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About This Item
Empirical Formula (Hill Notation):
C6H13N3O2S
CAS Number:
Molecular Weight:
191.25
UNSPSC Code:
12352204
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
6844478
InChI
1S/C6H13N3O2S/c7-4(5(10)11)2-1-3-9-6(8)12/h4H,1-3,7H2,(H,10,11)(H3,8,9,12)/t4-/m0/s1
SMILES string
N[C@@H](CCCNC(N)=S)C(O)=O
InChI key
BKGWACHYAMTLAF-BYPYZUCNSA-N
assay
≥98.0%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
application(s)
peptide synthesis
storage temp.
−20°C
Gene Information
human ... NOS2(4843)
mouse ... Nos2(18126)
rat ... Nos1(24598), Nos2(24599)
Biochem/physiol Actions
Potent and selective inhibitor of neuronal and endothelial isoforms of nitric oxide synthase.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Yu Na Wu et al.
Pflugers Archiv : European journal of physiology, 472(12), 1743-1755 (2020-09-18)
Nitric oxide (NO) affects mitochondrial activity through its interactions with complexes. Here, we investigated regulations of complex I (C-I) and complex II (C-II) by neuronal NO synthase (nNOS) in the presence of fatty acid supplementation and the impact on left
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