Conformationally Restrained Analogs of Sympathomimetic Catecholamines. Synthesis, Conformational Analysis, and Adrenergic Activity of Isochroman Derivatives

DOI: 10.1021/jm00073a006

Source and publish data:

Journal of Medicinal Chemistry p. 3077 - 3086 (1993)

Update date:2022-08-04

Topics:

Authors:

Macchia, Bruno

Balsamo, Aldo

Breschi, Maria Cristina

Chiellini, Grazia

Lapucci, Annalina

et al. et al.

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

Article abstract of DOI:10.1021/jm00073a006

In previous papers dealing with the study of the conformations and the biopharmalogical activity of conformationally restrained analogs of sympathomimetic catecholamines (NE and ISO), proposals were advanced for the three-dimensional molecular models A, B

Full text of DOI:10.1021/jm00073a006

Products guided by the article

Product name:(2,3-dimethoxyphenyl)oxirane

Cas No:144923-98-8

R&D Labs maybe for 144923-98-8

Linyi VIHO Chemical Co.,Ltd

Contact:86-15588110016

Address:LINYI CITY,SHANDONG PROVINCE,CHINA
Shanghai FWD Chemicals ltd

website:http://www.fwdchem.com

Contact:86-21-54450828

Address:Room 802,Lotus Tower ,159 Tianzhou Road,Xuhui District,Shanghai
Anhui Hope-Chem Co., Ltd.

Contact:86-551-63540590

Address:No 1388 Furong Rd., Hefei, Anhui, China
Wuhan Soleado Technology Co.,Ltd.

Contact:86-2783341481 18971291927

Address:RM2405 Unit 1 Builing 1, Taiyin Tower, Changqing Road,Wuhan China
Angel Yeast Co., Ltd.

Contact:+86-717-6370352

Address:168 Chengdong Avenue, Yichang, Hubei 443003, P. R.China

Relevant to this article

Synthesis of 3-(4-Methyl-phenyl)-2-phenyl-3,4-dihydro-2H-benzo[e][1,3,2] oxazaphosphinine and Its Chalcogenides

Doi:10.14233/ajchem.2013.13937
(2013)
Metal-Free Visible-Light-Mediated Aromatization of 1,2–Dihydronaphthalenes

Doi:10.1002/ejoc.201901410
(2020)
Cyclopropane-based conformational restriction of GABA by a stereochemical diversity-oriented strategy: Identification of an efficient lead for potent inhibitors of GABA transports

Doi:10.1016/j.bmc.2013.06.063
(2013)
A convenient synthesis of lubeluzole and its enantiomer: Evaluation as chemosensitizing agents on human ovarian adenocarcinoma and lung carcinoma cells

Doi:10.1016/j.bmcl.2013.06.077
(2013)
Carbon-Carbon Bond Formation via N-Tosyliminium Ions

Doi:10.1016/S0040-4020(01)88321-6
(1992)
A novel one-pot synthesis of 7-methoxy-2-arylthieno[3,2-b]pyridine-3-ols in domino fashion

Doi:10.1016/j.tetlet.2013.07.024
(2013)

Article Doi