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MilliporeSigma

I18008

Sigma-Aldrich

Isonipecotic acid

97%

Sinónimos:

4-Piperidinecarboxylic acid, Hexahydroisonicotinic acid

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About This Item

Fórmula empírica (notación de Hill):
C6H11NO2
Número de CAS:
Peso molecular:
129.16
Beilstein/REAXYS Number:
112553
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

mp

>300 °C (lit.)

SMILES string

OC(=O)C1CCNCC1

InChI

1S/C6H11NO2/c8-6(9)5-1-3-7-4-2-5/h5,7H,1-4H2,(H,8,9)

InChI key

SRJOCJYGOFTFLH-UHFFFAOYSA-N

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Application

Reactant for synthesis of:
  • Antibiotic nitroxoline derivatives for cathepsin B inhibition
  • Sphingosine-1-phosphate receptor agonists
  • RhoA inhibitors for cardiovascular disease therapy
  • Alkyl piperidine and piperazine hydroxamic acids as HDAC inhibitors
  • CHK1 inhibitors
  • IKK2 inhibitors for investigations into rheumatoid arthritis treatment

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Journal of molecular graphics & modelling, 85, 171-181 (2018-09-17)
Inhibition of 4-aminobutanoic acid (GABA) uptake is a strategy for enhancing GABA transmission. The utility of this approach is demonstrated by the successful development of such agents for the treatment of epilepsy and pain. Existing reports on acute brain slice
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Phedias Diamandis et al.
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The identification of self-renewing and multipotent neural stem cells (NSCs) in the mammalian brain holds promise for the treatment of neurological diseases and has yielded new insight into brain cancer. However, the complete repertoire of signaling pathways that governs the

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