Journal of Medicinal Chemistry p. 4660 - 4669 (1995)
Update date:2022-07-29
Topics:
Matsoukas
Agelis
Wahhab
Hondrelis
Panagiotopoulos
Yamdagni
Wu
Mavromoustakos
Maia
Ganter
Moore
Type I angiotensin II antagonists with O-methyl-L-homoserine [HSer(γ- OMe)] and δ-methoxy-L-norvaline [Nva(δ-OMe)] at position 8 have been prepared by the solid-phase method, purified by reverse-phase HPLC, and bioassayed in the rat uterus, and their backbone conformational properties were investigated by nuclear Overhauser effect (NOE) spectroscopy. [Sar1,HSer-(γ-OMe)8]ANGII, [HSer(γ-OMe)8]ANGII, [Des1,HSer(γ- OMe)8]ANGII, [Sar1,Nva(δ-OMe)8]-ANGII, and [Des1,Nva(δ-OMe)8]ANGII had, respectively, the following antagonist activities, pA2: 7.6, 7.5, <6.0, 7.1, and 6.9. Analogs of [Sar1]ANGII with δ-hydroxy-L-norvaline [Nva(δ- OH)], δ-methoxy-L-norvaline [Nva(δ-OMe)], 4'-carboxyphenylalanine [Phe(4'- COOH)], and 4'-(trifluoromethyl)phenylalanine [Phe(4'-CF3)] at position 4 were also prepared by solid phase and bioassayed in the rat uterus. [Sar1,Nva(δ-OH)4]ANGII, [Aib1,Nva(δ-OMe)4]ANGII, [Sar1, DL-Phe(4'- COOH)4]ANGII, and [Sar1,DL-Phe(4'-CF3)4]ANGII had, respectively, agonist activities as follows: 4%, 1.5%, 3%, <0.1%, and <0.1%. These data emphasize that replacement of Ile8 in Sarilesin with the higher homologs HSer(γ-OMe) and Nva(δ-OMe) does not greatly alter the structural requirements necessary for expression of type I antagonist activity, while replacement of the tyrosine hydroxyl in [Sar1]ANGII by the carboxylate or the trifluoromethyl group abolishes activity, suggesting that the tyrosinate pharmacophore cannot be replaced by any negatively charged or electronegative group. Conformational investigation of the ANGII type I antagonists [HSer(γ- OMe)8]ANGII and [Sar1 Nva(δ-OMe)8]ANGII in DMSO by 1D-NOE spectroscopy revealed that the Tyr-Ile-His bend, a conformational property found in ANGII and [Sar1]ANGII (J. Biol. Chem. 1994, 269, 5303) is not present in type I antagonists, providing for the first time an important conformational difference between angiotensin II agonists and type I antagonists.
View MoreHubei Onward Bio-Development Co., Ltd.
Contact:+86-718-8417012
Address:No.517,Shizhou Avenue,Enshi City,Hubei Province,China,445002
Winchem Industrial Co. Ltd.(expird)
Contact:86-574-83851061 86-574-87083208
Address:Room 905, No.3 Building,East Business Center, 456 Xingning Road, Ningbo City,China
Shandong Dayi Chemical Co., Ltd.
website:http://www.dayi.com.cn
Contact:+86- 535-7388728. 15306386031
Address:No 1 Danya west road, Laiyang City, Shandong province
Shenzhen ZheYi Chemicals Co.,LTD(Shanghai Branch)
Contact:+86-21-54159691
Address:Room1002,Building No.2, Lane 98 Bixiu Road,Minhang District, Shanghai,China 201100
Yangzhou Zhongbao Pharmaceutical Co.,Ltd
Contact:+86-514-88290838
Address:Jiangsu Baoying county economic develpment zone in baoying avenue91
Doi:10.1039/c3tb20156b
(2013)Doi:10.1016/0008-6215(95)00014-K
(1995)Doi:10.1007/BF01177015
(1995)Doi:10.1016/S0008-6215(00)80197-4
(1967)Doi:10.1021/om970923b
(1998)Doi:10.1021/acs.joc.1c00553
(2021)