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Otoba parvifolia

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ff728684ea503082024
Scientific name Otoba parvifolia
Authority (Markgr.) A.H.Gentry
First published in Taxon 28: 417 (1979)

Description Top

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Synonyms Top

Scientific name Authority First published in
Dialyanthera parvifolia Markgr. Notizbl. Bot. Gart. Berlin-Dahlem 9: 964 (1926)
Myristica otoba var. glaucescens A.DC. Fl. Bras. 5(1): 122 (1860)

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
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000388977
Tropicos 21800182
KEW urn:lsid:ipni.org:names:586389-1
The Plant List kew-2397718
Open Tree Of Life 377620
NCBI Taxonomy 224906
IPNI 586389-1
GBIF 3743713
EOL 5036546

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
Understanding different dominance patterns in western Amazonian forests Matas‐Granados L, Draper FC, Cayuela L, de Aledo JG, Arellano G, Saadi CB, Baker TR, Phillips OL, Honorio Coronado EN, Ruokolainen K, García‐Villacorta R, Roucoux KH, Guèze M, Sandoval EV, Fine PV, Amasifuen Guerra CA, Gomez RZ, Stevenson Diaz PR, Monteagudo‐Mendoza A, Martinez RV, Socolar JB, Disney M, del Aguila Pasquel J, Llampazo GF, Arenas JV, Huaymacari JR, Grandez Rios JM, Macía MJ Ecol Lett 18-Dec-2023
PMCID:PMC10952671
doi:10.1111/ele.14351
PMID:38111128
The Use of Natural Bioactive Nutraceuticals in the Management of Tick-Borne Illnesses Shor SM, Schweig SK Microorganisms 05-Jul-2023
PMCID:PMC10384908
doi:10.3390/microorganisms11071759
PMID:37512931
Response of dung beetle diversity to remediation of soil ecosystems in the Ecuadorian Amazon Pozo-Rivera WE, Quiloango-Chimarro C, Paredes X, Landívar M, Chiriboga C, Hidalgo D, García K, Villacís J PeerJ 14-Mar-2023
PMCID:PMC10022510
doi:10.7717/peerj.14975
PMID:36935915
The Symbiotic Fungus Leucoagaricus gongylophorus (Möller) Singer (Agaricales, Agaricaceae) as a Target Organism to Control Leaf-Cutting Ants Araújo S, Seibert J, Ruani A, Alcántara-de la Cruz R, Cruz A, Pereira A, Zandonai D, Forim M, Silva MF, Bueno O, Fernandes J Insects 06-Apr-2022
PMCID:PMC9029082
doi:10.3390/insects13040359
PMID:35447801
Enzyme Activity of Natural Products on Cytochrome P450 Zuo HL, Huang HY, Lin YC, Cai XX, Kong XJ, Luo DL, Zhou YH, Huang HD Molecules 14-Jan-2022
PMCID:PMC8779343
doi:10.3390/molecules27020515
PMID:35056827
The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E Front Pharmacol 08-Jun-2021
PMCID:PMC8248671
doi:10.3389/fphar.2021.690432
PMID:34220515
DNA barcoding of fogged caterpillars in Peru: A novel approach for unveiling host-plant relationships of tropical moths (Insecta, Lepidoptera) Hausmann A, Diller J, Moriniere J, Höcherl A, Floren A, Haszprunar G PLoS One 30-Jan-2020
PMCID:PMC6992181
doi:10.1371/journal.pone.0224188
PMID:31999713
Comparative phylogeography of five widespread tree species: Insights into the history of western Amazonia Honorio Coronado EN, Dexter KG, Hart ML, Phillips OL, Pennington RT Ecol Evol 11-Jun-2019
PMCID:PMC6662334
doi:10.1002/ece3.5306
PMID:31380054
Herb–Drug Interaction Potential of Anti-Borreliae Effective Extracts from Uncaria tomentosa (Samento) and Otoba parvifolia (Banderol) Assessed In Vitro Weiss J Molecules 31-Dec-2018
PMCID:PMC6337116
doi:10.3390/molecules24010137
PMID:30602711
The anti-borreliae efficacy of phytochemicals and micronutrients: an update Goc A, Rath M Ther Adv Infect Dis 04-Jul-2016
PMCID:PMC4971593
doi:10.1177/2049936116655502
PMID:27536352
Exploring indigenous landscape classification across different dimensions: a case study from the Bolivian Amazon Riu-Bosoms C, Vidal-Amat T, Duane A, Fernandez-Llamazares A, Guèze M, Luz AC, Macía MJ, Paneque-Gálvez J, Reyes-García V Landsc Res 01-Jan-2015
PMCID:PMC4374147
doi:10.1080/01426397.2013.829810
PMID:25821282
The Colletotrichum gigasporum species complex Liu F, Cai L, Crous PW, Damm U Persoonia 29-Aug-2014
PMCID:PMC4312939
doi:10.3767/003158514X684447
PMID:25737595
Are ecologically important tree species the most useful? A case study from indigenous people in the Bolivian Amazon Guèze M, Luz AC, Paneque-Gálvez J, Macía MJ, Orta-Martínez M, Pino J, Reyes-García V Econ Bot 01-Mar-2014
PMCID:PMC4471144
doi:10.1007/s12231-014-9257-8
PMID:26097243
Further farnesyl-homogentisic acid derivatives from Otoba parvifolia A Ferreira Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(95)00368-H
Farnesyl-homogentisic acid derivatives from Otoba parvifolia A.Gilberto Ferreira, Mario Motidome, Otto R. Gottlieb, João B. Fernandes, Paulo C. Vieira, Miriam Cojocaru, Hugo E. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80055-X

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 / Phenol esters
(2,5-Dihydroxyphenyl) 3-methylbut-2-enoate 163189954 Click to see CC(=CC(=O)OC1=C(C=CC(=C1)O)O)C 208.21 unknown https://doi.org/10.1016/0031-9422(95)00368-H
> Lignans, neolignans and related compounds / Aryltetralin lignans
9-(1,3-benzodioxol-5-yl)-7,8-dimethyl-7,8-dihydro-6H-benzo[g][1,3]benzodioxol-9-ol 163011568 Click to see CC1CC2=C(C3=C(C=C2)OCO3)C(C1C)(C4=CC5=C(C=C4)OCO5)O 340.40 unknown https://doi.org/10.1016/0031-9422(95)00368-H
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(1R,3aS,4S,6aS)-4-(1,3-Benzodioxol-5-yl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2-methoxyphenol 44144290 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown https://doi.org/10.1016/0031-9422(95)00368-H
4-[(3aS,6aR)-6-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 138114568 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC 372.40 unknown https://doi.org/10.1016/0031-9422(95)00368-H
4-[(3R,3aR,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol 11348830 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown https://doi.org/10.1016/0031-9422(89)80055-X
https://doi.org/10.1016/0031-9422(95)00368-H
4-[(3S,3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol 5315338 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown https://doi.org/10.1016/0031-9422(95)00368-H
https://doi.org/10.1016/0031-9422(89)80055-X
Phillygenol; Epipinoresinol methyl ether; (+)-Phillygenin 4166098 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC 372.40 unknown https://doi.org/10.1016/0031-9422(95)00368-H
https://doi.org/10.1016/0031-9422(89)80055-X
Sylvatesmin 3083590 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC 372.40 unknown https://doi.org/10.1007/BF02266969
https://doi.org/10.1016/0031-9422(95)00368-H
https://doi.org/10.1016/0031-9422(89)80055-X
Xanthoxylol 130679 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown https://doi.org/10.1016/0031-9422(95)00368-H
https://doi.org/10.1016/0031-9422(89)80055-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
methyl (3S)-3-[(1R,2S)-2-hydroxy-4-oxo-1-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]cyclopentyl]-3-methoxypropanoate 163037808 Click to see CC(=CCCC(=CCCC(=CCC1(CC(=O)CC1O)C(CC(=O)OC)OC)C)C)C 420.60 unknown https://doi.org/10.1016/0031-9422(89)80055-X
methyl (3S)-3-ethoxy-3-[(1R,2S)-2-hydroxy-4-oxo-1-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]cyclopentyl]propanoate 162934379 Click to see CCOC(CC(=O)OC)C1(CC(=O)CC1O)CC=C(C)CCC=C(C)CCC=C(C)C 434.60 unknown https://doi.org/10.1016/0031-9422(89)80055-X
methyl 2-[(1R,5R)-5-acetyloxy-2-oxo-1-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]cyclohex-3-en-1-yl]acetate 101683230 Click to see CC(=CCCC(=CCCC(=CCC1(CC(C=CC1=O)OC(=O)C)CC(=O)OC)C)C)C 430.60 unknown https://doi.org/10.1016/0031-9422(95)00368-H
methyl 2-[(1R,5R)-5-hydroxy-2-oxo-1-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]cyclohex-3-en-1-yl]acetate 101683228 Click to see CC(=CCCC(=CCCC(=CCC1(CC(C=CC1=O)O)CC(=O)OC)C)C)C 388.50 unknown https://doi.org/10.1016/0031-9422(95)00368-H
methyl 2-[(1S,5S)-5-hydroxy-2-oxo-1-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]cyclohex-3-en-1-yl]acetate 101683229 Click to see CC(=CCCC(=CCCC(=CCC1(CC(C=CC1=O)O)CC(=O)OC)C)C)C 388.50 unknown https://doi.org/10.1016/0031-9422(95)00368-H
Methyl 2-[5-acetyloxy-2-oxo-1-(3,7,11-trimethyldodeca-2,6,10-trienyl)cyclohex-3-en-1-yl]acetate 163058807 Click to see CC(=CCCC(=CCCC(=CCC1(CC(C=CC1=O)OC(=O)C)CC(=O)OC)C)C)C 430.60 unknown https://doi.org/10.1016/0031-9422(95)00368-H
Methyl 2-[5-hydroxy-2-oxo-1-(3,7,11-trimethyldodeca-2,6,10-trienyl)cyclohex-3-en-1-yl]acetate 163053319 Click to see CC(=CCCC(=CCCC(=CCC1(CC(C=CC1=O)O)CC(=O)OC)C)C)C 388.50 unknown https://doi.org/10.1016/0031-9422(95)00368-H
Methyl 3-[2-hydroxy-4-oxo-1-(3,7,11-trimethyldodeca-2,6,10-trienyl)cyclopentyl]-3-methoxypropanoate 163037807 Click to see CC(=CCCC(=CCCC(=CCC1(CC(=O)CC1O)C(CC(=O)OC)OC)C)C)C 420.60 unknown https://doi.org/10.1016/0031-9422(89)80055-X
Methyl 3-ethoxy-3-[2-hydroxy-4-oxo-1-(3,7,11-trimethyldodeca-2,6,10-trienyl)cyclopentyl]propanoate 162934378 Click to see CCOC(CC(=O)OC)C1(CC(=O)CC1O)CC=C(C)CCC=C(C)CCC=C(C)C 434.60 unknown https://doi.org/10.1016/0031-9422(89)80055-X
> 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/10.1016/0031-9422(95)00368-H
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/0031-9422(95)00368-H
2,5-Dihydroxy-3-(3,7,11-trimethyldodeca-2,6,10-trienyl)benzaldehyde 129684342 Click to see CC(=CCCC(=CCCC(=CCC1=C(C(=CC(=C1)O)C=O)O)C)C)C 342.50 unknown https://doi.org/10.1016/0031-9422(89)80055-X
2,5-dihydroxy-3-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]benzaldehyde 14259035 Click to see CC(=CCCC(=CCCC(=CCC1=C(C(=CC(=C1)O)C=O)O)C)C)C 342.50 unknown https://doi.org/10.1016/0031-9422(89)80055-X
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/0031-9422(95)00368-H
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,5R,8S)-8-hydroxy-5-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-2-oxabicyclo[3.3.1]nonane-3,6-dione 101683232 Click to see CC(=CCCC(=CCCC(=CCC12CC(C(CC1=O)O)OC(=O)C2)C)C)C 374.50 unknown https://doi.org/10.1016/0031-9422(95)00368-H
(1S,5S,8R)-8-hydroxy-5-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-2-oxabicyclo[3.3.1]nonane-3,6-dione 101683233 Click to see CC(=CCCC(=CCCC(=CCC12CC(C(CC1=O)O)OC(=O)C2)C)C)C 374.50 unknown https://doi.org/10.1016/0031-9422(95)00368-H
(1S,5S)-5-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-2-oxabicyclo[3.3.1]non-7-ene-3,6-dione 101683235 Click to see CC(=CCCC(=CCCC(=CCC12CC(C=CC1=O)OC(=O)C2)C)C)C 356.50 unknown https://doi.org/10.1016/0031-9422(95)00368-H
(3aR,7aR)-3a-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-4,7a-dihydro-3H-1-benzofuran-2,5-dione 14259037 Click to see CC(=CCCC(=CCCC(=CCC12CC(=O)C=CC1OC(=O)C2)C)C)C 356.50 unknown https://doi.org/10.1016/0031-9422(89)80055-X
(4R,4aR,7aR)-4-ethoxy-4a-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-4,5,7,7a-tetrahydro-3H-cyclopenta[b]pyran-2,6-dione 14259041 Click to see CCOC1CC(=O)OC2C1(CC(=O)C2)CC=C(C)CCC=C(C)CCC=C(C)C 402.60 unknown https://doi.org/10.1016/0031-9422(89)80055-X
(4R,4aR,7aR)-4-methoxy-4a-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-4,5,7,7a-tetrahydro-3H-cyclopenta[b]pyran-2,6-dione 14259039 Click to see CC(=CCCC(=CCCC(=CCC12CC(=O)CC1OC(=O)CC2OC)C)C)C 388.50 unknown https://doi.org/10.1016/0031-9422(89)80055-X
3a-(3,7,11-trimethyldodeca-2,6,10-trienyl)-4,7a-dihydro-3H-1-benzofuran-2,5-dione 163086753 Click to see CC(=CCCC(=CCCC(=CCC12CC(=O)C=CC1OC(=O)C2)C)C)C 356.50 unknown https://doi.org/10.1016/0031-9422(89)80055-X
4-ethoxy-4a-(3,7,11-trimethyldodeca-2,6,10-trienyl)-4,5,7,7a-tetrahydro-3H-cyclopenta[b]pyran-2,6-dione 162851554 Click to see CCOC1CC(=O)OC2C1(CC(=O)C2)CC=C(C)CCC=C(C)CCC=C(C)C 402.60 unknown https://doi.org/10.1016/0031-9422(89)80055-X
4-methoxy-4a-(3,7,11-trimethyldodeca-2,6,10-trienyl)-4,5,7,7a-tetrahydro-3H-cyclopenta[b]pyran-2,6-dione 163010714 Click to see CC(=CCCC(=CCCC(=CCC12CC(=O)CC1OC(=O)CC2OC)C)C)C 388.50 unknown https://doi.org/10.1016/0031-9422(89)80055-X
5-(3,7,11-Trimethyldodeca-2,6,10-trienyl)-2-oxabicyclo[3.3.1]non-7-ene-3,6-dione 73810148 Click to see CC(=CCCC(=CCCC(=CCC12CC(C=CC1=O)OC(=O)C2)C)C)C 356.50 unknown https://doi.org/10.1016/0031-9422(95)00368-H
8-Hydroxy-5-(3,7,11-trimethyldodeca-2,6,10-trienyl)-2-oxabicyclo[3.3.1]nonane-3,6-dione 162912961 Click to see CC(=CCCC(=CCCC(=CCC12CC(C(CC1=O)O)OC(=O)C2)C)C)C 374.50 unknown https://doi.org/10.1016/0031-9422(95)00368-H
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0031-9422(95)00368-H
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(95)00368-H
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(95)00368-H

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