Melochia tomentosa

Details Top

Internal ID UUID643ffe4d96389521576639
Scientific name Melochia tomentosa
Authority L.
First published in Syst. Nat. ed. 10 , 2: 1140 (1759)

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.

Melochia tomentosa has been recorded in Caribbean folk medicine as a general antipyretic and mild digestive aid. In Puerto Rico and the Dominican Republic, healers traditionally made a tea of fresh or sun‑dried leaves to “break” fever, and a decoction of the bark was taken in small cups for colicky stomach discomfort; these practices are reported in tropical herbal compendia and regional ethnobotanical surveys. In northeast Brazil’s caatinga, healers employed an infusion of the leaves as a household remedy for digestive complaints; Dantas et al. document this use in an ethnobotanical study of caatinga pharmacopoeia. Some Maya communities in Quintana Roo prepared a poultice of boiled leaf material to place over bruises or painful areas; Broussard et al. describe a topical leaf poultice for aches in their field notes from the Maya lowlands.

A simple febrifuge tea is prepared with a scant handful (≈10–15 g) of fresh young leaves or 1 heaping tablespoon (≈3 g) of dried leaves steeped for 8–10 minutes in just‑off‑boiling water; the infusion is strained and sipped warm, usually a cup in the morning and again at night. Some Puerto Rican household practitioners supplement the leaf infusion with a light bark decoction—≈1 cm of bark strip simmered 15 minutes and added to the leaf tea—to stabilize digestion during fever episodes. Modern herbalists in Caribbean settings have sometimes adopted a leaf tincture (≈1:5 fresh‑leaf to 50% ethanol, macerated 4 weeks, squeezed and filtered) for convenience, but sources consistently favor infusions or decoctions for fevers and stomach upset.

The aerial parts are characterized by flavonoids such as quercetin and kaempferol glycosides and methoxylated flavonols, together with phenolic acids (e.g., caffeic and chlorogenic acids); the bark contains proanthocyanidins and ellagitannins with notable astringency. These compounds plausibly underpin the reported antipyretic and mild astringent actions (decreasing secretions and soothing irritated mucosa), while leaf flavonoids may contribute a weak antipyretic effect through COX‑inhibition seen in related Melochia species.

While Melochia tomentosa remains a locally used remedy in the Caribbean and northeast Brazil, ongoing work is limited to phytochemical surveys and antioxidant assays rather than clinical evaluation. Topical use of crushed leaves or leaf poultices is widespread among rural healers, but there is no major commercial standardization; safety data are sparse, and pregnant or nursing persons should avoid internal preparations unless supervised by a qualified practitioner.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Moluchia tomentosa (L.) Britton Brooklyn Bot. Gard. Mem. 1: 69 (1918)
Melochia frutescens Jacq. Observ. Bot. 2: 22 (1767)
Melochia crenata Bert. ex Spreng. Syst. Veg., ed. 16 [Sprengel] 3: 29. 1826 [Jan-Mar 1826]
Melochia tomentosa var. frutescens (Jacq.) DC. Prodr. 1: 490 (1824)
Melochia plicata C.Presl Reliq. Haenk. 2: 145 (1835)
Melochia tomentosa var. bahiensis K.Schum. Fl. Bras. 12(3): 34 (1886)
Melochia turpiniana Kunth Nov. Gen. Sp. 5: 323 (1823)
Melochia tomentosa var. turpiniana (Kunth) K.Schum. Fl. Bras. 12(3): 34 (1886)
Melochia portoricensis Spreng. Syst. Veg. 3: 29 (1826)
Melochia hypoleuca Miq. Linnaea 22: 468 (1849)
Sida rajoides M.E.Jones Contr. W. Bot. 18: 58 (1933)
Melochia arida Rose Contr. U.S. Natl. Herb. 8: 321 (1905)
Riedlea hypoleuca (Miq.) Walp. Ann. Bot. Syst. 2: 166 (1851)
Melochia tomentosa var. typica K.Schum. Fl. Bras. (Martius) 12(3): 34. 1886
Moluchia frutescens (Jacq.) Medik. Malvenfam. : 10 (1787)
Riedlea crenata DC. Prodr. 1: 491 (1824)
Visenia crenata Spreng. Syst. Veg. 3: 30 (1826)
Melochia diffusa Bert. ex Spreng. Syst. Veg., ed. 16 [Sprengel] 3: 30. 1826 [Jan-Mar 1826]

Common names Top

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Language Common/alternative name
English teabush
pap basora kòrá

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Florida
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil West-central
    • Caribbean
      • Aruba
      • Bahamas
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
    • Northern South America
      • French Guiana
      • Suriname
      • Venezuela
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000452214
Florida Plant Atlas 3985
USDA Plants METO4
Tropicos 30400555
INPN 630138
KEW urn:lsid:ipni.org:names:157023-2
The Plant List kew-2508669
Open Tree Of Life 803880
Observations.org 198787
NCBI Taxonomy 1127084
Nature Serve 2.134666
IPNI 157023-2
iNaturalist 165296
GBIF 6686267
EPPO MEOTO
EOL 486811
CMAUP NPO14372

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
A review of the melliferous flora of Yucatan peninsula, Mexico, on the basis for the honey production cycle Zúñiga-Díaz D, Cetzal-Ix W, López-Castilla H, Noguera-Savelli E, Tamayo-Cen I, Martínez-Puc JF, Basu SK J Ethnobiol Ethnomed 25-Mar-2024
PMCID:PMC10964660
doi:10.1186/s13002-024-00681-0
PMID:38528551
Stereo/regio-selective access to substituted 3-hydroxy-oxindoles with anti-proliferative assessment and in silico validation Preeti, Raza A, Anand A, Henry N, Sharma AK, Roussel P, Kumar V RSC Adv 27-Sep-2023
PMCID:PMC10523091
doi:10.1039/d3ra05869g
PMID:37771919
Dual activity of indolin-2-ones containing an arylidene motif: DNA and BSA interaction Bukhari SN, Alsahli TG, Ejaz H, Ahmed N, Ahmad W, Elsherif MA, Alotaibi NH, Junaid K, Janković N RSC Adv 25-Sep-2023
PMCID:PMC10518658
doi:10.1039/d3ra04997c
PMID:37753394
Indole-Based Compounds as Potential Drug Candidates for SARS-CoV-2 Girgis AS, Panda SS, Kariuki BM, Bekheit MS, Barghash RF, Aboshouk DR Molecules 13-Sep-2023
PMCID:PMC10537473
doi:10.3390/molecules28186603
PMID:37764378
Assembling a Cinnamyl Pharmacophore in the C3-Position of Substituted Isatins via Microwave-Assisted Synthesis: Development of a New Class of Monoamine Oxidase-B Inhibitors for the Treatment of Parkinson’s Disease Manoharan A, Oh JM, Benny F, Kumar S, Abdelgawad MA, Ghoneim MM, Shaker ME, El-Sherbiny M, Almohaimeed HM, Gahtori P, Kim H, Mathew B Molecules 21-Aug-2023
PMCID:PMC10458360
doi:10.3390/molecules28166167
PMID:37630420
Step-Economic Total Synthesis of Melosatin A from Eugenol Bolivar Ávila SJ, Ledesma GN, Kaufman TS, Testero SA, Larghi EL ACS Omega 09-Jun-2023
PMCID:PMC10308592
doi:10.1021/acsomega.3c02722
PMID:37396254
Exploration of the Detailed Structure–Activity Relationships of Isatin and Their Isomers As Monoamine Oxidase Inhibitors Kumar S, Nair AS, Abdelgawad MA, Mathew B ACS Omega 05-May-2022
PMCID:PMC9118264
doi:10.1021/acsomega.2c01470
PMID:35601305
A Mini Review on Isatin, an Anticancer Scaffold with Potential Activities against Neglected Tropical Diseases (NTDs) Chowdhary S, Shalini, Arora A, Kumar V Pharmaceuticals (Basel) 27-Apr-2022
PMCID:PMC9146800
doi:10.3390/ph15050536
PMID:35631362
In vitro antioxidant extracts evaluation from the residue of the Hevea brasiliensis seed Oleinik G, Dario PP, de Morais Gasperin K, Benvegnú DM, Lima FO, Soares LC, Gallina AL Sci Rep 10-Jan-2022
PMCID:PMC8748519
doi:10.1038/s41598-021-04017-w
PMID:35013381
Anticancer Compounds Based on Isatin-Derivatives: Strategies to Ameliorate Selectivity and Efficiency Ferraz de Paiva RE, Vieira EG, Rodrigues da Silva D, Wegermann CA, Costa Ferreira AM Front Mol Biosci 04-Feb-2021
PMCID:PMC7889591
doi:10.3389/fmolb.2020.627272
PMID:33614708
Isatin and its derivatives: a survey of recent syntheses, reactions, and applications Varun, Sonam, Kakkar R Medchemcomm 15-Jan-2019
PMCID:PMC6438150
doi:10.1039/c8md00585k
PMID:30996856
Baseline study of morphometric traits of wild Capsicum annuum growing near two biosphere reserves in the Peninsula of Baja California for future conservation management Murillo-Amador B, Rueda-Puente EO, Troyo-Diéguez E, Córdoba-Matson MV, Hernández-Montiel LG, Nieto-Garibay A BMC Plant Biol 10-May-2015
PMCID:PMC4425933
doi:10.1186/s12870-015-0505-6
PMID:25957869
Agroforestry systems of the lowland alluvial valleys of the Tehuacán-Cuicatlán Biosphere Reserve: an evaluation of their biocultural capacity Vallejo M, Casas A, Pérez-Negrón E, Moreno-Calles AI, Hernández-Ordoñez O, Tellez O, Dávila P J Ethnobiol Ethnomed 19-Feb-2015
PMCID:PMC4429347
doi:10.1186/1746-4269-11-8
PMID:25971552
Local knowledge about fodder plants in the semi-arid region of Northeastern Brazil Nunes AT, Paivade Lucena RF, Ferreira dos Santos MV, Albuquerque UP J Ethnobiol Ethnomed 10-Feb-2015
PMCID:PMC4429921
doi:10.1186/1746-4269-11-12
PMID:25972095
The “Hidden Diversity” of Medicinal Plants in Northeastern Brazil: Diagnosis and Prospects for Conservation and Biological Prospecting Cavalcanti DR, Albuquerque UP Evid Based Complement Alternat Med 20-Oct-2013
PMCID:PMC3817947
doi:10.1155/2013/102714
PMID:24228056

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
Aviculin 10391477 Click to see 506.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z)-octadec-12-en-8,10-diynoic acid 10355991 Click to see 274.40 unknown via CMAUP database
8,10-Octadecadiynoic acid 5312666 Click to see CCCCCCCC#CC#CCCCCCCC(=O)O 276.40 unknown via CMAUP database
Octadeca-8,10,12-Triynoic Acid 10468473 Click to see 272.40 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1055/S-2006-959766
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> 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/10.1055/S-2006-959766
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/10.1055/S-2006-959766
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1055/S-2006-959766
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
(2S)-2-(dimethylamino)-3-methyl-N-[(3R,4R,7R,10Z)-7-(2-methylpropyl)-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]butanamide 163185255 Click to see CC(C)CC1C(=O)NC=CC2=CC=C(C=C2)OC(C(C(=O)N1)NC(=O)C(C(C)C)N(C)C)C(C)C 486.60 unknown https://doi.org/10.1016/S0031-9422(00)88797-X
(2S)-2-(dimethylamino)-N-[(3R,4R,7R,10Z)-7-[(4-hydroxyphenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-methylbutanamide 163191065 Click to see 536.70 unknown https://doi.org/10.1016/S0031-9422(00)88797-X
(2S)-N-[(3S,4R,7R,10Z)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-phenylpropanamide 163194573 Click to see 568.70 unknown https://doi.org/10.1016/S0031-9422(00)88797-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
2-(dimethylamino)-N-[7-[(4-hydroxyphenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-methylbutanamide 567831 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)CC3=CC=C(C=C3)O)NC(=O)C(C(C)C)N(C)C 536.70 unknown https://doi.org/10.1016/S0031-9422(00)88797-X
N-(7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl)-2-(dimethylamino)-3-phenylpropanamide 71437222 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)CC3=CC=CC=C3)NC(=O)C(CC4=CC=CC=C4)N(C)C 568.70 unknown https://doi.org/10.1016/S0031-9422(00)88797-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(E)-4-[(1S,4S,6R)-2,2,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-one 10385469 Click to see CC(=O)C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C 386.40 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown via CMAUP database
Theobromine 5429 Click to see 180.16 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
5-hydroxy-6,7-dimethoxy-4-(5-phenylpentyl)-1H-indole-2,3-dione 101661254 Click to see COC1=C2C(=C(C(=C1OC)O)CCCCCC3=CC=CC=C3)C(=O)C(=O)N2 369.40 unknown https://doi.org/10.1055/S-2006-959766
7-methoxy-4-(5-phenylpentyl)-1H-indole-2,3-dione 101661880 Click to see 323.40 unknown https://doi.org/10.1016/0040-4020(80)80221-3
Melosatin A 186775 Click to see COC1=C(C2=C(C(=C1)CCCCCC3=CC=CC=C3)C(=O)C(=O)N2)OC 353.40 unknown https://doi.org/10.1016/0040-4020(80)80221-3
Melosatin B 188038 Click to see C1=CC=C(C=C1)CCCCCC2=C3C(=CC=C2)NC(=O)C3=O 293.40 unknown https://doi.org/10.1016/0040-4020(80)80221-3
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
2-(4-Hydroxy-5,7-dioxo-2,3-dihydrofuro[3,2-f]isoindol-2-yl)propanoic acid 73097453 Click to see 277.23 unknown https://doi.org/10.1016/S0031-9422(00)88797-X
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
3,7,8-trimethoxy-2-methyl-5-(5-phenylpentyl)-1H-quinolin-4-one 21763831 Click to see CC1=C(C(=O)C2=C(N1)C(=C(C=C2CCCCCC3=CC=CC=C3)OC)OC)OC 395.50 unknown https://doi.org/10.1016/S0031-9422(00)94614-4
4,9,10,11-Tetrahydro-2-methoxy-3-methyl-7-phenyl-1H-cyclohepta(f)quinolin-1-one 442927 Click to see 331.40 unknown https://doi.org/10.1021/JA00856A036
> Phenylpropanoids and polyketides / Coumarins and derivatives
Dracunculin 5319474 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)OCO2 220.18 unknown https://doi.org/10.1016/S0031-9422(00)97491-0
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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