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    Review

    An Updated Review on Phytochemistry of Plumeria alba L. (Apocynaceae)

    Satyavarapu Veera Venkata Naga Satya Maha Lakshmi1, Katam Teja Sri1, Kokku Naveen Kumar1, Kolepaka Supraja1, Koppujola Manisha1 Corresponding author

    1. 1Department of Pharmacognosy, Vishnu Institute of Pharmaceutical Education and Research, Narsapur, Medak, Telangana, INDIA.

    CORRESPONDENCE

    Satyavarapu Veera Venkata Naga Satya Maha Lakshmi

    Associate Professor, Department of Pharmacognosy, Vishnu Institute of Pharmaceutical Education and Research (VIPER), Narsapur, Medak-502313, Telangana, INDIA.

    lakshmi.svvnsm@viper.ac.in

    Received: 22-01-2026; Revised: 03-02-2026; Accepted: 16-04-2026.

    Volume 18, Issue 3 · pp. 679–697 · PUBLISHED Jul-Sep 2026 · DOI: 10.5530/pres.20260257

    View on Pharmacogn. Res. original site ↗

    ABSTRACT

    Plumeria alba L. (Apocynaceae) is an ornamental tree widely distributed in tropical and subtropical regions and is well recognized in traditional medicine. Over the decades, extensive phytochemical investigations have been conducted on different parts of the plant, resulting in the identification of diverse secondary metabolites. This review aims to systematically compile and organize phytochemical data on Plumeria alba L. reported between 1960 and 2024, focusing on the identification and classification of secondary metabolites from different plant parts. By highlighting major and frequently reported compounds, the review provides a consolidated chemical profile to support future studies on isolation, characterization, and further scientific exploration. Key classes include iridoids, flavonoids, alkaloids, phenolics, coumarins, terpenoids (mono-, sesqui-, di-, and triterpenes), fatty acids, hydrocarbons, alkanes, alkenes, alkynes, esters, aldehydes, carboxylic acids and other miscellaneous compounds. Floral essential oils were rich in monoterpenes and sesquiterpenes, while leaves contained abundant flavonoids, phenolic acids, sugars, and amino acids. Major compounds such as plumieride, plumericin, ursolic acid, and quercetin were frequently reported. Although many of these constituents are known to possess biological activities, this review focuses solely on their chemical identification. The data provide a valuable foundation for future studies aimed at isolating, characterizing, and evaluating the bioactivity of these compounds to support potential therapeutic applications.

    KEYWORDS

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    FULL TEXT

    INTRODUCTION

    Plumeria L. from the Apocynaceae family, are lactiferous, deciduous shrubs found in tropical regions from southern Mexico to northern South America, the Pacific islands, the Caribbean, and India (Rudrappa et al., 2022). The family comprises 366 genera, with about 133 Plumeria species listed, taxonomic revisions based on morphological and molecular data currently recognize only 11 validly accepted species (Bruna et al., 2024).

    Plumeria alba is an ornamental evergreen plant in gardens because of its fragrant flower. It is a medium-sized tree that can reach a height of 5-8 feet, with many branches on the upper part. The leaves are lanceolate to oblanceolate; the flowers are white in color and fragrant in corymbose fascicles (Kumari et al., 2022). A few reviews on the phytochemical and pharmacological profile of the plant have been made. However, a systematic review comprising all updated information is required. Therefore, in the present review, a comprehensive summary of the phytochemistry of Plumeria alba was made. It includes a detailed classification of phytoconstituents isolated from different part of the plant by various extraction and isolation techniques reported in the literature till June, 2025. The aerial parts and bark of Plumeria alba containing alkaloids, carbohydrates, flavonoids, phenolic compounds, and tannins (Imrana et al., 2020). Traditionally, many parts of the plant considered medicinal. Its parts such as bark, leaves, latex, and flowers engage in various biological activities such as antibacterial (Radha et al., 2008), antioxidant (Kirsty et al., 2023), antitumor (Rudrappa et al., 2022), antiarthritic (Choudhary et al., 2014), hepatoprotective, and antidiabetic activities (Chowdhury et al., 2010). The bark is used as purgative, emmenagogue, and febrifuge. The latex of the plant has rubefacient and purgative properties (Kumari et al., 2012). It bears edible fruit; the seeds have demonstrated hemostatic properties. Latex has been used to treat herpes, ulcers, and scabies, and the powdered bark has been used as a plaster applied on hard tumors (Sura et al., 2016), while the other species of the Plumeria are used for cardiotonic, purgative, hypotensive, and diuretic applications (Gupta et al., 2016).

    METHODOLOGY

    A detailed literature search was conducted on this plant for its phytochemistry in different search engines like PubMed, PubMed Central, SciFinder, Google Scholar, J-gate, Library Search, Science Direct, Elsevier, Semantic Scholar, PubMed Central, ResearchGate and primary sources were searched since 1960 to June, 2025. Literature searches were performed using keywords such as “Plumeria alba phytochemistry,” “iridoids,” “essential oil composition”, etc. Only peer-reviewed articles reporting compound isolation or chemical characterization were included. Duplicate reports and secondary citations were excluded wherever possible. To plot the phytochemistry flow diagram, we have used XmindAI software.

    RESULTS

    Over the past seven decades, extensive phytochemical investigations on Plumeria alba have revealed a wide range of secondary metabolites isolated from different plant parts using diverse solvent systems and analytical techniques. Identified compounds include iridoids, flavonoids, terpenoids, alkaloids, phenolics, sterols, hydrocarbons, and other metabolites. Structural elucidation was achieved through NMR, MS, IR spectroscopy, and chemical degradation or biosynthetic studies. More than 200 compounds have been reported from roots, leaves, stems, bark, flowers, and aerial parts. The compiled phytochemical data are summarized in Tables 1-10 and Figure 1, many of which exhibit notable pharmacological relevance.

    Figure 1: Major classes of secondary metabolites present in Plumeria alba.

    Iridoids

    Iridoids represent major secondary metabolites of Plumeria alba, showing wide distribution across plant parts. Plumieride and related derivatives were reported by Afifi et al., 2006, Leena et al., 2023, and Rangaswami et al., 1960 from bark, stems, and leaves, while John et al., 1983 identified plumericin from roots. Zhou et al., 2024 recently isolated novel iridoids including allamancins A and B from flowers, highlighting continued chemical discovery and pharmacological relevance. Details of reported iridoids are summarized in Table 1.

    Table 1: Iridoids reported from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    1PlumierideChloroform:methanol:water (80:20:2) fraction of ethylacetate extractStem barkAfifi et al., 2006
    Chloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al., 2023
    Petroleum etherBarkRangaswami et al., 1960
    2Plumieride acidEthylacetate:methanol:water (100:16.5:13.5) fraction of n-butanol extractLeavesAfifi et al., 2006
    3Plumieride glucosideChloroform:ethanol (2:1)BarkRangaswami et al., 1960
    4PlumieridecoumarateMethanolRoots, stem, leavesJohn et al., 1983
    N/ALeaves and stem barkBramadhayalaselvam et al., 1997
    5Plumieride coumerate glucosideMethanolRoots, stem, leaves, flowersJohn et al., 1983
    6PlumericinMethanolRootsJohn et al., 1983
    7IsoplumericinMethanolRootsJohn et al., 1983
    8Fulvoplumierin coumaroneN/ALeaves and barkAnggoro et al., 2020
    9Resinic acidN/ALeaves and barkAnggoro et al., 2020
    10Protoplumericin AEthylacetate-methanol-water (100: 16.5:13.5) fraction of n-butanol extractStem bark and leavesAfifi et al., 2006
    11Allamancins AN/AFlowersXin et al., 2024
    12allamancins BN/AFlowersXin et al., 2024
    133-O-methyallamancinN/AFlowersXin et al., 2024

    Flavonoids

    Flavonoids have been consistently reported from methanolic leaf and floral extracts of Plumeria alba. Hassan et al., 2015 identified kaempferol derivatives and glycosides, while Santhi et al., 2009 confirmed quercetin, rutin, apigenin, catechin, and epicatechin in leaf extracts. These compounds are associated with antioxidant, anti-inflammatory, and antimicrobial activities. The identified flavonoids are summarized in Table 2.

    Table 2: Flavonoids identified from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    Flavonoids
    14QuercetinMethanolLeavesHassan et al., 2015
    15KaempferolMethanolLeavesHassan et al., 2015
    Diethyl ether fraction of ethanol extractFlowersSanthi et al., 2009
    16Kaempferol 4’-O-glucosideEthyl acetate fraction of ethanol extractFlowersSanthi et al., 2009
    17RutinMethanolLeavesHassan et al., 2015
    18HerperetinMethanolLeavesHassan et al., 2015
    19NarenniginMethanolLeavesHassan et al., 2015
    20CatechinMethanolLeavesHassan et al., 2015
    21EpicatechinMethanolLeavesHassan et al., 2015
    22ApigeninMethanolLeavesHassan et al., 2015
    23DiosmitinMethanolLeavesHassan et al., 2015

    Terpenes and sterols

    Monoterpenes dominate essential oils of leaves and flowers. Kirsty et al., 2023 reported linalool, geraniol, and α-terpineol, whereas Lawal et al., 2014 identified citronellol, sabinene, and limonene with ecological significance. El-Shiekh et al., 2024 confirmed floral volatiles such as geranyl benzoate and nerol through headspace analysis.

    Sesquiterpenes are abundant in floral and leaf essential oils. Lawal et al., 2014 identified β-caryophyllene and (E)-nerolidol, while Sahoo et al., 2021 and Mamattah et al., 2023 reported germacrene B and muurolol. Additional sesquiterpenes including farnesol were detected by Rakhmawati et al., 2022 and Malik et al., 2023.These findings highlight the therapeutic and chemotaxonomic value of Plumeria alba mono and sesquiterpenes.

    Diterpenes occur less frequently but remain biologically significant. Mamattah et al., 2023 and Lawal et al., 2014 identified phytol from essential oils, whereas Sahoo et al., 2021 reported (Z,E)-geranyl linalool. Their occurrence supports the use of Plumeria alba in skin and wound-healing preparations.

    Triterpenes including lupeol, ursolic acid, lupenone, and amyrin derivatives were reported from stems, bark, and leaves by Leena et al., 2023, Rangaswami et al., 1960, and Bramadhayalaselvam et al., 1997. Leena et al., 2023 further identified acylated derivatives such as lup-20(29)-ene-3-yl-hexanoate and related compounds. These findings suggest that triterpenes contribute significantly to the anti-inflammatory, hepatoprotective, and antidiabetic properties attributed to the plant. Terpenoidal derivatives represent acylated triterpenes, which are often associated with enhanced lipophilicity and bioavailability.

    Sterols were also reported widely, with β-sitosterol first identified by Rangaswami et al., 1960 and α-sitosterol derivatives later characterized by Leena et al., 2023. Terpenes and sterols are summarized in Table 3.

    Table 3: Terpenoids and sterols reported from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    Monoterpenes
    243,7-dimethyl-2,6-OctadienolSteam distilled essential oilFlowersKirsty et al., 2023
    251,6-Octadien-3-ol, 3,7-dimethyl-Steam distilled essential oilLeavesKirsty et al., 2023
    262,6-octadien-1-ol, 3,7-dimethyl-, acetate, (Z)-/neryl acetateMethanolflowersMalik et al., 2023
    27LinaloolSteam distilled essential oilFlowersKirsty et al., 2023
    Steam distilled essential oilLeaves and flowersLawal et al., 2014
    Essential oil extracted with water by headspaceFlowersEI-Shiekh et al., 2024
    Steam distilled essential oilFlowersSahoo et al., 2021
    28GeraniolSteam distilled essential oilFlowersKirsty et al., 2023
    Steam distilled essential oilLeaves and flowersLawal et al., 2014
    29CitronellolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    30α and β -PineneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    31SabineneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    32δ-2-CareneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    33α and β-PhellandreneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    34LimoneneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    35(E)-β-OcimeneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    36γ-TerpineneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    37Cis-VerbenolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    38LavandulolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    39Terpinen-4-olSteam distilled essential oilLeaves and flowersLawal et al., 2014
    40p-Cymen-8-olSteam distilled essential oilLeaves andflowersLawal et al., 2014
    41α-TerpineolSteam distilled essential oilFlowersKirsty et al., 2023
    ButanolFlowersMohammad 2020
    Steam distilled essential oilLeaves and flowersLawal et al., 2014
    Steam distilled essential oilFlowersSahoo et al., 2021
    42GeranialSteam distilled essential oilLeaves and flowersLawal et al., 2014
    43Geranyl benzoateSteam distilled essential oilFlowersEI-Shiekh et al., 2024
    Steam distilled essential oilFlowersSahoo et al., 2021
    44Neryl acetateSteam distilled essential oilLeaves and flowersLawal et al., 2014
    45Neryl acetoneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    46Trans-sabinene hydrate acetateSteam distilled essential oilFlowersSahoo et al., 2021
    47NerolSteam distilled essential oilFlowersSahoo et al., 2021
    Sesquiterpenes
    48MuurololSteam distilled essential oilLeavesKirsty et al., 2023
    49Nerolidol 2HexaneFlowersMohammad et al., 2020
    501,6,10-dodecatrien-3-ol, 3,7,11-trimethyl-, [S-(Z)]-MethanolflowersMalik et al., 2023
    51d-NerolidolEthanolFlowersRakhmawati et al.
    521,6,10-Dodecatrien-3-olEthanolFlowersRakhmawati et al.
    53FarnesolEthanolFlowersRakhmawati et al.
    Steam distilled essential oilFlowersSahoo et al., 2021
    543,7,11-Trimethyl-3-hydroxy-6,10-dodecadien-1-yl acetateSteam distilled essential oilFlowersKirsty et al., 2023
    55(Z,E)-FarnesolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    Steam distilled essential oilFlowersSahoo et al., 2021
    56α-BisabololSteam distilled essential oilLeaves and flowersLawal et al., 2014
    Steam distilled essential oilFlowersSahoo et al., 2021
    57δ-CadinolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    58Caryophyllene oxideSteam distilled essential oilLeaves and flowersLawal et al., 2014
    59SpathulenolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    60Γ and δ -CadineneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    61β-SesquiphellandreneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    62(E)-NerolidolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    63ViridiflorolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    646,10,14-Trimethyl-2-pentadecanoneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    65(E)-β-IononeSteam distilled essential oilLeaves and flowersLawal et al., 2014
    66ZingibereneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    67α-ChamigreneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    68(E,E)-α-FarneseneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    69α-BulneseneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    70β-BisaboleneSteam distilled essential oilLeaves andflowersLawal et al., 2014
    71β-CaryophylleneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    72Trans-α-BergamoteneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    73β-SantaleneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    74γ-MuuroleneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    75β-ElemeneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    76ElemolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    77Germacrene BSteam distilled essential oilFlowersSahoo et al., 2021
    788-cedren-13-olSteam distilled essential oilFlowersSahoo et al., 2021
    Diterpenes
    79PhytolSteam distilled essential oilLeavesKirsty et al., 2023
    Steam distilled essential oilLeaves and flowersLawal et al., 2014
    80LedolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    81(Z, E)-geranyl linaloolSteam distilled essential oilFlowersSahoo et al., 2021
    Triterpenes
    82AmyrinPetroleum etherBarkRangaswami et al., 1960
    83Amyrin acetatePetroleum ether13EI-Shiekh et al., 2024
    N/ALeaves and stem barkBramadhayalaselvam et al., 1997
    84BetulinN/ALeaves and barkAnggoro et al., 2020
    85LupeolChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al., 2023
    86LupenoneChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al., 2023
    87FriedelineN/ALeaves and barkAnggoro et al.
    88TaraxerolN/ALeaves and barkAnggoro et al.
    893-O-acetylbetulinN/ALeaves and barkAnggoro et al.
    90Ursolic acidChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al., 2023
    Leaves and stem barkBramadhayalaselvam et al., 1997
    91SqualeneHexaneFlowersMohammad et al., 2020
    EthanolFlowersRakhmawati et al., 2022
    Triterpenoid derivatives
    92Lup-20(29)-ene-3-yl-hexanoateChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al.
    933β-O-acety lolean-12-eneChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al.
    943 β -O-acetyl-lup-20(29)-eneChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al.
    Sterols
    95ß-sitosterolPetroleum etherBarkRangaswami et al., 1960
    96α-sitosterol glucosideChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al.
    97α-sitosterolChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al.

    Alkaloids

    Floral alkaloids were extensively characterized by Sibi et al., 2014 using petroleum ether fractions of ethanol extracts. Compounds including voacamine, curine, syrosingopine, and tubocurarine chloride, along with rare nitrogenous derivatives, demonstrated significant chemical diversity and pharmaceutical potential. They also identified rare nitrogenous compounds like benzo[f]quinazoline and naphthalenedione derivatives, indicating high chemical diversity. A comprehensive list of alkaloids reported from flowers of Plumeria alba was provided in Table 4. These findings highlight the pharmaceutical potential of floral alkaloids and expand the phytochemical profile of Plumeria alba beyond iridoids and terpenoids.

    Table 4: Alkaloids identified from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    98VoacaminePetroleum ether fraction of ethanol extractFlowersSibi et al., 2024
    991,3-Di(4-bromophenyl) benzo[f]quinazolinePetroleum ether fraction of ethanol extractFlowersSibi et al.
    100Vobtusine, 2',3'-didehydro-2'-deoxyPetroleum ether fraction of ethanol extractFlowersSibi et al.
    101CurinePetroleum ether fraction of ethanol extractFlowersSibi et al., 2024
    102Pyrrolidine 1-[3.alpha., 7.alpha., 12.alpha.-tris(trimethylsiloxy)-5.beta.-cholan-24-oyl]Petroleum ether fraction of ethanol extractFlowersSibi et al., 2024
    103SyrosingopinePetroleum ether fraction of ethanol extractFlowersSibi et al., 2024
    1041,4-Naphthalenedione, 2-(3,7,11,15,19,23,27,31-octamethyl-2,6,10,14,18,22,26,30 dotriacontaoctaenyl), (all-E)-Petroleum ether fraction of ethanol extractFlowersSibi et al., 2024
    105Cycleanine, O7, O7’-didemethyl-, (1.alpha., 1’.alpha.)Petroleum ether fraction of ethanol extractFlowersSibi et al., 2024
    106EvoninePetroleum ether fraction of ethanol extractFlowersSibi et al., 2024
    107Evonimine, 8-(acetyloxy)-O2-benzoyl-O2-deacetyl-8-deoxo-26-hydroxy-, (8.alpha.)Petroleum ether fraction of ethanol extractFlowersSibi et al., 2024
    108Tubocurarine chloridePetroleum ether fraction of ethanol extractFlowersSibi et al., 2024

    Phenolics, courmarins and aromatic compounds

    Phenolic acids such as rosmarinic, ferulic, ellagic, and p-coumaric acids were identified from methanolic leaf extracts by Hassan et al., 2015, while Kirsty et al., 2023 reported volatile phenolics including 2-methoxy-4-vinylphenol. Coumarins including scopoletin were reported by Malik et al., 2023, Rangaswami et al., 1960, and Leena et al., 2023 from stems, bark, and flowers.

    Benzene derivatives such as catechol and hydroquinone were identified by Kirsty et al., 2023, while Lawal et al., 2014 reported aromatic essential oil constituents. Furan derivatives including furfural and hydroxymethylfurfural were reported from aqueous flower extracts by Sahoo et al., 2021. Aromatic acids such as salicylic acid and benzoic acid were detected by Hassan et al., 2015 and Rakhmawati et al., 2022. These detailed list constituents were summarized in Table 5.

    Table 5: Phenolics, coumarins, and aromatic compounds reported from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    Phenolic compounds
    109PhenolMethanolFlowersMalik et al., 2023
    1102-Methoxy-4-vinyl phenolSteam distilled essential oilLeavesKirsty et al., 2023
    111Phenol, 2,4-bis (1,1-dimethyl ethyl)Steam distilled essential oilLeavesKirsty et al., 2023
    112PyrogallolMethanolLeavesHassan et al., 2015
    113Rosamarinic acidMethanolLeavesHassan et al., 2015
    114Ferulic acidMethanolLeavesHassan et al., 2015
    115Vanilic acidMethanolLeavesHassan et al., 2015
    116Ellagic acidMethanolLeavesHassan et al., 2015
    117Protocatechuic acidMethanolLeavesHassan et al., 2015
    118P-coumaric acidMethanolLeavesHassan et al., 2015
    119Methyl eugenolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    120ZingeroneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    Coumarinand its glycoside
    121Benzofuran, 2,3-dihydroMethanolFlowersMalik et al., 2023
    Steam distilled essential oilLeavesKirsty et al., 2023
    DichloromethaneFlowersMohammad et al., 2020
    122ScopoletinChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al., 2023
    EtherBarkRangaswami et al., 1960
    Benzene derivatives
    123CatecholMethanolFlowersMalik et al., 2023
    DichloromethaneFlowersMohammad et al., 2020
    124HydroquinoneMethanolflowersMalik et al., 2023
    125Benzene, 1-isocyano-3-methylSteam distilled essential oilFlowersKirsty et al., 2023
    Furan derivatives
    126FurfuralWaterFlowersMohammad et al., 2020
    1275-HydroxymethylfurfuralWaterFlowersMohammad et al., 2020
    1282-FuranmethanolWaterFlowersMohammad et al., 2020
    Aromatic carboxylic acids
    129Benzoic acidEthanolFlowersRakhmawati et al., 2022
    130Salicylic acidMethanolLeavesHassan et al., 2015
    1311,2-Benzenedicarboxylic acidEthanolFlowersRakhmawati et al., 2022

    Hydrocarbons

    Hydrocarbons including decane, heptadecane, and n-heneicosane were reported from essential oils by Kirsty et al., 2023 and Lawal et al., 2014. Long-chain alkanes such as hexadecane and hentriacontane were confirmed by Lawal et al., 2014, Kirsty et al., 2023, Anggoro et al., 2020, and Sahoo et al., 2021. Alkenes including cetene and docosene were reported by Lawal et al., 2014 and Kirsty et al., 2023, whereas alkynes such as 1,8-nonadiyne were identified by Sahoo et al., 2021. Non-polar hydrocarbon constituents identified primarily from essential oil fractions were compiled in Table 6.

    Table 6: Hydrocarbon constituents identified from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    Alkanes
    1321,3-propanediamine, N-methyl-MethanolFlowersMalik et al., 2023
    133DodecaneSteam distilled essential oilLeavesKirsty et al., 2023
    134HexadecaneSteam distilled essential oilLeavesKirsty et al., 2023
    EthanolFlowersRakhmawati et al., 2022
    135OctadecaneSteam distilled essential oilLeavesKirsty et al., 2023
    136TetradecaneSteam distilled essential oilLeavesKirsty et al., 2023
    EthanolFlowersRakhmawati et al., 2022
    137HexacosaneSteam distilled essential oilLeavesKirsty et al., 2023
    138DocosaneSteam distilled essential oilLeavesKirsty et al., 2023
    Steam distilled essential oilFlowersSahoo et al., 2021
    139TetracosaneSteam distilled essential oilLeavesKirsty et al., 2023
    140HentriacontaneSteam distilled essential oilLeavesKirsty et al., 2023
    141OctacosaneSteam distilled essential oilLeavesKirsty et al., 2023
    142EicosaneSteam distilled essential oilLeavesKirsty et al., 2023
    HexaneFlowersMohammad et al., 2020
    143n-TridecaneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    144Oxacyclotetradecane-2EthanolFlowersRakhmawati et al., 2022
    145n-NonadecaneSteam distilled essential oilFlowersSahoo et al., 2021
    146n-TricosaneSteam distilled essential oilFlowersSahoo et al., 2021
    1473,7,11-tridecatrienenitrile, 4,8,12-trimethylMethanolflowersMalik et al., 2023
    148HeptadecaneMethanolFlowersMalik et al., 2023
    149DecaneSteam distilled essential oilLeavesKirsty et al., 2023
    150n-heneicosaneSteam distilled essential oilFlowersSahoo et al., 2021
    Alkenes
    151CeteneSteam distilled essential oilLeavesKirsty et al., 2023
    1521-DocoseneSteam distilled essential oilLeavesKirsty et al., 2023
    15310-HeneicoseneSteam distilled essential oilFlowersKirsty et al., 2023
    1543-TetradeceneSteam distilled essential oilFlowersKirsty et al., 2023
    1554-NoneneEthanolFlowersRakhmawati et al., 2022
    1561-NoneneEthanolFlowersRakhmawati et al., 2022
    1571-DeceneEthanolFlowersRakhmawati et al., 2022
    1584-methyl-1,5-heptadieneMethanolflowersMalik et al., 2023
    AlkynesRakhmawati et al., 2022
    1591,8-NonadiyneEthanolFlowersRakhmawati et al., 2022
    1609-OctadecyneMethanolFlowersMalik et al., 2023
    Aromatic hydrocarbons
    161m-dimethylbenzeneSteam distilled essential oilFlowersKirsty et al., 2023
    1621-Ethyl-2-heptylcyclopropaneSteam distilled essential oilFlowersKirsty et al., 2023

    Fatty Acids and their Derivatives

    Fatty acids including octadecanoic, hexadecanoic, oleic, and linolenic acids were reported from solvent and essential oil extracts by Lawal et al., 2014 and Sahoo et al., 2021. Fatty acids and related carboxylic acid derivatives identified from solvent extracts were presented in Table 7. Kirsty et al., 2023 added 9,12,15-octadecatrienoic acid methyl ester and geranic acid, highlighting the plant’s rich lipid profile.

    Table 7: Fatty acids and organic acids reported from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    163Acetic acidEthanolFlowersRakhmawati et al., 2022
    164Octadecanoic acidSteam distilled essential oilLeavesKirsty et al., 2023
    165EthanolFlowersRakhmawati et al., 2022
    166Methyl octadecanoateSteam distilled essential oilLeaves and flowersLawal et al., 2014
    1672-Propenyl octanoateEthanolFlowersRakhmawati et al., 2022
    168Pentadecanoic acidEthanolFlowersRakhmawati et al., 2022
    169Octanoic acidEthanolFlowersRakhmawati et al., 2022
    170Tetradecanoic acidEthanolFlowersRakhmawati et al., 2022
    171Cyclopentaneundecanoic acidEthanolFlowersRakhmawati et al., 2022
    172Oleic acidEthanolFlowersRakhmawati et al., 2022
    173Hexanoic acidEthanolFlowersRakhmawati et al., 2022
    1749-Hexadecenoic acidEthanolFlowersRakhmawati et al., 2022
    175Tricosanoic acidChloroform:acetone fraction of dichloromethane:methanol (1:1) extractStems and leavesLeena et al., 2023
    176Neric acidButanolFlowersMohammad et al., 2020
    177Geranic acidHexaneFlowersMohammad et al., 2020
    1789,12,15-Octadecatrienoic acid, methyl ester, (Z,Z,Z)MethanolflowersMalik et al., 2023
    1792-Propenyl hexanoateEthanolFlowersRakhmawati et al., 2022
    1809,12,15-Octadecatrienoic acidEthanolFlowersRakhmawati et al., 2022
    1819,12-Octadecadienoic acidEthanolFlowersRakhmawati et al., 2022
    182Hexadecanoic acidSteam distilled essential oilLeaves and flowersLawal et al., 2014
    EthanolFlowersRakhmawati et al., 2022
    183Hexadecanoic acid, 15-methyl-, methyl esterMethanolflowersMalik et al., 2023
    184Hexadecanoic acid methyl esterHexaneFlowersMohammad et al., 2020
    1859-Octadecenoic acid (Z)- methyl esterHexaneFlowersMohammad et al., 2020
    1861-PentadecanalSteam distilled essential oilFlowersKirsty et al., 2023
    1871-HexadecanolSteam distilled essential oilLeavesKirsty et al., 2023
    1881-NonanolEthanolFlowersRakhmawati et al., 2022
    1891-EicosanolEthanolFlowersRakhmawati et al., 2022
    1901-TetracosanolEthanolFlowersRakhmawati et al., 2022
    1911-Hexadecen-1-olEthanolFlowersRakhmawati et al., 2022
    1921-HexacosanolEthanolFlowersRakhmawati et al., 2022
    193Trans-2-TridecenalEthanolFlowersRakhmawati et al., 2022
    194(E,E)-2,4-HeptadienalSteam distilled essential oilLeaves and flowersLawal et al., 2014
    195n-NonanalSteam distilled essential oilLeaves and flowersLawal et al., 2014
    196(E,Z)-2,6-NonadienalSteam distilled essential oilLeaves and flowersLawal et al., 2014
    197(E)-2-NonenalSteam distilled essential oilLeaves and flowersLawal et al., 2014
    198Non-2-en-1-olSteam distilled essential oilLeaves and flowersLawal et al., 2014
    199(E)-2-DecenalSteam distilled essential oilLeaves and flowersLawal et al., 2014
    200(E,E)-2,4-DecadienalSteam distilled essential oilLeaves and flowersLawal et al., 2014
    201TetradecanalSteam distilled essential oilLeaves and flowersLawal et al., 2014
    202Methyl octadecanoateSteam distilled essential oilLeaves and flowersLawal et al., 2014
    203Methyl linoleateSteam distilled essential oilLeaves and flowersLawal et al., 2014
    204Methyl palmitateSteam distilled essential oilLeaves and flowersLawal et al., 2014
    205Isopropyl myristateSteam distilled essential oilLeaves andflowersLawal et al., 2014
    2061-DodecanolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    207n-DecanalSteam distilled essential oilLeaves and flowersLawal et al., 2014

    Oxygenated volatile constituents

    Oxygenated constituents including cyclic ketones, alcohols, aldehydes, esters, and pyranone derivatives were reported from solvent and essential oil extracts. Kirsty et al., 2023, Lawal et al., 2014, Rangaswami et al., 1960, and Sahoo et al., 2021 documented multiple aroma-active and antimicrobial compounds contributing to fragrance and biological activity. Though present in low amounts, their volatility and reactivity may contribute to both aroma and antimicrobial activity. Aliphatic carboxylic acids which are known for its antioxidant potential and UV-protective effects. Esters commonly used in perfumery for their fragrance-fixative properties. Oxygenated volatile compounds, including alcohols, aldehydes, ketones, esters, were detailed in Table 8.

    Table 8: Oxygenated volatile constituents identified from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    Cyclic ketones
    2082-Cyclopenten-1-one, 2-hydroxyMethanolflowersMalik et al., 2023
    209CyclononanoneMethanolflowersMalik et al., 2023
    2104,5-Dihydro-2 (1H)-pentalenoneSteam distilled essential oilFlowersKirsty et al., 2023
    211Ethanone, 1-(6,6-dimethylbicyclo [3.1.0] hex-2-en-2-yl)-Steam distilled essential oilFlowersKirsty et al., 2023
    2123,3l-DimethoxybenzilMethanolFlowersMalik et al., 2023
    2135-Methyl-1,3-cyclohexanedioneEthanolFlowersRakhmawati et al., 2022
    2148a-Hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dioneN/ALeaves and barkAnggoro et al., 2020
    2152,3-Dihydro-3,5-dihydroxy-6-methyl-4HPyran-4-oneDichloromethaneFlowersMohammad et al., 2020
    Alcohols
    216Phenyl ethyl alcoholSteam distilled essential oilFlowersKirsty et al., 2023
    Steam distilled essential oilLeaves and flowersLawal et al., 2014
    2172-Methyl benzyl alcoholSteam distilled essential oilFlowersKirsty et al., 2023
    218Benzyl alcoholMethanolFlowersMalik et al., 2023
    ButanolFlowersMohammad et al., 2020
    2192-EthylhexanolSteam distilled essential oilLeaves and flowersLawal et al., 2014
    220CyclohexanolEthanolFlowersRakhmawati et al., 2022
    221CyclopentadecanolEthanolFlowersRakhmawati et al., 2022
    2221-Decanol, 2-hexylMethanolFlowersMalik et al., 2023
    223cis-Linalool oxideSteam distilled essential oilLeaves and flowersLawal et al., 2014
    Aldehyde
    224E-15-heptadecenalSteam distilled essential oilLeavesKirsty et al., 2023
    225BenzaldehydeEthanolFlowersRakhmawati et al., 2022
    226Phenyl acetaldehydeSteam distilled essential oilLeaves and flowersLawal et al., 2014
    Esters
    227Norborneol acetateSteam distilled essential oilLeaves and flowersLawal et al., 2014
    228Benzyl salicylateSteam distilled essential oilFlowersSahoo et al., 2021
    229Benzyl benzoateSteam distilled essential oilFlowersSahoo et al., 2021
    230Sulfurous acid, dodecyl 2-propyl esterSteam distilled essential oilFlowersKirsty et al., 2023

    Primary metabolites

    Hassan et al., 2015 reported sugars including fucose, rhamnose, arabinose, glucose, and mannose along with polysaccharide complexes from hot water leaf extracts. The same study identified seventeen amino acids within protein-bound polysaccharides, indicating nutritional relevance. Primary metabolites such as sugars, amino acids, and polysaccharide complexes identified from aqueous leaf extracts are summarized in Table 9.

    Table 9: Primary metabolites (sugars and amino acids) reported from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    Sugars
    231FucoseNaOH as eluent for Hot water extractLeavesHassan et al., 2015
    232RhamnoseNaOH as eluent for Hot water extractLeavesHassan et al., 2015
    233ArabinoseNaOH as eluent for Hot water extractleavesHassan et al., 2015
    234GalactoseNaOH as eluent for Hot water extractleavesHassan et al., 2015
    235GlucoseNaOH as eluent for Hot water extractleavesHassan et al., 2015
    236MannoseNaOH as eluent for Hot water extractleavesHassan et al., 2015
    237Polysaccharide complexNaOH as eluent for Hot water extractleavesHassan et al., 2015
    Amino acidsHassan et al., 2015
    238Aspartic acidProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    239ThreonineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    240Glutamic acidProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    241SerineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    242ValineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    243AlanineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    244GlycineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    245ArginineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    246HistidineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    247LeucineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    248PhenylalanineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    249ProlineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    250ValineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    251LysineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    252TyrosineProtein bound polysaccharide in hot water extractleavesHassan et al., 2015
    253IsoleucineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    254CysteineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015
    255MethionineProtein bound polysaccharide complex in hot water extractleavesHassan et al., 2015

    Miscellaneous Compounds

    A small but diverse group of miscellaneous compounds has been identified in Plumeria alba, highlighting its broad phytochemical profile. These include lignans, vitamin E, aromatic ethers, apocarotenoids, sulfur compounds, and pyranone derivatives were reported by Rangaswami and Rao, 1960; Anggoro et al., 2020; Kirsty et al., 2023; and Sahoo et al., 2021. Phthalate esters were also detected in floral extracts by Lawal et al., 2014 and Sahoo et al., 2021. These constituents, though present in low amounts, add to the plant’s pharmacological and industrial relevance. The list of phytoconstituents under this category were presented in Table 10.

    Table 10: Miscellaneous compounds reported from Plumeria alba L.
    Compound No.CategoryName of the compoundExtractPart of the plantReferences
    256Lignin(+/-)-1,4-O-diferuloylsecoisolariciresionolN/ALeaves and barkAnggoro et al., 2020
    257VitaminVitamin EN/ALeaves and barkAnggoro et al., 2020
    258cyclohexane derivative1,4-cyclohexanedimethanamineMethanolflowersMalik et al., 2023
    259Ketone derivative2-Butanone, 4-[2-isopropyl-5-methyl-5-(2-methyl-5-oxocyclopentyl) cyclopentenyl]-Steam distilled essential oilFlowersKirsty et al., 2023
    260cyclic aromatic ether3,5-DimethylanisoleMethanolFlowersMalik et al., 2023
    261GlyceroneDihydroxyacetoneWaterFlowersMohammad et al., 2020
    262Apocarotenoidβ-CyclocitralSteam distilled essential oilLeaves and flowersLawal et al., 2014
    263Naphthalene derivativeα-MethylnaphthaleneSteam distilled essential oilLeaves and flowersLawal et al., 2014
    264Pentene derivative2-Pentene, 4-bromoEthanolFlowersRakhmawati et al., 2022
    265Inorganic compoundSilaneEthanolFlowersRakhmawati et al., 2022
    266Organic disulfaneDi-2-Benzothiazole disulfaneEthanolFlowersRakhmawati et al., 2022
    267Pyranone4H-pyran-4-one, 2,3-dihydro-3,5-dihydroxy-6-methylMethanolFlowersMalik et al., 2023
    268PyranoneGlycerin 2,3-dihydro-3,5-dihydroxy-6-methyl-4(H)-pyran-4-oneWaterFlowersMohammad et al., 2020
    269Pthalate ester1,2-Benzenedicarboxylic acid, butyl 8-methyl nonyl esterSteam distilled essential oilLeavesKirsty et al., 2023
    270Pthalate esterBis(2-ethylhexyl) phthalateEthyl acetateFlowersMohammad et al., 2020

    DISCUSSION

    The compiled phytochemical evidence establishes Plumeria alba L. as a metabolically rich Apocynaceae species characterized by a consistent secondary metabolite profile. Iridoids, particularly plumieride, plumericin, and related derivatives, represent defining chemotaxonomic markers of the genus, consistent with biosynthetic patterns observed in closely related taxa such as Allamanda. Several iridoids and terpenoids exhibit defined stereochemical configurations influencing biological activity, as demonstrated by NMR and optical rotation studies; however, stereochemical characterization remains limited for many recently reported metabolites.

    Flavonoids and phenolic compounds, predominantly localized in leaves and flowers, indicate a conserved antioxidant framework, while mono- and sesquiterpenes in floral essential oils emphasize ecological roles in pollinator attraction and defense. Polar solvents such as methanol and ethanol preferentially extracted flavonoids, phenolics, sugars, and amino acids, whereas non-polar solvents including petroleum ether and hexane favored sterols, triterpenes, hydrocarbons, and fatty acids, with essential oil constituents primarily obtained through steam distillation. Accordingly, leaves and flowers represent the most chemically diverse and pharmacologically promising plant parts.

    The presence of triterpenes, sterols, alkaloids, and modified terpenoid derivatives further expands the chemical space of P. alba, although most studies remain descriptive with limited mechanistic evaluation. Overall, the phytochemical consistency across plant parts and decades supports its placement within iridoid- and terpenoid-rich Apocynaceae and highlights opportunities for bioactivity-guided and translational research.

    CONCLUSION

    This comprehensive review highlights the diverse phytochemical profile of Plumeria alba, as reported in literature spanning from the 1960s to recent years. Major compound classes include iridoids, flavonoids, terpenoids (mono-, sesqui-, di-, and triterpenes), alkaloids, phenolics, coumarins, and fatty acids, each contributing distinct pharmacological activities. Numerous volatile compounds such as aldehydes, alcohols, esters, and hydrocarbons enhance its aromatic and therapeutic value. Floral parts were especially rich in volatile oils and alkaloids, while leaves yielded abundant phenolics and fatty acids. Several bioactive molecules, including scopoletin, ursolic acid, quercetin, and plumericin, support traditional medicinal uses. Antimicrobial, antioxidant, anti-inflammatory, and cytoprotective properties were commonly associated across classes. The presence of rare and structurally diverse compounds like apocarotenoids, sulfur derivatives, and lignans further adds to its pharmacological potential. Many constituents also suggest applications in cosmetics, perfumery, and nutraceuticals. The findings lay a solid foundation for future research aimed exploring their biological effects through well-designed pharmacological and mechanistic studies. Establishing robust links between specific phytochemicals and their bioactivities will be crucial for validating the therapeutic potential of Plumeria alba and guiding its applications in medicine, cosmetics, and nutraceuticals.

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    Lakshmi, S. V. V. N. S. M., Sri, K. T., Kumar, K. N., Supraja, K., & Manisha, K. (2026). An Updated Review on Phytochemistry of Plumeria alba L. (Apocynaceae). Pharmacognosy Research, 18(3), 679–697. https://doi.org/10.5530/pres.20260257