Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mariana C. F. C. B. Damião"'
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 11, Pp o1700-o1700 (2013)
The title compound, C14H13NO4S, an analogue of capsaicin, differs from the latter by having a 1,3-benzodioxole ring rather than a 2-methoxyphenol moiety, and having a benzenesulfonamide group instead of an aliphatic amide chain. The five-membered rin
Externí odkaz:
https://doaj.org/article/05169db58e864d08b78b37370db7fc88
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 3, Pp o332-o332 (2013)
In the title compound, C16H15NO3, the five-membered 1,3-dioxole ring is in an envelope conformation with the methylene C atom as the flap atom [lying 0.202 (3) Å out of the plane formed by the other four atoms]. The benzene ring makes a dihedral ang
Externí odkaz:
https://doaj.org/article/aab31c49e2854e3ea114b0f34d96846f
Publikováno v:
Reaction Chemistry & Engineering. 5:865-872
Herein, the urate anion exchange transporter 1 (URAT1) inhibitor lesinurad is synthesized from commercially available building blocks by a five-step linear continuous flow sequence. Our previously developed continuous flow platform was successfully a
Autor:
Julio Cezar Pastre, Mariana C. F. C. B. Damião, Renan Galaverna, Alan P. Kozikowski, James H. Eubanks
Publikováno v:
Reaction Chemistry & Engineering. 2:896-907
We report herein the successful application of continuous flow micro reactors to prepare important building blocks based on the 3-thio-1,2,4-triazole core. A telescoped continuous flow process was developed based on the condensation of hydrazides and
Autor:
Mariana C F C B, Damião, Kerly F M, Pasqualoto, Adilson K, Ferreira, Sarah F, Teixeira, Ricardo A, Azevedo, José A M, Barbuto, Fanny, Palace-Berl, Gilberto C, Franchi-Junior, Alexandre E, Nowill, Maurício T, Tavares, Roberto, Parise-Filho
Publikováno v:
Archiv der Pharmazie. 347(12)
A novel class of benzo[d][1,3]dioxol-5-ylmethyl alkyl/aryl amide and ester analogues of capsaicin were designed, synthesized, and evaluated for their cytotoxic activity against human and murine cancer cell lines (B16F10, SK-MEL-28, NCI-H1299, NCI-H46