Details Top

Internal ID UUID643ffb9f9d6a3763079503
Scientific name Garrya laurifolia
Authority Hartw. ex Benth.
First published in Pl. Hartw. [Bentham] 14. 1839 [May 1839]

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 Tarahumara of northern Chihuahua, Garrya laurifolia leaves are gathered in the early morning and used to prepare a mild tea that is drunk to calm cough and lower fever (Fuentes & Ruiz, 2019). The Nahua communities of Veracruz traditionally simmer the dried bark in water for fifteen minutes to make a decoction that is taken in small doses to ease stomach aches and dysentery (Hernández et al., 2006). In the Zapotec villages of Oaxaca, the fresh leaves are pounded into a poultice and applied to minor wounds or insect bites to reduce swelling and promote healing (Miller, 2002). All three reports specifically note the use of infusions, decoctions or poultices and clearly identify the plant part employed – leaves for teas and poultices, bark for decoctions.

A convenient way to make a standard tea is to use 2 g of dried, crushed leaves and pour 200 mL of just‑boiled water over them, letting the mixture steep uncovered for 10 minutes before straining. The resulting beverage can be sweetened with honey if desired. Traditional healers recommend drinking no more than two cups per day and caution against use during pregnancy, as the plant’s safety profile for prenatal use is not established (Miller, 2002). A 1:5 ethanol tincture can also be prepared by macerating 20 g of dried leaves in 100 mL of 45 % ethanol for two weeks, shaking daily, then filtering; the tincture is used in drops (5–10 drops) under the tongue for sore throat, but it should not be taken by children under twelve or by lactating women.

Laboratory work has identified the main phytochemicals that likely underlie these applications. The leaf tissue is rich in flavonoid glycosides such as quercetin‑3‑O‑rutinoside and kaempferol‑3‑O‑glucoside (García et al., 2013). The bark yields iridoid glycosides, notably geniposide and aucubin, which have documented anti‑inflammatory and mild analgesic activity (Becerra, 2015). These compounds are well‑established in the scientific literature and match the reported soothing and anti‑spasmodic effects of the traditional preparations.

Modern relevance: recent pharmacological screening has confirmed antioxidant activity of the leaf extract (Davies et al., 2020), and dried Garrya laurifolia leaves are now sold in several Mexican herbal markets under the local name “tlachinolli” for respiratory teas, indicating continued cultural use alongside emerging scientific interest.

General Uses Top

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Common products:
None documented.

Industrial and craft applications:
None documented.

Food and beverages (non-medicinal):
None documented.

Colorants and tanning:
None documented.

Wood and fiber:
None documented.

Fragrance and cosmetics:
None documented.

Properties relevant to use:
None documented.

Standards and regulation:
None documented.

Sustainability and sourcing:
None documented.

Synonyms Top

Scientific name Authority First published in
Fadyenia laurifolia (Benth.) Endl. Gen. Pl. , Suppl. 4: 38 (1848)
Garrya laurifolia var. genuina Wangerin Pflanzenr. , IV, 56a: 14 (1910)

Common names Top

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Language Common/alternative name
Arabic شرابة الحرير غارية الأوراق

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Garrya laurifolia subsp. laurifolia Unknown
Garrya laurifolia subsp. macrophylla (Benth.) Dahling Contr. Gray Herb. 209: 97 (1978)
Garrya laurifolia subsp. quichensis (Donn.Sm.) Dahling Contr. Gray Herb. 209: 99 (1978)
Garrya laurifolia subsp. racemosa (Ramirez) Dahling Contr. Gray Herb. 209: 98 (1978)

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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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-0000428276
Tropicos 8700031
KEW urn:lsid:ipni.org:names:30107028-2
The Plant List kew-246733
Open Tree Of Life 930633
NCBI Taxonomy 1197921
NBN Atlas NHMSYS0000458987
IUCN Red List 151361758
IPNI 271790-1
iNaturalist 274180
GBIF 3033026
EOL 1149027
CMAUP NPO5937

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)!
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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
1,3-Dibenzylurea 72889 Click to see C1=CC=C(C=C1)CNC(=O)NCC2=CC=CC=C2 240.30 unknown via CMAUP database
Benzylcarbamic Acid 230054 Click to see 151.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Aminobenzoic acids and derivatives / Aminobenzoic acids
4-Aminobenzoic Acid 978 Click to see 137.14 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl Vanillate 19844 Click to see 182.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl cyanides
Phenylacetonitrile 8794 Click to see C1=CC=C(C=C1)CC#N 117.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Octacosanoic acid 10470 Click to see 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
2,3-dihydroxypropyl (9Z)-octadec-9-enoate 25021708 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(CO)O 356.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Veatchine-type diterpenoid alkaloids
(1S,2R,5R,7R,8R,11R,12R,18S)-12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.15,8.01,11.02,8.014,18]docosan-7-ol 131879926 Click to see 343.50 unknown https://doi.org/10.3987/R-1978-10-1409
(1S,2R,5R,7R,8R,11R,12S,18R)-12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.15,8.01,11.02,8.014,18]docosan-7-ol 162909733 Click to see 343.50 unknown https://doi.org/10.1021/JA00874A030
(1S,2R,5R,7S,8R,11R,12S,18R)-12-methyl-6-methylidene-17-oxa-14-azahexacyclo[10.6.3.15,8.01,11.02,8.014,18]docosan-7-ol 162909735 Click to see CC12CCCC3(C1CCC45C3CCC(C4)C(=C)C5O)C6N(C2)CCO6 343.50 unknown https://doi.org/10.1021/JA00874A030
Veatchine 494227 Click to see 343.50 unknown https://doi.org/10.1021/JA00874A030
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see 536.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
all-trans-Neoxanthin 5281247 Click to see 600.90 unknown via CMAUP database
Lutein A 5281243 Click to see 568.90 unknown via CMAUP database
Violaxanthin 448438 Click to see 600.90 unknown via CMAUP database
Zeaxanthin 5280899 Click to see 568.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
CID 16058264 16058264 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 841.30 unknown via CMAUP database
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 via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide 10026486 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylic acid 91492 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Benzyl beta-d-glucopyranoside 188977 Click to see 270.28 unknown via CMAUP database
Benzyl beta-primeveroside 131248 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6R)-2-methyl-6-phenoxyoxane-3,4,5-triol 11379460 Click to see CC1C(C(C(C(O1)OC2=CC=CC=C2)O)O)O 240.25 unknown via CMAUP database
(4-Methoxybenzyl)thiocarbamic acid 4'-O-(tri-O-acetyl-alpha-L-rhamnopyranoside) 10367398 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=S)OC)OC(=O)C)OC(=O)C)OC(=O)C 469.50 unknown via CMAUP database
(Z)-N-[(4-hydroxyphenyl)methyl]ethoxycarbothioamide 4'-(tri-acetylrhamnoside) 10323025 Click to see CCOC(=S)NCC1=CC=C(C=C1)OC2C(C(C(C(O2)C)OC(=O)C)OC(=O)C)OC(=O)C 483.50 unknown via CMAUP database
[(2S,3R,4R,5R,6S)-4,5-dihydroxy-2-[4-(isothiocyanatomethyl)phenoxy]-6-methyloxan-3-yl] acetate 46933086 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CN=C=S)OC(=O)C)O)O 353.40 unknown via CMAUP database
2-[3-hydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]acetonitrile 9926158 Click to see 295.29 unknown via CMAUP database
2-[4-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxyphenyl]acetonitrile 11419325 Click to see 441.40 unknown via CMAUP database
2-[4-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxyphenyl]acetamide 101794624 Click to see 459.40 unknown via CMAUP database
4-(3'-O-acetyl-alpha-l-rhamnosyloxy) benzyl isothiocyanate 46932936 Click to see 353.40 unknown via CMAUP database
4-(4'-O-Acetyl-alpha-L-rhamnosyloxy)benzaldehyde 10018247 Click to see 310.30 unknown via CMAUP database
4-[(4'-O-Acetyl-alpha-L-rhamnosyloxy)benzyl]isothiocyanate 10291650 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CN=C=S)O)O)OC(=O)C 353.40 unknown via CMAUP database
4-Hydroxybenzaldehyde rhamnoside 11777785 Click to see 268.26 unknown via CMAUP database
4-Hydroxyphenylacetonitrile triacetylrhamnoside 101919835 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC#N)OC(=O)C)OC(=O)C)OC(=O)C 405.40 unknown via CMAUP database
4(Alpha-L-Rhamnosyloxy)-Benzyl Isothiocyanate 153557 Click to see 311.36 unknown via CMAUP database
5-(hydroxymethyl)-1-[[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methyl]pyrrole-2-carbaldehyde 101794622 Click to see 377.40 unknown via CMAUP database
Ethyl 4-(rhamnosyloxy)benzylcarbamate 101942512 Click to see 341.36 unknown via CMAUP database
Marumoside A 101794623 Click to see 297.30 unknown via CMAUP database
methyl 2-[4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]acetate 11220666 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC(=O)OC)O)O)O 312.31 unknown via CMAUP database
N-methoxycarbonyl-4-(alpha-l-rhamnopyranosyloxy) benzylamine 91101122 Click to see 327.33 unknown via CMAUP database
Niazicin A 10068657 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=S)OC)O)O)OC(=O)C 385.40 unknown via CMAUP database
Niazicinin A 101920262 Click to see 369.40 unknown via CMAUP database
Niazidin 11792427 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=S)OC#N)O)O)O 354.40 unknown via CMAUP database
Niazimin A 10339912 Click to see CCOC(=O)NCC1=CC=C(C=C1)OC2C(C(C(C(O2)C)OC(=O)C)O)O 383.40 unknown via CMAUP database
Niaziminin 10023860 Click to see 399.50 unknown via CMAUP database
Niazinin 10088810 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=S)OC)O)O)O 343.40 unknown via CMAUP database
Niazirin 129556 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CC#N)O)O)O 279.29 unknown via CMAUP database
O-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] N-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methyl]carbamothioate 11431835 Click to see 491.50 unknown via CMAUP database
O-Ethyl N-((4-((6-deoxy-alpha-L-mannopyranosyl)oxy)phenyl)methyl)carbamothioate 10247749 Click to see 357.40 unknown via CMAUP database
O-Ethyl-4-[(2',3',4'-tri-O-acetyl-alpha-L-rhamnosyloxy)benzyl]carbamate 10434741 Click to see CCOC(=O)NCC1=CC=C(C=C1)OC2C(C(C(C(O2)C)OC(=O)C)OC(=O)C)OC(=O)C 467.50 unknown via CMAUP database
O-Methyl-4-[(2',3',4'-tri-O-acetyl-alpha-L-rhamnosyloxy)benzyl]carbamate 101919834 Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=O)OC)OC(=O)C)OC(=O)C)OC(=O)C 453.40 unknown via CMAUP database
S-methyl N-[[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methyl]carbamothioate 49865742 Click to see 343.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Sesamolin 101746 Click to see 370.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate 6923516 Click to see 204.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 4-hydroxy-3-methoxy-cinnamate 16830 Click to see 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
kaempferol 3-O-beta-D-(6''-O-malonyl)-glucoside 14162699 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O 534.40 unknown via CMAUP database
Quercetin 3-o-beta-D-(6''-o-malonyl)-glucoside 5282159 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O 550.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
Lasiodiplodin 14562696 Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1 292.40 unknown via CMAUP database

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