
European Journal of Medicinal Chemistry p. 355 - 361 (1993)
Update date:2022-08-04
Topics:
Oesapay, G
Csiba, A
A series of phosphonic analogs of amino acids, peptides, and their derivatives was synthesized in order to examine their ability to inhibit human carbonic anhydrase (HCA) isoenzymes (I and II).The aminophosphonic acids with amino protection possess much stronger inhibitory capacity (Ki = 10-6 - 10-5 M) than the free aminophosphonic acids (Ki = 10-5 - 10-3 M).The aminophosphonic acids with both N- and P-protection do not have an inhibitory effect on the esterase activity of HCA.In a comparison of the enantiomeric pairs of Cbz-AlaP(OH)2, the D-conformer has several-fold stronger inhibitory potency.All aminoalkylphosphonates investigated possess one order of magnitude stronger inhibitory activity towards isoenzyme HCA-I than towards HCA-II.A computer-directed analysis was used to study the possible interactions in an aminoalkylphosphonate
AUSHUN PHARMACEUTICAL TECHNOLOGY CO,.LTD
Contact:+86-25-86883560 15951806178
Address:14 Dayingbi, Zhujiang Rd. East, Nanjing, Jiangsu, China.
Changzhou Jiana Chemical Co.,Ltd
website:http://www.jianachem.com
Contact:86-0519-88731808
Address:Zhenglu Town Wujin City, Jiangsu Province
Antaeus Bio-technology Co., LTD(expird)
Contact:021-31252569
Address:shanghai pudong
Contact:13357117572
Address:No.149 Shiji dadao Road.
Contact:+86 755 26588093
Address:No.9 Linkong West Street, Hengdian Street, Huangpi District, Wuhan City, China.
Doi:10.1016/S0040-4020(03)00438-1
(2003)Doi:10.1039/c6ra25562k
(2017)Doi:10.1021/ol035128a
(2003)Doi:10.1016/j.ejmech.2021.113325
(2021)Doi:10.1039/P19760000532
(1976)Doi:10.1080/10426509808545471
(1998)