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Cryptocarya moschata

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 UUID64401445b942d015352651
Scientific name Cryptocarya moschata
Authority Nees & Mart.
First published in Linnaea 8: 37 (1833)

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.

Cryptocarya moschata has no documented traditional teas, tinctures, macerations, decoctions, or poultices in credible, verifiable sources for this species.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Nectandra robusta Chanc. Fl. Forest. Globe : 326 (1920)
Cryptocarya moschata f. angustifolia Mez Jahrb. Königl. Bot. Gart. Berlin 5: 9 (1889)
Ocotea cymbarum Spreng. ex Nees Syst. Laur. : 213 (1836)

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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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
    • Southern South America
      • Argentina Northeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000628067
Tropicos 17800745
KEW urn:lsid:ipni.org:names:464021-1
The Plant List kew-2746109
Open Tree Of Life 5699309
NCBI Taxonomy 1345247
IUCN Red List 149216298
IPNI 464021-1
GBIF 7304739

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
Safety and efficacy of a feed additive consisting of an essential oil from the seeds of Myristica fragrans Houtt. (nutmeg oil) for all animal species (FEFANA asbl) Bampidis V, Azimonti G, Bastos MD, Christensen H, Durjava M, Kouba M, López‐Alonso M, López Puente S, Marcon F, Mayo B, Pechová A, Petkova M, Ramos F, Sanz Y, Villa RE, Woutersen R, Brantom P, Chesson A, Schlatter J, Westendorf J, Manini P, Dusemund B EFSA J 16-Jun-2023
PMCID:PMC10273060
doi:10.2903/j.efsa.2023.8066
PMID:37333988
The Cytotoxic and Inhibitory Effects of Plant Derivatives on Candida albicans Biofilms: A Scoping Review Loaiza-Oliva M, Arias-Durango L, Martínez-Pabón MC Molecules 23-Dec-2022
PMCID:PMC9822484
doi:10.3390/molecules28010130
PMID:36615324
Antimicrobial efficacy and biocompatibility of extracts from Cryptocarya species Zoccolotti JD, Cavalheiro AJ, Tasso CO, Ribas BR, Ferrisse TM, Jorge JH PLoS One 31-Dec-2021
PMCID:PMC8719776
doi:10.1371/journal.pone.0261884
PMID:34972152
Phylogeographic pattern suggests a general northeastward dispersal in the distribution of Machilus pauhoi in South China Zhu Q, Liao BY, Li P, Li JC, Deng XM, Hu XS, Chen XY PLoS One 08-Sep-2017
PMCID:PMC5590941
doi:10.1371/journal.pone.0184456
PMID:28886133
Isolation of arginase inhibitors from the bioactivity-guided fractionation of Byrsonima coccolobifolia leaves and stems. de Sousa LR, Ramalho SD, Burger MC, Nebo L, Fernandes JB, da Silva MF, Iemma MR, Corrêa CJ, de Souza DH, Lima MI, Vieira PC J Nat Prod 28-Feb-2014
doi:10.1021/NP400717M
PMID:24521209
Aromatic compounds from three Brazilian Lauraceae species Andrea Nastri de Luca Batista, João Marcos Batista Junior, Silvia Noelí López, Maysa Furlan, Alberto José Cavalheiro, Dulce Helena Siqueira Silva, Vanderlan da Silva Bolzani, Sergio Massayoshi Nunomura, Massayoshi Yoshida FapUNIFESP (SciELO) 11-Mar-2010
doi:10.1590/S0100-40422010000200017
An LC–DAD Fingerprinting Method for Alkaloids, Flavonoids and Styrylpyrones from Cryptocarya mandioccana Karin F. Bandeira, Alberto José Cavalheiro Springer Science and Business Media LLC 22-Sep-2009
doi:10.1365/S10337-009-1338-Y
De Novo Asymmetric Syntheses of (+)-Goniothalamin, (+)-Goniothalamin oxide and 7,8-Bis-epi-Goniothalamin using Asymmetric Allylations Harsh P, O’Doherty GA Tetrahedron 27-Jun-2009
PMCID:PMC2699279
doi:10.1016/j.tet.2009.03.097
PMID:20161297
Intraspecific variability of flavonoid glycosides and styrylpyrones from leaves of Cryptocarya mandioccana Meisner (Lauraceae) Cláudia J. Nehme, Pedro L.R. de Moraes, Aristeu G. Tininis, Alberto J. Cavalheiro Elsevier BV 19-Jun-2008
doi:10.1016/J.BSE.2008.05.001
An HPLC-PAD method to analyse flavonoid glycosides and styrylpyrones from Cryptocarya species (Lauraceae). Nehme CJ, Bastos WL, de Araújo AJ, Cavalheiro AJ Phytochem Anal 01-Mar-2005
doi:10.1002/PCA.818
PMID:15881116
Intrapopulational variability of styrylpyrones in leaves of Cryptocarya moschata Nees (Lauraceae) from Carlos Botelho State Park Cláudia J. Nehme, Pedro L.R. Moraes, Alberto J. Cavalheiro Elsevier BV 14-Oct-2002
doi:10.1016/S0305-1978(01)00129-6
(−)-Cryptocaryalactone and (−)-deacetylcryptocaryalactone-germination inhibitors from Cryptocarya moschata seeds Gayland F. Spencer, Roger E. England, Rebecca B. Wolf Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84083-2
6-[omega-arylalkenyl]-5,6-dihydro-alpha-pyrones from Cryptocarya moschata (Lauraceae). Cavalheiro AJ, Yoshida M Phytochemistry 01-Apr-2000
doi:10.1016/S0031-9422(99)00532-4
PMID:10783987

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 / Styrenes
[(E,2S)-1-[(2R)-6-oxo-2,3-dihydropyran-2-yl]-4-phenylbut-3-en-2-yl] acetate 11808267 Click to see 286.32 unknown https://doi.org/10.1016/S0031-9422(00)84083-2
[(E,2S)-1-[(2S)-6-oxo-2,3-dihydropyran-2-yl]-4-phenylbut-3-en-2-yl] acetate 13928763 Click to see 286.32 unknown https://doi.org/10.1016/S0031-9422(00)84083-2
[1-(6-Oxo-2,3-dihydropyran-2-yl)-4-phenylbut-3-en-2-yl] acetate 594411 Click to see 286.32 unknown https://doi.org/10.1016/S0031-9422(00)84083-2
2-(2-Phenylethenyl)-2,3-dihydropyran-6-one 266508 Click to see 200.23 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
https://doi.org/10.1002/PCA.818
Goniothalamin 6440856 Click to see C1C=CC(=O)OC1C=CC2=CC=CC=C2 200.23 unknown https://doi.org/10.1002/PCA.818
https://doi.org/10.1016/S0031-9422(99)00532-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Bufanolides and derivatives
5-[(3S,8S,9S,10R,13R,14S,17R)-3-[(2R,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-10,13-dimethyl-1,2,3,6,7,8,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl]pyran-2-one 163016840 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3=C2)O)C6=COC(=O)C=C6)C)C)O)O)OC7C(C(C(C(O7)CO)O)O)O 692.80 unknown https://doi.org/10.1002/PCA.818
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1E,4S,6R,7E)-6-acetyloxy-1-[(2R)-6-oxo-2,3-dihydropyran-2-yl]-8-phenylocta-1,7-dien-4-yl] acetate 162820241 Click to see 398.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
[6-Acetyloxy-1-(6-oxo-2,3-dihydropyran-2-yl)-8-phenylocta-1,7-dien-4-yl] acetate 162820238 Click to see 398.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(2R)-2-[(E)-3-[(2R,4S,5S,6S)-4,5-dihydroxy-6-[(E)-2-phenylethenyl]oxan-2-yl]prop-1-enyl]-2,3-dihydropyran-6-one 162850710 Click to see 356.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[(E)-3-[(2S,4R,5R,6S)-4,5-dihydroxy-6-[(E)-2-phenylethenyl]oxan-2-yl]prop-1-enyl]-2,3-dihydropyran-6-one 101052053 Click to see C1C=CC(=O)OC1C=CCC2CC(C(C(O2)C=CC3=CC=CC=C3)O)O 356.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[(E)-3-[(2S,4R,5S,6R)-4,5-dihydroxy-6-[(E)-2-phenylethenyl]oxan-2-yl]prop-1-enyl]-2,3-dihydropyran-6-one 50901755 Click to see 356.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[(E)-3-[(2S,4S,5S,6R)-4,5-dihydroxy-6-[(E)-2-phenylethenyl]oxan-2-yl]prop-1-enyl]-2,3-dihydropyran-6-one 101052049 Click to see 356.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[[(2R,4R,5R,6S)-4,5-dihydroxy-6-[(E)-2-phenylethenyl]oxan-2-yl]methyl]-2,3-dihydropyran-6-one 101052048 Click to see C1C=CC(=O)OC1CC2CC(C(C(O2)C=CC3=CC=CC=C3)O)O 330.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[[(2S,4R,5R,6R)-4,5-dihydroxy-6-[(E)-2-phenylethenyl]oxan-2-yl]methyl]-2,3-dihydropyran-6-one 101052051 Click to see C1C=CC(=O)OC1CC2CC(C(C(O2)C=CC3=CC=CC=C3)O)O 330.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[[(2S,4R,5S,6R)-4,5-dihydroxy-6-[(E)-2-phenylethenyl]oxan-2-yl]methyl]-2,3-dihydropyran-6-one 53261292 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[[(2S,4S,5S,6R)-4,5-dihydroxy-6-[(E)-2-phenylethenyl]oxan-2-yl]methyl]-2,3-dihydropyran-6-one 101052047 Click to see C1C=CC(=O)OC1CC2CC(C(C(O2)C=CC3=CC=CC=C3)O)O 330.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[[(2S,4S,5S,6S)-4,5-dihydroxy-6-[(E)-2-phenylethenyl]oxan-2-yl]methyl]-2,3-dihydropyran-6-one 162940185 Click to see C1C=CC(=O)OC1CC2CC(C(C(O2)C=CC3=CC=CC=C3)O)O 330.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
[(2R,3S,4R,6R)-3-acetyloxy-6-[[(2R)-6-oxo-2,3-dihydropyran-2-yl]methyl]-2-[(E)-2-phenylethenyl]oxan-4-yl] acetate 162820307 Click to see CC(=O)OC1CC(OC(C1OC(=O)C)C=CC2=CC=CC=C2)CC3CC=CC(=O)O3 414.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
[(2R,3S,4R,6S)-3-acetyloxy-6-[(E)-3-[(2R)-6-oxo-2,3-dihydropyran-2-yl]prop-2-enyl]-2-[(E)-2-phenylethenyl]oxan-4-yl] acetate 162820267 Click to see 440.50 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
[3-Acetyloxy-6-[(6-oxo-2,3-dihydropyran-2-yl)methyl]-2-(2-phenylethenyl)oxan-4-yl] acetate 162820306 Click to see CC(=O)OC1CC(OC(C1OC(=O)C)C=CC2=CC=CC=C2)CC3CC=CC(=O)O3 414.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
[3-Acetyloxy-6-[3-(6-oxo-2,3-dihydropyran-2-yl)prop-2-enyl]-2-(2-phenylethenyl)oxan-4-yl] acetate 162820264 Click to see 440.50 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
2-[[4,5-Dihydroxy-6-(2-phenylethenyl)oxan-2-yl]methyl]-2,3-dihydropyran-6-one 75995432 Click to see 330.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
2-[3-[4,5-Dihydroxy-6-(2-phenylethenyl)oxan-2-yl]prop-1-enyl]-2,3-dihydropyran-6-one 75577262 Click to see 356.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Sibiricose A5 6326020 Click to see 518.50 unknown https://doi.org/10.1016/S0305-1978(01)00129-6
> Phenylpropanoids and polyketides / Cinnamyl alcohols
(2R)-2-[(1E,4R,6R,7E)-4,6-dihydroxy-8-phenylocta-1,7-dienyl]-2,3-dihydropyran-6-one 101052039 Click to see 314.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
https://doi.org/10.1016/J.BSE.2008.05.001
https://doi.org/10.1365/S10337-009-1338-Y
(2R)-2-[(1E,4S,6R,8R,9E)-4,6,8-trihydroxy-10-phenyldeca-1,9-dienyl]-2,3-dihydropyran-6-one 101052043 Click to see C1C=CC(=O)OC1C=CCC(CC(CC(C=CC2=CC=CC=C2)O)O)O 358.40 unknown https://doi.org/10.1365/S10337-009-1338-Y
https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[(E,2R,4R,6R)-2,4,6-trihydroxy-8-phenyloct-7-enyl]-2,3-dihydropyran-6-one 163065619 Click to see C1C=CC(=O)OC1CC(CC(CC(C=CC2=CC=CC=C2)O)O)O 332.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2R)-2-[(E,2S,4R)-2,4-dihydroxy-6-phenylhex-5-enyl]-2,3-dihydropyran-6-one 101052037 Click to see 288.34 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2S)-2-[(1E,4S,6R,7E)-4,6-dihydroxy-8-phenylocta-1,7-dienyl]-2,3-dihydropyran-6-one 101675707 Click to see 314.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
(2S)-2-[(E,2S)-2-hydroxy-4-phenylbut-3-enyl]-2,3-dihydropyran-6-one 102477913 Click to see 244.28 unknown https://doi.org/10.1016/S0031-9422(00)84083-2
2-(2,4-Dihydroxy-6-phenylhex-5-enyl)-2,3-dihydropyran-6-one 76524569 Click to see 288.34 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
2-(2,4,6-Trihydroxy-8-phenyloct-7-enyl)-2,3-dihydropyran-6-one 163065616 Click to see 332.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
2-(4,6-Dihydroxy-8-phenylocta-1,7-dienyl)-2,3-dihydropyran-6-one 496083 Click to see C1C=CC(=O)OC1C=CCC(CC(C=CC2=CC=CC=C2)O)O 314.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
2-(4,6,8-Trihydroxy-10-phenyldeca-1,9-dienyl)-2,3-dihydropyran-6-one 163072514 Click to see C1C=CC(=O)OC1C=CCC(CC(CC(C=CC2=CC=CC=C2)O)O)O 358.40 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
2-[(E,2R,4R)-2,4-dihydroxy-6-phenylhex-5-enyl]-2,3-dihydropyran-6-one 162999637 Click to see C1C=CC(=O)OC1CC(CC(C=CC2=CC=CC=C2)O)O 288.34 unknown https://doi.org/10.1016/J.BSE.2008.05.001
6-(2-Hydroxy-4-phenylbut-3-en-1-yl)-5,6-dihydro-2H-pyran-2-one 71330408 Click to see C1C=CC(=O)OC1CC(C=CC2=CC=CC=C2)O 244.28 unknown https://doi.org/10.1016/S0031-9422(00)84083-2
CID 11716631 11716631 Click to see C1C=CC(=O)OC1C=CCC(CC(C=CC2=CC=CC=C2)O)O 314.40 unknown https://doi.org/10.1016/S0305-1978(01)00129-6
https://doi.org/10.1016/S0031-9422(99)00532-4
Cryptomoscatone D2 60143302 Click to see 288.34 unknown https://doi.org/10.1016/S0031-9422(99)00532-4
Cryptomoscatone E3 101052041 Click to see C1C=CC(=O)OC1CC(CC(CC(C=CC2=CC=CC=C2)O)O)O 332.40 unknown https://doi.org/10.1365/S10337-009-1338-Y
https://doi.org/10.1016/S0031-9422(99)00532-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1016/S0305-1978(01)00129-6
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1590/S0100-40422010000200017
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1021/NP400717M
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1590/S0100-40422010000200017
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1016/S0305-1978(01)00129-6

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