Literature DB >> 31512284

Morpholine as a privileged structure: A review on the medicinal chemistry and pharmacological activity of morpholine containing bioactive molecules.

Angeliki P Kourounakis1, Dimitrios Xanthopoulos1, Ariadni Tzara1.   

Abstract

Morpholine is a heterocycle featured in numerous approved and experimental drugs as well as bioactive molecules. It is often employed in the field of medicinal chemistry for its advantageous physicochemical, biological, and metabolic properties, as well as its facile synthetic routes. The morpholine ring is a versatile and readily accessible synthetic building block, it is easily introduced as an amine reagent or can be built according to a variety of available synthetic methodologies. This versatile scaffold, appropriately substituted, possesses a wide range of biological activities. There are many examples of molecular targets of morpholine bioactive in which the significant contribution of the morpholine moiety has been demonstrated; it is an integral component of the pharmacophore for certain enzyme active-site inhibitors whereas it bestows selective affinity for a wide range of receptors. A large body of in vivo studies has demonstrated morpholine's potential to not only increase potency but also provide compounds with desirable drug-like properties and improved pharamacokinetics. In this review we describe the medicinal chemistry/pharmacological activity of morpholine derivatives on various therapeutically related molecular targets, attempting to highlight the importance of the morpholine ring in drug design and development as well as to justify its classification as a privileged structure.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  SAR; drug design; in vivo; molecular targets; morpholine; pharmacokinetics; scaffold

Mesh:

Substances:

Year:  2019        PMID: 31512284     DOI: 10.1002/med.21634

Source DB:  PubMed          Journal:  Med Res Rev        ISSN: 0198-6325            Impact factor:   12.944


  19 in total

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Authors:  John A Gilleran; Xin Yu; Alan J Blayney; Anthony F Bencivenga; Bing Na; David J Augeri; Adam R Blanden; S David Kimball; Stewart N Loh; Jacques Y Roberge; Darren R Carpizo
Journal:  J Med Chem       Date:  2021-02-04       Impact factor: 8.039

4.  From cyclic amines and acetonitrile to amidine zinc(ii) complexes.

Authors:  Nina Podjed; Barbara Modec; María M Alcaide; Joaquín López-Serrano
Journal:  RSC Adv       Date:  2020-05-13       Impact factor: 4.036

5.  Synthesis, X-ray crystal structure, Hirshfeld surface analysis, and molecular docking study of novel inhibitor of hepatitis B: methyl 4-fluoro-3-(morpholinosulfonyl)benzo[b]thiophene-2-carboxylate.

Authors:  Alexandre V Ivachtchenko; Oleg D Mitkin; Dmitry V Kravchenko; Sergiy M Kovalenko; Svitlana V Shishkina; Natalya D Bunyatyan; Irina S Konovalova; Irina G Dmitrieva; Vladimir V Ivanov; Thierry Langer
Journal:  Heliyon       Date:  2019-11-14

6.  Morpholine-based chalcones as dual-acting monoamine oxidase-B and acetylcholinesterase inhibitors: synthesis and biochemical investigations.

Authors:  Rani Sasidharan; Bo Hyun Eom; Jeong Hyun Heo; Jong Eun Park; Mohamed A Abdelgawad; Arafa Musa; Nicola Gambacorta; Orazio Nicolotti; Sreedharannair Leelabaiamma Manju; Bijo Mathew; Hoon Kim
Journal:  J Enzyme Inhib Med Chem       Date:  2021-12       Impact factor: 5.051

7.  An acidic morpholine derivative containing glyceride from thraustochytrid, Aurantiochytrium.

Authors:  Kunimitsu Kaya; Fujio Shiraishi; Tetsuo Iida; Masaki Yamada; Tomoharu Sano
Journal:  Sci Rep       Date:  2021-03-25       Impact factor: 4.379

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Authors:  Winnie Deuther-Conrad; Daniel Diez-Iriepa; Isabel Iriepa; Francisco López-Muñoz; María Angeles Martínez-Grau; Michael Gütschow; José Marco-Contelles
Journal:  RSC Med Chem       Date:  2021-05-20

Review 9.  β-Carboline-based molecular hybrids as anticancer agents: a brief sketch.

Authors:  Jay Prakash Soni; Yogesh Yeole; Nagula Shankaraiah
Journal:  RSC Med Chem       Date:  2021-03-24

10.  Small-molecule activating SIRT6 elicits therapeutic effects and synergistically promotes anti-tumor activity of vitamin D3 in colorectal cancer.

Authors:  Jialin Shang; Zhehui Zhu; Yingyi Chen; Jinglue Song; Yuji Huang; Kun Song; Jie Zhong; Xinyuan Xu; Jiacheng Wei; Chengxiang Wang; Long Cui; Chen-Ying Liu; Jian Zhang
Journal:  Theranostics       Date:  2020-04-27       Impact factor: 11.556

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