about
Determination of non-steroidal anti-inflammatory drugs in pharmaceuticals and human serum by dual-mode gradient HPLC and fluorescence detectionVery small injected samples to study chloroquine and quinine in human serum using capillary-LC and native fluorescence.Determination of free amino acids in African gourd seed milks by capillary electrophoresis with light-emitting diode induced fluorescence and laser-induced fluorescence detection.Antioxidant, 5-lipoxygenase inhibitory and cytotoxic activities of compounds isolated from the Ferula lutea flowers.Antioxidant activity and hepatoprotective potential of Cedrelopsis grevei on cypermethrin induced oxidative stress and liver damage in male mice.Chemical composition and anticancer, antiinflammatory, antioxidant and antimalarial activities of leaves essential oil of Cedrelopsis grevei.Chemical composition and antioxidant, anti-inflammatory, and antiproliferation activities of pomegranate (Punica granatum) flowers.Assessment of antioxidant, anti-inflammatory, anti-cholinesterase and cytotoxic activities of pomegranate (Punica granatum) leaves.Chemical study and antimalarial, antioxidant, and anticancer activities of Melaleuca armillaris (Sol Ex Gateau) Sm essential oil.Synthesis, cytotoxic, anti-lipoxygenase and anti-acetylcholinesterase capacities of novel derivatives from harmine.Design, synthesis of novel pyranotriazolopyrimidines and evaluation of their anti-soybean lipoxygenase, anti-xanthine oxidase, and cytotoxic activities.Chemical composition and anticancer and antioxidant activities of Schinus molle L. and Schinus terebinthifolius Raddi berries essential oils.Two new unusual monoterpene acid glycosides from Acacia cyclops with potential cytotoxic activity.Synthesis of new isoxazoline derivatives from harmine and evaluation of their anti-Alzheimer, anti-cancer and anti-inflammatory activities.Oregano: chemical analysis and evaluation of its antimalarial, antioxidant, and cytotoxic activities.Pomegranate (Punica granatum) juices: chemical composition, micronutrient cations, and antioxidant capacity.Chemical composition, biological and cytotoxic activities of plant extracts and compounds isolated from Ferula lutea.Composition and anti-oxidant, anti-cancer and anti-inflammatory activities of Artemisia herba-alba, Ruta chalpensis L. and Peganum harmala L.Helichrysum gymnocephalum essential oil: chemical composition and cytotoxic, antimalarial and antioxidant activities, attribution of the activity origin by correlations.Chemical Composition and In Vitro Evaluation of Antimicrobial, Antioxidant and Antigerminative Properties of the Seed Oil from the Tunisian Endemic Ferula tunetana Pomel ex Batt.Synthesis and antiplasmodial activity of new indolone N-oxide derivatives.Chemical Composition and Behavioral Effects of Five Plant Essential Oils on the Green Pea Aphid Acyrthosiphon pisum (Harris) (Homoptera: Aphididae).Preliminary in vitro and in vivo evaluation of antidiabetic activity of Ducrosia anethifolia Boiss. and its linear furanocoumarins.Amelioration of prallethrin-induced oxidative stress and hepatotoxicity in rat by the administration of Origanum majorana essential oil.The influence of organ, season and drying method on chemical composition and antioxidant and antimicrobial activities of Juniperus phoenicea L. essential oils.Chemical composition and antimicrobial and antioxidant activities of essential oils and various extracts of Juniperus phoenicea L. (Cupressacees).Comparison between supercritical CO2 extraction and hydrodistillation for two species of eucalyptus: yield, chemical composition, and antioxidant activity.Bioactive flavones isolated from Tunisian Artemisia campestris L. Leaves.Comparison of different methods for extraction from Tetraclinis articulata: yield, chemical composition and antioxidant activity.Antimutagenic effect of Origanum majorana L. essential oil against prallethrin-induced genotoxic damage in rat bone marrow cells.New cytotoxic sesquiterpene lactones from Achillea cretica L. growing in Tunisia.Cytotoxicity of new secondary metabolites, fatty acids and tocols composition of seeds of Ducrosia anethifolia (DC.) Boiss.Alpha-phenyl-N-tert-butyl nitrone (PBN) derivatives: synthesis and protective action against microvascular damages induced by ischemia/reperfusion.Understanding Kombucha Tea Fermentation: A Review.Season's variation impact on Citrus aurantium leaves essential oil: chemical composition and biological activities.Synthesis of novel diazaphosphinanes coumarin derivatives with promoted cytotoxic and anti-tyrosinase activities.Synthesis and biological evaluation of novel pyrazolopyrimidines derivatives as anticancer and anti-5-lipoxygenase agents.Synthesis of a Series of γ-Keto Allyl Phosphonates.Phytochemical composition, protective and therapeutic effect on gastric ulcer and α-amylase inhibitory activity of Achillea biebersteinii Afan.Chemical Composition and in vitro Antimicrobial and Antioxidant Activities of Citrus aurantium L. Flowers Essential Oil (Neroli Oil)
P50
Q28218764-4680F3B5-FC4F-4B4D-87FC-406BABEEA8AEQ33269434-37777572-F6F0-40B8-9155-8131CE5AC114Q34822342-8F0E3868-2065-4B04-98D9-C6BB1FA977E7Q35360641-9342CEF2-4CFC-49BF-BB10-B2D64BDFA114Q35713068-5CBEF06C-4782-47D2-81C3-57097353EDB4Q38086388-45CB57EF-92BE-4EED-BE09-AD6E612EDAD8Q38453855-9B123B69-A652-4723-90A0-68ED3DC77DD1Q38455516-7AB372D8-1F69-40BE-A27C-F4C147B1979EQ38464363-7C1EC061-B561-4D4D-BF6D-1EF2A2F988AEQ38782393-0B9A8542-F6DC-4C5B-A2E2-45DD4FA82CD1Q38810796-3E2CC222-BF34-41D4-B91C-FC54DF29A213Q38903288-67AA2041-A3D9-4B64-B2A9-2D91BE89CE8DQ38969697-96E3BC9E-F004-4628-AAEC-C6F1C7D3416CQ38971088-49F10D61-818E-4F63-AC11-E14F4394023AQ38984156-5BE2E39F-4D4B-4190-9D60-021AC03BA3B8Q38984853-7538F4C0-9007-4C83-86C1-EC9D7E5100FAQ39020196-45A98C89-B03A-424E-98A5-E32B72E778C2Q39208042-0AD1618B-CA0B-4DCF-A19E-CE647487CECBQ39465644-16CFAF4E-F6CC-4322-A935-DA20E1890AB9Q39633145-4CF262AD-65A7-4555-90D2-8956C6440925Q39762661-D6A9D3AB-2978-4485-A695-0DDE44A56DBDQ41361112-A222F0CE-96C3-43B7-A3B6-574A4B58867DQ41697551-D1CE40EE-A326-4FE0-9017-FE0DB8487FFFQ41893667-DD24D249-0318-42E5-A38C-7C126A05B3F2Q43114070-4F399BB1-9C3B-4BF8-9863-1D05313D9263Q43246971-18A285E4-F380-4E2C-9F38-321171B90374Q43476206-DCF87C6C-0490-4FA4-B4F5-EC2D953B5CE9Q46247482-EA018B25-28F5-4762-98A5-DC6CE80E04C8Q46302014-E161043B-44C8-4AF0-97EA-16E971D62433Q46748897-B5BAC759-67C6-4328-8782-553FEB1A7195Q46792356-8EE65B1D-21DC-4BF3-B0AF-5388EC9FEEF4Q46941290-389BC8AA-9DB2-4640-961D-39A1BEA61FF8Q51798779-7E62367B-0081-4627-8D4B-CF0DA3DA7933Q52365970-A9032C6B-5DD1-4796-A983-D78CE940FF1FQ52741905-0B2E88CB-1460-4383-B3CC-AC2C6BA3D6DFQ52847230-802CF129-ADB7-45C3-92BF-8C851349B72DQ53763035-190B69D4-60C2-4B52-B526-5DDC08F1EA6CQ53772704-D2C5DDB0-952E-438C-8603-86A9D8147592Q53812580-23825B35-6AD8-40EB-B4B5-CEFC7A5CBE03Q59276702-B500B4BF-F29C-494A-9C84-D67540F62995
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jalloul Bouajila
@ast
Jalloul Bouajila
@en
Jalloul Bouajila
@es
Jalloul Bouajila
@nl
type
label
Jalloul Bouajila
@ast
Jalloul Bouajila
@en
Jalloul Bouajila
@es
Jalloul Bouajila
@nl
prefLabel
Jalloul Bouajila
@ast
Jalloul Bouajila
@en
Jalloul Bouajila
@es
Jalloul Bouajila
@nl
P106
P1153
16199832400
P31
P496
0000-0002-2439-5145