- Ultrafast singlet - singlet energy transfer in self-assembled via metal - ligand axial coordination of free-base porphyrin - zinc phthalocyanine and free-base porphyrin - zinc naphthalocyanine Dyads
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Singlet - singlet energy transfer in self-assembled via axial coordination of imidazole-appended (at different positions of one of the meso-phenyl entities) free-base tetraphenylporphyrin, H2PIm, to either zinc phthalocyanine, ZnPc, or zinc nap
- Maligaspe, Eranda,Kumpulainen, Tatu,Lemmetyinen, Helge,Tkachenko, Nikolai V.,Subbaiyan, Navaneetha K.,Zandler, Melvin E.,D'Souza, Francis
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Read Online
- Magnetically retrievable lepidocrocite supported copper oxide nanocatalyst (Fe-CuO) for N-arylation of imidazole
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A simple and efficient lepidocrocite-supported copper oxide catalyst (Fe-CuO) has been successfully prepared by a simple precipitation method in aqueous medium from readily available inexpensive starting materials and was used as a heterogeneous nanocatal
- Sivakami,Babu, S. Ganesh,Dhanuskodi,Karvembu
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p. 8571 - 8578
(2015/03/03)
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- P2X4 RECEPTOR MODULATING COMPOUNDS
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Provided herein are P2X4 receptor modulating compounds, methods of their synthesis, pharmaceutical compositions comprising the compounds, and methods of their use. The compounds provided herein are useful for the treatment, prevention, and/or management of various disorders, including but not limited to, chronic pain, neuropathy, inflammatory diseases and central nervous system disorders.
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Paragraph 00248
(2015/06/25)
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- Synthesis and characterization of Sant-75 derivatives as Hedgehog-pathway inhibitors
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Sant-75 is a newly identified potent inhibitor of the hedgehog pathway. We designed a diversity-oriented synthesis program, and synthesized a series of Sant-75 analogues, which lays the foundation for further investigation of the structure-activity relationship of this important class of hedgehog-pathway inhibitors.
- Che, Chao,Li, Song,Yang, Bo,Xin, Shengchang,Yu, Zhixiong,Shao, Taofeng,Tao, Chuanye,Lin, Shuo,Yang, Zhen
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scheme or table
p. 841 - 849
(2012/07/28)
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- Imidazol-1-yl and Pyridin-3-yl Derivatives of 4-Phenyl-1,4-dihydropyridines Combining Ca2+ Antagonism and Thromboxane A2 Synthase Inhibition
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A series of derivatives of 4-phenyl-1,4-dihydropyridine bearing imidazol-1-yl or pyridin-3-yl moieties on the phenyl ring were synthesized with the aim of combining Ca2+ antagonism and thromboxane A2 (Tx A2) synthase inhib
- Cozzi, Paolo,Carganico, Germano,Fusar, Domenico,Grossoni, Mauro,Menichincheri, Maria,et al.
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p. 2964 - 2972
(2007/10/02)
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