Bimane fluorogenic substrates for microdetermination of angiotensin converting enzyme level in serum

DOI: 10.1248/cpb.39.2146

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 2146 - 2148 (1991)

Update date:2022-07-29

Topics:

Authors:

Sato Sato

Hattori Hattori

Nishikawa

Kanaoka Kanaoka

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

Article abstract of DOI:10.1248/cpb.39.2146

The fluorescence of 9,10-dioxa-syn-3,4,6,7-tetramethylbimane (bimane) was found to be quenched in the presence of nitrated aromatic amino acid. Bimane peptides containing nitrated amino acid (1a, b) were shown to be useful fluorogenic substrates for the a

Full text of DOI:10.1248/cpb.39.2146

NII-Electronic Library Service

Products guided by the article

Product name:(S)-1-((S)-3-(6-Nitro-1H-indol-3-yl)-2-{(S)-3-phenyl-2-[2-(2,6,7-trimethyl-3,5-dioxo-3H,5H-pyrazolo[1,2-a]pyrazol-1-ylmethylsulfanyl)-acetylamino]-propionylamino}-propionyl)-pyrrolidine-2-carboxylic acid

Cas No:138329-98-3

R&D Labs maybe for 138329-98-3

UNION PHARMPRO CO.,LTD

Contact:18710867521(wechat)

Address:Rm10516,Galaxy Tech Building #2,No.25 Tangyan Rd,Hi-Tech Zone,Xi'an, China
Qingdao S. H. Huanyu Imp. & Exp. Co., Ltd.

Contact:86-532-88250866

Address:Room 615, World Trade Centre Building B, Hongkong Middle Roda 6#, Qingdao, Shandong, China
Quhua Zhongxing Refrigeration Technology Co.,Ltd.

Contact:+86-5708886618

Address:318 Bulding 2, No.866 Quhua Rd.,Kecheng District
Jinan Hongfangde Pharmatech Co.LTD

Contact:0531-88870908

Address:F Bldg,750#,Shunhua Rd,New&High-tech Zone,Jinan,Shandong,China 250101
Rayfull Holding Co., Ltd

Contact:+86-577-65618087-605

Address:Room 402, Unit 4 Xinhu Bldg. Waitan Ruian City, Zhejiang China.

Relevant to this article

Synthesis of α,γ-peptide hybrids by selective conversion of glutamic acid units

Doi:10.1021/ol301552c
(2012)
One-pot deracemization of sec-alcohols: Enantioconvergent enzymatic hydrolysis of alkyl sulfates using stereocomplementary sulfatases

Doi:10.1002/anie.201209946
(2013)
X=Y-ZH systems as potential 1,3-dipoles. Part 34. Generation of nitrones from oximes. Tandem Michael addition-1,3-dipolar cycloaddition reactions. Class 2 processes utilising bifunctional Michael acceptor-dipolarophile components

Doi:10.1016/S0040-4020(01)91022-1
(1991)
First stereoselective total synthesis of Phomolide G and H via RCM protocol

Doi:10.1016/j.tetlet.2012.04.118
(2012)
O-Tolyl/benzyl dithiocarbonates of phosphorus(III) and (V): Syntheses and characterization

Doi:10.1007/s00706-011-0704-2
(2012)
2,2-disubstituted 1,3-oxathianes as potential drugs

Doi:10.1002/ardp.2503241211
(1991)

Article Doi