Tag: 100-200

On July 31, 1996, Lombardini, John B. published an article.Safety of Pyridine-3-sulfonic acid The title of the article was Quantitative analysis of the combination dose-effects of taurine and taurine analogs on the phosphorylation of an ∼44-Kd protein present in a mitochondrial subfraction of rat heart. And the article contained the following:

Combinations of taurine and analogs of taurine that partially contain the N-C-C-S moiety within a semirigid saturated ring structure were tested for their effects on the phosphorylation of an ∼44-Kd protein present in the mitochondrial fraction of rat heart. (±)-Piperidine-3-sulfonic acid (PiP), an inhibitor of the phosphorylation of the ∼44-Kd protein with activity approx. similar to that of taurine, was observed to be mutually exclusive with taurine, i.e., to have a similar mode of action. The combination of taurine plus PiP in a fixed ratio mixture of 1:1 was slightly antagonistic at all concentrations (±)-Aminotetrahydrothiopyran-1,1-dioxide (APS), a sulfone derivative of taurine with a net pos. charge, also has approx. the same inhibitory activity as taurine. However, APS was mutually nonexclusive with taurine when tested in combination and thus appears to act independently of taurine. Taurine plus APS in a fixed ratio mixture of 3:1 was highly antagonistic at low concentrations of the mixture, approached an additive relation at 50% saturation, and became synergistic at high concentrations of the mixture Three analogs of taurine, pyridine-3-sulfonic acid (PyS), quinoline-8-sulfonic acid (QS), and 2-aminobenzenesulfonic acid (ABS), that have the basic taurine structure (N-C-C-S) partially in a semirigid unsaturated ring structure stimulate the phosphorylation of the ∼44-Kd protein. Due to the unsaturated ring structure, these analogs of taurine have a net neg. charge at physiol. pH and are not zwitterions. When PyS, QS, or ABS was titrated in the presence of a fixed concentration of taurine (10 mM), there was a competitive relation even through their electronic nature is quite different than that of taurine. The combination of QS plus PyS (1:5) appears to progress through a transition from being synergistic at low concentrations of the fixed ratio mixture, additive at 50% saturation, and finally antagonistic at high concentration of the fixed ratio mixture The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Safety of Pyridine-3-sulfonic acid

The Article related to taurine analog heart protein structure activity, Pharmacology: Structure-Activity and other aspects.Safety of Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On October 31, 1991, Kaczmarek, Lukasz; Nantka-Namirski, Pawel; Klodzinska, Aleksandra; Bujak, Barbara; Tatarczynska, Ewa published an article.Name: [2,2′-Bipyridine]-3,3′-diamine The title of the article was Synthesis and pharmacological properties of some dipyrido[1,3]diazepinones. And the article contained the following:

The synthesis of two isomeric dipyrido[1,3]diazepinones (I and II, R = e.g., Bu, 3-dimethylaminopropyl) and N-monosubstituted derivatives of I by cyclocondensation of corresponding bipyridinediamines with urea was described. The alkylation of these compounds with alkyl halides in K2CO3/DMF/TBAB system gave N,N’-disubstituted compounds Dipyrido[1,3]diazepinones and I showed a weak general depressive action on the central nervous system and they were also devoid of antidepressant, anxiolytic, anticonvulsant and serotoninolytic or serotoninomimetic properties. The experimental process involved the reaction of [2,2′-Bipyridine]-3,3′-diamine(cas: 75449-26-2).Name: [2,2′-Bipyridine]-3,3′-diamine

The Article related to dipyridodiazepinone pharmacol preparation, Pharmacology: Structure-Activity and other aspects.Name: [2,2′-Bipyridine]-3,3′-diamine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On December 1, 1995, Tanaka, Shunitz; Kodama, Kokoro; Kaneta, Takashi; Nakamura, Hiroshi published an article.Application In Synthesis of Pyridine-3-sulfonic acid The title of the article was Migration behavior of niacin derivatives in capillary electrophoresis. And the article contained the following:

The migration behavior of niacin derivatives was investigated by capillary zone electrophoresis (CZE) and micellar electrokinetic chromatog. (MEKC). When the pH of the buffer solution is lower than the pKa of the pyridine ring in the niacin derivatives, they are pos. charged by protonation on the pyridine ring and migrate electrophoretically. The mobilities of niacin derivatives in CZE were controlled by the pH of the migrating buffer. Good separation of 13 niacin derivatives was achieved at pH 2.8. Further, to shorten the anal. time and to achieve a more complete separation, an investigation by MEKC using SDS micelles was performed. All 13 niacin derivatives were eluted within 30 min and a satisfactory separation was achieved. 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 niacin derivative migration capillary zone electrophoresis, micellar electrokinetic chromatog niacin derivative, Biochemical Methods: Electrical and other aspects.Application In Synthesis of Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Xing, Kai; Fan, Rui-Qing; Liu, Xiao-Yuan; Gai, Shuang; Chen, Wei; Yang, Yu-Lin; Li, Jing published an article in 2020, the title of the article was A self-calibrating dual responsive platform for the sensitive detection of sulfite and sulfonic derivatives based on a robust Hf(IV) metal-organic framework.Name: Pyridine-3-sulfonic acid And the article contains the following content:

A robust hafnium-based metal organic framework, Hf-PBTA, with sensitive and self-calibrating dual-emissive fluorescence response towards sulfite and sulfonic derivatives, including antibiotic sulfamethazine, has been developed, which shows fast detection of sulfite ions at a concentration as low as 76 ppb. The opposite response tendency from two radiative pathways towards aromatic sulfonic mols. and sulfite anions stems from the synergistic effect of the pyridine protonation effect, π-π stacking interaction and intramol. twist motion. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Name: Pyridine-3-sulfonic acid

The Article related to fluorescent sensor sulfite sulfonic derivative metal organic framework, Organic Analytical Chemistry: Determinations and other aspects.Name: Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On August 13, 2012, Zhao, Hong-Wu; Li, Hai-Long; Yue, Yuan-Yuan; Qin, Xiao; Sheng, Zhi-Hui; Cui, Jin; Su, Shi; Song, Xiu-Qing; Yan, Hong; Zhong, Ru-Gang published an article.Safety of [2,2′-Bipyridine]-3,3′-diamine The title of the article was Design, synthesis and use of novel 3,3′-disubstituted 2,2′-bipyridine-based chiral ligands: asymmetric catalysis in direct aldol reactions. And the article contained the following:

A wide range of chiral ligands based on the 2,2′-bipyridine scaffold were designed and synthesized. In complexation with metal Lewis acids, the reactivity and stereoselectivity of the prepared chiral ligands were examined in asym. catalytic direct aldol reactions, thus providing the desired products with high stereoselectivities. The experimental process involved the reaction of [2,2′-Bipyridine]-3,3′-diamine(cas: 75449-26-2).Safety of [2,2′-Bipyridine]-3,3′-diamine

The Article related to bipyridine chiral ligand preparation asym aldol catalyst, General Organic Chemistry: Synthetic Methods and other aspects.Safety of [2,2′-Bipyridine]-3,3′-diamine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On October 15, 2021, Wang, Qiang; Wang, Yujia; Chen, Lin; Sun, Xuzhuo; Li, Bo; He, Shuanglin; Li, Jun; Wang, Ning published an article.Formula: C5H5NO3S The title of the article was Introducing electrostatic interaction into Ru(bda) complexes for promoting water-oxidation catalysis. And the article contained the following:

Ru(bda) (H2bda = 2,2′-bipyridine-6,6′-dicarboxylic acid) complex is a kind of well-known water oxidation catalyst, which goes through the bimol. I2M mechanism with an inter-catalyst O-O coupling step. Recently, we developed two facile strategies to accelerate O-O coupling via introducing the electrostatic interaction into Ru(bda)-catalyzed systems. In this work, a series of Ru(bda) complexes with different charged groups on different positions were synthesized to demonstrate the general applicability of these design strategies. It found these catalytic systems with attractive electrostatic interaction display much better activity, and the position of the charged substituents also has a significant influence on the catalytic activity. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Formula: C5H5NO3S

The Article related to ruthenium bipyridine complex electrostatic interaction water oxidation, Placeholder for records without volume info and other aspects.Formula: C5H5NO3S

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On February 28, 2019, Steinlechner, Christoph; Spannenberg, Anke; Junge, Henrik; Beller, Matthias published an article.Related Products of 109660-12-0 The title of the article was Tetracarbonyl[4,4-dimethyl-2-(pyridin-2-yl)-2-oxazoline-κ2N,N′]molybdenum(0). And the article contained the following:

In the title compound, [Mo(C10H12N2O)(CO)4], the molybdenum(0) center is surrounded by a bidentate diimine [4,4-dimethyl-2-(pyridin-2-yl)-2-oxazoline] and four carbonyl ligands in a distorted octahedral coordination geometry. The diimine ligand coordinates via the two nitrogen atoms. The experimental process involved the reaction of 2-(4,5-Dihydro-4,4-dimethyl-2-oxazolyl)pyridine(cas: 109660-12-0).Related Products of 109660-12-0

The Article related to tetracarbonyl dimethyl pyridinyl oxazoline molybdenum crystallization, Placeholder for records without volume info and other aspects.Related Products of 109660-12-0

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On January 31, 2020, Jin, Lei; Yang, Jia-Qiang; Yang, Fang-Zu; Wu, De-Yin; Tian, Zhong-Qun published an article.Application In Synthesis of Pyridine-3-sulfonic acid The title of the article was Electrochemistry and coordination behaviors of hypoxanthine-Au (III) ion in the cyanide-free gold electrodeposition. And the article contained the following:

Alkaloid hypoxanthine is a novel complexant for green cyanide-free Au(III) electrodeposition. The electrochem. and coordination behaviors of hypoxanthine-Au(III) ion in the green cyanide-free bath were studied. The electrochem. behavior confirms that hypoxanthine-Au(III) ion is in the irreversible two-step electro-reductions with the 1st controlled by diffusion and the 2nd by diffusion and electrochem. The stability constant of hypoxanthine-Au(III) ion is 4.8 × 1030. DFT calculations further indicate that the optimal coordination structure is N3-Au-N7 with the N-Au average bond energy of 11.03 eV. The bath component of K citrate plays almost no influence, whereas the additive of sulfocompounds shows a significant effect on the electro-reduction of hypoxanthine-Au(III) ion. Based on the cyanide-free Au(III) electrodeposition bath, the obtained Au coating is fine and compact in grains without organic inclusion and in the resistivity of 2.84 × 10-8 Ω m. 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 electrochem coordination hypoxanthine gold electrodeposition, Placeholder for records without volume info and other aspects.Application In Synthesis of Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Lombardini, J. B.; Props, C. published an article in 1997, the title of the article was Analogs of taurine as inhibitors of the phosphorylation of an ≈20 K molecular weight protein present in a mitochondrial fraction of the rat retina.Computed Properties of 636-73-7 And the article contains the following content:

It was previously demonstrated that taurine inhibits the phosphorylation of a ≈20 K apparent mol. weight protein present in the mitochondrial fraction of the rat retina. Analogs of taurine were tested for their inhibitory activity on the phosphorylation of this 20 K protein. The most potent analogs were (±)trans-2-aminocyclopentanesulfonic acid (TAPS) and 1,2,3,4-tetrahydroquinoline-8-sulfonic acid (THQS), which were 21 and 7 times more potent than the parent compound, taurine, resp. Median-effect plots were used to calculate the inhibitory median effect and combination index values for the combined effects of taurine and taurine analogs. It was determined that the inhibitory taurine analogs were antagonistic to taurine when used in combination with taurine to inhibit the phosphorylation of the 20 K apparent mol. weight protein. It was concluded that the distance between the N and S atoms in the taurine structure was important for inhibitory activity. If the N atom was either within or attached to an unsaturated ring structure, the inhibitory potency was decreased. If both the S and N atoms were present within the ring structure, the analog has no activity. 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 retina protein phosphorylation inhibition taurine analog, General Biochemistry: Subcellular Processes and other aspects.Computed Properties of 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

On August 15, 1997, Lee, Hon Cheung; Aarhus, Robert published an article.Quality Control of Pyridine-3-sulfonic acid The title of the article was Structural determinants of nicotinic acid adenine dinucleotide phosphate important for its calcium-mobilizing activity. And the article contained the following:

Nicotinic acid adenine dinucleotide phosphate (NAADP) mobilizes Ca2+ through a mechanism totally independent of cyclic ADP-ribose or inositol trisphosphate. The structural determinants important for its Ca2+ release activity were investigated using a series of analogs. It is shown that changing the 3-carboxyl group of the nicotinic acid (NA) moiety in NAADP to either an uncharged carbinol or from the 3-position to the 4-position of the pyridine ring totally eliminates the Ca2+ release activity. Conversion of the 3-carboxyl to other neg. charged groups, either 3-sulfonate, 3-acetate, or 3-quinoline carboxylate, retains the Ca2+ release activity, although their half-maximal effective concentrations (EC50) are 100-200-fold higher. Changing the 6-amino group of the adenine to a hydroxyl group results in more than a 1000-fold decrease in the Ca2+ release activity. Conversion of the 2′-phosphate to 2′,3′-cyclic phosphate or 3′-phosphate likewise increases the EC50 by about 5- and 20-fold, resp. Similar to NAADP, all of the active analogs can also desensitize the Ca2+ release mechanism at subthreshold concentrations, suggesting that this novel property is intrinsic to the release mechanism. The series of analogs used was produced by using ADP-ribosyl cyclase to catalyze the exchange of the nicotinamide group of various analogs of NADP with various analogs of NA. An important determinant in NA that is crucial to the base exchange reaction was shown to be the 2-position of the pyridine ring. Neither pyridine-2-carboxylate nor 2-methyl-NA support the exchange reaction. The neg. charge and the position of the 3-carboxyl group ware nonessential since both pyridine-3-carbinol and pyridine-4-carboxylate support the base exchange reaction. In addition to the information on the structure-activity relationships of NAADP and NA, this study also demonstrates the utility of the base exchange reaction as a general approach for synthesizing NAADP analogs. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Quality Control of Pyridine-3-sulfonic acid

The Article related to naadp na calcium transport cyclase, General Biochemistry: Subcellular Processes and other aspects.Quality Control of Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem