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2-methylharmine, also known as 9H-beta-carboline, is a member of the beta-carboline class that is substituted by a methoxy group at position 7 and methyl groups at positions 1 and 2. It is a semisynthetic derivative of harmine and has been shown to exhibit significant anti-HIV activity.

6519-18-2

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6519-18-2 Usage

Uses

Used in Pharmaceutical Industry:
2-methylharmine is used as an anti-HIV agent for its significant anti-HIV activity, making it a potential candidate for the development of new therapeutic agents against HIV infection.
Used in Drug Development:
2-methylharmine is used as a lead compound in drug development for its potential to be further modified and optimized for enhanced therapeutic effects and reduced side effects. Its unique chemical structure and biological activity make it a valuable starting point for the design of new drugs targeting various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 6519-18-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,1 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6519-18:
(6*6)+(5*5)+(4*1)+(3*9)+(2*1)+(1*8)=102
102 % 10 = 2
So 6519-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2O/c1-9-14-12(6-7-16(9)2)11-5-4-10(17-3)8-13(11)15-14/h4-8H,1-3H3

6519-18-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N2-methylharmine

1.2 Other means of identification

Product number -
Other names 2-methylharmine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6519-18-2 SDS

6519-18-2Upstream product

6519-18-2Downstream Products

6519-18-2Relevant academic research and scientific papers

Spectroscopic study of molecular associations between FMN and β-carbolines

Codoner, Armando,Medina, Piedad,Jover, Enrique,Sanchez, Jesus A.

, p. 1793 - 1800 (2007/10/02)

The spectrophotometric and thermodynamic properties of molecular complexes of flavin mononucleotide (FMN) (riboflavin 5'-phosphate) with some β-carboline derivatives have been investigated in aqueous solution.The molecular associations have been examined by means of electronic absorption spectra, since in each a new charge-transfer band has been located, and also the variation of the fluorescenece emission of FMN on the solutions has been observed.The formation constants for the molecular complexes were determined from absorption data using the Foster-Hammick-Wardley method.The quenching phenomenon observed in FMN fluorescence is related to the concentration of the β-carboline derivatives, allowing the calculation of the quenching constants for FMN-β-carboline complexes.Thermodynamic parameters have been determined from the values of association constants for the molecular complexes at various temperatures.The influence of substituents in the β-carboline molecule on the stability of the complexes formed was also investigated.

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