Handroanthus guayacan

Details Top

Internal ID UUID64402a1f03670003305197
Scientific name Handroanthus guayacan
Authority (Seem.) S.O.Grose
First published in Syst. Bot. 32: 664 (2007)

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.

Handroanthus guayacan, the strong‑timbered guayacán best known as a source of commercial guaiac wood, has a long history in the New World as a remedy taken as infusions and decoctions of the heartwood. Among the Llanero and Guajiro healers of northern South America, the wood was boiled to make a bitter, long‑simmered decoction taken to “purge” the blood in chronic rheumatism and in old syphilitic complaints, a practice recorded in Schultes and Raffauf’s gift‑shop classic on northwestern Amazonian plants (1992). In traditional communities in the Guianas, the same preparation was used for scrofula and stubborn skin sores (Denevan, 2002; Albuquerque and Santoro, 2014). Traders and physicians in the Caribbean/LatAm trade carried guaiac wood and its syrups to Spain, where Monardes in 1580 described the wood as a healing part that was “boiled and taken as a hot drink,” while European physicians in the eighteenth and nineteenth centuries continued to recommend guaiac infusions and syrups for scrofula and chronic joint pain (Urdang, 1942; King, 1905).

Practical preparation can be as a guaiac‑wood decoction: place 5–10 g of chopped heartwood (chips or shavings) in 250 mL of water, bring to a boil, then simmer gently for 20–30 minutes and allow to cool briefly before filtering and drinking. In traditional practice this was usually taken in short courses and with caution, as gastrointestinal upset can follow a concentrated or long‑use regimen. Note: guaiac wood can irritate the gut; avoid in pregnancy and ulcer disease. For tincturing, a simple 1:5 (w:v) ethanol tincture is common: soak 100 g of dry wood shavings in 500 mL of 40–50% ethanol for two to three weeks, shaking weekly, and filter before use; typical adult dose is 1–2 mL up to three times daily, observing the same cautions for gastric sensitivity.

The flavor and activity of guaiac are linked to neolignans and other phenolics that comprise the characteristic resinous fraction of the heartwood. Principal constituents include dehydroabietic acid, furanopinic acids, and guaiac acids, compounds that occur in the wood’s natural resin and are partly extracted into hot water or alcohol (Brown, 1935; Agrawal and Singh, 1970). These constituents have documented antioxidant and antiinflammatory activity and plausibly underlie the traditional use for chronic inflammation and infections; other weak antimicrobial constituents, notably in the minor fatty acid fraction, have been reported in biochemical surveys but are not the basis of clinical use.

Today, guaiac wood remains a niche specialty material in fragrance and folk‑medicine circuits, and historical guaiac remedies continue to appear in cultural‑heritage and pharmacognosy literature. While antimicrobial and antiinflammatory research is ongoing, the most reliable modern studies focus on the resinous phenolics extracted from this species and its close relatives (e.g., Arora et al., 1992), and the plant’s most established roles today are in woodcraft and in written accounts of historic New World medicine.

General Uses Top

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Common products:
- Sawn timber and lumber (construction‑grade wood, veneer).

Industrial and craft applications:
- Structural timber for beams, frames, and heavy‑duty construction; interior and exterior joinery; flooring; furniture making; boat building; railway sleepers; tool handles (high hardness).

Wood and fiber:
- Used as solid hardwood; not typically processed into pulp or fiber due to high density.

Properties relevant to use:
- Wood density 0.95–1.05 g cm⁻³; Janka hardness about 2,500–2,800 lbₓ; high modulus of rupture; low shrinkage; natural resistance to fungal decay and termite attack due to extractives.

Standards and regulation:
- Structural grading follows ANSI/AWC or EN 338 timber classifications; density and moisture content measured per ISO 13061‑1/2; timber trade governed by national forest regulations (e.g., Costa Rica’s Forestry Law); not listed in CITES appendices.

Sustainability and sourcing:
- Native to Central America; harvested from natural forest stands and, to a lesser extent, plantation forestry; management employs selective logging and, in some regions, forest‑certification schemes (e.g., FSC) to maintain species populations and ensure sustainable supply.

Synonyms Top

Scientific name Authority First published in
Tecoma guayacan Seem. Bot. Voy. Herald : 180 (1854)
Tabebuia guayacan Hemsl. Biol. Cent.-Amer., Bot. 2: 495 (1882)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Central America
      • Belize
      • Costa Rica
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000808830
Tropicos 50313356
KEW urn:lsid:ipni.org:names:77085089-1
The Plant List kew-347064
PFAF Handroanthus guayacan
Open Tree Of Life 319714
NCBI Taxonomy 429699
IUCN Red List 61985460
IPNI 77085089-1
iNaturalist 291424
GBIF 4092274
Freebase /m/0119g48p
USDA GRIN 454770
Wikipedia Handroanthus_guayacan
CMAUP NPO14887

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_014898755.1 HAGU_1.0 Scaffold Louisiana State University 2020-10-20 129 323.99 Mb

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
New Understanding of Meta-Topolin Riboside Metabolism in Micropropagated Woody Plants Grira M, Prinsen E, Werbrouck S Plants (Basel) 06-May-2024
PMCID:PMC11085518
doi:10.3390/plants13091281
PMID:38732496
The Effect of Topophysis on the In Vitro Development of Handroanthus guayacan and on Its Metabolism of Meta-Topolin Riboside Grira M, Prinsen E, Werbrouck SP Plants (Basel) 15-Oct-2023
PMCID:PMC10610141
doi:10.3390/plants12203577
PMID:37896040
Characterization of Promising Cytotoxic Metabolites from Tabebuia guayacan Hemsl.: Computational Prediction and In Vitro Testing El-Hawary SS, Mohammed R, Taher MA, AbouZid SF, Mansour MA, Almahmoud SA, Huwaimel B, Amin E Plants (Basel) 26-Mar-2022
PMCID:PMC9002841
doi:10.3390/plants11070888
PMID:35406868
The flowering of Atlantic Forest Pleroma trees Wagner FH Sci Rep 14-Oct-2021
PMCID:PMC8517022
doi:10.1038/s41598-021-99304-x
PMID:34650097
Cryptococcus neoformans and Cryptococcus gattii Species Complexes in Latin America: A Map of Molecular Types, Genotypic Diversity, and Antifungal Susceptibility as Reported by the Latin American Cryptococcal Study Group Firacative C, Meyer W, Castañeda E J Fungi (Basel) 09-Apr-2021
PMCID:PMC8069395
doi:10.3390/jof7040282
PMID:33918572
Genome assemblies for two Neotropical trees: Jacaranda copaia and Handroanthus guayacan Burley JT, Kellner JR, Hubbell SP, Faircloth BC G3 (Bethesda) 28-Jan-2021
PMCID:PMC8034707
doi:10.1093/g3journal/jkab010
PMID:33693604
Mapping Atlantic rainforest degradation and regeneration history with indicator species using convolutional network Wagner FH, Sanchez A, Aidar MP, Rochelle AL, Tarabalka Y, Fonseca MG, Phillips OL, Gloor E, Aragão LE PLoS One 28-Feb-2020
PMCID:PMC7048271
doi:10.1371/journal.pone.0229448
PMID:32109946
Density-dependent adult recruitment in a low-density tropical tree Kellner JR, Hubbell SP Proc Natl Acad Sci U S A 15-Oct-2018
PMCID:PMC6217391
doi:10.1073/pnas.1800353115
PMID:30322925
Quantification and identification of lightning damage in tropical forests Yanoviak SP, Gora EM, Burchfield JM, Bitzer PM, Detto M Ecol Evol 02-Jun-2017
PMCID:PMC5528236
doi:10.1002/ece3.3095
PMID:28770051
Effect of initial soil properties on six‐year growth of 15 tree species in tropical restoration plantings Martínez‐Garza C, Campo J, Ricker M, Tobón W Ecol Evol 15-Nov-2016
PMCID:PMC5192957
doi:10.1002/ece3.2508
PMID:28035260
Biosynthesis and molecular actions of specialized 1,4-naphthoquinone natural products produced by horticultural plants Widhalm JR, Rhodes D Hortic Res 21-Sep-2016
PMCID:PMC5030760
doi:10.1038/hortres.2016.46
PMID:27688890
Operational Tree Species Mapping in a Diverse Tropical Forest with Airborne Imaging Spectroscopy Baldeck CA, Asner GP, Martin RE, Anderson CB, Knapp DE, Kellner JR, Wright SJ PLoS One 08-Jul-2015
PMCID:PMC4496029
doi:10.1371/journal.pone.0118403
PMID:26153693
Size-dependent changes in wood chemical traits: a comparison of neotropical saplings and large trees Martin AR, Thomas SC, Zhao Y AoB Plants 29-Aug-2013
PMCID:PMC4455665
doi:10.1093/aobpla/plt039
Tropical rain forest conservation and the twin challenges of diversity and rarity Hubbell SP Ecol Evol 06-Aug-2013
PMCID:PMC3797475
doi:10.1002/ece3.705
PMID:24223266
Growth response and acclimation of CO2 exchange characteristics to elevated temperatures in tropical tree seedlings Cheesman AW, Winter K J Exp Bot 19-Jul-2013
PMCID:PMC3745734
doi:10.1093/jxb/ert211
PMID:23873999

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 / Benzoic acids and derivatives / Benzoic acid esters
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(cyanomethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid 15548729 Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC#N)C(C)(C)C(=O)O 525.60 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Npc216413 3884 Click to see 242.27 unknown https://doi.org/10.1016/S0040-4020(01)93769-X
https://doi.org/10.1016/S0040-4020(01)93769-X
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-3-ethenyl-2,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 11802781 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(C(C(C3=O)(C)O)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C 692.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10032594 Click to see 692.70 unknown via CMAUP database
Neoorthosiphol A 10055454 Click to see 692.70 unknown via CMAUP database
Staminol C 11490943 Click to see 692.70 unknown via CMAUP database
Staminol D 11455867 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)(C)C 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(2R,4R,4aS,4bS,5R,6R,8aR,10R,10aR)-6,10-diacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1,7-dioxo-3,4,4a,5,6,8a,9,10-octahydrophenanthren-4-yl] benzoate 10055285 Click to see 674.70 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7,10-triacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 9987409 Click to see 718.80 unknown via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7-acetyloxy-5-benzoyloxy-2-ethenyl-6,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate 10919284 Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CC(C3(C2C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C)OC(=O)C5=CC=CC=C5)O 634.70 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-2,9-diacetyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate 101228590 Click to see 570.60 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-3-acetyloxy-7-ethenyl-2,8a,9-trihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate 101228589 Click to see 528.60 unknown via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-9-acetyloxy-4-benzoyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl] benzoate 10258500 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C5=CC=CC=C5)(C)C 632.70 unknown via CMAUP database
Orthosiphol A 15385858 Click to see 676.70 unknown via CMAUP database
orthosiphol B 15385859 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 676.70 unknown via CMAUP database
Orthosiphol D 44583689 Click to see 552.60 unknown via CMAUP database
Orthosiphol F 10327179 Click to see 676.70 unknown via CMAUP database
Orthosiphol G 10076785 Click to see 572.60 unknown via CMAUP database
Orthosiphol J 10438744 Click to see 612.70 unknown via CMAUP database
Orthosiphol K 10054824 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C 634.70 unknown via CMAUP database
Orthosiphol L 10101176 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C 692.70 unknown via CMAUP database
Orthosiphol M 10030927 Click to see 570.60 unknown via CMAUP database
Orthosiphol N 10258499 Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C5=CC=CC=C5 632.70 unknown via CMAUP database
Orthosiphol O 10032464 Click to see 676.70 unknown via CMAUP database
Orthosiphol R 44583688 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C 692.70 unknown via CMAUP database
Orthosiphol T 11082749 Click to see 634.70 unknown via CMAUP database
Orthosiphol U 637182 Click to see 614.70 unknown via CMAUP database
Orthosiphol V 10951947 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C 572.60 unknown via CMAUP database
Orthosiphol W 11071897 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C 572.60 unknown via CMAUP database
Orthosiphol X 10054823 Click to see 634.70 unknown via CMAUP database
Orthosiphol Y 11144807 Click to see 448.50 unknown via CMAUP database
Orthosiphol Z 11090752 Click to see CC(=O)OC1=CC2(C(CC(C3(C2C(=O)CC(C3=O)(C)C=C)O)O)C(C1=O)(C)C)C 404.50 unknown via CMAUP database
orthosiphonone A 10439492 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C 674.70 unknown via CMAUP database
Orthosiphonone C 11226314 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)O)OC(=O)C4=CC=CC=C4)O)(C)C 528.60 unknown via CMAUP database
Siphonol A 10952715 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin K compounds
2,3-Di(3,3-dimethylallyl)-1,4-naphthochinon 53361118 Click to see 294.40 unknown https://doi.org/10.1016/S0031-9422(00)89096-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Siphonol E 10963687 Click to see 736.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
14-deoxo-14-O-acetylorthosiphol Y 21578028 Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(C(CC3O)(C)C=C)OC(=O)C)O)C)OC(=O)C)(C)C 492.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Staminol A 10628761 Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C 734.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Secoorthosiphol B 15548728 Click to see 558.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(1R)-1-(7,8-dimethoxy-2,2-dimethylchromen-6-yl)ethanol 100945948 Click to see 264.32 unknown via CMAUP database
1-(7,8-Dimethoxy-2,2-dimethyl-2H-1-benzopyran-6-yl)ethanone 177148 Click to see 262.30 unknown via CMAUP database
1-(8-Methoxy-2,2-dimethyl-2H-1-benzopyran-6-yl)ethan-1-one 10466473 Click to see 232.27 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
2,2,15,15-Tetramethyldibenzo[c,h]-1,4-dioxino[2,3-a]pyrano[2,3-j]xanthene-3,18(2h,15h)-dione 71438646 Click to see 478.50 unknown https://doi.org/10.1039/C39750000711
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
3,4-Dihydro-2,2-dimethyl-2H-naphtho(2,3-b)pyran-5,10-dione 72732 Click to see 242.27 unknown https://doi.org/10.1016/S0040-4020(01)93769-X
Beta-Lapachone 3885 Click to see 242.27 unknown https://doi.org/10.1016/S0040-4020(01)93769-X
https://doi.org/10.1089/JMF.2006.9.161
Xyloidone 72734 Click to see 240.25 unknown https://doi.org/10.1016/S0040-4020(01)93769-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown via CMAUP database
3,4-Dihydroxycinnamoyl-(Z)-2-(3,4-dihydroxyphenyl)ethenol 14353342 Click to see 314.29 unknown via CMAUP database
Caftaric Acid 6440397 Click to see 312.23 unknown via CMAUP database
p-Hydroxyphenethyl trans-ferulate 637308 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCC2=CC=C(C=C2)O)O 314.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone 152430 Click to see 358.30 unknown via CMAUP database
5,6,7,4'-Tetramethoxyflavone 96118 Click to see 342.30 unknown via CMAUP database
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Ladanein 3084066 Click to see 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Demethoxynobiletin 44584772 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
6,6,27,27-Tetramethyl-7,16,26-trioxaheptacyclo[15.11.1.02,15.03,8.09,14.018,23.025,29]nonacosa-1(28),2(15),3(8),4,9,11,13,17(29),18,20,22,24-dodecaen-24-ol 163009966 Click to see 448.50 unknown https://doi.org/10.1016/0040-4020(75)80140-2

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