New human renin inhibitory peptides: Angiotensinogen transition-state analogues containing novel Leu-Val replacement and a retro-inverso amide bond

DOI: 10.1248/cpb.36.2278

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2278 - 2281 (1988)

Update date:2022-09-26

Topics:

Authors:

Iizuka Iizuka

Kamijo Kamijo

Harada Harada

Akahane Akahane

Kubota Kubota

Shimaoka

Umeyama Umeyama

Kiso Kiso

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1248/cpb.36.2278

Full text of DOI:10.1248/cpb.36.2278

NII-Electronic Library Service

Products guided by the article

Product name:2-[1-Naphthalen-1-yl-meth-(Z)-ylidene]-N-phenethyl-succinamic acid

Cas No:103632-72-0

R&D Labs maybe for 103632-72-0

WUXI KINGHAN BIO-MEDICAL&CHEMICAL INC.

Contact:13861062998

Address:Room 1316,No.1619 Huishan Avenue,Wuxi,China
Wuhan Chemchemical Co., Ltd.(expird)

Contact:15973022782

Address:7-5-6218,Incubation Centre,Guandong Industry Park, East Lake High-Tech Development Zone,Wuhan City.
Liaoning Yufeng Chemical Co.,Ltd.

Contact:86-0419-3418888

Address:The metallurgical industrial zone,shoushan town, Liaoyang, Liaoning, China
Yingkou Sanzheng Organic Chemical Co. Ltd.

Contact:+86-417-3638818

Address:25 Gengxinli Village, Daqing Road, Yingkou, Liaoning, China
Chongqing Werlchem Fine Chemical Co. Ltd

Contact:+86-23-67521957

Address:NO.15,Fortune Road,Yubei District,401121,Chongqing,China

Relevant to this article

Pd-Cu catalyzed heterocyclization during Sonogashira coupling: synthesis of 2-benzylimidazo[1,2-a]pyridine

Doi:10.1016/j.tetlet.2008.03.141
(2008)
Cram-selective Addition of α-Allyl Sulphinyl Anion to Chiral Aldehydes: Synthesis of (E)-1,4-Dihydroxyalk-2-enes

Doi:10.1039/c39860000366
(1986)
Structure-based optimization and biological evaluation of human 20α-hydroxysteroid dehydrogenase (AKR1C1) salicylic acid-based inhibitors

Doi:10.1016/j.ejmech.2010.08.052
(2010)
Effects of modifications of the linker in a series of phenylpropanoic acid derivatives: Synthesis, evaluation as PPARα/γ dual agonists, and X-ray crystallographic studies

Doi:10.1016/j.bmc.2008.03.043
(2008)
A simple method for semi-synthesis of peptidyl-argininals as potent inhibitors of trypsin-like proteases.

Doi:10.1248/cpb.34.1748
(1986)
Supramolecular substitution reactions between hydrazide-based molecular duplex strands: Complexation induced nonsymmetry and dynamic behavior

Doi:10.1021/jo801139p
(2008)

Article Doi