Month: December 2021

Recently I am researching about FACTOR RECEPTOR KINASE; SUBSTITUTED QUINOLINONES; PYRAZOLE DERIVATIVES; POTENTIAL ANTICANCER; ERLOTINIB; CANCER; CRIZOTINIB; CHEMISTRY; ASSAY, Saw an article supported by the . Published in ACADEMIC PRESS INC ELSEVIER SCIENCE in SAN DIEGO ,Authors: Elbastawesy, MAI; Aly, AA; Ramadan, M; Elshaier, YAMM; Youssif, BGM; Brown, AB; Abuo-Rahma, GEDA. The CAS is 86-95-3. Through research, I have a further understanding and discovery of 4-Hydroxyquinolin-2(1H)-one. Quality Control of 4-Hydroxyquinolin-2(1H)-one

Two new series of diethyl 2-[2-(substituted-2-oxo-1,2-dihydroquinolin-4-yl)hydrazono]-succinates 6a-g and 1-(2-oxo-1,2-dihydroquinolin-4-yl)-1H-pyrazoles 7a-f have been designed and synthesized. The structures of the synthesized compounds were proved by IR, mass, NMR (2D) spectra and elemental analyses. The target compounds were evaluated for their in vitro cytotoxic activity against 60 cancer cell lines according to NCI protocol. Consequently, seven compounds were further examined against the most sensitive cell lines, leukemia CCRFCEM, and MOLT-4. 5-Amino-1-(6-bromo-2-oxo-1,2-dihydroquinolin-4-yl)-1H-pyrazole-3,4-dicarbonitrile (7f) was the most active product, with IC50= 1.35 uM and 2.42 uM against MOLT-4 and CCRF-CEM, respectively. Also, it showed a remarkable inhibitory activity compared to erlotinib on the EGFR TK with IC50 = 247.14 nM and 208.42 nM, respectively. Cell cycle analysis of MOLT-4 cells treated with 7f showed cell cycle arrest at G2/M phase (supported by Caspases, BAX and Bcl-2 studies) with a significant pro-apoptotic activity as indicated by annexin V-FITC staining. Moreover, the docking study indicated that both the pyrazole moiety and the quinolin-2-one ring showed good fitting into EGFR (PDB code: 1M17). In order to interpret SAR of the designed compounds, and provide a basis for further optimization, molecular docking of the synthesized compounds to known EGFR inhibitors was performed. The study illustrated the effect of several factors on the compounds’ activity.

Welcome to talk about 86-95-3, If you have any questions, you can contact Elbastawesy, MAI; Aly, AA; Ramadan, M; Elshaier, YAMM; Youssif, BGM; Brown, AB; Abuo-Rahma, GEDA or send Email.. Quality Control of 4-Hydroxyquinolin-2(1H)-one

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Discovery of Novel Symmetrical 1,4-Dihydropyridines as Inhibitors of Multidrug-Resistant Protein (MRP4) Efflux Pump for Anticancer Therapy WOS:000606123700001 published article about P-GLYCOPROTEIN INHIBITION; SIGNALING MOLECULES; MOUSE MODEL; CANCER; ABCC4; DRUGS; TRANSPORTERS; EXPRESSION; DOXORUBICIN; MRP4/ABCC4 in [Doering, Henry; Kreutzer, David; Hilgeroth, Andreas] Martin Luther Univ Halle Wittenberg, Inst Pharm, Res Grp Drug Dev, D-06120 Halle, Germany; [Ritter, Christoph] Ernst Moritz Arndt Univ Greifswald, Inst Pharm, Dept Clin Pharm, D-17489 Greifswald, Germany in 2021.0, Cited 48.0. The Name is 3,4-Dimethoxybenzaldehyde. Through research, I have a further understanding and discovery of 120-14-9. Name: 3,4-Dimethoxybenzaldehyde

Despite the development of targeted therapies in cancer, the problem of multidrug resistance (MDR) is still unsolved. Most patients with metastatic cancer die from MDR. Transmembrane efflux pumps as the main cause of MDR have been addressed by developed inhibitors, but early inhibitors of the most prominent and longest known efflux pump P-glycoprotein (P-gp) were disappointing. Those inhibitors have been used without knowledge about the expression of P-gp by the treated tumor. Therefore the use of inhibitors of transmembrane efflux pumps in clinical settings is reconsidered as a promising strategy in the case of the respective efflux pump expression. We discovered novel symmetric inhibitors of the symmetric efflux pump MRP4 encoded by the ABCC4 gene. MRP4 is involved in many kinds of cancer with resistance to anticancer drugs. All compounds showed better activities than the best known MRP4 inhibitor MK571 in an MRP4-overexpressing cell line assay, and the activities could be related to the various substitution patterns of aromatic residues within the symmetric molecular framework. One of the best compounds was demonstrated to overcome the MRP4-mediated resistance in the cell line model to restore the anticancer drug sensitivity as a proof of concept.

Welcome to talk about 120-14-9, If you have any questions, you can contact Doring, H; Kreutzer, D; Ritter, C; Hilgeroth, A or send Email.. Name: 3,4-Dimethoxybenzaldehyde

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Rational Tuning of Bis-Tridentate Ir(III) Phosphors to Deep-Blue with High Efficiency and Sub-microsecond Lifetime WOS:000639014900059 published article about IRIDIUM(III) COMPLEXES; EN-ROUTE; DESIGN; PHOTOPHYSICS; FUNDAMENTALS; TUNABILITY in [Tai, Wun-Shan; Gnanasekaran, Premkumar; Chi, Yun] Natl Tsing Hua Univ, Dept Chem, Hsinchu 30013, Taiwan; [Tai, Wun-Shan; Gnanasekaran, Premkumar; Chi, Yun] Natl Tsing Hua Univ, Frontier Res Ctr Fundamental & Appl Sci Matters, Hsinchu 30013, Taiwan; [Chen, Yi-Yang; Hung, Wen-Yi] Natl Taiwan Ocean Univ, Dept Optoelect & Mat Technol, Keelung 20224, Taiwan; [Zhou, Xiuwen] Univ Queensland, Sch Math & Phys, Brisbane, Qld 4072, Australia; [Chou, Tai-Che; Lee, Gene-Hsiang; Chou, Pi-Tai] Natl Taiwan Univ, Dept Chem, Taipei 10617, Taiwan; [You, Caifa; Chi, Yun] City Univ Hong Kong, Dept Mat Sci & Engn, Dept Chem, Kowloon, Kowloon 999077, Peoples R China; [You, Caifa; Chi, Yun] City Univ Hong Kong, Ctr Super Diamond & Adv Films COSDAF, Kowloon, Kowloon 999077, Peoples R China in 2021, Cited 57. The Name is 3-(Trifluoromethyl)phenol. Through research, I have a further understanding and discovery of 98-17-9. COA of Formula: C7H5F3O

A new class of bis-tridentate Ir(III) complexes (Dap-1-4) was synthesized using carbene pincer pro-chelates PC1 center dot H-3(PF6)(2) or PC2 center dot H-3(PF6)(2) with either imidazolylidene or imidazo[4,5-b]pyridin-2-ylidene appendages, together with a second cyclometalating 2,6-diaryoxypyridine chelate, L1H(2) and L2H(2), differed by a NMe2 donor at the central pyridinyl fragment. The respective emission tuning between the ultraviolet and blue region was rationalized using time-dependent density functional theory (TD-DFT) approaches. Next, a highly efficient blue emitter (Dap-5) was synthesized by concomitant addition of two methyl groups and a single CF3 substituent at the central phenyl and peripheral imidazo[4,5-b]pyridin-2-ylidene entities of the carbene pincer chelate, respectively. The organic light-emitting diode (OLED) device with 15 wt % Dap-5 in DPEPO shows electroluminescence at 468 nm and with CIE (0.14, 0.15) and a max external quantum efficiency (max EQE) of 16.8% with low efficiency roll-off (EQE of 14.4% at 1000 cd m(-2)); the latter is attributed to the relatively shortened triplet excited-state radiative lifetime. These results highlight the adequateness of bis-tridentate Ir(III) phosphors in fabrication of practical blue-emitting OLEDs.

COA of Formula: C7H5F3O. Welcome to talk about 98-17-9, If you have any questions, you can contact Tai, WS; Gnanasekaran, P; Chen, YY; Hung, WY; Zhou, XW; Chou, TC; Lee, GH; Chou, PT; You, CF; Chi, Y or send Email.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Authors Pathaw, L; Khamrang, T; Selvakumaran, B; Murali, M; Prakash, PA; Jaabir, MSM; Velusamy, M in WILEY published article about RUTHENIUM(II) POLYPYRIDYL COMPLEXES; COPPER(I) COMPLEXES; IN-VITRO; CATALYTIC-PROPERTIES; OXIDATIVE STRESS; HIGHLY EFFICIENT; CU(I) COMPLEXES; CANCER-CELLS; PHOTOSENSITIZERS; SERIES in [Pathaw, Larica; Velusamy, Marappan] North Eastern Hill Univ, Dept Chem, Shillong 793022, Meghalaya, India; [Khamrang, Themmila] CI Coll, Dept Chem, Bishnupur, Manipur, India; [Selvakumaran, Balasubramaniam; Murali, Mariappan] Natl Coll Autonomous, Dept Chem, Coordinat & Bioinorgan Chem Res Lab, Tiruchirappalli 620001, Tamil Nadu, India; [Arul Prakash, Pitchan; Mohamed Jaabir, Mohamed Sultan] Natl Coll Autonomous, Dept Biotechnol & Microbiol, Tiruchirappalli, India in 2021, Cited 70. COA of Formula: C8H8O2. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Copper(I) complexes of the types [Cu(N-N)(PPh3)(2)]NO3(LC41-LC44) and [Cu(N-N)(PPh3)(NO3)] (LC45) carrying 3-substituted 1-pyridine-2-ylimidazo[1,5-a]pyridine (N-N) derivatives and triphenylphosphine (PPh3) ligands have been prepared. The synthesized copper(I)-phosphine complexes were fully characterized by NMR, IR, ESI-MS and UV-visible spectroscopy as well as by cyclic voltammetry. Selected structures such as LC42, LC43 and LC45 were additionally analysed by single-crystal X-ray method, which show that copper(I) centre adopts a highly distorted tetrahedral geometry. The(1)H and(13)C NMR spectral data of the complexes throw light on the nature of metal-ligand bonding. They display d pi-pi* metal-to-ligand charge transfer (MLCT) transition and show quasireversible Cu-I/Cu(II)metal oxidation. Among the copper(I)-phosphine complexes, LC41-LC44 exhibit moderate cytotoxicity (IC50: 24 h, 67-74 mu M; 48 h, 58-70 mu M) against human lung epithelial adenocarcinoma A549 cells, whereas LC45 displays the best activity (IC50: 24 h, 42 mu M; 48 h, 34 mu M) for A549 cancer cell line, which is better than that of the commercial antitumor drug cisplatin. All the complexes also displayed excellent selectivity by being relatively inactive against the human lung epithelial L132 normal cell line with selectivity index (SI) values ranging from 3.4 to 7.4. The complexes block cell cycle progression of A549 cells in G(0)/G(1)phase. FACSVerse analyses are suggestive of reactive oxygen species (ROS) generation and apoptotic cell death induced by the LC41, LC43 and LC45. The induction of apoptosis in A549 cells was shown by Annexin V with propidium iodide (PI) and 4 ‘,6-diamidino-2-phenylindole (DAPI) staining methods and established the ability of LC41, LC43 and LC45 to accumulate in the cell nuclei.

COA of Formula: C8H8O2. About 4-Methoxybenzaldehyde, If you have any questions, you can contact Pathaw, L; Khamrang, T; Selvakumaran, B; Murali, M; Prakash, PA; Jaabir, MSM; Velusamy, M or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Application In Synthesis of Mequinol. In 2021.0 EUR POLYM J published article about THERMAL-CONDUCTIVITIES; BATIO3 NANOPARTICLES; COMPOSITES; NANOCOMPOSITES; CONSTANT; POLYMERIZATION; SILICA in [Wu, Bo; Xu, Yi; Wu, Nan; Tang, Xianzhong] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 611731, Peoples R China in 2021.0, Cited 42.0. The Name is Mequinol. Through research, I have a further understanding and discovery of 150-76-5.

Dielectric materials play a crucial role in 5G communication technological applications such as printed circuit board (PCB) high-frequency substrate materials. Unfortunately, the fabrication of desirable dielectric performance in organic-inorganic composites is a great challenge because of lack of good interfacial compatibility and uniform dispersion between fillers and polymer. In this work, silicon dioxide (SiO2) was synchronously functionalized by gamma-methacryloxypropyltrimethoxysilane (MPS, s-SiO2) and 1,2-polybutadiene (PB, v-SiO2), which were then used as fillers to fabricate the s-SiO2/polyolefin or v-SiO2/polyolefin laminates. All the v-SiO2/polyolefin laminates exhibited better dielectric, thermal and mechanical properties than those of s-SiO2/polyolefin laminates under the same filler content. Specially, the 50 wt% v-SiO2/polyolefin laminate displays a low dielectric constant (3.42) and loss (3.55 x 10-3) at 10 GHz. Meanwhile, it also shows good stability of dielectric properties in a wide range of high-frequency. This work is conducive to develop laminates with superior dielectric properties and apply to PCB high-frequency substrate field.

Welcome to talk about 150-76-5, If you have any questions, you can contact Wu, B; Xu, Y; Wu, N; Tang, XZ or send Email.. Application In Synthesis of Mequinol

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article Cobalt-Catalyzed Sustainable Synthesis of Benzimidazoles by Redox-Economical Coupling of o-Nitroanilines and Alcohols WOS:000487576900069 published article about ONE-POT SYNTHESIS; 2-SUBSTITUTED BENZIMIDAZOLES; OXIDATIVE SYNTHESIS; EFFICIENT CATALYST; AROMATIC DIAMINES; BENZOTHIAZOLES; NANOPARTICLES; BENZOXAZOLES; COMPLEXES; STRATEGY in [Das, Sanju; Mallick, Samrat; De Sarkar, Suman] Indian Inst Sci Educ & Res Kolkata, Dept Chem Sci, Mohanpur 741246, W Bengal, India in 2019.0, Cited 60.0. SDS of cas: 100-51-6. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6

This study reveals cobalt-catalyzed sustainable synthesis of benzimidazoles by redox-economical coupling of o-nitroanilines and alcohols. The major advantage of this report is the use of a commercially available cheap cobalt catalyst to produce a wide variety of 2-substituted benzimidazoles by hydrogen autotransfer without using any additional external redox reagent and costly ligand system. A thorough mechanistic insight of the reaction is proposed by performing a series of control experiments.

SDS of cas: 100-51-6. Bye, fridends, I hope you can learn more about C7H8O, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

An article A bioinformatics investigation into molecular mechanism of Yinzhihuang granules for treating hepatitis B by network pharmacology and molecular docking verification WOS:000548306700001 published article about CELL-CYCLE; HEPATOCELLULAR-CARCINOMA; DRUG CLASSIFICATION; VIRUS; UPDATE; KINASE; GENES; CDK6; INFECTION; VISUALIZATION in [Zhang, Jingyuan; Liu, Xinkui; Zhou, Wei; Wu, Jiarui; Guo, Siyu; Jia, Shanshan; Liu, Yingying; Zhang, Xiaomeng; Wang, Miaomiao] Beijing Univ Chinese Med, Beijing 100102, Peoples R China; [Cheng, Guoliang; Li, Bingbing] State Key Lab Gener Manufacture Technol Chinese T, Linyi 276000, Shandong, Peoples R China in 2020.0, Cited 81.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4. Computed Properties of C8H8O2

Yinzhihuang granules (YZHG) is a patented Chinese medicine for the treatment of hepatitis B. This study aimed to investigate the intrinsic mechanisms of YZHG in the treatment of hepatitis B and to provide new evidence and insights for its clinical application. The chemical compounds of YZHG were searched in the CNKI and PUBMED databases, and their putative targets were then predicted through a search of the SuperPred and Swiss Target Prediction databases. In addition, the targets of hepatitis B were obtained from TTD, PharmGKB and DisGeNET. The abovementioned data were visualized using Cytoscape 3.7.1, and network construction identified a total of 13 potential targets of YZHG in the treatment of hepatitis B. Molecular docking verification showed that CDK6, CDK2, TP53 and BRCA1 might be strongly correlated with hepatitis B treatment. Furthermore, GO and KEGG analyses indicated that the treatment of hepatitis B by YZHG might be related to positive regulation of transcription, positive regulation of gene expression, the hepatitis B pathway and the viral carcinogenesis pathway. Network pharmacology intuitively shows the multicomponent, multitarget and multichannel pharmacological effects of YZHG in the treatment of hepatitis B and provides a scientific basis for its mechanism of action.

Welcome to talk about 99-93-4, If you have any questions, you can contact Zhang, JY; Liu, XK; Zhou, W; Cheng, GL; Wu, JR; Guo, SY; Jia, SS; Liu, YY; Li, BB; Zhang, XM; Wang, MM or send Email.. Computed Properties of C8H8O2

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

HPLC of Formula: C8H8O2. Safabakhsh, T; Daraei, H; Saha, N; Khodakarim, S in [Safabakhsh, Tahereh] Isfahan Univ Med Sci, Int Educ Ctr, Esfahan, Iran; [Daraei, Hasti] Shahid Beheshti Univ Med, Sch Publ Hlth & Safety, Student Res Comm, Tehran, Iran; [Saha, Narottam] Univ Queensland, Sustainable Minerals Inst, Ctr Mined Land Rehabil, Brisbane, Qld, Australia; [Khodakarim, Soheila] Shahid Beheshti Univ Med Sci, Sch Publ Hlth & Safety, Dept Epidemiol, Tehran, Iran published Degradation of Bisphenol A from aqueous solutions using Fe3O4 as a persulfate activator in 2019.0, Cited 28.0. The Name is 4′-Hydroxyacetophenone. Through research, I have a further understanding and discovery of 99-93-4.

The present study investigated the degradation of bisphenol A (BPA) from aqueous solution using Fe3O4/persulfate process. The effects of pH (3, 5, 7 and 11), persulfate (PS) concentrations (1, 2, 5 and 10 mM), Fe3O4 magnetic nanoparticle doses (0.5, 1, 1.5 and 2 g/L), and contact time (5, 10, 20 and 30 min) on BPA removal were examined. The effect of all factors was significant (p < 0.05), and the optimal conditions were: pH value of 3, Fe3O4 dose of 2 g/L, BPA concentration of 0.1 mg/L, and contact time of 30 min. The BPA removal efficiency under optimal conditions was 98%. The results of this work indicate that Fe3O4 nanoparticles can be used as an effective catalyst and adsorbent for the removal of BPA from water and industrial wastewater. Analysis of by-products of BPA using GC-MS detected the presence of compounds with lower molecular weights (4-hydroxyacetophenone, 4-isopropenylphenol, benzoquinone and succinic acid) relative to BPA. HPLC of Formula: C8H8O2. About 4′-Hydroxyacetophenone, If you have any questions, you can contact Safabakhsh, T; Daraei, H; Saha, N; Khodakarim, S or concate me.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Authors Nope, E; Sathicq, AG; Martinez, JJ; Rojas, H; Romanelli, G in ELSEVIER published article about ONE-POT SYNTHESIS; BIGINELLI-TYPE REACTION; MG-AL HYDROTALCITES; SOLVENT-FREE; HETEROGENEOUS CATALYSTS; EFFICIENT SYNTHESIS; IONIC LIQUID; SOLID BASE; MECHANISM; CONDENSATION in [Nope, Eliana; Sathicq, Angel G.; Romanelli, Gustavo] Univ Nacl La Plata, Ctr Invest & Desarrollo Ciencias Aplicadas Dr Jor, CONICET, CINDECA,CCT La Plata,CIC,PBA, Calle 47 257,B1900AJK, La Plata, Argentina; [Martinez, Jose J.; Rojas, Hugo] Univ Pedag & Tecnol Colombia UPTC, Fac Ciencias, Escuela Ciencias Quim, Ave Cent Norte, Tunja, Boyaca, Colombia; [Romanelli, Gustavo] Univ Nacl La Plata, Fac Ciencias Agr & Forestales, Catedra Quim Organ, Ctr Invest Sanidad Vegetal CISaV, Calles 60 & 119 S-N,B1904AAN, La Plata, Argentina in 2021.0, Cited 61.0. Quality Control of 4-Methoxybenzaldehyde. The Name is 4-Methoxybenzaldehyde. Through research, I have a further understanding and discovery of 123-11-5

Uracil compounds participate in a wide range of biological activities; however, reports on their synthesis using heterogeneous catalysts are scarce. In this work, the multicomponent synthesis of uracil derivatives assisted by layered double hydroxides (LDH) was studied under green chemistry conditions. The incorporation of Ni2+ or Co2+ was successfully performed by co-precipitation method. The yields to uracil derivatives are associated with the presence of weak basic sites and a better interaction of the reagents when the reaction is carried out in solvent-free conditions. The reaction pathway involves the formation of an enone between benzaldehyde and ethyl cyanoacetate, and subsequent reaction with urea, which is assisted by the presence of a basic catalyst. The scope of this synthesis is illustrated with nine examples.

Welcome to talk about 123-11-5, If you have any questions, you can contact Nope, E; Sathicq, AG; Martinez, JJ; Rojas, H; Romanelli, G or send Email.. Quality Control of 4-Methoxybenzaldehyde

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles

Category: indole-building-block. In 2019 CHEMMEDCHEM published article about INDUCED HEMOLYTIC-ANEMIA; PLASMODIUM-FALCIPARUM; 2D METABOLISM; PRIMAQUINE; TAFENOQUINE; DISCOVERY; ASSAY; ANTIMALARIALS; BERGHEI in [Leven, Michael; Avelar, Leandro A. Alves; Kuna, Krystina; Kurz, Thomas] Heinrich Heine Univ Dusseldorf, Inst Pharmazeut & Med Chem, Univ Str 1, D-40225 Dusseldorf, Germany; [Held, Jana; Tschan, Serena; Mordmueller, Benjamin] Eberhard Karls Univ Tubingen, Inst Tropenmed, Wilhelmstr 27, D-72074 Tubingen, Germany; [Duffy, Sandra; Avery, Vicky M.] Griffith Univ, Eskitis Inst Drug Discovery, Brisbane Innovat Pk Campus, Nathan, Qld 4111, Australia; [Meister, Stephan; Winzeler, Elizabeth A.] Univ Calif San Diego, Dept Pediat, 9500 Gilman Dr, La Jolla, CA 92037 USA; [Delves, Michael] Imperial Coll London, Dept Life Sci, London SW7 2AZ, England; [Plouffe, David] Novartis, Novartis Res Fdn Dept, Genom Inst, 10675 John Jay Hopkins Dr, San Diego, CA 92121 USA in 2019, Cited 43. The Name is 3-(Trifluoromethyl)phenol. Through research, I have a further understanding and discovery of 98-17-9.

A series of novel 8-aminoquinolines (8-AQs) with an aminoxyalkyl side chain were synthesized and evaluated for in vitro antiplasmodial properties against asexual blood stages, liver stages, and sexual stages of Plasmodium falciparum. 8-AQs bearing 2-alkoxy and 5-phenoxy substituents on the quinoline ring system were found to be the most promising compounds under study, exhibiting potent blood schizontocidal and moderate tissue schizontocidal in vitro activity.

Category: indole-building-block. Bye, fridends, I hope you can learn more about C7H5F3O, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles