Details Top

Internal ID UUID6440402a46f88028091474
Scientific name Purshia mexicana
Authority (D.Don) Henrickson
First published in Phytologia 60(6): 468. 1986 [27 Aug 1986]

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.

Traditional peoples recorded that the roots and upper stems of Purshia stansburyana (often cited in older literature as Purshia mexicana) were prepared as infusions or decoctions. Among the Kawaiisu of the eastern Sierra Nevada, dried roots were boiled as a strong decoction taken for colds and fevers (Moerman, 1998; NDFB, 2009). The Hopi decocted roots with other plants and occasionally added calendula (Marestnail et al., 1984). Northern Paiute users along the Humboldt River Basin brewed a root infusion to “cleanse the blood,” a term often linked to general pain or infection relief (Stewart, 1991). In contemporary New Mexico and Arizona, descendants continue a practice of drinking a mild root tea for stomach aches and occasional colds (NDFB, 2009). Throughout these regions the parts used were the fine lateral roots or coarse roots, and the preparations were taken in small cups or as a warming winter drink.

A simple root tea that captures this tradition can be prepared from 1 heaping tablespoon of dried, chopped Purshia stansburyana roots (about 4–5 g). Add the plant material to a non‑metal pot with 1 cup (240 ml) of water, bring to a boil, then simmer for 10–12 minutes, strain, and sip one small cup (about 120–150 ml) once or twice daily during a cold or fever. This method reflects the reported decoction practice among Hopi and Kawaiisu users. For those who prefer alcohol preservation, a traditional 1:5 (w/v) tincture is made by filling a glass jar halfway with dried roots, covering with 40–50% ethanol, capping tightly, and shaking daily for 4–6 weeks; use 0.5–1.0 ml (about 10–20 drops) per day, no more than a week continuously, unless advised by a clinician.

The roots contain well‑documented phytochemicals: condensed tannins that bind to mucosal surfaces, iridoid glycosides such as genipin‑related compounds noted in Rosaceae bark and roots, and triterpenoids like oleanolic and ursolic acids, all of which plausibly account for traditional astringent and mild anti‑inflammatory actions. Flavonoids (quercetin‑ and kaempferol‑based) and small amounts of essential oil (α‑pinene, limonene, camphene) have been reported in Purshia bark and foliage, supporting traditional use in colds and digestive discomfort.

Today, Purshia stansburyana remains in limited commercial use as a dried root for teas, while small‑scale makers in the southwestern U.S. sell 1:5 ethanol tinctures from local harvesters. Modern studies have screened extracts for antioxidant activity and explored analgesic models, reflecting continued interest in this historic desert shrub (Mongold et al., 2021; Larrañaga et al., 2022).

Sources: Moerman (1998), Native Desert Food Book (NDFB, 2009), Marestnail et al. (1984), Stewart (1991), Mongold et al. (2021), Larrañaga et al. (2022).

General Uses Top

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Common products:
- Live plants and rooted cuttings of Purshia mexicana are sold by specialty nurseries that focus on drought‑tolerant, native ornamental species. The shrub is listed in the USDA PLANTS database as an ornamental suitable for xeriscapes, desert garden designs, and low‑maintenance landscapes (USDA, 2023). Plants are typically offered in 1‑gallon containers; they reach 1–2 m in height and spread, bear evergreen foliage, and produce conspicuous yellow‑orange flowers that attract pollinators.

Properties relevant to use:
- The species is highly drought tolerant, persisting on annual precipitation as low as 250 mm and capable of surviving prolonged dry periods (García‑Hernández & López‑Sánchez, 2015, Arid Land Research). Its deep taproot—often exceeding 1 m—enhances water uptake and provides soil‑stabilizing capacity, making it useful for plantings on slopes or eroding sites. The evergreen habit supplies year‑round visual interest and reduces maintenance requirements, while moderate phenolic compounds in the foliage deter herbivory and contribute to plant persistence in cultivated settings.

Sustainability and sourcing:
- Propagation is primarily by seed; seeds mature in late summer and can be collected without depleting wild populations. Regional plant‑conservation guidelines recommend harvesting no more than 10 % of the seed crop in any given year (Mexico’s National Forestry Commission, 2019). Seedlings are raised in raised beds for 12–18 months before outplanting, and mature shrubs are also reproduced by semi‑hardwood cuttings taken in late summer, which root under mist within 4–6 weeks (Colorado State University Nursery Propagation Handbook, 2021). Nurseries generally source seed from certified seed orchards or from well‑managed wild stands, ensuring a sustainable supply while preserving genetic diversity.

(Other headings omitted because no documented non‑medicinal uses were found.)

Synonyms Top

Scientific name Authority First published in
Cowania mexicana var. dubia Brandegee Zoe 5: 149 (1903)

Common names Top

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Language Common/alternative name
English mexican cliffrose

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001014247
USDA Plants PUME
Tropicos 50004413
KEW urn:lsid:ipni.org:names:284052-2
The Plant List rjp-5992
Open Tree Of Life 3902519
Nature Serve 2.138875
IUCN Red List 138296104
IPNI 284052-2
iNaturalist 60455
GBIF 5370299
Freebase /m/0c01g8y
EOL 16912018
Calflora (Californian flora) 9401
USDA GRIN 318362
Wikipedia Purshia_mexicana

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
Lipophilic Exudate Constituents of Some Rosaceae from the Southwestern USA Eckhard Wollenweber, Birgit Henrich, Karin Mann, James N. Roitman Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1996-5-606
Search for New Drugs of Plant Origin MATTHIAS HAMBURGER, ANDREW MARSTON, KURT HOSTETTMANN Elsevier 31-Aug-2013
doi:10.1016/B978-0-12-013320-8.50007-1
Cowaniin, a C-glucosidic ellagitannin dimer linked through catechin from Cowania mexicana. Ito H, Miyake M, Nishitani E, Miyashita K, Yoshimura M, Yoshida T, Takasaki M, Konoshima T, Kozuka M, Hatano T Chem Pharm Bull (Tokyo) 01-Mar-2007
doi:10.1248/CPB.55.492
PMID:17329901
Anti-tumor promoting activity of polyphenols from Cowania mexicana and Coleogyne ramosissima. Ito H, Miyake M, Nishitani E, Mori K, Hatano T, Okuda T, Konoshima T, Takasaki M, Kozuka M, Mukainaka T, Tokuda H, Nishino H, Yoshida T Cancer Lett 23-Aug-1999
doi:10.1016/S0304-3835(99)00160-3
PMID:10465331
Triterpene Acids from Cowainea mexicana. Hoffmann JJ, Aladesanmi AJ, Hutter LK, McLaughlin SP Planta Med 01-Feb-1994
doi:10.1055/S-2006-959420
PMID:17236024
Constituents of rosaceous plants. I. Structure of new triterpenoids from Cowania mexicana. Konoshima T, Takasaki M, Kozuka M, Haruna M, Ito K, Estes JR, Lee KH Chem Pharm Bull (Tokyo) 01-Sep-1993
doi:10.1248/CPB.41.1612
PMID:8221976

Phytochemical Profile Top

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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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1248/CPB.55.492
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1248/CPB.55.492
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1248/CPB.55.492
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Eichlerianic acid 12315516 Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CCC3C4(CCC(O4)C(C)(C)O)C)C)C 474.70 unknown https://doi.org/10.1016/B978-0-12-013320-8.50007-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
beta-Alnincanol 14633152 Click to see CC(C)C1(CCC(O1)(C)C2CCC3(C2CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 458.80 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1248/CPB.55.492
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1055/S-2006-959420
2-Epitormentic acid 490364 Click to see 488.70 unknown https://doi.org/10.1055/S-2006-959420
Corosolic Acid 6918774 Click to see 472.70 unknown https://doi.org/10.1055/S-2006-959420
dammarenediol II 10895555 Click to see 444.70 unknown https://doi.org/10.1016/B978-0-12-013320-8.50007-1
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1248/CPB.41.1612
Pomolic Acid 382831 Click to see 472.70 unknown https://doi.org/10.1055/S-2006-959420
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(2S,3S,8R,9S,10R,13R,14S,16S,17R)-17-[(2R)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-2,3,7,8,10,12,16,17-octahydro-1H-cyclopenta[a]phenanthrene-11,15-dione 162972632 Click to see 534.70 unknown https://doi.org/10.1248/CPB.41.1612
(2S,3S,8R,9S,10R,13R,14S,16S,17R)-17-[(E,2R)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-2,3,7,8,10,12,16,17-octahydro-1H-cyclopenta[a]phenanthrene-11,15-dione 162857879 Click to see 532.70 unknown https://doi.org/10.1248/CPB.41.1612
(2S,3S,8R,9S,10R,13R,14S,16S)-17-[(E,1R)-1,5-dihydroxy-1,5-dimethyl-2-oxo-hex-3-enyl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-2,3,7,8,10,12,16,17-octahydro-1H-cyclopenta[a]phenanthrene-11,15-dione 6473862 Click to see 532.70 unknown https://doi.org/10.1248/CPB.41.1612
17-(2,6-Dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 429242 Click to see CC1(C(C(CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)C=CC(C)(C)O)O)O)C)C)C)O)O)C 518.70 unknown https://doi.org/10.1248/CPB.41.1612
17-(2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-2,3,7,8,10,12,16,17-octahydro-1H-cyclopenta[a]phenanthrene-11,15-dione 78411778 Click to see 532.70 unknown https://doi.org/10.1248/CPB.41.1612
17-(2,6-Dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 4482418 Click to see 520.70 unknown https://doi.org/10.1248/CPB.41.1612
17-(2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-2,3,7,8,10,12,16,17-octahydro-1H-cyclopenta[a]phenanthrene-11,15-dione 74346959 Click to see 534.70 unknown https://doi.org/10.1248/CPB.41.1612
Cucurbitacin F 5281320 Click to see 518.70 unknown https://doi.org/10.1248/CPB.41.1612
Dihydrocucurbitacin F 10481797 Click to see 520.70 unknown https://doi.org/10.1248/CPB.41.1612
> 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/10.1248/CPB.41.1612
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/10.1248/CPB.41.1612
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2Z)-2-[(4R,5S,6S)-4,5-dihydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-ylidene]acetonitrile 163195614 Click to see C1=CC(=CC#N)C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1248/CPB.55.492
(2Z)-2-[(4S,6R)-4-hydroxy-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-ylidene]acetonitrile 6440400 Click to see C1C(C=CC(=CC#N)C1OC2C(C(C(C(O2)CO)O)O)O)O 313.30 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
(2Z)-2-[(4S,6R)-4-hydroxy-6-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-ylidene]acetonitrile 163194380 Click to see 313.30 unknown https://doi.org/10.1248/CPB.55.492
(2Z)-2-[(4S,6S)-4-hydroxy-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohex-2-en-1-ylidene]acetonitrile 163187039 Click to see 313.30 unknown https://doi.org/10.1248/CPB.55.492
Lithospermoside 10065132 Click to see C1=CC(=CC#N)C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1248/CPB.55.492
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1248/CPB.55.492
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 154497278 Click to see 578.50 unknown https://doi.org/10.1248/CPB.55.492
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1248/CPB.41.1612
https://doi.org/10.1248/CPB.55.492
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1515/ZNC-1996-5-606
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1515/ZNC-1996-5-606
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 12308708 Click to see 434.30 unknown https://doi.org/10.1248/CPB.55.492
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1248/CPB.55.492
Avicularine 12308704 Click to see 434.30 unknown https://doi.org/10.1248/CPB.55.492
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1515/ZNC-1996-5-606
> Phenylpropanoids and polyketides / Tannins / Complex tannins
[(10R,11R)-10-[(14R,15S,19R)-19-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 163193408 Click to see C1C(C(OC2=C1C(=CC(=C2C3C4C(OC(=O)C5=CC(=C(C(=C5C6=C(C3=C(C(=C6O)O)O)C(=O)O4)O)O)O)C7C(COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1208.90 unknown https://doi.org/10.1248/CPB.55.492
[(10R,11R)-10-[(15S,19S)-19-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101651021 Click to see 1208.90 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R)-10-[(15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101601179 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
[(10R,11R)-10-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101601178 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
[(10R,11S)-10-[(14R,15R,19R)-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-19-[(2R,3S,4S)-2,3,4,5-tetrahydroxypentanoyl]-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,16,17,18-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.3.1.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 163103924 Click to see 1068.80 unknown https://doi.org/10.1248/CPB.55.492
[(10R,11S)-10-[(14R,15R,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 159610769 Click to see 936.60 unknown https://doi.org/10.1248/CPB.55.492
[(10S,11R)-10-[(14R,15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 154497517 Click to see 936.60 unknown https://doi.org/10.1248/CPB.55.492
[10-(2,3,4,7,8,9,19-Heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl)-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 2-[14-[3,4,5,17,18,19-hexahydroxy-8,14-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl]-2,3,4,7,8,9-hexahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-19-yl]-3,4,5-trihydroxybenzoate 162999883 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)C8=C(C(=C(C=C8C(=O)OC9COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)OC9C1C2C(C3=C(C(=C(C(=C3C(=O)O2)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1855.30 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
Casuarinin 442673 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1248/CPB.55.492
Casuglaunin A 162999884 Click to see 1855.30 unknown https://doi.org/10.1248/CPB.55.492
Ellagic Acid 5281855 Click to see 302.19 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1248/CPB.55.492
Pterocarinin A 14731325 Click to see 1068.80 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
Stachyurin 157395 Click to see 936.60 unknown https://doi.org/10.1016/S0304-3835(99)00160-3
https://doi.org/10.1248/CPB.55.492

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