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Mortonia greggii

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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 UUID64405b358f927933507255
Scientific name Mortonia greggii
Authority A.Gray
First published in Smithsonian Contr. Knowl. 3(5): 35 (1852)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mortonia effusa Turcz. Bull. Soc. Imp. Naturalistes Moscou 31(I): 453 (1858)

Common names Top

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Language Common/alternative name
English gregg's saddlebush

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
  • Northern America
    • Mexico
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
    • South-central U.S.A.
      • Texas

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001292671
USDA Plants MOGR2
Tropicos 6600592
KEW urn:lsid:ipni.org:names:162242-1
The Plant List tro-6600592
Open Tree Of Life 755538
NCBI Taxonomy 123436
Nature Serve 2.160732
IPNI 162242-1
iNaturalist 165530
GBIF 5414282
EOL 489457

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
Natural Products/Bioactive Compounds as a Source of Anticancer Drugs Asma ST, Acaroz U, Imre K, Morar A, Shah SR, Hussain SZ, Arslan-Acaroz D, Demirbas H, Hajrulai-Musliu Z, Istanbullugil FR, Soleimanzadeh A, Morozov D, Zhu K, Herman V, Ayad A, Athanassiou C, Ince S Cancers (Basel) 15-Dec-2022
PMCID:PMC9777303
doi:10.3390/cancers14246203
PMID:36551687
Role of Plant-Derived Active Constituents in Cancer Treatment and Their Mechanisms of Action Khan AW, Farooq M, Haseeb M, Choi S Cells 13-Apr-2022
PMCID:PMC9031068
doi:10.3390/cells11081326
PMID:35456005
The Therapeutic Potential of Celastrol in Central Nervous System Disorders: Highlights from In Vitro and In Vivo Approaches Schiavone S, Morgese MG, Tucci P, Trabace L Molecules 03-Aug-2021
PMCID:PMC8347599
doi:10.3390/molecules26154700
PMID:34361850
Recent Updates on Anti-Inflammatory and Antimicrobial Effects of Furan Natural Derivatives Alizadeh M, Jalal M, Hamed K, Saber A, Kheirouri S, Pourteymour Fard Tabrizi F, Kamari N J Inflamm Res 19-Aug-2020
PMCID:PMC7443407
doi:10.2147/JIR.S262132
PMID:32884326
Lupeol, A Novel Anti-inflammatory and Anti-cancer Dietary Triterpene Saleem M Cancer Lett 22-May-2009
PMCID:PMC2764818
doi:10.1016/j.canlet.2009.04.033
PMID:19464787
Chemical correlation of mortonins A, C and D sesquiterpenoids from mortonia genus L. Rodríguez-Hahn, M. Martínez, M. Mora, C. Rodríguez, E. Díaz, M. Soriano-García, H. Campana Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(01)91125-1
The sesquiterpene constituents of Mortonia hidalgensis M. Martínez, A. Romo de Vivar, E. Díaz, M. Jiménez, L. Rodriguez-Hahn Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)80137-4

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/10.1016/0031-9422(82)80137-4
https://doi.org/10.1016/S0040-4020(01)91125-1
[(1R,2R,5R,6R,7R)-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-11,13-dioxatricyclo[5.4.2.01,6]tridec-8-en-5-yl] benzoate 163007139 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/10.1016/0031-9422(82)80137-4
[(1R,2S,5S,6S,7R)-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-11,13-dioxatricyclo[5.4.2.01,6]tridec-8-en-5-yl] benzoate 21680410 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/10.1016/0031-9422(82)80137-4
[(1S,2R,4S,5S,6R,7S)-4-acetyloxy-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-11,13-dioxatricyclo[5.4.2.01,6]tridec-8-en-5-yl] benzoate 162909596 Click to see CC(=O)OC1CC(C23C(=O)OC(C2(C1OC(=O)C4=CC=CC=C4)C)C=CC(O3)(C)C)(C)O 444.50 unknown https://doi.org/10.1016/0031-9422(82)80137-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(7-Benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl) benzoate 162928926 Click to see CC1(C2CC(C3(C(CCC(C3(C2=O)O1)(C)O)OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C 492.60 unknown https://doi.org/10.1016/0031-9422(82)80137-4
[(1R,2S,4R,5R,6R,7R,9S)-4-acetyloxy-5-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162909035 Click to see CC(=O)OC1CC(C23C(=O)C(CC(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C(O3)(C)C)(C)O 550.60 unknown https://doi.org/10.1016/0031-9422(82)80137-4
[(1R,2S,5S,6S,7S,9S)-7-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] benzoate 162928928 Click to see CC1(C2CC(C3(C(CCC(C3(C2=O)O1)(C)O)OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C 492.60 unknown https://doi.org/10.1016/0031-9422(82)80137-4

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