SOME CHEMICAL AND PHYSIOLOGICAL PROPERTIES OF NITRIC OXIDE: A MINI REVIEW

Nitric oxide (NO) is a simple odd-electron molecule that is a primary pollutant. It transmits signals between neurons; playing a role in blood flow and sexual arousal. In this mini review we try to make accessible the properties and functions of this lipophilic molecule to non-specialists

SOME CHEMICAL AND PHYSIOLOGICAL PROPERTIES OF NITRIC OXIDE: A MINI REVIEW

Nitric oxide (NO) is a simple odd-electron molecule that is a primary pollutant. It transmits signals between neurons; playing a role in blood flow and sexual arousal. In this mini review we try to make accessible the properties and functions of this lipophilic molecule to non-specialists

Antiplasmodial Activity shown by Secondary Metabolites Extracted from the Seeds ofPentaclethramacrophyllaBenth

Oil extracts from the African oil bean seed (PentaclethramacrophyllaBenth.) was analyzed for its phytochemical and mineral content and proximate, physicochemical and antimicrobial analyses were also performed. Phytochemical analysis showed the presence of tannins, saponins, quinones, terpenoids, phenols and coumarins in the oil sample. Mineral determination of the cotyledon showed the presence of iron (Fe) (with the highest concentration), Cu, Zn, Mn, Cr, Pb and Cd; while proximate analysis gave the following result: moisture (14.2%), ash content (1.5%), crude fibre (4.9%), crude proteins (12.8%), oil contents (4.9%), and carbohydrate (61.8%). GC-MS analysis of the partitioned petroleum ether and chloroform fractions of the oil revealed the presence of 9-Octadecenoic acid, 9,12- Octadecadienoic acid and their methyl esters,cis-9-Hexadecenal among the many components of the oil extract. Physicochemical analysis of the oil indicateda saponification value (148.67 mg KOH/g), peroxide value(8.0 meq/g), iodine value (10.41 mg iodine/g) and free fatty acid (8.98 mg KOH/g). The need for the development of new drugs for malaria led to our study of the antiplasmodial activity of the oil from the seeds of Pentaclethramacrophylla. Toxicological studies were carried out to determine the LD50with chloroquinediphosphate as positive control and normal saline as negative control. Using the Peter’s 4 day suppressive test a parasite inhibition rate of 47.72% (25 mg/kg), 63.63% (50 mg/kg) and 61.36% (100 mg/kg) on day 4 after treatment was recorded. A 95.45% chemo-suppression was observed for animals treated with 10 mg/kg chloroquine. This resultis an indication that the extract had appreciable signs of chemosuppression

ANTIBACTERIAL ACTIVITY OF MODERATELY VOLATILE COMPONENTS OF THE OIL EXTRACTED FROM THE SEEDS OF DACRYODES EDULIS G. LAM

Objectives: Dacryodes edulis is a versatile plant in many African countries, as its various parts are employed to treat several diseases. Like most plants used in traditional medicine, the possible mechanism by which D. edulis functions is still unknown. This study was designed to investigate the components of the plant seed with a view of justifying its use as traditional medicine. Methods: The seed oil of D. edulis was exhaustively extracted with a Soxhlet extractor from 500 g seeds and 200 g seeds of D. edulis using ethanol and petroleum ether as solvent, respectively. The extraction solvent was removed to obtain the oil which was then subjected to antimicrobial activity test to determine its activity against the following clinical isolates namely Pseudomonas aeruginosa, Staphylococcus aureus, Bacillus cereus, and Escherichia coli using gentamycin as positive control. Phytochemical screening and gas chromatography-mass spectrometry (GC-MS) analyses were carried out following standard methods Results: Ethanolic extract resulted in a higher percentage of oil yield (11.6%) than petroleum ether (5.3%). D. edulis seed oil showed remarkable activity against Gram-negative and Gram-positive isolates: E. coli, Bacillus spp, and S. aureus but not against P. aeruginosa. The presence of saponins, quinones, cardiac glycosides, terpenoids, and phenol was confirmed during qualitative phytochemical screening, and the preliminary results from GC-MS analysis show the presence of terpinen-4-ol, 4,6,6-trimethyl bicyclo[3.1.1]hept-3-en-2-one, ethyl 14-methyl-hexadecanoate, methyl 19-methyleicosanoate, squalene, C-14 to C-18 fatty acids, and their esters. Conclusion: The study, therefore, confirms that the use of D. edulis as component of traditional medicine may be justified

A review on the chemistry and pharmacological properties of benzodiazepine motifs in drug design

Benzodiazepines are an important class of heterocyclic compounds in organic chemistry. They are known for their diverse physicochemical and biological properties. Some benzodiazepine derivates are well-known drugs with diverse and strong pharmacophoric moiety. An immense number of pharmacological research on benzodiazepine heterocycles and their derivatives have recently been conducted to explore its numerous pharmacological potentials as better therapeutic candidates for the treatment of various disorders, benzodiazepines, however, are one of the main sources of interest for many medicinal chemists. Researchers are drawn to the benzodiazepine nucleus for the synthesis of new drugs because of its potent pharmacophoric moiety and ring shape. Due to the emergence of new pathogenic strains’ resistance to the presently available drugs, there has been a constant demand for more effective and selective drugs. Benzodiazepine moiety has all the desired qualities for selective drug candidates used as useful therapeutic agents. Given the importance of benzodiazepine moiety, the current review aims to assess benzodiazepine syntheses as well as their pharmacological properties for potential molecular targets in therapeutic development