Category: 104-10-9

Recently I am researching about MAGNETIC-RESONANCE-SPECTROSCOPY; POSITRON-EMISSION-TOMOGRAPHY; PROSTATE-CANCER; RADIATION-DOSIMETRY; LUNG-CANCER; IN-VITRO; METABOLISM; F-18-FLUOROCHOLINE; DIAGNOSIS; CELLS, Saw an article supported by the Czech Science FoundationGrant Agency of the Czech Republic [19-01602S]; Ministry of Health of the Czech RepublicMinistry of Health, Czech Republic [16-30544A]; Ministry of Education, Youth and Sports of the Czech RepublicMinistry of Education, Youth & Sports – Czech Republic [LM2015064 EATRIS-CZ, LO1304, CZ.02.1.01/0.0/0.0/16_013/0001818, CZ.02.1.01/0.0/0.0/16_019/0000868]; Technology Agency of the Czech Republic [TE01020028]; Charles University Grant Agency [766119]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Svec, P; Novy, Z; Kucka, J; Petrik, M; Sedlacek, O; Kuchar, M; Liskova, B; Medvedikova, M; Kolouchova, K; Groborz, O; Loukotova, L; Konefal, RL; Hajduch, M; Hruby, M. The CAS is 104-10-9. Through research, I have a further understanding and discovery of 2-(4-Aminophenyl)ethanol. SDS of cas: 104-10-9

We present a novel series of radioiodinated tracers and potential theranostics for diseases accompanied by pathological function of proteins involved in choline transport. Unlike choline analogues labeled with C-11 or F-18 that are currently used in the clinic, the iodinated compounds described herein are applicable in positron emission tomography, single-photon emission computed tomography, and potentially in therapy, depending on the iodine isotope selection. Moreover, favorable half-lives of iodine isotopes result in much less challenging synthesis by isotope exchange reaction. Six of the described compounds were nanomolar ligands, and the best compound possessed an affinity 100-fold greater than that of choline. Biodistribution data of I-125-labeled ligands in human prostate carcinoma bearing (PC-3) mice revealed two compounds with a biodistribution profile superior to that of [F-18]fluorocholine.

About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Svec, P; Novy, Z; Kucka, J; Petrik, M; Sedlacek, O; Kuchar, M; Liskova, B; Medvedikova, M; Kolouchova, K; Groborz, O; Loukotova, L; Konefal, RL; Hajduch, M; Hruby, M or concate me.. SDS of cas: 104-10-9

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

Computed Properties of C8H11NO. I found the field of Biochemistry & Molecular Biology; Chemistry very interesting. Saw the article C-N Coupling of DNA-Conjugated (Hetero)aryl Bromides and Chlorides for DNA-Encoded Chemical Library Synthesis published in 2020, Reprint Addresses Chen, YC; Simmons, N (corresponding author), Baylor Coll Med, Ctr Drug Discovery, Dept Pathol & Immunol, Houston, TX 77030 USA.. The CAS is 104-10-9. Through research, I have a further understanding and discovery of 2-(4-Aminophenyl)ethanol.

DNA-encoded chemical library (DECL) screens are a rapid and economical tool to identify chemical starting points for drug discovery. As a robust transformation for drug discovery, palladium-catalyzed C-N coupling is a valuable synthetic method for the construction of DECL chemical matter; however, currently disclosed methods have only been demonstrated on DNA-attached (hetero)aromatic iodide and bromide electrophiles. We developed conditions utilizing an N-heterocyclic carbene-palladium catalyst that extends this reaction to the coupling of DNA-conjugated (hetero)aromatic chlorides with (hetero)aromatic and select aliphatic amine nucleophiles. In addition, we evaluated steric and electronic effects within this catalyst series, carried out a large substrate scope study on two representative (hetero)aryl bromides, and applied this newly developed method within the construction of a 63 million-membered DECL.

Computed Properties of C8H11NO. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Chen, YC; Faver, JC; Ku, AF; Miklossy, G; Riehle, K; Bohren, KM; Ucisik, MN; Matzuk, MM; Yu, ZF; Simmons, N or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

COA of Formula: C8H11NO. In 2021.0 CHEMBIOCHEM published article about TRANSCRIPTION; GENE in [Huang, Jinguo; Zhao, Ruiqi; Qin, Shanshan; Yang, Shixi; Li, Wei; Mo, Jing; Du, Yuhao; Weng, Xiaocheng; Zhou, Xiang] Wuhan Univ, Hubei Prov Key Lab Allergy & Immunol, Minist Educ, Coll Chem & Mol Sci,Key Lab Biomed Polymers, Wuhan 430072, Hubei, Peoples R China; [Wang, Fang] Wuhan Univ, Sch Pharmaceut Sci, Wuhan 430071, Peoples R China in 2021.0, Cited 27.0. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9.

Peroxidase-generated proximity labeling is in widespread use to study subcellular proteomes and the protein interaction networks in living cells, but the development of subcellular RNA labeling is limited. APEX-seq has emerged as a new method to study subcellular RNA in living cells, but the labeling of RNA still has room to improve. In this work, we describe 4-thiouridine (s(4)U)-enhanced peroxidase-generated biotinylation of RNA with high efficiency. The incorporation of s(4)U could introduce additional sites for RNA labeling, enhanced biotinylation was observed on monomer, model oligo RNA and total RNA. Through the s(4)U metabolic approach, thein vivoRNA biotinylation efficiency by peroxidase catalysis was also dramatically increased, which will benefit RNA isolation and study for the spatial transcriptome.

COA of Formula: C8H11NO. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Huang, JG; Zhao, RQ; Qin, SS; Yang, SX; Li, W; Mo, J; Wang, F; Du, YH; Weng, XC; Zhou, X or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

An article A-ring and E-ring modifications of the cytotoxic alkaloid Luotonin A: Synthesis, computational and biological studies WOS:000523307500003 published article about TOPOISOMERASE-I INHIBITOR; S-PHASE; DNA; ARREST; CAMPTOTHECIN; DOXORUBICIN; INDUCTION; EFFICIENT; APOPTOSIS; DERIVATIVES in [Ibric, Amra; Battisti, Verena; Deckardt, Sophie; Haller, Anna Veronika; Lee, Calvin; Proetsch, Corinna; Langer, Thierry; Haider, Norbert] Univ Vienna, Dept Pharmaceut Chem, Althanstr 14, A-1090 Vienna, Austria; [Heffeter, Petra; Schueffl, Hemma Henrike; Marian, Brigitte] Med Univ Vienna, Inst Canc Res, Borschkegasse 8a, A-1090 Vienna, Austria; [Heffeter, Petra; Schueffl, Hemma Henrike; Marian, Brigitte] Med Univ Vienna, Comprehens Canc Ctr, Borschkegasse 8a, A-1090 Vienna, Austria in 2020.0, Cited 56.0. Category: amides-buliding-blocks. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9

A series of new Luotonin A derivatives with substituents at rings A and E was synthesized, together with some E-ring-unsubstituted derivatives. Subsequently, the compound library was examined in silico for their binding into a previously proposed site in the DNA/topoisomerase I binary complex. Whereas no convincing correlation between docking scores and biological data from in vitro assays could be found, one novel 4,9-diamino Luotonin A derivative had strong antiproliferative activity based on massive G2/M phase arrest. As this biological activity clearly differs from the reference compound Camptothecin, this strongly indicates that at least some Luotonin A derivatives may be potent antiproliferative agents, however with a different mode of action.

About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Ibric, A; Battisti, V; Deckardt, S; Haller, AV; Lee, C; Protsch, C; Langer, T; Heffeter, P; Schueffl, HH; Marian, B; Haider, N or concate me.. Category: amides-buliding-blocks

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

Authors Giampietro, L; Laghezza, A; Cerchia, C; Florio, R; Recinella, L; Capone, F; Ammazzalorso, A; Bruno, I; De Filippis, B; Fantacuzzi, M; Ferrante, C; Maccallini, C; Tortorella, P; Verginelli, F; Brunetti, L; Cama, A; Amoroso, R; Loiodice, F; Lavecchia, A in AMER CHEMICAL SOC published article about BINDING; MECHANISMS; INSIGHTS; ACID in [Giampietro, Letizia; Florio, Rosalba; Recinella, Lucia; Ammazzalorso, Alessandra; Bruno, Isabella; De Filippis, Barbara; Fantacuzzi, Marialuigia; Ferrante, Claudio; Maccallini, Cristina; Verginelli, Fabio; Brunetti, Luigi; Cama, Alessandro; Amoroso, Rosa] Univ G dAnnunzio, Dept Pharm, Via Vestini 31, I-66100 Chieti, Italy; [Laghezza, Antonio; Tortorella, Paolo; Loiodice, Fulvio] Univ Bari Aldo Moro, Dept Pharm Drug Sci, Via E Orabona 4, I-70126 Bari, Italy; [Cerchia, Carmen; Capone, Fabio; Lavecchia, Antonio] Univ Napoli Federico II, Drug Discovery Lab, Dept Pharm, Via D Montesano 49, I-80131 Naples, Italy; [Florio, Rosalba; Verginelli, Fabio; Cama, Alessandro] Univ G dAnnunzio, Ctr Aging Sci & Translat Med CeSI MeT, Via Luigi Polacchi 11, I-66100 Chieti, Italy in 2019.0, Cited 30.0. Name: 2-(4-Aminophenyl)ethanol. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9

The development of PPAR alpha/gamma dual or PPAR alpha/gamma/S pan-agonists could represent an efficacious approach for a simultaneous pharmacological intervention on carbohydrate and lipid metabolism. Two series of new phenyldiazenyl fibrate derivatives of GL479, a previously reported PPAR alpha/gamma dual agonist, were synthesized and tested. Compound 12a was identified as a PPAR pan-agonist with moderate and balanced activity on the three PPAR isoforms (alpha, gamma, delta). Moreover, docking experiments showed that 12a adopts a different binding mode in PPARy compared to PPARa or PPARS, providing a structural basis for further structure-guided design of PPAR pan-agonists. The beneficial effects of 12a were evaluated both in vitro, on the expression of PPAR target key metabolic genes, and ex vivo in two rat tissue inflammatory models. The obtained results allow considering this compound as an interesting lead for the development of a new class of PPAR pan-agonists endowed with an activation profile exploitable for therapy of metabolic syndrome.

Name: 2-(4-Aminophenyl)ethanol. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Giampietro, L; Laghezza, A; Cerchia, C; Florio, R; Recinella, L; Capone, F; Ammazzalorso, A; Bruno, I; De Filippis, B; Fantacuzzi, M; Ferrante, C; Maccallini, C; Tortorella, P; Verginelli, F; Brunetti, L; Cama, A; Amoroso, R; Loiodice, F; Lavecchia, A or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

Authors Brown, PD; Lawrence, AL in ROYAL SOC CHEMISTRY published article about BIOMIMETIC SYNTHESIS; INCARVIDITONE; INCARVILLEATONE; ALKALOIDS; DIMER in [Brown, Patrick D.; Lawrence, Andrew L.] Univ Edinburgh, Sch Chem, EaStCHEM, Joseph Black Bldg,David Brewster Rd, Edinburgh EH9 3FJ, Midlothian, Scotland in 2019.0, Cited 28.0. Application In Synthesis of 2-(4-Aminophenyl)ethanol. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9

Synthetic studies into the origins of the alkaloid incargranine A have resulted in the development of a four-step (longest linear sequence) total synthesis. This synthesis has been scaled-up to provide gram-scale quantities of material, which would alternatively require extraction of several metric-tons of dried-whole Chinese Trumpet-Creeper plants (Incarvillea mairei var. grandiflora).

Application In Synthesis of 2-(4-Aminophenyl)ethanol. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Brown, PD; Lawrence, AL or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

Quality Control of 2-(4-Aminophenyl)ethanol. In 2020.0 J MED CHEM published article about FATTY LIVER-DISEASE; DIET-INDUCED OBESITY; OXIDATIVE-PHOSPHORYLATION; METABOLIC-INHIBITORS; INSULIN-RESISTANCE; CANCER-CELLS; DINITROPHENOL; PROTON; MECHANISM; BIOENERGETICS in [Hargett, Stefan R.; Hoehn, Kyle L.] Univ Virginia, Dept Pharmacol, Charlottesville, VA 22908 USA; [Hargett, Stefan R.; Hoehn, Kyle L.] Univ Virginia, Dept Med, Charlottesville, VA 22908 USA; [Chen, Sing-Young; Beretta, Martina; Alexopoulos, Stephanie J.; Shah, Divya P.; Olzomer, Ellen M.; Hoehn, Kyle L.] Univ New South Wales, Sch Biotechnol & Biomol Sci, Kensington, NSW 2033, Australia; [Salamoun, Joseph M.; Garcia, Christopher J.; Murray, Jacob H.; Santos, Webster L.] Virginia Tech, Dept Chem, Blacksburg, VA 24061 USA; [Salamoun, Joseph M.; Garcia, Christopher J.; Murray, Jacob H.; Santos, Webster L.] Virginia Tech, Virginia Tech Ctr Drug Discovery, Blacksburg, VA 24061 USA; [Tucker, Simon P.] Continuum Biosci Pty Ltd, Sydney, NSW 2035, Australia; [Tucker, Simon P.] Continuum Biosci Inc, Boston, MA 02116 USA in 2020.0, Cited 93.0. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9.

Small molecule mitochondrial uncouplers have recently garnered great interest for their potential in treating nonalcoholic steatohepatitis (NASH). In this study, we report the structure-activity relationship profiling of a 6-amino[1,2,5]oxadiazolo[3,4-b]pyrazin-5-ol core, which utilizes the hydroxy moiety as the proton transporter across the mitochondrial inner membrane. We demonstrate that a wide array of substituents is tolerated with this novel scaffold that increased cellular metabolic rates in vitro using changes in oxygen consumption rate as a readout. In particular, compound SHS4121705 (12i) displayed an EC50 of 4.3 mu M in L6 myoblast cells and excellent oral bioavailability and liver exposure in mice. In the STAM mouse model of NASH, administration of 12i at 25 mg kg(-1) day(-1) lowered liver triglyceride levels and improved liver markers such as alanine aminotransferase, NAFLD activity score, and fibrosis. Importantly, no changes in body temperature or food intake were observed. As potential treatment of NASH, mitochondrial uncouplers show promise for future development.

About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Salamoun, JM; Garcia, CJ; Hargett, SR; Murray, JH; Chen, SY; Beretta, M; Alexopoulos, SJ; Shah, DP; Olzomer, EM; Tucker, SP; Hoehn, KL; Santos, WL or concate me.. Quality Control of 2-(4-Aminophenyl)ethanol

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

I found the field of Polymer Science very interesting. Saw the article Synthesis, characterization, and antibacterial activities of a new lignocellulosic material carrying aryl triazole moiety published in 2019.0. Formula: C8H11NO, Reprint Addresses Zerrouki, R (corresponding author), Univ Limoges, Lab Chim Subst Nat, EA 1069, 123 Ave Albert Thomas, F-87060 Limoges, France.. The CAS is 104-10-9. Through research, I have a further understanding and discovery of 2-(4-Aminophenyl)ethanol

Contamination of surfaces by bacteria and the emergence of antimicrobial resistant strains are very worrying issues. One of ways to limit the bacterial proliferation is to develop antimicrobial materials. We reported herein the development of new antimicrobial support by grafting different aryl azide onto propargylated Kraft Pulp, using the copper (I)-catalyzed alkyne-azide 1,3-dipolar cycloaddition (CuAAC) reaction, forming 1,2,3-triazole aryl. These novel materials have been investigated for their antibacterial properties against Escherichia coli and Staphylococcus aureus. The developed materials acquire its antimicrobial potential only after grafting via triazole link. Depending on the substituent of the grafted aryl, the elaborated materials showed a bacteriostatic or even bactericidal activity.

Formula: C8H11NO. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Khaldi, Z; Besse, C; Keki, JKNT; Ouk, TS; Gloaguen, V; Zerrouki, R or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

An article Enantioselective Hydrative para-Dearomatization of Sulfonanilides by an Indanol-based Chiral Organoiodine Catalyst WOS:000641165200001 published article about HYPERVALENT IODINE REAGENTS; OXIDATIVE SPIROLACTONIZATION; SPIROCYCLIZATION; DIARYLAMINES; FLUORINATION; ANILINES; PHENOLS in [Shimazaki, Yuto; Maruoka, Keiji] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Kyoto 6068502, Japan; [Wata, Chisato; Hashimoto, Takuya] Chiba Univ, Chiba Iodine Resource Innovat Ctr, Inage Ku, 1-33 Yayoi, Chiba 2638522, Japan; [Wata, Chisato; Hashimoto, Takuya] Chiba Univ, Dept Chem, Grad Sch Sci, Inage Ku, 1-33 Yayoi, Chiba 2638522, Japan; [Maruoka, Keiji] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Panyu District, Peoples R China; [Maruoka, Keiji] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan in 2021.0, Cited 89.0. The Name is 2-(4-Aminophenyl)ethanol. Through research, I have a further understanding and discovery of 104-10-9. Application In Synthesis of 2-(4-Aminophenyl)ethanol

We report herein the development of an enantioselective oxidative para-dearomatization of sulfonanilides with water by use of an indanol-based chiral organoiodine catalyst, originally developed in our group. This reaction proceeds efficiently by the use of N-mesyl-protected anilines as substrates, giving functionalized p-quinol imines in good yields and moderate to high enantioselectivities.

Application In Synthesis of 2-(4-Aminophenyl)ethanol. About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Shimazaki, Y; Wata, C; Hashimoto, T; Maruoka, K or concate me.

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics

Recently I am researching about DNA; CATALYSIS; RECOGNITION, Saw an article supported by the Japan Society for the Promotion of Science (JSPS)Ministry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of Science [16H06356]; KAKENHI programMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [18K05315]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Yum, JH; Sugiyama, H; Park, S. The CAS is 104-10-9. Through research, I have a further understanding and discovery of 2-(4-Aminophenyl)ethanol. Category: amides-buliding-blocks

Asymmetric synthesis based on DNA scaffolds has been actively exploited because of the advantages of DNA such as diverse tertiary structures, chemical stability, and easy handling. Since duplex DNA-based hybrid catalysts have demonstrated this remarkable capability, efforts have been made to investigate new biomolecular scaffolds. Herein, we report modular quadruplex-duplex (QD) hybrid DNA catalysts containing bipyridine ligands and hydrogen donor moieties. The conformation, thermal stability, and metal-binding ability of modified QD hybrid DNA were characterized using spectroscopy. The QD hybrid-based DNA catalysts were successfully applied to asymmetric Michael addition reactions (86% conversion and 76% ee). This study describes a new type of DNA hybrid catalyst produced by the construction of a cooperative active site with a Lewis acid and a H-bond donor.

About 2-(4-Aminophenyl)ethanol, If you have any questions, you can contact Yum, JH; Sugiyama, H; Park, S or concate me.. COA of Formula: C8H11NO

Reference:
Amide – Wikipedia,
,Amide – an overview | ScienceDirect Topics