A method for elucidating the relative configuration of acyclic organic compounds was developed on the basis of carbon-proton spin-coupling constants ((2,3)J(C,H)) and interproton spin-coupling constants ((3)J(H,H)). This method is based on the theory that, in acyclic systems, the conformation of adjacent asymmetric centers is represented by staggered rotamers, and their relative stereochemistry can be determined using (2,3)J(C,H) and (3)J(H,H), because the combined use of these J values enables the identification of the predominant staggered rotamer(s) out of the six possible derived from threo and erythro configurations. Detailed conformational analysis for model compounds 1-4 revealed that this method is useful in most cases for assignment of the configuration of acyclic structures occurring in natural products, in which stereogenic methine carbons are often substituted with a methyl or a hydroxy (alkoxy) group. This J-based configuration analysis was applied to the stereochemical elucidation of carboxylic acid 5 derived from zooxanthellatoxin and proven to be a practical method even for natural products with complicated structures.

it has two spirofused six-membered ketal ring systems in place of the more commonly encountered spiroketal involving six-and fixe-membered rings. The presence of two fused tetrahydropyran rings (D, E) is also unique.Acanthifolicin exhibits ED50's of 2.8 X 10"4, 2.1 X 10"3, and 3.9 X 10"3 9mcg/mL, respectively, against P388, KB, and L1210 cell lines. In vivo antitumor tests and other biological activity evaluation are in progress.Efforts are under way to isolate microorganisms associated with P. acanthifolium that may produce acanthifolicin. In this connection it may be noted that a macrolide polyether antibiotic, aplasmomycin, has been isolated from a marine bacterium.10 Acknowledgment. This investigation was supported by Grant CA-17256, CA-17562, and Contract N01-CM-67108 awarded by the National Cancer Institute, DHEW. We thank Ms. Lin Craft for sponge identification and assistance in sample collection. 360-MHz NMR spectra were obtained at the Purdue Biochemical Magnetic Resonance Laboratory supported by NIH Grant RR 01077. Supplementary Material Available: A listing of the final parameters, bond angles, torsion angles, structure factors, bond lengths, and Bijvoet differences is available (40 pages). Ordering information is given on any current masthead page.

Low-temperature plasma physics and technology are diverse and interdisciplinary fields. The plasma parameters can span many orders of magnitude and applications are found in quite different areas of daily life and industrial production. As a consequence, the trends in research, science and technology are difficult to follow and it is not easy to identify the major challenges of the field and their many sub-fields. Even for experts the road to the future is sometimes lost in the mist. Journal of Physics D: Applied Physics is addressing this need for clarity and thus providing guidance to the field by this special Review article, The 2012 Plasma Roadmap. Although roadmaps are common in the microelectronic industry and other fields of research and development, constructing a roadmap for the field of low-temperature plasmas is perhaps a unique undertaking. Realizing the difficulty of this task for any individual, the plasma section of the Journal of Physics D Board decided to meet the challenge of developing a roadmap through an unusual and novel concept. The roadmap was divided into 16 formalized short subsections each addressing a particular key topic. For each topic a renowned expert in the sub-field was invited to express his/her individual visions on the status, current and future challenges, and to identify advances in science and technology required to meet these challenges. Together these contributions form a detailed snapshot of the current state of the art which clearly shows the lifelines of the field and the challenges ahead. Novel technologies, fresh ideas and concepts, and new applications discussed by our authors demonstrate that the road to the future is wide and far reaching. We hope that this special plasma science and technology roadmap will provide guidance for colleagues, funding agencies and government institutions. If successful in doing so, the roadmap will be periodically updated to continue to help in guiding the field.

We have isolated a novel cell-cell adhesion system localized at cadherin-based adherens junctions (AJs). This system consists of at least nectin, a Ca 2؉ -independent immunoglobulin-like adhesion molecule, and afadin, an actin filament-binding protein, that connects nectin to the actin cytoskeleton. Nectin constitutes a family consisting of two members, nectin-1 and -2. We have isolated here a third member of the nectin family and named it nectin-3. Nectin-3 has three splicing variants, nectin-3␣ (biggest), -3␤ (middle), and -3␥ (smallest). Like nectin-1 and -2, nectin-3␣ consists of three extracellular immunoglobulin-like domains, a transmembrane segment, and a cytoplasmic region with the C-terminal consensus motif for binding to the PDZ domain. Nectin-3␣ formed a cis-homo-dimer and showed Ca 2؉ -independent trans-homo-interaction to cause homophilic cell-cell adhesion. Nectin-3␣ furthermore showed trans-hetero-interaction with nectin-1 or -2 but did not form a cis-hetero-dimer with nectin-1 or -2. Nectin-1 did not show trans-heterointeraction with nectin-2. The affinity of trans-heterointeraction of nectin-3␣ with nectin-1 or -2 was higher than that of trans-homo-interaction of nectin-1, -2, or -3␣. Nectin-2 and -3 were ubiquitously expressed, whereas nectin-1 was abundantly expressed in brain. Nectin-3␣ was colocalized with nectin-2 at cadherinbased AJs and interacted with afadin. These results indicate that the nectin family consists of at least three members, nectin-1, -2, and -3, all of which show homophilic and heterophilic cell-cell adhesion activities and are localized at cadherin-based AJs.