10123-90-7Relevant articles and documents
Solvent Compatibility of Poly(dimethylsiloxane)-Based Microfluidic Devices
Lee, Jessamine Ng,Park, Cheolmin,Whitesides, George M.
, p. 6544 - 6554 (2003)
The compatibility of poly(dimethylsiloxane) (PDMS) with organic solvents, e.g., benzene, chloroform, acetonitrile, phenol, and methanol, was studied, which is important in considering the potential of PDMS-based microfiuidic devices in various application
Direct interaction between amphotericin B and ergosterol in lipid bilayers as revealed by 2H NMR spectroscopy
Matsumori, Nobuaki,Tahara, Kazuaki,Yamamoto, Hiroko,Morooka, Atsushi,Doi, Mototsugu,Oishi, Tohru,Murata, Michio
supporting information; experimental part, p. 11855 - 11860 (2009/12/08)
Although amphotericin B (AmB) is thought to exert its antifungal activity by forming transmembrane ion-permeable self-assemblies together with ergosterol, no previous study has directly proven AmB-ergosterol interaction. To establish the interaction, we m
IMPROVED SYNTHESIS OF 1,2,4-TRIAZOLINE-3,5-DIONE DERIVATIVES OF ERGOSTEROL AND A NEW METHOD FOR THEIR RECONVERSION TO ERGOSTEROL
Barton, Derek H. R.,Lusinchi, Xavier,Ramirez, Jesus Sandoval
, p. 2995 - 2998 (2007/10/02)
The ergosterol diene system reacts in excellent yield with a series of 4-substituted 1,2,4-triazoline-3,5-diones generated by in situ oxidation of the appropriate hydrazides with phenylseleninic anhydride or phenylseleninic acid.Diaryltelluroxide and diphenylselenoxide are also efficient oxidants.The diene system can be smoothly regenerated by alkaline hydrolysis.
Unsaturated Steroids. Part 10. The mechanism of the Anthrasteroid Rearrangement: The Conformation of Anthrasteroids
Emke, Alice,Midgley, John M.,Whalley, W. Basil
, p. 1779 - 1781 (2007/10/02)
The mechanism previously suggested for the conversion of the adducts of steroidal 5,7-dienes with 4-phenyl-1,2,4-triazoline-3,5-dione into anthrasteroids has been substantiated.The conformation of the anthrasteroids has been clarified using c.d. and n.m.r. studies.