Protectin D1, neuroprotectin D1 when generated by neural cells, is a member of a new family of bioactive products generated from docosahexaenoic acid. The complete stereochemistry of protectin D1 (10,17S-docosatriene), namely, chirality of the carbon-10 alcohol and geometry of the conjugated triene, required for bioactivity remained to be assigned. To this end, protectin D1/neuroprotectin D1 (P...

Tumor resistance to antitubulin drugs resulting from P-glycoprotein (Pgp) drug-efflux activity, increased expression of the βIII tubulin isotype, and alterations in the drug-binding sites are major obstacles in cancer therapy. Consequently, novel antitubulin drugs that overcome these challenges are of substantial interest. Here, we study a novel chemotype named furan metotica that localizes to ...

Food products from ruminants are the major dietary source of conjugated linoleic acids (CLA) for humans. The uniqueness of CLA in ruminant fat relates to the biohydrogenation of dietary unsaturated fatty acids by rumen bacteria. The CLA are intermediates in the biohydrogenation, and a portion escape the rumen and are incorporated into milk fat and body fat. In addition, the animal itself synthe...

Styrene 7,8-oxide, which reacts preferentially at the N-7 position of guanine, yielded two pairs of diastereomers 7-(1'-hydroxy-2'-phenylethyl)-dGMP (the alpha-isomer) and 7-(2-hydroxy-2-phenylethyl)-dGMP (the beta-isomer) on reaction with deoxyguanosine-3'-monophosphate (3'-dGMP). The alpha- and beta-isomers were formed in the ratio 32:68. T4 polynucleotide kinase preferentially mediated label...

Alzheimer's disease (AD) is the most common type of senile dementia in aging populations. Amyloid β (Aβ)-mediated dysregulation of ionic homeostasis is the prevailing underlying mechanism leading to synaptic degeneration and neuronal death. Aβ-dependent ionic dysregulation most likely occurs either directly via unregulated ionic transport through the membrane or indirectly via Aβ binding to cel...

Benidipine is a dihydropyridine calcium antagonist that has been used clinically as an antihypertensive and antianginal agent. It is used clinically as a racemate, containing the (-)-alpha and (+)-alpha isomers of benidipine. This study was performed to elucidate the metabolism of benidipine and its enantiomers in human liver microsomes (HLMs) and to characterize the cytochrome P450 (P450) enzy...

The chemical composition of the essential oil from the whole plant of Acalypha segetalis Muell. Arg. was analyzed by GC and GC/MS. Nineteen volatile constituents were identified. The main compounds were alpha-pinene (8.5%), neophytadiene, isomer II (14.7%) and neophytadiene, isomer III (33.6%). Toxicity and larvicidal assays revealed that the plant had LC50 values of 14.0 microg/mL and 45.4 mic...

The trifluoromethylation of a higher fullerene mixture followed by HPLC separation allowed the isolation and X-ray structural characterization of C1-C88(CF3)18 and D2-C92(CF3)16 compounds that turned out to be the derivatives of C2-C88 (isomer 33) and D2-C92 (isomer 82), respectively.

The algal excretion product geranylacetone was proved to be an effective and novel inhibitor of carotene synthesis in Synechoccus 6911. The application of geranylacetone resulted in an ac­ cumulation of phytofluene, indicating an inhibition of the conversion of this compound into fcarotene. The cts-isomer of geranylacetone was as effective as the natural irans-isomer. The chloro­ phyll synthesi...

A novel type of anti and syn isomers of a pentacyclic compound consisting of two thiophene rings and one pyrrole ring were efficiently synthesized from benzo[b]thiophene, and the anti isomer exhibits better charge transport and OFET properties compared with the syn isomer and its N-hexyl substitution.