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Empirische Formel (Hill-System):
C7H4BrN3O2
CAS-Nummer:
Molekulargewicht:
242.03
UNSPSC Code:
12352202
PubChem Substance ID:
MDL number:
assay
≥98% (TLC)
form
powder
color
light yellow
solubility
ethanol: 25 mg/mL, DMSO: soluble
storage temp.
2-8°C
SMILES string
[O-][N+](=O)c1cccc2c(Br)n[nH]c12
InChI
1S/C7H4BrN3O2/c8-7-4-2-1-3-5(11(12)13)6(4)9-10-7/h1-3H,(H,9,10)
InChI key
NFSTZPMYAZRZPC-UHFFFAOYSA-N
Biochem/physiol Actions
A potent inhibitor of all nitric oxide synthase isoforms. Shows substantial neuroprotective effects against hypoxic damage (such as stroke) and animal models of Parkinson′s disease.
A potent inhibitor of all nitric oxide synthase isoforms. Shows substantial neuroprotective effects against hypoxic damage (such as stroke) and animal models of Parkinson′s disease. Crystallographic studies show that inhibition of eNOS is due to an induced cascade of conformation changes that ultimately dissociates the tetrahydrobiopterin cofactor from the enzyme.
signalword
Danger
hcodes
Hazard Classifications
Repr. 1B
Lagerklasse
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Recent studies have pointed to protein S-nitrosylation as a critical regulator of cellular redox homeostasis. For example, S-nitrosylation of peroxiredoxin-2 (Prx2), a peroxidase widely expressed in mammalian neurons, inhibits both enzymatic activity and protective function against oxidative stress. Here, using
