about
Solution structure of an acyl carrier protein domain from a fungal type I polyketide synthaseInteractions of saprophytic yeasts with a nor mutant of Aspergillus flavus.Enzymatic function of the nor-1 protein in aflatoxin biosynthesis in Aspergillus parasiticus.Interrogation of global active site occupancy of a fungal iterative polyketide synthase reveals strategies for maintaining biosynthetic fidelity.Norsolorinic acid from Aspergillus nidulans inhibits the proliferation of human breast adenocarcinoma MCF-7 cells via Fas-mediated pathwayNorsolorinic acid inhibits proliferation of T24 human bladder cancer cells by arresting the cell cycle at the G0/G1 phase and inducing a Fas/membrane-bound Fas ligand-mediated apoptotic pathway.Precursor recognition by kinetic pulse-labeling in a toxigenic aflatoxin B1-producing strain of Aspergillus.Identification of averantin as an aflatoxin B1 precursor: placement in the biosynthetic pathway.HypC, the anthrone oxidase involved in aflatoxin biosynthesis.Mutagenicity of fungal metabolites related to aflatoxin biosynthesis.One gene to whole pathway: the role of norsolorinic acid in aflatoxin research.The preparation of an enzyme associated with aflatoxin biosynthesis by affinity chromatography.Initial characterization of a type I fatty acid synthase and polyketide synthase multienzyme complex NorS in the biosynthesis of aflatoxin B(1).Demonstration of the catalytic roles and evidence for the physical association of type I fatty acid synthases and a polyketide synthase in the biosynthesis of aflatoxin B1.The affinity purification and characterization of a dehydrogenase from Aspergillus parasiticus involved in aflatoxin B1 biosynthesis.Inhibition of aflatoxin biosynthesis by phenolic compoundsIsolation of the anthraquinone norsolorinic acid from Cinchona ledgerianaIsolation of microorganisms and substances inhibitory to aflatoxin productionA note on the relevance of norsolorinic acid as a chemopreventive agent for the treatment of bladder cancer
P921
Q27659607-998E6F1A-0DA9-4FCA-A15D-546B71458750Q33985150-73A2F135-E8E6-4C8C-A5F7-FD36ECF7A883Q33986357-0D406D20-3049-4718-862D-44754E967937Q35906588-096A65B2-319F-4AD1-B5D7-788EDDCE316AQ37124453-A7BC4E79-CD99-42D8-A79B-C17DD4813C41Q39955256-68AEEC09-C766-4123-A61B-5E24B6786A0DQ40080894-45D9F395-08F1-4D0A-B60D-C8C0876F8F84Q40321540-00940A4C-B410-4977-B18B-7251D19105BBQ40527307-7E82BB07-711B-4292-8C1A-C0DCB4E7BF91Q40813064-F0D95B12-AD02-464E-A1B3-271BFA48F0BDQ41650502-DCDC2A7F-CB80-4465-B1DD-0E3EB2C96D70Q41775236-7F5D18E8-2069-44C3-BDEB-D9C305F8E737Q44152735-EA1DA01C-968B-4822-84BB-21727EB5739FQ52521222-7ED8D791-EFD9-4EE4-AF2D-EAB6E3E89CADQ53868394-8779F4B8-30FC-4A1D-9997-E04E1113228AQ73424134-DD105341-99F6-462B-8A69-7F4644841174Q79694530-FCDE24DD-BD44-4DBF-8740-E451156E16B2Q81978597-1E9A0CAC-C591-440C-9F27-4B6A0F0EB1D7Q84209362-A7B4AFC8-999D-4701-9099-24708F968CDF
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
norsolorinic acid
@en
type
label
norsolorinic acid
@en
prefLabel
norsolorinic acid
@en
P661
P662
P683
P1579
P2067
P231
10254-99-6
P233
CCCCCC(=O)C1=C(C=C2C(=C1O)C(=O)C3=C(C=C(C=C3C2=O)O)O)O
P234
1S/C20H18O7/c1-2-3-4-5-12(22)1 ...... 23/h6-8,21,23-24,27H,2-5H2,1H3
P235
XIJDBHLQUYAZJI-UHFFFAOYSA-N
P274
P2840
P3117
DTXSID00145263
P652
Q1W7A6D0J6