115627-41-3 Usage
Uses
Used in Pharmaceutical Research and Development:
N-(3-INDOLYLFORMYL)-L-PHENYLALANINE is used as a building block for the synthesis of novel peptidomimetics, which are designed to mimic the structure and function of peptides, offering improved stability and bioavailability for therapeutic applications.
Used in Medicinal Chemistry:
N-(3-INDOLYLFORMYL)-L-PHENYLALANINE is used as a precursor to biologically active compounds, contributing to the development of new drugs with potential applications in various therapeutic areas.
Used in Anti-inflammatory Applications:
N-(3-INDOLYLFORMYL)-L-PHENYLALANINE is studied for its anti-inflammatory properties, which may be harnessed in the treatment of conditions characterized by inflammation.
Used in Anti-tumor Applications:
N-(3-INDOLYLFORMYL)-L-PHENYLALANINE is investigated for its anti-tumor activities, suggesting its potential use in cancer therapy to inhibit tumor growth and progression.
Used in Drug Delivery Systems:
N-(3-INDOLYLFORMYL)-L-PHENYLALANINE is being explored for its potential use in the development of targeted drug delivery systems, which aim to improve the efficacy and specificity of drug action while reducing side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 115627-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,2 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 115627-41:
(8*1)+(7*1)+(6*5)+(5*6)+(4*2)+(3*7)+(2*4)+(1*1)=113
113 % 10 = 3
So 115627-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H16N2O3/c21-17(14-11-19-15-9-5-4-8-13(14)15)20-16(18(22)23)10-12-6-2-1-3-7-12/h1-9,11,16,19H,10H2,(H,20,21)(H,22,23)/t16-/m0/s1
115627-41-3Relevant academic research and scientific papers
Palladium-Catalyzed Aminocarbonylation in Solid-Phase Peptide Synthesis: A Method for Capping, Cyclization, and Isotope Labeling
Skogh, Anna,Friis, Stig D.,Skrydstrup, Troels,Sandstr?m, Anja
supporting information, p. 2873 - 2876 (2017/06/07)
A new synthetic approach for introducing N-capping groups onto peptides attached to a solid support, combining aminocarbonylation under mild conditions using a palladacycle precatalyst and solid-phase peptide synthesis, is reported. The use of a silacarboxylic acid as an in situ CO-releasing molecule allowed the reaction to be performed in a single vial. The method also enables versatile substitution of side chains, side-chain-to-side-chain cyclizations, and selective [13C] acyl labeling of modified peptides.
