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Dovyalis hebecarpa

Dovyalis hebecarpa - 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 UUID644035ef86f19081247656
Scientific name Dovyalis hebecarpa
Authority (Gardner) Warb.
First published in Nat. Pflanzenfam. 3(6a): 44 (1893)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rumea hebecarpa Gardner Calcutta J. Nat. Hist. 7: 9 (1847)
Aberia gardneri Clos Ann. Sci. Nat., Bot. sér. 4, 8: 235. 1857
Aberia hebecarpa (Gardner) Kuntze Revis. Gen. Pl. 1: 43 (1891)

Common names Top

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Language Common/alternative name
English ceylon gooseberry
Arabic رامحة نضرة الثمار
Persian انگور فرنگی سیلان
Dutch ketembilla
Russian Кетембилла
Sinhala කැටඹිල්ල
Tamil கொக்கு வெட்டி
Chinese 木莓
Chinese 锡兰莓
Chinese 酸味果
Chinese 锡兰醋栗

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
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Marianas
    • South-central Pacific
      • Cook Islands
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Puerto Rico
    • Central America
      • El Salvador

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000925151
USDA Plants DOHE2
Tropicos 13201126
INPN 447218
KEW urn:lsid:ipni.org:names:111561-1
The Plant List kew-4776119
Open Tree Of Life 353906
NCBI Taxonomy 688332
IPNI 111561-1
iNaturalist 401513
GBIF 2874134
Freebase /m/077md3
EPPO DOVHE
EOL 486339
USDA GRIN 14617
Wikipedia Dovyalis_hebecarpa
CMAUP NPO29086

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
Bioactive Dairy-Fermented Products and Phenolic Compounds: Together or Apart Wróblewska B, Kuliga A, Wnorowska K Molecules 14-Dec-2023
PMCID:PMC10746084
doi:10.3390/molecules28248081
PMID:38138571
Evaluation of Bioactive Compounds and Antioxidant Activity in 51 Minor Tropical Fruits of Ecuador Coyago-Cruz E, Guachamin A, Villacís M, Rivera J, Neto M, Méndez G, Heredia-Moya J, Vera E Foods 11-Dec-2023
PMCID:PMC10742603
doi:10.3390/foods12244439
PMID:38137243
Tri‐trophic interactions among Fopius arisanus, Tephritid species and host plants suggest apparent competition Moquet L, Jobart B, Fontaine R, Delatte H Ecol Evol 11-Jan-2023
PMCID:PMC9834009
doi:10.1002/ece3.9742
PMID:36644698
Red Fruits: Extraction of Antioxidants, Phenolic Content, and Radical Scavenging Determination: A Review Hidalgo GI, Almajano MP Antioxidants (Basel) 19-Jan-2017
PMCID:PMC5384171
doi:10.3390/antiox6010007
PMID:28106822
Dovyalicin-type spermidine alkaloids from Dovyalis species. Rasmussen B, Nkurunziza AJ, Witt M, Oketch-Rabah HA, Jaroszewski JW, Staerk D J Nat Prod 01-Sep-2006
doi:10.1021/NP060204E
PMID:16989523

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
> Alkaloids and derivatives / Aporphines
Bulbocapnine 12441 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3 325.40 unknown via CMAUP database
Corydine 10153 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC 341.40 unknown via CMAUP database
Corytuberine 160500 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC 327.40 unknown via CMAUP database
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
Noscapine 275196 Click to see CN1CCC2=CC3=C(C(=C2C1C4C5=C(C(=C(C=C5)OC)OC)C(=O)O4)OC)OCO3 413.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(+)-Corypalmine 12304090 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)O)OC)C=C1)OC 341.40 unknown via CMAUP database
(+)-Isocorypalmine 71261649 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown via CMAUP database
(13aR)-3,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol 1152279 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown via CMAUP database
(S)-Canadine 21171 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
6,6aalpha,11,14-Tetrahydro-9-methoxy-6beta-methyl-12H-benzo[a]-1,3-benzodioxolo[4,5-g]quinolizin-8-ol 25050515 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC5=C4OCO5)OC)O 339.40 unknown via CMAUP database
Corybulbine 10316181 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)O)OC 355.40 unknown via CMAUP database
Corydaline 101301 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)OC)OC)OC 369.50 unknown via CMAUP database
D-Tetrahydropalmatine 969488 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
Dehydrocorydaline 34781 Click to see CC1=C2C=CC(=C(C2=C[N+]3=C1C4=CC(=C(C=C4CC3)OC)OC)OC)OC 366.40 unknown via CMAUP database
Tetrahydropalmatine 72301 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
Thalictricavine 12443379 Click to see CC1C2C3=CC4=C(C=C3CCN2CC5=C1C=CC(=C5OC)OC)OCO4 353.40 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
(-)-Corycavine 90478581 Click to see CC1C2=C(CN(CCC3=CC4=C(C=C3C1=O)OCO4)C)C5=C(C=C2)OCO5 367.40 unknown via CMAUP database
Corycavamine 12304036 Click to see CC1C2=C(CN(CCC3=CC4=C(C=C3C1=O)OCO4)C)C5=C(C=C2)OCO5 367.40 unknown via CMAUP database
Corycavidine 12304035 Click to see CC1C2=C(CN(CCC3=CC4=C(C=C3C1=O)OCO4)C)C(=C(C=C2)OC)OC 383.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[4-hydroxy-2-[[(1R)-1-hydroxy-6-oxocyclohex-2-ene-1-carbonyl]oxymethyl]phenoxy]-6-(hydroxymethyl)oxan-3-yl] benzoate 162889087 Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=CC=C4)O 544.50 unknown https://doi.org/10.1021/NP060204E
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-[[(1S)-1-hydroxy-6-oxocyclohex-2-ene-1-carbonyl]oxymethyl]phenoxy]oxan-3-yl] benzoate 92212918 Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=CC=C4)O 528.50 unknown https://doi.org/10.1021/NP060204E
[4,5-Dihydroxy-2-[4-hydroxy-2-[(1-hydroxy-6-oxocyclohex-2-ene-1-carbonyl)oxymethyl]phenoxy]-6-(hydroxymethyl)oxan-3-yl] benzoate 73238325 Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=CC=C4)O 544.50 unknown https://doi.org/10.1021/NP060204E
2'-O-benzoyl-salicortin 404838 Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=CC=C4)O 528.50 unknown https://doi.org/10.1021/NP060204E
Tremulacin 442544 Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=CC=C4)O 528.50 unknown https://doi.org/10.1021/NP060204E
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Hydrohydrastinine 22301 Click to see CN1CCC2=CC3=C(C=C2C1)OCO3 191.23 unknown via CMAUP database

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