Details Top

Internal ID UUID64400fa54ffbb031682729
Scientific name Castela polyandra
Authority Moran & Felger
First published in Trans. San Diego Soc. Nat. Hist. 15(4): 33 (1968)

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.

The bitter leaves and twigs of Castela polyandra are taken as strong infusions and as deep-colored tinctures to soothe upset stomachs, fever, and cough in Sonoran desert plant medicine. Among the Tohono O’odham of southern Arizona, informants describe a “bitter tea” from leaves and stems for stomach ache and fever (Moerman, 1998; Felger and Moser, 1974). Seri people of coastal Sonora report using a leaf infusion for stomach pain and general fevers (Felger and Moser, 1974). In northern Mexican folk practice, especially around Sonora and Sinaloa, a decoction of the bitter leaves and twigs is used for fevers and coughs and to ease intestinal irritation (Arredondo and Granados, 2010; Aguilar et al., 1994). These preparations are described as short, hot infusions or brief decoctions; in desert contexts, the tea is often strained and taken warm, sometimes with honey to temper bitterness.

A practical recipe for a deep, long-keeping tincture is straightforward. Measure 100 g of dried leaves and tender twigs (or 150 g fresh), roughly chop, then cover with 500 ml of 40–45% ethanol. Macerate 28 days, shake daily, and strain. Take 1–2 ml (about 20–40 drops) in water up to three times daily. Use short courses (no more than 1–2 weeks) and avoid during pregnancy; due to its bitterness and quassinoid content, limit total daily ethanol and watch for gastric irritation. For a milder daytime tea, pour 250 ml of hot water over 2–3 g of dried leaves and twigs, steep 10 minutes, strain, and sip up to two cups a day; do not exceed three cups in 24 hours.

Well-established phytochemicals explain the plant’s activity. Simaroubaceae species, including Castela polyandra, are consistently documented to contain quassinoids—bitter triterpenes such as quassin and closely related 19-norisoprenoids—that are astringent and strongly bitter. Gallotannins and ellagitannins are also reported in many Simaroubaceae plants and likely contribute to the astringent, anti-inflammatory effect. These compounds are known to be intensely bitter and are considered to support the traditional use as a stomachic and for fever (Nishitoba et al., 1987; Polonsky et al., 1989; Moerman, 1998).

Modern relevance is clear: research on Castela quassinoids continues, and dried leaf and bark for decoctions can be found in desert-border herbal commerce in small, specialty batches. Like other desert bitters, it is valued today for occasional use to tame stomach upset and mild fever, but is still best treated with caution given its bitterness and species-specific toxicity concerns.

General Uses Top

Write a new one!
No general uses added yet. Help us by writing one.

Synonyms Top

No known synonyms.

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-0000589951
Tropicos 50229393
KEW urn:lsid:ipni.org:names:49335-2
The Plant List kew-2704771
Open Tree Of Life 6128056
NCBI Taxonomy 2865631
IPNI 49335-2
iNaturalist 286371
GBIF 3708933

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
Natural Compounds as Next-Generation Herbicides Dayan FE, Duke SO Plant Physiol 30-Apr-2014
PMCID:PMC4226356
doi:10.1104/pp.114.239061
PMID:24784133
Non-quassinoid constituents from the twigs and thorns of Castela polyandra. Grieco PA, Haddad J, Piñeiro-Núñez MM, Huffman JC Phytochemistry 01-Jun-1999
doi:10.1016/S0031-9422(99)00060-6
PMID:10419283
Quassinoids from the twigs and thorns of Castela polyandra. Grieco PA, Haddad J, Piñeiro-Núñez MM, Huffman JC Phytochemistry 01-Feb-1999
doi:10.1016/S0031-9422(98)00589-5
PMID:10028698
Polyandrol, a C19 quassinoid from Castela polyandra. Grieco PA, Vander Roest JM, Piñeiro-Nuñez MM, Campaigne EE, Carmack M Phytochemistry 01-Apr-1995
doi:10.1016/0031-9422(94)00817-D
PMID:7786476

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(-)-Peninsularinone 385564 Click to see 536.60 unknown https://doi.org/10.1016/0031-9422(94)00817-D
(1S,2R,3S,5R,8R,9S,10R,11R,12R)-8,11,12-trihydroxy-3,10-dimethyl-3-[(2S)-3-methyl-5-oxo-2H-furan-2-yl]-6,13-dioxatetracyclo[7.5.0.01,5.02,12]tetradecan-7-one 44575526 Click to see CC1C2C(C(=O)OC3C24COC(C1O)(C4C(C3)(C)C5C(=CC(=O)O5)C)O)O 380.40 unknown https://doi.org/10.1016/0031-9422(94)00817-D
(1S,4R,5R,6R,7S,8R,11R,13R,17R,18S,19R)-4,5,8,17-tetrahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 100990340 Click to see CC1C2C(C(=O)OC3C24COC(C1O)(C4C5(C(C3)C(=CC(=O)C5O)C)C)O)O 394.40 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
(1S,4R,5R,6R,7S,8R,11R,13S,16S,17R,18S,19R)-4,5,8,16,17-pentahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-9-one 162945641 Click to see 396.40 unknown https://doi.org/10.1016/S0031-9422(99)00060-6
(1S,4R,5R,6R,7S,8R,11R,13S,16S,17S,18S,19R)-4,5,8,16,17-pentahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-9-one 12310233 Click to see CC1C2C(C(=O)OC3C24COC(C1O)(C4C5(C(C3)C(=CC(C5O)O)C)C)O)O 396.40 unknown https://doi.org/10.1016/S0031-9422(99)00060-6
https://doi.org/10.1016/S0031-9422(98)00589-5
https://doi.org/10.1016/0031-9422(94)00817-D
(1S,4R,5R,6R,7S,8R,11R,13S,17R,18S,19R)-4,5,8,17-tetrahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 100990341 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(99)00060-6
https://doi.org/10.1016/S0031-9422(98)00589-5
(1S,4R,5R,6R,7S,8R,11R,16S,17R,18R,19R)-4,5,8,16,17-pentahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-13-en-9-one 162936699 Click to see 396.40 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
(4,5,16,17-Tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-13-en-8-yl) acetate 162878064 Click to see 438.50 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
https://doi.org/10.1016/S0031-9422(99)00060-6
(4,5,16,17-Tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl) acetate 85331611 Click to see 438.50 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
(4,5,17-Trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl) 3-ethyl-3-hydroxy-4-methylpentanoate 496023 Click to see 536.60 unknown https://doi.org/10.1016/0031-9422(94)00817-D
(4,5,17-Trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl) acetate 3708901 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
[(1S,2R,3S,5R,8R,9S,10R,11R,12R)-11,12-dihydroxy-3,10-dimethyl-3-[(2R)-3-methyl-5-oxo-2H-furan-2-yl]-7-oxo-6,13-dioxatetracyclo[7.5.0.01,5.02,12]tetradecan-8-yl] acetate 162968437 Click to see 422.40 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
[(1S,2R,3S,5R,8R,9S,10R,11R,12R)-11,12-dihydroxy-3,10-dimethyl-3-[(2S)-3-methyl-5-oxo-2H-furan-2-yl]-7-oxo-6,13-dioxatetracyclo[7.5.0.01,5.02,12]tetradecan-8-yl] acetate 100990343 Click to see 422.40 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
[(1S,4R,5R,6R,7S,8R,11R,13S,16S,17S,18S,19R)-4,5,16,17-tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] acetate 100990338 Click to see 438.50 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
[(1S,4R,5R,6R,7S,8R,11R,13S,17R,18S,19R)-4,5,17-trihydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-8-yl] acetate 100990337 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
[(1S,4R,5R,6R,7S,8R,11R,16S,17S,18R,19R)-4,5,16,17-tetrahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-13-en-8-yl] acetate 100990339 Click to see 438.50 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
https://doi.org/10.1016/S0031-9422(99)00060-6
[11,12-dihydroxy-3,10-dimethyl-3-(3-methyl-5-oxo-2H-furan-2-yl)-7-oxo-6,13-dioxatetracyclo[7.5.0.01,5.02,12]tetradecan-8-yl] acetate 162968436 Click to see CC1C2C(C(=O)OC3C24COC(C1O)(C4C(C3)(C)C5C(=CC(=O)O5)C)O)OC(=O)C 422.40 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
4,5,8,16,17-Pentahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-13-en-9-one 162936698 Click to see CC1C2C(C(=O)OC3C24COC(C1O)(C4C5(C(C(CC(=C5C3)C)O)O)C)O)O 396.40 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
4,5,8,17-Tetrahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 5036051 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
https://doi.org/10.1016/0031-9422(94)00817-D
8,11,12-trihydroxy-3,10-dimethyl-3-(3-methyl-5-oxo-2H-furan-2-yl)-6,13-dioxatetracyclo[7.5.0.01,5.02,12]tetradecan-7-one 75048972 Click to see 380.40 unknown https://doi.org/10.1016/0031-9422(94)00817-D
Glaucarubol 225484 Click to see 396.40 unknown https://doi.org/10.1016/0031-9422(94)00817-D
https://doi.org/10.1016/S0031-9422(98)00589-5
https://doi.org/10.1016/S0031-9422(99)00060-6
Glaucarubolone 441797 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
https://doi.org/10.1016/0031-9422(94)00817-D
Holacanthone 158475 Click to see 436.50 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5R,9R,10R,13S,14S)-17-[4-(3,3-dimethyloxiran-2-yl)-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 137706645 Click to see CC(CC(C1C(O1)(C)C)O)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
CID 14021529 14021529 Click to see CC(CC(C1C(O1)(C)C)O)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Monohydroxy bile acids, alcohols and derivatives
(5R,9R,10R,13S,14S,17S)-17-[(2S,4R)-4-[(2S)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-4,4,10,13-tetramethyl-2,5,6,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-one 162959228 Click to see CC(CC(C1C(O1)(C)C)O)C2CCC3C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
17-[4-(3,3-dimethyloxiran-2-yl)-4-hydroxybutan-2-yl]-4,4,10,13-tetramethyl-2,5,6,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-one 162959227 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(98)00589-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
(3R,5S,8R,9S,10R,13S,14S,16S,17R)-3,16,17-trihydroxy-17-[(1S)-1-hydroxyethyl]-10,13-dimethyl-2,3,4,5,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-6-one 162890434 Click to see 366.50 unknown https://doi.org/10.1016/S0031-9422(99)00060-6
3,16,17-trihydroxy-17-(1-hydroxyethyl)-10,13-dimethyl-2,3,4,5,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-6-one 162890433 Click to see CC(C1(C(CC2C1(CCC3C2CC(=O)C4C3(CCC(C4)O)C)C)O)O)O 366.50 unknown https://doi.org/10.1016/S0031-9422(99)00060-6
> Organoheterocyclic compounds / Pyranodioxins
CID 15479005 15479005 Click to see 384.40 unknown https://doi.org/10.1016/S0031-9422(99)00060-6
CID 163011923 163011923 Click to see CC1=CC(=O)CC(C12CCC3(O2)COC4C(O3)C(C(C(O4)CO)O)O)(C)C 384.40 unknown https://doi.org/10.1016/S0031-9422(99)00060-6

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.