نتایج جستجو برای: 3 d pyrimidines

تعداد نتایج: 2219499  

Journal: :Organic & biomolecular chemistry 2015
Paolo Innocenti Hannah Woodward Lisa O'Fee Swen Hoelder

Fused pyrimidine cores are privileged kinase scaffolds, yet few examples of the 2-amino-pyrido[3,4-d]pyrimidine chemotype have been disclosed in the context of kinase inhibitor programs. Furthermore, no general synthetic route has been reported to access 2-amino-pyrido[3,4-d]pyrimidine derivatives. Here we report a versatile and efficient chemical approach to this class of molecules. Our strate...

2012
Veronika Škedelj Emilija Arsovska Tihomir Tomašić Ana Kroflič Vesna Hodnik Martina Hrast Marija Bešter-Rogač Gregor Anderluh Stanislav Gobec Julieanne Bostock Ian Chopra Alex J. O'Neill Christopher Randall Anamarija Zega

BACKGROUND ATP-dependent D-alanine:D-alanine ligase (Ddl) is a part of biochemical machinery involved in peptidoglycan biosynthesis, as it catalyzes the formation of the terminal D-ala-D-ala dipeptide of the peptidoglycan precursor UDPMurNAc-pentapeptide. Inhibition of Ddl prevents bacterial growth, which makes this enzyme an attractive and viable target in the urgent search of novel effective ...

Journal: :Molecules 2016
Rawda M Okasha Fawzia F Albalawi Tarek H Afifi Ahmed M Fouda Al-Anood M Al-Dies Ahmed M El-Agrody

Three new series of chromene molecules have been synthesized in order to explore their antimicrobial activity. The series encompass 2-substituted 14-(4-halophenyl)-12-methoxy-14H-benzo[h]chromeno[3,2-e][1,2,4]-triazolo[1,5-c]pyrimidines 7a-o, 9-benzylideneamino-7-(4-halo-phenyl)-5-methoxy-8-imino-7H-benzo-[h]chromeno[2,3-d]pyrimidines 8a-b and 3-ethoxycarbonyl-14-(4-halophenyl)-12-methoxy-14H-b...

Journal: :علوم دامی ایران 0
علی اکبر مسعودی استادیار دانشکده کشاورزی، دانشگاه تربیت مدرس، تهران میثاق مریدی دانشجوی کارشناسی ارشد دانشکده کشاورزی، دانشگاه تربیت مدرس، تهران جواد احمدپناه دانشجوی کارشناسی ارشد دانشکده کشاورزی، دانشگاه تربیت مدرس، تهران رسول واعظ ترشیزی دانشیار، دانشکده کشاورزی، دانشگاه تربیت مدرس، تهران حمیدرضا سید آبادی عضو هیئت علمی موسسة تحقیقات علوم دامی کشور، تهران

heat shock proteins (hsps), are highly important due to their association with such economically important traits in animals as resistance to temperature shock and mastitis. in the current study, to get a comprehensive information on molecular structure and evolution of the hsp70s, and the available hsp70 sequences of the cattle and other animals taken from ncbi and aligned together. then, nucl...

احمدپناه, جواد,

     In the current study, phylogenetic analysis and molecular evolution of the mammalian’s Leptin was investigated. Data was achieved and aligned by searching its genome database, while all examined mammals contained only a single copy of the Leptin. The nucleotide substitution rate of the sequences and molecular evolution of the Leptin were calculated by maximum likelihood and neighbor-joinin...

2012
Essam M. Hussein

Tetra-n-butyl ammonium bromide (TBAB) was found to be an efficient phase-transfer catalyst for the synthesis of pyrido[2,3-d]pyrimidines by one-pot reaction of 6-aminouracils, aromatic aldehydes, and malononitrile or ethyl cyanoacetate in water under ultrasonic irradiation. The advantages of this method are the use of an inexpensive and readily available catalyst, short reaction time, easy work...

Journal: :Bioorganic & medicinal chemistry letters 2006
Ha-Soon Choi Zhicheng Wang Wendy Richmond Xiaohui He Kunyong Yang Tao Jiang Donald Karanewsky Xiang-ju Gu Vicki Zhou Yi Liu Jianwei Che Christian C Lee Jeremy Caldwell Takanori Kanazawa Ichiro Umemura Naoko Matsuura Osamu Ohmori Toshiyuki Honda Nathanael Gray Yun He

A series of 2-amino-9-aryl-7H-pyrrolo[2,3-d]pyrimidines were designed and synthesized as focal adhesion kinase (FAK) inhibitors using molecular modeling in conjunction with a co-crystal structure. Chemistry was developed to introduce functionality onto the 9-aryl ring, which resulted in the identification of potent FAK inhibitors. In particular, compound 32 possessed single-digit nanomolar IC(5...

Journal: :Antimicrobial agents and chemotherapy 1974
M A Pfaller J J Marr

Allopurinol (4-hydroxypyrazolo[3,4-d]pyrimidine) has been shown to inhibit the growth of Leishmania braziliensis in vitro at concentrations which are attainable in human tissues and body fluids. This compound is believed to act by interdicting the de novo synthesis of pyrimidines, probably through the formation of allopurinol ribotide. Its lack of toxicity makes it a potential candidate for ani...

Journal: :Journal of Heterocyclic Chemistry 2021

Chalcone-derived pyrimidine is a well-known heterocyclic compound that commonly present in ribonucleic acid (RNA) and deoxyribonucleic (DNA) bio-isosteres. Pyrimidine derivatives are effective both the electronic industry drug industries. This review highlights synthesis of pyrimidines, namely mono-pyrimidine, bis-pyrimidine, fused pyrimidine, symmetric, asymmetric via one-pot two-pot methods. ...

Journal: :Journal of bacteriology 1996
S Y Ghim R L Switzer

A transcriptional attenuation mechanism for the regulation of pyr operon expression in Bacillus subtilis in which the PyrR regulatory protein binds pyr mRNA at three sites with similar sequences to cause transcription termination in response to elevated pyrimidine nucleotide pools has been proposed (R. J. Turner, Y. Lu, and R. L. Switzer, J. Bacteriol. 176:3708-3722, 1994). Twenty-seven mutants...

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