Details Top

Internal ID UUID6440044c3a72e474738465
Scientific name Swertia chirayta
Authority (Roxb.) H.Karst.
First published in Deut. Fl. : 1025 (1883)

Ethnobotanical Use Top

Write a new one!
No ethnobotanical data added yet. Help us by writing one.

General Uses Top

Suggest a correction!

Common products:
- Dried aerial parts of Swertia chirayita are marketed as a source of natural bitter extracts used in the production of alcoholic bitters and some non‑alcoholic tonic formulations.
- Amarogentin, a secoiridoid glycoside isolated from the aerial parts, is sold as a reference standard for bitterness by major chemical‑supply companies (e.g., Sigma‑Aldrich, Cayman Chemical).
- Bulk extracts standardized for amarogentin content are supplied to flavor‑and‑beverage manufacturers seeking natural bittering agents.

Scientific/model‑organism use:
- Amarogentin is employed internationally as the bitterness reference substance in sensory‑analysis laboratories, allowing quantitative comparison of taste thresholds across food and drink matrices.
- Swertia chirayita serves as a model system for research on secoridoid glycoside biosynthesis; key enzymes such as geraniol‑8‑hydroxylase (G8H) and amarogentin synthase have been cloned and expressed in heterologous hosts to study pathway regulation.

Food and beverages (non‑medicinal):
- Extracts of Swertia chirayita (dried, ground aerial parts) are incorporated as natural bittering components in the formulation of craft‑style alcoholic bitters and in experimental tonic beverages, providing a bitter taste without added synthetic compounds.
- The extracts are used to create “bitter” flavor profiles in certain specialty liqueurs where a sharp, clean bitterness is desired.

Properties relevant to use:
- Amarogentin belongs to the secoridoid glycoside class and exhibits an extremely low bitterness threshold of approximately 5 × 10⁻⁸ g L⁻¹, making it one of the most potent natural bitterants known.
- The compound is soluble in water and ethanol and remains stable under acidic conditions (pH 3–5) typical of many beverage applications.
- Total bitterness of plant extracts is routinely quantified by amarogentin equivalents, facilitating batch‑to‑batch consistency in commercial formulations.

Standards and regulation:
- Amarogentin is listed as a bitterness reference substance in ISO 4139 (Sensory analysis – Reference substances for bitterness), which is used by sensory panels worldwide.
- No specific regulatory approval exists for Swertia chirayita extracts as food additives; any use as a flavor must comply with national food‑additive regulations (e.g., EU Novel Food, U.S. GRAS) and requires safety assessment.
- Analytical‑grade amarogentin is provided as a certified reference material by organizations such as the United States Pharmacopeia (USP).

Sustainability and sourcing:
- The species occurs in sub‑Himalayan forests and is classified as Vulnerable on the IUCN Red List due to over‑harvest for medicinal and flavoring markets.
- Sustainable cultivation programs in India and Nepal have been established, employing seed propagation and tissue‑culture techniques to reduce pressure on wild populations.
- Certification initiatives such as FairWild promote responsible wild collection of Swertia chirayita, encouraging traceability and the implementation of harvest‑monitoring plans to safeguard long‑term availability.

Synonyms Top

Scientific name Authority First published in
Henricea pharmacearcha Lem.-Lis. Bull. Sci. Soc. Philom. Paris 11: 171 (1824)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000498214
IPNI 370833-1
iNaturalist 602692
GBIF 5596315
Elurikkus 553323
Open Tree Of Life 1000758

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)!
Title Authors Publication Released IDs
Crystal structure of 1,5,8-trihydroxyl-3-methoxy xanthone from Swertia chirayita GaoFeng Shi, RunHua Lu, YunShang Yang, ChunLei Li, AiMei Yang, LiXiang Cai Springer Science and Business Media LLC 05-Apr-2005
doi:10.1007/S10870-005-2802-7
X-Ray crystal structure of swertanone, a triterpene of new skeletal type from Swertia chirata Buch.-Ham. Ajit K. Chakravarty, Binayak Das, Satyesh C. Pakrashi, Donald R. McPhail, Andrew T. McPhail Royal Society of Chemistry (RSC) 01-Apr-2004
doi:10.1039/C39890000438
Unexpected Biosynthetic Precursors of Amarogentin − A Retrobiosynthetic13C NMR Study Chang-Zeng Wang, Ulrich H. Maier, Wolfgang Eisenreich, Petra Adam, Ingrid Obersteiner, Michael Keil, Adelbert Bacher, Meinhart H. Zenk Wiley 25-Aug-2002
doi:10.1002/1099-0690(200104)2001:8<1459::AID-EJOC1459>3.0.CO;2-0
Swertane triterpenoids from Swertia chirata Ajit Kumar Chakravarty, Sibabrata Mukhopadhyay, Binayak Das Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83473-X
Triterpenoids from Swertia petiolata Satesh Bhan, Rajive Kumar, Ashok K. Kalla, K.L. Dhar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83137-6
A xanthone from Swertia chirayita Rakesh K. Asthana, Narendra K. Sharma, Dinesh K. Kulshreshtha, Sunil K. Chatterjee Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)85308-M
Amarogentin, a naturally occurring secoiridoid glycoside and a newly recognized inhibitor of topoisomerase I from Leishmania donovani. Ray S, Majumder HK, Chakravarty AK, Mukhopadhyay S, Gil RR, Cordell GA J Nat Prod 01-Jan-1996
doi:10.1021/NP960018G
PMID:8984149
Hypoglycemic effect of swerchirin from the hexane fraction of Swertia chirayita. Bajpai MB, Asthana RK, Sharma NK, Chatterjee SK, Mukherjee SK Planta Med 01-Apr-1991
doi:10.1055/S-2006-960041
PMID:1891489
Chemical constituents of the gentianaceae V: tetraoxygenated xanthones of Swertia chirata Buch.-Ham. Ghosal S, Sharma PV, Chaudhuri RK, Bhattacharya SK J Pharm Sci 01-Jun-1973
doi:10.1002/JPS.2600620614
PMID:4712626
[Studies on the constituents of Swertia japonica. V. On the xanthone constituents of the plants of Swertia ssp]. Tomimori T, Komatsu M Yakugaku Zasshi 01-Jan-1970
doi:10.1248/YAKUSHI1947.89.3_410
PMID:5815804

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[2-[[(4aR)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 2,4-dihydroxy-6-(3-hydroxyphenyl)benzoate 137795174 Click to see 586.50 unknown https://doi.org/10.1021/NP960018G
Amarogentin 115149 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O 586.50 unknown https://doi.org/10.1021/NP960018G
https://doi.org/10.1002/1099-0690(200104)2001:8<1459::AID-EJOC1459>3.0.CO;2-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Mohangic acid D 127047614 Click to see CC(CC(C)C(C(C)C=CC=CC=CC(CC(=O)O)O)O)C(CC(C1=CC=C(C=C1)NC(=O)C)O)O 503.60 unknown https://doi.org/10.1248/YAKUSHI1947.89.3_410
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
4,4,6a,6b,8a,9,9,14b-octamethyl-2,4a,5,7,8,10,11,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 72745637 Click to see 424.70 unknown https://doi.org/10.1039/C39890000438
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-hexamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-9-ol 12309610 Click to see CC(=C)C1CCC2(C1CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
5a,5b,8,8,11a,13b-Hexamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-9-ol 604951 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Methyl 6-hydroxy-2,6-dimethylocta-2,7-dienoate 72728877 Click to see 198.26 unknown https://doi.org/10.1016/0031-9422(91)83473-X
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aR,6aR,6aS,8aS,12aR,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 162931943 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol 344467 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-16-Gammaceren-3beta-ol 14447659 Click to see CC1(CCCC2(C1=CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
(3R,4aR,6aS,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,8a,9,9,14b-octamethyl-1,2,3,4a,5,7,8,10,11,12,12a,13,14,14a-tetradecahydropicen-3-ol 101619548 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
(3R,4aR,6aS,6bS,8aS,12aR,14aS,14bR)-4,4,6a,6b,8a,9,9,14b-octamethyl-1,2,3,4a,5,7,8,10,11,12,12a,13,14,14a-tetradecahydropicen-3-ol 163021778 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
(3S,4aS,6aS,6bS,8aS,12aR,14aS,14bR)-4,4,6a,6b,8a,9,9,14b-octamethyl-1,2,3,4a,5,7,8,10,11,12,12a,13,14,14a-tetradecahydropicen-3-ol 163021780 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
(4aR,6aS,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,8a,9,9,14b-octamethyl-2,4a,5,7,8,10,11,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 15127586 Click to see 424.70 unknown https://doi.org/10.1039/C39890000438
(4aR,6aS,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,8a,9,9,14b-octamethyl-2,4a,5,7,8,10,11,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 102285187 Click to see 424.70 unknown https://doi.org/10.1039/C39890000438
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(88)83137-6
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholest-4-en-3-one 15596633 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(3S,4aR,6aR,6aR,6bR,12aR,14aR,14bR)-4,4,6a,6b,10,10,12a,14b-octamethyl-1,2,3,4a,5,6,6a,7,9,11,12,13,14,14a-tetradecahydropicen-3-ol 14831162 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(91)83473-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxy-2,3,4,5-tetramethoxyxanthone 5318357 Click to see 332.30 unknown https://doi.org/10.1007/S10870-005-2802-7
1-Hydroxy-2,3,4,7-tetramethoxyxanthone 5318358 Click to see 332.30 unknown https://doi.org/10.1007/S10870-005-2802-7
1-Hydroxy-3,5-dimethoxy-xanthen-9-one 5479773 Click to see COC1=CC=CC2=C1OC3=CC(=CC(=C3C2=O)O)OC 272.25 unknown https://doi.org/10.1007/S10870-005-2802-7
1-Hydroxy-3,5,8-trimethoxyxanthone 5378285 Click to see 302.28 unknown https://doi.org/10.1002/JPS.2600620614
1,8-Dihydroxy-3,7-dimethoxyxanthone 5281653 Click to see 288.25 unknown https://doi.org/10.1002/JPS.2600620614
3,8-Dihydroxy-1,4-dimethoxyxanthone 86108288 Click to see 288.25 unknown https://doi.org/10.1248/YAKUSHI1947.89.3_410
Bellidifolin 5281623 Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)O)O)O 274.22 unknown https://doi.org/10.1007/S10870-005-2802-7
Chiratol 10356746 Click to see 288.25 unknown https://doi.org/10.1016/0031-9422(91)85308-M
Swerchirin 5281660 Click to see 288.25 unknown https://doi.org/10.1016/0031-9422(91)85308-M
https://doi.org/10.1007/S10870-005-2802-7
https://doi.org/10.1055/S-2006-960041

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.