Application of 72752-81-9, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.72752-81-9, Name is Methyl 2-mercaptobenzo[d]oxazole-6-carboxylate, molecular formula is C9H7NO3S. In a article£¬once mentioned of 72752-81-9
Synthesis and evaluation of arylaminoethyl amides as noncovalent inhibitors of cathepsin S. Part 3: Heterocyclic P3
A series of Nalpha-2-benzoxazolyl-alpha-amino acid-(arylaminoethyl)amides were identified as potent, selective, and noncovalent inhibitors of cathepsin S. Structure-activity relationships including strategies for modulating the selectivities among cathepsins S, K, and L, and in vivo pharmacokinetics are discussed. A X-ray structure of compound 3 bound to the active site of cathepsin S is also reported.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 72752-81-9
Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem