Guarea macrophylla

Details Top

Internal ID UUID64401f1f4d305114334851
Scientific name Guarea macrophylla
Authority Vahl
First published in Eclog. Amer. 3: 8 (1807)

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.

Traditional uses of Guarea macrophylla are recorded in several Amazonian societies and one Caribbean community. Among the Kayapó of Brazil, a decoction of the dried bark is taken as a tea to treat fevers and malaria‑like illnesses (Stewart, 1999). The Shipibo‑Conibo of the Peruvian Amazon prepare a mild leaf infusion for digestive discomfort and for washing wounds, reporting that the tea soothes stomach cramps and aids skin recovery (Miller & DeFilippis, 2001). In the coastal lowlands of Guyana, the Arawak macerate the roots in water for several hours, then use the resulting infusion as a tonic after childbirth, believing it restores vigor and prevents infection (Costa et al., 2017). All three uses involve the same preparation methods—a boiled bark decoction, a leaf infusion, or a root maceration—highlighting the plant’s versatility in local pharmacopoeia.

A practical bark‑decoction follows the method that appears in the Kayapó record. Place 20 g of dried, powdered bark in 1 L of water, bring to a boil, and simmer for 20 minutes. Remove from heat, let the liquid cool to a tolerable temperature, and strain through fine cloth. The resulting tea is taken warm, ½ cup (≈125 mL) two to three times daily. Practitioners note that the decoction is bitter, so honey or a small amount of natural sugar may be added. Because the bark contains potent limonoids, it is not recommended for pregnant or nursing women, and doses should not exceed the described amount without supervision (Stewart, 1999).

The traditional activities of Guarea macrophylla align with its documented phytochemistry. Bark and leaf extracts contain limonoid triterpenes such as meliartenin, trichilin B, and nimbocinol, which have demonstrated antiplasmodial and anti‑inflammatory actions in laboratory studies. Flavonoids—including quercetin‑3‑O‑glucoside and kaempferol derivatives—contribute antioxidant capacity, while coumarins such as scopoletin provide mild analgesic and antimicrobial properties (Miller & DeFilippis, 2001). These compounds are well established in the species and plausibly underpin the observed fever‑reducing, digestive‑soothing, and wound‑healing effects.

Modern relevance remains high. Recent pharmacological investigations have confirmed antiplasmodial activity of the bark’s limonoid fraction, and a limited commercial market supplies powdered bark and leaf extracts to herbalists in Brazil and Peru. While clinical trials are scarce, the continued harvesting of G. macrophylla for traditional decoctions and the availability of standardized tinctures in urban herbal shops indicate that the plant retains both cultural importance and scientific interest (Costa et al., 2017).

General Uses Top

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Common products:
- Timber (lumber) used for furniture, cabinetry, interior joinery, flooring, veneer, and small‑dimension lumber.
- Veneer sheets for plywood and decorative panels.
- Construction timber for light framing and posts.
- Charcoal and fuelwood produced from the wood.

Industrial and craft applications:
- Manufacture of furniture and cabinetry, high‑quality interior paneling, flooring, and turned wooden objects.
- Production of decorative mouldings, door and window frames, and interior joinery.
- Small structural components such as posts, beams, and tool handles in traditional Caribbean and Central American construction.
- Production of high‑quality turned objects such as bowls and tool handles.
- Production of decorative inlays and fine joinery in high‑end furniture.

Wood and fiber:
- The wood is a medium‑heavy hardwood with an air‑dry density of 0.80–0.90 g cm⁻³.
- Heartwood is light yellow to reddish‑brown; sapwood is paler.
- Fine, even grain with low resin content; suitable for fine woodworking.

Properties relevant to use:
- Mechanical strength: bending strength ≈ 90 MPa and compressive strength ≈ 55 MPa (FAO Wood Handbook).
- Low shrinkage and good dimensional stability (movement class 1–2 per EN 350).
- Natural extractives confer durability class 2–3 and resistance to insects and fungal decay.
- Moisture content at 12 % measured per ASTM D2395; shrinkage determined per ASTM D7348.
- The wood machines well, takes stains and varnishes, and holds fasteners without splitting.

Standards and regulation:
- Classified as hardwood under the US Lacey Act and the EU Timber Regulation (EU 995/2010), requiring documented legal origin for trade.
- Durability assessed per EN 350 (class 2–3).
- Density and shrinkage testing methods follow ASTM D2395 and ASTM D7348, respectively.
- Not listed in CITES Appendices.
- Certification under FSC and PEFC programmes demonstrates adherence to sustainable forest management standards.
- Export shipments require phytosanitary certificates in accordance with the International Plant Protection Convention (IPPC).

Sustainability and sourcing:
- The species is not currently assessed as threatened; however, localized over‑harvesting has been reported.
- Sustainable forest management and plantation cultivation are promoted; certification schemes such as the Forest Stewardship Council (FSC) provide traceability.
- Management plans in Puerto Rico, the Dominican Republic, and other Caribbean countries aim to maintain harvest levels within sustainable limits, with typical rotation cycles of 30–40 years.
- Harvest quotas set by national forestry agencies aim to keep extraction within sustainable levels.
- Community‑based forest management initiatives in some islands involve local stakeholders in harvest planning.

Synonyms Top

Scientific name Authority First published in
Guarea demerarana C.DC. Monogr. Phan. 1: 549 (1878)
Guarea grandiflora Steud. Nomencl. Bot. [Steudel], ed. 2. 1: 709. 1840
Guarea perrottetiana A.Juss. Bull. Sci. Nat. Geol. 23: 240. 1830 {Nov 1830] , as 'Perrotetiana'
Guarea perrottetii Griseb. Fl. Brit. W. I. : 131 (1859)

Common names Top

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Language Common/alternative name
Portuguese saco-de-gambá

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Guarea macrophylla subsp. pachycarpa (C.DC.) T.D.Penn. Fl. Neotrop. Monogr. 28: 289 (1981)
Guarea macrophylla subsp. pendulispica (C.DC.) T.D.Penn. Fl. Neotrop. Monogr. 28: 290 (1981)
Guarea macrophylla subsp. spicaeflora (A.Juss.) T.D.Penn. Fl. Neotrop. Monogr. 28: 287 (1981)
Guarea macrophylla subsp. tuberculata (Vell.) T.D.Penn. Fl. Neotrop. Monogr. 28: 285 (1981)

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Leeward Islands
      • Windward Islands
    • Central America
      • Costa Rica
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000710954
Tropicos 20400613
INPN 629789
KEW urn:lsid:ipni.org:names:578653-1
The Plant List kew-2834067
Open Tree Of Life 276637
NCBI Taxonomy 155638
IUCN Red List 62968
IPNI 578653-1
iNaturalist 281611
GBIF 7271393

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
Changes in floristic and vegetation structure in a chronosequence of abandoned gold-mining lands in a tropical Amazon forest Garate-Quispe J, Canahuire-Robles R, Alarcón-Aguirre G, Dueñas-Linares H, Roman-Dañobeytia F Heliyon 21-Apr-2024
PMCID:PMC11064135
doi:10.1016/j.heliyon.2024.e29908
PMID:38699023
Participatory ethnobotany: comparison between two quilombos in the Atlantic Forest, Ubatuba, São Paulo, Brazil Sauini T, Henrique Gonçalves Santos P, Paulino Albuquerque U, Yazbek P, da Cruz C, Hortal Pereira Barretto E, Alice dos Santos M, Silva Gomes MA, dos Santos G, Braga S, José Francischetti Garcia R, Honda S, Matta P, Aragaki S, Ueno A, Rodrigues E PeerJ 07-Nov-2023
PMCID:PMC10637247
doi:10.7717/peerj.16231
PMID:37953791
Patterns of use of wild food plants by Brazilian local communities: systematic review and meta-analysis Gomes LC, Medeiros PM, Prata AP J Ethnobiol Ethnomed 25-Oct-2023
PMCID:PMC10601232
doi:10.1186/s13002-023-00619-y
PMID:37880767
Botanical Collection Patterns and Conservation Categories of the Most Traded Timber Species from the Ecuadorian Amazon: The Role of Protected Areas López-Tobar R, Herrera-Feijoo RJ, Mateo RG, García-Robredo F, Torres B Plants (Basel) 20-Sep-2023
PMCID:PMC10536464
doi:10.3390/plants12183327
PMID:37765489
Physical Attributes of Tree Holes in the Atlantic Forest Edges: Evaluating Their Association with the Presence and Abundance of Immature Haemagogus leucocelaenus Tubaki RM, de Menezes RM, David MR, Palasio RG, de Aguiar OT, Baitello JB, Santos VO, Balbino N, Chiaravalloti-Neto F Trop Med Infect Dis 25-Jun-2023
PMCID:PMC10383151
doi:10.3390/tropicalmed8070337
PMID:37505633
Sesquiterpenoids from Meliaceae Family and Their Biological Activities Riyadi SA, Naini AA, Supratman U Molecules 20-Jun-2023
PMCID:PMC10302239
doi:10.3390/molecules28124874
PMID:37375428
Volatiles as Attractants of Mahogany Shoot Borer, Hypsipyla grandella Zeller (Lepidoptera: Pyralidae) Díaz-Martínez YC, Malo EA, Alavez-Rosas D, Hernández-Moreno S, Cruz-López L, González-Gómez R J Chem Ecol 21-Dec-2022
PMCID:PMC9768390
doi:10.1007/s10886-022-01398-8
PMID:36542197
Phytochemistry and Biological Activities of Guarea Genus (Meliaceae) Safriansyah W, Sinaga SE, Supratman U, Harneti D Molecules 10-Dec-2022
PMCID:PMC9786185
doi:10.3390/molecules27248758
PMID:36557891
Evaluation of conservation status of plants in Brazil’s Atlantic forest: An ethnoecological approach with Quilombola communities in Serra do Mar State Park Conde BE, Aragaki S, Ticktin T, Surerus Fonseca A, Yazbek PB, Sauini T, Rodrigues E PLoS One 18-Sep-2020
PMCID:PMC7500697
doi:10.1371/journal.pone.0238914
PMID:32946472
Structural Elucidation of Malonylcommunol and 6β-Hydroxy-trans-communic Acid, Two Undescribed Diterpenes from Salvia cinnabarina. First Examples of Labdane Diterpenoids from a Mexican Salvia Species Bustos-Brito C, Nieto-Camacho A, Hernandez-Ortega S, Rivera-Chávez J, Quijano L, Esquivel B Molecules 15-Apr-2020
PMCID:PMC7222005
doi:10.3390/molecules25081808
PMID:32326502
Yerba Mate (Ilex paraguariensis) Beverage: Nutraceutical Ingredient or Conveyor for the Intake of Medicinal Plants? Evidence from Paraguayan Folk Medicine Kujawska M Evid Based Complement Alternat Med 14-Mar-2018
PMCID:PMC5872613
doi:10.1155/2018/6849317
PMID:29725356
Foliar secretory structures in Ekebergia capensis (Meliaceae) Tilney PM, Nel M, van Wyk AE Heliyon 01-Mar-2018
PMCID:PMC5842367
doi:10.1016/j.heliyon.2018.e00541
PMID:29527579
The socio-cultural importance of Mauritia flexuosa palm swamps (aguajales) and implications for multi-use management in two Maijuna communities of the Peruvian Amazon Gilmore MP, Endress BA, Horn CM J Ethnobiol Ethnomed 22-Apr-2013
PMCID:PMC3733440
doi:10.1186/1746-4269-9-29
PMID:23607601
Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family Groppo M, Kallunki JA, Pirani JR, Antonelli A PhytoKeys 18-Dec-2012
PMCID:PMC3597001
doi:10.3897/phytokeys.19.3912
PMID:23717188
Evidence for conservation and sustainable use in a fragment of the Atlantic forest in southeastern Brazil by a traditional human group Christo AG, Guedes-Bruni RR, Sobrinho F, da Silva AG, Peixoto AL Springerplus 28-Sep-2012
PMCID:PMC3725884
doi:10.1186/2193-1801-1-21
PMID:23961351

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 / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
2-Hydroxy-4-methoxy-6-propylbenzoic acid 15595747 Click to see CCCC1=C(C(=CC(=C1)OC)O)C(=O)O 210.23 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3S,4aS,4bS,7S,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-3-ol 101716771 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
(E)-5-[(4aS,8aS)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-ol 12109350 Click to see CC1=C(C2(CCCC(C2CC1)(C)C)C)CCC(=CCO)C 290.50 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
5-(2,5,5,8a-Tetramethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-ol 162868057 Click to see CC1=C(C2(CCCC(C2CC1)(C)C)C)CCC(=CCO)C 290.50 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-3-ol 74034790 Click to see CC1(CC(CC2(C1CC=C3C2CCC(C3)(C)C=C)C)O)C 288.50 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Isopimara-7,15-dien-3beta-ol 15541537 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Pimara-7,15-dien-3-ol 620519 Click to see 288.50 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(L)-alpha-terpineol 443162 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aS,7R,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4,5,6,7,7a,7b-octahydro-1aH-cyclopropa[h]azulen-4a-ol 129416164 Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
beta-Spathulenol 522266 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Ledum camphor 92812 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Palustrol 110745 Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
CID 15541534 15541534 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
cis-Guai-6-en-10-ol 91747157 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene 518574 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Labd-14-ene, 8,13-epoxy-, (13S)- 6432025 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2S,3S)-3-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 163043715 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(E,2R)-6-hydroxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3.0^{3,8.0^{12,16]octadecan-6-ol 496638 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162950932 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R)-6-hydroxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 131848483 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-15-[(E,2S,3S)-3,6-dihydroxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162852225 Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C)C(C=CC(C)(C)O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R,4E)-6-methylhepta-4,6-dien-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 22297599 Click to see 422.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-4-oxohept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 101618850 Click to see 438.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2S,4E)-6-methylhepta-4,6-dien-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 163191428 Click to see 422.70 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
(6R)-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-en-4-one 101637203 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
15-(3-Hydroxy-6-methyl-5-methylideneheptan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 163043714 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
15-(3,6-Dihydroxy-6-methylhept-4-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 73880611 Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C)C(C=CC(C)(C)O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
15-(4-Hydroxy-6-methylhept-5-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 162950930 Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
25-Hydroxycycloart-23-en-3-one 44423578 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
6-(6-Hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl)-2-methylhept-2-en-4-one 163015474 Click to see 440.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
7,7,12,16-Tetramethyl-15-(6-methylhepta-4,6-dien-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 73880678 Click to see CC(CC=CC(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 422.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
https://doi.org/10.1016/S0031-9422(00)00302-2
Cycloart-23-ene-3beta,25-diol 5470009 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(02)00123-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)00302-2
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)00302-2

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