Literature DB >> 23195843

Antibacterial and antifungal activities of neocryptolepine, biscryptolepine and cryptoquindoline, alkaloids isolated from Cryptolepis sanguinolenta.

K Cimanga1, T De Bruyne, L Pieters, J Totte, L Tona, K Kambu, D V Berghe, A J Vlietinck.   

Abstract

From the 80% EtOH extract of Cryptolepis sanguinolenta (Lindl.) Schlechter (Periplocaeae) root bark, a cryptolepine isomer named neocryptolepine, and two dimeric alkaloids named biscryptolepine and cryptoquindoline were isolated. These compounds were tested for their putative antibacterial and antifungal activities. Results have indicated that neocryptolepine showed an antibacterial activity against Gram-positive bacteria (MIC < 100 μg/ml), but was less acive against Gram-negative bacteria. It also inhibited the growth of the yeast C. albicans. Biscryptolepine exhibited only an activity against some Gram-positive bacteria (MIC = 62.5 or 31 μg/ml) while cryptoquindoline did not shown an activity against all selected microorganisms. The antibacterial activity of neocryptolepine and biscryptolepine is bacteriostatic rather than bactericidal. No antifungal activity could be observed for all alkaloids in our test system at the highest test concentration of 100 μg/ml.
Copyright © 1998 Gustav Fischer Verlag. Published by Elsevier GmbH.. All rights reserved.

Entities:  

Year:  1998        PMID: 23195843     DOI: 10.1016/S0944-7113(98)80030-5

Source DB:  PubMed          Journal:  Phytomedicine        ISSN: 0944-7113            Impact factor:   5.340


  11 in total

1.  Rh(II)2-catalyzed synthesis of α-, β-, or δ-carbolines from aryl azides.

Authors:  Ashley L Pumphrey; Huijun Dong; Tom G Driver
Journal:  Angew Chem Int Ed Engl       Date:  2012-04-26       Impact factor: 15.336

2.  Clinical efficacy of a tea-bag formulation of cryptolepis sanguinolenta root in the treatment of acute uncomplicated falciparum malaria.

Authors:  K A Bugyei; G L Boye; M E Addy
Journal:  Ghana Med J       Date:  2010-03

Review 3.  A review on potential of natural products in the management of COVID-19.

Authors:  Rudra Chakravarti; Rajveer Singh; Arijit Ghosh; Dhritiman Dey; Priyanka Sharma; Ravichandiran Velayutham; Syamal Roy; Dipanjan Ghosh
Journal:  RSC Adv       Date:  2021-05-12       Impact factor: 4.036

4.  Expedient one-pot synthesis of indolo[3,2-c]isoquinolines via a base-promoted N-alkylation/tandem cyclization.

Authors:  Huy H Nguyen; James C Fettinger; Makhluf J Haddadin; Mark J Kurth
Journal:  Tetrahedron Lett       Date:  2015-09-30       Impact factor: 2.415

5.  Antifertility activity of Cryptolepis sanguinolenta leaf ethanolic extract in male rats.

Authors:  Ayodeji F Ajayi; Roland E Akhigbe
Journal:  J Hum Reprod Sci       Date:  2012-01

6.  Mineral Fertilization Influences the Growth, Cryptolepine Yield, and Bioefficacy of Cryptolepis sanguinolenta (Lindl.) Schlt.

Authors:  Jacqueline Naalamle Amissah; Forgive Enyonam Alorvor; Benjamin Azu Okorley; Chris Mpere Asare; Dorcas Osei-Safo; Regina Appiah-Opong; Ivan Addae-Mensah
Journal:  Plants (Basel)       Date:  2022-01-01

Review 7.  Advancements in the synthesis of fused tetracyclic quinoline derivatives.

Authors:  Ramadan A Mekheimer; Mariam A Al-Sheikh; Hanadi Y Medrasi; Kamal U Sadek
Journal:  RSC Adv       Date:  2020-05-27       Impact factor: 4.036

Review 8.  Comprehensive review of α-carboline alkaloids: Natural products, updated synthesis, and biological activities.

Authors:  Deping Li; Renze Yang; Jun Wu; Bin Zhong; Yan Li
Journal:  Front Chem       Date:  2022-08-26       Impact factor: 5.545

9.  Synthesis and Evaluation of the Tetracyclic Ring-System of Isocryptolepine and Regioiso-Mers for Antimalarial, Antiproliferative and Antimicrobial Activities.

Authors:  Katja S Håheim; Emil Lindbäck; Kah Ni Tan; Marte Albrigtsen; Ida T Urdal Helgeland; Clémence Lauga; Théodora Matringe; Emily K Kennedy; Jeanette H Andersen; Vicky M Avery; Magne O Sydnes
Journal:  Molecules       Date:  2021-05-30       Impact factor: 4.411

Review 10.  Phytochemical and Pharmacological Review of Cryptolepis sanguinolenta (Lindl.) Schlechter.

Authors:  Newman Osafo; Kwesi Boadu Mensah; Oduro Kofi Yeboah
Journal:  Adv Pharmacol Sci       Date:  2017-10-15
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