Literature DB >> 25054213

Peganumine A, a β-carboline dimer with a new octacyclic scaffold from Peganum harmala.

Kai-Bo Wang1, Ying-Tong Di, Yu Bao, Chun-Mao Yuan, Gang Chen, Da-Hong Li, Jiao Bai, Hong-Ping He, Xiao-Jiang Hao, Yue-Hu Pei, Yong-Kui Jing, Zhan-Lin Li, Hui-Ming Hua.   

Abstract

Peganumine A (1), a new dimeric β-carboline alkaloid characterized by a unique 3,9-diazatetracyclo[6.5.2.0(1,9).0(3,8)]pentadec-2-one scaffold, was isolated from the seeds of Peganum harmala. The structure including the absolute configuration was determined by spectroscopic data, X-ray crystallography, ECD calculation, and CD exciton chirality approaches. Compound 1 showed moderate cytotoxic activity against MCF-7, PC-3, and HepG2 cells and selective effects on HL-60 cells with an IC50 value of 5.8 μM.

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Year:  2014        PMID: 25054213     DOI: 10.1021/ol501856v

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  11 in total

1.  MCR synthesis of a tetracyclic tetrazole scaffold.

Authors:  Pravin Patil; Kareem Khoury; Eberhardt Herdtweck; Alexander Dömling
Journal:  Bioorg Med Chem       Date:  2014-12-20       Impact factor: 3.641

2.  Three new alkaloids from the roots of Sophora tonkinensis.

Authors:  Chun Wu; Lijun He; Xue Yi; Juan Qin; Yaolan Li; Yubo Zhang; Guocai Wang
Journal:  J Nat Med       Date:  2019-04-26       Impact factor: 2.343

3.  Structurally Diverse Alkaloids from the Seeds of Peganum harmala.

Authors:  Kai-Bo Wang; Da-Hong Li; Yu Bao; Fei Cao; Wen-Jing Wang; Clement Lin; Wen Bin; Jiao Bai; Yue-Hu Pei; Yong-Kui Jing; Danzhou Yang; Zhan-Lin Li; Hui-Ming Hua
Journal:  J Nat Prod       Date:  2017-01-27       Impact factor: 4.050

4.  Unified Synthesis of Polycyclic Alkaloids by Complementary Carbonyl Activation*.

Authors:  Guoli He; Benjamin List; Mathias Christmann
Journal:  Angew Chem Int Ed Engl       Date:  2021-05-01       Impact factor: 15.336

5.  Synthesis, Biological Activity, and Apoptotic Properties of NO-Donor/Enmein-Type ent-Kauranoid Hybrids.

Authors:  Dahong Li; Xu Hu; Tong Han; Shengtao Xu; Tingting Zhou; Zhenzhong Wang; Keguang Cheng; Zhanlin Li; Huiming Hua; Wei Xiao; Jinyi Xu
Journal:  Int J Mol Sci       Date:  2016-05-24       Impact factor: 5.923

Review 6.  Application of the Asymmetric Pictet-Spengler Reaction in the Total Synthesis of Natural Products and Relevant Biologically Active Compounds.

Authors:  Majid M Heravi; Vahideh Zadsirjan; Masumeh Malmir
Journal:  Molecules       Date:  2018-04-18       Impact factor: 4.411

Review 7.  Recent Advances in the Synthesis of β-Carboline Alkaloids.

Authors:  Tímea Szabó; Balázs Volk; Mátyás Milen
Journal:  Molecules       Date:  2021-01-27       Impact factor: 4.411

8.  Diastereoselective approach to rationally design tetrahydro-β-carboline-isatin conjugates as potential SERMs against breast cancer.

Authors:  Bharvi Sharma; Amandeep Singh; Liang Gu; Sourav Taru Saha; Ashona Singh-Pillay; Nosipho Cele; Parvesh Singh; Mandeep Kaur; Vipan Kumar
Journal:  RSC Adv       Date:  2019-03-28       Impact factor: 4.036

Review 9.  Peganum spp.: A Comprehensive Review on Bioactivities and Health-Enhancing Effects and Their Potential for the Formulation of Functional Foods and Pharmaceutical Drugs.

Authors:  Javad Sharifi-Rad; Cristina Quispe; Jesús Herrera-Bravo; Prabhakar Semwal; Sakshi Painuli; Beraat Özçelik; Furkan Ediz Hacıhasanoğlu; Shabnum Shaheen; Surjit Sen; Krishnendu Acharya; Marjan Amirian; Carla Marina Salgado Castillo; María Dolores López; Mauricio Schoebitz; Miquel Martorell; Tamar Goloshvili; Ahmed Al-Harrasi; Ahmed Al-Rawahi; Manoj Kumar; Hafiz Ansar Rasul Suleria; William C Cho
Journal:  Oxid Med Cell Longev       Date:  2021-06-27       Impact factor: 6.543

10.  A Series of β-Carboline Alkaloids from the Seeds of Peganum harmala Show G-Quadruplex Interactions.

Authors:  Kai-Bo Wang; Da-Hong Li; Ping Hu; Wen-Jing Wang; Clement Lin; Jian Wang; Bin Lin; Jiao Bai; Yue-Hu Pei; Yong-Kui Jing; Zhan-Lin Li; Danzhou Yang; Hui-Ming Hua
Journal:  Org Lett       Date:  2016-06-24       Impact factor: 6.005

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