Solid-phase synthesis and anti-infective activity of a combinatorial library based on the natural product anisomycin.Low-dose anisomycin sensitizes melanoma cells to TRAIL induced apoptosisInhibition of protein synthesis and JNK activation are not required for cell death induced by anisomycin and anisomycin analogues.Synergistic induction of TRAIL-mediated apoptosis by anisomycin in human hepatoma cells via the BH3-only protein Bid and c-Jun/AP-1 signaling pathway.In vitro and in vivo evaluation of anisomycin against Ehrlich ascites carcinoma.Structure-activity relationships of synthetic antibiotic analogues of anisomycin.In vivo toxicological evaluation of Anisomycin.Effects of nalidixic acid, chloramphenicol, cycloheximide, and anisomycin on structure and development of plastids and mitochondria in greening Euglena gracilis
P921
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P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
Anisomycine
@fr
Anizomicin
@sh
Anizomicin
@sr
anisomycin
@en
انیزومایسن
@azb
انیزومایسن
@fa
type
label
Anisomycine
@fr
Anizomicin
@sh
Anizomicin
@sr
anisomycin
@en
انیزومایسن
@azb
انیزومایسن
@fa
altLabel
1,4,5-Trideoxy-1,4-imino-5-(p-methoxyphenyl)-D-xylo-pentitol 3-acetate
@en
2-(p-Methoxybenzyl)-3,4-pyrrolidinediol 3-acetate
@en
2-p-Methoxyphenylmethyl-3-acetoxy-4-hydroxypyrrolidine
@en
Anisomycin
@en
prefLabel
Anisomycine
@fr
Anizomicin
@sh
Anizomicin
@sr
anisomycin
@en
انیزومایسن
@azb
انیزومایسن
@fa
P2868
P638
P486
P592
P6366
P646
P661
P662
P665
P683
P1579
P2017
CC(=O)O[C@@H]1[C@H](CN[C@@H]1CC2=CC=C(C=C2)OC)O
P2067
P231
22862-76-6
P232
P233
CC(=O)OC1C(CNC1CC2=CC=C(C=C2)OC)O
P234
1S/C14H19NO4/c1-9(16)19-14-12( ...... 7-8H2,1-2H3/t12-,13+,14+/m1/s1
P235
YKJYKKNCCRKFSL-RDBSUJKOSA-N