نتایج جستجو برای: aza cope rearrangement

تعداد نتایج: 64605  

Journal: :Blood 1985
T Motoji T Hoang D Tritchler E A McCulloch

Blast cells from patients with acute myeloblastic leukemia were exposed to 5-azacytidine (5-aza) and its analogues 5-aza 2'-deoxycytidine (5-aza-dr) and 6-azacytidine (6-aza). Simple negative exponential survival curves were obtained for the three drugs, but the sensitivity varied; 5-aza-dr was most toxic, 6-aza was least toxic, and 5-aza was intermediate. Colonies surviving drug exposure were ...

Journal: :Antimicrobial agents and chemotherapy 2016
Jonathan M O Rawson Michele B Daly Jiashu Xie Christine L Clouser Sean R Landman Cavan S Reilly Laurent Bonnac Baek Kim Steven E Patterson Louis M Mansky

5-Azacytidine (5-aza-C) is a ribonucleoside analog that induces the lethal mutagenesis of human immunodeficiency virus type 1 (HIV-1) by causing predominantly G-to-C transversions during reverse transcription. 5-Aza-C could potentially act primarily as a ribonucleotide (5-aza-CTP) or as a deoxyribonucleotide (5-aza-2'-deoxycytidine triphosphate [5-aza-dCTP]) during reverse transcription. In ord...

Understanding the mechanism of tumor resistance is critical for cancer therapy. In this study, we investigated the effect of carcinoembryonic antigen (CEA) overexpression on UV-and 5-fluorouracil (5-FU)-induced apoptosis and autophagy in colorectal cancer cells. We used histone deacetylase (HDAC) inhibitor, NaB and DNA demethylating agent, 5- azacytidine (5-AZA) to induce CEA expression in HT29...

2002
Holger Butenschön

Tricarbonylchromium complexes of benzocyclobutenone, benzocyclobutenedione, and 1,3-indandione are readily prepared by hydrolysis of the complexes of the corresponding acetals. Reduction of the benzocyclobutenone complex gives rise to an oxyanion-driven ring opening to the corresponding ortho-quinodimethane intermediate, which can be trapped with dienophiles. Addition of 1-ethoxy-1-lithioethene...

Journal: :international journal of molecular and cellular medicine 0
ebrahim eftekhar department of biochemistry, shiraz university of medical sciences, school of medicine, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) hajar jaberi department of biochemistry, shiraz university of medical sciences, school of medicine, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences) fakhraddin naghibalhossaini autoimmune research center, shiraz university of medical sciences, school of medicine, shiraz, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی شیراز (shiraz university of medical sciences)

understanding the mechanism of tumor resistance is critical for cancer therapy. in this study, we investigated the effect of carcinoembryonic antigen (cea) overexpression on uv-and 5-fluorouracil (5-fu)-induced apoptosis and autophagy in colorectal cancer cells. we used histone deacetylase (hdac) inhibitor, nab and dna demethylating agent, 5- azacytidine (5-aza) to induce cea expression in ht29...

ES FARBOUD, M ADRANGUI,

In this study the influence of azelaic acid (AZA) 20% cream on the sebum excretion rate (SER) of 80 volunteers having mild to moderate acne vulgaris was demonstrated. Absorbent paper and Sebutape were used to collect the sebum and quantification was carried out by direct gravimetric method. It was shown that topical application of AZA creams could reduce the SER and number of acneic lesions...

2014
Brendan T. Parr Huw M. L. Davies

Stereoselective synthesis of a cyclopentane nucleus by convergent annulation constitutes a significant challenge for synthetic chemists. Although a number of biologically relevant cyclopentane natural products are known, more often than not, the cyclopentane core is assembled in a stepwise manner because of the lack of efficient annulation strategies. Here we report the rhodium-catalysed reacti...

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