Synthesis and cytotoxic activities of 1-benzylidine substituted β-carboline derivatives

R Cao, W Yi, Q Wu, X Guan, M Feng, C Ma… - Bioorganic & Medicinal …, 2008 - Elsevier
A series of new β-carboline derivatives, bearing a benzylidine substituent at position-1, has
been prepared and evaluated in vitro against a panel of human cell lines. The N2 …

[引用][C] Synthesis and Activity of Carbazole Derivatives Against Mycobacterium tuberculosis

TA Choi, R Czerwonka, W Fröhner… - ChemMedChem …, 2006 - Wiley Online Library
Infecting one-third of the world's inhabitants, Mycobacterium tuberculosis (MTB) is deemed a
serious public health concern.[1] Failure to follow the current regimen along with the HIV …

Primary discovery of 1-aryl-5-substituted-1H-1, 2, 3-triazole-4-carboxamides as promising antimicrobial agents

N Pokhodylo, N Manko, N Finiuk, O Klyuchivska… - Journal of Molecular …, 2021 - Elsevier
Three series of novel 1H-1, 2, 3-triazole-4-carboxamides: 1-aryl-5-alkyl/aryl-1H-1, 2, 3-
triazole-4-carboxamides, 1-aryl-5-amino-1H-1, 2, 3-triazole-4-carboxamides and 1, 2, 3 …

Indole‐3‐carbaldehyde Semicarbazone Derivatives: Synthesis, Characterization, and Antibacterial Activities

F Carrasco, W Hernández, O Chupayo… - Journal of …, 2020 - Wiley Online Library
Four indole‐3‐carbaldehyde semicarbazone derivatives, 2‐((5‐bromo‐1H‐indol‐3‐yl)
methylene) hydrazinecarboxamide (1), 2‐((5‐chloro‐1H‐indol‐3‐yl) methylene) …

Syntheses of novel β-carboline derivatives and the activities against five tumor-cell lines

B Bai, XY Li, L Liu, Y Li, HJ Zhu - Bioorganic & Medicinal Chemistry Letters, 2014 - Elsevier
A series of β-carbolines possessing the aryl group at C-1 position has been synthesized
from tryptophan. The newly synthesized compounds were screened for their in vitro …

Design, synthesis of new β-carboline derivatives and their selective anti-HIV-2 activity

P Ashok, S Chander, J Balzarini… - Bioorganic & medicinal …, 2015 - Elsevier
In the present study, a new series of β-carboline derivatives were synthesized and evaluated
for inhibition activity against both HIV-1 and HIV-2 strains. Among these reported analogues …

Direct biomimetic synthesis of β-carboline alkaloids from two amino acids

ZX Wang, JC Xiang, Y Cheng, JT Ma… - The Journal of …, 2018 - ACS Publications
The increasing importance of enzyme mimics in organic synthesis inspired us to design a
novel biomimetic synthesis of β-carboline alkaloids directly from tryptophan and a second …

Synthesis, acute toxicities, and antitumor effects of novel 9-substituted β-carboline derivatives

R Cao, Q Chen, X Hou, H Chen, H Guan, Y Ma… - Bioorganic & medicinal …, 2004 - Elsevier
A series of novel 9-substituted β-carboline derivatives was synthesized from harmine and l-
tryptophan, respectively. Cytotoxic activities of these compounds in vitro were investigated …

Synthesis and antimycobacterial evaluation of N-substituted 5-chloropyrazine-2-carboxamides

B Servusová, J Vobicková, P Paterová… - Bioorganic & medicinal …, 2013 - Elsevier
To develop new potential antimycobacterial drugs, a series of pyrazinamide derivatives was
designed, synthesized and tested for their ability to inhibit the growth of selected …

Recent advances on the synthesis and application of tetrahydro-γ-carbolines

H Mei, K Aradi, L Kiss, J Han - Chinese Chemical Letters, 2023 - Elsevier
Tetrahydro-γ-carbolines (THγ Cs) constitute one of the most important subtypes of indole
alkaloids. In addition to being substructures of natural products, these structural motifs and …