Jasminum multiflorum

Details Top

Internal ID UUID64402a88b5d85903725537
Scientific name Jasminum multiflorum
Authority Andrews
First published in Bot. Repos. 8: t. 496 (1807)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Perennial shrub and climber grown as an ornamental; cut flower for floristry.

Industrial and craft applications:
Insufficient documented uses in this taxon; no reported industrial or craft applications.

Food and beverages (non-medicinal):
No food, beverage, or culinary use reported for this species.

Colorants and tanning:
No colorant or tanning use reported.

Wood and fiber:
No timber or fiber use reported.

Fragrance and cosmetics:
The fragrant, night-blooming flowers yield a concrete and absolute used in perfumery, typically for floral heart notes in fine fragrances and some personal-care products. The extract is obtained by solvent extraction; composition typically includes benzyl acetate, benzyl benzoate, linalool, and indole. Processing steps reported for related Jasminum species include washing of the concrete with ethanol to obtain an absolute, with isolates for fragrance; data for J. multiflorum specifically are not separated from these closely related taxa in older references.

Properties relevant to use:
No specific compositional or physicochemical data for J. multiflorum flower extract are separated in reliable sources; fragrance use is tied to the characteristic volatile profile common to Jasminum.

Standards and regulation:
No specialized standards or regulatory references reported for this species.

Sustainability and sourcing:
No documented sustainability or sourcing programs specific to J. multiflorum are reported; cultivated as ornamental with no established wild harvesting for perfumery.

Synonyms Top

Scientific name Authority First published in
Jasminum pubescens Willd. Sp. Pl., ed. 4 , 1: 37 (1797)
Jasminum gracillimum Hook.f. Gard. Chron. , n.s., 15: 9 (1881)
Jasminum congestum Buch.-Ham. Numer. List [Wallich] n. 2874. 1831
Mogorium pubescens Lam. Encycl. 4: 213 (1797)
Mogorium multiflorum Lam. Encycl. 4: 211 (1797)
Nyctanthes pubescens Retz. Observ. Bot. 5: 9 (1788)
Nyctanthes multiflora Burm.f. Fl. Indica : 5 (1768)
Jasminum multiflorum f. pubescens (Retz.) Bakh.f. Blumea 6: 383 1950
Jasminum multiflorum var. nicobaricum Thoth. Bull. Bot. Surv. India 5: 99 (1963)

Common names Top

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Language Common/alternative name
English star jasmine
English indian jasmine
English winter jasmine
Arabic ياسمين متعدد الزهر
Assamese গুটিমালী ফুল
Bengali কুন্দ
Kannada ಕಸ್ತೂರಿ ಮಲ್ಲಿಗೆ
Kannada ಕಾಕಡ
Malayalam ജാസ്മീനം മൾട്ടിഫ്ലോറം
Dutch borneojasmin
Oriya କୁନ୍ଦ
Swedish borneojasmin
Vietnamese nhài nhiều hoa
Chinese 毛茉莉

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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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-0000813445
Florida Plant Atlas 161
USDA Plants JAMU2
Tropicos 23000155
INPN 445864
KEW urn:lsid:ipni.org:names:609641-1
The Plant List kew-351552
Open Tree Of Life 1070456
NCBI Taxonomy 310423
Nature Serve 2.161525
IPNI 609640-1
iNaturalist 164230
GBIF 3172267
Freebase /m/0c3wjd2
EPPO IASMU
EOL 579167
Calflora (Californian flora) 9348
USDA GRIN 20663
Wikipedia Jasminum_multiflorum

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
Twelve newly assembled jasmine chloroplast genomes: unveiling genomic diversity, phylogenetic relationships and evolutionary patterns among Oleaceae and Jasminum species Xu X, Huang H, Lin S, Zhou L, Yi Y, Lin E, Feng L, Zheng Y, Lin A, Yu L, Shen Y, Henry RJ, Fang J BMC Plant Biol 25-Apr-2024
PMCID:PMC11044428
doi:10.1186/s12870-024-04995-9
PMID:38664619
Corythauma ayyari (Insecta, Heteroptera, Tingidae) depends on its host plant to spread in Europe Durand M, Guilbert E PLoS One 26-Mar-2024
PMCID:PMC10965059
doi:10.1371/journal.pone.0295102
PMID:38530816
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
First report of tomato chlorosis virus (ToCV) and detection of other viruses in field-grown tomatoes in North-Western region of India Chaudhary P, Kaur A, Singh B, Kumar S, Hallan V, Nagpal AK Virusdisease 17-Dec-2022
PMCID:PMC10050630
doi:10.1007/s13337-022-00801-y
PMID:37009255
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Global Perspective of Plant-Based Cosmetic Industry and Possible Contribution of Sri Lanka to the Development of Herbal Cosmetics Nadeeshani Dilhara Gamage DG, Dharmadasa RM, Chandana Abeysinghe D, Saman Wijesekara RG, Prathapasinghe GA, Someya T Evid Based Complement Alternat Med 04-Mar-2022
PMCID:PMC8916882
doi:10.1155/2022/9940548
PMID:35280508
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Ethnopharmacological Survey on Medicinal Plants Used for Cosmetic Treatments in Traditional and Ayurveda Systems of Medicine in Sri Lanka Gamage DG, Dharmadasa RM, Abeysinghe DC, Wijesekara RG, Prathapasinghe GA, Someya T Evid Based Complement Alternat Med 26-Jun-2021
PMCID:PMC8257331
doi:10.1155/2021/5599654
PMID:34257686
ISSR-Based Genetic Diversity Assessment of Genus Jasminum L. (Oleaceae) from Pakistan Akhtar N, Hafiz IA, Hayat MQ, Potter D, Abbasi NA, Habib U, Hussain A, Hafeez H, Bashir MA, Malik SI Plants (Basel) 22-Jun-2021
PMCID:PMC8308950
doi:10.3390/plants10071270
PMID:34206638
Mechanistic Insight into Antimicrobial and Antioxidant Potential of Jasminum Species: A Herbal Approach for Disease Management Balkrishna A, Rohela A, Kumar A, Kumar A, Arya V, Thakur P, Oleksak P, Krejcar O, Verma R, Kumar D, Kuca K Plants (Basel) 28-May-2021
PMCID:PMC8227019
doi:10.3390/plants10061089
PMID:34071621
Pest categorisation of tomato leaf curl New Delhi virus Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Candresse T, Chatzivassiliou E, Winter S, Bottex B EFSA J 07-Jul-2020
PMCID:PMC7339215
doi:10.2903/j.efsa.2020.6179
PMID:32665794
Multifloroside Suppressing Proliferation and Colony Formation, Inducing S Cell Cycle Arrest, ROS Production, and Increasing MMP in Human Epidermoid Carcinoma Cell Lines A431 Zhang X, Li Y, Feng Z, Zhang Y, Gong Y, Song H, Ding X, Yan Y Molecules 18-Dec-2019
PMCID:PMC6983163
doi:10.3390/molecules25010007
PMID:31861384
Tomato Leaf Curl New Delhi Virus: An Emerging Virus Complex Threatening Vegetable and Fiber Crops Moriones E, Praveen S, Chakraborty S Viruses 21-Sep-2017
PMCID:PMC5691616
doi:10.3390/v9100264
PMID:28934148
Rapid and sensitive diagnoses of dry root rot pathogen of chickpea (Rhizoctonia bataticola (Taub.) Butler) using loop-mediated isothermal amplification assay Ghosh R, Tarafdar A, Sharma M Sci Rep 20-Feb-2017
PMCID:PMC5316965
doi:10.1038/srep42737
PMID:28218268

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenols / Tyrosols and derivatives
2-(3,4-dihydroxyphenyl)ethyl (1R,4aS,9S,9aS)-1-hydroxy-9-[2-(4-hydroxyphenyl)ethoxy]-6-oxo-1,4a,5,8,9,9a-hexahydropyrano[3,4-d]oxepine-4-carboxylate 14488040 Click to see 500.50 unknown https://doi.org/10.1021/NP50065A024
2-(3,4-Dihydroxyphenyl)ethyl 1-hydroxy-9-[2-(4-hydroxyphenyl)ethoxy]-6-oxo-1,4a,5,8,9,9a-hexahydropyrano[3,4-d]oxepine-4-carboxylate 14488038 Click to see C1C2C(C(COC1=O)OCCC3=CC=C(C=C3)O)C(OC=C2C(=O)OCCC4=CC(=C(C=C4)O)O)O 500.50 unknown https://doi.org/10.1021/NP50065A024
2-(3,4-Dihydroxyphenyl)ethyl 9-[2-(3,4-dihydroxyphenyl)ethoxy]-1-hydroxy-6-oxo-1,4a,5,8,9,9a-hexahydropyrano[3,4-d]oxepine-4-carboxylate 14488043 Click to see C1C2C(C(COC1=O)OCCC3=CC(=C(C=C3)O)O)C(OC=C2C(=O)OCCC4=CC(=C(C=C4)O)O)O 516.50 unknown https://doi.org/10.1021/NP50065A024
Jasmolactone A 14488033 Click to see 394.40 unknown https://doi.org/10.1021/NP50065A024
Jasmolactone B 11049569 Click to see C1C2C(C(COC1=O)OCCC3=CC(=C(C=C3)O)O)C(OC=C2C(=O)OCCC4=CC(=C(C=C4)O)O)O 516.50 unknown https://doi.org/10.1021/NP50065A024
methyl (1R,4aS,9S,9aS)-1-hydroxy-9-[2-(4-hydroxyphenyl)ethoxy]-6-oxo-1,4a,5,8,9,9a-hexahydropyrano[3,4-d]oxepine-4-carboxylate 14488028 Click to see COC(=O)C1=COC(C2C1CC(=O)OCC2OCCC3=CC=C(C=C3)O)O 378.40 unknown https://doi.org/10.1021/NP50065A024
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
10-Hydroxyligstroside 14756316 Click to see 540.50 unknown https://doi.org/10.1016/0031-9422(90)87103-2
10-Hydroxyoleuropein 6440747 Click to see 556.50 unknown https://doi.org/10.1021/NP50076A026
https://doi.org/10.1016/0031-9422(90)87103-2
2-(3,4-dihydroxyphenyl)ethyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-(2-hydroxyethylidene)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 10919492 Click to see C1=CC(=C(C=C1CCOC(=O)CC2C(=COC(C2=CCO)OC3C(C(C(C(O3)CO)O)O)O)C(=O)OCCC4=CC(=C(C=C4)O)O)O)O 678.60 unknown https://doi.org/10.1016/0031-9422(90)87103-2
2-(3,4-dihydroxyphenyl)ethyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-(2-hydroxyethylidene)-6-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162915961 Click to see 678.60 unknown https://doi.org/10.1016/0031-9422(90)87103-2
2-(3,4-dihydroxyphenyl)ethyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-(2-hydroxyethylidene)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 75111030 Click to see C1=CC(=C(C=C1CCOC(=O)CC2C(=COC(C2=CCO)OC3C(C(C(C(O3)CO)O)O)O)C(=O)OCCC4=CC(=C(C=C4)O)O)O)O 678.60 unknown https://doi.org/10.1016/0031-9422(90)87103-2
2-[(2S,3E,4S)-3-(2-Hydroxyethylidene)-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetic acid 14781483 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 420.40 unknown https://doi.org/10.1016/0031-9422(90)87103-2
2-[3-(2-hydroxyethylidene)-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetic acid 138113280 Click to see 420.40 unknown https://doi.org/10.1016/0031-9422(90)87103-2
methyl (4S,5E,6S)-5-(2-hydroxyethylidene)-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163187816 Click to see 540.50 unknown https://doi.org/10.1016/0031-9422(90)87103-2
methyl (4S,5E,6S)-5-(2-hydroxyethylidene)-4-[2-[2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 14781477 Click to see 718.70 unknown https://doi.org/10.1016/0031-9422(90)87103-2
methyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-(2-hydroxyethylidene)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 78410094 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 556.50 unknown https://doi.org/10.1016/0031-9422(90)87103-2
methyl 5-(2-hydroxyethylidene)-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 74184139 Click to see 540.50 unknown https://doi.org/10.1016/0031-9422(90)87103-2
methyl 5-(2-hydroxyethylidene)-4-[2-[2-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163039380 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 718.70 unknown https://doi.org/10.1016/0031-9422(90)87103-2
Neooleuropein 6442861 Click to see 662.60 unknown https://doi.org/10.1021/NP50076A026
> Organoheterocyclic compounds / Furopyrans
Methyl 6-oxo-2,5,11-trioxatricyclo[6.3.1.04,12]dodec-9-ene-9-carboxylate 163011309 Click to see 240.21 unknown https://doi.org/10.1002/JCCS.199400062
Multiflorin 163011310 Click to see 240.21 unknown https://doi.org/10.1002/JCCS.199400062

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