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Isonipecotic acid

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Catalog No. T22348Cas No. 498-94-2
Alias Hexahydroisonicotinic acid, 4-Piperidinecarboxylic acid, 4-Carboxypiperidine

Isonipecotic acid (4-Piperidinecarboxylic acid) is a heterocyclic compound. Isonipecotic acid mainly characterized as a GABAA receptor partial agonist.

Isonipecotic acid

Isonipecotic acid

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Purity: 99.82%
Catalog No. T22348Alias Hexahydroisonicotinic acid, 4-Piperidinecarboxylic acid, 4-CarboxypiperidineCas No. 498-94-2
Isonipecotic acid (4-Piperidinecarboxylic acid) is a heterocyclic compound. Isonipecotic acid mainly characterized as a GABAA receptor partial agonist.
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1 g$29-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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Purity:99.82%
Appearance:solid
Color:White
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Product Introduction

Isonipecotic acid AI Summary
Isonipecotic acid exhibits a wide range of bioactivities. It acts as an agonist on human Gamma-aminobutyric acid A (GABAA) receptor subtypes, demonstrating varying potency (EC50 values) on subtypes such as alpha-1-beta-3-gamma-2, alpha-2-beta-3-gamma-2, alpha-3-beta-3-gamma-2, alpha-4-beta-3-gamma-2, alpha-5-beta-3-gamma-2, and alpha-6-beta-3-gamma-2. It also shows agonist activity against the GABA-C receptor derived from bovine retinal RNA with a binding affinity (Kb) greater than 100,000 nM and significant inhibitory effects on GABA binding in rat brain synaptosomal membranes with an IC50 of 330 nM. Despite its extensive receptor interactions, Isonipecotic acid shows weak anticonvulsive activity in the bicuculline (BIC) test, with an effective dose (ED50) of greater than 1000 umol.kg-1. Additionally, it demonstrates inhibitory activity against the N-methyl-D-aspartate glutamate receptor 1 with an IC50 of 94100 nM and has distinct effects on the input resistance of cultured spinal cord neurons. Furthermore, Isonipecotic acid exhibits antiplasmodial activity against Plasmodium falciparum with an IC50 of 15848.93 nM and differential inhibition of various Plasmodium falciparum strains. It also modulates activity for several other receptors and enzymes such as Thyroid Stimulating Hormone Receptor, Human Peripheral Myelin Protein 22 (PMP22), Acetylcholine Muscarinic M1 Receptor, and other enzymes like Histone Lysine Methyltransferase G9a and Mammalian Selenoprotein Thioredoxin Reductase 1. Additionally, it shows inhibition of virus entry for Lassa Virus and Marburg Virus and enhances Arylsulfatase A (ASA1) activity. In terms of neuronal interactions, Isonipecotic acid exhibits moderate affinity for GABAA receptors with Ki values around 500 nM and acts as an agonist at several subtypes with varying EC50 values, demonstrating considerable efficacy compared to GABA. It also moderately inhibits human PAT1-mediated L-[3H]proline uptake in human Caco2 cells with a Ki value of 2300000.0 nM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Isonipecotic acid (4-Piperidinecarboxylic acid) is a heterocyclic compound. Isonipecotic acid mainly characterized as a GABAA receptor partial agonist.
SynonymsHexahydroisonicotinic acid, 4-Piperidinecarboxylic acid, 4-Carboxypiperidine
Chemical Properties
Molecular Weight129.16
FormulaC6H11NO2
Cas No.498-94-2
SmilesOC(=O)C1CCNCC1
Relative Density.1.125 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 25 mg/mL (193.56 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM7.7423 mL38.7117 mL77.4234 mL387.1168 mL
5 mM1.5485 mL7.7423 mL15.4847 mL77.4234 mL
10 mM0.7742 mL3.8712 mL7.7423 mL38.7117 mL
20 mM0.3871 mL1.9356 mL3.8712 mL19.3558 mL
50 mM0.1548 mL0.7742 mL1.5485 mL7.7423 mL
100 mM0.0774 mL0.3871 mL0.7742 mL3.8712 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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