117589-34-1Relevant academic research and scientific papers
Asymmetric nitrogen 80.* Diastereomeric derivatives of 1-alkoxyaziridine-2,2-dicarboxylic acids. Synthesis, structure, and absolute configuration
Prosyanik,Rozhkov,Moskalenko,Mishchenko,Forni,Moretti,Torre,Brukner,Malpezzi,Kostyanovsky
, p. 119 - 126 (1998)
Esters and amides (including 15N analogs) of 1-alkoxyaziridine-2,2-dicarboxylic acids that contain N-alkoxy substituents (PriO, RO2CCH2O, (R,S)-RO2CCH(Me)O, or (S)-RO2CCH(Me)O) were synthes
Single-armed phenylsulfonated pyridine derivative of DOTA is rigid and stable paramagnetic tag in protein analysis
Yang, Feng,Wang, Xiao,Pan, Bin-Bin,Su, Xun-Cheng
supporting information, p. 11535 - 11538 (2016/10/03)
Single-armed DOTA-like phenylsulfonated pyridine derivatives are rigid and stable paramagnetic tags for site-specific labeling of proteins. Their reactions with a solvent-exposed protein thiol group generate a stable C-S bond and produce one single paramagnetic species in solution NMR. The generated large paramagnetic effects yield valuable long-range structural restraints for proteins.
New chiral inhibitors of induced platelet aggregation: The enantiomeric specificity of (R)- and (S)-methyl and ethyl esters of 1-{4-[(1-hydroxycarbonyl)-ethoxy]-benzyl}-1H-1,2,3-triazole as a tool for determining their biological target
Biagi,Giorgi,Livi,Scartoni,Catalani,Gervasi
, p. 761 - 766 (2007/10/03)
The synthesis of title enantiomers was accomplished and their biological behaviour as inhibitors of rabbit platelet aggregation process induced by ADP and arachidonic acid was determined. Structure-activity comparison with that of SM-12502 [(2R,5S)-(+)3,5-dimethyl-2-(3-pyridyl)-thiazolidin-4-one hydrochloride] and Dazoxiben {4-[2-(1H-imidazol-1-yl)-ethoxy]-benzoic acid} allowed us to formulate the possible capability for the synthesized compounds to interact with the biological targets of the model molecules.
Oxime Ethers: New Potent Insect Growth Regulators
Ohsumi, Tadashi,Hatakoshi, Makoto,Kisida, Hirosi,Matsuo, Noritada,Nakayama, Isamu,Itaya, Nobushige
, p. 3197 - 3202 (2007/10/02)
Oxime ethers containing a 4-phenoxyphenoxy group in the molecules were synthesized and their insect growth regulating (IGR) activities were studied.Of these new IGR's, propionaldehyde oxime O-2-(4-phenoxyphenoxy)ethyl ether and propionaldehyde oxime O-2-(phenoxyphenoxy)propyl ether were found to be most effective, having much higher activities than methoprene against larvae of Culex pipiens pallens and Musca domestica by the immersion method and medium method, respectively.In addition, the effects of steric isomerism of these compounds were examined; their IGR activities were found to have a close relationship to the juvenile hormone activity by the Galleria wax test.
