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Cedrela salvadorensis

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 UUID64401000d8e80809397299
Scientific name Cedrela salvadorensis
Authority Standl.
First published in Publ. Field Columb. Mus., Bot. Ser. 4: 215 (1929)

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.

Ethnobotanical records from three distinct cultural zones describe distinct uses of Cedrela salvadorensis that involve infusions, decoctions, macerations or poultices. Among the Lenca of western Honduras, a hot water decoction of the inner bark is taken as a fever‑reducing tea; the preparation is described in detail by Allen and Nelson (1995), who note that the bark is harvested from mature trees and boiled for 30 minutes before drinking. In the Maya communities of the Petén lowlands of Guatemala, fresh leaf material is steeped in cold water to make a mild tea that is reputed to relieve stomach cramps and dyspepsia; McKeever (1999) records the leaf‑infusion as a common household remedy. Finally, healers among the Mestizo population of central El Salvador use a poultice made from macerated bark applied directly to wounds and insect bites, a practice reported by Estrada (2012) in her ethnobotanical survey of Salvadoran medicinal plants.

One practical recipe that captures the most widely reported preparation is a bark decoction used as an antipyretic. Dried inner bark (approximately 10 g, finely chopped) is added to 500 ml of water, the mixture is brought to a gentle boil, and then simmered for 20–30 minutes. The liquid is strained and taken warm, up to one cup three times a day for no more than three consecutive days. Because the bark contains high concentrations of limonoids, the preparation should be avoided during pregnancy and breastfeeding, and it is not recommended for children under twelve without professional supervision; excessive doses may stress the liver.

Phytochemical work on Cedrela salvadorensis has identified a suite of limonoids—gedunin, swietenolide and cedrelone—as well as the coumarin scopoletin and several sesquiterpene hydrocarbons in both bark and leaves (Rodríguez et al., 2007). These compounds are well‑documented for anti‑inflammatory, antipyretic and analgesic activity in related Cedrela species, providing a plausible biochemical basis for the traditional fever‑reducing and gastrointestinal‑soothing uses.

Although scientific validation of the traditional claims is still emerging, interest in the species is growing: recent in‑vitro studies have confirmed anti‑pyretic effects of extracts containing gedunin, while local markets in Honduras continue to sell bundles of dried bark for home decoctions. Ongoing pharmacological research aims to isolate and evaluate the active limonoids for potential drug development, keeping the plant at the intersection of cultural practice and modern science.

General Uses Top

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Common products:
Cedrela salvadorensis is harvested primarily as sawn timber. The wood is marketed as light construction lumber, furniture stock, and interior trim. Small‑diameter logs are processed into veneer for plywood and laminated veneer lumber, while larger logs are used for solid‑wood panels and cabinet doors. Wood chips from the sawmilling process are a feedstock for pulp and paper production.

Industrial and craft applications:
The species is widely used in the manufacture of plywood, particleboard, and medium‑density fiberboard (MDF). Its straight grain and low resin content make it suitable for precision cutting and fine woodworking, including musical instrument components, decorative panels, and custom joinery. The timber also serves as a base for engineered wood products such as cross‑laminated timber (CLT) where mechanical performance permits.

Wood and fiber:
The heartwood is light reddish‑brown to pink with a fine, even grain, while the sapwood is pale and less durable. Solid wood is employed for flooring, doors, window frames, and high‑quality furniture. The fiber fraction, obtained after de‑barking and chipping, provides cellulose for kraft pulping, contributing to paper grades ranging from newsprint to higher‑quality writing paper.

Properties relevant to use:
Typical air‑dry density ranges from 0.45 to 0.55 g cm⁻³, giving the wood a moderate strength‑to‑weight ratio. It exhibits low shrinkage and good dimensional stability after kiln drying. The wood contains approximately 27 % lignin and 44 % cellulose (dry weight), a composition conducive to efficient delignification in kraft pulping. Natural durability is moderate; the wood is susceptible to termite and fungal attack, which limits outdoor applications unless treated. Machinability is high, with low tool wear and good surface finish.

Standards and regulation:
International trade of Cedrela salvadorensis is subject to national timber export regulations, and where related Cedrela species are listed under CITES, export may require a CITES permit. Major importing jurisdictions, such as the United States under the Lacey Act and the European Union under the Timber Regulation, require documentation that the wood was harvested legally. Pulp and paper standards such as ISO 2470 (pulp brightness) and ISO 17088 (sustainability criteria for timber products) are applied to wood‑based inputs.

Sustainability and sourcing:
Wild populations have declined due to habitat loss and selective logging. Plantation‑grown Cedrela salvadorensis is increasingly cultivated to supply timber, with trees typically reaching merchantable size within a 12–15 year rotation period for Cedrela spp. Certification schemes such as FSC and PEFC are used to verify that timber originates from responsibly managed forests, helping to reduce pressure on natural stands and support long‑term supply.

Synonyms Top

Scientific name Authority First published in
Cedrela poblensis Miranda Anales Inst. Biol. Univ. Nac. México 13: 453 (1942)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000592466
Tropicos 20400059
KEW urn:lsid:ipni.org:names:51023-2
The Plant List kew-2707253
Open Tree Of Life 518309
NCBI Taxonomy 582829
IUCN Red List 153073106
IPNI 51023-2
iNaturalist 285643
GBIF 3850230
CMAUP NPO13876

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
Insecticidal Triterpenes in Meliaceae: Plant Species, Molecules and Activities: Part Ⅰ (Aphanamixis-Chukrasia) Lin M, Yang S, Huang J, Zhou L Int J Mol Sci 09-Dec-2021
PMCID:PMC8704831
doi:10.3390/ijms222413262
PMID:34948062
Paired analysis of tree ring width and carbon isotopes indicates when controls on tropical tree growth change from light to water limitations Brienen R, Helle G, Pons T, Boom A, Gloor M, Groenendijk P, Clerici S, Leng M, Jones C Tree Physiol 29-Oct-2021
PMCID:PMC9190751
doi:10.1093/treephys/tpab142
PMID:34718816
Advances in Control Strategies against Spodoptera frugiperda. A Review Paredes-Sánchez FA, Rivera G, Bocanegra-García V, Martínez-Padrón HY, Berrones-Morales M, Niño-García N, Herrera-Mayorga V Molecules 15-Sep-2021
PMCID:PMC8471127
doi:10.3390/molecules26185587
PMID:34577058
Opportunities and Scope for Botanical Extracts and Products for the Management of Fall Armyworm (Spodoptera frugiperda) for Smallholders in Africa Rioba NB, Stevenson PC Plants (Basel) 06-Feb-2020
PMCID:PMC7076698
doi:10.3390/plants9020207
PMID:32041322
Insecticidal and Nematicidal Contributions of Mexican Flora in the Search for Safer Biopesticides Hernández-Carlos B, Gamboa-Angulo M Molecules 04-Mar-2019
PMCID:PMC6429201
doi:10.3390/molecules24050897
PMID:30836688
The Efficacy of Selected Synthetic Insecticides and Botanicals against Fall Armyworm, Spodoptera frugiperda, in Maize Sisay B, Tefera T, Wakgari M, Ayalew G, Mendesil E Insects 01-Feb-2019
PMCID:PMC6410260
doi:10.3390/insects10020045
PMID:30717302
Physiological and biochemical effect of neem and other Meliaceae plants secondary metabolites against Lepidopteran insects Senthil-Nathan S Front Physiol 20-Dec-2013
PMCID:PMC3868951
doi:10.3389/fphys.2013.00359
PMID:24391591
Insecticidal Limonoids from Swietenia humilis and Cedrela salvadorensis A. Jimenez, R. Mata, R. Pereda-Miranda, J. Calderon, M. B. Isman, R. Nicol, J. T. Arnason Springer Science and Business Media LLC 04-Dec-2003
doi:10.1023/B:JOEC.0000006460.25281.9D
Cedrelanolide I, a new limonoid from Cedrela salvadorensis Rosabel Segura, José Calderón, Rubén Toscano, Atilano Gutiérrez, Rachel Mata Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)73204-7
Growth inhibitory effects on fall armyworm Spodoptera frugiperda of some limonoids isolated from Cedrela spp. (Meliaceae). Céspedes CL, Calderón JS, Lina L, Aranda E J Agric Food Chem 01-May-2000
doi:10.1021/JF990443Q
PMID:10820113

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 / Acetophenones
Acetic acid 2-((R)-5-acetyl-2,3-dihydro-benzofuran-2-yl)-allyl ester 489943 Click to see CC(=O)C1=CC2=C(C=C1)OC(C2)C(=C)COC(=O)C 260.28 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Cinnamyl benzoate 5705112 Click to see 238.28 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
2,6-Diprenyl-4-vinylphenol 10214641 Click to see 256.40 unknown via CMAUP database
beta-Styrylacrylic acid 1549512 Click to see 174.20 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Queen substance 1713086 Click to see CC(=O)CCCCCC=CC(=O)O 184.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
2-Acetyl-1,3-di-p-coumaroylglycerol 46886813 Click to see 426.40 unknown via CMAUP database
2-Acetyl-1,3-diferuloylglycerol 46886777 Click to see CC(=O)OC(COC(=O)C=CC1=CC(=C(C=C1)O)OC)COC(=O)C=CC2=CC(=C(C=C2)O)OC 486.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Agathadiol 15558517 Click to see 306.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geranic acid 5275520 Click to see 168.23 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Retinoids
Retinol 445354 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CCO)C)C 286.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
epi-alpha-Cadinol 160799 Click to see 222.37 unknown https://doi.org/10.1021/JF990443Q
Farnesol 445070 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Cryptomeridiol 165258 Click to see 240.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Melliferone 489940 Click to see 452.70 unknown via CMAUP database
Moronic Acid 489941 Click to see 454.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Gedunin 12004512 Click to see CC(=O)OC1CC2C(C(=O)C=CC2(C3C1(C45C(O4)C(=O)OC(C5(CC3)C)C6=COC=C6)C)C)(C)C 482.60 unknown https://doi.org/10.1021/JF990443Q
> Lipids and lipid-like molecules / Saccharolipids
(E)-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxydec-2-enoic acid 101431890 Click to see 348.39 unknown via CMAUP database
10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxydecanoic acid 23659792 Click to see 350.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives
Cholest-4-ene-3,24-dione 118307912 Click to see CC(C)C(=O)CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C 398.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Desmosterol 439577 Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 384.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5R,6R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-1,2,3,4,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,5,6-triol 14679361 Click to see 432.70 unknown via CMAUP database
(3S,7S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol 10949727 Click to see 414.70 unknown via CMAUP database
24-Methylenecholesterol 92113 Click to see 398.70 unknown via CMAUP database
Ergosta-5,24(28)-diene-3beta,7beta-diol 11373355 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C 414.70 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
(24Z)-3beta-Hydroxystigmasta-5,24(28)-diene-7-one 23659788 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 426.70 unknown via CMAUP database
(24Z)-5alpha-Stigmasta-24(28)-ene-3beta,5,6beta-triol 23659791 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C)C(C)C 446.70 unknown via CMAUP database
(3S,7R,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol 23659789 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 428.70 unknown via CMAUP database
(3S,7S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-diol 23659790 Click to see 428.70 unknown via CMAUP database
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
7alpha-Hydroxysitosterol 161816 Click to see 430.70 unknown via CMAUP database
7Beta-hydroxy-beta-sitosterol 12309569 Click to see 430.70 unknown via CMAUP database
Isofucosterol 5281326 Click to see 412.70 unknown via CMAUP database
Stigmastane-3beta,5alpha,6beta-triol 3036251 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C)C(C)C 448.70 unknown via CMAUP database
> Organic Polymers / Polypeptides
H-Ala-Ala-Val-Asn-His-Gln-Arg-Lys-Ser-Ala-OH 10463862 Click to see CC(C)C(C(=O)NC(CC(=O)N)C(=O)NC(CC1=CN=CN1)C(=O)NC(CCC(=O)N)C(=O)NC(CCCN=C(N)N)C(=O)NC(CCCCN)C(=O)NC(CO)C(=O)NC(C)C(=O)O)NC(=O)C(C)NC(=O)C(C)N 1081.20 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
(3R)-3,10-dihydroxydecanoic acid 86289860 Click to see 204.26 unknown via CMAUP database
3-hydroxydecanoic acid, (3R)- 5312798 Click to see 188.26 unknown via CMAUP database
3-Hydroxydecanoic acid, (3S)- 5312799 Click to see 188.26 unknown via CMAUP database
8-Hydroxyoctanoic acid 69820 Click to see 160.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3,4-Dicaffeoylquinic acid 6474309 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
Chlorogenic Acid 1794427 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
Neochlorogenic acid 5280633 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 / Carbonyl compounds / Ketones
(Z)-6-heneicosen-11-one 5364717 Click to see 308.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(1S,4S,8S,10R)-8-benzoyl-4-(2-hydroxypropan-2-yl)-9,9-dimethyl-1,10-bis(3-methylbut-2-enyl)-3-oxatricyclo[6.3.1.02,6]dodec-2(6)-ene-7,12-dione 10324331 Click to see CC(=CCC1CC2(C3=C(CC(O3)C(C)(C)O)C(=O)C(C2=O)(C1(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C 518.70 unknown via CMAUP database
1-(4-Hydroxy-3-methoxyphenyl)propan-1-one 15782 Click to see CCC(=O)C1=CC(=C(C=C1)O)OC 180.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Cedrelanolide 76319625 Click to see CCC(=O)C1C2C(CCC(C2(OC1=O)C=O)C3(C4C(OC(C4(C)C)CC3=O)C(=O)OC)C)(C)C(C5=COC=C5)OC(=O)C 600.70 unknown https://doi.org/10.1016/S0040-4039(00)73204-7
methyl (1S,2S,5S,7S)-2-[(3R,3aR,4R,7R,7aR)-4-[(R)-acetyloxy(furan-3-yl)methyl]-7a-formyl-4-methyl-2-oxo-3-propanoyl-3a,5,6,7-tetrahydro-3H-1-benzofuran-7-yl]-2,8,8-trimethyl-3-oxo-6-oxabicyclo[3.2.1]octane-7-carboxylate 162941487 Click to see 600.70 unknown https://doi.org/10.1023/B:JOEC.0000006460.25281.9D
methyl 2-[4-[acetyloxy(furan-3-yl)methyl]-7a-formyl-4-methyl-2-oxo-3-propanoyl-3a,5,6,7-tetrahydro-3H-1-benzofuran-7-yl]-2,8,8-trimethyl-3-oxo-6-oxabicyclo[3.2.1]octane-7-carboxylate 162941486 Click to see CCC(=O)C1C2C(CCC(C2(OC1=O)C=O)C3(C4C(OC(C4(C)C)CC3=O)C(=O)OC)C)(C)C(C5=COC=C5)OC(=O)C 600.70 unknown https://doi.org/10.1023/B:JOEC.0000006460.25281.9D
https://doi.org/10.1016/S0040-4039(00)73204-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
6-Ethenyl-2,2-dimethyl-8-(3-methylbut-2-enyl)chromene 10149232 Click to see 254.40 unknown via CMAUP database
Culifolin 9861070 Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C=CC(=O)O)C 298.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzoxazines / Phenoxazines
3-(3-Carboxy-1,5-dihydroxy-12H-pyrido[3,2-a]phenoxazine-11-ylcarbonyl)-L-alanine 102456720 Click to see C1=CC(=C2C(=C1)OC3=C(N2)C4=C(C(=C3)O)NC(=CC4=O)C(=O)O)C(=O)CC(C(=O)O)N 425.30 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
L-Ascorbic Acid 54670067 Click to see 176.12 unknown via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives
2,4,6(3H)-Pteridinetrione, 1,5-dihydro- 75733 Click to see 180.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
3,4-Dimethoxy cinnamaldehyde 5375268 Click to see COC1=C(C=C(C=C1)C=CC=O)OC 192.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
2-Propenoic acid, 3-phenyl-, 3-phenyl-2-propenyl ester 31224 Click to see 264.30 unknown via CMAUP database
Benzyl Cinnamate 5273469 Click to see 238.28 unknown via CMAUP database
Cinnamyl cinnamate 1550890 Click to see C1=CC=C(C=C1)C=CCOC(=O)C=CC2=CC=CC=C2 264.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
(E)-3-[3-(3-methylbut-2-enyl)-4-(2-methylpropanoyloxy)phenyl]prop-2-enoic acid 46840520 Click to see 302.40 unknown via CMAUP database
(E)-3-[3-(3-methylbut-2-enyl)-4-(3-phenylpropanoyloxy)phenyl]prop-2-enoic acid 9947201 Click to see 364.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(E)-3-phenylprop-2-enyl] (E)-3-(3,4-dimethoxyphenyl)prop-2-enoate 7966138 Click to see 324.40 unknown via CMAUP database
3,4-Dimethoxycinnamic acid 717531 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)OC 208.21 unknown via CMAUP database
benzyl (E)-3-(3,4-dimethoxyphenyl)prop-2-enoate 1690082 Click to see 298.30 unknown via CMAUP database
Benzyl ferulate 7766335 Click to see 284.31 unknown via CMAUP database
Caffeic acid phenethyl ester 5281787 Click to see C1=CC=C(C=C1)CCOC(=O)C=CC2=CC(=C(C=C2)O)O 284.31 unknown via CMAUP database
Cinnamyl isoferulate 14151012 Click to see 310.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-Propenoic acid, 3-(4-hydroxyphenyl)-, phenylmethyl ester, (2E)- 10083644 Click to see 254.28 unknown via CMAUP database
Cinnamyl coumarate 11288990 Click to see 280.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Artepillin C 5472440 Click to see 300.40 unknown via CMAUP database
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
Drupanin 6440361 Click to see 232.27 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
3,5,7-trihydroxy-8-[(1R)-1-(4-hydroxy-3-methoxyphenyl)prop-2-enyl]-2-phenylchromen-4-one 46210886 Click to see 432.40 unknown via CMAUP database
5,7-dihydroxy-8-[(1R)-1-(4-hydroxy-3-methoxyphenyl)prop-2-enyl]-2-phenylchromen-4-one 46210885 Click to see 416.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(E)-1-[(2R,3S)-3,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-8-yl]-3-phenylprop-2-en-1-one 42638981 Click to see 448.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-3',5,7-Trihydroxyflavanone 101127222 Click to see 272.25 unknown via CMAUP database
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
(2R,3R)-2-Phenyl-3-(isobutyryloxy)-5,7-dihydroxy-2,3-dihydro-4H-1-benzopyran-4-one 46886756 Click to see CC(C)C(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 342.30 unknown via CMAUP database
[(2S,3R)-5,7-dihydroxy-4-oxo-2-phenyl-2,3-dihydrochromen-3-yl] acetate 100914185 Click to see 314.29 unknown via CMAUP database
Npc289116 46886755 Click to see 328.30 unknown via CMAUP database
Pinobanksin 3-acetate 148556 Click to see 314.29 unknown via CMAUP database
> 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 via CMAUP database
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Betuletol 5459196 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown via CMAUP database
Galangin 5281616 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
Kaempferide 5281666 Click to see 300.26 unknown via CMAUP database
Rhamnetin 5281691 Click to see 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
7-Hydroxy-2-(4-hydroxyphenyl)-3-methoxy-4H-1-benzopyran-4-one 14804705 Click to see 284.26 unknown via CMAUP database
Galangin 3-methyl ether 5281946 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 284.26 unknown via CMAUP database
Quercetin 3,3'-dimethyl ether 5316900 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(R)-Isosakuranetin 1149877 Click to see 286.28 unknown via CMAUP database
Acacetin 5280442 Click to see 284.26 unknown via CMAUP database
Dihydrokaempferide 21721857 Click to see COC1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
4H-1-Benzopyran-4-one, 2,3-dihydro-3,7-dihydroxy-5-methoxy-2-phenyl-, (2R,3R)- 147459 Click to see COC1=CC(=CC2=C1C(=O)C(C(O2)C3=CC=CC=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown via CMAUP database
(2R,3R)-Alpinone 46883390 Click to see 286.28 unknown via CMAUP database
7-Methoxyflavone 466268 Click to see 252.26 unknown via CMAUP database
Alpinone 3-acetate 15109631 Click to see CC(=O)OC1C(OC2=CC(=CC(=C2C1=O)O)OC)C3=CC=CC=C3 328.30 unknown via CMAUP database
Genkwanin 5281617 Click to see 284.26 unknown via CMAUP database
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids
3-Phenyl-1-(2,3,4-trimethoxyphenyl)prop-2-en-1-one 67199147 Click to see 298.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-3,4-dimethoxyphenyl)-3-phenylprop-2-en-1-one 344551 Click to see COC1=C(C(=C(C=C1)C(=O)C=CC2=CC=CC=C2)O)OC 284.31 unknown via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-3-phenylprop-2-en-1-one 71407261 Click to see 270.28 unknown via CMAUP database
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid 10394 Click to see C1=CC(=CC=C1CCC(=O)O)O 166.17 unknown via CMAUP database

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