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Senegalia berlandieri

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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 UUID643fd5f9291dc897913565
Scientific name Senegalia berlandieri
Authority (Benth.) Britton & Rose
First published in N.L.Britton & al. (eds.), N. Amer. Fl.23: 109 (1928)

Description Top

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Synonyms Top

Scientific name Authority First published in
Acacia berlandieri Benth. London J. Bot.1: 522 (1842)
Acacia tephroloba A.Gray Smithsonian Contr. Knowl.3(5): 65 (1852)

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000166114
KEW urn:lsid:ipni.org:names:234302-2
Open Tree Of Life 112136
NCBI Taxonomy 138013
IUCN Red List 152909937
GBIF 2980082
USDA GRIN 414830

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
The Fabaceae in Northeastern Mexico (Subfamily Caesalpinioideae, Mimosoideae Clade, Tribes Mimoseae, Acacieae, and Ingeae) Estrada-Castillón E, Villarreal-Quintanilla JÁ, Cuéllar-Rodríguez G, Encina-Domínguez JA, Martínez-Ávalos JG, Mora-Olivo A, Sánchez-Salas J Plants (Basel) 30-Jan-2024
PMCID:PMC10857220
doi:10.3390/plants13030403
PMID:38337936
Effect of Replacing Sorghum Stubble with Tillandsia recurvata (L.) on Liveweight Change, Blood Metabolites, and Hematic Biometry of Goats Gámez-Vázquez HG, Rosales-Nieto CA, Urrutia-Morales J, Mellado M, Meza-Herrera CA, Vázquez-García JM, Hernández-Arteaga LE, Negrete-Sánchez LO, Loredo-Osti C, Rivas-Jacobo MA, Beltrán-López S Biology (Basel) 28-Mar-2022
PMCID:PMC9032657
doi:10.3390/biology11040517
PMID:35453716
Pharmacological assessment of the heartwood of Acacia raddiana Willd for antifungal potential Singh R, Choudhary A, Ram R Mater Today Proc 14-Mar-2022
PMCID:PMC8919969
doi:10.1016/j.matpr.2022.03.133
PMID:35311216
Metabarcoding of the phytotelmata of Pseudalcantarea grandis (Bromeliaceae) from an arid zone Herrera-García JA, Martinez M, Zamora-Tavares P, Vargas-Ponce O, Hernández-Sandoval L, Rodríguez-Zaragoza FA PeerJ 27-Jan-2022
PMCID:PMC8801176
doi:10.7717/peerj.12706
PMID:35127281
Phytochemicals: Potential Therapeutic Modulators of Radiation Induced Signaling Pathways Jit BP, Pradhan B, Dash R, Bhuyan PP, Behera C, Behera RK, Sharma A, Alcaraz M, Jena M Antioxidants (Basel) 27-Dec-2021
PMCID:PMC8773162
doi:10.3390/antiox11010049
PMID:35052553
Hypoglycemic Effects of Plant Flavonoids: A Review Sok Yen F, Shu Qin C, Tan Shi Xuan S, Jia Ying P, Yi Le H, Darmarajan T, Gunasekaran B, Salvamani S Evid Based Complement Alternat Med 08-Dec-2021
PMCID:PMC8674047
doi:10.1155/2021/2057333
PMID:34925525
Impacts of land cover change on the plant resources of an endangered pollinator Gómez-Ruiz EP, Lacher Jr TE, Moreno-Talamantes A, Flores Maldonado JJ PeerJ 05-Oct-2021
PMCID:PMC8500086
doi:10.7717/peerj.11990
PMID:34707921
Phytochemicals With Anti 5-alpha-reductase Activity: A Prospective For Prostate Cancer Treatment Azizi A, Mumin NH, Shafqat N F1000Res 06-Jul-2021
PMCID:PMC8276191
doi:10.12688/f1000research.51066.1
PMID:34316358
High Throughput Profiling of Flavonoid Abundance in Agave lechuguilla Residue-Valorizing under Explored Mexican Plant Morreeuw ZP, Castillo-Quiroz D, Ríos-González LJ, Martínez-Rincón R, Estrada N, Melchor-Martínez EM, Iqbal HM, Parra-Saldívar R, Reyes AG Plants (Basel) 03-Apr-2021
PMCID:PMC8067008
doi:10.3390/plants10040695
PMID:33916866
T N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771678
doi:10.1016/B978-0-7020-7463-9.50028-8
Antidiabetic Potential of Medicinal Plants and Their Active Components Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J Biomolecules 30-Sep-2019
PMCID:PMC6843349
doi:10.3390/biom9100551
PMID:31575072
Pharmacokinetic and Pharmacodynamic Aspects of Peyote and Mescaline: Clinical and Forensic Repercussions Dinis-Oliveira RJ, Pereira CL, Dias da Silva D Curr Mol Pharmacol 01-Aug-2019
PMCID:PMC6864602
doi:10.2174/1874467211666181010154139
PMID:30318013
Optimal leaf water status regulation of plants in drylands Ratzmann G, Zakharova L, Tietjen B Sci Rep 06-Mar-2019
PMCID:PMC6403219
doi:10.1038/s41598-019-40448-2
PMID:30842586
Targeting Cancer with Phytochemicals via Their Fine Tuning of the Cell Survival Signaling Pathways Chirumbolo S, Bjørklund G, Lysiuk R, Vella A, Lenchyk L, Upyr T Int J Mol Sci 12-Nov-2018
PMCID:PMC6274856
doi:10.3390/ijms19113568
PMID:30424557
Biotechnology, In Vitro Production of Natural Bioactive Compounds, Herbal Preparation, and Disease Management (Treatment and Prevention) Alamgir AN Therapeutic Use of Medicinal Plants and their Extracts: Volume 2 24-Jun-2018
PMCID:PMC7123938
doi:10.1007/978-3-319-92387-1_7

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
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.1021/JF00120A008
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Candicine 23135 Click to see C[N+](C)(C)CCC1=CC=C(C=C1)O 180.27 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
Hordenine 68313 Click to see CN(C)CCC1=CC=C(C=C1)O 165.23 unknown https://doi.org/10.2527/1993.712467X
https://doi.org/10.1016/S0031-9422(97)00240-9
Mescaline 4076 Click to see COC1=CC(=CC(=C1OC)OC)CCN 211.26 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
N-Methylmescaline 138365 Click to see CNCCC1=CC(=C(C(=C1)OC)OC)OC 225.28 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
N-Methylphenethylamine 11503 Click to see CNCCC1=CC=CC=C1 135.21 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
N-Methyltyramine 9727 Click to see CNCCC1=CC=C(C=C1)O 151.21 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
Phenethylamine 1001 Click to see C1=CC=C(C=C1)CCN 121.18 unknown https://doi.org/10.2527/1993.712467X
https://doi.org/10.1016/S0031-9422(97)00240-9
Tyramine 5610 Click to see C1=CC(=CC=C1CCN)O 137.18 unknown https://doi.org/10.2527/1993.712467X
https://doi.org/10.1016/S0031-9422(97)00240-9
> Benzenoids / Benzene and substituted derivatives / Phenethylamines / Amphetamines and derivatives
4-(2-Aminopropyl)phenol 3651 Click to see CC(CC1=CC=C(C=C1)O)N 151.21 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
4-Methoxyamphetamine 31721 Click to see CC(CC1=CC=C(C=C1)OC)N 165.23 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
Amphetamine 3007 Click to see CC(CC1=CC=CC=C1)N 135.21 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
Methamphetamine 10836 Click to see CC(CC1=CC=CC=C1)NC 149.23 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
> Benzenoids / Benzene and substituted derivatives / Toluenes / Nitrotoluenes / Dinitrotoluenes
Musk ambrette 6753 Click to see CC1=C(C=C(C(=C1[N+](=O)[O-])OC)C(C)(C)C)[N+](=O)[O-] 268.27 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
> Benzenoids / Dibenzocycloheptenes
Nortriptyline 4543 Click to see CNCCC=C1C2=CC=CC=C2CCC3=CC=CC=C31 263.40 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
> Benzenoids / Phenols / Benzenediols / Catechols / Catecholamines and derivatives
5-(2-Aminoethyl)-3-methoxybenzene-1,2-diol 54382520 Click to see COC1=CC(=CC(=C1O)O)CCN 183.20 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
Deoxyepinephrine 4382 Click to see CNCCC1=CC(=C(C=C1)O)O 167.20 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
Dopamine 681 Click to see C1=CC(=C(C=C1CCN)O)O 153.18 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
> Benzenoids / Phenols / Methoxyphenols
4-(2-Aminoethyl)-2-methoxyphenol 1669 Click to see COC1=C(C=CC(=C1)CCN)O 167.20 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
4-(2-Aminoethyl)-2,6-dimethoxyphenol 533955 Click to see COC1=CC(=CC(=C1O)OC)CCN 197.23 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1021/JF00120A008
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
Mimosine methyl ester 186729 Click to see COC(=O)C(CN1C=CC(=O)C(=C1)O)N 212.20 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
1-Phenylethylamine 7408 Click to see CC(C1=CC=CC=C1)N 121.18 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
https://doi.org/10.2527/1993.712467X
> Organoheterocyclic compounds / Oxolanes
2-Furanmethanol, 5-ethenyltetrahydro-alpha,alpha,5-trimethyl-, cis- 11116492 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown https://doi.org/10.1021/JF00120A008
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
3-(1-Methylpyrrolidin-2-yl)pyridine 942 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
Nicotine 89594 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(9S)-8-ethyl-4-methoxy-9-methyl-7,9-dihydro-6H-[1,3]dioxolo[4,5-h]isoquinoline 101017032 Click to see CCN1CCC2=CC(=C3C(=C2C1C)OCO3)OC 249.30 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
Anhalamine 69510 Click to see COC1=C(C(=C2CNCCC2=C1)O)OC 209.24 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
Anhalidine 2752318 Click to see CN1CCC2=CC(=C(C(=C2C1)O)OC)OC 223.27 unknown https://doi.org/10.1016/S0031-9422(97)00240-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (2S)-3-hydroxy-2-methylpropanoate 163030082 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)OC6C(C(C(C(O6)COC(=O)C(C)CO)O)O)O 842.70 unknown https://doi.org/10.1016/S0031-9422(97)00240-9

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