Gelsemium rankinii, also known as Rankin's trumpetflower or swamp jessamine, is a climbing vine found in the southeastern United States. It can reach heights of up to 6 meters and has attractive glossy green leaves and bright yellow flowers. This plant is a member of the Gelsemiaceae family and is native to states such as Louisiana and the Carolinas.

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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Filter by language:

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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No subvariety added yet.

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

Northern America click to expand
- 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!
You can also contribute to this by clicking here.

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 CC=C1CN(C2C3C1CC(C4(C2O)C5=CC=CC=C5N(C4=O)OC)OC3)C	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 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
(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 CC=C1CNC2CC3(C4CC1(C2CO4)O)C5=CC=CC=C5N(C3=O)OC	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 CCC1CNC2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC	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 CN1C2C3COC4CC3C(C2C45C6=CC=CC=C6N(C5=O)OC)(C1=O)C=C	366.40	unknown	https://doi.org/10.1021/NP50045A017 https://doi.org/10.1016/J.TET.2010.06.032
(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 CN1CC2(C3CC4C5(C2C1C3CO4)C6=CC=CC=C6N(C5=O)OC)C=C	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
1-Methoxygelsemine	572828	Click to see CN1CC2(C3CC4C5(C2C1C3CO4)C6=CC=CC=C6N(C5=O)OC)C=C	352.40	unknown	https://doi.org/10.1016/J.TET.2010.06.032 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 CCC1CNC2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC	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 CC=C1CNC2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC	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 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
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 CC=C1CN(C2C3C1CC(C4(C2O)C5=CC=CC=C5N(C4=O)OC)OC3)C	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 CC=C1CNC2CC3(C4CC1(C2CO4)O)C5=CC=CC=C5N(C3=O)OC	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
Gelsevirine	14217344	Click to see CN1CC2(C3CC4C5(C2C1C3CO4)C6=CC=CC=C6N(C5=O)OC)C=C	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 CC=C1CN2C3CC4=C(C2(CC1C3CO)O)NC5=CC=CC=C45	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 CC=C1CN2C3CC4=C(C2(CC1C3CO)O)NC5=CC=CC=C45	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 CC1=CC(=O)C(CC1)C(C)(CC=CC(C)(C)O)O	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 CC=C1CN=C2CC3(C4CC1C2CO4)C5=CC=CC=C5N(C3=O)OC	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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Gelsemium rankinii

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top