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

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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.

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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