Category: 150-19-6

HPLC of Formula: C7H8O2. In 2019.0 EUR J MED CHEM published article about VASCULAR DISRUPTING AGENTS; INHIBITORS; COMPLEX; DESIGN in [Bueno, Oskia; Gargantilla, Marta; Jose Camarasa, Maria; Perez-Perez, Maria-Jesus; Priego, Eva-Maria] CSIC, IQM, Juan Cierva 3, Madrid 28006, Spain; [Estevez-Gallego, Juan; Fernando Diaz, J.] CSIC, CIB, Ramiro Maeztu 9, Madrid 28040, Spain; [Martins, Solange; Liekens, Sandra] Katholieke Univ Leuven, Rega Inst Med Res, Herestr 49, B-3000 Leuven, Belgium in 2019.0, Cited 39.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

Microtubule targeting agents represent a very active arena in the development of anticancer agents. In particular, compounds binding at the colchicine site in tubulin are being deeply studied, and the structural information recently available on this binding site allows structure-directed design of new ligands. Structural comparison of our recently reported high resolution X-Ray structure of the cyclohexanedione derivative TUB075 bound to tubulin and the tubulin-DAMA-colchicine complex has revealed a conformational change in the alpha T5 loop. By a grid-based computational analysis of the tubulin-DAMA-colchicine binding site, we have identified a new favourable binding area in the colchicine-site that was unexplored by our lead TUB075. Thus, based on a structure-guided design, new cyclohexanedione derivatives have been synthesized and tested for tubulin binding and in cellular assays. As a result, we have identified diphenyl ether derivatives with IC50 values around 10-40 nM against three different tumor cell lines and affinity constants for tubulin similar to that of colchicine around 10(7) M-1. As expected, they halted the cell cycle progression at G2/M phase at concentrations as low as 0.08 mu M. (C) 2019 Elsevier Masson SAS. All rights reserved.

HPLC of Formula: C7H8O2. About m-Methoxyphenol, If you have any questions, you can contact Bueno, O; Gargantilla, M; Estevez-Gallego, J; Martins, S; Diaz, JF; Camarasa, MJ; Liekens, S; Perez-Perez, MJ; Priego, EM 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 Vonlanthen, M; Rojas-Montoya, SM; Cuetara-Guadarrama, F; Martiez-Serrano, RD; Burillo, G; Rivera, E in WILEY-V C H VERLAG GMBH published article about RECENT PROGRESS; RADIATION; SENSOR; FILM; IMMOBILIZATION; POLYMERS; PYRENE; UNITS in [Vonlanthen, Mireille; Rojas-Montoya, Sandra M.; Cuetara-Guadarrama, Fabian; Martinez-Serrano, Ricardo D.; Rivera, Ernesto] Univ Nacl Autonoma Mexico, Inst Invest Mat, Circuito Exterior Ciudad Univ, Mexico City 04510, DF, Mexico; [Burillo, Guillermina] Univ Nacl Autonoma Mexico, Inst Ciencias Nucl, Circuito Exterior Ciudad Univ, Mexico City 04510, DF, Mexico in 2020.0, Cited 39.0. Quality Control of m-Methoxyphenol. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6

A coumarin-based chemosensor is synthesized and grafted onto a polyethylene (PE) surface by means of gamma radiation. The obtained polymeric film results to work as test-paper-like colorimetric sensor for the detection of Cu(2+)ions. After immersion of the grafted PE film into a solution of Cu(2+)in chloroform/methanol (8/2), a color change from colorless to green is observed by naked eye together with a quenching of the fluorescence emission. Control experiment with methoxy-grafted PE films shows no response after the immersion in the same Cu(2+)solution. The polymeric sensor can be washed and reused over several cycles for the detection of Cu2+. Moreover, the obtained polymeric sensor is used to detect Zn(2+)by means of photoinduced electron transfer (PET) quenching disrupting mechanism. The fluorescence emission increases about three times after immersion in a solution containing Zn2+. A similar behavior is observed in the presence of acidic protons.

Quality Control of m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact Vonlanthen, M; Rojas-Montoya, SM; Cuetara-Guadarrama, F; Martiez-Serrano, RD; Burillo, G; Rivera, E 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 Saka, ET; Kahriman, N in ELSEVIER SCIENCE SA published article about THIN-FILMS; COBALT PHTHALOCYANINE; ZINC PHTHALOCYANINE; CYCLOHEXENE OXIDATION; SELECTIVE OXIDATION; SUBSTITUTED CO(II); FE(II); 2,6-DI-TERT-BUTYLPHENOL; AUTOXIDATION; DEGRADATION in [Saka, Ece Tugba; Kahriman, Nuran] Karadeniz Tech Univ, Fac Sci, Dept Chem, TR-61080 Trabzon, Turkey in 2019.0, Cited 43.0. Application In Synthesis of m-Methoxyphenol. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6

Phenols from various man-made activities pose threats to public health and aquatic ecosystems. A number of technologies (e.g., adsorption, oxidation, and biological methods) have been proposed and tested to remove phenolic compounds from different sources. Among these technologies, oxidation process is considered one of the most efficient tools for abating phenolic compounds because of low cost, easy scalability, and ecofriendly production. In this work, we aim to synthesize and characterize potential catalysts (Co(II) and Cu(II) phthalocyanines 6 and 7) for phenolic compounds oxidation. Different parameters influenced the oxidation process were determined and phenolic compounds oxidize to the less harmful products with high conversion and yield in the presence of Co(II) and Cu(II) phthalocyanine catalysts. (c) 2019 Elsevier B.V. All rights reserved.

About m-Methoxyphenol, If you have any questions, you can contact Saka, ET; Kahriman, N or concate me.. Application In Synthesis of m-Methoxyphenol

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 Nickel catalyzed intramolecular oxidative coupling: synthesis of 3-aryl benzofurans WOS:000542724200063 published article about ONE-POT SYNTHESIS; MARINE SPONGE; BIOLOGICAL-ACTIVITY; EFFICIENT SYNTHESIS; TERMINAL ALKYNES; O-ALKYNYLPHENOLS; FACILE SYNTHESIS; ALKENYL PHENOLS; C-C; MICROWAVE in [Aggarwal, Sakshi; Srinivas, Dasari; Sreenivasulu, Chinnabattigalla; Satyanarayana, Gedu] Indian Inst Technol, Dept Chem, Hyderabad 502285, Telangana, India in 2020.0, Cited 81.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6. Application In Synthesis of m-Methoxyphenol

Recent research has been focused on the transition metal-catalyzed reactions. Herein we have developed nickel-catalyzed synthesis of 3-aryl benzofurans fromortho-alkenyl phenolsviaintramolecular dehydrogenative coupling. Notably, simple O(2)gas served as an oxidant, without using any sacrificial hydrogen acceptor. The strategy enabled the synthesis of 3-aryl benzofurans in good to excellent yields.

Application In Synthesis of m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact Aggarwal, S; Srinivas, D; Sreenivasulu, C; Satyanarayana, G 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

SDS of cas: 150-19-6. In 2020.0 ANGEW CHEM INT EDIT published article about SHAPE-PERSISTENT MACROCYCLES; BOTTOM-UP SYNTHESIS; NANOHOOPS; ARYLENE in [Wang, Jinyi; Chen, Muqing; Lu, Dapeng; Huang, Qiang; Jia, Hongxing; Cui, Shengsheng; Yang, Shangfeng; Du, Pingwu] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, CAS Key Lab Mat Energy Convers, Dept Mat Sci & Engn,iChEM Collaborat Innovat Ctr, Hefei 230026, Anhui, Peoples R China; [Zhuang, Guilin] Zhejiang Univ Technol, Coll Chem Engn, 18 Chaowang Rd, Hangzhou 310032, Zhejiang, Peoples R China; [Li, Zhe; Shao, Xiang] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Dept Chem Phys, Hefei 230026, Anhui, Peoples R China in 2020.0, Cited 68.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

Carbon nanotubes (CNTs) have unusual physical properties that are valuable for nanotechnology and electronics, but the chemical synthesis of chirality- and diameter-specific CNTs and pi-conjugated CNT segments is still a great challenge. Reported here are the selective syntheses, isolations, characterizations, and photophysical properties of two novel chiral conjugated macrocycles ([4]cyclo-2,6-anthracene; [4]CAn(2,6)), as (-)/(+)-(12,4) carbon nanotube segments. These conjugated macrocyclic molecules were obtained using a bottom-up assembly approach and subsequent reductive elimination reaction. The hoop-shaped molecules can be directly viewed by a STM technique. In addition, chiral enantiomers with (-)/(+) helicity of the [4]CAn(2,6) were successfully isolated by HPLC. The new tubular CNT segments exhibit large absorption and photoluminescence redshifts compared to the monomer unit. The carbon enantiomers are also observed to show strong circularly polarized luminescence (g(lum)approximate to 0.1). The results reported here expand the scope of materials design for bottom-up synthesis of chiral macrocycles and enrich existing knowledge of their optoelectronic properties.

About m-Methoxyphenol, If you have any questions, you can contact Wang, JY; Zhuang, GL; Chen, MQ; Lu, DP; Li, Z; Huang, Q; Jia, HX; Cui, SS; Shao, X; Yang, SF; Du, PW or concate me.. SDS of cas: 150-19-6

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 m-Methoxyphenol. I found the field of Chemistry very interesting. Saw the article Synthesis of N,N-Disubstituted Thiocarbamates from Thiocarbamoyl Fluorides with Alcohols/Phenols/Thiophenols/Thioalcohols Through Copper Catalysis published in 2019.0, Reprint Addresses Jiang, LQ (corresponding author), East China Normal Univ China, Sch Chem & Mol Engn, 500 Dongchuan Rd, Shanghai 200241, Peoples R China.. The CAS is 150-19-6. Through research, I have a further understanding and discovery of m-Methoxyphenol.

Traditional methods for preparing N,N-disubstituted thiocarbamates require highly toxic, flammable and volatile reagents, or their derivatives. Recently, we developed a general method for thiocarbamoyl fluorides from safe, cheap, and easily available starting materials. Reported reactions involving thioyl fluoride with nucleophiles are very scarce. In this report, copper catalyzed reaction of thiocarbamoyl fluorides with phenols/thiophenols/alcohols/thioalcohols under Na2CO3 at 50 degrees C or at 80 degrees C in CH3CN were first developed, affording the corresponding N,N-disubstituted thiocarbamates in moderate to excellent yields. When alcohols are cheap and their boiling points are less than 120 degrees C or they are water-soluble, CuCl catalyzed reaction of thiocarbamoyl fluorides with alcohols at 50 degrees C was also developed. The reaction has good functional group tolerance. Methoxy, methyl, chloro, bromo, nitro, even ester functional groups were all tolerated. Control reactions demonstrated that copper catalyst played the key role on the success of these novel reactions.

About m-Methoxyphenol, If you have any questions, you can contact Yang, J; Zhen, L; Jiang, LQ or concate me.. Application In Synthesis of m-Methoxyphenol

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. Authors Jia, RF; Zhang, J; Bertagnin, C; Cherukupalli, S; Ai, W; Ding, X; Li, Z; Zhang, JW; Ju, H; Ma, XL; Loregian, A; Huang, B; Zhan, P; Liu, XY in ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER published article about in [Jia, Ruifang; Cherukupalli, Srinivasulu; Ai, Wei; Ding, Xiao; Li, Zhuo; Zhang, Jiwei; Ju, Han; Zhan, Peng; Liu, Xinyong] Shandong Univ, Cheeloo Coll Med, Sch Pharmaceut Sci, Dept Med Chem,Key Lab Chem Biol,Minist Educ, 44 West Culture Rd, Jinan 250012, Shandong, Peoples R China; [Zhang, Jian] Shandong Univ, Hosp 2, Cheeloo Coll Med, Inst Med Sci, Jinan 250033, Shandong, Peoples R China; [Bertagnin, Chiara; Loregian, Arianna] Univ Padua, Dept Mol Med, Via Gabelli 63, I-35121 Padua, Italy; [Ma, Xiuli; Huang, Bing] Shandong Acad Agr Sci, Inst Poultry Sci, 1 Jiaoxiao Rd, Jinan 250023, Shandong, Peoples R China; [Zhan, Peng; Liu, Xinyong] China Belgium Collaborat Res Ctr Innovat Antivira, 44 West Culture Rd, Jinan 250012, Shandong, Peoples R China in 2021, Cited 41. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6

Encouraged by our earlier discovery of N1-selective inhibitors, the 150-cavity of influenza virus neuraminidases (NAs) could be further exploited to yield more potent oseltamivir derivatives. Herein, we report the design, synthesis and biological evaluation of a series of novel oseltamivir derivatives via the structural modifications at C-5-NH2 of oseltamivir targeting 150-cavity. Among them, compound 5c bearing 4-(3-methoxybenzyloxy)benzyl group exhibited the most potent activity, which was lower or modestly improved activities than oseltamivir carboxylate (OSC) against N1 (H1N1), N1 (H5N1) and N1 (H5N1-H274Y). Specifically, there was 30-fold loss of activity against the wild-type strain H1N1. However, 5c displayed 4.85-fold more potent activity than OSC against H5N1-H274Y NA. Also, 5c demonstrated low cytotoxicity in vitro and no acute toxicity in mice. Molecular docking studies provided insights into the high potency of 5c against N1 and N1-H274Y mutant NAs. Besides, the in silico prediction of physicochemical properties and CYP enzymatic inhibitory ability of representative compounds were conducted to evaluate their drug-like properties. (C) 2020 Elsevier Masson SAS. All rights reserved.

Category: indole-building-block. About m-Methoxyphenol, If you have any questions, you can contact Jia, RF; Zhang, J; Bertagnin, C; Cherukupalli, S; Ai, W; Ding, X; Li, Z; Zhang, JW; Ju, H; Ma, XL; Loregian, A; Huang, B; Zhan, P; Liu, XY 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

Recommanded Product: m-Methoxyphenol. In 2020 EUR J ORG CHEM published article about TRANSITION-METAL-FREE; ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE CONSTRUCTION; FLUORINATED ALCOHOLS; CROSS-COUPLINGS; CYCLOADDITION REACTIONS; PRIVILEGED STRUCTURES; NAZAROV CYCLIZATION; QUATERNARY CENTER; NATURAL-PRODUCTS in [Aota, Yusuke; Doko, Yuki; Kano, Taichi; Maruoka, Keiji] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Kyoto 6068502, Japan; [Maruoka, Keiji] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan; [Maruoka, Keiji] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China in 2020, Cited 164. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

Nucleophilic addition to the oxy-allyl cation intermediate has emerged as a promising methodology for functionalization of the alpha-position of carbonyl compounds in an umpolung fashion. However, a structure of available carbon nucleophiles to trap the catalytically generated oxy-allyl cation has been limited to highly nucleophilic ones. Herein, we report the Bronsted acid-catalyzed alpha-arylation of ketones employing less explored phenolic nucleophiles as carbon nucleophiles in the oxy-allyl cation catalysis, affording ketones bearing an all carbon quaternary center at the alpha-position.

About m-Methoxyphenol, If you have any questions, you can contact Aota, Y; Doko, Y; Kano, T; Maruoka, K or concate me.. Recommanded Product: m-Methoxyphenol

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

Recommanded Product: m-Methoxyphenol. In 2020.0 RSC ADV published article about CARBONYLATION REACTIONS; ELEVATED-TEMPERATURES; COUPLING REACTIONS; CARBON-MONOXIDE; PALLADIUM; CHEMISTRY; SUFEX; CO in [Koeckinger, Manuel; Hone, Christopher A.; Kappe, C. Oliver] Res Ctr Pharmaceut Engn GmbH RCPE, Ctr Continuous Flow Synth & Proc CCFLOW, Inffeldgasse 13, A-8010 Graz, Austria; [Koeckinger, Manuel; Hone, Christopher A.; Kappe, C. Oliver] Karl Franzens Univ Graz, Inst Chem, NAWI Graz, Heinrichstr 28, A-8010 Graz, Austria; [Hanselmann, Paul; Hu, Guixian] Lanza AG, LPBN, R&D Chem, CH-3930 Visp, Switzerland in 2020.0, Cited 39.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

This communication describes the palladium-catalyzed reductive carbonylation of aryl fluorosulfonates (ArOSO2F) using syngas as an inexpensive and sustainable source of carbon monoxide and hydrogen. The conversion of phenols to aryl fluorosulfonates can be conveniently achieved by employing the inexpensive commodity chemical sulfuryl fluoride (SO2F2) and base. The developed continuous flow formylation protocol requires relatively low loadings for palladium acetate (1.25 mol%) and ligand (2.5 mol%). Good to excellent yields of aryl aldehydes were obtained within 45 min for substrates containing electron withdrawing substituents, and 2 h for substrates containing electron donating substituents. The optimal reaction conditions were identified as 120 degrees C temperature and 20 bar pressure in dimethyl sulfoxide (DMSO) as solvent. DMSO was crucial in suppressing Pd black formation and enhancing reaction rate and selectivity.

Recommanded Product: m-Methoxyphenol. About m-Methoxyphenol, If you have any questions, you can contact Kockinger, M; Hanselmann, P; Hu, GX; Hone, CA; Kappe, CO 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

Al Mahmud, H; Seo, H; Kim, S; Islam, MI; Sultana, OF; Nam, KW; Lee, BE; Sadu, VS; Lee, KI; Song, HY in [Al Mahmud, Hafij; Seo, Hoonhee; Kim, Sukyung; Islam, Md Imtiazul; Sultana, Omme Fatema; Song, Ho-Yeon] Soonchunhyang Univ, Sch Med, Dept Microbiol & Immunol, Cheonan 31151, Chungnam, South Korea; [Nam, Kung-Woo] Soonchunhyang Univ, Dept Life Sci & Biotechnol, Asan 31538, Chungnam, South Korea; [Lee, Byung-Eui] Soonchunhyang Univ, Sch Life Sci, Dept Chem, Asan 31538, Chungnam, South Korea; [Sadu, Venkata S.; Lee, Kee-In] Univ Sci & Technol, Major Green Chem & Environm Biotechnol, Daejeon 34113, South Korea; [Lee, Kee-In] Korea Res Inst Chem Technol, Green Chem Div, Daejeon 34114, South Korea published Synthesis and activity of BNF15 against drug-resistant Mycobacterium tuberculosis in 2021.0, Cited 41.0. Recommanded Product: 150-19-6. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.

Aim: Tuberculosis is the leading cause of mortality among infectious diseases worldwide. Finding a new competent anti tubercular therapy is essential. Materials & methods: We screened thousands of compounds and evaluated their efficacy against Mycobacterium tuberculosis. Results: Initially, 2-nitronaphtho[2,3-b]benzofuran-6,11-dione was active against M. tuberculosis. Next, among x15 newly synthesized derivatives, BNF15 showed promising effect against all drug-sensitive and drug-resistant M. tuberculosis (MIC: 0.02-0.78 mu g/ml). BNF15 effectively killed intracellular M. tuberculosis and nontuberculous mycobacteria. BNF15 exhibited a prolonged post antibiotic effect superior to isoniazid, streptomycin, and ethambutol and synergistic interaction with rifampicin. In acute oral toxicity test, BNF15 did not show toxic effect at a concentration up to 2000 mg/kg. Conclusion: These results highlight the perspective of BNF15 to treat drug-resistant M. tuberculosis.

Recommanded Product: 150-19-6. About m-Methoxyphenol, If you have any questions, you can contact Al Mahmud, H; Seo, H; Kim, S; Islam, MI; Sultana, OF; Nam, KW; Lee, BE; Sadu, VS; Lee, KI; Song, HY 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