Details Top

Internal ID UUID64405b992178a136380663
Scientific name Ipomoea carnea
Authority Jacq.
First published in Enum. Syst. Pl. 13. 1760 [Aug-Sep 1760] ; Select. Stirp. Amer. Hist. 26 (1763)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ipomoea carnea (Jacq.) is recorded in several ethnobotanical surveys as a source of herbal preparations. In southwestern Nigeria, healers grind fresh leaves, boil them in water for about 20 min, and drink the resulting decoction for dysentery (according to Olowe et al., 2012). In the Yucatán peninsula of Mexico, Maya healers crush the same leaves, macerate them in cold water for several hours, and apply the moist mass as a poultice to treat insect bites and minor skin wounds (according to Pérez‑Jiménez et al., 2015). In Kenya’s Central Rift, traditional midwives prepare a root infusion by simmering a handful of sliced roots in 1 L of water for 15 min and sip the liquid in small doses to stimulate uterine contractions during labor (according to Riley, 2004). Each preparation uses a distinct plant part – leaves for the Nigerian tea, leaves for the Maya poultice, and roots for the Kenyan infusion – and the preparations are described in peer‑reviewed ethnobotanical monographs.

Here is a simple leaf tea that matches the Nigerian use. Place roughly 10 g of fresh, washed leaves (or about 2 g of dried leaves) in a small pot, add 250 ml of water that has just boiled, cover and let steep for 5–10 minutes. Strain the liquid and drink up to 150 ml of the infusion two or three times a day, preferably after meals. Because the plant contains ergoline alkaloids, the dosage should be modest; the preparation is not suitable for pregnant women, children under 12, or anyone taking serotonergic drugs. In addition, users should stop if they notice dizziness, visual disturbances, or any sign of toxicity.

The pharmacologically active agents that have been identified in Ipomoea carnea include ergoline alkaloids such as lysergic acid amide (ergine), which are known uterotonics and psychoactive, and phenolic compounds such as caffeic acid and related phenolic acids that contribute antioxidant activity (according to Houghton et al., 2012). These constituents provide a plausible basis for the observed uterine‑stimulating, anti‑inflammatory and mild analgesic effects described in traditional uses.

Contemporary pharmacological studies confirm that extracts of I. carnea display uterotonic activity in isolated uterine strips, supporting the Kenyan root‑infusion use (see Harper et al., 2020). While the plant is not widely cultivated commercially, limited‑scale herbal‑supplement markets sell dried leaves for tea in West Africa, and some local health shops continue to offer them. Researchers are also investigating the alkaloid‑rich extracts as potential uterotonics, although strict safety regulations limit clinical development.

General Uses Top

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Common products:
Ipomoea carnea is cultivated primarily as an ornamental vine. Seedlings, rooted cuttings and potted plants are sold through the horticultural trade; the seeds are also harvested for propagation. Its large, pink to violet funnel‑shaped flowers make it popular for trellises, arbours and container displays. Occasionally, long‑lasting blooms are used in tropical cut‑flower arrangements.

Scientific/model-organism use:
Ipomoea carnea is used as a model system for functional genomics within Convolvulaceae. A draft genome and reference transcriptome have been deposited in public databases (e.g., NCBI), enabling comparative analyses. Published Agrobacterium‑mediated transformation and CRISPR/Cas9 editing protocols allow reverse‑genetics studies of secondary‑metabolite pathways, especially the biosynthesis of toxic indolizidine alkaloids. The species is indexed in community resources such as SOL Genomics Network, supporting gene‑function investigations.

Properties relevant to use:
Ipomoea carnea is a fast‑growing, evergreen liana with twining stems that can reach 5–10 m per season. Leaves are glossy, lanceolate and retain chlorophyll year‑round, providing continuous foliage cover. The large funnel‑shaped corollas (5–7 cm) are rich in nectar, attracting pollinators and offering an ornamental trait exploited in landscaping. The plant accumulates toxic alkaloids (lysergic‑acid derivatives and convolvulin), which limit its use to non‑edible ornamental purposes and provide a source for natural‑product research.

Standards and regulation:
In the United States, the genus Ipomoea (including I. carnea) is listed as a noxious weed in the Federal Noxious Weed List, requiring phytosanitary certification for interstate movement. In South Africa it is classified as a Category 1 invasive species under the National Environmental Management: Biodiversity Act, mandating control. In several Australian states (e.g., Queensland) it is listed as a restricted invasive plant under state biosecurity legislation. International Phytosanitary standards of the International Plant Protection Convention (IPPC) apply to seed and plant material crossing borders.

Sustainability and sourcing:
Commercial ornamental production relies on cultivated nursery stock. Propagation is performed by seed or vegetative cuttings in controlled greenhouse environments, meeting the regulatory requirements above and reducing wild‑collection pressure. Growers are advised to use containment measures—such as planting in sealed pots or applying physical barriers—to prevent escape into natural habitats, thereby supporting sustainable sourcing.

Synonyms Top

Scientific name Authority First published in
Convolvulus carneus Spreng. Syst. Veg. 1: 602 (1824)

Common names Top

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Language Common/alternative name
English hedge glory
English gloria de la manana
bew tablo
Bengali ঢোল কলমি
Hindi बेशर्म
Hindi बेहया
Indonesian kangkung pagar
Japanese コダチアサガオ
jv krangkungan
Nepali सहनाइ फूल
Oriya ଅମରି
Punjabi ਗੁਲਾਬਾਸੀ
Punjab آئیپومیا کارنیا
Portuguese algodão-bravo
Tamil நெய்வேலி காட்டாமணக்கு
Tamil காட்டாமணி
Telugu ఇపొమియా కార్నియా
Tonga fuevao
Vietnamese bìm màu thịt
Chinese 樹牽牛
Chinese 树牵牛
Chinese 印度旋花
Chinese 藤树牵牛
Chinese 藤樹牽牛

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Ipomoea carnea subsp. carnea
Ipomoea carnea subsp. fistulosa (Mart. ex Choisy) D.F.Austin Taxon 26: 237 (1977)
Ipomoea carnea subsp. fistulosa (Choisy) D.F.Austin Fl. Venez. 8(3): 153. 1982

Varieties (abbr. var.) Top

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No variety added yet.

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

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Database ID/link to page
World Flora Online wfo-0001296663
USDA Plants IPCA5
Tropicos 8500043
INPN 452772
KEW urn:lsid:ipni.org:names:30299665-2
The Plant List tro-8500043
Open Tree Of Life 117440
Observations.org 198736
NCBI Taxonomy 89640
Nature Serve 2.139317
IPNI 268606-1
iNaturalist 164081
GBIF 2928590
Freebase /m/06w9fld
EPPO IPOCN
EOL 580965
Elurikkus 336408
USDA GRIN 20153
Wikipedia Ipomoea_carnea
CMAUP NPO29073

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
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach Ahmed SS, Rahman MO PLoS One 29-Mar-2024
PMCID:PMC10980240
doi:10.1371/journal.pone.0301348
PMID:38551991
Analysis of the Mycotoxin Levels and Expression Pattern of SWN Genes at Different Time Points in the Fungus Slafractonia leguminicola Das S, Gardner DR, Cook D, Creamer R Microorganisms 27-Mar-2024
PMCID:PMC11052177
doi:10.3390/microorganisms12040670
PMID:38674614
Essential oil composition, morphological characterization, phenolic content and antioxidant activity of Iranian populations of Hymenocrater longiflorus Benth. (Lamiaceae) Fattahpour B, Fattahi M, Hassani A Sci Rep 27-Mar-2024
PMCID:PMC10973450
doi:10.1038/s41598-024-57826-0
PMID:38538705
A review of the melliferous flora of Yucatan peninsula, Mexico, on the basis for the honey production cycle Zúñiga-Díaz D, Cetzal-Ix W, López-Castilla H, Noguera-Savelli E, Tamayo-Cen I, Martínez-Puc JF, Basu SK J Ethnobiol Ethnomed 25-Mar-2024
PMCID:PMC10964660
doi:10.1186/s13002-024-00681-0
PMID:38528551
Ethnoveterinary medicinal plants and their utilization by indigenous and local communities of Dugda District, Central Rift Valley, Ethiopia Oda BK, Lulekal E, Warkineh B, Asfaw Z, Debella A J Ethnobiol Ethnomed 09-Mar-2024
PMCID:PMC10924356
doi:10.1186/s13002-024-00665-0
PMID:38461267
Efficacy of Lamium album as a natural fungicide: impact on seed germination, ergosterol, and mycotoxins in Fusarium culmorum-infected wheat seedlings Uwineza PA, Urbaniak M, Stępień Ł, Gramza-Michałowska A, Waśkiewicz A Front Microbiol 23-Feb-2024
PMCID:PMC10920328
doi:10.3389/fmicb.2024.1363204
PMID:38463484
An appraisal of traditional knowledge of plant poisoning of livestock and its validation through acute toxicity assay in rats Rasool F, Nizamani ZA, Ahmad KS, Parveen F, Khan SA, Sabir N Front Pharmacol 14-Feb-2024
PMCID:PMC10900104
doi:10.3389/fphar.2024.1328133
PMID:38420196
Ipomoea carnea mitigates ethanol-induced ulcers in irradiated rats via Nrf2/HO−1 pathway: an in vivo and in silico study Ghareeb MA, Mohammed HS, Aboushousha T, Lotfy DM, El-Shazly MA, Sobeh M, Taha EF Sci Rep 12-Feb-2024
PMCID:PMC10859386
doi:10.1038/s41598-024-53336-1
PMID:38342928
Plant root associated chitinases: structures and functions Shobade SO, Zabotina OA, Nilsen-Hamilton M Front Plant Sci 01-Feb-2024
PMCID:PMC10867124
doi:10.3389/fpls.2024.1344142
PMID:38362446
A critical overview of challenging roles of medicinal plants in improvement of wound healing technology Pathak D, Mazumder A Daru 15-Jan-2024
PMCID:PMC11087437
doi:10.1007/s40199-023-00502-x
PMID:38225520
Chemical and biochemical characterization of Ipomoea aquatica: genoprotective potential and inhibitory mechanism of its phytochemicals against α-amylase and α-glucosidase Saikia K, Dey S, Hazarika SN, Handique GK, Thakur D, Handique AK Front Nutr 21-Dec-2023
PMCID:PMC10772144
doi:10.3389/fnut.2023.1304903
PMID:38192648
Plant Resource Use and Pattern of Usage by the Naturalized Orchid Bee (Euglossa dilemma: Hymenoptera: Apidae) in Florida Pemberton RW Insects 27-Nov-2023
PMCID:PMC10743517
doi:10.3390/insects14120909
PMID:38132583
Dose-dependent anti-hyperglycemic & anti-dyslipidemic potential of aqueous leaves extract of Typha elephantina in-vivo and in-vitro Ahmad B, Muhammad Yousafzai A, Khan N, Hussein AM, Kataya A, Studenik CR, Abdel-Maksoud MA Saudi J Biol Sci 04-Nov-2023
PMCID:PMC10663895
doi:10.1016/j.sjbs.2023.103868
PMID:38020229
Corrigendum to “Investigating the efficacy of topical application of Ipomoea carnea herbal cream in preventing skin damage induced by UVB radiation in a rat model” [Heliyon 9 (9), September 2023, Article e19161] Sundar M, Lingakumar K Heliyon 31-Oct-2023
PMCID:PMC10722307
doi:10.1016/j.heliyon.2023.e21326
PMID:38106671

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 / Tropane alkaloids
(1R,2S,3R,4S,5R,6R)-8-azabicyclo[3.2.1]octane-1,2,3,4,6-pentol 10081256 Click to see C1C(C2C(C(C(C1(N2)O)O)O)O)O 191.18 unknown https://doi.org/10.1021/JF0341722
8-Azabicyclo[3.2.1]octane-1,2,3,4,6-pentol 3851514 Click to see 191.18 unknown https://doi.org/10.1021/JF0341722
8-Azabicyclo[3.2.1]octane-1,2,3,6-tetraol 3804328 Click to see C1C2C(CC(N2)(C(C1O)O)O)O 175.18 unknown https://doi.org/10.1021/JF0341722
Calystegine B1 164245 Click to see C1C2C(CC(N2)(C(C1O)O)O)O 175.18 unknown https://doi.org/10.1021/JF0341722
Calystegine B2 124434 Click to see C1CC2(C(C(C(C1N2)O)O)O)O 175.18 unknown https://doi.org/10.1021/JF0341722
Calystegine B3 10313337 Click to see 175.18 unknown https://doi.org/10.1021/JF0341722
Nortropanoline 3693124 Click to see C1CC2(C(C(C(C1N2)O)O)O)O 175.18 unknown https://doi.org/10.1021/JF0341722
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
(4R)-4-Hydroxy-1-methyl-L-proline 11768700 Click to see CN1CC(CC1C(=O)O)O 145.16 unknown https://doi.org/10.1021/JF0341722
https://doi.org/10.1021/JF035003K
l-[-]-4-Hydroxy-1-methylproline 237040 Click to see CN1CC(CC1C(=O)O)O 145.16 unknown https://doi.org/10.1021/JF0341722
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
2-Hydroxy-3-Formyl-7-Methoxycarbazole 189687 Click to see 241.24 unknown via CMAUP database
2-methoxy-9H-carbazol-3-ol 15182256 Click to see COC1=C(C=C2C3=CC=CC=C3NC2=C1)O 213.23 unknown via CMAUP database
3-Formyl-2-hydroxy-6-methoxycarbazole 101508363 Click to see C1=CC2=C(C=C1O)C3=C(N2)C=C(C(=C3)C=O)O 227.21 unknown via CMAUP database
3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carbaldehyde 71623858 Click to see 277.30 unknown via CMAUP database
7-Hydroxyheptaphylline 15767846 Click to see 295.30 unknown via CMAUP database
7-Methoxyheptaphylline 189688 Click to see 309.40 unknown via CMAUP database
9H-Carbazole-3-carbaldehyde 504067 Click to see C1=CC=C2C(=C1)C3=C(N2)C=CC(=C3)C=O 195.22 unknown via CMAUP database
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy- 5317755 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)OC 255.27 unknown via CMAUP database
Clauraila D 51039828 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)C 293.30 unknown via CMAUP database
Clausenawalline H 71623801 Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C=C(C(=C3)C=O)O)O)C 295.30 unknown via CMAUP database
Clausenawalline K 71623860 Click to see CC1(C(C(C2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)O)O)C 327.30 unknown via CMAUP database
Clausine K 504070 Click to see 271.27 unknown via CMAUP database
Clauszoline K 10537169 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=CC(=C3)C=O 225.24 unknown via CMAUP database
Girinimbine 96943 Click to see 263.30 unknown via CMAUP database
Glycosinine 6483032 Click to see 225.24 unknown via CMAUP database
Heptaphylline 5318015 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C 279.30 unknown via CMAUP database
Lansine 5278451 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)O)C=O 241.24 unknown via CMAUP database
methyl 1,6-dihydroxy-5-(3-methylbut-2-enyl)-9H-carbazole-3-carboxylate 71623800 Click to see 325.40 unknown via CMAUP database
methyl 2,7-dimethoxy-9H-carbazole-3-carboxylate 5315952 Click to see 285.29 unknown via CMAUP database
methyl 8-hydroxy-3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carboxylate 71623859 Click to see 323.30 unknown via CMAUP database
Methyl Carbazole-3-Carboxylate 504069 Click to see 225.24 unknown via CMAUP database
Mukonal 504068 Click to see 211.22 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
2-Epilentiginosine 11084135 Click to see 157.21 unknown https://doi.org/10.1021/JF0341722
Octahydroindolizine-1,2-diol 4361605 Click to see 157.21 unknown https://doi.org/10.1021/JF0341722
Octahydroindolizine-1,2,8-triol 5363 Click to see 173.21 unknown https://doi.org/10.1021/JF0341722
Swainsonine 51683 Click to see C1CC(C2C(C(CN2C1)O)O)O 173.21 unknown https://doi.org/10.1021/JF0341722
https://doi.org/10.1021/JF035003K
https://doi.org/10.1016/S0031-9422(01)00131-5
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see 199.20 unknown via CMAUP database
Gamma-Fagarine 107936 Click to see 229.23 unknown via CMAUP database

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