Scientific name	Authority	First published in
Laurus multiflora	Ruiz ex Meisn.	Prodr. 15(1): 150 (1864)
Nectandra guaporensis	Coe-Teix.	Acta Amazonica 5: 163 (1975)
Nectandra ambigua	Meisn.	Prodr. 15(1): 158 (1864)
Nectandra pallida	Nees	Linnaea 21: 510 (1848)
Nectandra urophylla	Meisn.	Prodr. 15(1): 157 (1864)
Nectandra bombycina	S.Moore	Trans. Linn. Soc. London, Bot. 4: 449 (1895)
Nectandra amazonum var. latifolia	Meisn.	A.P.de Candolle, Prodr. 15(1): 150 (1864)
Nectandra canescens	Meisn.	A.P.de Candolle, Prodr. 15(1): 147 (1864)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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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

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil West-central
- Northern South America
  - Guyana
  - Suriname
  - Venezuela
- Western South America
  - Bolivia
  - Colombia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000379445
Tropicos	17801027
KEW	urn:lsid:ipni.org:names:466626-1
The Plant List	kew-2379536
Open Tree Of Life	545877
NCBI Taxonomy	128645
IUCN Red List	143819265
IPNI	466626-1
GBIF	7304432

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

Current State of Knowledge Regarding WHO High Priority Pathogens—Resistance Mechanisms and Proposed Solutions through Candidates Such as Essential Oils: A Systematic Review

Romanescu M, Oprean C, Lombrea A, Badescu B, Teodor A, Constantin GD, Andor M, Folescu R, Muntean D, Danciu C, Dalleur O, Batrina SL, Cretu O, Buda VO

Int J Mol Sci

04-Jun-2023

PMCID:	PMC10253476
doi:	10.3390/ijms24119727
PMID:	37298678

Generating Flavor Molecules Using Scientific Machine Learning

Queiroz LP, Rebello CM, Costa EA, Santana VV, Rodrigues BC, Rodrigues AE, Ribeiro AM, Nogueira IB

ACS Omega

15-Mar-2023

PMCID:	PMC10061502
doi:	10.1021/acsomega.2c07176
PMID:	37008127

Chemical characteristics of the sesquiterpenes and diterpenes from Lauraceae family and their multifaceted health benefits: A review

Feng H, Jiang Y, Cao H, Shu Y, Yang X, Zhu D, Shao M

Heliyon

07-Dec-2022

PMCID:	PMC9801090
doi:	10.1016/j.heliyon.2022.e12013
PMID:	36590503

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

Toxic Potential of Cerrado Plants on Different Organisms

Rocha JD, Carneiro FM, Fernandes AS, Morais JM, Borges LL, Chen-Chen L, de Almeida LM, Bailão EF

Int J Mol Sci

22-Mar-2022

PMCID:	PMC8998518
doi:	10.3390/ijms23073413
PMID:	35408775

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

Antifungal Activity against Fusarium oxysporum of Botanical End-Products: An Integration of Chemical Composition and Antifungal Activity Datasets to Identify Antifungal Bioactives

Cárdenas-Laverde D, Barbosa-Cornelio R, Coy-Barrera E

Plants (Basel)

24-Nov-2021

PMCID:	PMC8705217
doi:	10.3390/plants10122563
PMID:	34961034

Effect of essential oils on Leishmania amazonensis: a systematic review

de Lara da Silva CE, Oyama J, Ferreira FB, de Paula Lalucci-Silva MP, Lordani TV, de Lara da Silva RC, de Souza Terron Monich M, Teixeira JJ, Lonardoni MV

Parasitology

03-Aug-2020

PMCID:	PMC10317781
doi:	10.1017/S0031182020001304
PMID:	32741424

Chemical Diversity and Biological Activities of Essential Oils from Licaria, Nectrandra and Ocotea Species (Lauraceae) with Occurrence in Brazilian Biomes

Xavier JK, Alves NS, Setzer WN, da Silva JK

Biomolecules

05-Jun-2020

PMCID:	PMC7356694
doi:	10.3390/biom10060869
PMID:	32517106

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

In Vitro antileishmania activity of sesquiterpene-rich essential oils from Nectandra species

Bosquiroli LS, dos Santos Ferreira AC, Farias KS, da Costa EC, Matos MD, Kadri MC, Rizk YS, Alves FM, Perdomo RT, Carollo CA, Pinto de Arruda CC

Pharm Biol

29-Nov-2017

PMCID:	PMC6130651
doi:	10.1080/13880209.2017.1407803
PMID:	29185382

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

Responses to flooding of plant water relations and leaf gas exchange in tropical tolerant trees of a black-water wetland

Herrera A

Front Plant Sci

01-May-2013

PMCID:	PMC3640197
doi:	10.3389/fpls.2013.00106
PMID:	23641246

Errata: Three New 7.3′,8.5′-Connected Bicyclo[3.2.1]octanoids and Other Neolignans from Leaves of Nectandra amazonum NEES. (Lauraceae) [Chem. Pharm. Bull. 57(6): 639-642 (2009)]

Ericsson David Coy Barrera, Luis Enrique Cuca Suárez

Pharmaceutical Society of Japan

02-Dec-2009

doi:	10.1248/CPB.57.1437

Drought responses of flood-tolerant trees in Amazonian floodplains

Parolin P, Lucas C, Piedade MT, Wittmann F

Ann Bot

31-Oct-2009

PMCID:	PMC2794061
doi:	10.1093/aob/mcp258
PMID:	19880423

Phytochemical Profile Top

Add a new one!

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 / Methoxybenzenes / Dimethoxybenzenes
(6R)-7-(3,4-dimethoxyphenyl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one	5318743	Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC(=C(C=C3)OC)OC	358.40	unknown	https://doi.org/10.1248/CPB.57.639
Kadsurenin C	45487142	Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC(=C(C=C3)OC)OC	358.40	unknown	https://doi.org/10.1248/CPB.57.639
> Benzenoids / Phenol ethers / Anisoles
(1R,2R,5S,6S,7R,8S)-1,5-dimethoxy-6-methyl-3-prop-2-enyl-7-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-3-ene-2,8-diol	102508302	Click to see CC1C(C2(C(C(=CC1(C2O)OC)CC=C)O)OC)C3=CC(=C(C(=C3)OC)OC)OC	420.50	unknown	https://doi.org/10.1248/CPB.57.1437
(1R,5S,8R,9R)-5-methoxy-9-methyl-3-prop-2-enyl-8-(3,4,5-trimethoxyphenyl)-6-oxabicyclo[3.2.2]non-3-ene-2,7-dione	10573162	Click to see CC1C(C2C(=O)C(=CC1(OC2=O)OC)CC=C)C3=CC(=C(C(=C3)OC)OC)OC	402.40	unknown	https://doi.org/10.1248/CPB.57.1437 https://doi.org/10.1248/CPB.57.639
(1S,4R,5S,6S,7S)-4-hydroxy-1-methoxy-7-methyl-3-prop-2-enyl-6-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-2-en-8-one	6325565	Click to see CC1C(C2C(C(=CC1(C2=O)OC)CC=C)O)C3=CC(=C(C(=C3)OC)OC)OC	388.50	unknown	https://doi.org/10.1248/CPB.57.639
(1S,5R,6R,7R,8R)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enyl-7-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-3-en-2-one	163081554	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/10.1248/CPB.57.1437
(1S,5S,6S,7R,8R)-8-hydroxy-1,5-dimethoxy-6-methyl-3-prop-2-enyl-7-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-3-en-2-one	44130496	Click to see CC1C(C2(C(C1(C=C(C2=O)CC=C)OC)O)OC)C3=CC(=C(C(=C3)OC)OC)OC	418.50	unknown	https://doi.org/10.1248/CPB.57.639 https://doi.org/10.1248/CPB.57.1437
(1S,5S,6S,7R,8S)-8-hydroxy-1,5-dimethoxy-6-methyl-3-prop-2-enyl-7-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-3-en-2-one	44130497	Click to see CC1C(C2(C(C1(C=C(C2=O)CC=C)OC)O)OC)C3=CC(=C(C(=C3)OC)OC)OC	418.50	unknown	https://doi.org/10.1248/CPB.57.1437
1,5-Dimethoxy-6-methyl-3-prop-2-enyl-7-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-3-ene-2,8-diol	46186918	Click to see CC1C(C2(C(C(=CC1(C2O)OC)CC=C)O)OC)C3=CC(=C(C(=C3)OC)OC)OC	420.50	unknown	https://doi.org/10.1248/CPB.57.1437
4-Hydroxy-1-methoxy-7-methyl-3-prop-2-enyl-6-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-2-en-8-one	75116725	Click to see CC1C(C2C(C(=CC1(C2=O)OC)CC=C)O)C3=CC(=C(C(=C3)OC)OC)OC	388.50	unknown	https://doi.org/10.1248/CPB.57.1437
5-Methoxy-9-methyl-3-prop-2-enyl-8-(3,4,5-trimethoxyphenyl)-6-oxabicyclo[3.2.2]non-3-ene-2,7-dione	85190303	Click to see CC1C(C2C(=O)C(=CC1(OC2=O)OC)CC=C)C3=CC(=C(C(=C3)OC)OC)OC	402.40	unknown	https://doi.org/10.1248/CPB.57.1437
8-Hydroxy-1,5-dimethoxy-6-methyl-3-prop-2-enyl-7-(3,4,5-trimethoxyphenyl)bicyclo[3.2.1]oct-3-en-2-one	74929278	Click to see CC1C(C2(C(C1(C=C(C2=O)CC=C)OC)O)OC)C3=CC(=C(C(=C3)OC)OC)OC	418.50	unknown	https://doi.org/10.1248/CPB.57.1437
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/10.1248/CPB.57.1437
CID 173323	173323	Click to see CC1C(C2C(C(=CC1(C2=O)OC)CC=C)O)C3=CC(=C(C(=C3)OC)OC)OC	388.50	unknown	https://doi.org/10.1248/CPB.57.1437
Macrophyllin B	45487148	Click to see CC1C(C2C(C(=CC1(C2=O)OC)CC=C)O)C3=CC(=C(C(=C3)OC)OC)OC	388.50	unknown	https://doi.org/10.1248/CPB.57.639
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)97906-8
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,6E)-nerolidol	11241545	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)97906-8
Nerolidol	8888	Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)97906-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)97906-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol	11850	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1016/S0031-9422(00)97906-8
Hexitol	453	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1016/S0031-9422(00)97906-8
> Organoheterocyclic compounds / Benzodioxoles
Piperonylic acid	7196	Click to see C1OC2=C(O1)C=C(C=C2)C(=O)O	166.13	unknown	https://doi.org/10.1016/S0031-9422(00)97906-8
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Licarin A	6442393	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)O)OC	326.40	unknown	https://doi.org/10.1248/CPB.57.639 https://doi.org/10.1248/CPB.57.1437
(2S,3R,3aR)-2-(3,4-dimethoxyphenyl)-3a,7-dimethoxy-3-methyl-5-prop-2-enyl-2,3-dihydro-1-benzofuran-6-one	163041887	Click to see CC1C(OC2=C(C(=O)C(=CC12OC)CC=C)OC)C3=CC(=C(C=C3)OC)OC	386.40	unknown	https://doi.org/10.1248/CPB.57.1437
(2S,3S)-2-(3,4-dimethoxyphenyl)-3-methyl-5-prop-2-enyl-2,3-dihydro-1-benzofuran-6-ol	9973651	Click to see CC1C(OC2=C1C=C(C(=C2)O)CC=C)C3=CC(=C(C=C3)OC)OC	326.40	unknown	https://doi.org/10.1248/CPB.57.639
2-(1,3-Benzodioxol-5-yl)-3-methyl-5-prop-2-enyl-2,3-dihydro-1-benzofuran-6-ol	75116720	Click to see CC1C(OC2=C1C=C(C(=C2)O)CC=C)C3=CC4=C(C=C3)OCO4	310.30	unknown	https://doi.org/10.1248/CPB.57.1437
2-(3,4-Dimethoxyphenyl)-3a,7-dimethoxy-3-methyl-5-prop-2-enyl-2,3-dihydro-1-benzofuran-6-one	163041886	Click to see CC1C(OC2=C(C(=O)C(=CC12OC)CC=C)OC)C3=CC(=C(C=C3)OC)OC	386.40	unknown	https://doi.org/10.1248/CPB.57.1437
2-(3,4-Dimethoxyphenyl)-7-methoxy-3-methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran	53934174	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)OC)OC	340.40	unknown	https://doi.org/10.1248/CPB.57.1437
2-Methoxy-4-(7-methoxy-3-methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol	73548	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)O)OC	326.40	unknown	https://doi.org/10.1248/CPB.57.1437
Acuminatin	6441048	Click to see CC=CC1=CC2=C(C(=C1)OC)OC(C2C)C3=CC(=C(C=C3)OC)OC	340.40	unknown	https://doi.org/10.1248/CPB.57.639 https://doi.org/10.1248/CPB.57.1437
Denudatin B	442834	Click to see CC1C(OC2=CC(=O)C(=CC12OC)CC=C)C3=CC(=C(C=C3)OC)OC	356.40	unknown	https://doi.org/10.1248/CPB.57.639
Liliflol A	45487097	Click to see CC1C(OC2=C1C=C(C(=C2)O)CC=C)C3=CC4=C(C=C3)OCO4	310.30	unknown	https://doi.org/10.1248/CPB.57.1437

Biological Material Top

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Nectandra amazonum

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top