Takahashi, Eiki’s team published research in Bioorganic & Medicinal Chemistry Letters in 24 | CAS: 31719-76-3

Bioorganic & Medicinal Chemistry Letters published new progress about 31719-76-3. 31719-76-3 belongs to catalysis-chemistry, auxiliary class Carboxylic acid,Benzene,Ether, name is 4-(Phenoxymethyl)benzoic acid, and the molecular formula is C14H31NO2, HPLC of Formula: 31719-76-3.

Takahashi, Eiki published the artcileThe discovery of potent glycine transporter type-2 inhibitors: Design and synthesis of phenoxymethylbenzamide derivatives, HPLC of Formula: 31719-76-3, the publication is Bioorganic & Medicinal Chemistry Letters (2014), 24(18), 4603-4606, database is CAplus and MEDLINE.

The authors describe the discovery of phenoxymethylbenzamide derivatives as a novel class of glycine transporter type-2 (GlyT-2) inhibitors. The authors found a hit compound (human GlyT-2, IC50 = 4040 nM) in their library and converted its 1-[[(2-naphthalenyl)methyl]-4-piperidinyl]-3-pyrrolidine group to an 1-(N,N-dimethylaminopropyl)piperidine group and its tert-Bu group to a trifluoromethyl group to obtain N-[1-[3-(dimethylamino)propyl]-4-piperidinyl]-4-[[4-(trifluoromethyl)phenoxy]methyl]benzamide. This compound showed good inhibitory activity against human GlyT-2 (IC50 = 15.3 nM) and exhibited antiallodynia effects in a mouse neuropathic pain model. The title compounds thus formed included N-(1′-methyl[1,4′-bipiperidin]-4-yl)-4-[[4-(trifluoromethyl)phenoxy]methyl]benzamide, N-[1-[3-(dimethylamino)propyl]-4-piperidinyl]-4-[[4-(trifluoromethyl)phenoxy]methyl]benzamide. The synthesis of the target compounds was achieved by a reaction of 4-(phenoxymethyl)benzoic acid derivatives with amines, such as 1-[1-(phenylmethyl)-4-piperidinyl]-3-pyrrolidinamine, 1′-methyl-[1,4′-bipiperidin]-4-amine, 4-amino-N,N-dimethyl-1-piperidinepropanamine, 4-amino-1-piperidineethanol and similar compounds

Bioorganic & Medicinal Chemistry Letters published new progress about 31719-76-3. 31719-76-3 belongs to catalysis-chemistry, auxiliary class Carboxylic acid,Benzene,Ether, name is 4-(Phenoxymethyl)benzoic acid, and the molecular formula is C14H31NO2, HPLC of Formula: 31719-76-3.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Yokoyama, Masataka’s team published research in Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) in | CAS: 6972-05-0

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C14H28O5S, Computed Properties of 6972-05-0.

Yokoyama, Masataka published the artcileSynthesis of heterocycles using a new immonium salt derived from N,N-dimethylthiourea, Computed Properties of 6972-05-0, the publication is Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) (1982), 1059-62, database is CAplus.

Treatment of Me2NCSNH2 with NaH, CS2 and MeI in THF gave Me2NC(SMe):N+MeCS2Me I (I), which underwent cyclocondensation reactions with nucleophiles to give heterocycles including triazolines, an oxadiazole, a thiazole, a triazine, a benzoxadiazepine and a benzothiadiazepine. E.g., I was refluxed in EtOH with N2H4 for 4 h to give 74% triazolinethione II. Similar treatment of I with HSCH2CO2Et-LiN(CHMe2)2 in THF at -70° for 1 h and at room temperature for 1 h gave 47% thiazole III.

Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) published new progress about 6972-05-0. 6972-05-0 belongs to catalysis-chemistry, auxiliary class Thiourea,Amine,Aliphatic hydrocarbon chain,Amide, name is 1,1-Dimethylthiourea, and the molecular formula is C14H28O5S, Computed Properties of 6972-05-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Lindstedt, Philip R.’s team published research in ACS Central Science in 5 | CAS: 2051-95-8

ACS Central Science published new progress about 2051-95-8. 2051-95-8 belongs to catalysis-chemistry, auxiliary class Carboxylic acid,Benzene,Ketone, name is 3-Benzoylpropionicacid, and the molecular formula is C10H10O3, Related Products of catalysis-chemistry.

Lindstedt, Philip R. published the artcileEnhancement of the anti-aggregation activity of a molecular chaperone using a rationally designed post-translational modification, Related Products of catalysis-chemistry, the publication is ACS Central Science (2019), 5(8), 1417-1424, database is CAplus and MEDLINE.

Protein behavior is closely regulated by a plethora of post-translational modifications (PTMs). It is therefore desirable to develop approaches to design rational PTMs to modulate specific protein functions. Here, we report one such method, and we illustrate its successful implementation by potentiating the anti-aggregation activity of a mol. chaperone. Mol. chaperones are a multifaceted class of proteins essential to protein homeostasis, and one of their major functions is to combat protein misfolding and aggregation, a phenomenon linked to a number of human disorders. In this work, we conjugated a small-mol. inhibitor of the aggregation of α-synuclein, a process associated with Parkinson’s disease (PD), to a specific cysteine residue on human Hsp70, a mol. chaperone with five free cysteines. We show that this regioselective conjugation augments in vitro the anti-aggregation activity of Hsp70 in a synergistic manner. This Hsp70 variant also displays in vivo an enhanced suppression of α-synuclein aggregation and its associated toxicity in a Caenorhabditis elegans model of PD.

ACS Central Science published new progress about 2051-95-8. 2051-95-8 belongs to catalysis-chemistry, auxiliary class Carboxylic acid,Benzene,Ketone, name is 3-Benzoylpropionicacid, and the molecular formula is C10H10O3, Related Products of catalysis-chemistry.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Bardin, V. V.’s team published research in Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya in | CAS: 1206-46-8

Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya published new progress about 1206-46-8. 1206-46-8 belongs to catalysis-chemistry, auxiliary class Organic Silicones, name is Trimethyl(perfluorophenyl)silane, and the molecular formula is C9H9F5Si, Quality Control of 1206-46-8.

Bardin, V. V. published the artcilePolyfluorophenylation of halosilanes, -germanes and -stannanes, Quality Control of 1206-46-8, the publication is Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya (1989), 2153-4, database is CAplus.

Reaction of R3MX (R = Me, Et; M = Si, Ge, Sn; X = Cl, Br) with 4-R1C6F4Br (R1 = F, PrO, CF3) in pentane containing P(NEt2)3 gave 4-R1C6F4MR3. Thus, reaction of C6F5Br with Me3MCl (M = Si, Ge, Sn) gave 50-66% C6F5MMe3.

Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya published new progress about 1206-46-8. 1206-46-8 belongs to catalysis-chemistry, auxiliary class Organic Silicones, name is Trimethyl(perfluorophenyl)silane, and the molecular formula is C9H9F5Si, Quality Control of 1206-46-8.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Bardin, V. V.’s team published research in Zhurnal Obshchei Khimii in 60 | CAS: 1206-46-8

Zhurnal Obshchei Khimii published new progress about 1206-46-8. 1206-46-8 belongs to catalysis-chemistry, auxiliary class Organic Silicones, name is Trimethyl(perfluorophenyl)silane, and the molecular formula is C9H9F5Si, COA of Formula: C9H9F5Si.

Bardin, V. V. published the artcileReactions of (triethylgermyl)pentafluorobenzene and perfluorotetraphenylgermane with nucleophiles, COA of Formula: C9H9F5Si, the publication is Zhurnal Obshchei Khimii (1990), 60(8), 1820-6, database is CAplus.

Oxygen- or nitrogen-containing nucleophiles attack the Ge atom in Et3GeC6F5, while sulfur-, carbon-, and hydrogen-containing nucleophiles attack the C-4 atom of the C6F5 group. (C6F5)4Ge undergoes Caryl-Ge bond cleavage in reactions with O– and S-nucleophiles, while reactions with C-nucleophiles give complex mixtures of products from cleavage and defluorination. Piperidine reacts with (C6F5)4Ge by substitution of an F atom, apparently due to steric screening of Ge.

Zhurnal Obshchei Khimii published new progress about 1206-46-8. 1206-46-8 belongs to catalysis-chemistry, auxiliary class Organic Silicones, name is Trimethyl(perfluorophenyl)silane, and the molecular formula is C9H9F5Si, COA of Formula: C9H9F5Si.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Kuo, Ying Che’s team published research in Chemical & Pharmaceutical Bulletin in 30 | CAS: 1949-41-3

Chemical & Pharmaceutical Bulletin published new progress about 1949-41-3. 1949-41-3 belongs to catalysis-chemistry, auxiliary class Carboxylic acid,Benzene, name is 2-Methyl-4-phenylbutanoic acid, and the molecular formula is C11H14O2, Application In Synthesis of 1949-41-3.

Kuo, Ying Che published the artcileNew methods and reagents in organic synthesis. 26. Reductive desulfonylation of α-sulfonylacetates, Application In Synthesis of 1949-41-3, the publication is Chemical & Pharmaceutical Bulletin (1982), 30(8), 2787-92, database is CAplus.

α-Acyl-α-benzylsulfonyldiazomethanes RCOC(:N2)SO2CH2Ph (R = Ph, PhCH2CH2, Me2CH, cyclohexyl) have been converted to RCH(CO2H)SO2CH2Ph (I, same R) by Wolff rearrangement. Reductive removal of the benzylsulfonyl group of I (R = PhCH2CH2, Me2CH, cyclohexyl) can be achieved by Na-EtOH in THF. HO2CCRMeSO2CH2Ph (same R), prepared from benzyl α-benzylsulfonyl-α-substituted acetates, were also benzylsulfonylated under similar reductive conditions. The overall process, in combination with the Arndt-Eistert synthesis of α-sulfonylacetates from acyl chlorides and benzylsulfonyldiazomethane, provides a new, safe method for the homologation of carboxylic acids.

Chemical & Pharmaceutical Bulletin published new progress about 1949-41-3. 1949-41-3 belongs to catalysis-chemistry, auxiliary class Carboxylic acid,Benzene, name is 2-Methyl-4-phenylbutanoic acid, and the molecular formula is C11H14O2, Application In Synthesis of 1949-41-3.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Luo, Na’s team published research in Chemistry – An Asian Journal in 16 | CAS: 140-28-3

Chemistry – An Asian Journal published new progress about 140-28-3. 140-28-3 belongs to catalysis-chemistry, auxiliary class Benzenes, name is N1,N2-Dibenzylethane-1,2-diamine, and the molecular formula is C16H20N2, COA of Formula: C16H20N2.

Luo, Na published the artcileπ-Face Promoted Catalysis in Water: From Electron-deficient Molecular Cages to Single Aromatic Slides, COA of Formula: C16H20N2, the publication is Chemistry – An Asian Journal (2021), 16(22), 3599-3603, database is CAplus and MEDLINE.

Exploiting noncovalent π-interactions particularly emerging anion-π interactions to drive efficient catalysis is fascinating. Even with exciting progresses, can anion-π activation operate in water remains elusive. Herein, design, synthesis and catalytic studies of a class of water-soluble electron-deficient mol. cages and relevant aromatic slide compounds is reported. The prism-like cages contain three divided, long, cationic aromatic walls which constitute three highly electron-deficient V-shape cavities. They were efficiently synthesized in two steps from a parent triformyl cage in gram-scale. Crystal structure showed the π-walls bind to the counter bromide through strong anion-π interactions. Just 5 mol% of cages were effective in catalyzing decarboxylative Aldol reactions of aldehydes and malonic acid half thioesters in water but not in organic solvents, showing a pronounced hydrophobic amplification effect. Meantime, a series of single π-slides resembling the π-wall of the cage performed equally well, while those lacking an extended π-surface were ineffective, highlighting the essential role of electron-deficient π-face on promoting the conversion.

Chemistry – An Asian Journal published new progress about 140-28-3. 140-28-3 belongs to catalysis-chemistry, auxiliary class Benzenes, name is N1,N2-Dibenzylethane-1,2-diamine, and the molecular formula is C16H20N2, COA of Formula: C16H20N2.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Rao, K. Hanumantha’s team published research in Minerals & Metallurgical Processing in 7 | CAS: 2016-56-0

Minerals & Metallurgical Processing published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Computed Properties of 2016-56-0.

Rao, K. Hanumantha published the artcileFlotation of mica minerals and selectivity between muscovite and biotite while using mixed anionic/cationic collectors, Computed Properties of 2016-56-0, the publication is Minerals & Metallurgical Processing (1990), 7(3), 127-32, database is CAplus.

Selective flotation of muscovite from a material containing muscovite 15.4, biotite 13%, and quartz and feldspar gangue by using a mixed collector system of Na oleate and dodecylamine acetate is described. Muscovite floats in preference to biotite, when the pulp is initially conditioned with oleate followed by amine at basic pH values. A product containing 63% muscovite with a recovery of 93% was obtained, while using 75-150 oleate and 96 g/ton amine. The biotite grade and recovery are �0 and 20%, resp. High selectivity between muscovite and siliceous gangue is obtained. A final product containing 95% muscovite with an overall recovery of 75% is obtained when the flotation concentrate is subjected to magnetic separation The possibility of separating muscovite from biotite by using a mixture of collectors is discussed.

Minerals & Metallurgical Processing published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Computed Properties of 2016-56-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Rao, K. Hanumantha’s team published research in Transactions of Society for Mining, Metallurgy, and Exploration, Inc. in 288 | CAS: 2016-56-0

Transactions of Society for Mining, Metallurgy, and Exploration, Inc. published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Quality Control of 2016-56-0.

Rao, K. Hanumantha published the artcileFlotation of mica minerals and selectivity between muscovite and biotite while using mixed anionic/cationic collectors, Quality Control of 2016-56-0, the publication is Transactions of Society for Mining, Metallurgy, and Exploration, Inc. (1991), 127-32, database is CAplus.

Selective flotation of muscovite from a material containing muscovite (15.4%), biotite (13%), and siliceous gangue (quartz and feldspar), using a mixed collector system of Na oleate and dodecylamine acetate, is described. Muscovite floats in preference to biotite when the pulp is initially conditioned with oleate followed by amine at basic pH values. The results indicate that a product containing 63% muscovite with a recovery of 93% can be obtained while using 75-150 g oleate and 96 g amine per ton. The biotite grade and recovery are �0 and 20%, resp. A good selectivity between muscovite and siliceous gangue is obtained. A final product containing 95% muscovite with an overall recovery of 75% is obtained when the flotation concentrate is subjected to magnetic separation Thus, muscovite can be separated from biotite by using a mixture of collectors.

Transactions of Society for Mining, Metallurgy, and Exploration, Inc. published new progress about 2016-56-0. 2016-56-0 belongs to catalysis-chemistry, auxiliary class Active Esterification, name is Dodecylamineacetate, and the molecular formula is C14H31NO2, Quality Control of 2016-56-0.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia

Shaimol, T.’s team published research in World Journal of Pharmaceutical Research in 6 | CAS: 38260-01-4

World Journal of Pharmaceutical Research published new progress about 38260-01-4. 38260-01-4 belongs to catalysis-chemistry, auxiliary class Chelating Agents, name is N1,N1′-(Ethane-1,2-diyl)bis(ethane-1,2-diamine) dihydrochloride, and the molecular formula is C7H8BNO5, COA of Formula: C6H20Cl2N4.

Shaimol, T. published the artcileWilson disease-an overview, COA of Formula: C6H20Cl2N4, the publication is World Journal of Pharmaceutical Research (2017), 6(1), 154-175, database is CAplus.

A review. Wilson disease is a rare inherited disorder that prevents the body from getting rid of extra copper. Our body needs a small amount of copper from food to stay healthy. Too much copper is poisonous. The condition is due to mutations in the Wilson disease protein (ATP7B) gene. Normally liver releases extra copper into bile. With Wilson disease, the copper builds up in liver and it releases the copper directly into bloodstream. This can cause damage to brain, kidneys and eyes. Wilson disease is present at birth, but symptoms usually start between ages 5 and 35. It first attacks the liver, the central nervous system or both. The most characteristic sign is a rusty brown ring around the cornea of the eye. A phys. exam and laboratory tests can diagnose it. Treatment is with drugs to remove the extra copper from body. It needs to take medicine and follow a low-copper diet for the rest of life. WD is treated with medication that reduces copper absorption or removes the excess copper from the body, but occasionally a liver transplant is required. A single abnormal copy of the gene is present in 1 in 100 people, who do not develop any symptoms (they are carriers). If a child inherits the gene from both parents, the child may develop Wilson’s disease. Wilson’s disease occurs in 1 to 4 per 100,000 people.

World Journal of Pharmaceutical Research published new progress about 38260-01-4. 38260-01-4 belongs to catalysis-chemistry, auxiliary class Chelating Agents, name is N1,N1′-(Ethane-1,2-diyl)bis(ethane-1,2-diamine) dihydrochloride, and the molecular formula is C7H8BNO5, COA of Formula: C6H20Cl2N4.

Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia