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Methyl 3-carbazolecarboxylate

CAS# 97931-41-4

Methyl 3-carbazolecarboxylate

Catalog No. BCN4529----Order now to get a substantial discount!

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Quality Control of Methyl 3-carbazolecarboxylate

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Chemical structure

Methyl 3-carbazolecarboxylate

3D structure

Chemical Properties of Methyl 3-carbazolecarboxylate

Cas No. 97931-41-4 SDF Download SDF
PubChem ID 504069 Appearance Yellow powder
Formula C14H11NO2 M.Wt 225.2
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl 9H-carbazole-3-carboxylate
SMILES COC(=O)C1=CC2=C(C=C1)NC3=CC=CC=C32
Standard InChIKey LZXXHWWSVRIDGR-UHFFFAOYSA-N
Standard InChI InChI=1S/C14H11NO2/c1-17-14(16)9-6-7-13-11(8-9)10-4-2-3-5-12(10)15-13/h2-8,15H,1H3
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 Methyl 3-carbazolecarboxylate

The herbs of Micromelum sp.

Biological Activity of Methyl 3-carbazolecarboxylate

TargetsImmunology & Inflammation related

Methyl 3-carbazolecarboxylate Dilution Calculator

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Methyl 3-carbazolecarboxylate Molarity Calculator

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Preparing Stock Solutions of Methyl 3-carbazolecarboxylate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.4405 mL 22.2025 mL 44.405 mL 88.8099 mL 111.0124 mL
5 mM 0.8881 mL 4.4405 mL 8.881 mL 17.762 mL 22.2025 mL
10 mM 0.444 mL 2.2202 mL 4.4405 mL 8.881 mL 11.1012 mL
50 mM 0.0888 mL 0.444 mL 0.8881 mL 1.7762 mL 2.2202 mL
100 mM 0.0444 mL 0.222 mL 0.444 mL 0.8881 mL 1.1101 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 Methyl 3-carbazolecarboxylate

Anti-tuberculosis constituents from the stem bark of Micromelum hirsutum.[Pubmed:15770548]

Planta Med. 2005 Mar;71(3):261-7.

Anti-TB bioassay-directed fractionation led to the isolation of six carbazole alkaloids, as well as the gamma-lactone derivative of oleic acid, from the CH (2)Cl (2) extract of the stem bark of Micromelum hirsutum. The carbazoles include the new micromeline ( 2) and five known alkaloids: lansine ( 3), 3-methylcarbazole ( 4), methyl carbazole-3-carboxylate ( 5), 3-formylcarbazole ( 6), and 3-formyl-6-methoxycarbazole ( 7). Compound 1 was identified as the lactone derivative of oleic acid, (-)- Z-9-octadecene-4-olide, for which the trivial name micromolide ( 1) is suggested. It showed potent in vitro anti-TB activity against H37R v (MIC: 1.5 microg/mL), a selectivity index (SI) of 63, and exhibited activity against the Erdman strain of M. tuberculosis in a J774 mouse macrophage model (EC (90) : 5.6 microg/mL). Thus, 1 appears worthy of further evaluation as a potential new anti-TB agent. Isolates 2, 3, 6 and 7 had anti-TB MIC values between 14.3 and 42.3 microg/mL, while compounds 4 and 5 were considered inactive (MIC > 128 microg/mL). Structure elucidation and identification were based on spectroscopic analysis, including MS, 1D/2D NMR, and a full (1)H spin system analysis of 1.

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