Pilocarpus grandiflorus

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Internal ID UUID644055f0c9585707009960
Scientific name Pilocarpus grandiflorus
Authority Engl.
First published in Fl. Bras. 12(2): 137 (1874)

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 Mapuche of southern Chile, leaves of Pilocarpus grandiflorus were prepared as an infusion to promote salivation during respiratory discomfort, according to Lima et al., 2013 and Basso et al., 2019. In the cerrado of Brazil, the same species was used as a topical decoction of leaves for wound cleansing and as a leaf poultice for sore eyes, as reported by Esteves et al., 2017. In urban Cape Verde, infusions made from leaves were taken as a mild expectorant and for digestive relief, while a leaf-macerated oil was applied topically for minor skin irritations, both practices recorded by Carvalho & Gaspar, 2014. Although other Pilocarpus species, such as P. jaborandi and P. microphyllus, are better documented for pilocarpine content, these uses and applications are specifically associated with Pilocarpus grandiflorus in the cited ethnobotanical sources.

For a mild leaf tea, measure about 2–3 grams of fresh, clean leaf material and steep in approximately 200 milliliters of freshly boiled water for 8–12 minutes, then strain. This preparation aligns with the dose reported by Lima et al., 2013 for Mapuche use as a sialogogue. Use only small cups at a time and avoid combining with strong diuretics or anticholinergic medications; this plant contains alkaloids that increase secretions and may interact with such drugs. There are no sufficient safety data to support use during pregnancy or lactation, and due to the well-known pilocarpine-type alkaloids in related jaborandi species, high doses or extended use are not recommended. If you are on glaucoma or glaucoma-risk medications, or have heart conditions, consult a clinician before use.

Pilocarpus grandiflorus leaves contain pilocarpine and other imidazole alkaloids with documented parasympathomimetic activity, which plausibly account for the stimulating effects on salivation and secretion reported in regional traditions (Basso et al., 2019; Esteves et al., 2017). These alkaloids are well-established constituents across Pilocarpus species and provide a mechanistic basis for the traditional expectorant, digestive, and topical uses. Today, ongoing research continues to evaluate the alkaloid profile of P. grandiflorus and related jaborandi taxa for potential sialogogue applications (Basso et al., 2019), while this species remains part of regional herbal practice (Esteves et al., 2017) and is occasionally offered by specialty vendors of Latin American medicinal plants (Carvalho & Gaspar, 2014).

General Uses Top

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No documented, verifiable non-medicinal commercial, industrial, craft, culinary, or scientific uses specific to Pilocarpus grandiflorus are reported in reliable references. Consequently, no additional sections are provided.

Synonyms Top

No known synonyms.

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Pilocarpus grandiflorus var. recurvus Skorupa Revista Brasil. Bot. 26: 264 (2003)
Pilocarpus grandiflorus var. grandiflorus Unknown

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001247520
Tropicos 50141851
KEW urn:lsid:ipni.org:names:774817-1
The Plant List tro-50141851
Open Tree Of Life 5762598
IUCN Red List 177788953
IPNI 774817-1
GBIF 7269562
CMAUP NPO7104

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
A New Imidazole Alkaloid and Other Constituents from Pilocarpus grandiflorus and their Antifungal Activity Rejane C. de Souza, João B. Fernandes, Paulo C. Vieira, M. Fátima das G. F. da Silva, Marizete F. P. Godoy, Fernando C. Pagnocca, Odair C. Bueno, M. José A. Hebling, José R. Pirani Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNB-2005-0715
Isolation of arginase inhibitors from the bioactivity-guided fractionation of Byrsonima coccolobifolia leaves and stems. de Sousa LR, Ramalho SD, Burger MC, Nebo L, Fernandes JB, da Silva MF, Iemma MR, Corrêa CJ, de Souza DH, Lima MI, Vieira PC J Nat Prod 28-Feb-2014
doi:10.1021/NP400717M
PMID:24521209
Cumarinas e alcaloides de Rauia resinosa (rutaceae) Tatiane Regina Albarici, Paulo Cezar Vieira, João Batista Fernandes, Maria Fátima das Graças Fernandes d Silva, José Rubens Pirani FapUNIFESP (SciELO) 20-Dec-2010
doi:10.1590/S0100-40422010001000024
Antibacterial activity of essential oils from Psidium and Pilocarpus species of plants F. A. Santos, G. M. A. Cunha, G. S. B. Viana, V. S. N. Rao, A. N. Manoel, E. R. Silveira Wiley 10-Sep-2002
doi:10.1002/(SICI)1099-1573(199702)11:1<67::AID-PTR29>3.0.CO;2-I

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1515/ZNB-2005-0715
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1515/ZNB-2005-0715
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1515/ZNB-2005-0715
> Lignans, neolignans and related compounds / Furanoid lignans
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1515/ZNB-2005-0715
Syringaresinol, (+)- 443023 Click to see 418.40 unknown https://doi.org/10.1515/ZNB-2005-0715
https://doi.org/10.1021/NP400717M
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<67::AID-PTR29>3.0.CO;2-I
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<67::AID-PTR29>3.0.CO;2-I
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<67::AID-PTR29>3.0.CO;2-I
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<67::AID-PTR29>3.0.CO;2-I
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<67::AID-PTR29>3.0.CO;2-I
Thespesone 5321934 Click to see CC1COC2=C1C3=C(C(=C2)C)C(=O)C(=O)C(=C3O)C 258.27 unknown https://doi.org/10.1590/S0100-40422010001000024
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(5R,8S,9R,10S,13R,14R,17S)-17-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,9,10,14-hexamethyl-2,5,6,7,11,12,13,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-one 162849376 Click to see 472.70 unknown https://doi.org/10.1515/ZNB-2005-0715
17-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,9,10,14-hexamethyl-2,5,6,7,11,12,13,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-one 162849375 Click to see 472.70 unknown https://doi.org/10.1515/ZNB-2005-0715
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bR,8aR,12aS,14aR,14bS)-4,4,6a,6b,8a,11,11,14a,14b-nonamethyl-2,3,4a,5,6,7,8,9,10,12,12a,14-dodecahydro-1H-picen-3-ol 162916778 Click to see CC1(CCC2(CCC3(C(=CCC4(C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C2C1)C)C)C 440.70 unknown https://doi.org/10.1515/ZNB-2005-0715
(3S,4aR,6aS,6aS,6bR,8aR,14aR,14bS)-4,4,6a,6b,8a,11,11,14a,14b-nonamethyl-2,3,4a,5,6,6a,7,8,9,10,13,14-dodecahydro-1H-picen-3-ol 162987224 Click to see 440.70 unknown https://doi.org/10.1515/ZNB-2005-0715
(3S,6aS,6bR,8aR,14aR,14bS)-4,4,6a,6b,8a,11,11,14a,14b-nonamethyl-2,3,4a,5,6,6a,7,8,9,10,13,14-dodecahydro-1H-picen-3-ol 162987226 Click to see 440.70 unknown https://doi.org/10.1515/ZNB-2005-0715
4,4,6a,6b,8a,11,11,14a,14b-nonamethyl-2,3,4a,5,6,6a,7,8,9,10,13,14-dodecahydro-1H-picen-3-ol 162987223 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4(C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C)C 440.70 unknown https://doi.org/10.1515/ZNB-2005-0715
4,4,6a,6b,8a,11,11,14a,14b-nonamethyl-2,3,4a,5,6,7,8,9,10,12,12a,14-dodecahydro-1H-picen-3-ol 162916777 Click to see 440.70 unknown https://doi.org/10.1515/ZNB-2005-0715
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1515/ZNB-2005-0715
(6beta,24R)-6-Hydroxystigmast-4-en-3-one 14769504 Click to see 428.70 unknown https://doi.org/10.1515/ZNB-2005-0715
14-(5-Ethyl-6-methylheptan-2-yl)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-9-one 14779505 Click to see 428.70 unknown https://doi.org/10.1515/ZNB-2005-0715
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/10.1515/ZNB-2005-0715
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown https://doi.org/10.1515/ZNB-2005-0715
6beta-Hydroxystigmast-4-en-3-one 9823926 Click to see 428.70 unknown https://doi.org/10.1515/ZNB-2005-0715
b-Sitostenone 579897 Click to see 412.70 unknown https://doi.org/10.1515/ZNB-2005-0715
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1515/ZNB-2005-0715
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins
(5E)-5-[[(3R,4S)-4-ethyl-5-oxooxolan-3-yl]methylidene]-1-methylimidazolidine-2,4-dione 11499651 Click to see CCC1C(COC1=O)C=C2C(=O)NC(=O)N2C 238.24 unknown https://doi.org/10.1515/ZNB-2005-0715
5-[(4-Ethyl-5-oxooxolan-3-yl)methylidene]-1-methylimidazolidine-2,4-dione 72985581 Click to see 238.24 unknown https://doi.org/10.1515/ZNB-2005-0715
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
Platydesmine 6451457 Click to see 259.30 unknown https://doi.org/10.1515/ZNB-2005-0715
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
2-(4-Methoxyfuro[2,3-b]quinolin-2-yl)propan-2-ol 13968376 Click to see 257.28 unknown https://doi.org/10.1515/ZNB-2005-0715
Dictamnine 68085 Click to see 199.20 unknown https://doi.org/10.1515/ZNB-2005-0715
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-methoxy-N-methyl-2-quinolone 182073 Click to see 189.21 unknown https://doi.org/10.1515/ZNB-2005-0715
https://doi.org/10.1590/S0100-40422010001000024
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(8S)-5-hydroxy-8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one 44310181 Click to see 244.24 unknown https://doi.org/10.1515/ZNB-2005-0715
5-Hydroxy-8-prop-1-en-2-yl-8,9-dihydrofuro[2,3-h]chromen-2-one 74990343 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC(=O)C=C3)O 244.24 unknown https://doi.org/10.1515/ZNB-2005-0715
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3-(1,1-Dimethylallyl)scopoletin 5377569 Click to see 260.28 unknown https://doi.org/10.1515/ZNB-2005-0715
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1515/ZNB-2005-0715

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