LAXATIVES. II. RELATIONSHIP BETWEEN STRUCTURE AND POTENCY.

DOI: 10.1002/jps.2600530918

Source and publish data:

Journal of Pharmaceutical Sciences p. 1067 - 1072 (1964)

Update date:2022-08-04

Topics:

Authors:

HUBACHER

DOERNBERG

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

Article abstract of DOI:10.1002/jps.2600530918

Full text of DOI:10.1002/jps.2600530918

Products guided by the article

Product name:Bis-<4-hydroxy-phenyl>-essigsaeure-<4-hydroxy-benzylidenhydrazid>

Cas No:1667-88-5

R&D Labs maybe for 1667-88-5

HEZE KINGVOLT CHEMICAL CO., LTD

Contact:86-573-82118911

Address:Juancheng Industry Park
Jiacheng-Chem Enterprises Limited(expird)

Contact:86-571-86711508

Address:19 Floor, CIBC Holley International Building, No. 198,Wuxing Road, Hangzhou, China,310020
Changzhou LanXu Chemical Co.,ltd.(expird)

Contact:86-0519-86330911,13656129734,15261186386

Address:Room 524, Depart.Chemical, Changzhou Science and Eductaion town, Jiangsu, China;Factory: Haian Fine Chemical Industry Park,Nantong,Jiangsu,China
ANTAI BIO-TECH CO LTD

website:http://www.antaibio.com

Contact:86-21-60939051,60939771

Address:Room 2108, Building 2，No. 489 Zhengli Road，200433
Jiande City Silibase Silicone New Material Manufacture Co., Ltd.

Contact:15967177856

Address:Genglou Industrial Development Area

Relevant to this article

Structure-guided discovery of 2-aryl/pyridin-2-yl-1H-indole derivatives as potent and selective hepsin inhibitors

Doi:10.1016/j.bmcl.2015.09.042
(2015)
Porphyrins with exocyclic rings. Part 12. Synthesis of meso,β-butano- and meso,β-pentanoporphyrins from cycloalka[b]pyrroles

Doi:10.1016/S0040-4020(98)00327-5
(1998)
Doi:10.1039/jr9380000445
(1938)
A redox-switchable hemilabile ligand: Electrochemical control of the coordination environment of a Rh^I complex

Doi:10.1002/anie.199516241
(1995)
Design, synthesis, and pharmacological evaluation of dual histamine H₂ and gastrin receptor antagonists

Doi:10.1016/S0960-894X(96)00248-X
(1996)
Organosilicon-mediated regioselective acetylation of carbohydrates

Doi:10.1039/c2cc31556d
(2012)

Article Doi