Literature DB >> 12713412

Antineoplastic agents. 485. Isolation and structure of cribrostatin 6, a dark blue cancer cell growth inhibitor from the marine sponge Cribrochalina sp.

George R Pettit1, Jeremiah C Collins, John C Knight, Delbert L Herald, Ronald A Nieman, Michael D Williams, Robin K Pettit.   

Abstract

Cribrostatin 6, a dark blue cancer cell growth inhibiting (P388 ED(50) 0.3 microg/mL) constituent of the Republic of Maldives marine sponge Cribrochalina sp., has been assigned structure 3 on the basis of a combination of HRMS, high-field (500 MHz, HMBC, and GOESY experiments) (15)N, (1)H, and (13)C NMR, and X-ray crystal structure analyses. Cribrostatin 6 also was found to inhibit the growth of a number of pathogenic bacteria and fungi.

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Year:  2003        PMID: 12713412     DOI: 10.1021/np020012t

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  9 in total

1.  Tandem Electrocyclic Ring Opening/Radical Cyclization: Application to the Total Synthesis of Cribrostatin 6.

Authors:  Daniel Knueppel; Stephen F Martin
Journal:  Tetrahedron       Date:  2011-12-23       Impact factor: 2.457

Review 2.  Antibacterials from the sea.

Authors:  Chambers C Hughes; William Fenical
Journal:  Chemistry       Date:  2010-11-08       Impact factor: 5.236

3.  Total synthesis of cribrostatin 6.

Authors:  Daniel Knueppel; Stephen F Martin
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

4.  Cribrostatin 6 induces death in cancer cells through a reactive oxygen species (ROS)-mediated mechanism.

Authors:  Mirth T Hoyt; Rahul Palchaudhuri; Paul J Hergenrother
Journal:  Invest New Drugs       Date:  2010-02-20       Impact factor: 3.850

5.  Multicomponent Reaction Based Synthesis of 1-Tetrazolylimidazo[1,5- a]pyridines.

Authors:  Santosh Kurhade; Elmar Diekstra; Fandi Sutanto; Katarzyna Kurpiewska; Justyna Kalinowska-Tłuścik; Alexander Dömling
Journal:  Org Lett       Date:  2018-06-26       Impact factor: 6.005

6.  Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes.

Authors:  Dmitrii A Aksenov; Nikolai A Arutiunov; Vladimir V Maliuga; Alexander V Aksenov; Michael Rubin
Journal:  Beilstein J Org Chem       Date:  2020-11-26       Impact factor: 2.883

7.  The synthesis of imidazo[1,5-a]quinolines via a decarboxylative cyclization under metal-free conditions.

Authors:  Zicong Yan; Changfeng Wan; Yu Yang; Zhenggen Zha; Zhiyong Wang
Journal:  RSC Adv       Date:  2018-06-25       Impact factor: 3.361

8.  Jorunnamycin A Suppresses Stem-Like Phenotypes and Sensitizes Cisplatin-Induced Apoptosis in Cancer Stem-Like Cell-Enriched Spheroids of Human Lung Cancer Cells.

Authors:  Somruethai Sumkhemthong; Supakarn Chamni; Gea U Ecoy; Pornchanok Taweecheep; Khanit Suwanborirux; Eakachai Prompetchara; Pithi Chanvorachote; Chatchai Chaotham
Journal:  Mar Drugs       Date:  2021-05-03       Impact factor: 5.118

9.  Chemistry of Renieramycins. Part 14: Total Synthesis of Renieramycin I and Practical Synthesis of Cribrostatin 4 (Renieramycin H).

Authors:  Masashi Yokoya; Keiichiro Kobayashi; Mitsuhiro Sato; Naoki Saito
Journal:  Mar Drugs       Date:  2015-08-06       Impact factor: 5.118

  9 in total

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