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Maytenus salicifolia

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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 UUID64405b3089584738141492
Scientific name Maytenus salicifolia
Authority Reissek
First published in Fl. Bras. 11(1): 10 (1861)

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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No germination or propagation data was added yet.

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-0001292540
Tropicos 6600217
KEW urn:lsid:ipni.org:names:162072-1
The Plant List tro-6600217
Open Tree Of Life 433225
NCBI Taxonomy 1081527
IPNI 162072-1
GBIF 3794167
EOL 8679617

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
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
Lupeol Stearate Accelerates Healing and Prevents Recurrence of Gastric Ulcer in Rodents Somensi LB, Costa P, Boeing T, Bolda Mariano LN, de Gregório E, E Silva AT, Longo B, Locatelli C, de Souza P, Magalhães CG, Pains Duarte L, da Silva LM Evid Based Complement Alternat Med 13-Apr-2022
PMCID:PMC9020945
doi:10.1155/2022/6134128
PMID:35463093
Antiangiogenic activity of PLGA-Lupeol implants for potential intravitreal applications Soares DC, de Paula Oliveira DC, Barcelos LS, Barbosa AS, Vieira LC, Townsend DM, Rubello D, de Barros AL, Duarte LP, Silva-Cunha A Biomed Pharmacother 27-May-2017
PMCID:PMC6522250
doi:10.1016/j.biopha.2017.05.093
PMID:28558353
Constituents of fruit pulp of Maytenus salicifolia and complete 1D/2D NMR data of 3β-hydroxy-D:B-friedo-olean-5-ene Frederico N. Valladao, Roqueline R. S. de Miranda, Gabriela S. de Oliveira, Gracia D. F. Silva, Lucienir P. Duarte, Sidney A. V. Filho Springer Science and Business Media LLC 05-Nov-2010
doi:10.1007/S10600-010-9716-0
Triterpene Esters Isolated from Leaves of <i>Maytenus salicifolia</i><scp>Reissek</scp> Roqueline Rodrigues Silva de Miranda, Grácia Divina de Fátima Silva, Lucienir Pains Duarte, Sidney Augusto Vieira Filho Wiley 19-Apr-2007
doi:10.1002/HLCA.200790068
Structural determination of 3beta-stearyloxy-urs-12-ene from Maytenus salicifolia by 1D and 2D NMR and quantitative 13C NMR spectroscopy. Miranda RR, Silva GD, Duarte LP, Fortes IC, Filho SA Magn Reson Chem 01-Feb-2006
doi:10.1002/MRC.1734
PMID:16358293

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl) octadecanoate 14486641 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 693.20 unknown https://doi.org/10.1002/HLCA.200790068
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-yl) octadecanoate 162976276 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)(C)C)C 693.20 unknown https://doi.org/10.1002/HLCA.200790068
(4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl) octadecanoate 5318378 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 693.20 unknown https://doi.org/10.1002/MRC.1734
https://doi.org/10.1002/HLCA.200790068
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] octadecanoate 14486643 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 693.20 unknown https://doi.org/10.1002/HLCA.200790068
[(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] octadecanoate 21159082 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 693.20 unknown https://doi.org/10.1002/MRC.1734
https://doi.org/10.1002/HLCA.200790068
[(3S,4aR,6aS,6aR,6bR,8aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-yl] octadecanoate 102079536 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5=CC(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)(C)C)C 693.20 unknown https://doi.org/10.1002/HLCA.200790068
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1002/MRC.1734
5-Glutinen-3-ol 12309493 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1007/S10600-010-9716-0
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1002/MRC.1734
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1007/S10600-010-9716-0
https://doi.org/10.1002/MRC.1734
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1002/MRC.1734
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/10.1002/MRC.1734
https://doi.org/10.1007/S10600-010-9716-0
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1002/MRC.1734
Friedelin 91472 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/10.1002/MRC.1734
https://doi.org/10.1007/S10600-010-9716-0
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1007/S10600-010-9716-0
Lup-20(29)-en-3-ol, (3beta)- 521518 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/10.1002/MRC.1734
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/10.1002/MRC.1734
Olean-12-en-3beta-ol 225689 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1007/S10600-010-9716-0
https://doi.org/10.1002/MRC.1734

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