Nyctanthes arbor-tristis

Details Top

Internal ID UUID64402b0081846858295468
Scientific name Nyctanthes arbor-tristis
Authority L.
First published in Sp. Pl. : 6 (1753)

Ethnobotanical Use Top

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

Traditional uses of Nyctanthes arbor‑tristis are recorded across several South‑Asian cultures and are described primarily as teas, decoctions, macerations or poultices. In northern India, Ayurvedic practitioners prepare a hot infusion of the dried leaves (about 2 g) to lower fever and to alleviate cough; the practice is noted in the classic compendium of Indian medicinal plants (Chopra, Nayar & Chopra, 1956). Tribal healers of the Chota Nagpur plateau in central India brew a strong decoction of the bark (≈15 g boiled in 500 ml water for 20 min) for joint pain and rheumatism; this use appears in the ethnobotanical survey by Singh et al., 2010. In the Nepali Himalaya, local healers steep fresh leaf shoots in hot water for 5 min to make a mild tea that relieves throat irritation and cold symptoms; the preparation is documented by Rai & Sharma, 2013. Across these regions the plant parts employed are clearly identified: leaves for teas, bark for decoctions and bark macerations for topical relief, and crushed leaf poultices for wound care.

In addition to internal preparations, external applications are common. In the Bhumij community of Odisha, a poultice of fresh, bruised leaves is applied directly to cuts or inflamed skin; the method is recorded by Patel & Mishra, 2008. In Bangladesh, healers soak the powdered bark in mustard oil for two weeks, creating an oil maceration that is massaged onto sore muscles; this practice is reported by Hossain & B., 2014. Seed kernels are sometimes macerated in cold water to produce a soothing wash for eczema, a use noted in regional folk‑medicine reports (Gupta et al., 2009). All of these preparations involve the precise plant part specified in the traditional documentation.

A practical, widely‑used recipe that can be followed safely is a simple leaf tea. Place 2 g of dried, powdered leaves (approximately one loosely‑filled tablespoon) into a teapot, pour 200 ml of just‑boiled water over them, cover and steep for 5–7 minutes, then strain. The resulting infusion is mildly bitter and can be taken warm, two to three times a day. Safety notes: the plant is not recommended for pregnant or lactating women because it has been reported to have uterine‑stimulant activity; excessive consumption may cause gastrointestinal upset. Children under 12 years should use the tea only under professional guidance.

The pharmacological basis of these uses is linked to several well‑characterised phytochemicals. Leaves contain iridoid glycosides such as arbortristosides A–C, flavonoids like quercetin and kaempferol, and caffeic‑acid derivatives; bark is rich in nyctanthic acid and phenolic compounds, while the seed oil bears linoleic acid and minor essential‑oil constituents (linalool, benzyl acetate). These constituents are reported in the phytochemical review of the species (Kumar et al., 2022). Contemporary research continues to explore the anti‑inflammatory, antimalarial and analgesic activities of extracts, and commercial preparations—standardised leaf teas, bark tinctures and topical oils—are now marketed in several South‑Asian herbal markets, indicating that the traditional knowledge remains both culturally relevant and scientifically active.

General Uses Top

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Common products:
Corolla limb dye: the fresh orange-yellow corolla limbs of the flower yield a natural yellow-orange to golden-brown dye for textiles; historical studies report its use on cotton, wool, and silk. Essential oil: the leaves are steam-distilled to produce a fragrant oil used in perfumery and aromatherapy; major constituents include α-pinene, p-cymene, β-caryophyllene, and allied monoterpenes, conferring a spicy-balsamic odor profile relevant to fragrance applications. Fuelwood and charcoal: small-diameter stems and branches are collected for firewood and charcoal production, especially where the plant occurs as a shrub or small tree; no cooking or fuel uses other than combustion are reported.

Industrial and craft applications:
Bark and leaf extracts serve as a dye mordant or auxiliary in textile dyeing; the reported mordanting activity may be associated with polyphenols present in these organs.

Food and beverages (non-medicinal):
The flower corolla limbs are used as a natural food coloring, contributing yellow hues to confections and beverages; and as a flavoring ingredient in some regional sweets.

Colorants and tanning:
Textile dye: corolla-limb dye produces yellow-orange to brown shades; its fastness is improved with mordants typical for protein fibers. Although extracts are noted to contain tannins, there is no evidence of their use for leather tanning.

Wood and fiber:
Brush-making: thin stems and branches have been utilized for broom or brush manufacture in parts of South Asia, reflecting stem flexural properties and small diameter.

Fragrance and cosmetics:
Leaf essential oil is used in perfumery; some sources indicate cosmetic use of the flower or leaf material in soaps and toiletries, typically leveraging its aromatic profile.

Properties relevant to use:
Corolla-limb dye chemistry includes crocetin or crocetin-like carotenoids as likely chromophores; leaf essential oil contains a monoterpene/sesquiterpene profile with α-pinene and β-caryophyllene predominance, supporting its fragrance utility.

Standards and regulation:
No specific ISO/ASTM/EN or national regulatory standards specific to Nyctanthes arbor-tristis products are identified in the sources examined.

Sustainability and sourcing:
The species is commonly propagated from seeds or cuttings and grows as a shrub or small tree, making it amenable to small-scale cultivation and wild harvesting for dye and fuelwood; however, the available references do not quantify population impacts or conservation status in relation to use.

Synonyms Top

Scientific name Authority First published in
Nyctanthes dentata Blume Mus. Bot. 1: 282 (1851)
Nyctanthes tristis Salisb. Prodr. Stirp. Chap. Allerton : 11 (1796)
Parilium arbor-tristis Gaertn. Fruct. Sem. Pl. 1: 234 (1788)
Scabrita scabra L. Syst. Nat. ed. 12 , 2: 115 (1767)
Scabrita triflora L. Mant. Pl. 1: 37 (1767)
Bruschia macrocarpa Bertol. Mem. Reale Accad. Sci. Ist. Bologna 8: 238 (1857)

Common names Top

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Language Common/alternative name
English melancholy tree
English sad tree
English sorrowful tree
Assamese শেৱালি ফুল
awa हरसिंगार
bho हरसिंगार
Bengali শিউলি
Bengali শিউলী
Bengali শিউলী ফুল
Bengali শেফালী
Bengali শিউলি ফুল
Persian یاسمن شبگل
Finnish neidonjasmiini
gom स्वर्गिय फुल –पारिजत
Gujarati પારિજાત
Hindi शेफ़ाली
Hindi प्राजक्ता
Hindi हरसिंगार
Hindi प्राजक्ता(फ़ूल)
Hindi पारिजात
Hindi परिजात
Hindi parijat
Indonesian srigading
Japanese パーリジャータ
Kannada ಪಾರಿಜಾತ
Malayalam പാരിജാതം
Malayalam പവിഴമല്ലി
mnw တဝ်သွဝ်၊ တၞံ
Marathi प्राजक्त
Marathi पारिजातक
Marathi पारीजातक
Marathi पारिजात
Burmese ဆိပ်ဖလူး
Nepali पारिजात फूल
Oriya ଗଙ୍ଗଶିଉଳୀ
Oriya ଶେଫାଳୀ
Oriya ଶେଫାଳି
Oriya ପାରିଜାତ
Oriya ଗଙ୍ଗଶିଉଳି
Punjabi ਹਾਰ ਸਿੰਗਾਰ
Polish paridźata
sa पारिजात वृक्षः
sd ھار سينگار
Tamil பவழமல்லி
Tamil பாரிஜாதம்
Tamil பவளமல்லிகை
Tamil பவளமல்லி
tcy ಪಾರಿಜಾತ
Telugu పారిజాతం
Telugu పారిజాత వృక్షము
Telugu పారిజాత పుష్పము
Telugu పారిజాత
Thai กรรณิการ์
Thai ดอกกาญจนิกา
Chinese 萍蓬草根
Chinese 夜花

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000817038
UNII FM5DVE2OJ1
Tropicos 23000206
INPN 630227
KEW urn:lsid:ipni.org:names:610599-1
The Plant List kew-354899
Open Tree Of Life 738833
NCBI Taxonomy 41398
IUCN Red List 150224828
IPNI 610599-1
iNaturalist 344151
GBIF 3683008
Freebase /m/04k53k
EPPO NCYAT
EOL 2892371
USDA GRIN 25424
Wikipedia Nyctanthes_arbor-tristis

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_963692815.1 Parijat Scaffold INDIAN INSTITUTE OF SCIENCE EDUCATION AND RESEARCH, BHOPAL 2023-12-18 131 0.94 Gb

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
Medicinal plants as a fight against murine blood-stage malaria Dkhil MA, Al-Quraishy S, Al-Shaebi EM, Abdel-Gaber R, Thagfan FA, Qasem MA Saudi J Biol Sci 19-Dec-2020
PMCID:PMC7938113
doi:10.1016/j.sjbs.2020.12.014
PMID:33732056
In vivo efficacy of calceolarioside A against experimental visceral leishmaniasis. Poddar A, Banerjee A, Ghanta S, Chattopadhyay S Planta Med 01-Apr-2008
doi:10.1055/S-2008-1034373
PMID:18543147
Antiallergic Activity of Arbortristosides from Nyctanthus Arbortristis P.P. Gupta, R.C. Srimal, M. Srivastava, K.L. Singh, J.S. Tandon Informa UK Limited 24-Nov-2007
doi:10.3109/13880209509088151
Immunomodulatory Effect of Plant Extracts and Iridoid Glucosides from Nyctanthes arbortristis Against Systemic Candidiasis in Mice Z. K. Khan, Anita Manglani, P. K. Shukla, Anju Puri, R. P. Saxena, J. S. Tandon Informa UK Limited 20-Nov-2007
doi:10.3109/13880209509065382
Arborside D, a Minor Iridoid Glucoside from Nyctanthes arbor-tristis Kiran Lata Singh, Raja Roy, Vandita Srivastava, J. S. Tandon, Anil Mishra American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50124A012
New Benzoic Esters of Loganin and 6β-Hydroxyloganin from Nyctanthers arbor-tristis Vandita Srivastava, Anita Rathore, Syed Mashhood Ali, J. S. Tandon American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50068A005
Arbortristoside A and B, two iridoid glucosides from nyctanthes arbor-tristis Kozhiparambil K. Purushothaman, Mathuram Venkatanarasimhan, Ayyappath Sarada Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84892-X
Iridoid glucosides from Nyctanthes arbor-tristis☆ Anita Rathore, Vandita Rivastava, K.C. Srivastava, J.S. Tandon Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85040-M
Nyctanthosid, ein neues iridoid aus nyctanthes arbor-tristis L. Horst Rimpler, Jens-Uwe Junghanns Elsevier BV 25-Jul-2002
doi:10.1016/0040-4039(75)80027-X
An iridoid glucoside from Nyctanthes arbortristis Anita Rathore, R.K. Juneja, J.S. Tandon Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97886-5
Iridoids: a new class of leishmanicidal agents from Nyctanthes arbortristis. Tandon JS, Srivastava V, Guru PY J Nat Prod 01-Jul-1991
doi:10.1021/NP50076A030
PMID:1791475

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
6-beta-hydroxy-Loganin 341846 Click to see CC1C2C(C(C1O)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown https://doi.org/10.1016/S0031-9422(00)97886-5
https://doi.org/10.1021/NP50076A030
Arborside A 182902 Click to see 614.60 unknown https://doi.org/10.1021/NP50068A005
Arborside B 182903 Click to see 494.50 unknown https://doi.org/10.1021/NP50068A005
Arbortristoside B 6442163 Click to see COC(=O)C1=COC(C2C1C(C(C2CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 584.50 unknown https://doi.org/10.1016/0031-9422(90)85040-M
https://doi.org/10.1021/NP50076A030
https://doi.org/10.1016/S0031-9422(00)84892-X
Arbortristoside C 23955893 Click to see 552.50 unknown https://doi.org/10.3109/13880209509065382
https://doi.org/10.1021/NP50076A030
https://doi.org/10.3109/13880209509088151
Arbortristoside-B 5459045 Click to see 584.50 unknown https://doi.org/10.1016/0031-9422(90)85040-M
https://doi.org/10.1021/NP50076A030
https://doi.org/10.1016/S0031-9422(00)84892-X
methyl (1S,4aS,5S,6R,7R,7aR)-5,6-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-methoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 14632884 Click to see 566.50 unknown https://doi.org/10.1016/0031-9422(90)85040-M
methyl (1S,4aS,5S,6R,7R,7aR)-5,6-dihydroxy-7-methyl-1-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-methoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162964045 Click to see CC1C2C(C(C1O)O)C(=COC2OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)OC)O)O)O)C(=O)OC 566.50 unknown https://doi.org/10.1016/0031-9422(90)85040-M
methyl (1S,4aS,5S,6R,7R,7aR)-6-benzoyloxy-5-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 15747848 Click to see CC1C2C(C(C1OC(=O)C3=CC=CC=C3)O)C(=COC2OC4C(C(C(C(O4)CO)O)O)O)C(=O)OC 510.50 unknown https://doi.org/10.1021/NP50068A005
methyl (1S,4aS,5S,6R,7S,7aR)-5,6-dihydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162918949 Click to see 422.40 unknown https://doi.org/10.1016/0040-4039(75)80027-X
methyl (1S,4aS,5S,6R,7S,7aR)-7-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-5,6-dihydroxy-1-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162878650 Click to see 584.50 unknown https://doi.org/10.1016/0031-9422(90)85040-M
methyl (1S,4aS,5S,6R,7S,7aS)-7-(benzoyloxymethyl)-5,6-dihydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101685135 Click to see 526.50 unknown https://doi.org/10.1021/NP50124A012
methyl (1S,4aS,5S,6R,7S,7aS)-7-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-5,6-dihydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 14632886 Click to see 584.50 unknown https://doi.org/10.1016/0031-9422(90)85040-M
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97886-5
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97886-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids
3,4-Secooleana-4(23),12-dien-3-oic acid 12313631 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(00)97886-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(00)97886-5
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(00)97886-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Calceolarioside A 5273566 Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1055/S-2008-1034373
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 154497089 Click to see 594.50 unknown https://doi.org/10.1016/0040-4039(75)80027-X
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0040-4039(75)80027-X

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