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The components of a nucleoside are: A pentose sugar(generally ribose or deoxyribose), and a nitrogenous base which may be Adenine/Guanine/Thymine/Cytosine/Uracil. It becomes a nucleotide on addition of a phosphate group.
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in laboratory bleaching powder can be prepare by shaking slaked lime with a gas jar of chloine on large bleaching poweder can be prepare on two methods 1: Hasenclever method 2: Beckmanns method
because mohar method gives the accurate result
it is a scientific method NOVANET
Nucleoside and nucleotide analogs inhibit viral replication by incorporating into the viral genome during replication. These analogs lack the necessary functional groups for further elongation of the viral genome, leading to termination of viral replication and inhibition of viral protein synthesis. This disruption ultimately stops the virus from spreading and replicating.
yes, nucleoside analogues are artificial nucleosides. The block the completion of new viral DNA chains, therefore, preventing the production of new viral bodies. This way the viral enzyme, reverse transcriptase is more likely to incorporate the nucleoside analogue into the DNA than the host's DNA polymerase.
They have a different mode of action in inhibiting the transcription of the viral DNA. The NRTI is actually a nucleoside that incorporates into the viral DNA but it does not have a 3-hydroxyl group so it inhibits and halts the continued growth of the viral DNA chain. The NNRTI's bind to the reverse transcriptase and inhibit its movement.
Guanine nucleoside analogues, Nucleoside analogues and Antiviral drugs
The number of nucleotides (and base pairs) varies from species to species. However, the number of DIFFERENT nucleotides is 4: - adenine nucleoside phosphate - cytosine nucleoside phosphate - guanine nucleoside phosphate - thymine nucleoside phosphate
A dog
These analogs include glucocorticoids, which are anti-inflammatory agents with a large number of other functions; mineralocorticoids, which control salt and water balance primarily through action on the kidneys; and corticotropins.
Current first line treatments for HSV-1 (Herpes Simplex Virus type I, usually in the mouth region) and HSV-2 (Herpes Simplex Virus type II, usually in the genital region) are Acyclovir, Valacyclovir and Famcicolovir. These drugs are nucleoside analogs. Their method of action is to prevent the production or new viral genetic material by inserting themselves into the viral DNA and terminating synthesis. Therefore, they are only functional against stopping the production of new viruses. These drugs cannot kill existing viruses lying dormant in the neuron. Currently no drug exists to kill dormant (non-replicating) HSV-1 or HSV-2 in the body.
The components of a nucleoside are: A pentose sugar(generally ribose or deoxyribose), and a nitrogenous base which may be Adenine/Guanine/Thymine/Cytosine/Uracil. It becomes a nucleotide on addition of a phosphate group.
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Nucleoside triphosphate. Network Time Protocol Notice To Proceed
Explosive or splitting action