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250 MG
¥11,550
1 G
¥36,050
この商品について
実験式(ヒル表記法):
C10H13NO2
CAS番号:
分子量:
179.22
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
208-643-0
MDL number:
Beilstein/REAXYS Number:
125804
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製品名
フザリン酸, from Gibberella fujikuroi
SMILES string
CCCCc1ccc(nc1)C(O)=O
InChI key
DGMPVYSXXIOGJY-UHFFFAOYSA-N
InChI
1S/C10H13NO2/c1-2-3-4-8-5-6-9(10(12)13)11-7-8/h5-7H,2-4H2,1H3,(H,12,13)
biological source
Gibberella fujikuroi
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
Quality Level
Gene Information
human ... DBH(1621)
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関連するカテゴリー
1 of 4
当該品目 | 55952 | 798673 | F0600000 |
|---|---|---|---|
| assay ≥98% (TLC) | assay ≥99.0% (HPLC) | assay ≥99% | assay - |
| form powder | form - | form powder | form - |
| Quality Level 200 | Quality Level 100 | Quality Level 100 | Quality Level - |
| storage temp. −20°C | storage temp. - | storage temp. - | storage temp. - |
| solubility ethanol: 49.00-51.00 mg/mL, clear, colorless to faintly yellow | solubility - | solubility - | solubility - |
| biological source Gibberella fujikuroi | biological source - | biological source - | biological source - |
Biochem/physiol Actions
ド-パミンβ-ヒドロキシラ-ゼインヒビタ-。
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.
General description
Chemical structure: pyridine
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
保管分類
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
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
Angélica Gutiérrez-Sánchez et al.
Toxins, 13(4) (2021-05-01)
Fusarium kuroshium is the fungal symbiont associated with the ambrosia beetle Euwallacea kuroshio, a plague complex that attacks avocado, among other hosts, causing a disease named Fusarium dieback (FD). However, the contribution of F. kuroshium to the establishment of this
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
Rouh-Mei Hu et al.
PloS one, 7(12), e51053-e51053 (2012-12-14)
Fusaric acid (5-butylpicolinic acid), a mycotoxin, is noxious to some microorganisms. Stenotrophomonas maltophilia displays an intrinsic resistance to fusaric acid. This study aims to elucidate the mechanism responsible for the intrinsic fusaric acid resistance in S. maltophilia. A putative fusaric
アクティブなフィルタ
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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