851314-56-2Relevant articles and documents
5-SUBSTITUTED DIFLUOROPIPERIDINE COMPOUND CAPABLE OF PASSING THROUGH BLOOD-BRAIN BARRIER
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, (2021/02/18)
The present invention discloses 5-substituted difluoropiperidine compounds having a capacity to cross the blood-brain barrier; the compound has the structural formula represented by formula (I): The 5-substituted difluoropiperidine compounds, derivatives
SUBSTITUTED QUINAZOLINE COMPOUND HAVING BLOOD-BRAIN BARRIER PENETRATION CAPABILITY
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, (2019/02/13)
The present invention discloses substituted quinazoline compounds having a capacity to cross the blood-brain barrier; the compound has the structural formula represented by formula (I): The quinazoline compounds, derivatives and pharmaceutically acceptabl
Quinazoline derivative salt-type crystal forms and preparation method and application thereof
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, (2019/10/29)
The invention discloses quinazoline derivative salt-type crystal forms and a preparation method and application thereof. The quinazoline derivative salt-type crystal forms are specifically the hydrochloride crystal forms A, B, C, D, F, H, I, the sulphate
HETEROCYCLIC COMPOUND
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, (2015/04/15)
The present invention provides a compound having a superior JAK inhibitory action, which is useful as an agent for the prophylaxis or treatment of autoimmune diseases (rheumatoid arthritis, psoriasis, inflammatory bowel disease, Sjogren's syndrome, Behcet's disease, multiple sclerosis, systemic lupus erythematosus, etc.), cancer (leukemia, uterine leiomyosarcoma, prostate cancer, multiple myeloma, cachexia, myelofibrosis, etc.) and the like, or a salt thereof. The present invention relates to a compound represented by the formula wherein each symbol is as defined in the specification, or a salt thereof.
FATTY ACID SYNTHASE INHIBITORS
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, (2014/01/18)
This invention relates to novel spirocyclic piperidines according to Formula (I) which are inhibitors of fatty acid synthase (FAS), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy for the treatment of cancers.
Discovery of spiropiperidine-based potent and selective Orexin-2 receptor antagonists
Fujimoto, Tatsuhiko,Tomata, Yoshihide,Kunitomo, Jun,Hirozane, Mariko,Marui, Shogo
, p. 6409 - 6413 (2011/11/29)
To generate novel human Orexin-2 Receptor (OX2R) antagonists, a spiropiperidine based scaffold was designed and a SAR study was carried out. Compound 4f possessed the highest OX2R antagonistic activity with an IC 50 value of 3 nM with 450-fold selectivity against Orexin-1 Receptor (OX1R).
New classes of potent and bioavailable human renin inhibitors
Remen, L'ubos,Bezencon, Olivier,Richard-Bildstein, Sylvia,Bur, Daniel,Prade, Lars,Corminboeuf, Olivier,Boss, Christoph,Grisostomi, Corinna,Sifferlen, Thierry,Strickner, Panja,Hess, Patrick,Delahaye, Stephane,Treiber, Alexander,Weller, Thomas,Binkert, Christoph,Steiner, Beat,Fischli, Walter
, p. 6762 - 6765 (2010/06/12)
New classes of de novo designed renin inhibitors are reported. Some of these compounds display excellent in vitro and in vivo activities toward human renin in a TGR model. The synthesis of these new types of mono- and bicyclic scaffolds are reported, and properties of selected compounds discussed.