R-(-)-β-O-methylsynephrine, a natural product, inhibits VEGF-induced angiogenesis in vitro and in vivo

R-(-)-β-O-methylsynephrine (OMe-Syn) is an active compound isolated from a plant of the Rutaceae family. We conducted cell proliferation assays on various cell lines and found that OMe-Syn more strongly inhibited the growth of human umbilical vein endothelial cells (HUVECs) than that of other normal and cancer cell lines tested. In angiogenesis assays, it inhibited vascular endothelial growth factor (VEGF)-induced invasion and tube formation of HUVECs with no toxicity. The anti-angiogenic activity of OMe-Syn was also validated in vivo using the chorioallantonic membrane (CAM) assay in growing chick embryos. Expression of the growth factors VEGF, hepatocyte growth factor, and basic fibroblast growth factor was suppressed by OMe-Syn in a dose-dependent manner. Taken together, our results indicate that this compound could be a novel basis for a small molecule targeting angiogenesis.     

An antiferromagnetically coupled trinuclear Cu(II) complex containing μ(O,O′), μ(O) carboxylates and μ(O) phenoxide bridges

The trinuclear complex [L₂Cu₃(CF₃CO₂)₄] (1) has been synthesized and its crystal structure determined. It consists of a linear arrangement of Cu(II) centers. The central copper atom is bonded to six oxygen atoms and has a tetragonally distorted octahedral geometry, while the terminal copper atoms are bonded to three oxygen and two nitrogen atoms and show a distorted square pyramidal geometry. The complex shows di-μ(O,O′) syn-syn carboxylate bridging as well as monoatomic (μ-O) bridging, along with phenolate (μ-O) oxygen bridging. Cryomagnetic investigations in the range 2-300 K revealed an antiferromagnetic spin exchange interaction with J = −95.7 cm⁻¹, based on the isotropic exchange model H_ex = −2J[S₁ · S₂ + S₂ · S₃].     

Révision systématiquedu genre Steginoporella smitt, 1873 (Bryozoa Cheilostomata)

Systematic revision of the genus Steginoporella: until now about eighty species were described. Only twenty recent species and thirty-four fossil ones are maintained. Several species and subspecies are new.The main interest of this revision is to establish a biostratigraphical scale: the settlement of this scale is based on the known stratigraphical distribution and on an attempt of phylogeny.The second advantage is ecological: all recent species live in marine tropical environment. The Steginoporella are good paleoecological indicators.At last, the establishment of a paleobiogeography, even incomplete and not definitive, allows to understand more easily recent distribution of Steginoporella connected with the great events of earth evolution.     

Nucleotide diversity and minisatellite in chloroplast Asp(GUC)–Thr(GGU) region in Elymus trachycaulus complex, Elymus alaskanus and Elymus caninus

Nucleotide variation in chloroplast Asp(GUC)–Thr(GGU) intergenic region and genetic relationships among this group were examined among Elymus trachycaulus complex, Elymus alaskanus and Elymus caninus. The estimates of nucleotide diversity (π) ranged from 0.00111 for Elymus virescens to 0.03086 for E. caninus. Highest nucleotide diversity was found for E. caninus among the taxa analyzed here and followed by Elymus hyperarcticus. E. virescens accessions are genetically very uniform. Phylogenetic analysis suggested that E. caninus is paraphyletic. Elymus violaceus is genetically distinct from both E. alaskanus and E. trachycaulus. Our result indicates that Asp (GUC)–Thr (GGU) intergenic region has a high rate of evolutionary in Elymus species. Large indels detected in this region appear to have a highly rate of evolution and are thus more prone to homoplasy. We also first reported a minisatellite discovered in Asp (GUC)–Thr (GGU) region in Elymus species. The minisatellite identified here is an excellent candidate marker for studying population structures of Elymus species.     

The effect of hydrogen bonding in two crystal modifications of aquabis(N,N-dimethylglycinato-κN,κO)copper(II): Experimental and theoretical study

From the crystals of trans aquabis(N,N-dimethylglycinato-κN,κO)copper(II) dihydrate (compound 1, space group P2₁2₁2₁) novel crystal structure of trans aquabis(N,N-dimethylglycinato-κN,κO)copper(II) (compound 2, space group Pbca) was obtained and analysed by X-ray diffraction. In the crystal structure 1, the O-H?O hydrogen bonds form three-dimensional network. In the crystal structure 2, two-dimensional layers stacking to each other are formed, with non-polar N,N-dimethyl groups placed on the opposite sides of the layers, and with the polar part in the middle forming CO?O-H and C-H?O hydrogen bonds. Different hydrogen bonding patterns in 1 and 2 do not pronouncedly affect molecular geometry of the title compound. Molecular mechanics force field suited for studying the properties of bis(amino acidato)copper(II) complexes in the solid state can follow the differences between the experimental molecular structures in the two diverse crystalline surroundings. To make possible direct comparison between crystal lattices, the force field was applied to predict unit cell packing of supposed anhydrous bis(N,N-dimethylglycinato)copper(II) in space group Pbca. Relative intermolecular energies of hypothetic anhydrous crystal and simulated 1 and 2 crystals are discussed. On the basis of experimental and theoretical results we conclude that the main effect of two water molecules of crystallisation in 1 is to stabilise the crystal packing via hydrogen bonding, whilst similar pyramidal copper(II) coordination geometry in 1 and 2 is due to axially coordinated water molecule and its intermolecular interactions.     

Leucocyanidin: Synthesis and properties of (2R,3S,4R)-(+)-3,4,5,7,3′,4′-hexahydroxyflavan

An isomer of leucocyanidin, (2R,3S,4R)-(+)-3,4,5,7,3′,4′-hexahydroxyflavan has been synthesized from (+)-taxifolin, isolated in its phe     

1,3-Bis(α-aminoisopropyl)benzene, meta-C6H4(CMe2NH2)2: An N,N-bridging and N,C,N-cyclometalating ligand

Saponification of the bis(carbamic acid ester) 1,3-C₆H₄(CMe₂NHCO₂Me)₂ (1), made by the addition of methanol to commercial 1,3-C₆H₄(CMe₂NCO)₂, yielded the meta-phenylene-based bis(tertiary carbinamine) 1,3-C₆H₄(CMe₂NH₂)₂ (2). Dinuclear [{(η⁴-1,5-C₈H₁₂)RhCl}₂{μ-1,3-C₆H₄(CMe₂NH₂)₂}] (3) resulted from the action of 2 on [{(η⁴-1,5-C₈H₁₂)Rh(μ-Cl)}₂] in toluene. Combination of 2 with PdCl₂ or K₂[PdCl₄] gave the dipalladium macrocycle trans,trans-[{μ-1,3-C₆H₄(CMe₂NH₂)₂}₂(PdCl₂)₂] (4) along with cyclometalated [{2,6-C₆H₃(CMe₂NH₂)₂-κN,κC¹,κN′}PdCl] (5). Substitution of PEt₃ for the labile chlorido ligand of 5 afforded [{2,6-C₆H₃(CMe₂NH₂)₂-κN,κC¹, κN′}Pd(PEt₃)]Cl (6). The crystal structures of the following compounds were determined: bis(carbamic acid ester) 1, ligand 2 as its bis(trifluoroacetate) salt [1,3-C₆H₄(CMe₂NH₃)₂](O₂CCF₃)₂, 2 · (HAc_f)₂, complexes 3 and 6, as well as 1,3-C₆H₄(CMe₂OH)₂ (the diol analogue of 2).     

Modification de la fonction antibiotique de deux diatomées marines, Asterionella japonica (Cleve) et Chaetoceros lauderi (Ralfs), par le dinoflagelléProrocentrum micans (Ehrenberg)

Two diatoms, Asterionella japonica (Cleve) and Chaetoceros lauderi (Ralfs), produced a similar lipidic antibiotic, whose activity increased after irradiation by visible light.In mixed cultures with the dinoflagellate Prorocentrum micans Ehrenberg, their cells contained higher amounts of the photoactivated antibiotic and a lower quantity of carotenoid pigments.These observations suggest the action of a chemical mediator released into the medium by P. micans, which inhibits the synthesis of pigments, thus leading to an increase of the photoactivation of the lipidic antibiotics in vivo. A similar inverse relationship between the concentration of carotenoids and the antibiotic activity was observed in several clones of Asterionella japonica isolated from different sea-water samples, and in cultures of the same diatom in the presence of diphenylamine. The importance of such phenomenon in a natural environment is discussed.     

Précisions morphologiques,structurales et systématiques sur Reptomulticava parviporosa CANU et LECOINTRE (Bryozoa,cyclostomata)

This miocene organism was described as an Alga (Lithophyllym vinassaiPATRINI, 1932 = Neosolenopora patriniiMASTRORILLI, 1955) and as a Bryozoan (Reptomulticava parviporosaCANU et LECOINTRE, 1934). This paper shows several salient features of Cyclostomatous Bryozoans (morphology, microstructure, zoarial brood chamber). The arguments for the classing of this organism among Algae are simultaneously refuted (pseudo-differentiation of the thallus, conceptacles).     

Contribution a la connaissancce des rhapydionininae (foraminifères, alveolinidae) crétacés

The formerly unknown microspheric form of Raadshoovenia salentina (Papetti and Tedeschi) and the new genus Cyclopseudedomia (type-species Cyclopseudedomia smouti n.g., n.sp.) are described from limestones of Campanian-Maastrichtian age from Gavrovo-Tripolitza zone in Greece. The new genus is distinguished from others of the sub-family RhapydionininaeKeijzer emend. Hamaoui and Fourcade by its almost entirely evolute test made of chambers tending to a cyclical stage (rapidly reached in the microspheric form).     

Heteroleptic κ(N,C)-2-phenylpyridine platinum complexes: The use of bis(pyrazolyl)borates as ancillary ligands

Luminescent platinum(II) bis(pyrazolyl)borate complexes bearing orthometalated phenylpyridines (based on 2-phenylpyridine, 3-hexyloxy-2-phenylpyridine and (4-(pyridine-2-yl)-phenyl)methanol) and bis(pyrazolyl)borate ligands (employed as potassium dihydridobis(pyrazolyl)borate and potassium dihydridobis(3,5-dimethylpyrazolyl)borate) have been synthesized and characterized. By reaction of K₂PtCl₄ with phenylpyridine ligands a precursor has been obtained which was further converted to the corresponding heteroleptic complexes. All platinum(II) bis(pyrazolyl)borate complexes have been investigated by nuclear magnetic resonance, Fourier transform infrared spectroscopy, thermal analysis and UV-Vis absorption spectroscopy. Luminescence as well as lifetime measurements in solution and in the solid state have been performed to establish a qualitative relationship between structure and luminescence properties. The absorption and emission properties of these complexes are governed by the nature of the orthometalating ligand with emission maxima ranging from 488 to 551 nm. Emission spectra at room temperature show well-resolved vibronic fine structures and a strong spin-orbit coupling. For the compounds under investigation the mixing of the excited states leads to apparent lifetimes in the microsecond regime (5.7-8.6 μs), rendering these materials phosphorescent.     

Ammonites diartianus d'Orbigny, 1850,Vascoceratidae du cénomanien supérieur de saint-calais (Sarthe)

Ammonites diartianus d'Orbigny is a Vascocerasoof late Cenomanian (Sciponoceras gracile Zone) age, occuring in both Sarthe (France) and southern England. It is the earliest vascoceratid known from France, and its recognition is of great significance, lending support to recent suggestions that the classic Vascoceras gamai - mundaeChoffat group are of Upper Cenomanian age.     

Crassostrea gryphoides et C. gingensis (Schlotheim, 1813) deux expressions morphologiques d'une même espèce (Miocène, Bivalvia)

The assemblages of Crassostrea gryphoïdes of the Loupian's quarry is constitued of differents morphotypes which result of ecological effects (population density, locality and position in the assemblage). The selection of individuals with her life position shows two lots of Ostreidae the morphology of which is statistically different. The observations about Crassostrea of outcrops of Rhone's Valley and Touraine confirm the relations between position (liable to population's density) and morphology. The two types which are point out are often recognize as different species describe by E.F. von Schlotheim, 1813: Crassostrea gryphoïdes and Crassostrea gingensis. Therefore this two species must be consider as synonymous.     

尾突角蟾Megophryscaudoprocta(两栖纲,角蟾科)的进一步记述

尾突角蟾(Megophrys caudoprocta Shen,1994)具有非常特殊的特征,它们的尾杆骨(urostyle)长,超过坐骨(ischium)后缘,支持着尾突(caudal projection);泄殖孔(cloacal pore)在股间后缘向腹面开口;上眼睑(upper eyelid)前部大,有一三角形突起向侧后突出.这些特征有别于角蟾属其他物种,有重要研究价值.近年来在模式标本产地又采到1雌2雄,先后共4号成体标本,本文对其形态特征,生物学资料和分布作了进一步记述,并拍摄到原色生态照片.     

Could pseudogenes be widespread in ants? Evidence of numts in the leafcutter ant Acromyrmex striatus (Roger, 1863) (Formicidae: Attini)

The incorporation of fragments of mitochondrial DNA (mtDNA) in the nuclear genome, known as numts (nuclear mitochondrial pseudogenes), undermines general assumptions concerning the use of mtDNA in phylogenetic and phylogeographic studies. Accidental amplifications of these nuclear copies instead of the mitochondrial target can lead to crucial misinterpretations, thus the correct identification of numts and their differentiation from true mitochondrial sequences are important in preventing this kind of error. Our goal was to describe the existence of cytochrome b (cytb) numts in the leafcutter ant Acromyrmex striatus (Roger, 1863). PCR products were directly sequenced using a pair of universal primers designed to amplify the cytb gene of these insects. Other species of leafcutter ants were also sequenced. The sequences were analyzed and the numts were identified by the presence of double peaks, indels and premature stop codons. Only A. striatus clearly showed the presence of numts, while the other species displayed the expected amplification of the mtDNA cytb gene target using the same primer pair. We hope that our report will highlight the benefits and challenges of using mtDNA in the molecular phylogenetic reconstruction and phylogeographic studies of ants, while establishing the importance of numts reports for future studies.     

Progress in antischistosomal N,N′-diaryl urea SAR

N,N′-Diaryl ureas have recently emerged as a new antischistosomal chemotype. We now describe physicochemical profiling, in vitro ADME, plasma exposure, and ex vivo and in vivo activities against Schistosoma mansoni for twenty new N,N′-diaryl ureas designed primarily to increase aqueous solubility, but also to maximize structural diversity. Replacement of one of the 4-fluoro-3-trifluoromethylphenyl substructures of lead N,N′-diaryl urea 1 with azaheterocycles and benzoic acids, benzamides, or benzonitriles decreased lipophilicity, and in most cases, increased aqueous solubility. There was no clear relationship between lipophilicity and metabolic stability, although all compounds with 3-trifluoromethyl-4-pyridyl substructures were metabolically stable. N,N′-diaryl ureas containing 4-fluoro-3-trifluoromethylphenyl, 3-trifluoromethyl-4-pyridyl, 2,2-difluorobenzodioxole, or 4-benzonitrile substructures had high activity against ex vivo S. mansoni and relatively low cytotoxicity. N,N-diaryl ureas with 3-trifluoromethyl-4-pyridyl and 2,2-difluorobenzodioxole substructures had the highest exposures whereas those with 4-fluoro-3-trifluoromethylphenyl substructures had the best in vivo antischistosomal activities. There was no direct correlation between compound exposure and in vivo activity.     

Synthesis of new (σ-N,N′-diazadiene)(η-alkene)platinum(0) compounds

Novel, thermally stable, dark-red to orange Pt⁰(σ²-N,N′-diazadiene)(η²-alkene) compounds have been synthesized in good yields from Pt⁰(COD)₂ or Pt⁰(NBE)₃, by stepwise substitution of the respective dienes or alkenes by an electron-poor alkene (dimethyl fumarate, maleic anhydride or fumaronitrile), followed by the appropriate diazadiene ligand in dry diethyl ether at 20 °C (diazadiene=various N,N′-disubstitued-1,4-diaza-1,3-dienes). The complex Pt(DBA)₂ is less suited as a precursor for the synthesis of Pt⁰(σ²-N,N′-diazadiene)(η²-alkene) compounds. These zerovalent Pt(diazadiene)(η²-alkene) compounds constitute a useful category of starting materials for synthetic organoplatinum chemistry and catalysis.