Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Article, Angewandte Chemie, International Edition called Sequence-specific DNA alkylation by hybrid molecules between segment A of Duocarmycin A and pyrrole/imidazole diamide, Author is Tao, Zhi-Fu; Fujiwara, Tsuyoshi; Saito, Isao; Sugiyama, Hiroshi, which mentions a compound: 180258-46-2, SMILESS is O=C(C1=NC(N)=CN1C)OCC.[H]Cl, Molecular C7H12ClN3O2, Recommanded Product: Ethyl 4-amino-1-methyl-1H-imidazole-2-carboxylate hydrochloride.
The authors decide the preparation of novel hybrid mols. between segment A of duocarmycin A and pyrrole/imidazole diamides. These hybrids primarily alkylate the 3′ end of A in AT-rich sequences, as does the parent compound, duocarmycin. These hybrids also alkylate G residues of predetermined DNA sequences efficiently and with high specificity by formation of a heterodimer with distamycin A.
If you want to learn more about this compound(Ethyl 4-amino-1-methyl-1H-imidazole-2-carboxylate hydrochloride)Recommanded Product: Ethyl 4-amino-1-methyl-1H-imidazole-2-carboxylate hydrochloride, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(180258-46-2).
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com