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Synsepalum dulcificum

Synsepalum dulcificum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fedff097c7845900498
Scientific name Synsepalum dulcificum
Authority (Schumach. & Thonn.) Daniell
First published in Pharm. J. Trans. 11: 446 (1852)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pouteria dulcifica (Schumach. & Thonn.) Baehni Candollea 9: 276 (1942)
Richardella dulcifica (Schumach. & Thonn.) Baehni Boissiera 11: 97 (1965)
Sideroxylon dulcificum (Schumach. & Thonn.) A.DC. Prodr. 8: 183 (1844)
Bakeriella dulcifica Dubard Ann. Mus. Colon. Marseille , sér. 2, 10: 28 (1912)
Bumelia dulcifica Schumach. & Thonn. Beskr. Guin. Pl. : 130 (1827)
Synsepalum glycydorum Wernham J. Bot. 55: 82 (1917)

Common names Top

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Language Common/alternative name
English miraculous berry
English miracle fruit
Spanish fruta mágica
Spanish fruta milagrosa
Spanish fruta magica
Spanish baya mágica
Spanish baya magica
Akan asawa
Catalan fruit miracle
Danish mirakelbær
Danish mirakelfrugt
Danish mirakelbær (plante)
German miracle fruit
German mirakelfrucht
German wunderbeere
Estonian magustav imemari
Persian میراکل
French fruit miracle
Hebrew פרי הפלא
Croatian miracolina
Italian frutto miracoloso
Japanese ミラクルベリー
Japanese ミラクルフルーツ
Korean 미라클프루트
ln mombungá
Malayalam മിറാക്കിൾ ഫ്രൂട്ട്
Malayalam മിറക്കിൾ ഫ്രൂട്ട്
Malayalam miracle fruit
Norwegian Bokmål mirakelbær
Norwegian Bokmål mirakelfrukt
Dutch mirakelbes
Dutch wonderbes
Polish synsepal słodki
Portuguese fruta-milagrosa
Portuguese fruta milagrosa
Russian Магический фрукт
Somali miraha mucjisada
Tamil அற்புதப் பழம்
Thai มิราเคิล
Vietnamese cây thần kỳ
Vietnamese thần kỳ (cây)
yi וואונדער־פרוכט
Chinese 神秘果
Chinese 變味果

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
  • Africa
    • West Tropical Africa
      • Benin
      • Ghana
      • Ivory Coast
      • Nigeria
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000318142
UNII 4B4S74M66K
USDA Plants SYDU
Tropicos 28700443
INPN 447605
KEW urn:lsid:ipni.org:names:789924-1
The Plant List kew-199113
Open Tree Of Life 208039
NCBI Taxonomy 3743
IUCN Red List 87719610
IPNI 789924-1
iNaturalist 426748
GBIF 2886039
Freebase /m/0czb6sl
EOL 1149984
USDA GRIN 36056
Wikipedia Synsepalum_dulcificum

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
Neuroscience of taste: unlocking the human taste code Hellekant G BMC Neurosci 21-Mar-2024
PMCID:PMC10956246
doi:10.1186/s12868-024-00847-2
PMID:38515045
A metagenomic investigation of phytoplasma diversity in Australian vegetable growing regions Rodrigues Jardim B, Gambley C, Tran-Nguyen LT, Webster C, Kehoe M, Kinoti WM, Bond S, Davis R, Jones L, Pathania N, Sharman M, Chapman T, Rodoni BC, Constable FE Microb Genom 06-Mar-2024
PMCID:PMC10999746
doi:10.1099/mgen.0.001213
PMID:38446015
Exploring the diversity, bioactivity of endophytes, and metabolome in Synsepalum dulcificum Liu S, Hou Y, Zheng K, Ma Q, Wen M, Shao S, Wu S Front Microbiol 27-Feb-2024
PMCID:PMC10929569
doi:10.3389/fmicb.2024.1258208
PMID:38476934
Antimicrobial, antioxidant and antiproliferative activities of a galactose-binding seed lectin from Manilkara zapota Podder MK, Hossain MM, Kabir SR, Asaduzzaman AK, Hasan I Heliyon 17-Jan-2024
PMCID:PMC10835259
doi:10.1016/j.heliyon.2024.e24592
PMID:38312555
Geometric entropy of plant leaves: A measure of morphological complexity Muraleedharan V, Rajan SC, R J PLoS One 02-Jan-2024
PMCID:PMC10760904
doi:10.1371/journal.pone.0293596
PMID:38166118
Effect of Regular Consumption of a Miraculin-Based Food Supplement on Taste Perception and Nutritional Status in Malnourished Cancer Patients: A Triple-Blind, Randomized, Placebo-Controlled Clinical Trial-CLINMIR Pilot Protocol López-Plaza B, Gil Á, Menéndez-Rey A, Bensadon-Naeder L, Hummel T, Feliú-Batlle J, Palma-Milla S Nutrients 01-Nov-2023
PMCID:PMC10648678
doi:10.3390/nu15214639
PMID:37960292
Challenges of current treatment and exploring the future prospects of nanoformulations for treatment of atopic dermatitis Kakkar V, Saini K, Singh KK Pharmacol Rep 05-Sep-2023
PMCID:PMC10539427
doi:10.1007/s43440-023-00510-3
PMID:37668937
Application of Zebrafish as a Model for Anti-Cancer Activity Evaluation and Toxicity Testing of Natural Products Shen Y, Sheng R, Guo R Pharmaceuticals (Basel) 01-Jun-2023
PMCID:PMC10305033
doi:10.3390/ph16060827
PMID:37375774
Editorial: Bioaccessibility of food-derived bioactive components and their health-promoting mechanisms Ren T Front Nutr 17-May-2023
PMCID:PMC10231672
doi:10.3389/fnut.2023.1191671
PMID:37266133
Biological Activities of Miracle Berry Supercritical Extracts as Metabolic Regulators in Chronic Diseases Wagner S, Gómez de Cedrón M, Navarro del Hierro J, Martín-Hernández D, Siles MD, Santoyo S, Jaime L, Martín D, Fornari T, Ramírez de Molina A Int J Mol Sci 09-Apr-2023
PMCID:PMC10138767
doi:10.3390/ijms24086957
PMID:37108121
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Miracle fruit seed as a potential supplement for the treatment of learning and memory disorders in Alzheimer’s disease Huang XY, Xue LL, Chen TB, Huangfu LR, Wang TH, Xiong LL, Yu CY Front Pharmacol 11-Jan-2023
PMCID:PMC9873977
doi:10.3389/fphar.2022.1080753
PMID:36712676
Microencapsulation of Probiotics for Food Functionalization: An Update on Literature Reviews Sbehat M, Mauriello G, Altamimi M Microorganisms 30-Sep-2022
PMCID:PMC9610121
doi:10.3390/microorganisms10101948
PMID:36296223
Natural sources and encapsulating materials for probiotics delivery systems: Recent applications and challenges in functional food development Singh S, Gupta R, Chawla S, Gauba P, Singh M, Tiwari RK, Upadhyay S, Sharma S, Chanda S, Gaur S Front Nutr 21-Sep-2022
PMCID:PMC9534265
doi:10.3389/fnut.2022.971784
PMID:36211518
A comparative study of nutrient composition, bioactive properties and phytochemical characteristics of Stauntonia obovatifoliola flesh and pericarp Li R, Ru Y, Feng L, Wang Z, He X, Zhang X Front Nutr 09-Sep-2022
PMCID:PMC9501892
doi:10.3389/fnut.2022.1013971
PMID:36159481

Phytochemical Profile Top

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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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1007/S10600-010-9639-9
> 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 https://doi.org/10.1007/S10600-010-9639-9
> 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 https://doi.org/10.1007/S10600-010-9639-9
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid 12575 Click to see COC1=C(C=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1007/S10600-010-9639-9
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown https://doi.org/10.1007/S10600-010-9639-9
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1007/S10600-010-9639-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
2-(3-Hydroxy-3,7,11,15-tetramethylhexadecyl)-3,5,6-trimethylcyclohexa-2,5-diene-1,4-dione 24205 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown https://doi.org/10.1007/S10600-010-9658-6
alpha-Tocopherolquinone 2734086 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown https://doi.org/10.1007/S10600-010-9658-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/S10600-010-9658-6
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1007/S10600-010-9658-6
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1007/S10600-010-9658-6
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1007/S10600-010-9658-6
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1007/S10600-010-9658-6
Lupeol Acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1007/S10600-010-9658-6
> 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/10.1007/S10600-010-9658-6
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/10.1007/S10600-010-9658-6
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/10.1007/S10600-010-9658-6
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/10.1007/S10600-010-9658-6
> Organoheterocyclic compounds / Lactones / Beta propiolactones
(R)-4-Hydroxyoxetan-2-one 133613436 Click to see C1C(OC1=O)O 88.06 unknown https://doi.org/10.1080/14786419.2010.482934
4-Hydroxyoxetan-2-one 59077943 Click to see C1C(OC1=O)O 88.06 unknown https://doi.org/10.1080/14786419.2010.482934
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(E)-3-(4-Hydroxy-3-methoxyphenyl)-N-(2-(4-hydroxy-3-methoxyphenyl)ethyl)-2-propenamide 134313 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1007/S10600-010-9639-9
n-cis-Feruloyltyramine 6440659 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1007/S10600-010-9639-9
N-Feruloyl-3-methoxytyramine, (Z)- 5322166 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1007/S10600-010-9639-9
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1007/S10600-010-9639-9
N-trans-feruloylmethoxytyramine 5352115 Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1007/S10600-010-9639-9

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