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SMB01336

Sigma-Aldrich

(±)-DIBOA

≥95% (HPLC)

Synonyme(s) :

DIBOA, 2,4-Dihydroxy-1,4-benzoxazin-3-one, 2,4-Dihydroxy-3,4-dihydro-2H-1,4-benzoxazin-3-one

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About This Item

Formule empirique (notation de Hill):
C8H7NO4
Numéro CAS:
Poids moléculaire :
181.15
Nomenclature NACRES :
NA.77

Niveau de qualité

Pureté

≥95% (HPLC)

Forme

solid

Pf

153—154 °C

Température de stockage

2-8°C

InChI

1S/C8H7NO4/c10-7-8(11)13-6-4-2-1-3-5(6)9(7)12/h1-4,8,11-12H

Clé InChI

COVOPZQGJGUPEY-UHFFFAOYSA-N

Description générale

DIBOA and its C-7-methoxy derivative DIMBOA are the predominant representatives of benzoxazinoids in plants. The end product of the benzoxazinoid biosynthesis is the glucoside form which has reduced toxicity compared to the aglucon. The toxic aglucon is produced upon disintegration of the cell due to pathogen or pest attack.

Application

Metabolomics research

Autres remarques

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Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3


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Hossein Hazrati et al.
Journal of agricultural and food chemistry, 68(39), 10609-10617 (2020-09-03)
Plants have evolved advanced chemical defense mechanisms, including root exudation, which enable them to respond to changes occurring in their surroundings rapidly. Yet, it remains unresolved how root exudation affects belowground plant-plant interactions. The objective of this study was to
Monika Frey et al.
Phytochemistry, 70(15-16), 1645-1651 (2009-07-07)
Benzoxazinoids are secondary metabolites that are effective in defence and allelopathy. They are synthesised in two subfamilies of the Poaceae and sporadically found in single species of the dicots. The biosynthesis is fully elucidated in maize; here the genes encoding
Ye Wang et al.
Oncotarget, 8(20), 33405-33415 (2017-04-20)
The non-receptor tyrosine kinase BMX has been reported in several solid tumors. However, the alternative splicing of BMX and its clinical relevance in lung cancer remain to be elucidated. Exon1.0 array was used to identify a novel alternative splicing of

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