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Fórmula lineal:
[HOC6H2(OCH3)2CH=N-]2
Número CAS:
Peso molecular:
360.36
NACRES:
NA.83
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
238-390-1
MDL number:
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Permítanos ayudarleNombre del producto
Syringaldazine, 98%
InChI key
YARKTHNUMGKMGS-LQGKIZFRSA-N
InChI
1S/C18H20N2O6/c1-23-13-5-11(6-14(24-2)17(13)21)9-19-20-10-12-7-15(25-3)18(22)16(8-12)26-4/h5-10,21-22H,1-4H3/b19-9+,20-10+
SMILES string
COc1cc(\C=N\N=C\c2cc(OC)c(O)c(OC)c2)cc(OC)c1O
assay
98%
form
powder or crystals
mp
209-210 °C (lit.)
solubility
DMF: 5%, clear to hazy
storage temp.
2-8°C
Quality Level
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Application
Syringaldazine has been used as a substrate to measure the enzymatic activity of recombinant laccase.
Biochem/physiol Actions
Syringaldazine (4-Hydroxy-3, 5-dimethoxybenzaldehyde azine) is a nonautooxidizable laccase-specific compound. It acts as a substrate for laccase and peroxidase in the presence of hydrogen peroxide (H2O2). Syringaldazine also acts as an electron donor in the prostaglandin H synthase (PGHS) reaction.
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W Bao et al.
Science (New York, N.Y.), 260(5108), 672-674 (1993-04-30)
Peroxidase has been thought to be the only enzyme that oxidizes monolignol precursors to initiate lignin formation in plants. A laccase was purified from cell walls of differentiating xylem of loblolly pine and shown to coincide in time and place
Y A Kuznetsova et al.
Applied biochemistry and biotechnology, 61(1-2), 205-209 (1996-10-01)
The prostaglandin H synthase (PGHS) reaction has been studied with syringaldazine as the electron donor. Kinetic parameters of the reaction agreed with those for commonly used electron donors. The sensitivity of the PGHS activity detection in the presence of syringaldazine
Use of syringaldazine for detection of laccase in sporophores of wood rotting fungi.
J M Harkin et al.
Mycologia, 66(3), 469-476 (1974-05-01)
S Molinari
Journal of nematology, 23(2), 254-258 (1991-04-01)
Isoperoxidases were detected in resistant Rossol and susceptible Roma VF tomato roots uninfected and infected by Meloidogyne incognita. Syringaldazine, guaiacol, p-phenylenediamine-pyrocatechol (PPD-PC), and indoleacetic acid (IAA) were used as substrates, and the corresponding peroxidative activities were detected either in cytoplasmic
Manickam Naresh Kumar et al.
Bioresource technology, 244(Pt 1), 353-361 (2017-08-07)
Inhibitor mediated intensified bio-pretreatment (IMBP) technology using natural cellulase inhibitor (NCI) for maximum cellulose recovery from paddy straw was studied. Pretreatment was carried out under solid state condition. Supplementation of 8% NCI in pretreatment medium improves cellulose recovery and delignification
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