Reference of 34253-02-6, 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.34253-02-6, Name is Methyl pyridazine-3-carboxylate, molecular formula is C6H6N2O2. In a article£¬once mentioned of 34253-02-6
INHIBITORS OF COLLAGEN PROLYL 4-HYDROXYLASE
Biheteroaryl dicarboxylates and esters, and salts thereof which are useful as modulators of CP4H activity and more particularly as inhibitors of CP4H. Compounds of formula: and salts thereof where: X is S, O, NH, or NR, where R is an alkyl group having 1-3 carbon atoms; R1 and R2 independently are ?OR7, or ?NHSO2R8, where R7 is selected from: hydrogen, alkyl, alkenyl, alkoxyalkyl, ?R??CO?R?, ?R??CO?O?R?, ?CO?R?, ?R??O?CO?R?, ?R??CO?NR?, ?CO?NR?, or ?R??O?CO?NR?, and R8 is selected from hydrogen, alkyl, aryl, arylalkyl; R3, R4 and R6 independently are hydrogen, alkyl, alkoxy, alkenyl, alkenoxy, halo alkyl, haloalkenyl, halogen, hydroxyl, hydroxyalkyl, hydroxyalkenyl, aryl, aryloxy, arylalkyl or arylalkyloxy; R5 is hydrogen, halogen, alkyl having 1-3 carbon atoms, or alkoxy having 1-3 carbon atoms; ?R?? is a divalent straight chain or branched alkylene, and ?R? is an alkyl, alkenyl, arylalkyl, or aryl group. Methods for inhibition of CP4H in vivo and in vitro.
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 34253-02-6
Reference£º
Pyridazine – Wikipedia,
Pyridazine | C4H4N795 – PubChem