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1H-Indole-3-carboxylic acid

CAS# 771-50-6

1H-Indole-3-carboxylic acid

2D Structure

Catalog No. BCN4324----Order now to get a substantial discount!

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Quality Control of 1H-Indole-3-carboxylic acid

3D structure

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1H-Indole-3-carboxylic acid

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Chemical Properties of 1H-Indole-3-carboxylic acid

Cas No. 771-50-6 SDF Download SDF
PubChem ID 69867 Appearance Powder
Formula C9H7NO2 M.Wt 161.2
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 1H-indole-3-carboxylic acid
SMILES C1=CC=C2C(=C1)C(=CN2)C(=O)O
Standard InChIKey KMAKOBLIOCQGJP-UHFFFAOYSA-N
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of 1H-Indole-3-carboxylic acid

The roots of Carpesium abrotanoides

Biological Activity of 1H-Indole-3-carboxylic acid

DescriptionIndole-3-carboxylic acid is a normal urinary indolic tryptophan metabolite which belongs to a class of organic compounds known as indolecarboxylic acids and derivatives.
Targets5-HT Receptor

Protocol of 1H-Indole-3-carboxylic acid

Structure Identification
Bioorg Med Chem Lett. 2008 Jul 15;18(14):3844-7.

Synthesis and structure-activity relationship of 1H-indole-3-carboxylic acid pyridine-3-ylamides: a novel series of 5-HT2C receptor antagonists.[Pubmed: 18602261]

A novel series of 1H-Indole-3-carboxylic acid pyridine-3-ylamides were synthesized and identified to show high affinity and selectivity for 5-HT(2C) receptor. Among them, 1H-Indole-3-carboxylic acid[6-(2-chloro-pyridin-3-yloxy)-pyridin-3-yl]-amide (15k) exhibits the highest affinity (IC(50)=0.5 nM) with an excellent selectivity (>2000 times) over other serotonin (5-HT(1A), 5-HT(2A), and 5-HT(6)) and dopamine (D(2)-D(4)) receptors.

1H-Indole-3-carboxylic acid Dilution Calculator

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1H-Indole-3-carboxylic acid Molarity Calculator

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Preparing Stock Solutions of 1H-Indole-3-carboxylic acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 6.2035 mL 31.0174 mL 62.0347 mL 124.0695 mL 155.0868 mL
5 mM 1.2407 mL 6.2035 mL 12.4069 mL 24.8139 mL 31.0174 mL
10 mM 0.6203 mL 3.1017 mL 6.2035 mL 12.4069 mL 15.5087 mL
50 mM 0.1241 mL 0.6203 mL 1.2407 mL 2.4814 mL 3.1017 mL
100 mM 0.062 mL 0.3102 mL 0.6203 mL 1.2407 mL 1.5509 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 1H-Indole-3-carboxylic acid

Synthesis and structure-activity relationship of 1H-indole-3-carboxylic acid pyridine-3-ylamides: a novel series of 5-HT2C receptor antagonists.[Pubmed:18602261]

Bioorg Med Chem Lett. 2008 Jul 15;18(14):3844-7.

A novel series of 1H-Indole-3-carboxylic acid pyridine-3-ylamides were synthesized and identified to show high affinity and selectivity for 5-HT(2C) receptor. Among them, 1H-Indole-3-carboxylic acid[6-(2-chloro-pyridin-3-yloxy)-pyridin-3-yl]-amide (15k) exhibits the highest affinity (IC(50)=0.5 nM) with an excellent selectivity (>2000 times) over other serotonin (5-HT(1A), 5-HT(2A), and 5-HT(6)) and dopamine (D(2)-D(4)) receptors.

Description

Indole-3-carboxylic acid is a normal urinary indolic tryptophan metabolite and has been found elevated in patients with liver diseases.

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