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L-Glutamic acid, N-[N-[(phenylmethoxy)carbonyl]-L-a-glutamyl]-, trimethyl ester is a chemical compound derived from glutamic acid, featuring a phenylmethoxy carbonyl group attached to the glutamic acid molecule. The addition of a trimethyl ester group enhances the compound's stability and solubility, making it a promising candidate for pharmaceutical applications and drug development.
Used in Pharmaceutical Applications:
L-Glutamic acid, N-[N-[(phenylmethoxy)carbonyl]-L-a-glutamyl]-, trimethyl ester is used as a prodrug form of glutamic acid for targeting specific receptors in the body. Its unique structure allows for potential use in drug development and further study in the field of pharmacology.
Used in Research Applications:
In the research industry, L-Glutamic acid, N-[N-[(phenylmethoxy)carbonyl]-L-a-glutamyl]-, trimethyl ester serves as a valuable tool for studying the properties and interactions of glutamic acid and its derivatives, contributing to the advancement of knowledge in biochemistry and molecular biology.

27169-29-5

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27169-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27169-29-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,6 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27169-29:
(7*2)+(6*7)+(5*1)+(4*6)+(3*9)+(2*2)+(1*9)=125
125 % 10 = 5
So 27169-29-5 is a valid CAS Registry Number.

27169-29-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Bz-Glu-γ-OMe-Glu-γ-OMe-OMe

1.2 Other means of identification

Product number -
Other names -

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

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More Details:27169-29-5 SDS

27169-29-5Relevant academic research and scientific papers

Comprehensive screening of octopus amphiphiles as DNA activators in lipid bilayers: Implications on transport, sensing and cellular uptake

Montenegro, Javier,Fin, Andrea,Matile, Stefan

, p. 2641 - 2647 (2011)

Dynamic octopus amphiphiles contain one charged "head," here a guanidinium cation, together several hydrophobic "tails" (or "tentacles") that can be attached and exchanged in situ by reversible hydrazone formation. Quite surprisingly, their ability to activate DNA as transporters in lipid bilayer membranes was found to increase with the number of tails (up to four) as well as with their length (up to eight carbons). Both encouraged and puzzled by these results, we decided that a comprehensive screening of octopus amphiphiles with regard to number (from one to six) and length (from three to eighteen carbons) of their tails would be appropriate at this point. For this purpose, we here report the synthesis of cationic hexahydrazide peptide dendrons together with that of aldehydes with long, saturated, unsaturated and branched hydrophobic tails. Comprehensive screening of the completed collection of tails and heads reveals that the ability of octopus amphiphiles to activate DNA transporters shifts with increasing number of tails to decreasing length of the tails. Moreover, cis-alkenyl and branched alkyl tails are more active than their linear analogs, branched aromatic tails are best. These overall very meaningful trends for octopus amphiphiles will be of importance for sensing applications and fragrant cellular uptake.

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