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Mortonia latisepala

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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 UUID64405955f37b2788196856
Scientific name Mortonia latisepala
Authority I.M.Johnst.
First published in J. Arnold Arbor. 21: 70 (1940)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mortonia scaberrima Rzed. Ciencia (Mexico) 15: 93 (1955)
Mortonia hidalgensis Standl. Contr. U.S. Natl. Herb. 23: 683 (1923)

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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-0001276650
Tropicos 50289851
KEW urn:lsid:ipni.org:names:164456-2
The Plant List tro-50289851
IPNI 164456-2
iNaturalist 284785
GBIF 5579549
Open Tree Of Life 50596

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)!
Title Authors Publication Released IDs
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
Minor polyhydroxyagarofuran derivatives from Mortonia hidalgensis L. Rodríguez-Hahn, L. Antúnez, M. Martínez, A.A. Sánchez, B. Esquivel, M. Soriano-García, A. Toscano Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81229-7
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/S0031-9422(00)81229-7
(5R,5aS,6S,9S,9aR)-5,6-dibenzoyloxy-9-hydroxy-2,2,5a,9-tetramethyl-5,6,7,8-tetrahydro-1-benzoxepine-9a-carboxylic acid 163012250 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/10.1016/S0040-4020(01)91125-1
(5S,5aS,6S,9S,9aS)-5,6-dibenzoyloxy-9-hydroxy-2,2,5a,9-tetramethyl-5,6,7,8-tetrahydro-1-benzoxepine-9a-carboxylic acid 163012249 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/10.1016/0031-9422(82)80137-4
(7-Benzoyloxy-2-hydroxy-2,6,9,10-tetramethyl-12-oxo-11,13-dioxatricyclo[8.2.1.01,6]tridecan-5-yl) benzoate 73823700 Click to see CC1CC(C2(C(CCC(C23C(=O)OC1(O3)C)(C)O)OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5 508.60 unknown https://doi.org/10.1016/S0031-9422(00)81229-7
[(1S,2S,5S,6S,7S)-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-11,13-dioxatricyclo[5.4.2.01,6]tridec-8-en-5-yl] benzoate 163007140 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
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/10.1016/0031-9422(82)80137-4
https://doi.org/10.1016/S0040-4020(01)91125-1
https://doi.org/10.1016/S0031-9422(00)81229-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
(4-Acetyloxy-5-benzoyloxy-2-hydroxy-2,6,10,10-tetramethyl-12-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) benzoate 162909033 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
https://doi.org/10.1016/S0031-9422(00)81229-7
(4-Acetyloxy-5-benzoyloxy-2,12-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl) benzoate 163049198 Click to see CC(=O)OC1CC(C23C(C(CC(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C(O3)(C)C)O)(C)O 552.60 unknown https://doi.org/10.1016/S0031-9422(00)81229-7
[(1S,2R,5S,6S,7S,9R)-5-acetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162972856 Click to see CC1CCC(C2(C13CC(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)COC(=O)C)OC(=O)C 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81229-7
[(1S,2S,4S,5R,6R,7S,9R,12R)-4-acetyloxy-5-benzoyloxy-2,12-dihydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 163049199 Click to see CC(=O)OC1CC(C23C(C(CC(C2(C1OC(=O)C4=CC=CC=C4)C)OC(=O)C5=CC=CC=C5)C(O3)(C)C)O)(C)O 552.60 unknown https://doi.org/10.1016/S0031-9422(00)81229-7
[5-Acetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162972855 Click to see CC1CCC(C2(C13CC(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)COC(=O)C)OC(=O)C 458.50 unknown https://doi.org/10.1016/S0031-9422(00)81229-7
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(2R)-2-hydroxy-N-[(2S,3S,4R)-1,3,4-trihydroxypentadecan-2-yl]pentacosanamide 15508081 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(CO)C(C(CCCCCCCCCCC)O)O)O 656.10 unknown https://doi.org/10.1016/0031-9422(82)80137-4

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