Identification of Chinese Herbal Compounds with Potential as JAK3 Inhibitors.

The Janus kinases (JAKs) consist of four similar tyrosine kinases and function as key hubs in the signaling pathways that are implicated in both innate and adaptive immunity. Among the four members, JAK3 is probably the more attractive target for treatment of inflammatory diseases because its inhibition demonstrates the greatest immunosuppression and most profound effect in the treatment of such disorders. Although many JAK3 inhibitors are already available, certain shortcomings have been identified, mostly acquired drug resistance or unwanted side effects.

[Non-covalent albumin conjugates of silicon (IV) phthalocyanines axially substituted with nucleoside: preparation and in vitro photodynamic activities].

The interactions of bovine serum albumin (BSA) with five novel silicon (N) phthalocyanines(SiPcl-5) axially modified by nucleosides (cytidine, 5-N-cytidine, methyl cytidine, uridine and methyl uridine) derivatives were studied by fluorescence spectroscopy. The results show that there are strong interactions between these silicon phthalocyanines and BSA with a binding constant of (4.90-83.

[Synthesis and photodynamic anticancer activity of silicon phthalocyanine axially modified by nucleoside derivatives].

A new axially modified silicon phthalocyanine, di [5'-(2', 3'-O-isopropyl)-5-methyl cytidineoxy] silicon phthalocyanine (SiPcG), was prepared and characterized by 1H NMR and HRMS. This compound is essentially nonaggregated in N,N-dimethyformamide and 1% cremophor EL aqueous solution. It shows a Qband at 676 nm and fluorescence emission at 685 nm in DMF, and exhibits a Q-band at 679 nm and fluorescence emission at 689 nm in 1% cremophor EL aqueous solution.

[Spectral properties, photodynamic anticancer activity and the interaction with albumin of silicon phthalocyanine axially modified by pyrimidine derivatives].

Photophysical photochemical properties, in vitro photodynamic anticancer activity and interaction with albumin of a new axially modified silicon phthalocyanine, i. e. di (2-amino-6-trifluoromethyl-4-pyrimidinyloxy) silicon phthalocyanine (SiPcF), were studied in the present paper.

[Synthesis, structure and special study of 1D cadmium sulfate-H2biim coordination polymer].

A novel cadmium complexes of {[Cd(H2 biim)2 (SO4)] x 3H2O}n(1) (H2 biim = 2,2'-biimidazole) was synthesized by hydrothermal reaction of 3CdSO4 x 8H2O and 2,2'-biimidazole ligand. The complex was built up by [Cd(H2 biim)2]2+ units bridged sequentially by SO4(2-) anions to form 1D zigzag chains parallel to the c-axis. The H2biim ligands were attached to the 1D chain as branches of the chain by coordinating to Cd2+ at two sides of the chain.

[Structural and spectral study of a novel lanthanide 2-hydroxynicotinic acid coordination polymer].

A novel lanthanide 2-hydroxynicotinic acid coordination polymer 1 {[LaL(HL) (H2O)3]1/3 (SO4)2/3 (H3O)2 H2O} (H2 L = 2-hydroxynicotinic acid) has been synthesized under hydrothermal condition and characterized by crystal X-ray diffraction, IR, UV, TGA, two-dimensional infrared (2D IR) correlation spectroscopy with magnetic and thermal perturbation. In 1, La ions are connected by 2-hydroxynicotinic acid through both carboxylate oxygen atoms and oxygen atoms from hydroxyl group in pyridine to generate a 2D layer in the ab plane, these layers are further connected by weak interactions to form a 3D framework along c axis. The response of out-of-plane bending vibrations of N-H and C-H are remarkable in the 2D IR correlation spectra under magnetic perturbation, this may attributes to the inducement of pi-electron cloud deformation under magnetic perturbation, v4 vibrations from SO4(2-) was also sensitive to magnetic perturbation.

[The structure and spectral research on Mn2 [V12 B16 O52 (OH)6 ] (en) 2 (H3O)6 (H2O)5 (en = ethylenediamine)].

A novel polyoxovanadium borate Mn2[V12B16O52 (OH)6](en)2 (H3O)6 (H2O)5 1(en = ethylenediamine) was hydrothermally synthesized and characterized by IR, two-dimensional infrared (2D IR) correlation spectroscopy with magnetic and thermal perturbation, and single crystal X-ray diffraction. In 1, it is interesting that each [V12B16O52 (OH)6]14- units is connected by four [Mn(H2O)2]2+ to generate a 2D layer on the ab plane. Along c axis, these layers are further linked by H-bond to form a 3D framework.

[Synthesis and spectroscopic properties of covalent albumin conjugates of phthalocyanine zincs substituted with metadicarboxyphenoxyl groups].

Four kinds of covalent serum albumin (BSA or HSA) conjugates of beta-tetrakis[(3,5-dicarboxy)phenoxy]-phthalocyaninatozinc (1) and beta-octakis [(3, 5-dicarboxy) phenoxy]-phthalocyaninatozinc (2) were synthesized by the approach of amide bond. The molar ratio of phthalocyanine to albumin in conjugates were found to be 6 - 7.1.

[Influence of albumin on the spectroscopic properties and existence state of mono-substituted phthalocyanine zinc (II)].

Interaction between 1-[4-(2-carboxyl-ethyl-)phenoxy] phthalocyanine Zinc(II) (ZnPcC1) and albumin (human serum albumin or bovine serum albumin) was studied. ZnPcC1 can be covalently bound to albumin through amide bond formation. The molar ratios of ZnPcC1 to albumins are found to be about 7 : 1 in the covalent bioconjugates.

[Synthesis, spectral analysis and photocatalysis of Ag/K4Nb6,O17 heterojunction catalysts].

K4Nb6O17 photocatalyst was successfully synthesized by low-temperature hydrothermal method with layer structure. Considering that a large number of hydroxyl (Nb-OH) and oxygen species (Nb==O, Nb--O-) exist on the surface of K4Nb6O17 synthesized by hydrothermal method, Ag(en)2+ precursors were employed to synthesize Ag/K4Nb6O17 heterostructure photo-catalysts with highly dispersed Ag. Photocatalytic performance evaluation results show that the photodegradation rate of MO for K4Nb6O17 was remarkably improved when a small amont of Ag was loaded.

[Syntheses and spectral study of novel metal zinc organic phosphonate].

Two novel Zn2+ organic phosphonate Zn(4,4'-bipy)(HBCP) 1 and [Zn2 (phen)2 (BCP)(H2 BCP)].H2O2 were hydrothermally synthesized. The compound 1 is with two-dimensional layer framework whereas the compound 2 is zero-dimensional structure.

[Structural and spectral study of a novel rare-earth and 3-bi-pyridine acid polymer].

A novel zero-dimension coordination polymer Gd2 (In)6 (H2O)4 (1) (In = 3-bipyridine acid) was synthesized under hydrothermal condition. By the analysis of single-crystal X-ray diffraction, the structure of the compound is that two Gd atoms connect with zero-dimension bi- nucleus cluster by the bridged carboxylate of four Ins. Based on the determination of the structure, the 2D correlation FTIR spectra with the perturbations of magnetism and thermal was applied.

[Studies on Ag-TiO2/KIT-6 composite nanosized photocatalyst].

In the present paper, ordered mesoporous silica (KIT-6) as support, nanosized TiO2 into KIT-6 was synthesized by titanium tetraisopropoxide hydrolysis. Then silver was loaded by deposition-precipitation method. Ag-TiO2/KIT-6 composite nanosized photocatalyst was firstly synthesized and a series of correlated catalysts were synthesized by the same preparation method.

[2D correlation spectral study of a coordination polymer [Eu(PCPOA)3 (H2O)]n].

A novel two dimensional coordination polymer [Eu(PCPOA)3 (H2O)], was synthesized under hydrothermal condition. Based on the determination of the structure, the 2D correlation FTIR spectra with the perturbation of magnetism and the 2D correlation fluorescence spectra with the perturbation of temperature were investigated. The energy bonds were calculated using CASTEP Program of Material studio.

[Study on the spectra of Au/alpha-Fe2O3 catalysts modified by ZrO2 and Nb2O5 promoters].

A series of Au/alpha-Fe2O3 catalysts promoted with ZrO2 and Nb2O5 were prepared by parallel co-precipitation method. Detailed characterizations were conducted by techniques including UV-Vis-DRS, XPS, TEM and XRF. Results indicated that the enrichment of Au, ZrO2 and Nb2O5 on the surface induced by the strong interaction between ZrO2 and Nb2O5 kept the nanoparticles apart, delaying sintering.

[Spectral study of two compounds of molybdate salt with beta-[Mo8O26] anion].

Two compounds of organic molybdate-alkali salt: [H(4,4'-bipy)]2[K2Mo8O26](I) and H3 [Na Mo8 O26] (4,4'-bipy)5 (H2O)4 (II), with beta-[Mo8O26]4- anion, were synthesized. The relationship between their properties and structures was studied by using FTIR, Raman, NIR-Vis and fluorescence etc. They possess isolating beta-[Mo8O26]4- anion, whose terminal O atoms combine with alkali.

[Spectral study of two Bi (III) contained heteropolymate compounds].

Two Bi (III) contained heteropolymate compounds Cos [Bi2 Co2 W20 O70 (H2O)6] x 44H2O (I)and Na3 H2 [Ce3 (H2O)18 Bi2 W22 O76] x 23H2O (II) have been synthesized under hydrothermal condition. The relationship between their properties and structures was studied by using FTIR, NIR FT-Raman, and UV-Vis DRS etc. The characteristic vibrational frequencies nu(as) (M = O(d)) and nu(s) (M-O(b)-M) is related to the structure of the materials.

[Synthesis and spectral study of three polyoxovanadium clusters].

Three polyoxovanadium clusters, [{Ni(phen)}2 V4O12] x H2O I, [N(CH2CH2)3NH]Na(H2O)6 {K4 (H2O)4 [V10 O28]} (H2O)4 II and [(CH3)4N]6 [V15 O36 Cl] III, have been synthesized under hydrothermal condition. The relationship between their properties and structures were studied by using FTIR, UV-Vis DRS and flurescence. The FTIR showed that the vibrational frequencies of the group are related to the structure of the materials.

[Spectral study of some polyoxovanadium borates].

Four novel polyoxovanadium borates with [(VO)12O6B18O42], namely (enH2)6 H3 [(VO)12O6B18O42].13H2O(1), [Ni (en)2]6 H3 [(VO)12 O6B18O42].8H2O(2), [Cu(en)2]5 H3 [(VO)12 O6B18 O42] [B(OH)3]2.

Barium divanadium(V) tellurite(IV).

A new three-dimensional bimetallic tellurite, BaV2TeO8, was synthesized by the hydrothermal reaction of Ba(OH)2, TeO2 and V2O5, and characterized by single-crystal X-ray diffraction. The three-dimensional framework is built up from anionic [V2TeO8]n(2n-) layers parallel to (101) and connected via Ba-O bonds. The anionic layers are formed by three types of polyhedra, namely VO5 tetragonal pyramids, VO(4) tetrahedra and TeO(4+2) 'folded square' polyhedra.

[Preparation and properties of organobentonites].

The chemistry organobentonites were synthesized by means of the ionexchange reaction between single-octadecyl trimethyl ammonium chloride(SOAC), di-octadecyl dimethyl ammonium chloride (DOAC) , tri-octadecyl methylammonium chloride (TOAC) quaternary ammonium salts and sodium base bentonies, respectively. The authors used FTIR, X-ray diffraction diagram and DSC thermograms to characterate the structure of the modified bentonites, and discussed the effect of different quaternary ammonium salt on the properties of organobentonites. The results showed that ion of the surfactants had entered into the chip layer of the bentonites, and changed the hydrophilic environment of the chip layer into hydrophobic environment and increased the distance among the chip layer, all of these had laid a base for the preparation of the nanometer composite material of high polymer/bentonite.

[Spectral study of the compound Zn(Pht):0.05 Sm].

Zn(Pht):0.05 Sm compounds have been synthesized by microwave. The compound was characterized by XRD, FTIR, NIR FT-Raman, DRS UV/Vis, fluorescence spectra, and TG analysis.

[Synthesis and spectroscopic studies of supermolecules of PW(x)V(12 - x)-MV].

A series of supermolecules of PW(x)V(12 - x)-MV (PW(x)V(12 - x): polyoxometalates x = 2, 4, 6, 8, 10; MV: methyl violet) with Keggin structure were prepared and their characters were studied by electronic spectra, infrared spectra and fluorescence spectra. As a result, the supermolecules were formed by the cooperating action between polyoxometalates and methyl violet. In the supermolecule, the structures of cation and anion are not destroyed.

[Spectroscopic studies of compounds with [(PO4)4Mo(V)O15]12- cluster].

Five novel organic-molybdenum phosphates with [(PO4)4Mo6(V)O15]12- cluster, Na x (H4TETA)3 x (H3O)5 x {Zn[(HPO4)2(PO4)2Mo6O15]2} (2), (H2en)7 x (H3O)4 x {Cu[(HPO4)2(PO4)2Mo6O15]2} x H2O (3), (H3DETA)2 x (H3O)3 x {Co0.5[(HPO4)2(PO4)2Mo6O15]} x H2O (4), [Co(H3TETA)]2{Co0.5[(HPO4)(PO4)3Mo6O15] x 3.

[Hydrothermal synthesis and spectra properties of compound Mn5(PO3(OH))2(PO4)2(H2O)4].

The title compound Mn5(PO3(OH))2(PO4)2(H2O)4 was synthesized under hydrothermal condition. Its crystal structure was determined by single-crystal X-ray diffraction. DRS, IR, fluorescence and TGA spectra were used to characterize the title compound.