نتایج جستجو برای: 4 amino pyrimidine

تعداد نتایج: 1477202  

2010
M. Kannan P. Manivel M. Sarathbabu R. Sathishkumar H. Surya Prakash Rao R. Krishna

In the title compound, C(19)H(22)N(4)O(2), the tetra-hydro-pyrimidine ring adopts an envelope conformation (with the N atom connected to the benzyl group representing the flap). This benzyl group occupies a quasi-axial position. The two benzyl groups lie over the tetra-hydro-pyridimidine ring. The amino group is a hydrogen-bond donor to the nitro group.

Journal: :Acta Crystallographica Section E Structure Reports Online 2009

2014
J. Sreeramulu

The synthesis and investigation of new Hetero Cyclic Dithicarbamate ligand and its solid metal complexes derived from 4-Amino-1,2,4triazole(ATAZ) and 2-Amino 4-Hydroxy-6-methyl pyrimidine (AHPY) by using different synthetic methods. The derived colored complexes are Au (III) and Ru (III) with above mentioned ligands. The structures and bio cancer activity were elucidated by different type of st...

Journal: :Molecules 2010
Markus K Dahlgren Christopher T Oberg Erika A Wallin Pär G Janson Mikael Elofsson

Salicylidene acylhydrazides are inhibitors of type III secretion in several gram-negative pathogens. To further develop the salicylidene acylhydrazides, scaffold hopping was applied to replace the core fragment of the compounds. The novel 2-(2-amino-pyrimidine)-2,2-difluoroethanol scaffold was identified as a possible analog to the salicylidene acylhydrazide core structure. The synthesis of a l...

2009
Hua Yang

Colourless crystals of the title mixed ligand complex, [Ag(C(5)H(7)N(3))(C(6)H(9)N(3))]ClO(4), were obtained from a solution of 2-amino-4-methyl-pyrimidine, 2-amino-4,6-dimethyl-pyrim-idine and silver perchlorate in water and methanol. The crystal structure is stabilized by inter-molecular N-H⋯O and N-H⋯N hydrogen bonds and π-π stacking inter-actions of the aromatic rings of the two ligands [in...

2013
Truong Hong Hieu Le Tuan Anh Anatoly T. Soldatenkov Vasily G. Vasil’ev Victor N. Khrustalev

The title compound, C33H35N3O5, is the product of the multicomponent condensation of 1-benzyl-4-eth-oxy-carbonyl-piperidin-3-one with 1,5-bis-(2-formyl-phen-oxy)-3-oxapentane and ammonium acetate. The mol-ecule comprises a penta-cyclic system containing the aza-14-crown-4-ether macrocycle, tetra-hydro-pyrimidine, tetra-hydro-pyridine and two benzene rings. The aza-14-crown-4-ether ring adopts a...

2009
Jacqui E. Hoffman Henry Cheng Arnold L. Rheingold Antonio DiPasquale Alex Yanovsky

The title compound, C(12)H(19)BrN(4)O, represents the minor component of the two products obtained in a series of transformations involving the Grignard reaction of tert-butoxy-carbonyl-protected 4-amino-cyclo-hexa-none with MeMgBr, and subsequent inter-action of the obtained amino-substituted cyclo-hexa-nol with 4-chloro-6-methyl-pyrimidin-2-amine followed by bromination with N-bromo-succinimi...

2013
Katarzyna Kiegiel Wojciech Starosta Janusz Leciejewicz

The crystal structure of the title compound, C5H4N2O2, is built of acid mol-ecules located on a mirror plane. They form sheets stacked along the b-axis direction. The mol-ecules inter-act via O-H⋯N hydrogen bonds, forming [001] chains, and weak van der Waals inter-actions.

2011
Shaaban Kamel Mohamed Mahmoud A. A. El-Remaily Atash V. Gurbanov Ali N. Khalilov Seik Weng Ng

There are two independent mol-ecules in the asymmetric unit of the title compound, C(13)H(13)N(5). In each mol-ecule, an amino N atom is connected to a benzimidazole fused-ring system and a pyrimidine ring [these are aligned at 1.3 (1)° in one independent mol-ecule and at 5.4 (1)° in the other]. The amino N atom of the fused ring forms an intra-molecular N-H⋯O hydrogen bond to a pyrimidine N at...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2014
Ryan Takahashi Shuguang Ma Alan Deese Qin Yue Heasook Kim-Kang Yijun Yi Michael Siu Kevin W Hunt Nicholas C Kallan Cornelis E C A Hop Xingrong Liu S Cyrus Khojasteh

We investigated an uncommon biotransformation of pyrimidine during the metabolism of GNE-892 ((R)-2-amino-1,3',3'-trimethyl-7'-(pyrimidin-5-yl)-3',4'-dihydro-2'H-spiro[imidazole-4,1'-naphthalen]-5(1H)-one), a β-secretase 1 inhibitor. Three novel metabolites, formed by conversion of pyrimidine to pyrazole, were observed in the (14)C-radiolabeled mass balance study in rats. Their structures were ...

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