4-1-75
6.3
[1]. Fabrizio Carta, et al. 5- and 6-membered (thio)lactones are prodrug type carbonic anhydrase inhibitors. Bioorg Med Chem Lett. 1 Jan 1;(1):67-7.
[]. Hagai Tavori, et al. Characterization of the PON1 active site using modeling simulation, in relation to PON1 lactonase activity. Bioorg Med Chem. Aug 1;16(15):754-9.
[3]. Jing Yang, et al. A novel approach to biodegradable block copolymers of epsilon-caprolactone and delta-valerolactone catalyzed by new aluminum metal complexes. Macromol Biosci. 4 Dec 15;4(1):19-14.
[4]. Leonid Gaidukov, et al. High affinity, stability, and lactonase activity of serum paraoxonase PON1 anchored on HDL with ApoA-I. Biochemistry. 5 Sep 6;44(35):1143-54.
[5]. Motofumi Osaki, et al. Switching of polymerization activity of cinnamoyl-alpha-cyclodextrin. Org Biomol Chem. 9 Apr 1;7():1646-51.
P6-P64-P-P31+P33+P331-P33+P361+P353-P34+P34-P35+P351+P33-P363-P45-P51
GHS5
365
1533 现货
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11634 现货
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