Literature DB >> 17687

The enkephalins and opiates: structure-activity relations.

A S Horn, J R Rodgers.   

Abstract

The X-ray structures of 9 "opiate" drugs which exhibit a range of pharmacological activity have been examined in detail leading to the theory that one of the reasons why the enkephalins and related peptides possess morphine-like activity is because they have a tyrosine, and hence a "tyramine", residue at the amino terminal position. This residue or a conformationally similar moiety, can be shown to be present in many opiates and analogues.

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Year:  1977        PMID: 17687     DOI: 10.1111/j.2042-7158.1977.tb11308.x

Source DB:  PubMed          Journal:  J Pharm Pharmacol        ISSN: 0022-3573            Impact factor:   3.765


  4 in total

1.  3D-QSAR studies of orvinol analogs as kappa-opioid agonists.

Authors:  Wei Li; Yun Tang; Qiong Xie; Wei Sheng; Zhui-Bai Qiu
Journal:  J Mol Model       Date:  2006-03-22       Impact factor: 1.810

2.  Conformation-activity relationships of opiate analgesics.

Authors:  J Martin; P Andrews
Journal:  J Comput Aided Mol Des       Date:  1987-04       Impact factor: 3.686

3.  Antagonistic effect of compound 48/80 on the inhibitory actions of morphine and methionine-enkephalin on electrically-induced contractions of the guinea-pig ileum.

Authors:  Y Kamikawa; Y Shimo
Journal:  Br J Pharmacol       Date:  1978-12       Impact factor: 8.739

4.  X-ray diffraction studies of enkephalins. Crystal structure of [(4'-bromo) Phe4,Leu5]enkephalin.

Authors:  T Ishida; M Kenmotsu; Y Mino; M Inoue; T Fujiwara; K Tomita; T Kimura; S Sakakibara
Journal:  Biochem J       Date:  1984-03-15       Impact factor: 3.857

  4 in total

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