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Bursera suntui

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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 UUID64400e56c434b572401391
Scientific name Bursera suntui
Authority C.A.Toledo
First published in Biótica 9: 446 (1984 publ. 1985)

Description Top

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Synonyms Top

No known synonyms.

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-0000576332
Tropicos 50337638
KEW urn:lsid:ipni.org:names:273575-2
The Plant List kew-2687663
Open Tree Of Life 841937
NCBI Taxonomy 80329
IUCN Red List 137373952
IPNI 273575-2
iNaturalist 276394
GBIF 3993908

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
Fruit Size and Structure of Zoochorous Trees: Identifying Drivers for the Foraging Preferences of Fruit-Eating Birds in a Mexican Successional Dry Forest Almazán-Núñez RC, Alvarez-Alvarez EA, Sierra-Morales P, Rodríguez-Godínez R Animals (Basel) 23-Nov-2021
PMCID:PMC8697955
doi:10.3390/ani11123343
PMID:34944120
Oxygenated verticillene derivatives from Bursera suntui. García-Gutiérrez HA, Cerda-García-Rojas CM, Hernández-Hernández JD, Román-Marín LU, Joseph-Nathan P Phytochemistry 01-Nov-2008
doi:10.1016/J.PHYTOCHEM.2008.09.013
PMID:18952247
Verticillane derivatives from Bursera suntui and Bursera kerberi. Hernández-Hernández JD, Román-Marín LU, Cerda-García-Rojas CM, Joseph-Nathan P J Nat Prod 01-Nov-2005
doi:10.1021/NP050323E
PMID:16309306

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(12-Hydroxy-8,12,15,15-tetramethyl-4-bicyclo[9.3.1]pentadeca-3,7-dienyl)methyl acetate 73981756 Click to see CC1=CCCC(=CCC2CCC(C(C2(C)C)CC1)(C)O)COC(=O)C 348.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
https://doi.org/10.1021/NP050323E
(1R,3E,7E,11R)-4,8,12,15,15-pentamethylbicyclo[9.3.1]pentadeca-3,7,12-triene 101382707 Click to see CC1=CCCC(=CCC2CC=C(C(C2(C)C)CC1)C)C 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
(1S,3E,7E,11S,12S)-4,8,12,15,15-pentamethylbicyclo[9.3.1]pentadeca-3,7-dien-12-ol 92000846 Click to see CC1=CCCC(=CCC2CCC(C(C2(C)C)CC1)(C)O)C 290.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
https://doi.org/10.1021/NP050323E
(1S,3Z,7E,11R)-(+)-verticilla-3,7,12(18)-triene 15939522 Click to see CC1=CCCC(=CCC2CCC(=C)C(C2(C)C)CC1)C 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
(1S,3Z,7E,11S,12S)-(+)-verticilla-3,7-dien-12,20-diol 20-acetate 5326321 Click to see CC1=CCCC(=CCC2CCC(C(C2(C)C)CC1)(C)O)COC(=O)C 348.50 unknown https://doi.org/10.1021/NP050323E
https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
(1S,3Z,7E,11S,12S)-4-(hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-12-ol 5324497 Click to see CC1=CCCC(=CCC2CCC(C(C2(C)C)CC1)(C)O)CO 306.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
https://doi.org/10.1021/NP050323E
(1S,5S,8Z,11S,14S)-8-(hydroxymethyl)-14,15,15-trimethyl-4-methylidenebicyclo[9.3.1]pentadec-8-ene-5,14-diol 102031323 Click to see CC1(C2CCC(C1CCC(=C)C(CCC(=CC2)CO)O)(C)O)C 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
(4E,8E,11S)-4,8,14,15,15-pentamethylbicyclo[9.3.1]pentadeca-1(14),4,8-triene 135082972 Click to see CC1=CCCC(=CCC2CCC(=C(C2(C)C)CC1)C)C 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
(7,12-Dihydroxy-12,15,15-trimethyl-8-methylidene-4-bicyclo[9.3.1]pentadec-3-enyl)methyl acetate 163010083 Click to see CC(=O)OCC1=CCC2CCC(C(C2(C)C)CCC(=C)C(CC1)O)(C)O 364.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
[(1S,3Z,7S,11S,12S)-7,12-dihydroxy-12,15,15-trimethyl-8-methylidene-4-bicyclo[9.3.1]pentadec-3-enyl]methyl acetate 163010084 Click to see CC(=O)OCC1=CCC2CCC(C(C2(C)C)CCC(=C)C(CC1)O)(C)O 364.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
4-(Hydroxymethyl)-8,12,15,15-tetramethylbicyclo[9.3.1]pentadeca-3,7-dien-12-ol 73981755 Click to see CC1=CCCC(=CCC2CCC(C(C2(C)C)CC1)(C)O)CO 306.50 unknown https://doi.org/10.1021/NP050323E
https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
4,8,12,15,15-Pentamethylbicyclo[9.3.1]pentadeca-3,7-dien-12-ol 620816 Click to see CC1=CCCC(=CCC2CCC(C(C2(C)C)CC1)(C)O)C 290.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
https://doi.org/10.1021/NP050323E
4,8,12,15,15-Pentamethylbicyclo[9.3.1]pentadeca-3,7,12-triene 73115868 Click to see CC1=CCCC(=CCC2CC=C(C(C2(C)C)CC1)C)C 272.50 unknown https://doi.org/10.1021/NP050323E
https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
4,8,14,15,15-Pentamethylbicyclo[9.3.1]pentadeca-1(14),4,8-triene 85382130 Click to see CC1=CCCC(=CCC2CCC(=C(C2(C)C)CC1)C)C 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
4,8,15,15-Tetramethyl-12-methylidenebicyclo[9.3.1]pentadeca-3,7-diene 73200959 Click to see CC1=CCCC(=CCC2CCC(=C)C(C2(C)C)CC1)C 272.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
https://doi.org/10.1021/NP050323E
8-(Hydroxymethyl)-14,15,15-trimethyl-4-methylidenebicyclo[9.3.1]pentadec-8-ene-5,14-diol 162912401 Click to see CC1(C2CCC(C1CCC(=C)C(CCC(=CC2)CO)O)(C)O)C 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(15-Hydroxy-4,15,16,16-tetramethyl-5-oxatricyclo[10.3.1.04,6]hexadec-9-en-9-yl)methyl acetate 163016639 Click to see CC(=O)OCC1=CCC2CCC(C(C2(C)C)CCC3(C(O3)CC1)C)(C)O 364.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
(1S,4S,6S,9Z,12S,15S)-9-(hydroxymethyl)-4,15,16,16-tetramethyl-5-oxatricyclo[10.3.1.04,6]hexadec-9-en-15-ol 102031322 Click to see CC1(C2CCC(C1CCC3(C(O3)CCC(=CC2)CO)C)(C)O)C 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
[(1S,4S,6S,9Z,12S,15S)-15-hydroxy-4,15,16,16-tetramethyl-5-oxatricyclo[10.3.1.04,6]hexadec-9-en-9-yl]methyl acetate 163016640 Click to see CC(=O)OCC1=CCC2CCC(C(C2(C)C)CCC3(C(O3)CC1)C)(C)O 364.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013
9-(Hydroxymethyl)-4,15,16,16-tetramethyl-5-oxatricyclo[10.3.1.04,6]hexadec-9-en-15-ol 162867107 Click to see CC1(C2CCC(C1CCC3(C(O3)CCC(=CC2)CO)C)(C)O)C 322.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.09.013

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