105752-11-2Relevant articles and documents
Synthesis of optically active ring-A substituted tryptophans as IDO inhibitors
Li, Xiaoyan,Yin, Wenyuan,Sarma, P.V.V. Srirama,Zhou, Hao,Jun Ma,Cook, James M.
, p. 8569 - 8573 (2004)
The first synthesis of optically active 7-methoxy-d-tryptophan as well as other ring-A substituted tryptophans is described.
3-AMINO-PYRIDINES AS GPBAR1 AGONISTS
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Page/Page column 128, (2012/09/21)
This invention relates to novel 3-aminopyridines of the formula (I) wherein B1, B2 and R1 to R6 are as defined in the description and in the claims, as well as pharmaceutically acceptable salts thereof. These compounds are GPBAR1 agonists and can be used as medicaments for the treatment of diseases such as type II diabetes.
The first porous MOF with photoswitchable linker molecules
Modrow, Antje,Zargarani, Dordaneh,Herges, Rainer,Stock, Norbert
supporting information; scheme or table, p. 4217 - 4222 (2011/06/18)
We synthesized a porous twofold interpenetrated MOF [Zn2(NDC) 2(1)] (coined CAU-5) using 3-azo-phenyl-4,4′-bipyridine (1), 2,6-naphthalenedicarboxylic acid, and Zn(NO3)2· 6H2O. The azo-functionality protrudes into the pores, and can be switched, by irradiation with UV light (365 nm), from the thermodynamically stable trans-isomer to the cis-isomer. Back-switching was achieved thermally and with an irradiation wavelength of λmax = 440 nm.
