FIELD: organic synthesis. SUBSTANCE: compound (see formula I: ) prepared by interaction of 2-amino-5,6,7,8-tetrahydroquinoline-3-carboxylic hydrazide acid with 5-nitrofurfurol exhibits bacteriostatic activity for gold staphylococci and colon bacteria with lethal dose LD50 = 1000 mg/ml. EFFECT: extended choice of bacteriostatics. 1 tbl
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2-CHLORO-5,6,7,8-TETRAHYDROQUINOLINE-4-CARBOXYLIC ACID 5-NITROFURFURYLIDENE HYDRAZIDE ELICITING AN ANTIBACTERIAL ACTIVITY |
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