Adenosine A1 antagonists. 3. Structure-activity relationships on amelioration against scopolamine- or N6-((R)-phenylisopropyl)adenosine-induced cognitive disturbance.

DOI: 10.1021/jm00069a009

Source and publish data:

Journal of medicinal chemistry p. 2508 - 2518 (1993)

Update date:2022-08-03

Topics:

Authors:

Suzuki Suzuki

Shimada Shimada

Shiozaki

Ichikawa

Ishii Ishii

Nakamura

Nonaka Nonaka

Kobayashi

Fuse Fuse

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

Article abstract of DOI:10.1021/jm00069a009

The effects of a variety of adenosine A1 and A2 antagonists on N6-((R)-phenylisopropyl)adenosine (R-PIA)- and scopolamine-induced amnesias were investigated in rodents in order to clarify the role of adenosine receptors in learning and memory. Some of the

Full text of DOI:10.1021/jm00069a009

Products guided by the article

Product name:N-[4-[2-(8-cyclopentyl-2,6-dioxo-1-propyl-7H-purin-3-yl)ethyl]phenyl]a cetamide

Cas No:149744-75-2

R&D Labs maybe for 149744-75-2

Tosta Enterprise Co., Ltd.

Contact:+86-134-5286-9121

Address:Add: Wing Tuck Commercial Centre, 177-183 Wing Lok Street, Hong Kong,
Lanling Hongchuang Flame Retardant Co., Ltd.

Contact:+86-531-68858132

Address:East Huafeichang Road, Cangshan County, Linyi, Shandong, China (Mainland)
Rely Chemicals Ltd.

Contact:+86-518-81061113

Address:No. 8 Lingzhou Road, Lianyungang, Jiangsu, China
Yangzhou Zhongbao Pharmaceutical Co.,Ltd

Contact:+86-514-88290838

Address:Jiangsu Baoying county economic develpment zone in baoying avenue91
Huangshi Shennong Chemical Technology Co., Ltd

Contact:+86-714-3072290

Address:Eastern industrial park , Tieshan district , Huangshi city ,Hubei province , China

Relevant to this article

Studies on the interaction of phosphate anions with N-functionalised polyaza[n]paracyclophanes: The role of N-methylation

Doi:10.1039/b315717b
(2004)
A new Schiff base compound N,N′-(2,2-dimetylpropane)- bis(dihydroxylacetophenone): Synthesis, experimental and theoretical studies on its crystal structure, FTIR, UV-visible, ¹H NMR and ¹³C NMR spectra

Doi:10.1016/j.saa.2011.05.080
(2011)
The chromiumtricarbonyl group as an electron acceptor in η⁶-complexes of stilbene and its derivatives

Doi:10.1016/0022-328X(93)83111-8
(1993)
Doi:10.1021/jo01265a119
(1968)
Stabilized Sulfur Ylide Mediated Cyclopropanations and Formal [4+1] Cycloadditions of 3-Acyl-2H-chromenones and Their Imines

Doi:10.1002/ejoc.201600759
(2016)
Potent in vitro and in vivo inhibitors of platelet aggregation based upon the Arg-Gly-Asp-Phe sequence of fibrinogen. A proposal on the nature of the binding interaction between the Arg-guanidine of RGDX mimetics and the platelet GP IIb-IIIa receptor

Doi:10.1021/jm00065a003
(1993)

Article Doi