Jacaratia spinosa - Unknown
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Internal ID UUID64402223583e5011562767
Scientific name Jacaratia spinosa
Authority (Aubl.) A.DC.
First published in Prodr. 15(1): 419 (1864)

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Synonyms Top

Scientific name Authority First published in
Jacaratia dodecaphylla f. longiflora Chodat Bull. Herb. Boissier 7(App. 1): 74 (1899)
Jacaratia dodecaphylla var. lucida Hassl. Bull. Herb. Boissier , sér. 2, 2: 745 (1902)
Carica dodecaphylla Vell. Fl. Flumin. 10: t. 132 (1829)
Carica spinosa Aubl. Hist. Pl. Guiane 2: 908 (1775)
Jacaratia dodecaphylla (Vell.) A.DC. Prodr. 15(1): 420 1864
Jacaratia costaricensis I.M.Johnst. Contr. Gray Herb. 70: 79 (1924)
Papaya spinosa DC. Encycl. 5: 3 (1804)

Common names Top

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Language Common/alternative name
Spanish jacarati á
Spanish yarakati-á
Spanish yarakati-a
Spanish yarakati á
Spanish yarakati a
Spanish yacaratia
Spanish papayo de monte
Spanish lagartillo
Spanish jacarati-á
Spanish jacarati-a
Spanish jacarati a
German jaracatiá
Esperanto jarakatiao
Esperanto jaracatiá
Esperanto dorna jarakatiao
Portuguese jaracatia spinosa
Portuguese mamãozinho
Portuguese mamoeiro-bravo
Portuguese mamoeiro-do-mato
Portuguese jaracatiá
Chinese 哈喀拉帝亞

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000734686
Tropicos 6100046
INPN 732868
KEW urn:lsid:ipni.org:names:30104966-2
The Plant List kew-2870238
Open Tree Of Life 131516
NCBI Taxonomy 1222208
IUCN Red List 56693194
iNaturalist 556969
GBIF 7269688
USDA GRIN 20606
Wikipedia Jacaratia_spinosa
CMAUP NPO27290
IPNI 30104966-2

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
Amazonian Invertebrates in the Traditional diet of the Paiter Suruí in Southeastern Brazil Molina AA, Ferreira MJ, Oyaxaka Suruí L, Norder LA, Costa Neto EM, Clement CR Hum Ecol Interdiscip J 28-Mar-2023
PMCID:PMC10044069
doi:10.1007/s10745-023-00402-3
PMID:37122818
Strengthening Structures in the Petiole–Lamina Junction of Peltate Leaves Wunnenberg J, Rjosk A, Neinhuis C, Lautenschläger T Biomimetics (Basel) 02-Apr-2021
PMCID:PMC8167582
doi:10.3390/biomimetics6020025
PMID:33918405
Ultra-long DNA molecule isolation from plant nuclei for ultra-long read genome sequencing Zerpa-Catanho D, Zhang X, Song J, Hernandez AG, Ming R STAR Protoc 17-Feb-2021
PMCID:PMC7902544
doi:10.1016/j.xpro.2021.100343
PMID:33665623
Edible Fruit Plant Species in the Amazon Forest Rely Mostly on Bees and Beetles as Pollinators Paz FS, Pinto CE, de Brito RM, Imperatriz-Fonseca VL, Giannini TC J Econ Entomol 13-Jan-2021
PMCID:PMC8042744
doi:10.1093/jee/toaa284
PMID:33440000
An integrative approach reveals five new species of highland papayas (Caricaceae, Vasconcellea) from northern Peru Tineo D, Bustamante DE, Calderon MS, Mendoza JE, Huaman E, Oliva M PLoS One 10-Dec-2020
PMCID:PMC7728213
doi:10.1371/journal.pone.0242469
PMID:33301452
Comparative analysis of chloroplast genomes in Vasconcellea pubescens A.DC. and Carica papaya L. Lin Z, Zhou P, Ma X, Deng Y, Liao Z, Li R, Ming R Sci Rep 25-Sep-2020
PMCID:PMC7519098
doi:10.1038/s41598-020-72769-y
PMID:32978465
Evaluation of conservation status of plants in Brazil’s Atlantic forest: An ethnoecological approach with Quilombola communities in Serra do Mar State Park Conde BE, Aragaki S, Ticktin T, Surerus Fonseca A, Yazbek PB, Sauini T, Rodrigues E PLoS One 18-Sep-2020
PMCID:PMC7500697
doi:10.1371/journal.pone.0238914
PMID:32946472
Yerba Mate (Ilex paraguariensis) Beverage: Nutraceutical Ingredient or Conveyor for the Intake of Medicinal Plants? Evidence from Paraguayan Folk Medicine Kujawska M Evid Based Complement Alternat Med 14-Mar-2018
PMCID:PMC5872613
doi:10.1155/2018/6849317
PMID:29725356
Management of Fruit Species in Urban Home Gardens of Argentina Atlantic Forest as an Influence for Landscape Domestication Furlan V, Pochettino ML, Hilgert NI Front Plant Sci 28-Sep-2017
PMCID:PMC5625568
doi:10.3389/fpls.2017.01690
PMID:29033964
Cognition, culture and utility: plant classification by Paraguayan immigrant farmers in Misiones, Argentina Kujawska M, Jiménez-Escobar ND, Nolan JM, Arias-Mutis D J Ethnobiol Ethnomed 25-Jul-2017
PMCID:PMC5526315
doi:10.1186/s13002-017-0169-4
PMID:28743302
Wild Edible Plants Used by the Polish Community in Misiones, Argentina Kujawska M, Łuczaj Ł Hum Ecol Interdiscip J 24-Nov-2015
PMCID:PMC4673098
doi:10.1007/s10745-015-9790-9
PMID:26691861
Genetic diversity analysis in a set of Caricaceae accessions using resistance gene analogues Sengupta S, Das B, Acharyya P, Prasad M, Ghose TK BMC Genet 10-Dec-2014
PMCID:PMC4271346
doi:10.1186/s12863-014-0137-0
PMID:25491793
Evidence for Emergence of Sex-Determining Gene(s) in a Centromeric Region in Vasconcellea parviflora Iovene M, Yu Q, Ming R, Jiang J Genetics 05-Dec-2014
PMCID:PMC4317651
doi:10.1534/genetics.114.173021
PMID:25480779
A comparative survey of genetic diversity among a set of Caricaceae accessions using microsatellite markers Sengupta S, Das B, Prasad M, Acharyya P, Ghose TK Springerplus 26-Jul-2013
PMCID:PMC3736075
doi:10.1186/2193-1801-2-345
PMID:23961410
Botany, Genetics and Ethnobotany: A Crossed Investigation on the Elusive Tapir's Diet in French Guiana Hibert F, Sabatier D, Andrivot J, Scotti-Saintagne C, Gonzalez S, Prévost MF, Grenand P, Chave J, Caron H, Richard-Hansen C PLoS One 03-Oct-2011
PMCID:PMC3185057
doi:10.1371/journal.pone.0025850
PMID:21991372

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see C1=CC(=C(C=C1O)C(=O)O)O 154.12 unknown via CMAUP database
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
3,5-Dihydroxybenzoic acid 7424 Click to see C1=C(C=C(C=C1O)O)C(=O)O 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
1,2-Ethanediol, 1-(4-hydroxy-3-methoxyphenyl)-, (R)- 688030 Click to see COC1=C(C=CC(=C1)C(CO)O)O 184.19 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(+)-Secoisolariciresinol 6336781 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
alpha-(beta-D-Glucopyranosyloxy)-trans-cinnamic acid 53385591 Click to see C1=CC=C(C=C1)C=C(C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)- 5274623 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2,3-Dihydro-5,7-dihydroxy-6-(beta-D-glucopyranosyl)-2beta-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one 45271033 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Eriodictyol-6-glucoside 102370911 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Hemiphloin 160711 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Eriodictyol-8-glucoside 122221847 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
1-[2,4,6-Trihydroxy-3-(beta-D-glucopyranosyloxy)phenyl]-3-(4-hydroxyphenyl)-1-propanone 102467789 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C(=C(C=C2O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 via CMAUP database
Isoquercetin 5280804 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 via CMAUP database
Quercetin 3-O-robinobioside 10371536 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Aspalathin 11282394 Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O)O 452.40 unknown via CMAUP database
Nothofagin 21722188 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown via CMAUP database

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