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Gelsemium rankinii

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 UUID64401d81c1bf3694118560
Scientific name Gelsemium rankinii
Authority Small
First published in Addisonia 13: 37 (1928)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Gelsemium sempervirens var. inodorum Nutt. Gen. N. Amer. Pl. 1: 171 1818

Common names Top

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Language Common/alternative name
English rankin's trumpetflower
English swamp jessamine
Persian یاسمن باتلاق
Japanese ランキンジャスミン
Malayalam സ്വാംപ് ജെസ്സാമൈൻ
Malayalam റാങ്കിൻസ് ട്രംപെറ്റ് ഫ്ളവർ
Malayalam ജെൽസിമിയം റാങ്കിനി

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
  • Northern America
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • Georgia
      • Louisiana
      • Mississippi
      • North Carolina
      • South Carolina

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000696052
Florida Plant Atlas 2997
Flora of Alabama 2569
USDA Plants GERA4
Tropicos 19000446
KEW urn:lsid:ipni.org:names:108096-2
The Plant List kew-2818734
Open Tree Of Life 257883
NCBI Taxonomy 427661
Nature Serve 2.128807
IPNI 108096-2
iNaturalist 163220
GBIF 3169515
EPPO GELRA
EOL 581132
Wikipedia Gelsemium_rankinii

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
Network Pharmacology and Experimental Verification to Unveil the Mechanism of N-Methyl-D-Aspartic Acid Rescue Humantenirine-Induced Excitotoxicity Qi XJ, Huang CY, Zuo MT, Gong MD, Huang SJ, Tang MH, Liu ZY Metabolites 28-Jan-2023
PMCID:PMC9966887
doi:10.3390/metabo13020195
PMID:36837814
Sex Differences in the In Vivo Exposure Process of Multiple Components of Gelsemium elegans in Rats Zuo MT, Gong MD, Ma X, Xu WB, Wang ZY, Tang MH, Wu Y, Liu ZY Metabolites 24-Dec-2022
PMCID:PMC9865510
doi:10.3390/metabo13010033
PMID:36676958
Excretion, Metabolism, and Tissue Distribution of Gelsemium elegans (Gardn. & Champ.) Benth in Pigs Ma X, Wang ZY, Zuo MT, Yang K, Sun ZL, Wu Y, Liu ZY Molecules 18-Apr-2022
PMCID:PMC9025967
doi:10.3390/molecules27082605
PMID:35458803
In Situ Visual Distribution of Gelsemine, Koumine, and Gelsenicine by MSI in Gelsemium elegans at Different Growth Stages Wu ZH, Su Y, Luo ZF, Sun ZL, Gong ZH, Xiao LT Molecules 10-Mar-2022
PMCID:PMC8952314
doi:10.3390/molecules27061810
PMID:35335173
Suppressive Effects of Gelsemine on Anxiety-like Behaviors Induced by Chronic Unpredictable Mild Stress in Mice Yu H, Tang MH, Zeng ZY, Huang SJ, Zheng XF, Liu ZY Brain Sci 30-Jan-2022
PMCID:PMC8870043
doi:10.3390/brainsci12020191
PMID:35203954
A network pharmacology-based investigation on the bioactive ingredients and molecular mechanisms of Gelsemium elegans Benth against colorectal cancer Que W, Chen M, Yang L, Zhang B, Zhao Z, Liu M, Cheng Y, Qiu H BMC Complement Med Ther 20-Mar-2021
PMCID:PMC7981997
doi:10.1186/s12906-021-03273-7
PMID:33743701
Gene expression profile analysis of ileum transcriptomes in pigs fed Gelsemium elegans plants Huang CY, Yang K, Cao JJ, Li YJ, Wang ZY, Yu H, Sun ZL, Zheng X, Liu ZY Sci Rep 31-Oct-2019
PMCID:PMC6823445
doi:10.1038/s41598-019-52374-4
PMID:31673142
Whole-genome sequencing and analysis of the Chinese herbal plant Gelsemium elegans Liu Y, Tang Q, Cheng P, Zhu M, Zhang H, Liu J, Zuo M, Huang C, Wu C, Sun Z, Liu Z Acta Pharm Sin B 16-Aug-2019
PMCID:PMC7016290
doi:10.1016/j.apsb.2019.08.004
PMID:32082980
A Potential Mechanism for the Anti-Apoptotic Property of Koumine Involving Mitochondrial Pathway in LPS-Mediated RAW 264.7 Macrophages Yuan ZH, Liang ZE, Wu J, Yi JE, Chen XJ, Sun ZL Molecules 01-Oct-2016
PMCID:PMC6273091
doi:10.3390/molecules21101317
PMID:27706063
Koumine Attenuates Lipopolysaccaride-Stimulated Inflammation in RAW264.7 Macrophages, Coincidentally Associated with Inhibition of NF-κB, ERK and p38 Pathways Yuan Z, Matias FB, Wu J, Liang Z, Sun Z Int J Mol Sci 22-Mar-2016
PMCID:PMC4813280
doi:10.3390/ijms17030430
PMID:27011173
Gelsemine alleviates both neuropathic pain and sleep disturbance in partial sciatic nerve ligation mice Wu YE, Li YD, Luo YJ, Wang TX, Wang HJ, Chen SN, Qu WM, Huang ZL Acta Pharmacol Sin 21-Sep-2015
PMCID:PMC4635333
doi:10.1038/aps.2015.86
PMID:26388157
Koumine enhances spinal cord 3α-hydroxysteroid oxidoreductase expression and activity in a rat model of neuropathic pain Qiu HQ, Xu Y, Jin GL, Yang J, Liu M, Li SP, Yu CX Mol Pain 09-Aug-2015
PMCID:PMC4529695
doi:10.1186/s12990-015-0050-1
PMID:26255228
New oxindole and indole alkaloids from Gelsemium rankinii Mariko Kitajima, Hiromi Kobayashi, Noriyuki Kogure, Hiromitsu Takayama Elsevier BV 21-Jun-2010
doi:10.1016/J.TET.2010.06.032
New humantenine-type indole alkaloids with iridoid unit from Gelsemium species Noriyuki Kogure, Hiromi Kobayashi, Naoko Ishii, Mariko Kitajima, Sumphan Wongseripipatana, Hiromitsu Takayama Elsevier BV 09-Apr-2008
doi:10.1016/J.TETLET.2008.03.148
21-Oxogelsevirine, a New Alkaloid from Gelsemium rankinii Yeh Schun, Geoffrey A. Cordell, Mark Garland American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50045A017

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 / Gelsemium alkaloids
(1R,2R,3R,4R,7Z,8R,9S)-7-ethylidene-3-hydroxy-1'-methoxy-5-methylspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 163189534 Click to see 370.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
(1R,2S,4S,7E,8R,9S)-7-ethylidene-1'-methoxy-5-methylspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 101520842 Click to see 354.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
(1R,2S,4S,7E,8S,9S)-7-ethylidene-1',6'-dimethoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 134611785 Click to see CC=C1CNC2CC3(C4CC1C2CO4)C5=C(C=C(C=C5)OC)N(C3=O)OC 370.40 unknown https://doi.org/10.1021/NP50047A007
(1R,2S,4S,7E,8S,9S)-7-ethylidene-8-hydroxy-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 101520840 Click to see 356.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
(1R,2S,4S,7R,8S,9S)-7-ethyl-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 163189459 Click to see 342.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
(1R,2S,4S,7Z,8R,9S)-5-[(Z)-[(3aS,4S,5S,6S,6aR)-4,6-dihydroxy-4-(hydroxymethyl)-5-methyl-2-oxo-3a,5,6,6a-tetrahydrocyclopenta[b]furan-3-ylidene]methyl]-7-ethylidene-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 101858926 Click to see CC=C1CN(C2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC)C=C6C7C(C(C(C7(CO)O)C)O)OC6=O 552.60 unknown https://doi.org/10.1016/J.TETLET.2008.03.148
(1R,2S,4S,7Z,8R,9S)-7-ethylidene-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 101855843 Click to see CC=C1CNC2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC 340.40 unknown https://doi.org/10.1021/NP50047A007
https://doi.org/10.1016/J.TET.2010.06.032
(1R,2S,5S,6S,7S,8R,11S)-2-ethenyl-1'-methoxy-4-methylspiro[9-oxa-4-azatetracyclo[6.3.1.02,6.05,11]dodecane-7,3'-indole]-2',3-dione 162876182 Click to see 366.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
https://doi.org/10.1021/NP50045A017
(1R,2S,5S,6S,7S,8R,11S)-2-ethenyl-1'-methoxyspiro[9-oxa-4-azatetracyclo[6.3.1.02,6.05,11]dodecane-7,3'-indole]-2'-one 162962774 Click to see CON1C2=CC=CC=C2C3(C1=O)C4CC5C(CO4)C6C3C5(CN6)C=C 338.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
(1R,2S,5S,6S,7S,8R)-2-ethenyl-1'-methoxy-4-methylspiro[9-oxa-4-azatetracyclo[6.3.1.02,6.05,11]dodecane-7,3'-indole]-2'-one 137345981 Click to see 352.40 unknown https://doi.org/10.1021/NP50045A017
(1S,2S,4R,7Z,8S,9R)-7-ethylidene-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 163187214 Click to see CC=C1CNC2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC 340.40 unknown https://doi.org/10.1021/NP50047A007
(1S,2S,4S,7Z,8R,9S,12S)-7-ethylidene-12-hydroxy-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 162989062 Click to see CC=C1CNC2CC3(C4C(C1C2CO4)O)C5=CC=CC=C5N(C3=O)OC 356.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
(1S,2S,5S,6S,7S,8R,11R)-2-ethenyl-1'-methoxy-4-methylspiro[9-oxa-4-azatetracyclo[6.3.1.02,6.05,11]dodecane-7,3'-indole]-2',3-dione 102450893 Click to see CN1C2C3COC4CC3C(C2C45C6=CC=CC=C6N(C5=O)OC)(C1=O)C=C 366.40 unknown https://doi.org/10.1021/NP50045A017
2-Ethenyl-1'-methoxyspiro[9-oxa-4-azatetracyclo[6.3.1.02,6.05,11]dodecane-7,3'-indole]-2'-one 162962773 Click to see CON1C2=CC=CC=C2C3(C1=O)C4CC5C(CO4)C6C3C5(CN6)C=C 338.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
21-Oxogelsevirine 184299 Click to see CN1C2C3COC4CC3C(C2C45C6=CC=CC=C6N(C5=O)OC)(C1=O)C=C 366.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
5-[[4,6-Dihydroxy-4-(hydroxymethyl)-5-methyl-2-oxo-3a,5,6,6a-tetrahydrocyclopenta[b]furan-3-ylidene]methyl]-7-ethylidene-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 163020258 Click to see CC=C1CN(C2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC)C=C6C7C(C(C(C7(CO)O)C)O)OC6=O 552.60 unknown https://doi.org/10.1016/J.TETLET.2008.03.148
7-Ethyl-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 163049342 Click to see 342.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
7-Ethylidene-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 129606 Click to see 340.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
7-Ethylidene-1',6'-dimethoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 78385037 Click to see CC=C1CNC2CC3(C4CC1C2CO4)C5=C(C=C(C=C5)OC)N(C3=O)OC 370.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
7-Ethylidene-12-hydroxy-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 162989061 Click to see 356.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
7-Ethylidene-3-hydroxy-1'-methoxy-5-methylspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 163048275 Click to see 370.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
7-Ethylidene-8-hydroxy-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 163038986 Click to see 356.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
CID 75055101 75055101 Click to see CC=C1CN(C2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC)C 354.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
Gelsemine, 1-methoxy- 572828 Click to see 352.40 unknown https://doi.org/10.1021/NP50045A017
https://doi.org/10.1016/J.TET.2010.06.032
Gelsevirine 14217344 Click to see 352.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
Humantenine 44593672 Click to see CC=C1CN(C2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC)C 354.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
Humantenirine 11132403 Click to see CC=C1CNC2CC3(C4CC1C2CO4)C5=C(C=C(C=C5)OC)N(C3=O)OC 370.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
> Alkaloids and derivatives / Macroline alkaloids
(1R,12S,13S,14S,15Z)-15-ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-1-ol 163190977 Click to see 310.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
15-Ethylidene-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2(10),4,6,8-tetraen-1-ol 162956541 Click to see 310.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Lippidulcine A 11673265 Click to see 252.35 unknown https://doi.org/10.1021/NP50047A007
> Organoheterocyclic compounds / Indoles and derivatives
(1R,2S,7Z,8R,9S)-7-ethylidene-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodec-4-ene-2,3'-indole]-2'-one 102477482 Click to see CC=C1CN=C2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC 338.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
7-Ethylidene-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodec-4-ene-2,3'-indole]-2'-one 162897159 Click to see 338.40 unknown https://doi.org/10.1016/J.TET.2010.06.032
> Organoheterocyclic compounds / Indolizidines
(1S,2S,8S,9S)-9-methoxy-14-oxa-7-azatetracyclo[6.6.1.01,11.02,7]pentadec-11-en-13-one 21601587 Click to see COC1CC2=CC(=O)OC23CC1N4C3CCCC4 249.30 unknown https://doi.org/10.1021/NP50047A007

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