152120-61-1Relevant articles and documents
Synthesis and characterization of 4(R)-epimer impurities of zanamivir and laninamivir octanoate
Duan, Chuanqi,Liu, Weiyuan,Bi, Siju,Chen, Liang,Pan, Jing,Zhou, Ting,Lin, Kuaile,Zhou, Weicheng
, p. 569 - 576 (2021/12/09)
The synthesis and characterization of compounds 7c and 8d, the 4(R)-epimer impurities of zanamivir and laninamivir octanoate, were reported for the first time. Their structures were confirmed by NMR and MS and distinguished from their corresponding active pharmaceutical ingredient (API) by coupling constant in 1H NMR and HPLC spectra. This work is of great significance for the drug-related substances analysis in zanamivir and laninamivir octanoate.
Synthesis of acylguanidine zanamivir derivatives as neuraminidase inhibitors and the evaluation of their bio-activities
Lin, Chien-Hung,Chang, Tsung-Che,Das, Anindya,Fang, Ming-Yu,Hung, Hui-Chen,Hsu, Kai-Cheng,Yang, Jinn-Moon,Von Itzstein, Mark,Mong, Kwok Kong T.,Hsu, Tsu-An,Lin, Chun-Cheng
supporting information, p. 3943 - 3948 (2013/07/05)
A series of acylguanidine-modified zanamivir analogs were synthesized and their inhibitory activities against the NAs of avian influenza viruses (H1N1 and H3N2) were evaluated. In particular, zanamivir derivative 3j, with a hydrophobic naphthalene substituent, exhibits the best inhibitory activity against group-1 NA with an IC50 of 20 nM. The Royal Society of Chemistry 2013.
Preparation of N-alkyl-N′-carboalkoxy guanidines: unexpected effective trans-alkoxylation transforming the 2,2,2-trichloroethoxycarbonyl into various carbamates
Schroif-Grégoire, Cosima,Barale, Karine,Zaparucha, Anne,Al-Mourabit, Ali
, p. 2357 - 2359 (2007/10/03)
A range of N-alkyl-N′-Boc guanidines was simply synthezized from monoprotected Boc-1H-pyrazole-1-carboxamidine by reaction with primary amines. Synthesis of the hindered (R)-N-methylbenzyl-N′-Troc guanidine was achieved from the corresponding thiourea by