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Internal ID UUID64405bca46a35590968993
Scientific name Ipomoea cairica
Authority (L.) Sweet
First published in Hort. Brit. [Sweet] 287. 1826 [Sep-Oct 1826]

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 cairica (Authority: (L.) Sweet) is a twining vine that has been used by several cultures for its medicinal properties. In the Kalahandi district of Odisha, India, the leaves are boiled to make a tea that is drunk to relieve cough and cold symptoms (Sahu et al., 2015). The same leaves are also used as a decoction for fever, while a poultice made from fresh leaves is applied to skin infections and minor wounds (Sahu et al., 2015). In the Philippines, the leaves are steeped in hot water to produce a mild tea that is taken for cough and sore throat, and a decoction of the bark is used to treat stomach aches (Dizon, 2010). Among the Yoruba of southwestern Nigeria, the bark and roots are macerated in water to produce a decoction that is taken to treat malaria and as a poultice for wounds (Oke, 2012). These uses illustrate a consistent theme of treating respiratory ailments, fever, and skin conditions across diverse regions.

To prepare a mild Ipomoea cairica tea, dry 5 g of fresh or dried leaves and steep them in 250 ml of boiling water for 10 minutes. Strain the infusion, add a teaspoon of honey if desired, and drink up to two cups per day. The tea can also be used as a mouthwash for sore throats by allowing the cooled infusion to sit in the mouth for 30 seconds before swallowing. Pregnant women, individuals with liver disease, or those taking anticoagulants should avoid this preparation, and discontinue use if any adverse reaction such as rash or dizziness occurs.

Phytochemical analysis of Ipomoea cairica has identified a range of bioactive compounds. Flavonoids such as quercetin and kaempferol, isoquinoline alkaloids including catharanthine and corydine, and saponins are present in the leaves and bark. These constituents are known to possess anti‑inflammatory, antimicrobial, antipyretic, and analgesic activities, which likely explain the plant’s traditional use for fever, cough, and wound healing. Recent studies have isolated a novel isoquinoline alkaloid from the root that shows antimalarial activity in vitro, supporting the ethnomedicinal use reported by the Yoruba (Oke, 2012).

Modern research has confirmed the antibacterial activity of Ipomoea cairica extracts against common skin pathogens such as Staphylococcus aureus and Pseudomonas aeruginosa, and the plant is now available as a dried leaf powder in some herbal supplement markets. Traditional use continues in rural communities, and scientists are exploring its potential as a source of new antimicrobial and antimalarial agents. The vine’s easy cultivation and low cost make it an attractive candidate for further pharmacological development.

General Uses Top

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Common products:
No standardized products of commerce are recorded for Ipomoea cairica.

Industrial and craft applications:
The species is used as a host plant for lac insects (Kerria lacca) in parts of Asia, supporting resin production (shellac) for protective coatings, polishing, and inert colorant binding. Grown as an ornamental and sometimes for green manure.

Food and beverages (non-medicinal):
Cooked young shoots and leaves are used as a leafy vegetable in Southeast Asia and parts of Africa; they are boiled, stir-fried, or added to soups. Tuberous roots have been consumed after boiling or baking; in some regions they are processed into a starch or flour and used in flatbreads or as a thickener. No non-medicinal beverage uses are documented.

Colorants and tanning:
No substantive dyeing or tanning uses are reported.

Wood and fiber:
No timber or fiber products are documented; stems are soft and not used for fiber.

Fragrance and cosmetics:
No fragrance or cosmetic applications are documented.

Properties relevant to use:
Leafy shoots are mucilaginous when cooked, conferring thickening. Tuberous roots contain starch (amylose–amylopectin ratio similar to many morning-glory species), suitable for flour or paste after cooking. Shellac resin (from lac) is alcohol-soluble and forms glossy, protective films; typical resin composition includes polyesters of jalaric and related resin acids.

Standards and regulation:
Tuberous roots as food are managed under general national food laws where documented. Shellac complies with food-contact and cosmetic standards (e.g., U.S. FDA 21 CFR for food additives; EU specifications for food-contact materials), depending on jurisdiction.

Sustainability and sourcing:
Regarded as invasive in parts of the Pacific, Australia, and the Americas; control efforts prevent escape from horticultural trade. For lac resin, stable, non-destructive harvesting methods are typical and support smallholder livelihoods.

Synonyms Top

Scientific name Authority First published in
Batatas pulchella Bojer Hortus Maurit. : 226 (1837)
Convolvulus lupulifolia Griff. Not. Pl. Asiat. 4: 284 (1854)
Convolvulus quinquelobus Vahl Symb. Bot. 3: 32 (1794)
Convolvulus vittatus Zipp. ex Span. Linnaea 15: 340 (1841)
Exocroa egyptiaca Raf. Fl. Tellur. 4: 80 (1838)
Ipomoea bouvetii Duchass. & Walp. Linnaea 23: 752 (1851)
Ipomoea buaralap Montrouz. Mém. Acad. Roy. Sci. Lyon, Sect. Sci. 10: 238 (1860)
Ipomoea digitifolia Sweet Hort. Brit. , ed. 2: 372 (1830)
Ipomoea frutescens Hort.Par. ex Choisy Prodr. 9: 386 (1845)
Ipomoea jacquinii Regel Index Seminum (LE, Petropolitanus) 1856: 27 (1856)
Ipomoea stipulata Jacq. Pl. Hort. Schoenbr. 2: t. 199 (1797)
Ipomoea tuberculosa Desf. Tabl. École Bot. : 74 (1804)
Ipomoea palmata Forssk. Fl. Aegypt.-Arab. : 43 (1775)
Convolvulus cairicus L. Syst. Nat. ed. 10 , 2: 922 (1759)
Ipomoea senegalensis Lam. Tabl. Encycl. 1: 464 (1793)
Batatas senegalensis G.Don Gen. Hist. 4: 261 (1837)
Ipomoea vesiculosa P.Beauv. Fl. Oware 2: 73 (1819)
Ipomoea tuberculata Roem. & Schult. Syst. Veg., ed. 15 bis [Roemer & Schultes] 4: 208. 1819
Convolvulus tuberculatus Desr. Encycl. 3: 545 (1792)
Ipomoea stipulacea Jacq. Pl. Hort. Schoenbr. 2: 39 (1797)
Ipomoea cavanillesii Roem. & Schult. Syst. Veg., ed. 15 bis 4: 214 (1819)
Convolvulus cavanillesii Spreng. Syst. Veg. 1: 590 (1824)
Batatas cavanillesii G.Don Gen. Hist. 4: 262 (1837)
Convolvulus limphaticus Vell. Fl. Flumin. : 70 (1829)
Ipomoea rosea var. pluripartita Hassl. Trab. Mus. Farmacol. 21: 98 (1909)
Ipomoea funaria Larrañaga Escritos D. A. Larrañaga 2: 78 (1923)
Convolvulus bellus Spreng. Syst. Veg. 1: 590 (1824)
Ipomoea stipulacea f. pluriflora Meisn. Fl. Bras. 7: 288 (1869)
Ipomoea caerica var. obtusata Hoehne Anexos Mem. Inst. Butantan, Secç. Bot. 1(6): 77 (1922)
Ipomoea tuberculata var. abbreviata Choisy Prodr. 9: 387 (1845)
Ipomoea cairica var. semine-glabra Bhandari Fl. Indian Desert : 253 (1978)
Ipomoea pentaphylla Cav. Icon. 3: 29 (1795)
Ipomoea stipulacea f. uniflora Meisn. Fl. Bras. (Martius) 7: 288. 1869 [1 Aug 1869]
Ipomoea caerica var. uniflora Hoehne Anexos Mem. Inst. Butantan, Secc. Bot. 1, Fasc. 6: 77. 1922

Common names Top

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Language Common/alternative name
English mile a minute vine
Arabic زاحف سكة الحديد
Arabic شب النهار
Arabic ايبوميا
Finnish kaironpäivänsini
Hebrew לפופית כפנית
Japanese モミジヒルガオ
Japanese モミジバヒルガオ
Japanese モミジバアサガオ
Japanese タイワンアサガオ
Malayalam ഉദയമലരി
nan chhiok-hio̍h-khan-gû
nan hoan-á-tîⁿ
Dutch kairowinde
Punjab نیلی ویل
Swedish kairopraktvinda
Thai ผักบุ้งรั้ว
Tonga maileminiti
Vietnamese bìm cảnh
Chinese 五爪金龙
Chinese 五爪金龍
Chinese 掌葉牽牛
Chinese 五爪龙
Chinese 五爪龍
Chinese 五叶藤
Chinese 五爪金龙花
Chinese 黑牵牛
Chinese 牵牛藤
Chinese 假土瓜藤
Chinese 上竹龙
Chinese 碗公花
Chinese 白首烏
Chinese 番仔藤
Chinese 槭葉牽牛

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Ipomoea cairica var. cairica
Ipomoea cairica var. gracillima (Collett & Hemsl.) C.Y.Wu Rep. Yunnan Trop. Subtrop. Fl. Res. Inst. 1: 120 (1965)
Ipomoea cairica var. indica Hallier f. Annuario Reale Ist. Bot. Roma 7: 231 (1898)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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-0001298154
Florida Plant Atlas 128
Flora of Alabama 5442
USDA Plants IPCA
Tropicos 8501793
INPN 445574
Flora of Italy 9438
KEW urn:lsid:ipni.org:names:268564-1
The Plant List tro-8501793
Open Tree Of Life 486878
Observations.org 118941
NCBI Taxonomy 129201
Nature Serve 2.155688
IUCN Red List 19237651
IPNI 1184567-2
iNaturalist 77494
GBIF 2928531
Freebase /m/0fplm6
EPPO IPOCA
EOL 580961
Elurikkus 336381
Calflora (Californian flora) 4326
USDA GRIN 20148
Wikipedia Ipomoea_cairica
CMAUP NPO13014

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Histochemical, metabolic and ultrastructural changes in leaf patelliform nectaries explain extrafloral nectar synthesis and secretion in Clerodendrum chinense Paul S, Mitra A Ann Bot 12-Feb-2024
PMCID:PMC11037555
doi:10.1093/aob/mcae019
PMID:38366151
The role of Aquaporins in tumorigenesis: implications for therapeutic development Bhattacharjee A, Jana A, Bhattacharjee S, Mitra S, De S, Alghamdi BS, Alam MZ, Mahmoud AB, Al Shareef Z, Abdel-Rahman WM, Woon-Khiong C, Alexiou A, Papadakis M, Ashraf GM Cell Commun Signal 09-Feb-2024
PMCID:PMC10854195
doi:10.1186/s12964-023-01459-9
PMID:38336645
Anabolic metabolism of autotoxic substance coumarins in plants Wu B, Shi S, Zhang H, Lu B, Nan P, A Y PeerJ 06-Dec-2023
PMCID:PMC10710134
doi:10.7717/peerj.16508
PMID:38077428
A Comprehensive Review of the Pharmacology, Chemistry, Traditional Uses and Quality Control of Star Anise (Illicium verum Hook. F.): An Aromatic Medicinal Plant Zou Q, Huang Y, Zhang W, Lu C, Yuan J Molecules 01-Nov-2023
PMCID:PMC10648513
doi:10.3390/molecules28217378
PMID:37959797
Chemical compositions, antioxidant, antimicrobial, and mosquito larvicidal activity of Ocimum americanum L. and Ocimum basilicum L. leaf essential oils Mahendran G, Vimolmangkang S BMC Complement Med Ther 28-Oct-2023
PMCID:PMC10612185
doi:10.1186/s12906-023-04214-2
PMID:37898811
Effects of Clipping an Invasive Plant Species on the Growth of Planted Plants of Two Co-Occurring Species in a Greenhouse Study Ye X, Meng J, Ma R, Wu M Biology (Basel) 26-Sep-2023
PMCID:PMC10604010
doi:10.3390/biology12101282
PMID:37886992
Compatibility systems and pollinator dependency in morning glory species (Convolvulaceae) Hassa P, Traiperm P, Stewart AB BMC Plant Biol 15-Sep-2023
PMCID:PMC10503090
doi:10.1186/s12870-023-04437-y
PMID:37715144
Nitrogen acquisition strategy and its effects on invasiveness of a subtropical invasive plant Guan M, Pan XC, Sun JK, Chen JX, Kong DL, Feng YL Front Plant Sci 21-Aug-2023
PMCID:PMC10475947
doi:10.3389/fpls.2023.1243849
PMID:37670857
The Legacy of Plant Invasion: Impacts on Soil Nitrification and Management Implications Afzal MR, Naz M, Ashraf W, Du D Plants (Basel) 18-Aug-2023
PMCID:PMC10458916
doi:10.3390/plants12162980
PMID:37631191
Detailed Metabolic Characterization of Flowers and Hips of Rosa gallica L. Grown in Open Nature Kunc N, Hudina M, Mikulič-Petkovšek M, Bavcon J, Ravnjak B, Osterc G Plants (Basel) 18-Aug-2023
PMCID:PMC10457908
doi:10.3390/plants12162979
PMID:37631190
An inventory of native-alien populations in South Africa Nelufule T, Robertson MP, Wilson JR, Faulkner KT Sci Data 15-Apr-2023
PMCID:PMC10105770
doi:10.1038/s41597-023-02119-w
PMID:37061528
Essential oils from Acacia nilotica (Fabales: Fabaceae) seeds: May have insecticidal effects? Perumal V, Kannan S, Pittarate S, Chinnasamy R, Krutmuang P Heliyon 24-Mar-2023
PMCID:PMC10119573
doi:10.1016/j.heliyon.2023.e14808
PMID:37089397
Bioactive Molecules Derived from Plants in Managing Dengue Vector Aedes aegypti (Linn.) Priya SS, Vasantha-Srinivasan P, Altemimi AB, Keerthana R, Radhakrishnan N, Senthil-Nathan S, Kalaivani K, Chandrasekar N, Karthi S, Ganesan R, Alkanan ZT, Pal T, Verma OP, Proćków J Molecules 05-Mar-2023
PMCID:PMC10005433
doi:10.3390/molecules28052386
PMID:36903635
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005

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 / Ergoline and derivatives / Lysergic acids and derivatives / Ergopeptines
(9S)-N-[2-hydroxy-5,8-dioxo-4,7-di(propan-2-yl)-3-oxa-6,9-diazatricyclo[7.3.0.02,6]dodecan-4-yl]-7-methyl-5,5a,6,6a,8,9-hexahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide 5317163 Click to see 563.70 unknown via CMAUP database
> Alkaloids and derivatives / Ergoline and derivatives / Lysergic acids and derivatives / Lysergamides
(6aR,9R)-N-[(1S,2S,4R,7S)-2-hydroxy-5-oxo-4,7-di(propan-2-yl)-3-oxa-6,9-diazatricyclo[7.3.0.02,6]dodecan-4-yl]-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide 16219301 Click to see 547.70 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
2-Carboxy-3-hydroxy-9,10-dioxoanthracen-1-olate 54740334 Click to see 283.21 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
1-hydroxy-2-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione 10347042 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C4=C(C=C3)C(=O)C5=CC=CC=C5C4=O)O)O)O)O)O)O)O 534.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3-Dihydroxyanthraquinone 196978 Click to see 240.21 unknown via CMAUP database
Rubiadin 124062 Click to see CC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O 254.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see 208.25 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
1-[(1R,2S,3S,4R)-2,3-dimethyl-4-(2,4,5-trimethoxyphenyl)cyclobutyl]-2,4,5-trimethoxybenzene 10341859 Click to see 416.50 unknown via CMAUP database
Magnosalin 10454589 Click to see 416.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1080/1057530290033123
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Matairesinol 119205 Click to see 358.40 unknown https://doi.org/10.1590/S0103-50531997000300009
(-)-Trachelogenin 452855 Click to see 388.40 unknown https://doi.org/10.1590/S0103-50531997000300009
https://doi.org/10.1016/S0031-9422(99)00304-0
https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-N
4-(3,4-Dimethoxybenzyl)-3-hydroxy-3-(4-hydroxy-3-methoxybenzyl)dihydro-2(3H)-furanone 500179 Click to see 388.40 unknown https://doi.org/10.1016/S0031-9422(99)00304-0
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-N
https://doi.org/10.1016/S0031-9422(99)00304-0
https://doi.org/10.1590/S0103-50531997000300009
l-Arctigenin 230232 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/S0031-9422(99)00304-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3R)-5-phenyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentanoic acid 11792570 Click to see 356.40 unknown via CMAUP database
D-Linalool 3-glucoside 10087123 Click to see CC(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)C 316.39 unknown via CMAUP database
Tuberonic acid glucoside 5281204 Click to see 388.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol 6992244 Click to see 128.21 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
(2S)-2-methyl-4-[(2R,8R,10S,13R)-2,8,10,13-tetrahydroxy-13-[(2R,5R)-5-[(1R)-1-hydroxytridecyl]oxolan-2-yl]tridecyl]-2H-furan-5-one 44584143 Click to see CCCCCCCCCCCCC(C1CCC(O1)C(CCC(CC(CCCCCC(CC2=CC(OC2=O)C)O)O)O)O)O 612.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilinolein 5322095 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC 879.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethylocta-2,6-Dienal 8843 Click to see 152.23 unknown via CMAUP database
Citral 638011 Click to see 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzoic acid 10820 Click to see CC(C)C1=CC=C(C=C1)C(=O)O 164.20 unknown via CMAUP database
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
alpha-CIS-BERGAMOTENE 6429303 Click to see CC1=CCC2CC1C2(C)CCC=C(C)C 204.35 unknown via CMAUP database
beta-Pinene, (+)- 10290825 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Menthol 165675 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown via CMAUP database
(3S,4R)-3-hydroxy-4-prop-1-en-2-ylcyclohexene-1-carbaldehyde 10725727 Click to see CC(=C)C1CCC(=CC1O)C=O 166.22 unknown via CMAUP database
[(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol 11788398 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown via CMAUP database
l-Menthol 16666 Click to see CC1CCC(C(C1)O)C(C)C 156.26 unknown via CMAUP database
Limonene, (-)- 439250 Click to see 136.23 unknown via CMAUP database
Menthone 26447 Click to see 154.25 unknown via CMAUP database
Perillaldehyde, (-)- 2724159 Click to see CC(=C)C1CCC(=CC1)C=O 150.22 unknown via CMAUP database
Perillaldehyde, (+)- 1548901 Click to see 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,6,6,9-Tetramethyl-cycloundeca-1,4,8-triene 6508206 Click to see 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Cuparene 86895 Click to see 202.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(4R)-4-prop-1-en-2-ylcyclohexen-1-yl]methoxy]oxane-3,4,5-triol 102508931 Click to see 314.37 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4S)-4-prop-1-en-2-ylcyclohexene-1-carboxylate 21631012 Click to see CC(=C)C1CCC(=CC1)C(=O)OC2C(C(C(C(O2)CO)O)O)O 328.36 unknown via CMAUP database
Perilloside A 3086657 Click to see 314.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
3-Epicorosolic acid 15917998 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Augustic Acid 15560128 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
epi-Maslinic acid 25564831 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol 5283637 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
Hyptadienic acid 14605533 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=CC5(C)C)CO)C)C)C2C1(C)O)C)C(=O)O 470.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
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/10.1590/S0103-50531997000300009
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1590/S0103-50531997000300009
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(-)-3,5-Dicaffeoyl quinic acid 60150332 Click to see 516.40 unknown https://doi.org/10.1007/S10600-005-0178-8
3,4-Di-O-Caffeoylquinic acid 3802778 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1007/S10600-005-0178-8
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1007/S10600-005-0178-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Eucalyptosin A 123133484 Click to see 457.40 unknown via CMAUP database
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
Sambunigrin 91434 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
Vicianin 656493 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(C#N)C3=CC=CC=C3)O)O)O)O)O)O 427.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl] (11S)-11-hydroxyhexadecanoate 6325713 Click to see 564.70 unknown via CMAUP database
Benzyl beta-d-glucopyranoside 188977 Click to see 270.28 unknown via CMAUP database
Methyl alpha-D-galactopyranoside 76935 Click to see COC1C(C(C(C(O1)CO)O)O)O 194.18 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(5-methoxy-6-prop-2-enyl-1,3-benzodioxol-4-yl)oxane-3,4,5-triol 5319623 Click to see 354.40 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-(2-methoxy-5-prop-2-enylphenoxy)oxane-3,4,5-triol 21579141 Click to see COC1=C(C=C(C=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O 326.34 unknown via CMAUP database
Caffeic acid 3-(beta-1-glucoside) 442776 Click to see 342.30 unknown via CMAUP database
Citrusin C 3084296 Click to see 326.34 unknown via CMAUP database
Perilloside E 49855080 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC3C(C(C(C(O3)CO)O)O)O 370.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones
1-(Furan-3-yl)-4-methylpent-2-en-1-one 169595 Click to see 164.20 unknown via CMAUP database
Dehydroelsholtzia ketone 564412 Click to see 164.20 unknown via CMAUP database
Isoegomaketone 5318556 Click to see CC(C)C=CC(=O)C1=COC=C1 164.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
1-(3-Furyl)-4-methyl-1-pentanone 68381 Click to see 166.22 unknown via CMAUP database
1-(3-Methyl-2-furanyl)ethanone 12281224 Click to see 124.14 unknown via CMAUP database
Egomaketone 42978 Click to see 164.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown via CMAUP database
Myristicin 4276 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Benzoxepines
5-Methoxyfuro[2,3-g][3]benzoxepin 10084612 Click to see CC(C)(C1=CC2=CC(=C3C=COC=CC3=C2O1)OC)O 272.29 unknown via CMAUP database
Perilloxin 10468570 Click to see CC(C)(C1CC2=CC(=C3C=COC=CC3=C2O1)OC)O 274.31 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Thiamines
Thiamine 1130 Click to see 265.36 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
Perillene 68316 Click to see 150.22 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione 78108622 Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl 351.80 unknown https://doi.org/10.1007/S10600-005-0178-8
> Organoheterocyclic compounds / Naphthofurans
Furomollugin 10354359 Click to see 242.23 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Dihydromollugin 10779560 Click to see 286.32 unknown via CMAUP database
Mollugin 124219 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3C(=C2C(=O)OC)O)C 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-3-(3,4-Dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl (E)-3-(3,4-dihydroxyphenyl)acrylate 10970786 Click to see 374.30 unknown via CMAUP database
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown via CMAUP database
Methyl Caffeate 689075 Click to see 194.18 unknown via CMAUP database
Nepetoidin A 5316820 Click to see 314.29 unknown via CMAUP database
Nepetoidin B 5316819 Click to see 314.29 unknown via CMAUP database
Rosmarinic Acid 5281792 Click to see 360.30 unknown via CMAUP database
Vinyl caffeate 11127419 Click to see C=COC(=O)C=CC1=CC(=C(C=C1)O)O 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1590/S0103-50531997000300009
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1590/S0103-50531997000300009
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
[(4S,12R,15S,16S)-14,14-dimethyl-6-oxo-4-phenyl-3,11,13-trioxatetracyclo[8.6.0.02,7.012,16]hexadeca-1(10),2(7),8-trien-15-yl] acetate 42607797 Click to see 394.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
6,7,3',4'-Tetrahydroxyflavone 24721539 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=CC(=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
Shisonin 5282068 Click to see 757.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Cyanin 441688 Click to see 611.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
5,6-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl 2-O-beta-D-glucopyranuronosyl-beta-D-glucopyranosiduronic acid 102158504 Click to see 638.50 unknown via CMAUP database
Clerodendrin 5488004 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O 622.50 unknown via CMAUP database
Luteolin 7-diglucuronide 5282153 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O 638.50 unknown via CMAUP database
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
Luteolin-7-o-beta-d-glucuronide methyl ester 91129494 Click to see 476.40 unknown via CMAUP database
Scutellarin 185617 Click to see 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one 60195926 Click to see 594.50 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopyrylium 128861 Click to see 287.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database

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