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Cryptocarya latifolia

Cryptocarya latifolia - 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 UUID64401440ee959933519105
Scientific name Cryptocarya latifolia
Authority Sond.
First published in Linnaea 23: 101 (1850)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Afrikaans breëblaarkweper

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

Area

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© OpenStreetMap
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000628000
Tropicos 17800732
KEW urn:lsid:ipni.org:names:463966-1
The Plant List kew-2746045
Open Tree Of Life 5232060
Observations.org 457710
NCBI Taxonomy 1041618
IPNI 463966-1
iNaturalist 583084
GBIF 4175963
EOL 5398136
Elurikkus 480540

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
A Review of Plant-Based Therapies for the Treatment of Urinary Tract Infections in Traditional Southern African Medicine Cock I, Mavuso N, Van Vuuren S Evid Based Complement Alternat Med 29-Jul-2021
PMCID:PMC8346297
doi:10.1155/2021/7341124
PMID:34367307
South Africa’s Best BARK Medicines Prescribed at the Johannesburg Muthi Markets for Skin, Gut, and Lung Infections: MIC’s and Brine Shrimp Lethality Khumalo GP, Sadgrove NJ, Van Vuuren SF, Van Wyk BE Antibiotics (Basel) 07-Jun-2021
PMCID:PMC8227155
doi:10.3390/antibiotics10060681
PMID:34200286
African Plant-Based Natural Products with Antivirulence Activities to the Rescue of Antibiotics Mahavy CE, Duez P, ElJaziri M, Rasamiravaka T Antibiotics (Basel) 19-Nov-2020
PMCID:PMC7699609
doi:10.3390/antibiotics9110830
PMID:33228261
The traditional use of southern African medicinal plants for the treatment of bacterial respiratory diseases: A review of the ethnobotany and scientific evaluations Cock IE, Van Vuuren SF J Ethnopharmacol 27-Jul-2020
PMCID:PMC7383173
doi:10.1016/j.jep.2020.113204
PMID:32730881
PHYTOCHEMICAL, ELEMENTAL AND BIOTECHNOLOGICAL STUDY OF CRYPTOCARYA LATIFOLIA Hamza MF, Shaik S, Moodley R Afr J Tradit Complement Altern Med 03-Jul-2016
PMCID:PMC5566154
doi:10.21010/ajtcam.v13i4.11
PMID:28852722
A Unified Synthetic Strategy to the Cryptocarya Family of Natural Products Exploiting Anion Relay Chemistry (ARC) Melillo B, Smith AB III Org Lett 24-Apr-2013
PMCID:PMC3671372
doi:10.1021/ol400857k
PMID:23614670
De Novo Synthesis of Natural Products via the Asymmetric Hydration of Polyenes Wang Y, Xing Y, Zhang Q, O’Doherty GA Chem Commun (Camb) 11-May-2011
PMCID:PMC5815319
doi:10.1039/c1cc11791b
PMID:21559534
α-Pyrones and their derivatives from two Cryptocarya species Siegfried E. Drewes, Marion M. Horn, Robert Scott Shaw Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)92696-6
α-Pyrone from Cryptocarya latifolia—A structural isomer of umuravumbolide Siegried E. Drewes, Marion M. Horn, C. Saroja Wijewardene Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(96)81093-4
5,6-dihydro-α-pyrones and two bicyclic tetrahydro-α-pyrone derivatives from Cryptocarya latifolia Siegfried E. Drewes, Bethuel M. Sehlapelo, Marion M. Horn, Robert Scott-Shaw, Peter Sandor Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(94)00828-H
A 6-substituted 5,6-dihydro-α-pyrone from two species of Cryptocarya Bethuel M. Sehlapelo, Siegfried E. Drewes, Robert Scott-Shaw Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90368-6

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 / Styrenes
Goniothalamin 6440856 Click to see C1C=CC(=O)OC1C=CC2=CC=CC=C2 200.23 unknown https://doi.org/10.1016/0031-9422(95)92696-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(2R,4R,6S)-4,6-diacetyloxy-7-[(2R)-6-oxo-2,3-dihydropyran-2-yl]heptan-2-yl] acetate 162988652 Click to see CC(CC(CC(CC1CC=CC(=O)O1)OC(=O)C)OC(=O)C)OC(=O)C 370.40 unknown https://doi.org/10.1016/0031-9422(94)00828-H
[4,6-Diacetyloxy-7-(6-oxo-2,3-dihydropyran-2-yl)heptan-2-yl] acetate 85387158 Click to see CC(CC(CC(CC1CC=CC(=O)O1)OC(=O)C)OC(=O)C)OC(=O)C 370.40 unknown https://doi.org/10.1016/0031-9422(94)00828-H
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(2R,4R)-4-acetyloxy-5-[(1R,3S,5S)-7-oxo-2,6-dioxabicyclo[3.3.1]nonan-3-yl]pentan-2-yl] acetate 162957292 Click to see CC(CC(CC1CC2CC(O1)CC(=O)O2)OC(=O)C)OC(=O)C 328.36 unknown https://doi.org/10.1016/0031-9422(94)00828-H
[(2R,4R)-4-acetyloxy-5-[(2R)-6-oxo-2,3-dihydropyran-2-yl]pentan-2-yl] acetate 72189089 Click to see CC(CC(CC1CC=CC(=O)O1)OC(=O)C)OC(=O)C 284.30 unknown https://doi.org/10.1016/0031-9422(94)00828-H
[4-Acetyloxy-5-(6-oxo-2,3-dihydropyran-2-yl)pentan-2-yl] acetate 85313065 Click to see CC(CC(CC1CC=CC(=O)O1)OC(=O)C)OC(=O)C 284.30 unknown https://doi.org/10.1016/0031-9422(94)00828-H
[4-Acetyloxy-5-(7-oxo-2,6-dioxabicyclo[3.3.1]nonan-3-yl)pentan-2-yl] acetate 72771708 Click to see CC(CC(CC1CC2CC(O1)CC(=O)O2)OC(=O)C)OC(=O)C 328.36 unknown https://doi.org/10.1016/0031-9422(94)00828-H
Cryptocaryolone diacetate 11771797 Click to see CC(CC(CC1CC2CC(O1)CC(=O)O2)OC(=O)C)OC(=O)C 328.36 unknown https://doi.org/10.1016/0031-9422(94)00828-H
https://doi.org/10.1016/0031-9422(95)92696-6
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(1R,5S,7R)-7-[(2S,4S)-2,4-dihydroxypentyl]-2,6-dioxabicyclo[3.3.1]nonan-3-one 163067647 Click to see CC(CC(CC1CC2CC(O1)CC(=O)O2)O)O 244.28 unknown https://doi.org/10.1016/0031-9422(94)00828-H
7-(2,4-Dihydroxypentyl)-2,6-dioxabicyclo[3.3.1]nonan-3-one 72775623 Click to see CC(CC(CC1CC2CC(O1)CC(=O)O2)O)O 244.28 unknown https://doi.org/10.1016/0031-9422(94)00828-H
https://doi.org/10.1016/0031-9422(95)92696-6
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
[(E,2R)-1-[(2R)-6-oxo-2,3-dihydropyran-2-yl]hept-4-en-2-yl] acetate 162908382 Click to see CCC=CCC(CC1CC=CC(=O)O1)OC(=O)C 252.31 unknown https://doi.org/10.1016/0031-9422(96)81093-4
1-(6-Oxo-2,3-dihydropyran-2-yl)hept-4-en-2-yl acetate 162908381 Click to see CCC=CCC(CC1CC=CC(=O)O1)OC(=O)C 252.31 unknown https://doi.org/10.1016/0031-9422(96)81093-4
> Phenylpropanoids and polyketides / Cinnamyl alcohols
2-(4,6-Dihydroxy-8-phenylocta-1,7-dienyl)-2,3-dihydropyran-6-one 496083 Click to see C1C=CC(=O)OC1C=CCC(CC(C=CC2=CC=CC=C2)O)O 314.40 unknown https://doi.org/10.1016/S0031-9422(00)90368-6
CID 11716631 11716631 Click to see C1C=CC(=O)OC1C=CCC(CC(C=CC2=CC=CC=C2)O)O 314.40 unknown https://doi.org/10.1016/0031-9422(95)92696-6

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