Title : Crystallographic and molecular mechanics calculations on the anti-tumor drugs N-[(2-dimethylamino)ethyl]-and N-[(2-dimethyl-amino)butyl]-9-aminoacridine-4-carboxamides and their dications: implications for models of DNA-binding.

Pub. Date : 1987 Aug

PMID : 3271463






4 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Both are in the free base form and have an intramolecular-hydrogen bond between N10 of the acridine and the nitrogen atom of the carboxamide substituent. Hydrogen nuclear receptor subfamily 4 group A member 1 Homo sapiens
2 Both are in the free base form and have an intramolecular-hydrogen bond between N10 of the acridine and the nitrogen atom of the carboxamide substituent. Acridines nuclear receptor subfamily 4 group A member 1 Homo sapiens
3 Both are in the free base form and have an intramolecular-hydrogen bond between N10 of the acridine and the nitrogen atom of the carboxamide substituent. Nitrogen nuclear receptor subfamily 4 group A member 1 Homo sapiens
4 Both are in the free base form and have an intramolecular-hydrogen bond between N10 of the acridine and the nitrogen atom of the carboxamide substituent. carboxamide nuclear receptor subfamily 4 group A member 1 Homo sapiens