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F6513

Fusaric acid

From Gibberella fujikuroi, ≥98% (TLC), Dopamine β-hydroxylase inhibitor, powder

Synonym(s):

5-Butylpicolinic acid, 5-Butylpyridine-2-carboxylic acid

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Pack SizeSKUAvailabilityPrice
250 mg
Please contact Customer Service for Availability
CZK 2,480.00
1 g
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CZK 7,710.00

About This Item

Empirical Formula (Hill Notation):
C10H13NO2
CAS Number:
Molecular Weight:
179.22
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
208-643-0
MDL number:
Beilstein/REAXYS Number:
125804
Assay:
≥98% (TLC)
Form:
powder
Quality level:

CZK 2,480.00


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Product Name

Fusaric acid, from Gibberella fujikuroi

biological source

Gibberella fujikuroi

Quality Level

assay

≥98% (TLC)

form

powder

mp

95-97  °C

solubility

ethanol: 49.00-51.00 mg/mL, clear, colorless to faintly yellow

antibiotic activity spectrum

Gram-positive bacteria

mode of action

enzyme | inhibits

storage temp.

−20°C

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This Item
55952798673F0600000
form

powder

form

-

form

powder

form

-

assay

≥98% (TLC)

assay

≥99.0% (HPLC)

assay

≥99%

assay

-

Quality Level

200

Quality Level

100

Quality Level

100

Quality Level

-

solubility

ethanol: 49.00-51.00 mg/mL, clear, colorless to faintly yellow

solubility

-

solubility

-

solubility

-

storage temp.

−20°C

storage temp.

-

storage temp.

-

storage temp.

-

biological source

Gibberella fujikuroi

biological source

-

biological source

-

biological source

-

General description

Chemical structure: pyridine

Biochem/physiol Actions

Dopamine β-hydroxylase inhibitor.

Features and Benefits

This compound is featured on the Dopamine, Norepinephrine and Epinephrine Synthesis page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Geneviève Girard et al.
Microbiology (Reading, England), 157(Pt 2), 398-407 (2010-10-30)
The triggering of antibiotic production by various environmental stress molecules can be interpreted as bacteria's response to obtain increased fitness to putative danger, whereas the opposite situation - inhibition of antibiotic production - is more complicated to understand. Phenazines enable
Daren W Brown et al.
Fungal genetics and biology : FG & B, 49(7), 521-532 (2012-06-02)
The genus Fusarium is of concern to agricultural production and food/feed safety because of its ability to cause crop disease and to produce mycotoxins. Understanding the genetic basis for production of mycotoxins and other secondary metabolites (SMs) has the potential
Brahim Bouizgarne et al.
Molecular plant-microbe interactions : MPMI, 19(5), 550-556 (2006-05-06)
Fusarium spp. are ubiquitous fungi found in soil worldwide as both pathogenic and nonpathogenic strains. The signals leading to disease or the absence of disease are poorly understood. We recently showed that fusaric acid (FA), a nonspecific toxin produced by
H Wang et al.
Life sciences, 65(9), 849-856 (1999-08-28)
This review article aims at summarizing research findings on the various pharmacological activities of fusaric acid (5-butylpicolinic acid), a mycotoxin produced by several Fusarium species which commonly infect cereal grains and other agricultural commodities. The actions of the toxin on
A Moretti et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 27(5), 718-728 (2010-03-31)
In a survey carried out on 87 rotted fig fruits samples collected in the Apulia region of Italy, the authors isolated 126 Fusarium strains identified as F. ramigenum (69 strains), F. solani (49), F. proliferatum (five) and three not identified.

Global Trade Item Number

SKUGTIN
F6513-250MG04061838354525
F6513-1G04061833618639

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