4-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline derivatives. II. Their renal vasodilation activity and structure-activity relationship

DOI: 10.1248/cpb.44.1865

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1865 - 1870 (1996)

Update date:2022-08-05

Topics: Structure-Activity Relationship

Authors:

Anan, Hideki

Tanaka, Akihiro

Tsuzuki, Ryuji

Yokota, Masaki

Yatsu, Takeyuki

Fujikura, Takashi

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

Article abstract of DOI:10.1248/cpb.44.1865

A series of 4-(3,4-dihydroxyphenyl)-1,2,3,4-tetrahydroisoquinoline derivatives showed potent DA₁ agonistic activities. We investigated the structure-activity relationship of the racemic compounds of this series. 4- (3,4-Dihydroxyphenyl)-7-metha

Full text of DOI:10.1248/cpb.44.1865

NII-Electronic Library Service

Products guided by the article

Product name:Benzoic acid, 3-[(ethylsulfonyl)amino]-, ethyl ester

Cas No:849410-09-9

R&D Labs maybe for 849410-09-9

Shanghai Demand Chemical Co., ltd，China

Contact:86-021-55237578/55239122

Address:Room 3H, No.578, Yingkou Road, Yangpu District, Shanghai, China
Shandong Shouguang Songchuan Industrial Additives Co.,Ltd

Contact:+86-536-8566856

Address:Shouguang,Shandong,China
Beyond Pharmaceutical Co., Ltd

Contact:+86-571-8195-3185

Address:No. 13-1, Liansheng Road, Yuhang District
HAORUI ENTERPRISES LLC

Contact:(1) 206-3550089

Address:5115 NE 8TH PL, Renton, WA 98059 USA
Landz International Company Ltd.

Contact:0086-21-58891610

Address:985 Dongfang Road, Pudong, Shanghai 200122 China

Relevant to this article

A Kinetic Investigation of Carbon Dioxide Insertion Processes Involving Anionic Tungsten-Alkyl and -Aryl Derivatives: Effects of CO2 Pressure, Counterions, and Ancillary Ligands.

Doi:10.1021/ja00311a040
(1985)
<3.3>Orthocyclophanes with Facing Benzene and Naphtahalene Rings

Doi:10.1021/jo00389a004
(1987)
Application of the Intramolecular Aza-Wittig Reaction to the Synthesis of Vinylogous Urethanes and Amides

Doi:10.1021/jo00225a066
(1985)
Doi:10.1039/CT9130301768
(1913)
Surfactant-mediated solvent-free dealkylative cleavage of ethers and esters and trans-alkylation under neutral conditions

Doi:10.1016/j.tetlet.2005.11.048
(2006)
Design, synthesis and anticancer activity of a new series of n-aryl-n^′-[4-(Pyridin-2-ylmethoxy)benzyl]urea derivatives

Doi:10.3390/molecules26123496
(2021)

Article Doi