Tag: 100-200

On April 12, 2019, Wu, Fengshou; Yue, Liangliang; Zhu, Sizhe; Wang, Kai; Sun, Qi published a patent.Quality Control of [2,2′-Bipyridine]-3,3′-diamine The title of the patent was Preparation method of metal ruthenium nano material, and its application as antitumor drug. And the patent contained the following:

The preparation method of metal ruthenium nano material includes (1) preparing metal ruthenium coordination compound by using amino-containing polypyridine ligands (5-amino-1,10-phenanthroline, 2-amino-1,10-phenanthroline, etc.) and ruthenium trichloride, dissolving in citric acid solution, malic acid solution or oxalic acid solution, and ultrasonically dispersing for 10-40 min to obtain mixture A; (2) heating at 140-220°C for 1-5 h to obtain mixture B; (3) adjusting pH to 6.8-7.4 with alk. reagent, dialyzing for 2-48 h, collecting dialyzate, and freeze drying to obtain final product. The metal ruthenium nano material can be used to prepare antitumor drug. The ruthenium nano material has good water solubility, strong light stability, high fluorescence quantum yield, good photodynamic therapy effect for tumors, and good biocompatibility. The experimental process involved the reaction of [2,2′-Bipyridine]-3,3′-diamine(cas: 75449-26-2).Quality Control of [2,2′-Bipyridine]-3,3′-diamine

The Article related to ruthenium nano material preparation antitumor drug, Inorganic Chemicals and Reactions: Coordination Compounds and other aspects.Quality Control of [2,2′-Bipyridine]-3,3′-diamine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Sgaragli, Gianpietro; Frosini, Maria; Palmi, Mitri; Dixon, Henry B. F.; Desmond-Smith, Nicholas; Bianchi, Loria; Della Corte, Laura published an article in 1996, the title of the article was Role of taurine in thermoregulation and motor control: behavioral and cellular studies.HPLC of Formula: 636-73-7 And the article contains the following content:

Taurine may have a role in the striatonigral system of the rat. Considering that, whether a neurotransmitter or a neuromodulator, taurine must be recognized before initiating its action, in the present contribution a structure-activity relationship study is presented which gives some information on the nature of a possible recognition site in the rabbit brain, helping to explain the role of endogenous taurine in the central mechanisms of thermoregulation. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).HPLC of Formula: 636-73-7

The Article related to thermoregulation taurine structure activity relationship, Mammalian Biochemistry: General Physiological Chemistry and other aspects.HPLC of Formula: 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On November 30, 2007, Wu, Chang-Ju; Chen, Ju-Na; Shi, Jing-Min published an article.Recommanded Product: 75449-26-2 The title of the article was Tris(3,3′-diamino-2,2′-bipyridine)zinc(II) dinitrate. And the article contained the following:

In the title complex, [Zn(C10H10N4)3](NO3)2, the six-coordinate ZnII atom lies at the intersection of three 2-fold axes in a slightly distorted octahedral coordination environment. The N atom of a nitrate anion is located on a 3-fold axis. In the crystal structure, intermol. N-H···N and N-H···O H bonds between cations and anions form a two-dimensional network perpendicular to the c axis. Crystallog. data and at. coordinates are given. The experimental process involved the reaction of [2,2′-Bipyridine]-3,3′-diamine(cas: 75449-26-2).Recommanded Product: 75449-26-2

The Article related to mol structure zinc aminobipyridine nitrate, crystal structure zinc aminobipyridine nitrate, hydrogen bond zinc aminobipyridine nitrate, Crystallography and Liquid Crystals: Crystal Structure and other aspects.Recommanded Product: 75449-26-2

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On May 31, 1999, Decristoforo, Clemens; Mather, Stephen J. published an article.Product Details of 636-73-7 The title of the article was 99M-technetium-labelled peptide-HYNIC conjugates: Effects of lipophilicity and stability on biodistribution. And the article contained the following:

The aim of this study was to explore the effects of lipophilicity and stability on the biodistribution of 99mTc labeled peptides through the use of different co-ligands. 6-Hydrazinopyridine-3-carboxylic acid (HYNIC) was coupled to the somatostatin analog RC160 and radiolabeled using a range of ethylenediaminediacetic acid (EDDA) and EDTA derivatives as well as tricine and pyridine/tricine as co-ligands. After labeling with technetium-99m, chromatog., stability, protein-binding, and rat biodistribution studies were performed. For most co-ligands, biodistribution correlated well with in vitro properties. Lipophilic substitution on EDDA resulted in higher protein binding, increased liver uptake, and intestinal excretion. Stabilization of tricine with pyridines reduced blood levels and lowered liver uptake. EDTA derivatives showed high instability in vitro and in vivo. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Product Details of 636-73-7

The Article related to technetium 99m somatostatin analog complex biodistribution, rc160 hynic technetium 99m complex biodistribution, Radiation Biochemistry: Disease Diagnosis and Therapy and other aspects.Product Details of 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On January 7, 2011, Mueller, Marion K.; Petkau, Katja; Brunsveld, Luc published an article.Related Products of 75449-26-2 The title of the article was Protein assembly along a supramolecular wire. And the article contained the following:

Discotic mols. self-assemble into supramol. wires that act as platforms for directed protein assembly via appended biotin functionalities. The experimental process involved the reaction of [2,2′-Bipyridine]-3,3′-diamine(cas: 75449-26-2).Related Products of 75449-26-2

The Article related to protein assembly supramol wire biotin streptavidin discotic monomer, General Biochemistry: Proteins and Their Constituents and other aspects.Related Products of 75449-26-2

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On May 24, 1991, Karaman, Rafik; Bruice, Thomas C. published an article.Computed Properties of 636-73-7 The title of the article was Synthesis and characterization of the first water-soluble closely interspaced cofacial porphyrin dimer. And the article contained the following:

The only documented example of a quadruply-bridged, closely-interspaced cofacial porphyrin dimer was synthesized by Kagan (1977). The target of this communication is the synthesis and characterization of the first water soluble quadruply-bridged, closely-interspaced cofacial porphyrin I (R = R1). Reaction of meso-tetrakis(3-bromomethylphenyl)porphyrin with m-pyridinesulfonamide provides the closely-interspaced cofacial porphyrin dimer I (R = R2) which on quaternization with MeI provides the water soluble I (R = R1). Reactions of I with Zn(OAc)2 provided the corresponding bis-zinc complexes I. Porphyrins I and their bis-zinc complexes, exist in a closed down conformation with closely approaching porphyrin planes or in an open conformation. It was established, on the basis of 1H-NMR UV/vis, and emission spectrophotometries, and I (R = R2) exists in a closed down conformation in DMSO or acetone and a more open conformation is CHCl3. With zinc complexes of I (or protonated I) the conformation is open regardless of the solvent. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Computed Properties of 636-73-7

The Article related to porphyrin dimer quadruply bridged conformation, tetrakisbromoethylphenylporphyrin alkylation pyridinesulfonamide, Biomolecules and Their Synthetic Analogs: Corrinoids, Porphyrins, and Bilines and other aspects.Computed Properties of 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On August 31, 2011, Chisholm, Danielle M.; McDonald, Robert; McIndoe, J. Scott published an article.Recommanded Product: [2,2′-Bipyridine]-3,3′-diamine The title of the article was 3,3′-N,N’-Bis(amino)-2,2′-bipyridine – An unusually methylation-resistant amine. And the article contained the following:

Methylation of aromatic amino groups is usually straightforward, but the formation of two intramol. hydrogen bonds in 3,3′-N,N’-bis(amino)-2,2′-bipyridine and (or) the potential for ring methylation prevents the clean tetramethylation of this mol. Numerous attempts to make 3,3′-N,N’-bis(dimethylamino)-2,2′-bipyridine produced only complex mixtures of variously methylated products, and the only isolated mol. was 3,3′-N,N’-bis(methylamino)-2,2′-bipyridine, for which an X-ray crystal structure was obtained. The experimental process involved the reaction of [2,2′-Bipyridine]-3,3′-diamine(cas: 75449-26-2).Recommanded Product: [2,2′-Bipyridine]-3,3′-diamine

The Article related to bisaminobipyridine methylation resistant amine, Physical Organic Chemistry: Addition, Elimination, and Substitution Reactions and other aspects.Recommanded Product: [2,2′-Bipyridine]-3,3′-diamine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On June 3, 1992, Karaman, Rafik; Blasko, Andrei; Almarsson, Orn; Arasasingham, Ramesh; Bruice, Thomas C. published an article.Electric Literature of 636-73-7 The title of the article was Symmetrical and unsymmetrical quadruply aza-bridged, closely interspaced, cofacial bis(5,10,15,20-tetraphenylporphyrin)s. 2. Synthesis, characterization, and conformational effects of solvents. And the article contained the following:

Title compounds I [X = NR, R = 3-pyridylsulfonyl (R1), 1-methylpyridinium-3-sulfonyl (R2), CONH2, cyano, tosyl; X = OCO2, R = R1, cyano] have been synthesized and fully characterized by 2-dimensional 1H-1H NMR (COSY), 2-dimensional 13C-1H NMR, fast-atom-bombardment mass spectrometry, UV/vis, IR, and fluorescence spectral techniques. It was established, on the basis of 1H NMR, UV/vis, and emission spectrophotometries, that I (X = NR, R = R1, R2, tosyl) exist in more than one conformational in DMSO and in only one sym. conformation in CHCl3. Their biszinc complexes and tetraprotonated derivatives exist in one conformation regardless of the solvent. These observations have been attributed to an interaction between DMSO and the pyrrolic N-H protons of the porphyrin cores which is inhibited by metalation or protonation. Mol. dynamics calculations reveal that the intracavity interactions of I (X = NR, R = R1) with DMSO are more important than the intercavity interactions which result in discrete, unsym. conformations of the dimer. In contrast, I (X = OCO2, R = R1, cyano; X = NR, R = cyano, CONH2) do not show any conformational changes upon switching from CHCl3 to DMSO. This is attributed to the long interplanar distances calculated for the porphyrin dimers which prevent intracavity coordination of DMSO with both porphyrin moieties. 1H NMR variable-temperature experiments of I (X = NR, R = R1) in DMSO show that the conformation of the dimer is greatly affected by temperature While at room temperature I (X = NR, R = R1) exists in more than one conformation, at higher temperatures (150°) only one conformation is populated. It is proposed that at room temperature, the existence of a H-bonding network between DMSO and the dimer results in more than one conformation, while at higher temperatures the network is destroyed to furnish an average conformation. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Electric Literature of 636-73-7

The Article related to porphyrin dimer preparation conformation, Biomolecules and Their Synthetic Analogs: Corrinoids, Porphyrins, and Bilines and other aspects.Electric Literature of 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On March 31, 2008, Ramya, G.; Renugadevi, C.; Rao, Chepuri R. K.; Trivedi, D. C. published an article.Application In Synthesis of Pyridine-3-sulfonic acid The title of the article was Investigations on pyridine-3-sulfonic acid doped polyaniline and polypyrrole: Metal loading through dopant molecules. And the article contained the following:

Polyniline and polypyrrole were chem. and electrochem. synthesized in presence of pyridine-3-sulfonic acid. These conducting polymers were characterized by FT-IR, UV-vis, XRD, TGA and SEM techniques. Polyaniline showed a conductivity of 4 × 10-4 S/cm while polypyrrole exhibited a conductivity of 6.2 × 10-2 S/cm. The presence of pyridine ring in the dopant enabled the polymers to anchor Pd/or PdO through which the composite can work as catalytic material. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Application In Synthesis of Pyridine-3-sulfonic acid

The Article related to pyridine sulfonic acid dopant polyaniline polypyrrole metal conductivity elec, Plastics Manufacture and Processing: Physical Properties and Testing Methods and other aspects.Application In Synthesis of Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On August 10, 2004, Winther-Jensen, Bjorn; Chen, Jun; West, Keld; Wallace, Gordon published an article.Application In Synthesis of Pyridine-3-sulfonic acid The title of the article was Vapor Phase Polymerization of Pyrrole and Thiophene Using Iron(III) Sulfonates as Oxidizing Agents. And the article contained the following:

Vapor phase polymerization is a versatile technique that can be used to obtain highly conducting coatings of conjugated polymer on both conducting and nonconducting substrates. This is demonstrated here by preparation of polypyrrole, polybithiophene, and polyterthiophene, coatings that otherwise must be prepared electrochem. in order to achieve the desired high conjugation. The method is based on the use of organic ferric sulfonates as oxidant as these salts easily form smooth, noncrystalline films. By proper choice of the sulfonate anion, the oxidizing power of the ferric salt can be varied over a wide range. The described technique can easily be adapted to different patterning techniques. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Application In Synthesis of Pyridine-3-sulfonic acid

The Article related to pyrrole thiophene vapor phase polymerization iron sulfonate oxidant, Chemistry of Synthetic High Polymers: Ring-Opening and Other Polymerizations and other aspects.Application In Synthesis of Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem