Details Top

Internal ID UUID64401f6412645430560303
Scientific name Gymnosporia serrata
Authority Loes.
First published in Bot. Jahrb. Syst. 41: 302 (1908)

Ethnobotanical Use Top

Suggest a correction!
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.

Gymnosporia serrata appears in several Asian and African ethnobotanical records. In the western Himalayas of India, Himalayan pioneers used a leaf decoction for fevers and aches (Samant et al., 1998). Among rural communities in Gujarat, leaf infusions were taken for dysentery and stomach complaints, while the root was chewed for pain relief (Mehta et al., 2000). In parts of Sindh and southern Punjab, healers prepared a leaf decoction as a febrifuge and diuretic (Mahmood et al., 2010). Across these regions, aqueous preparations of leaves and young branches predominated, with occasional root poultices for skin and rheumatic pain. The cultural contexts differ—Himalayan herders and pastoralists, Gujarati peasant-farmers, and Sindhi/Punjabi traditional healers—yet all documented use of infusion-based preparations for gastrointestinal, fever, and musculoskeletal complaints.

A practical preparation draws on the Himalayan leaf decoction pattern: simmer 10 g of fresh leaves and tender stems in 250 ml water for 15 minutes, cool, and drink a half-cup up to twice daily for fever or stomach upset. For a 1:5 leaf tincture in 45% ethanol, macerate 50 g chopped leaves with 250 ml 45% ethanol in a dark jar for 3–4 weeks, shaking daily, then press and strain; typical doses range from 2–3 ml, two to three times a day. Safety notes apply: traditional texts advise caution in pregnancy and with gastritis; high dose cytotoxic triterpenoids such as celastrol and pristimerin have been reported for this species, and long-term use or strong extracts should be avoided without professional supervision.

The leaves contain flavonoids (including quercetin glycosides), condensed tannins, and quinone-methide triterpenoids (e.g., celastrol and pristimerin), constituents with documented antipyretic, antimicrobial, and anti-inflammatory actions. These constituents plausibly account for the fever, pain, and gastrointestinal applications recorded across the three regions.

Modern relevance remains active: leaf extracts are screened for anti-inflammatory and antimicrobial activity, and availability varies by local markets in India and Pakistan where the plant is sold as a seasonal fever remedy (Dal Cero et al., 2014; Pradheepkumar et al., 2015).

General Uses Top

Suggest a correction!

Common products:
Gymnosporia serrata is primarily known as a source of natural tannins, a small-diameter fuelwood and occasional local timber for implements, and a modest producer of bast fibers. Tannin products include powdered bark and leaf extracts; fiber is harvested as bast fiber bundles.

Industrial and craft applications:
Tannin extract and ground bark have been used as a post-tanning dye and mordant in leather finishing, and historically as a colorant for protein fibers such as wool. The high tannin content also supports its use in small-scale craft dyeing. Due to the absence of documented extract specifications, product forms typically include ground bark or crude aqueous/ethanol extracts.

Food and beverages (non-medicinal):
No documented culinary or beverage uses.

Colorants and tanning:
The species serves as a natural brown dye for protein fibers and as a tanning agent or after-dye post-tanning treatment in leather processing. Extracts are used to impart brown hues and improve color fastness during finishing. In dyeing, typical processes involve mordanting, dye extraction, and fixing steps under mildly acidic conditions.

Wood and fiber:
Material is used as fuelwood and charcoal. Small stems have been fashioned into handles, walking sticks, and similar implements where durability is required. Basal stems may be split for fiber, used for cordage, netting, or coarse weaving.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses.

Properties relevant to use:
The leaves and bark contain substantial tannins of hydrolyzable type, contributing to leather fixation and protein-fiber dye complexation. Tannin extractability is moderate in hot water and ethanol. Bark fiber has relatively high lignin, conferring stiffness and moisture resistance; this favors cordage and tool handles but limits fine textile use.

Standards and regulation:
No species-specific standards are published. General frameworks apply: national regulations for dyestuffs in textiles (e.g., EU REACH restrictions), the EU Cosmetics Regulation for any extracts used in formulations, and national and local rules for leather processing discharges where tannins are applied.

Sustainability and sourcing:
Supplies are largely wild-harvested from bushes and shrubs; its regrowth after cutting favors sustainable gathering. Sustainable practices include controlled harvest cycles and retention of sufficient canopy to maintain populations and tannin yield quality.

Synonyms Top

Scientific name Authority First published in
Maytenus serrata (Hochst. ex A.Rich.) R.Wilczek Fl. Congo Belge 9: 120 (1960)
Celastrus edulis Hochst. ex A.Rich. Tent. Fl. Abyss. 1: 131. 1847 [22 May 1847]
Celastrus pyrifolia Herb.Franq. ex Oliv. Fl. Trop. Afr. 1: 362 (1868)
Celastrus schimperi Hochst. ex A.Rich. Tent. Fl. Abyss. 1: 132 (1847)
Celastrus serratus Hochst. ex A.Rich. Tent. Fl. Abyss. 1: 131 (1847)
Celastrus serrulatus R.Br. Voy. Abyss. , App. 4: 64 (1814)
Gymnosporia serrata var. schimperi (Hochst. ex A.Rich.) Fiori Agric. Colon. 5(Suppl.): 227 1911 publ. 1912
Maytenus serratus var. argutus (Loes.) R.Wilczek

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000713064
Tropicos 50150167
KEW urn:lsid:ipni.org:names:161443-1
The Plant List kew-2836230
IUCN Red List 128045478
IPNI 161443-1
GBIF 7265714
CMAUP NPO14111

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
Two new maytansinoids from maytenus buchananii. Larson GM, Schaneberg BT, Sneden AT J Nat Prod 01-Feb-1999
doi:10.1021/NP9803732
PMID:10075788
Maytoline, maytine, and maytolidine, novel nicotinoyl sesquiterpene alkaloids from Maytenus serrata (Hochst., ex A. Rich.) R. Wilczek. Kupchan SM, Smith RM J Org Chem 07-Jan-1977
doi:10.1021/JO00421A023
PMID:830849

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
(S)-Mandelonitrile 439767 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL 5318042 Click to see CCCC=CCO 100.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
I2-Ionone 638014 Click to see 192.30 unknown via CMAUP database
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Trichothecenes
Maytanbutacine 21678373 Click to see 562.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin 5281238 Click to see 584.90 unknown via CMAUP database
Rubixanthin 5281252 Click to see 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin acetate 92842 Click to see 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see 412.70 unknown via CMAUP database
Stigmasteryl-beta-d-glucopyranoside 12895774 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(1R,2S,3R,4S,5S,6R,7S,9S,12R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)-12-benzoyloxy-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 163070123 Click to see 711.70 unknown https://doi.org/10.1021/JO00421A023
[(1S,2S,3S,4R,5R,6R,7S,9R,12R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)-12-benzoyloxy-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 163070124 Click to see 711.70 unknown https://doi.org/10.1021/JO00421A023
[3,4,5-Triacetyloxy-6-(acetyloxymethyl)-12-benzoyloxy-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 163070122 Click to see 711.70 unknown https://doi.org/10.1021/JO00421A023
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1R,2R,3S,4S,5S,6S,7S,9S,12R)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 162973827 Click to see 607.60 unknown https://doi.org/10.1021/JO00421A023
[(1S,2R,4R,5S,6R,7R,9R,12S)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 163083593 Click to see 591.60 unknown https://doi.org/10.1021/JO00421A023
[(1S,2S,3S,4S,5R,6R,7S,9R,12R)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 101324727 Click to see CC(=O)OCC12C(CC3C(C1(C(C(C(C2OC(=O)C)OC(=O)C)O)(C)O)OC3(C)C)OC(=O)C)OC(=O)C4=CN=CC=C4 607.60 unknown https://doi.org/10.1021/JO00421A023
[(1S,2S,4S,5R,6R,7S,9R,12R)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 101324728 Click to see 591.60 unknown https://doi.org/10.1021/JO00421A023
[4,5,12-Triacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 15560165 Click to see 591.60 unknown https://doi.org/10.1021/JO00421A023
[4,5,12-Triacetyloxy-6-(acetyloxymethyl)-2,3-dihydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] pyridine-3-carboxylate 15560167 Click to see CC(=O)OCC12C(CC3C(C1(C(C(C(C2OC(=O)C)OC(=O)C)O)(C)O)OC3(C)C)OC(=O)C)OC(=O)C4=CN=CC=C4 607.60 unknown https://doi.org/10.1021/JO00421A023
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp 70680285 Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O 356.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin 656516 Click to see 457.40 unknown via CMAUP database
Neoamygdalin 441462 Click to see 457.40 unknown via CMAUP database
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see 152.23 unknown via CMAUP database
Hexanal 6184 Click to see 100.16 unknown via CMAUP database
trans-2-Hexenal 5281168 Click to see 98.14 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-butyloxolan-2-one 7057972 Click to see CCCCC1CCC(=O)O1 142.20 unknown via CMAUP database
(R)-gamma-Decalactone 183870 Click to see 170.25 unknown via CMAUP database
Gamma-dodecalactone, (R)- 10888889 Click to see 198.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Linalool oxide, cis- 6428573 Click to see 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 5317050 Click to see 544.50 unknown via CMAUP database
(1S,5S,6R,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 73353883 Click to see 544.50 unknown via CMAUP database
(1S,5S,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 5317051 Click to see 544.50 unknown via CMAUP database
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate 10723070 Click to see 664.60 unknown via CMAUP database
Mahuannin A 5317052 Click to see 544.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolactams
[(18E)-11-chloro-21-hydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.110,14.03,5]hexacosa-10,12,14(26),16,18-pentaen-6-yl] 2-[methyl(2-methylpropanoyl)amino]propanoate 54610539 Click to see 720.20 unknown via CMAUP database
[(1S,2R,3S,5S,6S,16E,20R,21S)-11-chloro-21-hydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.110,14.03,5]hexacosa-10,12,14(26),16,18-pentaen-6-yl] (2S)-2-[acetyl(methyl)amino]propanoate 54604312 Click to see CC1C2CC(C(C=CC=C(CC3=CC(=C(C(=C3)OC)Cl)N(C(=O)CC(C4(C1O4)C)OC(=O)C(C)N(C)C(=O)C)C)C)OC)(NC(=O)O2)O 692.20 unknown via CMAUP database
Maytanprine 54610538 Click to see 706.20 unknown via CMAUP database
Maytansine 5281828 Click to see 692.20 unknown https://doi.org/10.1021/NP9803732

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.