Literature DB >> 24214836

Daphniphyllum alkaloids: recent findings on chemistry and pharmacology.

Haifeng Wu1, Xiaopo Zhang, Lisheng Ding, Shilin Chen, Junshan Yang, Xudong Xu.   

Abstract

The unique polycyclic fused ring systems of Daphniphyllum alkaloids, along with their extensive bioactivities, make this family of alkaloids especially attractive targets for total synthesis and biogenetic studies. Successive discoveries of new alkaloids with unprecedented skeletons have made a great contribution to structural diversities of alkaloids elaborated by plants of the genus Daphniphyllum. By the end of 2008, more than 200 alkaloids belonging to 14 different skeletal types have been isolated from different parts of plants of thirteen Daphniphyllum species. These alkaloids show cytotoxic, antioxidant, vasorelaxant, and antiplatelet activating factor effects. The plausible biosynthetic pathways for Daphniphyllum alkaloids have been proposed and biomimetic total syntheses of some alkaloids completed. To provide an update of the previous reviews published in 2009, new structures, synthesis, and bioactivity of Daphniphyllum alkaloids reported in recent years are presented in this article. In the meantime, an additional 54 novel alkaloids have been isolated and identified. Among them, some possess unprecedented frameworks. Several inspired organic syntheses were completed. Georg Thieme Verlag KG Stuttgart · New York.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 24214836     DOI: 10.1055/s-0033-1351024

Source DB:  PubMed          Journal:  Planta Med        ISSN: 0032-0943            Impact factor:   3.352


  8 in total

1.  Calyciphylline B-Type Alkaloids: Total Syntheses of (-)-Daphlongamine H and (-)-Isodaphlongamine H.

Authors:  Cedric L Hugelshofer; Vignesh Palani; Richmond Sarpong
Journal:  J Am Chem Soc       Date:  2019-05-16       Impact factor: 15.419

Review 2.  Synthetic Strategies toward Natural Products Containing Contiguous Stereogenic Quaternary Carbon Atoms.

Authors:  Martin Büschleb; Stéphane Dorich; Stephen Hanessian; Daniel Tao; Kyle B Schenthal; Larry E Overman
Journal:  Angew Chem Int Ed Engl       Date:  2016-02-02       Impact factor: 15.336

3.  Asymmetric total synthesis of yuzurimine-type Daphniphyllum alkaloid (+)-caldaphnidine J.

Authors:  Yan Zhang; Jingping Hu; Lian-Dong Guo; Chengqing Ning; Heyifei Fu; Yuye Chen; Jing Xu
Journal:  Nat Commun       Date:  2020-07-15       Impact factor: 14.919

4.  Five new alkaloids from the stem bark of Daphniphyllum macropodum.

Authors:  Yunyang Lu; Kai Gao; Xiaoyang Wang; Wei Zhang; Ning Ma; Haifeng Tang
Journal:  Molecules       Date:  2014-03-10       Impact factor: 4.411

5.  Calycindaphines A-J, Daphniphyllum alkaloids from the roots of Daphniphyllum calycinum.

Authors:  Ji Yang; Xin Liu; Jing Fu; Hao-Yuan Lyu; Li-Ping Bai; Zhi-Hong Jiang; Guo-Yuan Zhu
Journal:  RSC Adv       Date:  2021-03-01       Impact factor: 3.361

6.  Comparative toxicity, phytochemistry, and use of 53 Philippine medicinal plants.

Authors:  Lydia M Clemen-Pascual; Rene Angelo S Macahig; Nina Rosario L Rojas
Journal:  Toxicol Rep       Date:  2021-12-10

Review 7.  Samarium(ii) iodide-mediated reactions applied to natural product total synthesis.

Authors:  Majid M Heravi; Azadeh Nazari
Journal:  RSC Adv       Date:  2022-03-30       Impact factor: 3.361

8.  Synthetic studies toward longeracemine: a SmI2-mediated spirocyclization and rearrangement cascade to construct the 2-azabicyclo[2.2.1]heptane framework.

Authors:  Keita Komine; Kyle M Lambert; Quentin R Savage; Joshua B Cox; John L Wood
Journal:  Chem Sci       Date:  2020-07-30       Impact factor: 9.825

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.