Radosavljevic, Damjan et al. published their research in Medicinski Razgledi in 1978 | CAS: 7413-34-5

Sodium (S)-2-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino)benzamido)pentanedioate (cas: 7413-34-5) belongs to amides. Compared to amines, amides are very weak bases and do not have clearly defined acid–base properties in water. On the other hand, amides are much stronger bases than esters, aldehydes, and ketones. The presence of the amide group –C(=O)N– is generally easily established, at least in small molecules. It can be distinguished from nitro and cyano groups in IR spectra. Amides exhibit a moderately intense νCO band near 1650 cm−1. By 1H NMR spectroscopy, CONHR signals occur at low fields. In X-ray crystallography, the C(=O)N center together with the three immediately adjacent atoms characteristically define a plane.Related Products of 7413-34-5

Effect of cytostatics on the morphology of bacteria was written by Radosavljevic, Damjan. And the article was included in Medicinski Razgledi in 1978.Related Products of 7413-34-5 This article mentions the following:

Bacteriostatic concentrations of Oncovin (vincristine) [2068-78-2], adriablastin [23214-92-8], Endoxan [50-18-0], Velbe [143-67-9], 5-fluorouracil [51-21-8], Na methotrexate [7413-34-5], Antimit [55-86-7], oncotiotepa [52-24-4], and Dtic (dacarbazine [4342-03-4] inhibited cell division but did not inhibit the growth of bacterial cells. The resulting cells became enlarged, and were spherical or filamentous in shape. In the experiment, the researchers used many compounds, for example, Sodium (S)-2-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino)benzamido)pentanedioate (cas: 7413-34-5Related Products of 7413-34-5).

Sodium (S)-2-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino)benzamido)pentanedioate (cas: 7413-34-5) belongs to amides. Compared to amines, amides are very weak bases and do not have clearly defined acid–base properties in water. On the other hand, amides are much stronger bases than esters, aldehydes, and ketones. The presence of the amide group –C(=O)N– is generally easily established, at least in small molecules. It can be distinguished from nitro and cyano groups in IR spectra. Amides exhibit a moderately intense νCO band near 1650 cm−1. By 1H NMR spectroscopy, CONHR signals occur at low fields. In X-ray crystallography, the C(=O)N center together with the three immediately adjacent atoms characteristically define a plane.Related Products of 7413-34-5

Referemce:
Amide – Wikipedia,
Amide – an overview | ScienceDirect Topics