Antitumor agents. 203. Carbazole alkaloid murrayaquinone A and related synthetic carbazolequinones as cytotoxic agents.
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3-Bromo-methyl-4-meth-oxy-2-(2-nitro-phen-yl)-9-phenyl-sulfonyl-9H-carbazole9-Meth-oxy-5-phenyl-sulfonyl-5H-benzo[b]carbazole7,9-Dimethyl-5-phenyl-sulfonyl-5H-benzo[b]carbazole.1-Naphthyl 9H-carbazole-4-sulfonate.3-[2-(9-Ethyl-9H-carbazol-3-yl)-6-methyl-3-quinol-yl]propan-1-ol6-Meth-oxy-9-phenyl-sulfonyl-2-(2-thien-yl)-9H-thieno[2,3-b]carbazole.9-p-Tolyl-9H-carbazole-3-carbonitrile.Crystal structure of (E)-N-(3,3-di-phenyl-allyl-idene)-9-ethyl-9H-carbazol-3-amineCrystal structure of (E)-N-[(2-chloro-6-meth-oxy-quinolin-3-yl)methyl-idene]-9-ethyl-9H-carbazol-3-amine.Leaves extract of murraya koenigii linn for anti-inflammatory and analgesic activity in animal modelsMurrayafoline A Induces a G0/G1-Phase Arrest in Platelet-Derived Growth Factor-Stimulated Vascular Smooth Muscle Cells.Crystal structure of ethyl 2-phenyl-9-phenyl-sulfonyl-9H-carbazole-3-carboxyl-ate.2-(4-Chloro-2-nitro-phen-yl)-9-phenyl-sulfonyl-9H-carbazole-3-carbaldehyde.Crystal structures of two new carbazole derivatives: 12-(4-nitro-phen-yl)-7-phenyl-sulfonyl-7H-benzofuro[2,3-b]carbazole and 2-methyl-4-(4-nitro-phen-yl)-9-phenyl-sulfonyl-9H-thieno[2,3-b]carbazole.Crystal structures of three carbazole derivatives: 12-ethyl-7-phenyl-sulfonyl-7H-benzofuro[2,3-b]carbazole, (1), 2-(4,5-dimeth-oxy-2-nitro-phen-yl)-4-hy-droxy-9-phenyl-sulfonyl-9H-carbazole-3-carbaldehyde, (2), and 12-phenyl-7-phenyl-sulfonyl-7H-benFunctional, electrophysiological and molecular docking analysis of the modulation of Cav 1.2 channels in rat vascular myocytes by murrayafoline A.9-[4-(Azido-meth-yl)phen-yl]-9H-carbazole-3-carbo-nitrile.2-(4,5-Di-chloro-2-nitro-phen-yl)-4-meth-oxy-3-methyl-9-phenyl-sulfon-yl-9H-carbazole.2-(4-Chloro-2-nitro-phen-yl)-4-meth-oxy-9-phenyl-sulfonyl-9H-carbazole-3-carbaldehyde.2-(4-Fluoro-2-nitro-phen-yl)-4-hy-droxy-9-phenyl-sulfonyl-9H-carbazole-3-carbaldehyde2-(4,5-Dimeth-oxy-2-nitro-phen-yl)-4-meth-oxy-3-methyl-9-phenyl-sulfonyl-9H-carbazole.2-(4,5-Dimeth-oxy-2-nitro-phen-yl)-4-meth-oxy-9-phenyl-sulfonyl-9H-carbazole-3-carbaldehyde.Synthesis and biological evaluation of novel pyrano[3,2-c]carbazole derivatives as anti-tumor agents inducing apoptosis via tubulin polymerization inhibition.Cytotoxic compounds isolated from Murraya tetramera Huang.Apoptosis of HL-60 leukemia cells induced by carbazole alkaloids isolated from Murraya euchrestifolia.Four new carbazole alkaloids from Murraya koenigii that display anti-inflammatory and anti-microbial activities.A novel and facile synthesis of 3-(2-benzofuroyl)- and 3,6-bis(2-benzofuroyl)carbazole derivatives.Atrovirinone inhibits pro-inflammatory mediator release from murine macrophages and human whole blood.tert-Butyl 6-bromo-1,4-dimethyl-9H-carbazole-9-carboxyl-ate.Synthesis of 3-(quinolin-2-yl)- and 3,6-bis(quinolin-2-yl)-9H-carbazoles.Protonation Sites, Tandem Mass Spectrometry and Computational Calculations of o-Carbonyl Carbazolequinone Derivatives.8,9-Dimeth-oxy-5-phenyl-sulfonyl-5H-benzo[b]carbazole.In vitro and in vivo anti-angiogenic activity of girinimbine isolated from Murraya koenigii.Biarylic biscarbazole alkaloids: occurrence, stereochemistry, synthesis, and bioactivity.Synthesis of novel derivatives of murrayafoline A and their inhibitory effect on LPS-stimulated production of pro-inflammatory cytokines in bone marrow-derived dendritic cells.1-O-Substituted derivatives of murrayafoline A and their antifungal properties.Synthesis of carbazoloquinone natural products 'on-water'.Sensitization of cardiac Ca²⁺ release sites by protein kinase C signaling: evidence from action of murrayafoline A.
P2860
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P2860
Antitumor agents. 203. Carbazole alkaloid murrayaquinone A and related synthetic carbazolequinones as cytotoxic agents.
description
2000 nî lūn-bûn
@nan
2000 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Antitumor agents. 203. Carbazo ...... equinones as cytotoxic agents.
@ast
Antitumor agents. 203. Carbazo ...... equinones as cytotoxic agents.
@en
type
label
Antitumor agents. 203. Carbazo ...... equinones as cytotoxic agents.
@ast
Antitumor agents. 203. Carbazo ...... equinones as cytotoxic agents.
@en
prefLabel
Antitumor agents. 203. Carbazo ...... equinones as cytotoxic agents.
@ast
Antitumor agents. 203. Carbazo ...... equinones as cytotoxic agents.
@en
P2093
P356
P1476
Antitumor agents. 203. Carbazo ...... equinones as cytotoxic agents.
@en
P2093
Furukawa H
Itoigawa M
Kashiwada Y
Tachibana Y
P304
P356
10.1021/NP000020E
P577
2000-07-01T00:00:00Z