about
Metabolites contributing to Rhizoctonia solani AG-1-IA maturation and sclerotial differentiation revealed by UPLC-QTOF-MS metabolomics.Structure and tautomerism of tenuazonic acid--a synergetic computational and spectroscopic approach.Alternaria toxin-induced resistance in rose plants against rose aphid (Macrosiphum rosivorum): effect of tenuazonic acid.Biosynthesis of the mycotoxin tenuazonic acid by a fungal NRPS-PKS hybrid enzymeDraft Genome Sequence of Sorghum Grain Mold Fungus Epicoccum sorghinum, a Producer of Tenuazonic AcidNon-synergistic cytotoxic effects of Fusarium and Alternaria toxin combinations in Caco-2 cells.Emerging Mycotoxins: Beyond Traditionally Determined Food Contaminants.Biosynthetic approaches to creating bioactive fungal metabolites: Pathway engineering and activation of secondary metabolism.TeA is a key virulence factor for Alternaria alternata (Fr.) Keissler infection of its host.Minor contribution of alternariol, alternariol monomethyl ether and tenuazonic acid to the genotoxic properties of extracts from Alternaria alternata infested rice.Alternaria Species and Their Associated Mycotoxins.Natural occurrence of mycotoxins and toxigenic capacity of Alternaria strains from mouldy peppers.Survey of Alternaria Toxins and Other Mycotoxins in Dried Fruits in China.Blocking the QB-binding site of photosystem II by tenuazonic acid, a non-host-specific toxin of Alternaria alternata, activates singlet oxygen-mediated and EXECUTER-dependent signalling in Arabidopsis.Chloroplastic oxidative burst induced by tenuazonic acid, a natural photosynthesis inhibitor, triggers cell necrosis in Eupatorium adenophorum Spreng.Degradation kinetics of the Alternaria mycotoxin tenuazonic acid in aqueous solutions.Determination of tenuazonic acid in human urine by means of a stable isotope dilution assay.Effect of environmental factors on tenuazonic acid production by Alternaria alternata on soybean-based media.In vivo assessment of effect of phytotoxin tenuazonic acid on PSII reaction centers.Large-scale synthesis of isotopically labeled 13C2-tenuazonic acid and development of a rapid HPLC-MS/MS method for the analysis of tenuazonic acid in tomato and pepper products.Arginine acts as an inhibitor of the biosynthesis of several mycotoxins.Detection and Quantitative Analysis of the Non-cytotoxic allo-Tenuazonic Acid in Tomato Products by Stable Isotope Dilution HPLC-MS/MS.Quantitative Determination of Tenuazonic Acid in Pig and Broiler Chicken Plasma by LC-MS/MS and Its Comparative Toxicokinetics.Characterization of Phenolic Compounds from Early and Late Ripening Sweet Cherries and Their Antioxidant and Antifungal Activities.Water activity and temperature effects on growth and mycotoxin production by Alternaria alternata strains isolated from Malbec wine grapes.Evaluation of an enzyme immunoassay for the detection of the mycotoxin tenuazonic acid in sorghum grains and sorghum-based infant foodDevelopment of analytical methods for the determination of tenuazonic acid analogues in food commoditiesContent of the Alternaria mycotoxin tenuazonic acid in food commodities determined by a stable isotope dilution assayDevelopment of a Stable Isotope Dilution Assay for Tenuazonic AcidEffect of Wheat Milling Process on the Distribution of ToxinsIn vitro characterization of hepatic toxicity of Alternaria toxinsEnzyme immunoassay for tenuazonic acid in apple and tomato productsNatural occurrence of four Alternaria mycotoxins in tomato- and citrus-based foods in ChinaNatural occurrence of tenuazonic acid and Phoma sorghina in Brazilian sorghum grains at different maturity stagesDetermination of Exposure to the Alternaria Mycotoxin Tenuazonic Acid and Its Isomer allo-Tenuazonic Acid in a German Population by Stable Isotope Dilution HPLC-MS(3)
P921
Q33657932-F38F58C4-4279-4213-B0F9-EBDB8CDAA346Q34615446-F74A7B03-B2DD-4C98-A8D9-616B3D1E3BC4Q35443390-8306D6B6-D116-4EEE-9EAA-895CA9D67379Q36266912-650C57DE-651E-417D-A1BD-64C22F4C28B1Q37610235-A0CF1DA5-E77B-4166-B33A-1EB5D287B985Q38822510-ADE4D82B-F2A0-458C-87B3-19FF90975DC6Q38947510-C14CC079-D7CA-4CBE-A656-7B1C50460CFCQ39014282-06C06CD4-AE8C-4314-A695-1F7DCBFD820EQ39119434-68C4A7D2-1CB5-4056-A1E7-5151681AF997Q39294502-62260358-F5BE-4206-A2EF-271F14EA5218Q40421042-BA815472-DEEA-4A70-B44F-A59ADF540EF6Q40578036-E9F4C6AD-19E5-4E9D-80F1-B2BBBB1A3A3FQ41174972-261A0019-B554-48B9-8627-45BAF737FB8BQ41712280-7562DCF5-7E68-49BD-BBFB-D9EBAEAFA465Q43212760-9E6B6F50-6957-4ACC-A95B-93C65BA4C8E9Q43235115-5A475788-D33C-4A35-9CA0-EF44E9CEBD9FQ44069219-82310135-521D-45EB-BAED-B2E1C0C68AC8Q45987715-ADA061DA-0A45-4C1E-A1F6-7C104E660BDBQ46122439-D8C7C317-4234-46B4-850A-B670EAC6DC3FQ46232752-A5F08601-521B-43E7-9D08-8C8310E468F4Q46518117-6F3C665F-07F0-4E6F-8156-876532550C34Q46628766-9E8244B7-A90A-433D-A9CE-7A656FEC83CAQ46669534-84319542-C0A5-4994-ABD4-90ECFEBA43BDQ48278449-A89F44BE-FB45-4D17-B200-14BEEF561852Q50273122-7DB77FCD-C134-494F-9585-79DE71ADAB79Q58233408-60A003A7-D7C1-4C6A-8C93-A435BC264558Q58233512-292164C2-CFC8-474C-B8F9-AE0EDCB8B880Q58233571-B358BF6E-A0A8-407C-9B12-F2E97856B18BQ58233624-39D52DB5-0410-408D-A111-81DB60D3DC87Q64085122-43C80E04-9069-4E3D-8C5C-310C7864C9A5Q64388504-68ADE3D5-7E01-452E-B620-5D84E114E1B9Q82350320-384D01AF-2190-4F5C-AAAC-35BA8B3D82D6Q86330365-029A5297-9DDD-4511-90F4-81AAB6084605Q87830587-0CC569BB-3392-4592-AB7D-8B470A9F7835Q87990031-E47DA67F-F179-4E9E-9AD5-4E94306BE41C
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
Tenuazonic acid
@en
type
label
Tenuazonic acid
@en
altLabel
Pyrrole-2,4-diol, 3-acetyl-5-sec-butyl-
@en
prefLabel
Tenuazonic acid
@en
P486
P661
P662
P665
P683
P2017
CC[C@H](C)[C@H]1C(=O)C(C(=O)N1)C(=O)C
P2064
P2067
197.105193
P231
27778-66-1
P233
CCC(C)C1C(=O)C(C(=O)N1)C(=O)C
P234
1S/C10H15NO3/c1-4-5(2)8-9(13)7 ...... -3H3,(H,11,14)/t5-,7?,8-/m0/s1
P235
KLBSRSYHIIAQTG-PZICIZFRSA-N
P274
P3117
DTXSID30893265