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Scutia buxifolia

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64404d49b9188451691732
Scientific name Scutia buxifolia
Authority Reissek
First published in Fl. Bras. 11(1): 93 (1861)

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 Uruguay’s traditional healers, dried leaf infusions have been used for fevers and for calming gastrointestinal cramps and general colicky pain, and as a light diuretic, a usage recorded by Cabrera and Wesolowski (1984) and confirmed by Doménech (1960) in Argentine folk medicine. Across the Río de la Plata basin, including the inland pampas of Uruguay and nearby southern Brazil, similar leaf teas have been taken to ease indigestion and as a febrifuge; pharmacognostic surveys in Argentina and Brazil (Lorenzi, 1992; Larsen & Rodríguez, 1998) also note these uses. In northern Argentina, the same preparation has been employed topically as a compress for minor skin irritations and bruises, with indications reported by Di Giacomo (1960) and reviewed by Kovaleski (1967).

Leaves have been the main plant part in these preparations, sometimes gathered young and air‑dried in shade for storage. In northern Argentina and Uruguay, a simple hot infusion is made by pouring roughly 2 liters of boiling water over 30 g of dried leaves, covering and infusing 10–15 minutes, then straining. The tea is taken in 1‑ to 1‑cup servings two to three times daily for mild colic or fever, and not for long courses without professional supervision. A concentrated decoction can also be prepared by simmering the same 30 g of dried leaves in 1 liter of water for 20 minutes and letting it steep 5 minutes; it is strained and used in smaller, divided doses to treat fever. Most accounts warn against large or extended doses, and pregnant or nursing people are advised to avoid it; in Brazil folk references (Lorenzi, 1992) caution that it can be emetic in excess. Traditional texts also note that in some neighborhoods of Buenos Aires and Montevideo the leaves were once macerated in 30–40% ethanol for up to a month to produce a small tincture (1:5) used as a carminative stimulant, but modern-day sources emphasize milder, non‑alcoholic preparations (Bennett et al., 2021).

Well‑studied constituents reported for Scutia buxifolia include flavonoids such as quercetin‑ and kaempferol‑glycosides, along with triterpenic acids (ursolic, oleanolic), saponins, phenolics including catechin/epicatechin, and quinolizidine alkaloids that likely underpin the plant’s bitter tonic and digestive effects (Alonso & Desmarchelier, 2015; Larsen & Rodríguez, 1998). The quinolizidine alkaloids and tannins are consistent with the traditional use for colic and as a diuretic, while the flavonoids add antioxidant plausibility.

At present, the species is not widely sold as a commercial herbal medicine, but isolated tinctures and small batches of dried leaf have appeared in niche markets, and a few producers still harvest the leaves for local use. Ongoing phytochemical studies continue to profile its alkaloid and flavonoid profile, while Argentine and Uruguayan field surveys confirm that leaf teas remain in occasional domestic use as gentle remedies for fevers, colic, and upset stomach (Silva, 2019).

General Uses Top

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Common products:
Scutia buxifolia is used chiefly as a source of tannins extracted from the bark; these are applied in leather tanning and as natural brown dyes. Historically the species has also been managed as a source of firewood or small timber in regional silviculture.

Industrial and craft applications:
Bark tannins are used in leather tanning and impart brown coloration to vegetable-tanned leather and mordanted protein fibers; the tannin extract is compatible with standard tanning workflows (soaking, raising, finishing). Wood is utilized locally for posts and fuel; charcoal production occurs where permitted.

Colorants and tanning:
The bark yields tannins employed as natural brown colorants in leather and textile dyeing, typically with mordants to improve washfastness. Tannins are compatible with chromium-free tanning protocols and can be combined with other vegetable tannins to balance acidity and viscosity in tanning liquors.

Wood and fiber:
The wood is exploited for fence posts, agricultural implements, and fuel; it may be carbonized for charcoal. No significant fiber or resin uses are reported.

Properties relevant to use:
Tannins extracted from the bark have sufficient astringency to act as vegetable tanning agents and mordants for protein fibers. The wood is described as hard and heavy, indicating suitability for durable timber applications.

Standards and regulation:
Tanning extracts and dyed materials generally follow standard tannery and dyeing protocols; dyed leather may be evaluated under relevant ISO/ASTM/EU protocols (e.g., colorfastness, flex resistance). Compliance with national timber and charcoal regulations applies where the species is harvested.

Sustainability and sourcing:
Local and regional management in Argentina, Brazil, and Paraguay sustains timber and tannin use; selection of mature material is typical. As assessments indicate the species is not globally threatened, risk depends on local harvesting intensity and management practices.

Synonyms Top

Scientific name Authority First published in
Adolia buxifolia Kuntze Revis. Gen. Pl. 1: 117 (1891)
Scutia fiebrigii Perkins Bot. Jahrb. Syst. 45: 464 (1911)
Scutia buxifolia var. obtusifolia Reissek Fl. Bras. (Martius) 11(1): 93. 1861 [15 Feb 1861]
Scutia buxifolia var. acutifolia Reissek Fl. Bras. (Martius) 11(1): 93. 1861 [15 Feb 1861]
Rhamnus coronula Larrañaga Escritos D. A. Larrañaga 2: 94 (1923)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001130909
Tropicos 27500129
KEW urn:lsid:ipni.org:names:718854-1
The Plant List tro-27500129
Open Tree Of Life 1040250
NCBI Taxonomy 106710
IUCN Red List 160422005
IPNI 718854-1
iNaturalist 371186
GBIF 7273785
USDA GRIN 33434
CMAUP NPO4144

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
Plants and Their Derivatives as Promising Therapeutics for Sustainable Control of Honeybee (Apis mellifera) Pathogens Bava R, Castagna F, Ruga S, Nucera S, Caminiti R, Serra M, Bulotta RM, Lupia C, Marrelli M, Conforti F, Statti G, Domenico B, Palma E Pathogens 19-Oct-2023
PMCID:PMC10610010
doi:10.3390/pathogens12101260
PMID:37887776
Morphometric and genetic characterization as tools for selection of Apis mellifera (Hymenoptera: Apidae) stocks in an area of natural hybridization in Argentina Litvinoff L, Menescardi F, Porrini L, Russo R, Liendo MC, Nucci A, Lusarreta E, Ventura R, Espasadin L, Monmany-Garzia AC, Scannapieco AC, Galindo-Cardona A Front Insect Sci 17-Jan-2023
PMCID:PMC10926486
doi:10.3389/finsc.2022.1073999
PMID:38468812
Ancient Rhamnaceae flowers impute an origin for flowering plants exceeding 250-million-years ago He T, Lamont BB iScience 18-Jun-2022
PMCID:PMC9254029
doi:10.1016/j.isci.2022.104642
PMID:35800761
Novel land uses shape meta-community structures in neighbouring native forests: Dataset across Uruguay Säumel I, Ramírez LR Data Brief 16-May-2022
PMCID:PMC9130530
doi:10.1016/j.dib.2022.108267
PMID:35647241
Native forest metacommunity structures in Uruguay shaped by novel land‐use types in their surroundings Ramírez LR, Säumel I Ecol Evol 06-Mar-2022
PMCID:PMC8928906
doi:10.1002/ece3.8700
PMID:35342551
Chemical Profile, Antimicrobial and Antioxidant Activity Assessment of the Crude Extract and Its Main Flavonoids from Tartary Buckwheat Sprouts Zhong L, Lin Y, Wang C, Niu B, Xu Y, Zhao G, Zhao J Molecules 07-Jan-2022
PMCID:PMC8779668
doi:10.3390/molecules27020374
PMID:35056695
Biologically Active Extracts from Different Medicinal Plants Tested as Potential Additives against Bee Pathogens Pașca C, Matei IA, Diaconeasa Z, Rotaru A, Erler S, Dezmirean DS Antibiotics (Basel) 10-Aug-2021
PMCID:PMC8388991
doi:10.3390/antibiotics10080960
PMID:34439010
Geographic Area of Collection Determines the Chemical Composition and Antimicrobial Potential of Three Extracts of Chilean Propolis Alvear M, Santos E, Cabezas F, Pérez-SanMartín A, Lespinasse M, Veloz J Plants (Basel) 28-Jul-2021
PMCID:PMC8400560
doi:10.3390/plants10081543
PMID:34451588
Enhancing monitoring of rewilding progress through wildlife tracking and remote sensing Mata JC, Buitenwerf R, Svenning JC PLoS One 09-Jul-2021
PMCID:PMC8270134
doi:10.1371/journal.pone.0253148
PMID:34242225
Prolonged Diuretic and Renoprotective Effects of a Xanthone Obtained from Garcinia achachairu Rusby in Normotensive and Hypertensive Rats Bolda Mariano LN, Boeing T, Cechinel Filho V, Niero R, Gasparotto Junior A, Mota da Silva L, de Souza P Evid Based Complement Alternat Med 20-Apr-2021
PMCID:PMC8081593
doi:10.1155/2021/5510053
PMID:33995544
Targeting P2 receptors in purinergic signaling: a new strategy of active ingredients in traditional Chinese herbals for diseases treatment Ai X, Dong X, Guo Y, Yang P, Hou Y, Bai J, Zhang S, Wang X Purinergic Signal 22-Mar-2021
PMCID:PMC8155138
doi:10.1007/s11302-021-09774-x
PMID:33751327
A review study on the anti-trichomonas activities of medicinal plants Hashemi N, Ommi D, Kheyri P, Khamesipour F, Setzer WN, Benchimol M Int J Parasitol Drugs Drug Resist 12-Feb-2021
PMCID:PMC7902805
doi:10.1016/j.ijpddr.2021.01.002
PMID:33610966
Potential Anti-Tuberculosis Activity of the Extracts and Their Active Components of Anogeissus leiocarpa (DC.) Guill. and Perr. with Special Emphasis on Polyphenols Salih EY, Julkunen-Tiitto R, Luukkanen O, Sipi M, Fahmi MK, Fyhrquist PJ Antibiotics (Basel) 29-Jun-2020
PMCID:PMC7399890
doi:10.3390/antibiotics9070364
PMID:32610461
Helminth fauna of the screaming hairy armadillo Chaetophractus vellerosus from Argentina: the consequence of host isolation on parasite diversity Ezquiaga MC, Abba AM, Navone GT Heliyon 08-May-2019
PMCID:PMC6513779
doi:10.1016/j.heliyon.2019.e01605
PMID:31193013
Breeding latitude predicts timing but not rate of spring migration in a widespread migratory bird in South America Jahn AE, Cereghetti J, Cueto VR, Hallworth MT, Levey DJ, Marini MÂ, Masson D, Pizo MA, Sarasola JH, Tuero DT Ecol Evol 16-Apr-2019
PMCID:PMC6540664
doi:10.1002/ece3.5159
PMID:31160996

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
> 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
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 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
Hexacosanoic Acid 10469 Click to see 396.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 40522879 Click to see 272.40 unknown via CMAUP database
(1R,4aS,10aS)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 7075030 Click to see 300.40 unknown via CMAUP database
(1R,4aS,9R,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol 21604174 Click to see 288.40 unknown via CMAUP database
(1R,4aS,9R,10aR)-9-hydroxy-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carbaldehyde 10425915 Click to see CC1(CCCC2(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)C)C=O 316.40 unknown via CMAUP database
(1R,4aS,9S,10aR)-1-(hydroxymethyl)-7-(1-hydroxy-1-methyl-ethyl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 3009626 Click to see 318.40 unknown via CMAUP database
(1R,4aS,9S,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1,9-diol 100982592 Click to see 288.40 unknown via CMAUP database
(1S,4aS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 26183496 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
(1S,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-1-ol 26183495 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)O)C 272.40 unknown via CMAUP database
15-Hydroxydehydroabietic Acid 14487943 Click to see 316.40 unknown via CMAUP database
15,18-Dihydroxyabieta-8,11,13-trien-7-one 3009631 Click to see 316.40 unknown via CMAUP database
18-Nor-4,15-dihydroxyabieta-8,11,13-trien-7-one 3009629 Click to see CC12CCCC(C1CC(=O)C3=C2C=CC(=C3)C(C)(C)O)(C)O 302.40 unknown via CMAUP database
18-Norabieta-8,11,13-trien-4-ol 15605917 Click to see 272.40 unknown via CMAUP database
7-Oxo-15-Hydroxydehydroabietic Acid 14017925 Click to see 330.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see 300.40 unknown via CMAUP database
7alpha-Hydroxydehydroabieticacid 13370053 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C(=O)O)C 316.40 unknown via CMAUP database
7alpha,15-Dihydroxydehydroabietic acid 12047563 Click to see 332.40 unknown via CMAUP database
7Beta-Hydroxydehydroabietic Acid 13370052 Click to see 316.40 unknown via CMAUP database
7beta,15-Dihydroxydehydroabietic acid 21626423 Click to see CC12CCCC(C1CC(C3=C2C=CC(=C3)C(C)(C)O)O)(C)C(=O)O 332.40 unknown via CMAUP database
Aquilarabietic Acid H 71578077 Click to see 314.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
[(3S,5bR,8R,9R,11aR,13S,13aS)-8-ethyl-13-hydroxy-3,5b,8,11a,13a-pentamethyl-1-oxo-4,5,5a,6,7,7a,9,10,11,11b,12,13-dodecahydro-3H-phenanthro[2,1-e]isobenzofuran-9-yl] acetate 486510 Click to see 472.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
https://doi.org/10.1016/0031-9422(74)80259-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,15S,16R,19R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16,19-triol 9547211 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CC(C(C6)O)O)C)O)C)C)OC1 448.60 unknown https://doi.org/10.1002/CBER.19741070712
https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
https://doi.org/10.1016/0031-9422(71)85096-3
https://doi.org/10.1016/S0031-9422(00)81890-7
https://doi.org/10.1016/0031-9422(74)80118-4
https://doi.org/10.1016/0031-9422(94)00611-V
https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
(2R)-N-[(3R,4R,7R,10Z)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-1-[(2S)-2-(methylamino)-3-phenylpropanoyl]pyrrolidine-2-carboxamide 163185613 Click to see 651.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2R)-N-[(3R,4R,7S,10E)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-phenylpropanamide 163186784 Click to see 568.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2S,3R)-2-(dimethylamino)-3-hydroxy-N-[(3R,4R,7R,10Z)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 163194572 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)C(C3=CC=CC=C3)O)NC(=O)C(C(C4=CC=CC=C4)O)N(C)C 600.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
(2S,3S)-2-(dimethylamino)-N-[(3S,4R,7R,10Z)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-methylpentanamide 163190610 Click to see 550.70 unknown https://doi.org/10.1016/S0031-9422(00)81890-7
(2S,3S)-N-[(3S,4R,7R,10Z)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-methylpentanamide 163186693 Click to see 534.70 unknown https://doi.org/10.1002/CBER.19741070712
https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2S,4S)-2-(dimethylamino)-N-[(3R,4R,7R,10Z)-5,8-dioxo-7-[(1R)-1-phenylethyl]-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-4-methylhexanamide 163193062 Click to see 562.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
(2S,4S)-2-(dimethylamino)-N-[(3S,4R,7R,10Z)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-4-methylhexanamide 163188154 Click to see CCC(C)CC(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)C(C3=CC=CC=C3)O)C(C)C)N(C)C 564.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
(2S)-2-(dimethylamino)-N-[(3R,4R,7R,10Z)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 163187422 Click to see 584.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2S)-2-(dimethylamino)-N-[(3R,4R,7R,10Z)-7-[(S)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 122362221 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)C(C3=CC=CC=C3)O)NC(=O)C(CC4=CC=CC=C4)N(C)C 584.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
https://doi.org/10.1016/S0031-9422(00)81890-7
https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
(2S)-2-(dimethylamino)-N-[(3S,4R,7R,10Z)-5,8-dioxo-7-[(1R)-1-phenylethyl]-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 163189418 Click to see 582.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
(2S)-2-(dimethylamino)-N-[(3S,4S,7R,10Z)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 163187423 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)C(C3=CC=CC=C3)O)NC(=O)C(CC4=CC=CC=C4)N(C)C 584.70 unknown https://doi.org/10.1016/0031-9422(74)80118-4
(2S)-2-(dimethylamino)-N-[(3S,4S,7S,10Z)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 163187421 Click to see 584.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
https://doi.org/10.1016/S0031-9422(00)81890-7
https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
(2S)-N-[(3R,4S,7S,10Z)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-1-[(2S)-2-(methylamino)-3-phenylpropanoyl]pyrrolidine-2-carboxamide 163193919 Click to see 651.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2S)-N-[(3S,4R,7R,10Z)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-phenylpropanamide 163194573 Click to see 568.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2S)-N-[(3S,4S,7R,10Z)-7-benzyl-11-ethyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-1-[(2S)-2-(methylamino)-3-phenylpropanoyl]pyrrolidine-2-carboxamide 163195159 Click to see 679.80 unknown https://doi.org/10.1016/S0031-9422(00)86715-1
(2S)-N-[(3S,4S,7R,10Z)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-phenylpropanamide 163185777 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)CC3=CC=CC=C3)NC(=O)C(CC4=CC=CC=C4)N(C)C 568.70 unknown https://doi.org/10.1016/0031-9422(74)80118-4
(E)-N-[(3R,4R,7R,10Z)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylprop-2-enamide 163194281 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)C(C3=CC=CC=C3)O)NC(=O)C=CC4=CC=CC=C4 539.60 unknown https://doi.org/10.1016/0031-9422(74)80259-1
(E)-N-[(3R,4R,7S,10Z)-7-[(2S)-butan-2-yl]-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylprop-2-enamide 163186587 Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC(C(C(=O)N1)NC(=O)C=CC3=CC=CC=C3)C4=CC=CC=C4 523.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(E)-N-[(3S,4S,7S,10Z)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylprop-2-enamide 11421341 Click to see 539.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
(E)-N-[(3S,4S,7S,10Z)-7-[(S)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylprop-2-enamide 10370032 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)C(C3=CC=CC=C3)O)NC(=O)C=CC4=CC=CC=C4 539.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
(E)-N-[(7S,10E)-7-[(2R)-butan-2-yl]-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylprop-2-enamide 101378053 Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC(C(C(=O)N1)NC(=O)C=CC3=CC=CC=C3)C4=CC=CC=C4 523.60 unknown via CMAUP database
2-(dimethylamino)-N-[5,8-dioxo-7-(1-phenylethyl)-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 162873014 Click to see 582.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
2-(dimethylamino)-N-[5,8-dioxo-7-(1-phenylethyl)-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-4-methylhexanamide 162872948 Click to see 562.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
2-(dimethylamino)-N-[7-[hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-4-methylhexanamide 163033204 Click to see 564.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
N-(7-benzyl-11-ethyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl)-1-[2-(methylamino)-3-phenylpropanoyl]pyrrolidine-2-carboxamide 162986339 Click to see 679.80 unknown https://doi.org/10.1016/S0031-9422(00)86715-1
N-(7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl)-2-(dimethylamino)-3-methylpentanamide 76393281 Click to see 534.70 unknown https://doi.org/10.1002/CBER.19741070712
https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
https://doi.org/10.1016/S0031-9422(00)81890-7
https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
https://doi.org/10.1016/0031-9422(74)80259-1
N-(7-butan-2-yl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl)-3-phenylprop-2-enamide 162889452 Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC(C(C(=O)N1)NC(=O)C=CC3=CC=CC=C3)C4=CC=CC=C4 523.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
N-[(10Z)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-phenylpropanamide 56677554 Click to see 568.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(2R)-N-[(3R,4R,7S,10E)-7-[(2R)-butan-2-yl]-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-phenylpropanamide 162996764 Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC(C(C(=O)N1)NC(=O)C(CC3=CC=CC=C3)N(C)C)C4=CC=CC=C4 568.70 unknown https://doi.org/10.1016/S0031-9422(97)00491-3
(2R)-N-[(3R,4R,7S,10Z)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-phenylpropanamide 163014980 Click to see 568.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2R)-N-[(3S,4S,7S,10E)-7-[(2R)-butan-2-yl]-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(methylamino)-3-phenylpropanamide 162963782 Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC(C(C(=O)N1)NC(=O)C(CC3=CC=CC=C3)NC)C4=CC=CC=C4 554.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2S,3R)-N-[(3S,4S,7S,10E)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-methylpentanamide 102239804 Click to see 534.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
https://doi.org/10.1016/0031-9422(94)00611-V
(2S,3R)-N-[(3S,4S,7S,10Z)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-methylpentanamide 90473277 Click to see CCC(C)C(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)CC3=CC=CC=C3)C(C)C)N(C)C 534.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
https://doi.org/10.1016/S0031-9422(00)81890-7
https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
https://doi.org/10.1016/0031-9422(74)80259-1
(2S,3S)-2-(dimethylamino)-3-hydroxy-N-[(3R,4S,7R,10E)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 163033370 Click to see 600.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
(2S)-2-(dimethylamino)-N-[(3R,4R,7R,10E)-7-[(S)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 102239802 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)C(C3=CC=CC=C3)O)NC(=O)C(CC4=CC=CC=C4)N(C)C 584.70 unknown https://doi.org/10.1016/S0031-9422(97)00491-3
https://doi.org/10.1016/0031-9422(94)00611-V
(2S)-2-(dimethylamino)-N-[(3S,4R,7R,10Z)-7-[(R)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 162949225 Click to see 584.70 unknown https://doi.org/10.1002/CBER.19741070712
https://doi.org/10.1016/0031-9422(71)85096-3
https://doi.org/10.1016/0031-9422(94)00611-V
(2S)-2-(dimethylamino)-N-[(3S,4S,7R,10Z)-7-[(S)-hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 101938865 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)C(C3=CC=CC=C3)O)NC(=O)C(CC4=CC=CC=C4)N(C)C 584.70 unknown https://doi.org/10.1016/S0031-9422(97)00491-3
(2S)-2-(dimethylamino)-N-[(3S,4S,7S,10E)-7-[hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 102239803 Click to see 584.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
(2S)-N-[(3R,4S,7S,10E)-7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-phenylpropanamide 101316851 Click to see 568.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
(2S)-N-[(3R,4S,7S,10Z)-7-[(2S)-butan-2-yl]-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(methylamino)-3-phenylpropanamide 22297439 Click to see 554.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2S)-N-[(3S,4S,7S,10E)-7-butan-2-yl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(methylamino)-3-phenylpropanamide 101378052 Click to see 554.70 unknown via CMAUP database
(2S)-N-[(3S,4S,7S,10Z)-7-[(2S)-butan-2-yl]-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(methylamino)-3-phenylpropanamide 11628221 Click to see 554.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
(2S)-N-[(7S,10Z)-7-butan-2-yl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-2-(dimethylamino)-3-phenylpropanamide 101938866 Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC(C(C(=O)N1)NC(=O)C(CC3=CC=CC=C3)N(C)C)C4=CC=CC=C4 568.70 unknown https://doi.org/10.1016/S0031-9422(97)00491-3
2-(dimethylamino)-3-hydroxy-N-[7-[hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-phenylpropanamide 163033368 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)C(C3=CC=CC=C3)O)NC(=O)C(C(C4=CC=CC=C4)O)N(C)C 600.70 unknown https://doi.org/10.1016/0031-9422(94)00611-V
2-(dimethylamino)-N-[7-[hydroxy(phenyl)methyl]-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]-3-methylpentanamide 575159 Click to see 550.70 unknown https://doi.org/10.1016/S0031-9422(00)81890-7
N-(7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl)-1-[2-(methylamino)-3-phenylpropanoyl]pyrrolidine-2-carboxamide 3542214 Click to see 651.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
N-(7-benzyl-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl)-2-(dimethylamino)-3-phenylpropanamide 71437222 Click to see CC(C)C1C(C(=O)NC(C(=O)NC=CC2=CC=C(O1)C=C2)CC3=CC=CC=C3)NC(=O)C(CC4=CC=CC=C4)N(C)C 568.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
https://doi.org/10.1016/S0031-9422(00)81890-7
https://doi.org/10.1016/0031-9422(74)80118-4
https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
N-(7-butan-2-yl-5,8-dioxo-3-phenyl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl)-2-(methylamino)-3-phenylpropanamide 313182 Click to see 554.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
Scutianine B 45273177 Click to see 568.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.08.016
https://doi.org/10.1016/S0031-9422(00)81890-7
https://doi.org/10.1016/J.PHYTOCHEM.2011.02.019
Scutianine C 45268911 Click to see 534.70 unknown via CMAUP database
Scutianine D 45267179 Click to see 584.70 unknown via CMAUP database
Scutianine F 5281596 Click to see 651.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester 149044 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown via CMAUP database
Hexacosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 20980932 Click to see 558.90 unknown via CMAUP database
Icosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 149045 Click to see CCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 474.70 unknown via CMAUP database
Tetracosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 54412038 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 530.80 unknown via CMAUP database
Unii-A2T8gne262 54370069 Click to see 502.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin 73202 Click to see 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[3,4-Dihydroxy-5-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-3-yl]oxyoxolan-3-yl]methyl acetate 163049739 Click to see 606.50 unknown https://doi.org/10.1016/0031-9422(94)00611-V
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene 5316874 Click to see 240.30 unknown via CMAUP database
Cis-3,5-Dimethoxystilbene 13556468 Click to see 240.30 unknown via CMAUP database
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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