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Merck
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Documenti fondamentali

I18008

Sigma-Aldrich

Isonipecotic acid

97%

Sinonimo/i:

4-Piperidinecarboxylic acid, Hexahydroisonicotinic acid

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CHF 56.70
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CHF 105.00

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Cambia visualizzazione
25 G
CHF 56.70
100 G
CHF 105.00

About This Item

Formula empirica (notazione di Hill):
C6H11NO2
Numero CAS:
Peso molecolare:
129.16
Beilstein:
112553
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

CHF 56.70


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Livello qualitativo

Saggio

97%

Punto di fusione

>300 °C (lit.)

Stringa SMILE

OC(=O)C1CCNCC1

InChI

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

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Applicazioni

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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Jenna Elizabeth Hunt et al.
American journal of physiology. Gastrointestinal and liver physiology, 318(5), G980-G987 (2020-04-21)
Glucagon-like peptide (GLP)-1 and -2-secreting L cells have been shown to express the bile acid receptor Takeda G protein-receptor-5 (TGR5) and increase secretion upon receptor activation. Previous studies have explored GLP-1 secretion following acute TGR5 activation, but chronic activation and
Alicja Nowaczyk et al.
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
Michela Semeraro et al.
Clinica chimica acta; international journal of clinical chemistry, 440, 108-112 (2014-12-03)
Pipecolic acid (PA) is an important biochemical marker for the diagnosis of peroxisomal disorders. PA is also a factor responsible for hepatic encephalopathy and a possible biomarker for pyridoxine-dependent seizures. We developed an easy and rapid PA quantification method, by
Iris Thondorf et al.
Bioorganic & medicinal chemistry, 19(21), 6409-6418 (2011-10-01)
The proton-coupled amino acid transporter hPAT1 has recently gained much interest due to its ability to transport small drugs thereby allowing their oral administration. A three-dimensional quantitative structure-activity relationship (3D QSAR) study has been performed on its natural and synthetic
Jing Yuan et al.
Nature chemical biology, 5(10), 765-771 (2009-09-08)
Studies of gene function and molecular mechanisms in Plasmodium falciparum are hampered by difficulties in characterizing and measuring phenotypic differences between individual parasites. We screened seven parasite lines for differences in responses to 1,279 bioactive chemicals. Hundreds of compounds were

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