نتایج جستجو برای: benzyl thio

تعداد نتایج: 12199  

Journal: :Drug discoveries & therapeutics 2016
Md Ariful Islam Reiko Waki Aki Fujisaka Kosuke Ramon Ito Satoshi Obika

Phosphorothioate modification is one of the most widely investigated and promising chemical modifications in oligonucleotide (ON) based therapeutics. Structurally similar 5'-thio or phosphorothiolate-modified nucleotides, in which a 5'-bridging oxygen is replaced with a sulfur atom, are gaining importance for ON-based research. Several reports have been published describing the synthesis of 5'-...

2016
Tristan Neumann Inke Jess Christian Näther

The asymmetric unit of the polymeric title compound, {[Cd(NCS)2(C6H6N2S)]·2CH3OH} n , consists of one cadmium(II) cation that is located on a centre of inversion as well as one thio-cyanate anion, one pyridine-4-carbo-thio-amide ligand and one methanol mol-ecule in general positions. The Cd(II) cations are octa-hedrally coordinated by the pyridine N atom of two pyridine-4-carbo-thio-amide ligan...

2008
O. Estévez-Hernández J. Duque J. Ellena Rodrigo S. Corrêa

The title compound, C(11)H(10)N(2)O(3)S, was synthesized from furoyl isothio-cyanate and furfurylamine in dry acetone. The thio-urea group is in the thio-amide form. The trans-cis geometry of the thio-urea group is stabilized by intra-molecular hydrogen bonding between the carbonyl and cis-thio-amide and results in a pseudo-S(6) planar ring which makes dihedral angles of 2.5 (3) and 88.1 (2)° w...

2014
H. Cristina Geiger James S. Donohoe David K. Geiger

The title compound, C18H13Br3N2S2, was obtained via the reaction of N-bromo-succinamide with 5,6-dimethyl-2-(thio-phen-2-yl)-1-[(thio-phen-2-yl)meth-yl]-1H-benzimidazole. The compound exhibits rotational disorder of the 5-bromo-thio-phen-2-yl substituent with a refined major:minor occupancy ratio of 0.876 (7):0.124 (7). The 5-bromo-thio-phen-2-yl mean plane is canted to the benzimidazole plane ...

Journal: :Infection and immunity 1984
T A Cebula A N El-Hage V J Ferrans

Acute toxic interactions of intravenously administered benzyl alcohol and Escherichia coli O55:B5 (Boivin preparation) endotoxin were examined in rodents. Lethality studies in male CD-1 mice demonstrated that these agents were more toxic when administered in combination than when either was administered alone. Prophylactic treatment with diazepam (5 mg/kg intraperitoneally) protected against le...

Journal: :Berichte der deutschen chemischen Gesellschaft 1911

Journal: :The Biochemical journal 1988
R W MacKintosh C A Fewson

A quick, reliable, purification procedure was developed for purifying both benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase II from a single batch of Acinetobacter calcoaceticus N.C.I.B. 8250. The procedure involved disruption of the bacteria in the French pressure cell and preparation of a high-speed supernatant, followed by chromatography on DEAE-Sephacel, affinity chromatography o...

Journal: :The Journal of pharmacology and experimental therapeutics 2011
Gretchen Bain Daniel S Lorrain Karin J Stebbins Alex R Broadhead Angelina M Santini Pat Prodanovich Janice Darlington Christopher D King Catherine Lee Christopher Baccei Brian Stearns Yen Troung John H Hutchinson Peppi Prasit Jilly F Evans

The prostaglandin D(2) (PGD(2)) receptor type 2 (DP2) is a G protein-coupled receptor that has been shown to be involved in a variety of allergic diseases, including allergic rhinitis, asthma, and atopic dermatitis. In this study, we describe the preclinical pharmacological and pharmacokinetic properties of the small-molecule DP2 antagonist [2'-(3-benzyl-1-ethyl-ureidomethyl)-6-methoxy-4'-trifl...

Journal: :The Journal of organic chemistry 1996
Xinhua Li Donovan N. Chin George M. Whitesides

Two new tris-melamine derivatives, triazine-thio-M(3) (5) (C(3)N(3)-2,4,6-[SCH(2)C(6)H(4)-3-N(CH(2)C(6)H(4)-4-C(CH(3))(3))COC(6)N(3)-2-NHC(3)N(3)(NH(2))(NHCH(2)CH(2)C(CH(3))(3))-5-Br](3)) and benzene-thio-M(3) (6) (C(6)H(3)-1,3,5-[SCH(2)C(6)H(4)-3-N(CH(2)C(6)H(4)-4-C(CH(3))(3))COC(6)H(3)-2-NHC(3)N(3)(NH(2))(NHCH(2)CH(2)C(CH(3))(3))-5-Br](3)), were synthesized by reactions of 2,4,6-trithiocyanur...

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