(C=C54)OCO6 317.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Swertisin 124034 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.3987/COM-11-12257

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