Nucleoside Intermediates Deoxynucleotides and their analogs Nucleotides and their analogs
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Nucleoside drugs

Nucleoside Intermediates Deoxynucleotides and their analogs Nucleotides and their analogs
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Many of the purine pyrimidine nucleoside analogues, which are promising antiviral compounds, are antiviral in tissue culture and in vivo. The compounds with selective inhibition of the virus, low toxicity, and effective in animals develop into nuclei Glycosides antiviral drugs. Currently, nucleoside drugs that are effective in clinical applications, have commodities, and have been recognized include iodine glycosides, trifluorothymidine, cyclosine, a sugar adenosine, acyclovir and so on. Nucleoside drugs that have a certain effect in clinical trials, have goods in some countries, yet to be recognized include ribavirin, arabinosyl adenosine monophosphate, bromide uridine and so on. Clinical trials are under way to observe the effect include fluoro-iodine cytosine. The new anti-viral nucleoside compounds have been reported is still in research and development. Nucleoside analogs are nucleic acid antimetabolites that are structurally analogous to nucleic acid precursors, competing for nucleic acid synthase enzyme systems, replacing normal nucleic acid precursors, or inhibiting nucleic acid synthetases, blocking viral or cellular nucleic acid synthesis, selectively inhibiting viral nucleic acids , while have little effect on the synthesis of nucleic acid.

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Structure:
Chemical Name:
Cordyecepin
MF:
C10H13N5O3
Structure:
Chemical Name:
2-CHLOROINOSINE
CAS:
13276-43-2
MF:
C10H11ClN4O5
Structure:
Chemical Name:
3',5'-DIACETYL-5-IODO-2'-DEOXYURIDINE
CAS:
1956-30-5
MF:
C13H15IN2O7
Structure:
Chemical Name:
2-AMINOADENOSINE
CAS:
209-61-0
MF:
C10H6O
Structure:
Chemical Name:
6-MERCAPTOPURINE-2'-DEOXYRIBOSIDE
CAS:
2239-64-7
MF:
C10H12N4O3S
Structure:
Chemical Name:
ISOXANTHOPTERIN
CAS:
529-69-1
MF:
C6H5N5O2
Structure:
Chemical Name:
8-HYDROXYGUANOSINE
CAS:
3868-31-3
MF:
C10H13N5O6