Use of biological system for the preparation of chiral molecules. Part 7. Synthesis of the pheromone components of the grape borer Xylotrechus pyrrhoderus by microbiological reduction of an .alpha.-diketone

1989 ◽  
Vol 54 (13) ◽  
pp. 3221-3223 ◽  
Author(s):  
R. Bel-Rhlid ◽  
A. Fauve ◽  
H. Veschambre
Keyword(s):  
Biological System ◽  
Chiral Molecules ◽  
Pheromone Components ◽  
Xylotrechus Pyrrhoderus ◽  
Microbiological Reduction

Synthesis of the Deuterated Sex Pheromone Components of the Grape Borer,Xylotrechus pyrrhoderus

2009 ◽  
Vol 73 (10) ◽  
pp. 2252-2256 ◽  
Author(s):  
Ryutaro KIYOTA ◽  
Rei YAMAKAWA ◽  
Kikuo IWABUCHI ◽  
Keita HOSHINO ◽  
Tetsu ANDO
Keyword(s):  
Sex Pheromone ◽  
Sex Pheromone Components ◽  
Pheromone Components ◽  
Xylotrechus Pyrrhoderus

Metal-, and Organocatalyst-Free One-Pot Assembly of Chiral Aza-Tricyclic Molecules: Creating Six Contiguous Stereocenters from 2-D-Structures and an Amino Acid

2020 ◽  
Author(s):  
Dung Do
Keyword(s):  
Amino Acid ◽  
Chemical Space ◽  
Structural Diversity ◽  
Therapeutic Agents ◽  
Chiral Molecules ◽  
One Pot ◽  
Complex Molecules ◽  
Chiral Catalyst ◽  
Chiral Complex ◽  
Free Process

<p>Chiral molecules with their defined 3-D structures are of paramount importance for the study of chemical biology and drug discovery. Having rich structural diversity and unique stereoisomerism, chiral molecules offer a large chemical space that can be explored for the design of new therapeutic agents.<sup>1</sup> Practically, chiral architectures are usually prepared from organometallic and organocatalytic processes where a transition metal or an organocatalyst is tailor-made for desired reactions. As a result, developing a method that enables rapid assembly of chiral complex molecules under metal- and organocatalyst-free condition represents a daunting challenge. Here we developed a straightforward route to create a chiral 3-D structure from 2-D structures and an amino acid without any chiral catalyst. The center of this research is the design of a <a>special chiral spiroimidazolidinone cyclohexadienone intermediate</a>, a merger of a chiral reactive substrate with multiple nucleophillic/electrophillic sites and a transient organocatalyst. <a>This unique substrate-catalyst (“subcatalyst”) dual role of the intermediate enhances </a><a>the coordinational proximity of the chiral substrate and catalyst</a> in the key Aza-Michael/Michael cascade resulting in a substantial steric discrimination and an excellent overall diastereoselectivity. Whereas the “subcatalyst” (hidden catalyst) is not present in the reaction’s initial components, which renders a chiral catalyst-free process, it is strategically produced to promote sequential self-catalyzed reactions. The success of this methodology will pave the way for many efficient preparations of chiral complex molecules and aid for the quest to create next generation of therapeutic agents.</p>

Parameters for Measuring the Activity and Viability of Activated Sludge

1974 ◽  
Vol 9 (1) ◽  
pp. 235-249 ◽  
Author(s):  
S.G. Nutt ◽  
K.L. Murphy
Keyword(s):  
Organic Carbon ◽  
Activated Sludge ◽  
Biological System ◽  
Analytical Methods ◽  
Heterogeneous System ◽  
Removal Rate ◽  
Bacterial Species ◽  
Atp Content ◽  
Culture Studies ◽  
Activated Sludge System

Abstract Conventional wastewater parameters are accepted as inadequate estimates of the condition of activated sludge but numerous other indices have been suggested as specific measurements of the activity and viability of the biomass. Literature in the related fields of microbiology and biochemistry were reviewed in order to select the most appropriate activity parameters for application to a heterogeneous biological material. Modified analytical methods were applied to a well-controlled biological system containing a single predominant bacterial species to evaluate the relative merit of each as an indicator of viability and activity. The potential of each parameter in a complex heterogeneous system was determined by monitoring each index in a bench activated sludge system. The predominant culture studies indicated that the ATP content of the biomass and the dehydrogenase activity were potential indicators of cell viability in a simple system. However, in the complex activated sludge system, only the ATP content showed significant correlation to the organic carbon removal rate.

Neuropharmacological Screening of Chiral and Non-chiral Phthalimide- Containing Compounds in Mice: in vivo and in silico Experiments

2019 ◽  
Vol 15 (1) ◽  
pp. 102-118 ◽  
Author(s):  
Carolina Campos-Rodríguez ◽  
José G. Trujillo-Ferrara ◽  
Ameyali Alvarez-Guerra ◽  
Irán M. Cumbres Vargas ◽  
Roberto I. Cuevas-Hernández ◽  
...  
Keyword(s):  
Locomotor Activity ◽  
In Silico ◽  
Biological Properties ◽  
Chiral Molecules ◽  
Chiral Compounds ◽  
Plus Maze ◽  
In Silico Studies ◽  
The Central Nervous System

Background: Thalidomide, the first synthesized phthalimide, has demonstrated sedative- hypnotic and antiepileptic effects on the central nervous system. N-substituted phthalimides have an interesting chemical structure that confers important biological properties. Objective: Non-chiral (ortho and para bis-isoindoline-1,3-dione, phthaloylglycine) and chiral phthalimides (N-substituted with aspartate or glutamate) were synthesized and the sedative, anxiolytic and anticonvulsant effects were tested. Method: Homology modeling and molecular docking were employed to predict recognition of the analogues by hNMDA and mGlu receptors. The neuropharmacological activity was tested with the open field test and elevated plus maze (EPM). The compounds were tested in mouse models of acute convulsions induced either by pentylenetetrazol (PTZ; 90 mg/kg) or 4-aminopyridine (4-AP; 10 mg/kg). Results: The ortho and para non-chiral compounds at 562.3 and 316 mg/kg, respectively, decreased locomotor activity. Contrarily, the chiral compounds produced excitatory effects. Increased locomotor activity was found with S-TGLU and R-TGLU at 100, 316 and 562.3 mg/kg, and S-TASP at 316 and 562.3 mg/kg. These molecules showed no activity in the EPM test or PTZ model. In the 4-AP model, however, S-TGLU (237.1, 316 and 421.7 mg/kg) as well as S-TASP and R-TASP (316 mg/kg) lowered the convulsive and death rate. Conclusion: The chiral compounds exhibited a non-competitive NMDAR antagonist profile and the non-chiral molecules possessed selective sedative properties. The NMDAR exhibited stereoselectivity for S-TGLU while it is not a preference for the aspartic derivatives. The results appear to be supported by the in silico studies, which evidenced a high affinity of phthalimides for the hNMDAR and mGluR type 1.

ALLELOPATHIC EFFECTS OF PARTHENIUM HYSTEROPHORUS ON GERMINATION OF SORGHUM SEEDS

2018 ◽  
Vol 6 (26) ◽  
Author(s):  
Jitendra Rajpoot
Keyword(s):  
Biological System ◽  
Growth And Development ◽  
Plant Virus ◽  
Evolutionary Origin ◽  
Plant Interactions ◽  
Biological Organization ◽  
Plant Soil ◽  
System A ◽  
Allelopathic Effects ◽  
Plant Plant

International Allelopathy Society has redefined Allelopathy as any process involving secondary metabolities produced by plants, algae, bacteria, fungi and viruses that influences the growth and development of agricultural and biological system; a study of the functions of secondary metabolities, their significance in biological organization, their evolutionary origin and elucidation of the mechanisms involving plant-plant, plant-microorganisms, plant-virus, plant-insect, plant-soil-plant interactions.

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