Details Top

Internal ID UUID64404fd971dbb370201263
Scientific name Larrea tridentata
Authority (DC.) Coville
First published in Contr. U.S. Natl. Herb. 4: 75. 1893 [20 Nov 1893]

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.

In northern Mexico the Tarahumara and Yaqui traditionally drank infusions of Larrea tridentata leaves and young twigs for colds, flu, and stomach upset (Spier, 1987). Across the Sonoran Desert the Comcaac (Seri) chewed fresh leaves for sore throats and rubbed a leaf poultice on wounds and toothaches (Felger and Moser, 1985). In the southwestern United States, the Shoshone and related groups decocted leaves for fevers and colds, and the Pima prepared a similar decoction for gastrointestinal complaints (Moerman, 1998; 2009). Among the Cahuilla of southern California, leaves and twigs were simmered and taken as a tonic for colds and digestive upset (Bean and Saubel, 1972), while Mexican healers in Sonora made “mesquite tea” from Larrea to ease indigestion and stomachache (Nabhan et al., 2010). In the 19th and early 20th centuries American frontier herbalists frequently compounded a 1:5 ethanol tincture of leaves and tender stems for fevers and urinary infections, and classic Southwest guides record a “creosote tea” dosed sparingly for colds and stomach cramps (Moerman, 1998; 2009; Perry and Medrow, 2010; Bensen, 1995; Berry, 1977).

Two practical recipes illustrate how these preparations were made. A mild cold-and-stomach infusion uses 1–2 teaspoons (2–4 g) of dried leaves and young stems per cup (240 ml) of near-boiling water, infused 10–15 minutes and strained; traditional usage was one cup per day for up to a week, and caution is advised for people with liver or kidney disease, those taking hepatotoxic drugs, and during pregnancy and lactation. A 1:5 ethanol tincture is made with 20 g of dried leaf in 100 ml of 45–60% ethanol, macerating four to six weeks with daily shaking, then straining; typical dosing in old herbal texts is 1–2 ml diluted in water two to three times daily, with the same safety cautions about pregnancy, liver disease, and drug interactions.

Well-established phytochemicals include the lignan nordihydroguaiaretic acid (NDGA), flavonoids such as quercetin and kaempferol, and essential oils rich in sabinene and limonene. These constituents provide the plant’s antioxidant and antimicrobial profile that aligns with the documented uses for colds, fevers, stomach upset, and topical care. Modern relevance remains active: laboratory studies continue to explore antioxidant and antimicrobial properties of Larrea extracts, while herbalists and tribal members still prepare modest infusions and tinctures. NDGA has drawn particular attention for its pharmacology, but safety concerns require measured dosing and avoidance by those at risk for hepatotoxicity.

General Uses Top

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Common products:
Larrea tridentata is the primary natural source of nordihydroguaiaretic acid (NDGA), a phenolic antioxidant isolated from the plant’s leaves and small stems. NDGA is used as an antioxidant additive in specialty food applications (e.g., products rich in lipids) and in technical preparations where oxidation inhibition is needed. Commercial preparations are typically standardized leaf extracts that specify NDGA content and are sold under trade names (e.g., Masoprocol).

Industrial and craft applications:
NDGA and L. tridentata extracts function as antioxidants in industrial formulations, including metalworking and cutting fluids. Laboratory studies report NDGA as an inhibitor of corrosion for mild steel in acidic media under controlled conditions, indicating potential as a corrosion inhibitor additive in fluids and coatings where phenolic inhibition is desired. As an antioxidant, NDGA serves as a radical scavenger that slows oxidative deterioration of unsaturated components, thereby prolonging service life of products sensitive to oxidation.

Properties relevant to use:
NDGA exhibits strong radical-scavenging activity due to its catechol structure; this property underpins its role as an antioxidant in both food and non-food contexts. Extracts contain lignans and phenolics that contribute to this activity. Commercial standardization typically specifies NDGA concentration, which correlates with oxidative stability in formulations.

Scientific/model-organism use:
L. tridentata has a published nuclear genome assembly that serves as a reference for desert shrub biology, resin chemistry, and plant–environment interactions. It is used in physiological and ecological research on drought adaptation, secondary metabolism, and co-occurring desert flora.

Standards and regulation:
NDGA is regulated as a food additive in certain jurisdictions (e.g., U.S. 21 CFR 172.140) with specifications for purity and usage levels; NDGA-containing extracts for technical uses must be labeled in accordance with national chemical and safety regulations.

Synonyms Top

Scientific name Authority First published in
Covillea glutinosa (Engelm.) Rydb. N. Amer. Fl. 25: 108 (1910)
Covillea tridentata (DC.) Vail Bull. Torrey Bot. Club 26(6): 302. 1899 [17 Jun 1899]
Guaiacum mexicanum Baill. Traité Bot. Méd. Phan. 2: 886 (1884)
Larrea mexicana Moric. Pl. Nouv. Amér. : 71 (1839)
Larrea tridentata var. glutinosa (Rydb.) Jeps. Man. Fl. Pl. Calif. : 604 (1925)
Larrea divaricata subsp. tridentata (DC.) Felger J. Arizona Acad. Sci. 6: 84 (1970)
Zygophyllum tridentatum ex DC. Prodr. 1: 706 (1824)
Larrea glutinosa Engelm. in Wisl. Mem. Tour N. Mexico : 93 (1848)
Schroeterella glutinosa Briq. Veröff. Geobot. Inst. Rübel Zürich iii. 664 (1925).
Neoschroetera glutinosa (Engelm.) Briq. Candollea 2: 514 (1926)
Neoschroetera tridentata (DC.) Briq. Candollea 2: 514 (1926)
Schroeterella tridentata (DC.) Briq. Veröff. Geobot. Inst. Rübel Zürich heft 3: 664. 1925
Larrea divaricata var. arenaria (L.D.Benson) Felger Fl. Gran Desierto & Río Colorado Northwest. Mexico : 467 (2000)
Larrea tridentata var. arenaria L.D.Benson Trees & Shrubs of Southw. Deserts , ed. 3: 123 (1981)
Larrea tridentata subsp. glutinosa (Engelm.) A.E.Murray Kalmia 12: 21 (1982)

Common names Top

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Language Common/alternative name
English chaparral
English greasewood
English creosote bush
Arabic حشيشة الشحم
Catalan arbust de creosota
Czech larea trojzubá
German kreosotbusch
Persian بوته قطران
Finnish kreosoottipensas
Hebrew לראה משולשת
Japanese クレオソートブッシュ
Japanese メキシコハマビシ
Norwegian Bokmål kreosotbusk
Dutch creosootstruik
Russian Ларрея трёхзубчатая
Ukrainian Креозотовий кущ
Chinese 石炭酸灌木
Chinese 墨西哥三齿拉瑞阿
Chinese 墨西哥三齒拉瑞阿

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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-0001146325
UNII B755J144H1
USDA Plants LATR2
Tropicos 34600049
KEW urn:lsid:ipni.org:names:873322-1
The Plant List tro-34600049
PFAF Larrea tridentata
Open Tree Of Life 185815
NCBI Taxonomy 66636
Nature Serve 2.159827
IPNI 135649-2
iNaturalist 68205
GBIF 5421118
Freebase /m/0fclg
FEIS plants/shrub/lartri
EPPO LARTR
EOL 581850
Calflora (Californian flora) 4573
USDA GRIN 21509
Wikipedia Larrea_tridentata

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
Characterization of the Worthen Sparrow (Spizella wortheni)’s Nest Building Materials in Northeastern Mexico Suarez EB, Mellado M, Luna M, Lozano EA, Calderon G, Angel Y, Angel O, Medina ML, García JE Animals (Basel) 19-Apr-2024
PMCID:PMC11047681
doi:10.3390/ani14081230
PMID:38672377
Living on the edge: The sensitivity of arthropods to development and climate along an urban-wildland interface in the Sonoran Desert of central Arizona Uhey DA, Hofstetter RW, Earl S, Holden J, Sprague T, Rowe H PLoS One 18-Apr-2024
PMCID:PMC11025936
doi:10.1371/journal.pone.0297227
PMID:38635739
Plants from Arid and Semi-Arid Zones of Mexico Used to Treat Respiratory Diseases: A Review Dávila-Rangel IE, Charles-Rodríguez AV, López-Romero JC, Flores-López ML Plants (Basel) 11-Mar-2024
PMCID:PMC10974781
doi:10.3390/plants13060792
PMID:38592789
The desert woodrat (Neotoma lepida) induces a diversity of biotransformation genes in response to creosote bush resin Greenhalgh R, Klure DM, Orr TJ, Armstrong NM, Shapiro MD, Dearing MD Comp Biochem Physiol C Toxicol Pharmacol 28-Feb-2024
PMCID:PMC11006593
doi:10.1016/j.cbpc.2024.109870
PMID:38428625
Chemically Mediated Plant–Plant Interactions: Allelopathy and Allelobiosis Kong CH, Li Z, Li FL, Xia XX, Wang P Plants (Basel) 24-Feb-2024
PMCID:PMC10934397
doi:10.3390/plants13050626
PMID:38475470
Efficient photocatalytic bactericidal performance of green-synthesised TiO2/reduced graphene oxide using banana peel extracts Utami M, Yenn TW, Alam MW, Ravindran B, Husniati, Purnama I, Salmahaminati, Hidayat H, Dhetaya FN, Salsabilla SN Heliyon 17-Feb-2024
PMCID:PMC10901103
doi:10.1016/j.heliyon.2024.e26636
PMID:38420369
Roles of autophagy in killing of mycobacterial pathogens by host macrophages – Effects of some medicinal plants Tatano Y, Shimizu T, Sano C, Tomioka H Eur J Microbiol Immunol (Bp) 13-Feb-2024
PMCID:PMC10895364
doi:10.1556/1886.2023.00062
PMID:38349363
The PPO family in Nicotiana tabacum is an important regulator to participate in pollination Wei X, Tao K, Liu Z, Qin B, Su J, Luo Y, Zhao C, Liao J, Zhang J BMC Plant Biol 09-Feb-2024
PMCID:PMC10854075
doi:10.1186/s12870-024-04769-3
PMID:38331761
Plant macrofossil data for 48-0 ka in the USGS North American Packrat Midden Database, version 5.0 Strickland LE, Thompson RS, Shafer SL, Bartlein PJ, Pelltier RT, Anderson KH, Schumann RR, McFadden AK Sci Data 12-Jan-2024
PMCID:PMC10786896
doi:10.1038/s41597-023-02616-y
PMID:38216580
Indirect impacts of a highway on movement behavioral states of a threatened tortoise and implications for landscape connectivity Harju S, Cambrin S, Berg J Sci Rep 06-Jan-2024
PMCID:PMC10771453
doi:10.1038/s41598-024-51378-z
PMID:38184706
Comparative Transcriptome Analysis of High- and Low-Growth Genotypes of Eucalyptus urophylla in Response to Long-Term Nitrogen Deficiency Yang X, Xu F, Pan W, Zhang W, Liao H, Zhu B, Xu B, Chen X, Yang H Genes (Basel) 30-Dec-2023
PMCID:PMC10815775
doi:10.3390/genes15010060
PMID:38254950
Retraction: Transcriptome characterization of Larrea tridentata and identification of genes associated with phenylpropanoid metabolic pathways N/A PLoS One 19-Dec-2023
PMCID:PMC10729945
doi:10.1371/journal.pone.0296317
PMID:38113222
Numbers of wildlife fatalities at renewable energy facilities in a targeted development region Conkling TJ, Fesnock AL, Katzner TE PLoS One 15-Dec-2023
PMCID:PMC10723682
doi:10.1371/journal.pone.0295552
PMID:38100470
Plant Secondary Compounds Promote White Adipose Tissue Browning via Modulation of the Gut Microbiota in Small Mammals Ren S, Zhang L, Tang X, Fan C, Zhao Y, Cheng Q, Zhang Y Int J Mol Sci 13-Dec-2023
PMCID:PMC10743627
doi:10.3390/ijms242417420
PMID:38139249
The complete chloroplast genome sequence of Zygophyllum brachypterum (Zygophyllaceae) reveals its distinctive characteristics and evolutionary implication Wang X, Gao F, Li W, Zhou Y Mitochondrial DNA B Resour 08-Dec-2023
PMCID:PMC10783824
doi:10.1080/23802359.2023.2288920
PMID:38213390

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 / Naphthalenes / Naphthoquinones
Larreantin 10434387 Click to see 460.50 unknown https://doi.org/10.1021/JO00245A011
> Benzenoids / Phenols / Benzenediols / Catechols
4-[(2S,5S)-5-(4-hydroxyphenyl)-3,4-dimethyl-2,5-dihydrofuran-2-yl]benzene-1,2-diol 162866375 Click to see 298.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
4-[5-(4-Hydroxyphenyl)-3,4-dimethyl-2,5-dihydrofuran-2-yl]benzene-1,2-diol 45783179 Click to see CC1=C(C(OC1C2=CC=C(C=C2)O)C3=CC(=C(C=C3)O)O)C 298.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
> Lignans, neolignans and related compounds
(E)-1,4-bis(4-hydroxyphenyl)-2,3-dimethylbut-2-ene-1,4-dione 11197216 Click to see 296.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
https://doi.org/10.1248/CPB.59.1467
(Z)-1,4-bis(4-hydroxyphenyl)-2,3-dimethylbut-2-ene-1,4-dione 101356830 Click to see CC(=C(C)C(=O)C1=CC=C(C=C1)O)C(=O)C2=CC=C(C=C2)O 296.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
[1,4-Bis(4-hydroxyphenyl)-2,3-dimethyl-2-butene-1,4-dione] 85431897 Click to see 296.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
https://doi.org/10.1248/CPB.59.1467
> Lignans, neolignans and related compounds / Aryltetralin lignans
(5R,6R,7R)-5-(4-hydroxy-3-methoxyphenyl)-3-methoxy-6,7-dimethyl-5,6,7,8-tetrahydronaphthalen-2-ol 11404691 Click to see 328.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
(5R,6R,7R)-5-(4-hydroxyphenyl)-3-methoxy-6,7-dimethyl-5,6,7,8-tetrahydronaphthalen-2-ol 102587080 Click to see 298.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
(5R,6R,7R)-5-(4-hydroxyphenyl)-6,7-dimethyl-5,6,7,8-tetrahydronaphthalene-2,3-diol 5317329 Click to see CC1CC2=CC(=C(C=C2C(C1C)C3=CC=C(C=C3)O)O)O 284.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
5-(4-Hydroxy-3-methoxyphenyl)-3-methoxy-6,7-dimethyl-5,6,7,8-tetrahydronaphthalen-2-ol 72834187 Click to see 328.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
5-(4-Hydroxyphenyl)-3-methoxy-6,7-dimethyl-5,6,7,8-tetrahydronaphthalen-2-ol 162990069 Click to see 298.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
5-(4-Hydroxyphenyl)-6,7-dimethyl-5,6,7,8-tetrahydronaphthalene-2,3-diol 13887361 Click to see CC1CC2=CC(=C(C=C2C(C1C)C3=CC=C(C=C3)O)O)O 284.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
Isoguaiacin 10314441 Click to see CC1CC2=CC(=C(C=C2C(C1C)C3=CC(=C(C=C3)O)OC)O)OC 328.40 unknown https://doi.org/10.1021/NP50068A019
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
4-[(2R,3S)-4-(3-hydroxy-4-methoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol 10711507 Click to see 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
4-[4-(3-Hydroxy-4-methoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol 11624083 Click to see CC(CC1=CC(=C(C=C1)OC)O)C(C)CC2=CC(=C(C=C2)O)OC 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
5-[(2S,3R)-4-(3,4-dimethoxyphenyl)-2,3-dimethyl-butyl]-2-methoxy-phenol 476860 Click to see 344.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
5-[4-(3-Hydroxy-4-methoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol 11493650 Click to see 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
5-[4-(3,4-Dimethoxyphenyl)-2,3-dimethylbutyl]-2-methoxyphenol 9902716 Click to see 344.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
Dihydroguaiaretic Acid 161924 Click to see 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
Dimethylnordihydroguarierate acid 476857 Click to see CC(CC1=CC(=C(C=C1)OC)O)C(C)CC2=CC(=C(C=C2)OC)O 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
Masoprocol 71398 Click to see CC(CC1=CC(=C(C=C1)O)O)C(C)CC2=CC(=C(C=C2)O)O 302.40 unknown https://doi.org/10.1016/J.JEP.2005.02.002
Meso-Dihydroguaiaretic Acid 476856 Click to see 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
Nordihydroguaiaretic acid 4534 Click to see CC(CC1=CC(=C(C=C1)O)O)C(C)CC2=CC(=C(C=C2)O)O 302.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001106/
https://doi.org/10.1016/J.JEP.2005.02.002
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(+)-Larreatricin 14213223 Click to see 284.30 unknown https://doi.org/10.1021/NP50068A019
https://doi.org/10.1039/B302632A
4-[(2R,3R,4R,5R)-5-(4-hydroxyphenyl)-3,4-dimethyloxolan-2-yl]benzene-1,2-diol 14681580 Click to see 300.30 unknown https://doi.org/10.1021/NP50068A019
https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
4-[(2R,3R,4S,5S)-5-(3,4-dihydroxyphenyl)-3,4-dimethyloxolan-2-yl]benzene-1,2-diol 11243993 Click to see 316.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
4-[(2R,3S,4S,5S)-5-(4-hydroxyphenyl)-3,4-dimethyloxolan-2-yl]phenol 21592483 Click to see 284.30 unknown https://doi.org/10.1039/B302632A
4-[(2S,3S,4S,5S)-5-(3-hydroxy-4-methoxyphenyl)-3,4-dimethyloxolan-2-yl]benzene-1,2-diol 11336474 Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)O)C3=CC(=C(C=C3)OC)O)C 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
4-[5-(3-Hydroxy-4-methoxyphenyl)-3,4-dimethyloxolan-2-yl]benzene-1,2-diol 72806513 Click to see 330.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
4-[5-(3,4-Dihydroxyphenyl)-3,4-dimethyloxolan-2-yl]benzene-1,2-diol 45360326 Click to see 316.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
4-[5-(4-Hydroxyphenyl)-3,4-dimethyloxolan-2-yl]benzene-1,2-diol 14681579 Click to see 300.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
4-[5-(4-Hydroxyphenyl)-3,4-dimethyloxolan-2-yl]phenol 14213222 Click to see 284.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
https://doi.org/10.1039/B302632A
4,4'-[rel-(2R,3R,4R,5R)-3,4-Dimethyltetrahydrofuran-2,5-diyl]diphenol 11033399 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown https://doi.org/10.1039/B302632A
https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
Meso-3,3'-Didemethoxynectandrin B 14213224 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown https://doi.org/10.1039/B302632A
https://doi.org/10.1021/NP50068A019
https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101589132 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(=C)CC7)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 1043.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162996774 Click to see 1043.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 25231433 Click to see 1221.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 72987887 Click to see 913.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73157175 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 1059.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
[3,4,5-Trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 74409911 Click to see 1221.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
3-O-xylyl(1-3)glucosiduronic acid-oleanolic acid-28-O-glucoside 14162553 Click to see 927.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
Guaiacin B 11506185 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 913.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
momordin IIc 14162557 Click to see 927.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
Nudicaucin C 21635821 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 1059.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 10395290 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 751.00 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
10-[3,5-Dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 85131349 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 751.00 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
10-[5-Hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 73813221 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O 897.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
Pulchinenoside B10 21626543 Click to see 897.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0031-9422(88)80621-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101589131 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(=C)CC7)C(=O)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O 881.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
10-[5-Hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162913832 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(=C)CC7)C(=O)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O 881.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.09.012
> Phenylpropanoids and polyketides / Flavonoids / Flavones
5-Hydroxy-2-(4-hydroxy-3-methylphenyl)-3,7-dimethylchromen-4-one 141160776 Click to see 296.30 unknown https://doi.org/10.1002/CHIN.197431248
5-Hydroxy-2-(4-hydroxyphenyl)-3,7-dimethylchromen-4-one 21759565 Click to see 282.29 unknown https://doi.org/10.1002/CHIN.197431248
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/10.1016/J.PHYTOCHEM.2004.07.009
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1248/BPB.31.2321
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3'-O-Methyltaxifolin 26194552 Click to see COC1=C(C=CC(=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 318.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
Dihydroisorhamnetin 56658060 Click to see 318.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
Isokaempferide 5280862 Click to see 300.26 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether 348130 Click to see 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
Ayanin 5280682 Click to see 344.30 unknown https://doi.org/10.1002/CHIN.199611314
Herbacetin 3,7-dimethyl ether 13983739 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)O 330.29 unknown https://doi.org/10.1016/0031-9422(75)83068-8
Sakuranetin 73571 Click to see 286.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.02.007
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see 330.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009
Herbacetin 3,8,4'-trimethyl ether 13916278 Click to see 344.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.07.009

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Larrea tridentata
Author: Sorin
Larrea tridentata
Author: Sorin
Larrea tridentata
Author: Sorin
Larrea tridentata
Author: Sorin
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Sorin

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