Synthesis and pharmacological properties of N-[3-{3-(1-piperidinylmethyl)phenoxy}propyl]-2-(2- hydroxyethylthio)acetamide and related compounds as antiulcer agents. I

DOI: 10.1248/cpb.38.3035

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 3035 - 3041 (1990)

Update date:2022-08-03

Topics:

Authors:

Ueda Ueda

Ishii Ishii

Shinozaki

Seiki Seiki

Arai Arai

Hatanaka

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

Article abstract of DOI:10.1248/cpb.38.3035

Full text of DOI:10.1248/cpb.38.3035

NII-Electronic Library Service

Products guided by the article

Product name:2-(2-Hydroxy-propylsulfanyl)-N-[3-(3-piperidin-1-ylmethyl-phenoxy)-propyl]-acetamide

Cas No:132794-06-0

R&D Labs maybe for 132794-06-0

Kraeber & Co GmbH

Contact:+49-4101-3053-0

Address:Waldhofstrasse 14 ,25474 Ellerbek Germany
ALPHA PHARMACEUTICAL CO，LTD JIANGSU

Contact:+86-527-84829968,+86-527-84829998

Address:suqian city
Hebei Fulong Import & Export Co., Ltd.

Contact:86-311-87795661

Address:15A19 Zhongyuan Building,368 Youyi North Street,Shijiazhuang 050070,China
Synchemie Co., Ltd.

website:http://www.synchemie.com/

Contact:+86-574-87642758

Address:Room 901, Yinyi Bund Building， 132 Renmin Road
Wuxi Forest Biological Co.,Ltd

Contact:+86-510-81602300

Address:Room 317,Building D, No.159 middle Chengjiang Road,Jiangyin Wuxi city.

Relevant to this article

Isopenicillin N Synthase Binds δ-(L-α-Aminoadipoyl)-L-Cysteinyl-D-Thia-allo-Isoleucine through both Sulfur Atoms

Doi:10.1002/cbic.201100149
(2011)
1,2-addition of allyl and 2-oxo-2H-pyran-6-ylcarbonyl groups to cyclic C=N double bonds by means of organotin reagent for alkaloids synthesis; a facile synthesis of 8-oxoprotoberberine and norkeoyobirine (demethoxycarbonyloxogambirtannine)

Doi:10.1246/bcsj.65.298
(1992)
THE UNCATALYZED DIELS-ALDER REACTION OF IMINES WITH BIS(PHENYLSULFONYL)SUBSTITUTED DIENES

Doi:10.1016/S0040-4039(00)99216-5
(1989)
4',5'-Unsaturated 5'-Halogenated Nucleosides. Mechanism-Based and Competitive Inhibitors of S-Adenosyl-L-homocysteine Hydrolase

Doi:10.1021/jm00106a028
(1991)
Design of HIV-1 integrase inhibitors targeting the catalytic domain as well as its interaction with LEDGF/p75: A scaffold hopping approach using salicylate and catechol groups

Doi:10.1016/j.bmc.2011.06.058
(2011)
General and scalable amide bond formation with epimerization-prone substrates using T3P and pyridine

Doi:10.1021/ol201875q
(2011)

Article Doi