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Mortonia diffusa

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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 UUID643ff5f5bacca436940509
Scientific name Mortonia diffusa
Authority Rose & Standl.
First published in Contr. U.S. Natl. Herb. 23: 683 (1923)

Description Top

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Synonyms Top

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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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Distribution (via POWO/KEW) Top

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-0000376790
Tropicos 50207538
KEW urn:lsid:ipni.org:names:164454-2
The Plant List kew-2372671
Open Tree Of Life 623426
NCBI Taxonomy 1034029
IPNI 164454-2
iNaturalist 284783
GBIF 5579561

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)!
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Title Authors Publication Released IDs
The Complete Chloroplast Genome of Catha edulis: A Comparative Analysis of Genome Features with Related Species Gu C, Tembrock LR, Zheng S, Wu Z Int J Mol Sci 09-Feb-2018
PMCID:PMC5855747
doi:10.3390/ijms19020525
PMID:29425128
Terpenoids from Montonia diffusa. Martínez V M, Corona MM, Vélez CS, Rodríguez-Hahn L, Joseph-Nathan P J Nat Prod 01-Jul-1988
doi:10.1021/NP50058A027
PMID:21401155

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 / Benzoic acid esters
(2-Hydroxy-2,6,10,10-tetramethyl-12-oxo-11,13-dioxatricyclo[5.4.2.01,6]tridec-8-en-5-yl) benzoate 14241007 Click to see CC1(C=CC2C3(C(CCC(C3(O1)C(=O)O2)(C)O)OC(=O)C4=CC=CC=C4)C)C 386.40 unknown https://doi.org/10.1021/NP50058A027
5,6-Dibenzoyloxy-9-hydroxy-2,2,5a,9-tetramethyl-5,6,7,8-tetrahydro-1-benzoxepine-9a-carboxylic acid 14108956 Click to see CC1(C=CC(C2(C(CCC(C2(O1)C(=O)O)(C)O)OC(=O)C3=CC=CC=C3)C)OC(=O)C4=CC=CC=C4)C 508.60 unknown https://doi.org/10.1021/NP50058A027
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4R,4aS,6aS,6aS,6bS,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 15559351 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP50058A027
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP50058A027
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/10.1021/NP50058A027

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Collections Top

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