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Beta-Carboline-1-propanoic acid

CAS# 89915-39-9

Beta-Carboline-1-propanoic acid

Catalog No. BCN5805----Order now to get a substantial discount!

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Beta-Carboline-1-propanoic acid: 5mg $690 In Stock
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Quality Control of Beta-Carboline-1-propanoic acid

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Chemical structure

Beta-Carboline-1-propanoic acid

3D structure

Chemical Properties of Beta-Carboline-1-propanoic acid

Cas No. 89915-39-9 SDF Download SDF
PubChem ID 5375436 Appearance Powder
Formula C14H12N2O2 M.Wt 240.3
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-(9H-pyrido[3,4-b]indol-1-yl)propanoic acid
SMILES C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)CCC(=O)O
Standard InChIKey CNUHEVWYPKFJHH-UHFFFAOYSA-N
Standard InChI InChI=1S/C14H12N2O2/c17-13(18)6-5-12-14-10(7-8-15-12)9-3-1-2-4-11(9)16-14/h1-4,7-8,16H,5-6H2,(H,17,18)
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 Beta-Carboline-1-propanoic acid

The wood of Picrasma quassioides

Biological Activity of Beta-Carboline-1-propanoic acid

Description1. Beta-Carboline-1-propanoic acid is a reference standard compound. 2. Beta-Carboline-1-propanoic acid is synthetic precursor compound.

Beta-Carboline-1-propanoic acid Dilution Calculator

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Beta-Carboline-1-propanoic acid Molarity Calculator

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Preparing Stock Solutions of Beta-Carboline-1-propanoic acid

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.1615 mL 20.8073 mL 41.6146 mL 83.2293 mL 104.0366 mL
5 mM 0.8323 mL 4.1615 mL 8.3229 mL 16.6459 mL 20.8073 mL
10 mM 0.4161 mL 2.0807 mL 4.1615 mL 8.3229 mL 10.4037 mL
50 mM 0.0832 mL 0.4161 mL 0.8323 mL 1.6646 mL 2.0807 mL
100 mM 0.0416 mL 0.2081 mL 0.4161 mL 0.8323 mL 1.0404 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 Beta-Carboline-1-propanoic acid

Fingerprinting and simultaneous determination of alkaloids in Picrasma quassioides from different locations by high performance liquid chromatography with photodiode array detection.[Pubmed:22888096]

J Sep Sci. 2012 Sep;35(17):2193-202.

A simple and sensitive method was developed and validated for profiling and simultaneous quantitation of seven alkaloids (6-hydroxy-beta-carboline-1-carboxylic acid, beta-carboline-1-carboxylic acid, Beta-Carboline-1-propanoic acid, 3-methylcanthin-5,6-dione, 5-hydroxy-4-methoxycanthin-6-one, 1-methoxycarbony-beta-carboline, and 4,5-dimethoxycanthin-6-one) in Picrasma quassioide grown in different locations by high-performance liquid chromatography with photodiode array detection. The analysis was conducted on a Phenomenex Gemini C(18) column at 35 degrees C with mobile phase of 25 mM aqueous ammonium acetate (pH 4.0, adjusted by glacial acetate acid) and acetonitrile. A common fingerprint chromatograph under 254 nm consisting of 27 peaks was constructed for the evaluation of the similarities among 31 P. quassioide samples. Samples from Guangdong and Guangxi Provinces were found to be within group linkage and showed significant difference from that of Jiangxi Province origin by using principal component analysis and hierarchical clustering analysis. In addition, the seven alkaloids were identified by electrospray ionization mass spectrometry and comparing with reference standards and literature data. All of them were determined simultaneously using the established HPLC method. This rapid and effective analytical method could be employed for quality assessment of P. quassioide, as well as pharmaceutical products containing this herbal material.

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