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Synthesis of halogenated 3-deazapurine and L-ascorbic acid derivatives (CROSBI ID 589946)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Stipković Babić, Maja ; Mintas, Mladen Synthesis of halogenated 3-deazapurine and L-ascorbic acid derivatives // ISMC 2012, XXIInd International Symposium on Medicinal Chemistry / Ortúzar, Natalia (ur.). Berlin: Wiley-VCH, 2012. str. 378-378

Podaci o odgovornosti

Stipković Babić, Maja ; Mintas, Mladen

engleski

Synthesis of halogenated 3-deazapurine and L-ascorbic acid derivatives

In research for antiviral and antitumor substances, many derivatives of natural nucleosides have been synthesized and used in treatment of viral, tumor and bacterial diseases. Numerous synthesized 3-deazapurine derivatives have shown signifficant biologial activity on the wide range of RNA and DNA viruses, broad leukemia tumor cells lines and as antituberculostatics. In light of these findings and based on our previous study, we efficiently synthesized a series of new derivatives of halogenated 3-deazapurines (A, B) and L-ascorbic (1-4, 7-8) or imino-L-ascorbic acid (5-6) as a substitute for sugar moiety to evaluate their antiviral and antitumor potency.

halogenirani 3-deazapurini; L-askorbinska kiselina

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Podaci o prilogu

378-378.

2012.

objavljeno

Podaci o matičnoj publikaciji

ISMC 2012, XXIInd International Symposium on Medicinal Chemistry

Ortúzar, Natalia

Berlin: Wiley-VCH

Podaci o skupu

ISMC 2012, XXIInd International Symposium on Medicinal Chemistry

poster

02.09.2012-06.09.2012

Berlin, Njemačka

Povezanost rada

Kemija