نتایج جستجو برای: functionalized piperidine

تعداد نتایج: 24245  

2015
B. K. Revathi D. Reuben Jonathan K. Kalai Sevi K. Dhanalakshmi G. Usha

In the title compound, 0.75C12H14ClNO2·0.25C12H14ClNO, which is an adduct comprising 0.75 4-hy-droxy-piperidin-1-yl or 0.25 4-piperidin-1-yl substituents on a common (4-chloro-phen-yl)methanone component; the dihedral angles between the benzene ring and the two piperidine rings are 51.6 (3) and 89.5 (7)°, respectively. The hy-droxy-piperidine ring is in a bis-ectional oriention (bi) with the ph...

2011
Jorge Gonzalez Roberto Atilano-Coral Ana Lilia Peraza-Campos David Ortegón-Reyna Eleuterio Álvarez

The title compound, C(15)H(30)N(2) (2+)·2Br(-)·H(2)O, was synthesized by reaction of 4-piperidino-piperidine with dibromo-pentane. The dication is built up from three linked piperidine rings, two of which have one quaternary N atom in common (azoniaspiro), whereas the third is N-C bonded to the azoniaspiro system and protonated on the N atom (piperidinium). All three piperidine rings adopt chai...

Journal: :Green Chemistry 2021

Solid Phase Peptide Synthesis (SPPS) is a key technology for the production of pharmaceutical grade peptides and replacement piperidine with alternative bases piece puzzle moving toward greener technology.

2011
Ana C. Mafud Maria Teresa P. Gambardella

The asymmetric unit of the title compound, Na(+)·C(6)H(10)NS(2) (-)·2H(2)O, is composed of a sodium cation, a piperidine-dithio-carbamate anion which exhibits positional disorder, and two lattice water mol-ecules. The atoms of the piperidine ring are divided over two sites with occupancy factors of 0.554 (6) and 0.446 (6). In the crystal, the sodium cation (coordination number of 6) and the pip...

Journal: :Journal of medicinal chemistry 2010
Daniel P Becker Thomas E Barta Louis J Bedell Terri L Boehm Brian R Bond Jeffery Carroll Chris P Carron Gary A Decrescenzo Alan M Easton John N Freskos Chris L Funckes-Shippy Marcia Heron Susan Hockerman Carol Pearcy Howard James R Kiefer Madeleine H Li Karl J Mathis Joseph J McDonald Pramod P Mehta Grace E Munie Teresa Sunyer Craig A Swearingen Clara I Villamil Dean Welsch Jennifer M Williams Ying Yu Jun Yao

α-Sulfone-α-piperidine and α-tetrahydropyranyl hydroxamates were explored that are potent inhibitors of MMP's-2, -9, and -13 that spare MMP-1, with oral efficacy in inhibiting tumor growth in mice and left-ventricular hypertrophy in rats and in the bovine cartilage degradation ex vivo explant system. α-Piperidine 19v (SC-78080/SD-2590) was selected for development toward the initial indication ...

Pain is probably the immediate stimulus for more visits to the Physician's office than all other complaints combined. Since pain serves as an alert to injury, it is often the first harbinger of disease. Piperidine has been extensively utilized for the synthesis of a wide range of therapeutic agents in general and analgetics in particular for the mitigation of pain. In a similar attempt, th...

Journal: :Acta Crystallographica Section E Structure Reports Online 2009

Journal: :Berichte der deutschen chemischen Gesellschaft 1915

Journal: :iranian journal of pathology 2014
zahra kiasalari mohsen khalili mehrdad roghani abbas ahmadi monireh mireie

background and objective: n-methyl-d-aspartate (nmda) antagonists such as piperidines are the most important antiepileptic drugs. considering the fact that piperidine derivatives such as phencyclidine (pcp) and its new derivative, 1-[1-(3-methoxyphenyl) (tetralyl)] piperidine (pcp1), have different potencies, the antiepileptic effects of mentioned drugs were investigated in the present study. ...

Journal: :Chemical & pharmaceutical bulletin 1987
H Setoi H Kayakiri H Takeno M Hashimoto

Polyhydroxylated pyrrolidine, piperidine, and indolizidine alkaloids are of great interest because of their specific glycosidase inhibitory activity." Moreover, it has recently been found in our laboratories that swainsonine (1), a representative of the polyhydroxylated indolizidine alkaloids, has an immunostimulating activity, possibly as a result of its glycosidase inhibitory activity.21 This...

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