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Diethyl N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamate is a synthetic compound that belongs to the class of antifolate drugs. It is characterized by a pteridine ring, which is crucial for its antifolate activity, and a glutamate moiety that aids in target specificity and cellular uptake. diethyl N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamate is commonly used in the production of chemotherapy drugs and plays a significant role in the development of new and improved cancer treatments.

43170-88-3

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43170-88-3 Usage

Uses

Used in Pharmaceutical Industry:
Diethyl N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamate is used as an active pharmaceutical ingredient for the development of chemotherapy drugs. It is effective in the treatment of various types of cancer, including leukemia, breast cancer, and lung cancer, due to its ability to inhibit the production of folic acid in cancer cells, thereby slowing down their growth and division.
Used in Cancer Research:
In the field of cancer research, diethyl N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamate serves as a valuable compound for studying the mechanisms of action of antifolate drugs. Its unique chemical structure and antifolate activity make it an important tool for understanding the molecular pathways involved in cancer cell growth and division, and for identifying potential targets for the development of novel cancer therapies.
Used in Drug Delivery Systems:
Diethyl N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamate can be incorporated into drug delivery systems to improve the efficacy and bioavailability of chemotherapy drugs. By encapsulating diethyl N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamate within nanoparticles or other carriers, researchers can enhance its delivery to cancer cells, reduce systemic side effects, and potentially overcome drug resistance in cancer treatment.
Overall, diethyl N-[4-[[(2,4-diamino-6-pteridinyl)methyl]methylamino]benzoyl]-L-glutamate is a versatile and promising compound in the fight against cancer, with applications in the development of chemotherapy drugs, cancer research, and drug delivery systems. Its unique chemical structure and antifolate activity make it an important component in the ongoing efforts to improve cancer treatment outcomes and patient quality of life.

Check Digit Verification of cas no

The CAS Registry Mumber 43170-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,7 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 43170-88:
(7*4)+(6*3)+(5*1)+(4*7)+(3*0)+(2*8)+(1*8)=103
103 % 10 = 3
So 43170-88-3 is a valid CAS Registry Number.
InChI:InChI=1/C24H30N8O5/c1-4-36-18(33)11-10-17(23(35)37-5-2)29-22(34)14-6-8-16(9-7-14)32(3)13-15-12-27-21-19(28-15)20(25)30-24(26)31-21/h6-9,12,17H,4-5,10-11,13H2,1-3H3,(H,29,34)(H4,25,26,27,30,31)/t17-/m0/s1

43170-88-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methotrexate diethyl ester

1.2 Other means of identification

Product number -
Other names JSF-1183

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:43170-88-3 SDS

43170-88-3Relevant academic research and scientific papers

An algorithm to determine the mechanism of drug distribution in lipid-core nanocapsule formulations

Oliveira, Catiuscia P.,Venturini, Cristina G.,Donida, Bruna,Poletto, Fernanda S.,Guterres, Silvia S.,Pohlmann, Adriana R.

, p. 1141 - 1150 (2013/03/28)

Aqueous solutions of lipid-core nanocapsules are interesting drug delivery systems for passive drug targeting. In this study, we hypothesized that the drug distribution mechanisms in lipid-core nanocapsule formulations could be categorized into six different types. To experimentally determine the type of drug distribution in these formulations, we proposed the use of an algorithm as an innovative strategy. The approach is shown to be a valuable tool to optimize and select formulations intended for drug delivery. The best physico-chemical parameter in terms of predicting the type of distribution was the log D value. In conclusion, the use of the algorithm developed in this study represents a simple and rapid approach through which it was possible to experimentally determine the drug distribution in colloidal formulations for eight drug models.

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