Bioisosterism is a process in drug design where one functional group or atom is substituted with another to maintain the desired pharmacological properties of a drug. The goal is to improve drug potency, selectivity, or pharmacokinetic properties while minimizing unwanted side effects. Bioisosteres are structurally similar but not identical compounds that can mimic the original pharmacophore.
Yes, pyrimidine and triazine rings are considered bioisosteres because they have similar geometries and sizes, allowing them to interact with biological targets in a comparable manner. They can be used interchangeably in drug design to modulate properties such as solubility, bioavailability, and potency.
Bioisosteres are molecules with a similar shape that have a similar biological effect. Their functional groups can be systematically replaced to investigate which structures have the desired properties such as high selectivity, less adverse effects, more metabolic stability, and less toxicity. The usage of bioisoteres can lead to a more simplified route to produce new drugs.
Which group is the group of death of soccer
a group a group a group a group and a big fat group and last but not least a groupA Group
Barrel group Bolt group Operating rod group Shoulder group Buttstock group Bipod group Feed tray group Receiver group
The -OH group is called the hydroxyl group
If at a competition group "a" defeats group "b", and group "b" defeats group "c" then group "a" will have to defeat group "C"
Carbon: group 14Sodium: group 1Neon: group 18Chlorine: group 17
Group A, Group B, Group AB, Group O
A -CH3 group is a methyl group. It consists of a carbon atom bonded to three hydrogen atoms, making it a simple alkyl group.
-COOH group is the carboxilic group.