Details Top

Internal ID UUID643fdafed8d2a815557639
Scientific name Saraca asoca
Authority (Roxb.) Willd.

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.

Among the traditions most closely associated with Saraca asoca is classical Ayurveda, where a bitter decoction of the dried stem bark is used to support “shothahara,” a property attributed to dampening excessive uterine bleeding and pelvic discomfort. Ashoka bark (asoka twak) is mentioned in pharmacopoeial texts as an internal remedy and is also part of standard decoctions and infusions used for menstrual regulation in Indian practice (Ayurvedic Pharmacopoeia of India, Part I, Vol. 2, 2001). In the Bengal ethnobotanical surveys, patients preparing a tea or decoction from small bark chips for menorrhagia and anemia were recorded in Bangladesh, showing continuity of bark use into living traditions (Yusuf et al., 2008). During South Asian household care, especially in Bangladesh and Assam, a mild infusion or decoction of Ashoka flowers—called “Ashoka pushpa”—is taken to support postpartum recovery and uterine cleansing after delivery, a practice noted in community studies in Bangladesh and a 2014 survey of medicinal plants in Assam (Abdul Malek, 2017; Neog et al., 2014). Across these regions, the plant part used is always the bark (and sometimes the flowers) and the preparation is consistently an aqueous infusion or decoction; this is clearly documented in pharmacopoeial and ethnobotanical sources rather than in general folklore alone.

A practical, time‑tested preparation is an Ashoka bark tea: measure 4–6 g of coarse, cut dried stem bark (roughly a heaping teaspoon), add to 250–300 mL of water, bring to a simmer for 10–12 minutes, then steep off the heat for 5–7 minutes and strain. This yields a lightly bitter, dark‑amber beverage whose bitterness signals the presence of tannins. For established formulations from the Ayurvedic Pharmacopoeia, a single dose of 5–10 g coarse bark in a decoction is recognized as a traditional range. Use no more than 1–2 cups per day for up to 10–14 days unless advised by a practitioner. Do not use during pregnancy or if you have hormone‑sensitive conditions; Ashoka is traditionally contraindicated in pregnancy in several Ayurvedic texts and should not be combined with anticoagulants or hormonal medications without professional guidance.

These traditional uses are aligned with the chemistry of the species. The bark contains high‑molecular‑weight tannins (including proanthocyanidins), simple phenolic acids such as gallic and ellagic acid, and flavonoids including quercetin and kaempferol glycosides; it also provides ketosteroids such as β‑sitosterol, a set of constituents that together can astringe mucus membranes, reduce bleeding, and dampen inflammation. Modern studies have begun to evaluate uterine‑calming and hemostatic actions of the extract and have confirmed the presence of those phytochemicals in Ashoka bark and flowers, offering plausible biochemical grounding for the centuries‑old decoction and infusion practices (Sultana et al., 2015; Dey et al., 2018). Today, Ashoka bark remains an ingredient in many women’s health tonics, is sold as a powdered bark for household decoctions, and continues to be collected and used in parts of South Asia, where artisans and herbal shops still prepare it to order, while research continues into its safety and efficacy.

General Uses Top

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Common products:
Saraca asoca yields timber, fuelwood, poles, a natural brown dyestuff for protein fibers, and bark tannins used in leather tanning. The species is widely cultivated as an avenue and garden tree.

Industrial and craft applications:
The wood is used for carpentry, furniture, tool handles, carved objects, and poles for fencing and light construction. It's also valued as fuelwood. Tannins from bark and wood are employed as a natural brown dye for wool and silk, producing fast shades suitable for leather finishing. Wood and bark are used for tanning leather; bark yields hydrolyzable tannins (~14–18% on air‑dry basis). Seed oil is explored as a non‑edible biodiesel feedstock, with high free fatty acid content enabling acid‑catalyzed transesterification.

Colorants and tanning:
Aqueous extracts of bark and wood produce brown dyes on protein fibers and are used in leather tanning. The dye class is based on hydrolyzable tannins (gallotannins/ellagitannins). Dyeing requires mordants typical of natural tannin dyes to achieve fast, brown shades on wool or silk.

Properties relevant to use:
Wood density is medium (~0.8 g/cm³), suitable for carving and carpentry. Bark tannins are hydrolyzable and effective in leather tanning formulations and as brown dyes. Seed oil is non‑edible and suitable for biodiesel production due to high free fatty acids and a favorable fatty‑acid profile for fuel properties.

Sustainability and sourcing:
The species is cultivated in South and Southeast Asia for ornament and, where permitted, for bark. Sustainable collection practices include controlled harvesting of bark from live trees, rotation intervals to allow regeneration, and avoidance of over‑harvesting. Loss of habitat and restricted natural populations are reported, warranting management of collection and planting programs.

Synonyms Top

Scientific name Authority First published in
Saraca indica sensu Bedd., non L.

Common names Top

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Language Common/alternative name
English ashoka tree
Arabic شجرة أشوكا
Assamese অশোক ফুল
Bengali অশোক
dv ނިކަބިލިއްސަގަސް
Finnish temppeliasoka
French arbre ashoka
French saraca indica
Gujarati અશોક
Hindi अशोक वृक्ष
Hungarian hindu asókafa
Hungarian saraca indica
Indonesian angsoka
Indonesian pohon asoka
Indonesian asoka
Japanese 無憂樹
Japanese ムユウジュ
jv kembang asoka
Kannada ಅಶೋಕ ವೃಕ್ಷ
Korean 사라카 아소카
Malayalam അശോക
Malayalam അശോകം
Marathi अशोक
Norwegian Bokmål asoka
Nepali अशोक वृक्ष
Dutch දියරතඔලා
Oriya ଅଶୋକ
Punjabi ਅਸ਼ੋਕ
Polish asioka
Polish saraca indica
Punjab اشوک رکھ
Portuguese açoca
Portuguese saraca indica
Russian saraca indica
Russian Ашока
sa अशोकवृक्षः
sa अशोकवृक्षम्
sa अश्वत्थः
Sinhala දියරතඔලා
Slovenian ašoka
Slovenian drevo ašoka
Tamil அசோகு
Tamil பிண்டி
Tamil அசோகம்
Tamil செயலை
Tamil ஆயில
tcy ಅಶೋಕ ಮರ
Telugu అశోక
Telugu అశోకవృక్షం
Thai อโศกน้ำ
Vietnamese saraca indica
Vietnamese vàng anh lá bé
Chinese 无忧树
Chinese 無憂樹
Chinese 无忧花树
Chinese 火焰花
Chinese 印度无忧花
Chinese 无忧花

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
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Myanmar
    • Malesia
      • Jawa
      • Malaya
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000193380
UNII OO7O919190
Tropicos 13062723
INPN 706773
KEW urn:lsid:ipni.org:names:517883-1
The Plant List ild-39965
PFAF Saraca asoca
Open Tree Of Life 757467
NCBI Taxonomy 1073321
IUCN Red List 34623
IPNI 517883-1
iNaturalist 181406
GBIF 5359545
Freebase /m/02205g
EOL 11244090
USDA GRIN 315038
Wikipedia Saraca_asoca

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_026873985.1 TDU_SM_1.0.fasta Contig The University of Trans-disciplinary Health Sciences and Technology 2022-12-13 50 1.54 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
Phytochemicals from Bark Extracts and Their Applicability in the Synthesis of Thermosetting Polymers: An Overview Szmechtyk T, Małecka M Materials (Basel) 30-Apr-2024
PMCID:PMC11084627
doi:10.3390/ma17092123
PMID:38730929
Response of Extremely Small Populations to Climate Change—A Case of Trachycarpus nanus in Yunnan, China Wang X, Wang X, Li Y, Wu C, Zhao B, Peng M, Chen W, Wang C Biology (Basel) 05-Apr-2024
PMCID:PMC11048604
doi:10.3390/biology13040240
PMID:38666852
An Investigation of Quorum Sensing Inhibitors against Bacillus cereus in The Endophytic Fungus Pithomyces sacchari of the Laurencia sp. Xiang SL, Xu KZ, Yin LJ, Jia AQ Mar Drugs 31-Mar-2024
PMCID:PMC11051030
doi:10.3390/md22040161
PMID:38667778
Plant-mediated synthesis of silver nanoparticles: unlocking their pharmacological potential–a comprehensive review Dhir R, Chauhan S, Subham P, Kumar S, Sharma P, Shidiki A, Kumar G Front Bioeng Biotechnol 09-Jan-2024
PMCID:PMC10803431
doi:10.3389/fbioe.2023.1324805
PMID:38264582
Phytochemical-Based Study of Ethanolic Extract of Saraca asoca in Letrozole-Induced Polycystic Ovarian Syndrome in Female Adult Rats Bu N, Jamil A, Hussain L, Alshammari A, Albekairi TH, Alharbi M, Jamshed A, Bazmi RR, Younas A ACS Omega 01-Nov-2023
PMCID:PMC10652831
doi:10.1021/acsomega.3c05274
PMID:38024692
In-vitro antibacterial, antioxidant and anti-inflammatory and In-silico ADMET, molecular docking study on Hardwickia binata phytocompunds with potential inhibitor of skin cancer protein Manimegalai P, Selvam K, Prakash P, Kirubakaran D, Shivakumar MS, SenthilNathan S In Silico Pharmacol 23-Sep-2023
PMCID:PMC10517914
doi:10.1007/s40203-023-00163-3
PMID:37750071
Implementation of machine learning in DNA barcoding for determining the plant family taxonomy Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA Heliyon 21-Sep-2023
PMCID:PMC10520734
doi:10.1016/j.heliyon.2023.e20161
PMID:37767518
Natural sensitizer extracted from Mussaenda erythrophylla for dye-sensitized solar cell Rajaramanan T, Heidari Gourji F, Elilan Y, Yohi S, Senthilnanthanan M, Ravirajan P, Velauthapillai D Sci Rep 24-Aug-2023
PMCID:PMC10449896
doi:10.1038/s41598-023-40437-6
PMID:37620519
Epigenetic manipulation for secondary metabolite activation in endophytic fungi: current progress and future directions Verma A, Tiwari H, Singh S, Gupta P, Rai N, Kumar Singh S, Singh BP, Rao S, Gautam V Mycology 08-Aug-2023
PMCID:PMC10769123
doi:10.1080/21501203.2023.2241486
PMID:38187885
Plant-derived nanomaterials (PDNM): a review on pharmacological potentials against pathogenic microbes, antimicrobial resistance (AMR) and some metabolic diseases Okeke ES, Nweze EJ, Anaduaka EG, Okoye CO, Anosike CA, Joshua PE, Ezeorba TP 3 Biotech 04-Aug-2023
PMCID:PMC10403488
doi:10.1007/s13205-023-03713-w
PMID:37547919
Effect of Peganum harmala Total Alkaloid Extract on Sexual Behavior and Sperm Parameters in Male Mice Derbak H, Imre K, Benabdelhak AC, Moussaoui M, Kribeche A, Kebbi R, Ayad A Vet Sci 02-Aug-2023
PMCID:PMC10459670
doi:10.3390/vetsci10080498
PMID:37624285
Structural and optical properties of silver supported α-Fe2O3 nanocomposite fabricated by Saraca asoca leaf extract for the effective photo-degradation of cationic dye Azure B Gautam N, Singh KB, Snigdha, Upadhyay DD, Pandey G RSC Adv 01-Aug-2023
PMCID:PMC10391326
doi:10.1039/d3ra03315e
PMID:37533787
An ethnobotanical survey on phytomedicines based on traditional knowledge in the Barpeta district, Assam, India Bhattacharjya DK, Akhtar J, Deka P, Bharadwaj A J Ayurveda Integr Med 19-Jul-2023
PMCID:PMC10371788
doi:10.1016/j.jaim.2023.100763
PMID:37478633
Diversity, astaxanthin production, and genomic analysis of Rhodotorula paludigena SP9-15 Phuengjayaem S, Kingkaew E, Hoondee P, Rojsitthisak P, Sritularak B, Thitikornpong W, Thompho S, Pornputtapong N, Tanasupawat S Heliyon 16-Jul-2023
PMCID:PMC10395543
doi:10.1016/j.heliyon.2023.e18280
PMID:37539266
DIMPSAR: Dataset for Indian medicinal plant species analysis and recognition B R P, Rani NS Data Brief 14-Jul-2023
PMCID:PMC10375553
doi:10.1016/j.dib.2023.109388
PMID:37520649

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
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 14521039 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1007/S11418-007-0182-3
(2R,3S,4S,5S)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 154497439 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(CO3)O)O)O)C4=CC(=C(C=C4)O)OC)O 492.50 unknown https://doi.org/10.1007/S11418-007-0182-3
(2R,3S,4S,5S)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 158384172 Click to see 552.60 unknown https://doi.org/10.1007/S11418-007-0182-3
(2S,3R,4R,5S)-2-[[(1R,2S,3S)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 158384171 Click to see 552.60 unknown https://doi.org/10.1007/S11418-007-0182-3
Nudiposide 14521040 Click to see 552.60 unknown https://doi.org/10.1007/S11418-007-0182-3
Schizandriside 14521043 Click to see 492.50 unknown https://doi.org/10.1007/S11418-007-0182-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 Click to see 576.80 unknown https://doi.org/10.1007/S11418-007-0182-3
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S11418-007-0182-3
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1007/S11418-007-0182-3
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 14015960 Click to see 562.50 unknown https://doi.org/10.1007/S11418-007-0182-3
3,3',4',5,7-Pentahydroxyflavan(4->8)-3,4',5,7-tetrahydroxyflavan 14015946 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC=C(C=C6)O)O 562.50 unknown https://doi.org/10.1515/ZNB-1985-0630
Epiafzelechin-(4beta->8)-epicatechin 14015948 Click to see 562.50 unknown https://doi.org/10.1515/ZNB-1985-0630
Proanthocyanidin B2 5320711 Click to see 578.50 unknown https://doi.org/10.1007/S11418-007-0182-3
https://doi.org/10.1515/ZNC-1985-7-812
Procyanidin B 130556 Click to see 578.50 unknown https://doi.org/10.1515/ZNB-1985-0630
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1515/ZNC-1985-7-812
Procyanidin B2 122738 Click to see 578.50 unknown https://doi.org/10.1515/ZNC-1985-7-812
https://doi.org/10.1515/ZNB-1985-0630
https://doi.org/10.1007/S11418-007-0182-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1515/ZNB-1985-0630
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/0304-3835(93)90031-4
https://doi.org/10.1515/ZNB-1985-0630
https://doi.org/10.1515/ZNC-1985-7-812
https://doi.org/10.1007/S11418-007-0182-3
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,3R,4S,5S,6R)-2-[2-[(2S)-1-hydroxy-3-(4-hydroxy-3-methoxyphenyl)propan-2-yl]-4-(3-hydroxypropyl)-6-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 159325252 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)C(CC3=CC(=C(C=C3)O)OC)CO)CCCO 524.60 unknown https://doi.org/10.1007/S11418-007-0182-3

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