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Guatteria blepharophylla

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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 UUID64401f2417702593065747
Scientific name Guatteria blepharophylla
Authority Mart.
First published in Fl. Bras. 13(1): 38 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Annona sessiliflora Benth. Hooker's J. Bot. Kew Gard. Misc. 5: 8 (1853)
Guatteria brevicuspis R.E.Fr. Acta Horti Berg. 12: 491 (1939)
Guatteria cylindrocarpa R.E.Fr. Ark. Bot. , a.s., 3: 601 (1957)
Guatteria dielsiana R.E.Fr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 719 (1938)
Guatteria oxycarpa Poepp. ex Mart. Fl. Bras. 13(1): 38 (1841)
Guatteria sessiliflora Saff. Contr. U.S. Natl. Herb. 18: 6 (1914)
Guatteria ucayaliana Diels Notizbl. Bot. Gart. Berlin-Dahlem 9: 138. 1924
Guatteriopsis blepharophylla R.E.Fr. Acta Horti Berg. 12: 110 (1934)
Guatteriopsis sessiliflora R.E.Fr. Acta Horti Berg. 12: 109 (1934)

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 West-central
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000711171
Tropicos 1600181
INPN 764902
KEW urn:lsid:ipni.org:names:73326-1
The Plant List kew-2834266
Open Tree Of Life 711596
Observations.org 273077
NCBI Taxonomy 402568
IUCN Red List 103430633
IPNI 73326-1
GBIF 3154197
Elurikkus 366487

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
Prospecting Plant Extracts and Bioactive Molecules with Antimicrobial Activity in Brazilian Biomes: A Review de Queiroz JC, Leite JR, Vasconcelos AG Antibiotics (Basel) 21-Feb-2023
PMCID:PMC10044579
doi:10.3390/antibiotics12030427
PMID:36978294
Antitumor Effect of Guatteria olivacea R. E. Fr. (Annonaceae) Leaf Essential Oil in Liver Cancer Galvão AF, Araújo MD, Silva VR, Santos LD, Dias RB, Rocha CA, Soares MB, da Silva FM, Koolen HH, Zengin G, Costa EV, Bezerra DP Molecules 09-Jul-2022
PMCID:PMC9319081
doi:10.3390/molecules27144407
PMID:35889279
Essential Oil of the Plants Growing in the Brazilian Amazon: Chemical Composition, Antioxidants, and Biological Applications Ferreira OO, Cruz JN, de Moraes ÂA, de Jesus Pereira Franco C, Lima RR, dos Anjos TO, Siqueira GM, do Nascimento LD, Cascaes MM, de Oliveira MS, Andrade EH Molecules 08-Jul-2022
PMCID:PMC9318482
doi:10.3390/molecules27144373
PMID:35889245
The Potential Application of Natural Photosensitizers Used in Antimicrobial Photodynamic Therapy against Oral Infections Afrasiabi S, Partoazar A, Chiniforush N, Goudarzi R Pharmaceuticals (Basel) 20-Jun-2022
PMCID:PMC9227410
doi:10.3390/ph15060767
PMID:35745686
Traditional Uses, Phytochemistry and Pharmacological Activities of Annonacae Al Kazman BS, Harnett JE, Hanrahan JR Molecules 27-May-2022
PMCID:PMC9182277
doi:10.3390/molecules27113462
PMID:35684400
Essential Oils from Annonaceae Species from Brazil: A Systematic Review of Their Phytochemistry, and Biological Activities Cascaes MM, Carneiro OD, do Nascimento LD, de Moraes ÂA, de Oliveira MS, Cruz JN, Guilhon GM, Andrade EH Int J Mol Sci 09-Nov-2021
PMCID:PMC8623146
doi:10.3390/ijms222212140
PMID:34830022
Natural Photosensitizers in Antimicrobial Photodynamic Therapy Polat E, Kang K Biomedicines 21-May-2021
PMCID:PMC8224061
doi:10.3390/biomedicines9060584
PMID:34063973
Role of Photoactive Phytocompounds in Photodynamic Therapy of Cancer Muniyandi K, George B, Parimelazhagan T, Abrahamse H Molecules 08-Sep-2020
PMCID:PMC7570746
doi:10.3390/molecules25184102
PMID:32911753
Biologically Active Isoquinoline Alkaloids covering 2014-2018 Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH Med Res Rev 29-Jul-2020
PMCID:PMC7554109
doi:10.1002/med.21703
PMID:32729169
A Review of Resistance Mechanisms of Synthetic Insecticides and Botanicals, Phytochemicals, and Essential Oils as Alternative Larvicidal Agents Against Mosquitoes Senthil-Nathan S Front Physiol 25-Feb-2020
PMCID:PMC7052130
doi:10.3389/fphys.2019.01591
PMID:32158396
Anti-Infective and Anti-Cancer Properties of the Annona Species: Their Ethnomedicinal Uses, Alkaloid Diversity, and Pharmacological Activities Nugraha AS, Damayanti YD, Wangchuk P, Keller PA Molecules 03-Dec-2019
PMCID:PMC6930583
doi:10.3390/molecules24234419
PMID:31816948
Antitumor Effect of the Essential Oil from the Leaves of Croton matourensis Aubl. (Euphorbiaceae) de Lima EJ, Alves RG, D´Elia GM, da Anunciação TA, Silva VR, Santos LD, Soares MB, Cardozo NM, Costa EV, da Silva FM, Koolen HH, Bezerra DP Molecules 14-Nov-2018
PMCID:PMC6278459
doi:10.3390/molecules23112974
PMID:30441836
Extracts from Annona Muricata L. and Annona Reticulata L. (Annonaceae) Potently and Selectively Inhibit Plasmodium Falciparum Yamthe LR, Fokou PV, Mbouna CD, Keumoe R, Ndjakou BL, Djouonzo PT, Mfopa AN, Legac J, Tsabang N, Gut J, Rosenthal PJ, Boyom FF Medicines (Basel) 30-Apr-2015
PMCID:PMC5533161
doi:10.3390/medicines2020055
PMID:28930201
The Seasonal Variation of the Chemical Composition of Essential Oils from Porcelia macrocarpa R.E. Fries (Annonaceae) and Their Antimicrobial Activity da Silva EB, Soares MG, Mariane B, Vallim MA, Pascon RC, Sartorelli P, Lago JH Molecules 01-Nov-2013
PMCID:PMC6269654
doi:10.3390/molecules181113574
PMID:24189296
Chemical constituents isolated from the bark of Guatteria blepharophylla (Annonaceae) and their antiproliferative and antimicrobial activities Emmanoel V. Costa, Francisco de Assis Marques, Maria Lúcia B. Pinheiro, Raquel M. Braga, Camila Delarmelina, Marta Cristina T. Duarte, Ana Lúcia T. G. Ruiz, João Ernesto de Carvalho, Beatriz H. L. N. S. Maia FapUNIFESP (SciELO) 16-Jun-2011
doi:10.1590/S0103-50532011000600016

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
(-)-N-nornuciferine 624491 Click to see COC1=C(C2=C3C(CC4=CC=CC=C42)NCCC3=C1)OC 281.30 unknown https://doi.org/10.1590/S0103-50532011000600016
5-Hydroxy-14,15,16-trimethoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2(7),3,5,9,11,13(17),14-octaen-8-one 135703596 Click to see COC1=C(C(=C2C3=C(C=C(C=C3)O)C(=O)C4=NC=CC1=C24)OC)OC 337.30 unknown https://doi.org/10.1590/S0103-50532011000600016
7H-Dibenzo(de,g)quinolin-7-one, 3-hydroxy-1,2-dimethoxy- 158503 Click to see COC1=C2C3=CC=CC=C3C(=O)C4=NC=CC(=C24)C(=C1OC)O 307.30 unknown https://doi.org/10.1590/S0103-50532011000600016
https://doi.org/10.1016/S0031-9422(00)81237-6
Homomoschatoline 145779 Click to see COC1=C(C(=C2C3=CC=CC=C3C(=O)C4=NC=CC1=C24)OC)OC 321.30 unknown https://doi.org/10.1590/S0103-50532011000600016
https://doi.org/10.1016/S0031-9422(00)81237-6
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1590/S0103-50532011000600016
https://doi.org/10.1016/S0031-9422(00)81237-6
Lysicamine 122691 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC 291.30 unknown https://doi.org/10.1590/S0103-50532011000600016
Nornuciferine 41169 Click to see COC1=C(C2=C3C(CC4=CC=CC=C42)NCCC3=C1)OC 281.30 unknown https://doi.org/10.1590/S0103-50532011000600016
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
2,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-3,11-diol 9549059 Click to see COC1=C(C=C2CC3C4=CC(=C(C=C4CCN3CC2=C1)O)OC)O 327.40 unknown https://doi.org/10.1590/S0103-50532011000600016
Isocoreximine 10616178 Click to see COC1=C(C=C2CC3C4=CC(=C(C=C4CCN3CC2=C1)O)OC)O 327.40 unknown https://doi.org/10.1590/S0103-50532011000600016
> Benzenoids / Phenol ethers / Anisoles
5H-Indeno[1,2-b]pyridin-5-one, 8-methoxy-4-methyl- 457723 Click to see CC1=C2C(=NC=C1)C3=C(C2=O)C=CC(=C3)OC 225.24 unknown https://doi.org/10.1016/S0031-9422(00)81862-2
https://doi.org/10.1016/S0031-9422(00)81237-6
6-Methoxy-4-methylindeno[2,3-b]pyridin-9-one 163025765 Click to see CC1=C2C3=C(C=CC(=C3)OC)C(=O)C2=NC=C1 225.24 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
> Lignans, neolignans and related compounds
(3S,14S,22R)-27-hydroxy-16,26-dimethoxy-4,21-dimethyl-12,29,37-trioxa-4,21-diazaoctacyclo[28.2.2.17,11.110,14.114,18.124,28.03,8.022,36]octatriaconta-1(33),7(38),8,10,16,18(36),24(35),25,27,30(34),31-undecaen-15-one 162892163 Click to see CN1CCC2=CC3=C4C=C2C1CC5=CC=C(C=C5)OC6=C(C(=CC(=C6)CC7C8=C(CCN7C)C=C(C(=O)C8(O4)CO3)OC)OC)O 622.70 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1590/S0103-50532011000600016
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1590/S0103-50532011000600016
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
1,1,7-Trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 522266 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1590/S0103-50532011000600016
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1590/S0103-50532011000600016
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,10S,13R,17R)-4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,15-diol 367561 Click to see CC(CCC=C(C)C)C1CC(C2(C1(CC=C3C2=CCC4C3(CCC(C4(C)C)O)C)C)C)O 440.70 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
(3S,5R,10S,13R,14R,15S,17R)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,15-diol 162874212 Click to see CC(CCC=C(C)C)C1CC(C2(C1(CC=C3C2=CCC4C3(CCC(C4(C)C)O)C)C)C)O 440.70 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,15-diol 3741069 Click to see CC(CCC=C(C)C)C1CC(C2(C1(CC=C3C2=CCC4C3(CCC(C4(C)C)O)C)C)C)O 440.70 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
CID 11697907 11697907 Click to see CC(CCC=C(C)C)C1CC(C2(C1(CC=C3C2=CCC4C3(CCC(C4(C)C)O)C)C)C)O 440.70 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1590/S0103-50532011000600016
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/10.1590/S0103-50532011000600016
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/10.1590/S0103-50532011000600016
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/10.1590/S0103-50532011000600016
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones
4-(hydroxymethyl)-1H-indeno[1,2-b]pyridine-2,5-dione 101062013 Click to see C1=CC=C2C(=C1)C3=C(C2=O)C(=CC(=O)N3)CO 227.21 unknown https://doi.org/10.1016/S0031-9422(00)81862-2
https://doi.org/10.1016/S0031-9422(00)81237-6
4-(hydroxymethyl)-1H-indeno[2,1-b]pyridine-2,9-dione 162846113 Click to see C1=CC=C2C(=C1)C3=C(C2=O)NC(=O)C=C3CO 227.21 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
4-methyl-1H-indeno[1,2-b]pyridine-2,5-dione 457731 Click to see CC1=CC(=O)NC2=C1C(=O)C3=CC=CC=C32 211.22 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
https://doi.org/10.1016/S0031-9422(00)81862-2
4-methyl-1H-indeno[2,1-b]pyridine-2,9-dione 163063015 Click to see CC1=CC(=O)NC2=C1C3=CC=CC=C3C2=O 211.22 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
4-Methylindeno[2,1-b]pyridin-9-one 14626439 Click to see CC1=C2C3=CC=CC=C3C(=O)C2=NC=C1 195.22 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
Onychine 72584 Click to see CC1=C2C(=NC=C1)C3=CC=CC=C3C2=O 195.22 unknown https://doi.org/10.1016/S0031-9422(00)81237-6
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Lichexanthone 5358904 Click to see CC1=CC(=CC2=C1C(=O)C3=C(C=C(C=C3O2)OC)O)OC 286.28 unknown https://doi.org/10.1590/S0103-50532011000600016
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines
Dielsiquinone 10445779 Click to see CC1=C(C(=O)NC2=C1C(=O)C3=CC=CC=C3C2=O)OC 269.25 unknown https://doi.org/10.1016/S0031-9422(00)81237-6

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