Synthesis of a netropsin conjugate of a water-soluble epi-quinocarcin analogue: The importance of stereochemistry at nitrogen

Bioorganic and Medicinal Chemistry

Volumn 8, Issue 3, 2000, Pages 523-532

  Herberich, Brad ^a   Scott, Jack D ^a   Williams, Robert M ^a  

^a Veterinary Dentistry and Oral Surgery   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; CONGOCIDINE; CONGOCIDINE DERIVATIVE; NITROGEN; QUINOCARCIN; QUINOCARCIN DERIVATIVE; SUPEROXIDE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CONJUGATE; CONTROLLED STUDY; DNA ALKYLATION; DNA CLEAVAGE; DNA DAMAGE; DRUG MECHANISM; DRUG SOLUBILITY; DRUG SYNTHESIS; FAST ATOM BOMBARDMENT MASS SPECTROMETRY; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY;

ALKYLATING AGENTS; ALKYLATION; ANTI-BACTERIAL AGENTS; ANTIBIOTICS, ANTINEOPLASTIC; ANTINEOPLASTIC AGENTS, ALKYLATING; ANTIVIRAL AGENTS; INDICATORS AND REAGENTS; ISOQUINOLINES; MOLECULAR STRUCTURE; NETROPSIN; NITROBLUE TETRAZOLIUM; OLIGODEOXYRIBONUCLEOTIDES; SOLUBILITY; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; SUPEROXIDES;

EID: 0034005126     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(99)00314-4     Document Type: Article

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