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1-Methoxycarbonyl-beta-carboline

CAS# 3464-66-2

1-Methoxycarbonyl-beta-carboline

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Quality Control of 1-Methoxycarbonyl-beta-carboline

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Chemical structure

1-Methoxycarbonyl-beta-carboline

3D structure

Chemical Properties of 1-Methoxycarbonyl-beta-carboline

Cas No. 3464-66-2 SDF Download SDF
PubChem ID 597266 Appearance Yellow powder
Formula C13H10N2O2 M.Wt 226.2
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl 9H-pyrido[3,4-b]indole-1-carboxylate
SMILES COC(=O)C1=NC=CC2=C1NC3=CC=CC=C23
Standard InChIKey FRNCTTUBAHKEBZ-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 1-Methoxycarbonyl-beta-carboline

The barks of Picrasma quassioides

Biological Activity of 1-Methoxycarbonyl-beta-carboline

Description1-Methoxycarbonyl-beta-carboline is a nantural product from Ailanthus altissima.

Protocol of 1-Methoxycarbonyl-beta-carboline

Structure Identification
Planta Medica 1989, 55(3):286-287.

A New beta-Carboline Alkaloid from Ailanthus altissima.[Reference: WebLink]

A new indole alkaloid, 1-methoxycarbonyl-4,8-dimethoxy-beta-carboline ( 1A) was isolated from the leaves of AILANTHUS ALTISSIMA and its structure elucidated by spectroscopic methods; 1-Methoxycarbonyl-beta-carboline ( 1B) was also identified.

1-Methoxycarbonyl-beta-carboline Dilution Calculator

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1-Methoxycarbonyl-beta-carboline Molarity Calculator

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Preparing Stock Solutions of 1-Methoxycarbonyl-beta-carboline

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.4209 mL 22.1043 mL 44.2087 mL 88.4173 mL 110.5217 mL
5 mM 0.8842 mL 4.4209 mL 8.8417 mL 17.6835 mL 22.1043 mL
10 mM 0.4421 mL 2.2104 mL 4.4209 mL 8.8417 mL 11.0522 mL
50 mM 0.0884 mL 0.4421 mL 0.8842 mL 1.7683 mL 2.2104 mL
100 mM 0.0442 mL 0.221 mL 0.4421 mL 0.8842 mL 1.1052 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 1-Methoxycarbonyl-beta-carboline

Chemical constituents of Arisaema franchetianum tubers.[Pubmed:23106482]

J Asian Nat Prod Res. 2013;15(1):71-7.

A novel pyrrolidine alkaloid, (2R*,3S*,5S*)-N,2-dimethyl-3-hydroxy-5-(10-phenyldecyl)pyrrolidine (1), and 17 known compounds were isolated from Arisaema franchetianum Engl. (Araceae) tubers. The 17 compounds were bergenin (2), emodin (3), caffeic acid (4), nobiletin (5), 3-O-beta-d-galactopyranosyl-hederagenin 28-O-beta-d-xylopyranosyl(1 --> 6)-beta-d-galactopyranosyl ester (6), coniferin (7), qingyangshengenin (8), methylconiferin (9), syringaresinol 4'-O-beta-d-glucopyranoside (10), gagaminine (11), perlolyrine (12), (S)-1-(1'-hydroxyethyl)-beta-carboline (13), 1-(beta-carboline-1-yl)-3,4,5-trihydroxy-1-pentanone (14), 1-Methoxycarbonyl-beta-carboline (15), indolo[2,3-alpha]carbazole (16), 4-hydroxycinnamic acid methyl ester (17), and methyl 4-[2-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-1-(hydroxymethyl)ethyl] ferulate (18). The inhibitory activities of compound 1 and its N-methyl derivative (1a) against porcine respiratory and reproductive syndrome virus (PRRSV), human leukemic K562 cells, and human breast cancer MCF-7 cells were evaluated. Compounds 1 [50% inhibited concentration (IC(50)) = 12.5 +/- 0.6 muM] and 1a (IC(50) = 15.7 +/- 0.9 muM) were cytotoxic against K562 cells. Compound 1a also had a weak effect on PRRSV with an IC(50) value of 31.9 +/- 6.0 muM [selectivity index (SI) = 18.7].

[Study on chemical constituents of Picrasma quassioides].[Pubmed:21761728]

Zhongguo Zhong Yao Za Zhi. 2011 Apr;36(7):886-90.

To study the chemical constituents of Picrasma quassioides. The chemical constituents were isolated and purified by chromatographic methods over Sephadex LH-20 and silica gel column, and structurally elucidated by spectral analysis, including UV, IR, MS, 1H-NMR, 13C-NMR. Fourteen compounds were obtained and identified as trifolirhizin(1), maackiain(2), 3', 7-dihydroxy-4'-methoxylisoflavone(3), umbelliferone(4), emodin(5), nigakilactone F(6), picrasin B(7),picraqualide B (8),4-methoxy-5-hydroxycanthin-6-one(9), 4,5-dimethoxycanthin-6-one (10),5-methoxycanthin-6-one(11), 11-hydroxycanthin-6-one(12) , 1-Methoxycarbonyl-beta-carboline(13), 1-hydroxymethyl-beta-carboline(14). Compounds 1-5 are reported from the first time for the genus Pricrasma.

A New beta-Carboline Alkaloid from Ailanthus altissima.[Pubmed:17262417]

Planta Med. 1989 Jun;55(3):286-7.

A new indole alkaloid, 1-methoxycarbonyl-4,8-dimethoxy-beta-carboline ( 1A) was isolated from the leaves of AILANTHUS ALTISSIMA and its structure elucidated by spectroscopic methods; 1-Methoxycarbonyl-beta-carboline ( 1B) was also identified.

Indole Alkaloids from Quassia amara.[Pubmed:17269024]

Planta Med. 1987 Jun;53(3):289-90.

Three beta-carboline alkaloids have been isolated for the first time from the wood of QUASSIA AMARA L. (Simarubaceae) and their structures were determined to be 1-vinyl-4,8-dimethoxy-beta-carboline ( 1), 1-Methoxycarbonyl-beta-carboline ( 2), and 3-methylcantin-2,6-dione ( 3) by spectral and chemical means.

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