Publications by authors named "Talla Emmanuel"

Propolis is a resinous material collected by different bee species from various plant exudates and used to seal holes in honeycombs, smoothen the internal walls, embalm intruders, improve health and prevent diseases. From its -hexane extract, eight compounds were isolated and characterised as: mangiferonic acid (); 1-hydroxymangiferonic acid (), new natural product; mangiferolic acid(); 27-hydroxymangiferolic acid (), reported here for the first time as propolis constituent; 27-hydroxymangiferonic acid (); -amyrin (); -amyrin () and lupeol (). The chemical structures of the isolated compounds were elucidated using spectroscopic methods, such as 1D and 2D-NMR, mass spectrometry and comparison with previous published reports.

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Ethnopharmacological Relevance: Commiphora kerstingii Engl is a tree which is 20-30 m in height and commonly called "ararrabi" in Hausa. It is found in the Sahelian region (Cameroon, Chad, and Nigeria) where it is utilized for the treatment of several ailments including cancer.

Aim Of The Study: This study was aimed at investigating the chemical constituents and cytotoxic effect of extracts and isolates from the stem barks and leaves of C.

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Article Synopsis
  • - The study investigates two natural compounds, TR2 and TR22, for their potential antioxidant and anticancer properties against two types of breast cancer cells (estrogen-sensitive MCF-7 and non-sensitive MDA-MB 231).
  • - TR2 demonstrated stronger antioxidant effects compared to standard antioxidants and effectively inhibited the growth and migration of breast cancer cells, while TR22 showed a more significant proliferation inhibition following acetylation.
  • - Molecular docking studies indicated that both compounds could inhibit receptor tyrosine kinases, suggesting their potential as effective agents in slowing cancer progression.
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The phytochemical study of L. led to the isolation, through chromatographic techniques, of a new triterpenoid saponin, 3--[--rhamnopyranosyl-(1→3)-(6--acetyl---glucopyranosyl)]-22-hydroxyolean-12-ene () namely Myxaoside A, together with three known compounds, Soyasaponine I (), oleanolic acid (), and 3--acetyl-oleanolic acid (). All structures were established, based on 1 & 2D-NMR spectroscopic analysis and comparison with previous published reports.

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Article Synopsis
  • Alzheimer's disease and diabetes impact global health, with specific enzymes targeted for treatment: acetylcholinesterase (AChE), butyrylcholinesterase (BChE) for AD, and α-amylase, α-glucosidase for diabetes.
  • A study isolated various compounds from a medicinal plant, identifying several derivatives of ellagic acid that showed moderate to strong inhibition of AChE and BChE, with 3,3'-di-O-methyl ellagic acid being the most potent.
  • In addition, some compounds effectively inhibited α-amylase and α-glucosidase, outperforming acarbose, indicating their potential as therapeutic agents for diabetes management.
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Background: Bacterial RNA polymerase holoenzyme requires sigma70 factors to start transcription by identifying promoter elements. Cyanobacteria possess multiple sigma70 factors to adapt to a wide variety of ecological niches. These factors are grouped into two categories: primary sigma factor initiates transcription of housekeeping genes during normal growth conditions, while alternative sigma factors initiate transcription of specific genes under particular conditions.

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The Nile tilapia is a widely consumed fish, its scales dumped in nature as waste have been recovered in the formulation of antiseptic creams because of its high content in chitin, precursor of chitosan. Creams have the advantage of being more comfortable on the skin and allow prolonged administration of the active ingredient. Chitosan is obtained with a yield of 21.

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Chemical investigation of L. (Boraginaceae) resulted in the isolation of the following ten known compounds: 1-naphthaleneacetic-5-carboxy-1,2,3,4,4a,7,8,8a-octahydro-1,2,4a-trimethyl-[1-(1,2, 4a,8a)]-acid (), hexacosanoate-1-glyceryl (), 3-urs-12,20(30)-diene-27,28-dioic acid (), 3-D-glucopyranosylurs-12,20(30)-diene-27,28-dioic acid (), stigmasterol (), stigmasterol-3---D-glucopyranoside (), oleanolic-acid (), 3--acetyl-oleanolic acid (), betulin () and spinasterol-3--D-glucopyranoside (). The isolated compounds were characterised by using spectroscopic methods, 1D and 2D NMR, mass spectroscopy (ESI-MS) and by comparison with the literature data.

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A rapid untargeted UHPLC-Q-TOF-ESI-MS/MS-Based metabolomic profiling of the medicinal plant was performed. A total of 18 metabolites were detected, of which 10 could not be identified. Based on this result, an extensive chemical investigation of the CHCl-MeOH (1:1) extract of this plant was carried out, leading to the isolation of a new ceramide, named entadamide (), together with nine known compounds: monomethyl kolavate (), 24-hydroxytormentic acid () chondrillasterol (), 3---D glucopyranosylstigmasterol (), 3---D glucopyranosylsitosterol (), quercetin 3'-methylether (), 2,3-dihydroxypropyl icosanoate (), 2,3-dihydroxy-propyl 23-hydroxytricosanoate () and 2,3-dihydroxy-propyl 24-hydroxytetracosanoate ().

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is a tropical plant noticeable for its variegated leaves and exploited for various medicinal purposes. In this study, seven compounds, including three furanolabdane diterpenoids, i.e.

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This research evaluated the metal-sulfide mineral, sphalerite, as an electron donor for autotrophic denitrification, with and without oyster shells (OS). Batch reactors containing sphalerite simultaneously removed NO and PO from groundwater. OS addition minimized NO accumulation and removed 100% PO in approximately half the time compared with sphalerite alone.

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The current study was conducted to isolate the phytoconstituents from leaves and stem bark and evaluate their inhibitory activity against α-glucosidase, digestive enzyme related to diabetes mellitus. Phytochemical investigation of the leaves resulted in the isolation of three saponins (3-5), two triterpenoids (7 and 8) and two steroids (10a and 10b) as inseparable mixture, while one saponin (6), one triterpenoid (9) and one mixture of two cinnamates (2a and 2b) were isolated from the stem bark. Except for compounds 2 b, 7, 8, 10a and 10 b all the isolated compounds are reported here for the first time from the genus .

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Diabetes mellitus is a metabolic disorder which is one of the leading causes of mortality and morbidities in elderly humans. Chronic diabetes can lead to kidney failure, blindness, limb amputation, heart attack and stroke. Physical activity, healthy diets and medications can reduce the incidence of diabetes, so the search for more efficient antidiabetic therapies, most especially from natural products, is a necessity.

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Background: Plants play an important role in cancer therapy. They are source of natural molecules which can induce apoptosis in cancer cells by affecting molecular mechanisms implicated in cancer progression. The MAP Kinase/ERK1/2 and PI3K/AKT signaling pathways are two classical signaling pathways implicated in cancer progression and constitute therapeutic targets against cancer.

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A phytochemical study was carried out on stem bark of F. Hoffm., a medicinal plant belonging to the Combretaceae family and used traditionally in the treatment of various ailments.

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Propolis is very popular for its beneficial health properties, such as antimicrobial activity and antioxidant effects. It is one of the most long-serving traditional medicines to mankind due to its interesting chemical diversity and therapeutic properties. The detailed chemical information of propolis samples is very necessary to guarantee its safety and for it to be accepted into health care systems.

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Background: Insertion sequences (ISs) are mobile repeat sequences and most of them can copy themselves to new host genome locations, leading to genome plasticity and gene regulation in prokaryotes. In this study, we present functional and evolutionary relationships between IS and neighboring genes in a large-scale comparative genomic analysis.

Results: IS families were located in all prokaryotic phyla, with preferential occurrence of IS3, IS4, IS481, and IS5 families in Alpha-, Beta-, and Gammaproteobacteria, Actinobacteria and Firmicutes as well as in eukaryote host-associated organisms and autotrophic opportunistic pathogens.

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The genetically regulated pattern of heterocyst formation in multicellular cyanobacteria represents the simplest model to address how patterns emerge and are established, the signals that control them, and the regulatory pathways that act downstream. Although numerous factors involved in this process have been identified, the mechanisms of action of many of them remain largely unknown. The aim of this study was to identify specific relationships between 14 factors required for cell differentiation and pattern formation by exploring their putative physical interactions in the cyanobacterium model Nostoc sp.

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An aliphatic alkene namely pentapentacontene () was isolated for the first time from a natural source, , along with fourteen other compounds including nonacosanol (), tetratriacontanol (), octatriacontanol (), -sitosterol () and stigmasterol (), daucosanol (), ursolic acid (), uvaol (), 3,19,23,24-tetrahydroxyurs-12-en-28-oic acid (), lupenone (), oleanolic acid (), vanillin (), vanillic acid () and D-mannitol (). -glucosidase inhibitory assay revealed that MeOH and EtOAc extracts of leaves had the best activity with IC of 9.65 and 20.

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A new glycoiridoid () together with seven (7) known compounds were isolated from the methanol crude extract of the root bark of using chromatography methods. Their structures were elucidated using HR-ESI-MS, 1 D- & 2 D-NMR spectroscopies in comparison with previous literature. The antioxidant activity was investigated by using FRAP, DPPH, ABTS and HRSA methods while the antibacterial activity was assays on (ATCC25922) and (ATCC14028) strains.

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Article Synopsis
  • A new diterpenoid called rubesanolidic acid was discovered alongside six known compounds from the roots of a particular plant using column chromatography.
  • Their structures were confirmed through various spectroscopic analyses and comparisons with prior research data.
  • The extract showed significant -amylase inhibition activity, outperforming individual compounds, with rubesanolidic acid displaying the highest inhibition among the isolated compounds, suggesting the plant has potential as a source for antidiabetic agents.
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The present work describes the isolation and anticancer activity of which is a hemi parasitic plant harvested on , the host plant. Phytochemical study afforded a new flavonoid glycoside, tapinantoside () isolated for the first time from natural source, alongside six known compounds (-). Structure of compounds were elucidated by extensive spectroscopic analyses including 1 D and 2 D NMR, mass spectrometry and by comparison with literature data.

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Background: Cancer incidence has been growing in an alarming rate worldwide and new therapeutics are needed, particularly for intractable and chemoresistant cases. We evaluated the cytotoxic effects of Combretum fragrans F. Hoffm (Combretaceae) on glioblastoma (U87MG and C6) and prostate (PC-3) cancer cell lines.

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This study investigated the performance and microbiome of cyclic denitrification filters (CDFs) for wood and sulfur heterotrophic-autotrophic denitrification (WSHAD) of saline wastewater. Wood-sulfur CDFs integrated into two pilot-scale marine recirculating aquaculture systems achieved high denitrification rates (103 ± 8.5 g N/(m·d)).

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Article Synopsis
  • A new alkaloid, 8,9-dimethoxy-5-phenanthridin-6-one, along with two flavonoids, was isolated for the first time from a natural source.
  • The compounds were characterized using advanced NMR spectroscopy and mass spectrometry to determine their structures.
  • Some fractions showed strong antifungal activity against certain yeast strains, suggesting that the source may have potential for developing antifungal drugs.
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