P9159

Piperidine-4-sulfonic acid

Name: Piperidine-4-sulfonic acid
Brand: SIGMA
Price: 133.45 EUR
Availability: InStock

Synonym(e):

P4S

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25 MG

133,45 €

250 MG

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Über diesen Artikel

Empirische Formel (Hill-System):

C₅H₁₁NO₃S

CAS-Nummer:

72450-62-5

Molekulargewicht:

165.21

NACRES:

NA.77

PubChem Substance ID:

24278165

UNSPSC Code:

12352106

MDL number:

MFCD00055097

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Unterstützung erhalten

InChI

1S/C5H11NO3S/c7-10(8,9)5-1-3-6-4-2-5/h5-6H,1-4H2,(H,7,8,9)

SMILES string

OS(=O)(=O)C1CCNCC1

InChI key

UGBJGGRINDTHIH-UHFFFAOYSA-N

form

powder

Quality Level

200

Gene Information

human ... GABRA1(2554), GABRA2(2555), GABRA3(2556), GABRA4(2557), GABRA5(2558), GABRA6(2559), GABRB1(2560), GABRB2(2561), GABRB3(2562)

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Dieser Artikel	D1262	P9625	D2531
Sigma-Aldrich P9159 Piperidine-4-sulfonic acid	Sigma-Aldrich D1262 P¹,P⁴-Di(adenosine-5′) tetraphosphate ammonium salt	Sigma-Aldrich P9625 Phenazin-Methosulfat	Sigma-Aldrich D2531 Dextromethorphan -hydrobromid Monohydrat
form powder	form powder	form powder	form powder
Gene Information human ... GABRA1(2554), GABRA2(2555), GABRA3(2556), GABRA4(2557), GABRA5(2558), GABRA6(2559), GABRB1(2560), GABRB2(2561), GABRB3(2562)	Gene Information human ... PLD1(5337), PLD2(5338), PLD3(23646), PLD4(122618), PLD5(200150)	Gene Information -	Gene Information human ... GRIN1(2902), GRIN2A(2903), GRIN2B(2904), GRIN2C(2905), GRIN2D(2906), GRIN3A(116443), GRIN3B(116444), SIGMAR1(10280)

Biochem/physiol Actions

GABA_A receptor agonist.

Features and Benefits

This compound is a featured product for Neuroscience research. Click here to discover more featured Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

0000379482

0000300095

0000234465

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Entropy as the predominant driving force of binding to human recombinant alpha(x)beta(3)gamma(2) GABA(A) receptors.

G Maksay et al.

European journal of pharmacology, 411(1-2), 55-60 (2001-01-04)

In order to study the correlation of the thermodynamic driving forces of binding with the efficacies of displacing ligands, the specific binding of [3H]SR 95531 [2-(3-carboxypropyl)3-amino-6-p-methoxyphenylpyridazinium bromide], a GABA(A) receptor antagonist, was studied in cell lines stably expressing human alpha(1)beta(3)gamma(2)

The apparent voltage dependence of GABAA receptor activation and modulation is inversely related to channel open probability.

Kate K O'Toole et al.

Molecular pharmacology, 81(2), 189-197 (2011-11-02)

The GABA type A receptor (GABA(A)R) is expressed ubiquitously throughout the brain and is a target for many therapeutic agents, including general anesthetics and benzodiazepines, which enhance receptor function by increasing the open probability (P(o)) of the ion channel. It

Pregnenolone sulfate block of GABA(A) receptors: mechanism and involvement of a residue in the M2 region of the alpha subunit.

G Akk et al.

The Journal of physiology, 532(Pt 3), 673-684 (2001-04-21)

Neurosteroids are produced in the brain, and can have rapid actions on membrane channels of neurons. Pregnenolone sulfate (PS) is a sulfated neurosteroid which reduces the responses of the [gamma]-aminobutyric acid A (GABA(A)) receptor. We analysed the actions of PS

Molecular pharmacology of gamma-aminobutyric acid type A receptor agonists and partial agonists in oocytes injected with different alpha, beta, and gamma receptor subunit combinations.

B Ebert et al.

Molecular pharmacology, 46(5), 957-963 (1994-11-01)

Using systematic combination of alpha 1, alpha 3, and alpha 5 with beta 1, beta 2, and beta 3, together with gamma 1, gamma 2, and gamma 3, we have investigated the contributions of the various alpha, beta, and gamma

Identifying agonistic and antagonistic mechanisms operative at the GABA receptor.

E Galvez-Ruano et al.

Journal of neuroscience research, 42(5), 666-673 (1995-12-01)

Based on our molecular modeling investigations of the glycinergic receptor, we expanded our studies to similarly investigate the GABAergic receptor. New data suggest there may exist a slightly different agonistic mechanism for the molecules described herein as compared to glycine.

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