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Ocotea macrophylla

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 UUID643ff6924598b530919261
Scientific name Ocotea macrophylla
Authority Kunth
First published in Nov. Gen. Sp. 2: 165 (1817)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Nectandra macrophylla (Kunth) Nees Syst. Laur. : 292 (1836)
Nectandra corzoana Lundell Wrightia 4(3): 102. 1969
Nectandra coryoana Lundell Wrightia 4: 102. 1969
Ocotea helicterifolia (Meisn.) Hemsl. Biol. Cent.-Amer., Bot. 3: 73 (1882)
Oreodaphne helicterifolia Meisn. Prodr. 15(1): 123 (1864)
Ocotea tenejapensis Lundell Wrightia 4: 108 (1969)
Persea macrophylla (Kunth) Spreng. Syst. Veg. 2: 270 (1825)
Phoebe helicterifolia (Meisn.) Mez Jahrb. Königl. Bot. Gart. Berlin 5: 193 (1889)
Phoebe corzoana (Lundell) Lundell Wrightia 4: 102 (1969)
Phoebe obtusata Lundell Contr. Univ. Michigan Herb. 6: 21 (1941)
Phoebe nectandroides Mez Jahrb. Königl. Bot. Gart. Berlin 5: 194 (1889)
Cinnamomum corzoanum (Lundell) Kosterm. Reinwardtia 10: 422. 1988
Cinnamomum helicterifolium (Meisn.) Kosterm. Reinwardtia 6: 21 (1961)
Cinnamomum obtusatum (Lundell) Kosterm. Reinwardtia 6: 22 (1961)
Ocotea mexicana (Meisn.) Hemsl. Biol. Cent.-Amer., Bot. 3: 73 (1882)
Oreodaphne mexicana Meisn. Prodr. 15(1): 118 (1864)
Oreodaphne mexicana var. longipes Meisn. Prodr. 15(1): 118 (1864)
Oreodaphne umbrosa var. bullata Meisn. Prodr. 15(1): 122 (1864)
Ocotea umbrosa var. bullata (Meisn.) Hemsl. Biol. Cent.-Amer., Bot. 3: 74 (1882)
Ocotea mexicana var. longipes (Meisn.) Hemsl. Biol. Cent.-Amer., Bot. 3: 73 (1882)
Laurus pubescens Willd. ex Nees Syst. Laur. : 293 (1836)
Oreodaphne mexicana var. subsessilis Meisn. Prodr. 15(1): 118 (1864)
Ocotea mexicana var. subsessilis (Meisn.) Hemsl. Biol. Cent.-Amer., Bot. 3: 73 (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
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000383017
Tropicos 17801204
KEW urn:lsid:ipni.org:names:326508-2
The Plant List kew-2386422
Open Tree Of Life 6027360
NCBI Taxonomy 1930893
IUCN Red List 151951595
IPNI 326508-2
GBIF 4179211

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
Characterization and Inhibitory Effects of Essential Oil and Nanoemulsion from Ocotea indecora (Shott) Mez in Aspergillus Species Pinto LD, Machado FP, Esteves R, Farias VM, Köptcke FB, Ricci-Junior E, Rocha L, Keller LA Molecules 13-Apr-2023
PMCID:PMC10142328
doi:10.3390/molecules28083437
PMID:37110671
Anti-Tuberculosis Mur Inhibitors: Structural Insights and the Way Ahead for Development of Novel Agents Mehta K, Khambete M, Abhyankar A, Omri A Pharmaceuticals (Basel) 01-Mar-2023
PMCID:PMC10058398
doi:10.3390/ph16030377
PMID:36986477
Ethyl acetate fractions of Myrciaria floribunda, Ocotea pulchella, and Ocotea notata exhibit promising in vitro activity against Sporothrix brasiliensis isolates with low susceptibility to itraconazole de Souza LC, Reis NF, Alcântara LM, da Silveira Souto SR, de Araújo Penna B, Santos RC, Robbs BK, Machado FP, Castro HC, Machado RL, Rocha L, de Souza Baptista AR Braz J Microbiol 26-Jan-2023
PMCID:PMC9944169
doi:10.1007/s42770-023-00904-8
PMID:36701111
Phylogeny and taxonomy of Cinnamomum (Lauraceae) Yang Z, Liu B, Yang Y, Ferguson DK Ecol Evol 01-Oct-2022
PMCID:PMC9526118
doi:10.1002/ece3.9378
PMID:36203627
Coagulation System Activation for Targeting of COVID-19: Insights into Anticoagulants, Vaccine-Loaded Nanoparticles, and Hypercoagulability in COVID-19 Vaccines Abdel-Bakky MS, Amin E, Ewees MG, Mahmoud NI, Mohammed HA, Altowayan WM, Abdellatif AA Viruses 24-Jan-2022
PMCID:PMC8876839
doi:10.3390/v14020228
PMID:35215822
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Antioxidant and Anti-Inflammatory Activities of Kigelia africana (Lam.) Benth. Nabatanzi A, Nkadimeng SM, Lall N, Kabasa JD, McGaw LJ Evid Based Complement Alternat Med 17-Jun-2020
PMCID:PMC7317318
doi:10.1155/2020/4352084
PMID:32655661
Antinociceptive Effect of Hinokinin and Kaurenoic Acid Isolated from Aristolochia odoratissima L. Montiel-Ruiz RM, Córdova-de la Cruz M, González-Cortázar M, Zamilpa A, Gómez-Rivera A, López-Rodríguez R, Lobato-García CE, Blé-González EA Molecules 24-Mar-2020
PMCID:PMC7145305
doi:10.3390/molecules25061454
PMID:32213823
Biphasic Dose-Response Induced by Phytochemicals: Experimental Evidence Jodynis-Liebert J, Kujawska M J Clin Med 06-Mar-2020
PMCID:PMC7141213
doi:10.3390/jcm9030718
PMID:32155852
Cell wall peptidoglycan in Mycobacterium tuberculosis: An Achilles’ heel for the TB-causing pathogen Maitra A, Munshi T, Healy J, Martin LT, Vollmer W, Keep NH, Bhakta S FEMS Microbiol Rev 10-Jun-2019
PMCID:PMC6736417
doi:10.1093/femsre/fuz016
PMID:31183501
Chemical Structures of Lignans and Neolignans Isolated from Lauraceae Li Y, Xie S, Ying J, Wei W, Gao K Molecules 30-Nov-2018
PMCID:PMC6321345
doi:10.3390/molecules23123164
PMID:30513687
Natural Products for Antithrombosis Chen C, Yang FQ, Zhang Q, Wang FQ, Hu YJ, Xia ZN Evid Based Complement Alternat Med 17-May-2015
PMCID:PMC4449941
doi:10.1155/2015/876426
PMID:26075003
Antimycobacterial and Nitric Oxide Production Inhibitory Activities of Ocotea notata from Brazilian Restinga Costa IF, Calixto SD, Heggdorne de Araujo M, Konno TU, Tinoco LW, Guimarães DO, Lasunskaia EB, Leal IR, Muzitano MF ScientificWorldJournal 19-Feb-2015
PMCID:PMC4350868
doi:10.1155/2015/947248
PMID:25789338
Tetrahydroisoquinolines affect the whole-cell phenotype of Mycobacterium tuberculosis by inhibiting the ATP-dependent MurE ligase Guzman JD, Pesnot T, Barrera DA, Davies HM, McMahon E, Evangelopoulos D, Mortazavi PN, Munshi T, Maitra A, Lamming ED, Angell R, Gershater MC, Redmond JM, Needham D, Ward JM, Cuca LE, Hailes HC, Bhakta S J Antimicrob Chemother 04-Feb-2015
PMCID:PMC4498294
doi:10.1093/jac/dkv010
PMID:25656411
Evaluation of the Leishmanicidal Activity of Rutaceae and Lauraceae Ethanol Extracts on Golden Syrian Hamster (Mesocricetus auratus) Peritoneal Macrophages Chávez Enciso NA, Coy-barrera ED, Patiño OJ, Cuca LE, Delgado G Indian J Pharm Sci 01-May-2014
PMCID:PMC4090825
PMID:25035529

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
> Alkaloids and derivatives / Aporphines
(+)-Glaucine 16754 Click to see 355.40 unknown https://doi.org/10.1016/0031-9422(75)85390-8
https://doi.org/10.1007/978-1-4899-1783-6_3
Dehydronantenine 151328 Click to see CN1CCC2=CC(=C(C3=C4C=C5C(=CC4=CC1=C23)OCO5)OC)OC 337.40 unknown https://doi.org/10.1016/0031-9422(75)85390-8
Lirinidine 31069 Click to see 281.30 unknown https://doi.org/10.1007/978-1-4899-1783-6_3
Nantenine 197001 Click to see 339.40 unknown https://doi.org/10.1016/0031-9422(75)85390-8
Thalictruberine 181743 Click to see 339.40 unknown https://doi.org/10.1016/0031-9422(75)85390-8
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(1S,5R,6R,7R,8S)-7-(3,4-dimethoxyphenyl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 44470608 Click to see 358.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
7-(3,4-Dimethoxyphenyl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 72962156 Click to see 358.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
> Benzenoids / Phenol ethers / Anisoles
(1S,5R,6R,7R,8S)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enyl-7-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-3-en-2-one 44470746 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC(=C(C(=C3)OC)OC)OC 388.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
8-Hydroxy-5-methoxy-6-methyl-3-prop-2-enyl-7-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-3-en-2-one 75055818 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC(=C(C(=C3)OC)OC)OC 388.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
> Organoheterocyclic compounds / Benzodioxoles
(1R,5R,6R,7R,8R)-7-(1,3-benzodioxol-5-yl)-8-hydroxy-3-methoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 101663174 Click to see 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
(1R,5R,6R,7R,8S)-7-(1,3-benzodioxol-5-yl)-8-hydroxy-3-methoxy-6-methyl-5-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 10893250 Click to see 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
(1S,5R,6R,7R,8R)-7-(1,3-benzodioxol-5-yl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 162937219 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC4=C(C=C3)OCO4 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
(1S,5R,6R,7R,8S)-7-(1,3-benzodioxol-5-yl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 44470607 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC4=C(C=C3)OCO4 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
2'-Epi-guianin 45487149 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)CC=C)O)C3=CC4=C(C=C3)OCO4 352.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
7-(1,3-Benzodioxol-5-yl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 75055817 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC4=C(C=C3)OCO4 342.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
Isoalvaxanthone 10596886 Click to see 396.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Licarin B 10860310 Click to see 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
(-)-Licarin-B 6441061 Click to see 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
5-(7-Methoxy-3-methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)-1,3-benzodioxole 3398496 Click to see 324.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
Ocophyllals A 44470605 Click to see 310.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010
Ocophyllals B 44470606 Click to see CC1=C(OC2=C1C=C(C=C2OC)C=O)C3=CC(=C(C(=C3)OC)OC)OC 356.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.07.010

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