Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Arani Chanda"'
Autor:
Farkhad Maksudov, Evgenii Kliuchnikov, Daniel Pierson, M.L. Ujwal, Kenneth A. Marx, Arani Chanda, Valeri Barsegov
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 31, Iss , Pp 631-647 (2023)
Elucidating the structure-function relationships for therapeutic RNA mimicking phosphorodiamidate morpholino oligonucleotides (PMOs) is challenging due to the lack of information about their structures. While PMOs have been approved by the US Food an
Externí odkaz:
https://doaj.org/article/a59037acee12490b9c56d8df91b65658
Autor:
Farid Benayoud, Masayuki Omori, Yuichi Suzuki, Arani Chanda, Kazunori Wakasugi, Yuzo Watanabe, Akio Kayano, Paschalis Dimopoulos, Yoichi Kita, Kunitoshi Takeda, Toshihiko Kaneko, Mitsuo Nagai, Noboru Yamamoto, Takafumi Motoki, Kazuhiro Yoshizawa, Christopher Neil Farthing, Lily Lu, Matthew J. Schnaderbeck, Khan Afzal, Tasuku Ishida, Huiming Zhang, Mamoru Takaishi, Markus Bracke, Branko Mitasev, Dae-Shik Kim, Francis G. Fang, Adrian Hall
Publikováno v:
Organic Process Research & Development. 26:804-816
Autor:
Arani Chanda, Shailendra Bordawekar, Samrat Mukherjee, John P. Higgins, Howard W. Ward, Mark A. LaPack, Adrian M. Daly, Bing-Shiou Yang, John D. Orr, James E. Morgado, Todd D. Maloney, George L. Reid, Aaron W. Garrett
Publikováno v:
Organic Process Research & Development. 19:1174-1185
The IQ Consortium reports on the current state of process analytical technology (PAT) for active pharmaceutical ingredient (API) manufacturing in branded pharmaceutical companies. The article describes the application of PAT in manufacturing and prov
Autor:
George Diabes, Jasper Van Kirk Thompson, Soumen Kundu, Arani Chanda, Sushil K. Khetan, Terrence J. Collins, Alexander D. Ryabov
Publikováno v:
Catalysis Science & Technology. 5:1775-1782
Nitrophenols (NPs) are widely prevalent recalcitrant anthropogenic pollutants. TAML activators in conjunction with peroxides have proven to be effective in the remediation of myriad organic pollutants. In the present study, we have discovered that on
Autor:
Duncan R. Thompson, Howard W. Ward, George L. Reid, Adrian M. Daly, Samrat Mukherjee, Mark A. LaPack, Arani Chanda, David A. Foley, John D. Orr
Publikováno v:
Organic Process Research & Development. 19:63-83
The IQ Consortium reports on the current state of process analytical technology (PAT) for active pharmaceutical ingredient (API) development in branded pharmaceutical companies. The article uses an API process workflow (process steps from raw materia
Publikováno v:
Environmental Science & Technology. 47:5319-5326
TAML activators are well-known for their ability to activate hydrogen peroxide to oxidize persistent pollutants in water. The trinitroaromatic explosives, 2,4,6-trinitrotoluene (TNT) and 1,3,5-trinitrobenzene (TNB), are often encountered together as
Publikováno v:
Journal of Coordination Chemistry. 63:2605-2618
Oxidative degradation of pinacyanol chloride (PNC) dye by H2O2, as catalyzed by the 1 FeIII-TAML activator (TAML = tetraamidomacrocyclic ligand), occurs rapidly in water, goes to completion, and exhibits noticeably complex kinetics at pH 11. The reac
Autor:
Alexander D. Ryabov, Anindya Ghosh, Arani Chanda, Erin C. Upham, Gregory J. Collins, Terrence J. Collins, Douglas A. Mitchell, Delia-Laura Popescu
Publikováno v:
Journal of the American Chemical Society. 130:15116-15126
Exceptionally high peroxidase-like and catalase-like activities of iron(III)-TAML activators of H 2O 2 ( 1: Tetra-Amidato-Macrocyclic-Ligand Fe (III) complexes [ F e{1,2-X 2C 6H 2-4,5-( NCOCMe 2 NCO) 2CR 2}(OH 2)] (-)) are reported from pH 6-12.4 and
Autor:
Eckard Münck, Delia-Laura Popescu, Alexander D. Ryabov, Emile L. Bominaar, Filipe Tiago de Oliveira, Matthew Stadler, Terrence J. Collins, Arani Chanda
Publikováno v:
Coordination Chemistry Reviews. 252:2050-2071
Introduced approximately two decades ago, macrocyclic deprotonated tetraamido (4 N ) and, nearly a decade earlier, acyclic diamidodialkoxido or diamidophenolato (2 N /2 O ) ligand systems have been used, among other things, for the synthesis of a wid
Autor:
Karl-Werner Schramm, Delia-Laura Popescu, Naima Chahbane, Douglas A. Mitchell, Alexander D. Ryabov, Dieter Lenoir, Terrence J. Collins, Arani Chanda
Publikováno v:
Green Chem.. 9:49-57
Oxidation of Orange II ([4-[(2-hydroxynaphtyl)azo]benzenesulfonic acid], sodium salt) by hydrogen peroxide catalyzed by iron(III) complexed to tetra amido macrocyclic ligands (FeIII–TAML activators) in aqueous solutions at pH 9–11 leads to CO2, C